Username

Password

Preview

Sign-in free and Explore the Exciting World of BiomedExperts:

Over 1.500.000 Profiles
More than 1.800 Organizations worldwide
State of the Art Network Visualizations

Manage your own Profile
Locate Experts in your Country/Region
Locate Experts in your 1. and 2. Level Network
Connect to Experts Worldwide

NetworkView

Margaret Pericak-Vance

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Concepts & Ideas

Procedures

Physiology

Disorders

Genes & Molecular Sequences

Chemicals & Drugs

Apolipoproteins E

Sign-in to see full Profile

Sign-in to see all Coauthors

Publications

TOP 3
Schnetz-Boutaud N C; Anderson B M; Brown K D; Wright H H; Abramson R K; Cuccaro M L; Gilbert J R; Pericak-Vance M A; Haines J L
Examination of tetrahydrobiopterin pathway genes in autism.
McCauley J L; Zuvich R L; Bradford Y; Kenealy S J; Schnetz-Boutaud N; Gregory S G; Hauser S L; Oksenberg J R; Mortlock D P; Pericak-Vance M A; Haines J L
Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.
De Jager Philip L; Jia Xiaoming; Wang Joanne; de Bakker Paul I W; Ottoboni Linda; Aggarwal Neelum T; Piccio Laura; Raychaudhuri Soumya; Tran Dong; Aubin Cristin; Briskin Rebeccah; Romano Susan; Baranzini Sergio E; McCauley Jacob L; Pericak-Vance Margaret A; Haines Jonathan L; Gibson Rachel A; Naeglin Yvonne; Uitdehaag Bernard; Matthews Paul M; Kappos Ludwig; Polman Chris; McArdle Wendy L; Strachan David P; Evans Denis; Cross Anne H; Daly Mark J; Compston Alastair; Sawcer Stephen J; Weiner Howard L; Hauser Stephen L; Hafler David A; Oksenberg Jorge R
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.

Sign-in to see all Publications

Sign in free and see...

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the visualized research activity
of experts around the globe

Sign-in to see more

Geonetwork of Margaret Pericak-Vance (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

Sign-in to see more

All Publications

2009: Schnetz-Boutaud N C; Anderson B M; Brown K D; Wright H H; Abramson R K; Cuccaro M L; Gilbert J R; Pericak-Vance M A; Haines J L
Examination of tetrahydrobiopterin pathway genes in autism.
Genes, brain, and behavior 2009;8(8):753-7.
2009: McCauley J L; Zuvich R L; Bradford Y; Kenealy S J; Schnetz-Boutaud N; Gregory S G; Hauser S L; Oksenberg J R; Mortlock D P; Pericak-Vance M A; Haines J L
Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.
Genes and immunity 2009;10(7):624-30.
2009: De Jager Philip L; Jia Xiaoming; Wang Joanne; de Bakker Paul I W; Ottoboni Linda; Aggarwal Neelum T; Piccio Laura; Raychaudhuri Soumya; Tran Dong; Aubin Cristin; Briskin Rebeccah; Romano Susan; Baranzini Sergio E; McCauley Jacob L; Pericak-Vance Margaret A; Haines Jonathan L; Gibson Rachel A; Naeglin Yvonne; Uitdehaag Bernard; Matthews Paul M; Kappos Ludwig; Polman Chris; McArdle Wendy L; Strachan David P; Evans Denis; Cross Anne H; Daly Mark J; Compston Alastair; Sawcer Stephen J; Weiner Howard L; Hauser Stephen L; Hafler David A; Oksenberg Jorge R
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.
Nature genetics 2009;41(7):776-82.
2009: Wang Gaofeng; Spencer Kylee L; Court Brenda L; Olson Lana M; Scott William K; Haines Jonathan L; Pericak-Vance Margaret A
Localization of age-related macular degeneration-associated ARMS2 in cytosol, not mitochondria.
Investigative ophthalmology & visual science 2009;50(7):3084-90.
2009: Anderson B M; Schnetz-Boutaud N C; Bartlett J; Wotawa A M; Wright H H; Abramson R K; Cuccaro M L; Gilbert J R; Pericak-Vance M A; Haines J L
Examination of association of genes in the serotonin system to autism.
Neurogenetics 2009;10(3):209-16.
2009: Edwards Todd L; Pericak-Vance Margaret; Gilbert Johnny R; Haines Jonathan L; Martin Eden R; Ritchie Marylyn D
An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009;150B(5):721-35.
2009: Beecham Gary W; Schnetz-Boutaud Nathalie; Haines Jonathan L; Pericak-Vance Margaret A
CALHM1 polymorphism is not associated with late-onset Alzheimer disease.
Annals of human genetics 2009;73(Pt 3):379-81.
2009: Ma Deqiong; Salyakina Daria; Jaworski James M; Konidari Ioanna; Whitehead Patrice L; Andersen Ashley N; Hoffman Joshua D; Slifer Susan H; Hedges Dale J; Cukier Holly N; Griswold Anthony J; McCauley Jacob L; Beecham Gary W; Wright Harry H; Abramson Ruth K; Martin Eden R; Hussman John P; Gilbert John R; Cuccaro Michael L; Haines Jonathan L; Pericak-Vance Margaret A
A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.
Annals of human genetics 2009;73(Pt 3):263-73.
2009: Wang Kai; Zhang Haitao; Ma Deqiong; Bucan Maja; Glessner Joseph T; Abrahams Brett S; Salyakina Daria; Imielinski Marcin; Bradfield Jonathan P; Sleiman Patrick M A; Kim Cecilia E; Hou Cuiping; Frackelton Edward; Chiavacci Rosetta; Takahashi Nagahide; Sakurai Takeshi; Rappaport Eric; Lajonchere Clara M; Munson Jeffrey; Estes Annette; Korvatska Olena; Piven Joseph; Sonnenblick Lisa I; Alvarez Retuerto Ana I; Herman Edward I; Dong Hongmei; Hutman Ted; Sigman Marian; Ozonoff Sally; Klin Ami; Owley Thomas; Sweeney John A; Brune Camille W; Cantor Rita M; Bernier Raphael; Gilbert John R; Cuccaro Michael L; McMahon William M; Miller Judith; State Matthew W; Wassink Thomas H; Coon Hilary; Levy Susan E; Schultz Robert T; Nurnberger John I; Haines Jonathan L; Sutcliffe James S; Cook Edwin H; Minshew Nancy J; Buxbaum Joseph D; Dawson Geraldine; Grant Struan F A; Geschwind Daniel H; Pericak-Vance Margaret A; Schellenberg Gerard D; Hakonarson Hakon
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Nature 2009;459(7246):528-33.
2009: Slifer Michael A; Martin Eden R; Gilbert John R; Haines Jonathan L; Pericak-Vance Margaret A
Resolving the relationship between ApolipoproteinE and depression.
Neuroscience letters 2009;455(2):116-9.
2009: Liang Xueying; Slifer Michael; Martin Eden R; Schnetz-Boutaud Nathalie; Bartlett Jackie; Anderson Brent; Züchner Stephan; Gwirtsman Harry; Gilbert John R; Pericak-Vance Margaret A; Haines Jonathan L
Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10.
Human mutation 2009;30(3):463-71.
2009: De Jager Philip L; Baecher-Allan Clare; Maier Lisa M; Arthur Ariel T; Ottoboni Linda; Barcellos Lisa; McCauley Jacob L; Sawcer Stephen; Goris An; Saarela Janna; Yelensky Roman; Price Alkes; Leppa Virpi; Patterson Nick; de Bakker Paul I W; Tran Dong; Aubin Cristin; Pobywajlo Susan; Rossin Elizabeth; Hu Xinli; Ashley Charles W; Choy Edwin; Rioux John D; Pericak-Vance Margaret A; Ivinson Adrian; Booth David R; Stewart Graeme J; Palotie Aarno; Peltonen Leena; Dubois Bénédicte; Haines Jonathan L; Weiner Howard L; Compston Alastair; Hauser Stephen L; Daly Mark J; Reich David; Oksenberg Jorge R; Hafler David A
The role of the CD58 locus in multiple sclerosis.
Proceedings of the National Academy of Sciences of the United States of America 2009;106(13):5264-9.
2009: Cukier Holly N; Pericak-Vance Margaret A; Gilbert John R; Hedges Dale J
Sample degradation leads to false-positive copy number variation calls in multiplex real-time polymerase chain reaction assays.
Analytical biochemistry 2009;386(2):288-90.
2009: Afshari Natalie A; Li Yi-Ju; Pericak-Vance Margaret A; Gregory Simon; Klintworth Gordon K
Genome-wide linkage scan in fuchs endothelial corneal dystrophy.
Investigative ophthalmology & visual science 2009;50(3):1093-7.
2009: Kwiatkowski T J; Bosco D A; Leclerc A L; Tamrazian E; Vanderburg C R; Russ C; Davis A; Gilchrist J; Kasarskis E J; Munsat T; Valdmanis P; Rouleau G A; Hosler B A; Cortelli P; de Jong P J; Yoshinaga Y; Haines J L; Pericak-Vance M A; Yan J; Ticozzi N; Siddique T; McKenna-Yasek D; Sapp P C; Horvitz H R; Landers J E; Brown R H
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.
Science (New York, N.Y.) 2009;323(5918):1205-8.
2009: Beecham Gary W; Martin Eden R; Li Yi-Ju; Slifer Michael A; Gilbert John R; Haines Jonathan L; Pericak-Vance Margaret A
Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease.
American journal of human genetics 2009;84(1):35-43.
2009: Züchner S; Wendland J R; Ashley-Koch A E; Collins A L; Tran-Viet K N; Quinn K; Timpano K C; Cuccaro M L; Pericak-Vance M A; Steffens D C; Krishnan K R; Feng G; Murphy D L
Multiple rare SAPAP3 missense variants in trichotillomania and OCD.
Molecular psychiatry 2009;14(1):6-9.
2009: Kajiwara Yuji; Akram Afia; Katsel Pavel; Haroutunian Vahram; Schmeidler James; Beecham Gary; Haines Jonathan L; Pericak-Vance Margaret A; Buxbaum Joseph D
FE65 binds Teashirt, inhibiting expression of the primate-specific caspase-4.
PloS one 2009;4(4):e5071.
2008: Anderson B M; Schnetz-Boutaud N; Bartlett J; Wright H H; Abramson R K; Cuccaro M L; Gilbert J R; Pericak-Vance M A; Haines J L
Examination of association to autism of common genetic variationin genes related to dopamine.
Autism research : official journal of the International Society for Autism Research 2008;1(6):364-9.
2008: Züchner S; Gilbert J R; Martin E R; Leon-Guerrero C R; Xu P-T; Browning C; Bronson P G; Whitehead P; Schmechel D E; Haines J L; Pericak-Vance M A
Linkage and association study of late-onset Alzheimer disease families linked to 9p21.3.
Annals of human genetics 2008;72(Pt 6):725-31.
2008: Barcellos L F; Ramsay P P; Caillier S J; Sawcer S; Haines J; Schmidt S; Pericak-Vance M; Compston D A S; Gabatto P; Hauser S L; Oksenberg J R
Genetic variation in nitric oxide synthase 2A (NOS2A) and risk for multiple sclerosis.
Genes and immunity 2008;9(6):493-500.
2008: Carney R M; Slifer M A; Lin P I; Gaskell P C; Scott W K; Potocky C F; Hulette C M; Welsh-Bohmer K A; Schmechel D E; Vance J M; Pericak-Vance M A
Longitudinal follow-up of late-onset Alzheimer disease families.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008;147B(5):571-8.
2008: Wang L; Hauser E R; Shah S H; Seo D; Sivashanmugam P; Exum S T; Gregory S G; Granger C B; Haines J L; Jones C J H; Crossman D; Haynes C; Kraus W E; Freedman N J; Pericak-Vance M A; Goldschmidt-Clermont P J; Vance J M
Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease.
Annals of human genetics 2008;72(Pt 4):443-53.
2008: Spencer Kylee L; Olson Lana M; Anderson Brent M; Schnetz-Boutaud Nathalie; Scott William K; Gallins Paul; Agarwal Anita; Postel Eric A; Pericak-Vance Margaret A; Haines Jonathan L
C3 R102G polymorphism increases risk of age-related macular degeneration.
Human molecular genetics 2008;17(12):1821-4.
2008: Beetz Christian; Schüle Rebecca; Deconinck Tine; Tran-Viet Khanh-Nhat; Zhu Hui; Kremer Berry P H; Frints Suzanna G M; van Zelst-Stams Wendy A G; Byrne Paula; Otto Susanne; Nygren Anders O H; Baets Jonathan; Smets Katrien; Ceulemans Berten; Dan Bernard; Nagan Narasimhan; Kassubek Jan; Klimpe Sven; Klopstock Thomas; Stolze Henning; Smeets Hubert J M; Schrander-Stumpel Constance T R M; Hutchinson Michael; van de Warrenburg Bart P; Braastad Corey; Deufel Thomas; Pericak-Vance Margaret; Schöls Ludger; de Jonghe Peter; Züchner Stephan
REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31.
Brain : a journal of neurology 2008;131(Pt 4):1078-86.
2008: Spencer Kylee L; Hauser Michael A; Olson Lana M; Schmidt Silke; Scott William K; Gallins Paul; Agarwal Anita; Postel Eric A; Pericak-Vance Margaret A; Haines Jonathan L
Deletion of CFHR3 and CFHR1 genes in age-related macular degeneration.
Human molecular genetics 2008;17(7):971-7.
2008: Thornton-Wells Tricia A; Moore Jason H; Martin Eden R; Pericak-Vance Margaret A; Haines Jonathan L
Confronting complexity in late-onset Alzheimer disease: application of two-stage analysis approach addressing heterogeneity and epistasis.
Genetic epidemiology 2008;32(3):187-203.
2008: Shuler R Keith; Schmidt Silke; Gallins Paul; Hauser Michael A; Scott William K; Caldwell Jennifer; Agarwal Anita; Haines Jonathan L; Pericak-Vance Margaret A; Postel Eric A
Peripheral reticular pigmentary change is associated with complement factor H polymorphism (Y402H) in age-related macular degeneration.
Ophthalmology 2008;115(3):520-4.
2008: Shuler R Keith; Schmidt Silke; Gallins Paul; Hauser Michael A; Scott William K; Caldwell Jennifer; Agarwal Anita; Haines Jonathan L; Pericak-Vance Margaret A; Postel Eric A
Phenotype analysis of patients with the risk variant LOC387715 (A69S) in age-related macular degeneration.
American journal of ophthalmology 2008;145(2):303-307.
2008: Liang Xueying; Schnetz-Boutaud Nathalie; Bartlett Jackie; Allen Melissa J; Gwirtsman Harry; Schmechel Don E; Carney Regina M; Gilbert John R; Pericak-Vance Margaret A; Haines Jonathan L
No association between SNP rs498055 on chromosome 10 and late-onset Alzheimer disease in multiple datasets.
Annals of human genetics 2008;72(Pt 1):141-4.
2008: Canter Jeffrey A; Olson Lana M; Spencer Kylee; Schnetz-Boutaud Nathalie; Anderson Brent; Hauser Michael A; Schmidt Silke; Postel Eric A; Agarwal Anita; Pericak-Vance Margaret A; Sternberg Paul; Haines Jonathan L
Mitochondrial DNA polymorphism A4917G is independently associated with age-related macular degeneration.
PloS one 2008;3(5):e2091.
2007: Cuccaro Michael L; Brinkley Jason; Abramson Ruth K; Hall Alicia; Wright Harry H; Hussman John P; Gilbert John R; Pericak-Vance Margaret A
Autism in African American families: clinical-phenotypic findings.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007;144B(8):1022-6.
2007: Xu Pu-Ting; Li Yi-Ju; Qin Xue-Jun; Kroner Charles; Green-Odlum Anya; Xu Hong; Wang Tian-Yuan; Schmechel Donald E; Hulette Christine M; Ervin John; Hauser Mike; Haines Jonathan; Pericak-Vance Margaret A; Gilbert John R
A SAGE study of apolipoprotein E3/3, E3/4 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease.
Molecular and cellular neurosciences 2007;36(3):313-31.
2007: Liang Xueying; Martin Eden R; Schnetz-Boutaud Nathalie; Bartlett Jackie; Anderson Brent; Züchner Stephan; Gwirtsman Harry; Schmechel Don; Carney Regina; Gilbert John R; Pericak-Vance Margaret A; Haines Jonathan L
Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease.
Human mutation 2007;28(11):1065-73.
2007: Brinkley Jason; Nations Laura; Abramson Ruth K; Hall Alicia; Wright Harry H; Gabriels Robin; Gilbert John R; Pericak-Vance Margaret A O; Cuccaro Michael L
Factor analysis of the aberrant behavior checklist in individuals with autism spectrum disorders.
Journal of autism and developmental disorders 2007;37(10):1949-59.
2007: Haines Jonathan L; Spencer Kylee M; Pericak-Vance Margaret A
Bringing the genetics of macular degeneration into focus.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(43):16725-6.
2007: Spencer Kylee L; Hauser Michael A; Olson Lana M; Schnetz-Boutaud Nathalie; Scott William K; Schmidt Silke; Gallins Paul; Agarwal Anita; Postel Eric A; Pericak-Vance Margaret A; Haines Jonathan L
Haplotypes spanning the complement factor H gene are protective against age-related macular degeneration.
Investigative ophthalmology & visual science 2007;48(9):4277-83.
2007: Gregory Simon G; Schmidt Silke; Seth Puneet; Oksenberg Jorge R; Hart John; Prokop Angela; Caillier Stacy J; Ban Maria; Goris An; Barcellos Lisa F; Lincoln Robin; McCauley Jacob L; Sawcer Stephen J; Compston D A S; Dubois Benedicte; Hauser Stephen L; Garcia-Blanco Mariano A; Pericak-Vance Margaret A; Haines Jonathan L;
Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis.
Nature genetics 2007;39(9):1083-91.
2007: Hafler David A; Compston Alastair; Sawcer Stephen; Lander Eric S; Daly Mark J; De Jager Philip L; de Bakker Paul I W; Gabriel Stacey B; Mirel Daniel B; Ivinson Adrian J; Pericak-Vance Margaret A; Gregory Simon G; Rioux John D; McCauley Jacob L; Haines Jonathan L; Barcellos Lisa F; Cree Bruce; Oksenberg Jorge R; Hauser Stephen L
Risk alleles for multiple sclerosis identified by a genomewide study.
The New England journal of medicine 2007;357(9):851-62.
2007: Ashley-Koch Allison E; Jaworski James; Ma De Qiong; Mei Hao; Ritchie Marylyn D; Skaar David A; Robert Delong G; Worley Gordon; Abramson Ruth K; Wright Harry H; Cuccaro Michael L; Gilbert John R; Martin Eden R; Pericak-Vance Margaret A
Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk.
Psychiatric genetics 2007;17(4):221-6.
2007: Spencer Kylee L; Hauser Michael A; Olson Lana M; Schmidt Silke; Scott William K; Gallins Paul; Agarwal Anita; Postel Eric A; Pericak-Vance Margaret A; Haines Jonathan L
Protective effect of complement factor B and complement component 2 variants in age-related macular degeneration.
Human molecular genetics 2007;16(16):1986-92.
2007: Beetz Christian; Zuchner Stephan; Ashley-Koch Allison; Auer-Grumbach Michaela; Byrne Paula; Chinnery Patrick F; Hutchinson Michael; McDermott Christopher J; Meijer Inge A; Nygren Anders O H; Pericak-Vance Margaret; Pyle Angela; Rouleau Guy A; Schickel Jörg; Shaw Pamela J; Deufel Thomas
Linkage to a known gene but no mutation identified: comprehensive reanalysis of SPG4 HSP pedigrees reveals large deletions as the sole cause.
Human mutation 2007;28(7):739-40.
2007: Scott William K; Schmidt Silke; Hauser Michael A; Gallins Paul; Schnetz-Boutaud Nathalie; Spencer Kylee L; Gilbert John R; Agarwal Anita; Postel Eric A; Haines Jonathan L; Pericak-Vance Margaret A
Independent effects of complement factor H Y402H polymorphism and cigarette smoking on risk of age-related macular degeneration.
Ophthalmology 2007;114(6):1151-6.
2007: Cuccaro Michael L; Nations Laura; Brinkley Jason; Abramson Ruth K; Wright Harry H; Hall Alicia; Gilbert John; Pericak-Vance Margaret A
A comparison of repetitive behaviors in Aspergers Disorder and high functioning autism.
Child psychiatry and human development 2007;37(4):347-60.
2007: Wang Liyong; Hauser Elizabeth R; Shah Svati H; Pericak-Vance Margaret A; Haynes Carol; Crosslin David; Harris Marco; Nelson Sarah; Hale A Brent; Granger Christopher B; Haines Jonathan L; Jones Christopher J H; Crossman David; Seo David; Gregory Simon G; Kraus William E; Goldschmidt-Clermont Pascal J; Vance Jeffery M
Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.
American journal of human genetics 2007;80(4):650-63.
2007: Ma D Q; Cuccaro M L; Jaworski J M; Haynes C S; Stephan D A; Parod J; Abramson R K; Wright H H; Gilbert J R; Haines J L; Pericak-Vance M A
Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
Molecular psychiatry 2007;12(4):376-84.
2007: Szatmari Peter; Paterson Andrew D; Zwaigenbaum Lonnie; Roberts Wendy; Brian Jessica; Liu Xiao-Qing; Vincent John B; Skaug Jennifer L; Thompson Ann P; Senman Lili; Feuk Lars; Qian Cheng; Bryson Susan E; Jones Marshall B; Marshall Christian R; Scherer Stephen W; Vieland Veronica J; Bartlett Christopher; Mangin La Vonne; Goedken Rhinda; Segre Alberto; Pericak-Vance Margaret A; Cuccaro Michael L; Gilbert John R; Wright Harry H; Abramson Ruth K; Betancur Catalina; Bourgeron Thomas; Gillberg Christopher; Leboyer Marion; Buxbaum Joseph D; Davis Kenneth L; Hollander Eric; Silverman Jeremy M; Hallmayer Joachim; Lotspeich Linda; Sutcliffe James S; Haines Jonathan L; Folstein Susan E; Piven Joseph; Wassink Thomas H; Sheffield Val; Geschwind Daniel H; Bucan Maja; Brown W Ted; Cantor Rita M; Constantino John N; Gilliam T Conrad; Herbert Martha; Lajonchere Clara; Ledbetter David H; Lese-Martin Christa; Miller Janet; Nelson Stan; Samango-Sprouse Carol A; Spence Sarah; State Matthew; Tanzi Rudolph E; Coon Hilary; Dawson Geraldine; Devlin Bernie; Estes Annette; Flodman Pamela; Klei Lambertus; McMahon William M; Minshew Nancy; Munson Jeff; Korvatska Elena; Rodier Patricia M; Schellenberg Gerard D; Smith Moyra; Spence M Anne; Stodgell Chris; Tepper Ping Guo; Wijsman Ellen M; Yu Chang-En; Rogé Bernadette; Mantoulan Carine; Wittemeyer Kerstin; Poustka Annemarie; Felder Bärbel; Klauck Sabine M; Schuster Claudia; Poustka Fritz; Bölte Sven; Feineis-Matthews Sabine; Herbrecht Evelyn; Schmötzer Gabi; Tsiantis John; Papanikolaou Katerina; Maestrini Elena; Bacchelli Elena; Blasi Francesca; Carone Simona; Toma Claudio; Van Engeland Herman; de Jonge Maretha; Kemner Chantal; Koop Frederieke; Langemeijer Marjolein; Hijmans Channa; Staal Wouter G; Baird Gillian; Bolton Patrick F; Rutter Michael L; Weisblatt Emma; Green Jonathan; Aldred Catherine; Wilkinson Julie-Anne; Pickles Andrew; Le Couteur Ann; Berney Tom; McConachie Helen; Bailey Anthony J; Francis Kostas; Honeyman Gemma; Hutchinson Aislinn; Parr Jeremy R; Wallace Simon; Monaco Anthony P; Barnby Gabrielle; Kobayashi Kazuhiro; Lamb Janine A; Sousa Ines; Sykes Nuala; Cook Edwin H; Guter Stephen J; Leventhal Bennett L; Salt Jeff; Lord Catherine; Corsello Christina; Hus Vanessa; Weeks Daniel E; Volkmar Fred; Tauber Maïté; Fombonne Eric; Shih Andy; Meyer Kacie J
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Nature genetics 2007;39(3):319-28.
2007: Lin Ping-I; Vance Jeffery M; Pericak-Vance Margaret A; Martin Eden R
No gene is an island: the flip-flop phenomenon.
American journal of human genetics 2007;80(3):531-8.
2007: Yeo Tai Wai; De Jager Philip L; Gregory Simon G; Barcellos Lisa F; Walton Amie; Goris An; Fenoglio Chiara; Ban Maria; Taylor Craig J; Goodman Reyna S; Walsh Emily; Wolfish Cara S; Horton Roger; Traherne James; Beck Stephan; Trowsdale John; Caillier Stacy J; Ivinson Adrian J; Green Todd; Pobywajlo Susan; Lander Eric S; Pericak-Vance Margaret A; Haines Jonathan L; Daly Mark J; Oksenberg Jorge R; Hauser Stephen L; Compston Alastair; Hafler David A; Rioux John D; Sawcer Stephen
A second major histocompatibility complex susceptibility locus for multiple sclerosis.
Annals of neurology 2007;61(3):228-36.
2007: Haines Jonathan L; Pericak-Vance Margaret A
Rapid dissection of the genetic risk of age-related macular degeneration: achieving the promise of the genomic era.
JAMA : the journal of the American Medical Association 2007;297(4):401-2.
2007: Shuler R Keith; Hauser Michael A; Caldwell Jennifer; Gallins Paul; Schmidt Silke; Scott William K; Agarwal Anita; Haines Jonathan L; Pericak-Vance Margaret A; Postel Eric A
Neovascular age-related macular degeneration and its association with LOC387715 and complement factor H polymorphism.
Archives of ophthalmology 2007;125(1):63-7.
2007: Motsinger Alison A; Brassat David; Caillier Stacy J; Erlich Henry A; Walker Karen; Steiner Lori L; Barcellos Lisa F; Pericak-Vance Margaret A; Schmidt Silke; Gregory Simon; Hauser Stephen L; Haines Jonathan L; Oksenberg Jorge R; Ritchie Marylyn D
Complex gene-gene interactions in multiple sclerosis: a multifactorial approach reveals associations with inflammatory genes.
Neurogenetics 2007;8(1):11-20.
2007: McCauley Jacob L; Kenealy Shannon J; Margulies Elliott H; Schnetz-Boutaud Nathalie; Gregory Simon G; Hauser Stephen L; Oksenberg Jorge R; Pericak-Vance Margaret A; Haines Jonathan L; Mortlock Douglas P
SNPs in Multi-species Conserved Sequences (MCS) as useful markers in association studies: a practical approach.
BMC genomics 2007;8():266.
2007: Liang Xueying; Schnetz-Boutaud Nathalie; Bartlett Jackie; Anderson Brent M; Gwirtsman Harry; Schmechel Don; Carney Regina; Gilbert John R; Pericak-Vance Margaret A; Haines Jonathan L
Association analysis of genetic polymorphisms in the CDC2 gene with late-onset Alzheimer disease.
Dementia and geriatric cognitive disorders 2007;23(2):126-32.
2006: Barcellos Lisa F; Kamdar Brinda B; Ramsay Patricia P; DeLoa Cari; Lincoln Robin R; Caillier Stacy; Schmidt Silke; Haines Jonathan L; Pericak-Vance Margaret A; Oksenberg Jorge R; Hauser Stephen L
Clustering of autoimmune diseases in families with a high-risk for multiple sclerosis: a descriptive study.
Lancet neurology 2006;5(11):924-31.
2006: Zuchner S; Cuccaro M L; Tran-Viet K N; Cope H; Krishnan R R; Pericak-Vance M A; Wright H H; Ashley-Koch A
SLITRK1 mutations in trichotillomania.
Molecular psychiatry 2006;11(10):887-9.
2006: de Bakker Paul I W; McVean Gil; Sabeti Pardis C; Miretti Marcos M; Green Todd; Marchini Jonathan; Ke Xiayi; Monsuur Alienke J; Whittaker Pamela; Delgado Marcos; Morrison Jonathan; Richardson Angela; Walsh Emily C; Gao Xiaojiang; Galver Luana; Hart John; Hafler David A; Pericak-Vance Margaret; Todd John A; Daly Mark J; Trowsdale John; Wijmenga Cisca; Vyse Tim J; Beck Stephan; Murray Sarah Shaw; Carrington Mary; Gregory Simon; Deloukas Panos; Rioux John D
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.
Nature genetics 2006;38(10):1166-72.
2006: Hauser Michael A; Sena Dayse Figueiredo; Flor Jason; Walter Jeff; Auguste Josette; Larocque-Abramson Karen; Graham Felicia; Delbono Elizabeth; Haines Jonathan L; Pericak-Vance Margaret A; Rand Allingham R; Wiggs Janey L
Distribution of optineurin sequence variations in an ethnically diverse population of low-tension glaucoma patients from the United States.
Journal of glaucoma 2006;15(5):358-63.
2006: Barcellos Lisa F; Sawcer Stephen; Ramsay Patricia P; Baranzini Sergio E; Thomson Glenys; Briggs Farren; Cree Bruce C A; Begovich Ann B; Villoslada Pablo; Montalban Xavier; Uccelli Antonio; Savettieri Giovanni; Lincoln Robin R; DeLoa Carolyn; Haines Jonathan L; Pericak-Vance Margaret A; Compston Alastair; Hauser Stephen L; Oksenberg Jorge R
Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis.
Human molecular genetics 2006;15(18):2813-24.
2006: Postel Eric A; Agarwal Anita; Caldwell Jennifer; Gallins Paul; Toth Cynthia; Schmidt Silke; Scott William K; Hauser Michael A; Haines Jonathan L; Pericak-Vance Margaret A
Complement factor H increases risk for atrophic age-related macular degeneration.
Ophthalmology 2006;113(9):1504-7.
2006: Saeed M; Siddique N; Hung W Y; Usacheva E; Liu E; Sufit R L; Heller S L; Haines J L; Pericak-Vance M; Siddique T
Paraoxonase cluster polymorphisms are associated with sporadic ALS.
Neurology 2006;67(5):771-6.
2006: Chen W; Saeed M; Mao H; Siddique N; Dellefave L; Hung W-Y; Deng H-X; Sufit R L; Heller S L; Haines J L; Pericak-Vance M; Siddique T
Lack of association of VEGF promoter polymorphisms with sporadic ALS.
Neurology 2006;67(3):508-10.
2006: Züchner Stephan; Wang Gaofeng; Tran-Viet Khanh-Nhat; Nance Martha A; Gaskell Perry C; Vance Jeffery M; Ashley-Koch Allison E; Pericak-Vance Margaret A
Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31.
American journal of human genetics 2006;79(2):365-9.
2006: Li Yi-Ju; Scott William K; Zhang Ling; Lin Ping-I; Oliveira Sofia A; Skelly Tara; Doraiswamy Maurali P; Welsh-Bohmer Kathleen A; Martin Eden R; Haines Jonathan L; Pericak-Vance Margaret A; Vance Jeffery M
Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases.
Neurobiology of aging 2006;27(8):1087-93.
2006: Lin P I; Martin E R; Bronson P G; Browning-Large C; Small G W; Schmechel D E; Welsh-Bohmer K A; Haines J L; Gilbert J R; Pericak-Vance M A
Exploring the association of glyceraldehyde-3-phosphate dehydrogenase gene and Alzheimer disease.
Neurology 2006;67(1):64-8.
2006: Collins Ann L; Ma Deqiong; Whitehead Patrice L; Martin Eden R; Wright Harry H; Abramson Ruth K; Hussman John P; Haines Jonathan L; Cuccaro Michael L; Gilbert John R; Pericak-Vance Margaret A
Investigation of autism and GABA receptor subunit genes in multiple ethnic groups.
Neurogenetics 2006;7(3):167-74.
2006: Lin Ping-I; Martin Eden R; Browning-Large Carrie A; Schmechel Donald E; Welsh-Bohmer Kathleen A; Doraiswamy P Murali; Gilbert John R; Haines Jonathan L; Pericak-Vance Margaret A
Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis.
Neurogenetics 2006;7(3):157-65.
2006: Schmidt S; Pericak-Vance M A; Sawcer S; Barcellos L F; Hart J; Sims J; Prokop A M; van der Walt J; DeLoa C; Lincoln R R; Oksenberg J R; Compston A; Hauser S L; Haines J L; Gregory S G;
Allelic association of sequence variants in the herpes virus entry mediator-B gene (PVRL2) with the severity of multiple sclerosis.
Genes and immunity 2006;7(5):384-92.
2006: Hauser Michael A; Allingham R Rand; Linkroum Kevin; Wang Jun; LaRocque-Abramson Karen; Figueiredo Dayse; Santiago-Turla Cecilia; del Bono Elizabeth A; Haines Jonathan L; Pericak-Vance Margaret A; Wiggs Janey L
Distribution of WDR36 DNA sequence variants in patients with primary open-angle glaucoma.
Investigative ophthalmology & visual science 2006;47(6):2542-6.
2006: Brassat D; Motsinger A A; Caillier S J; Erlich H A; Walker K; Steiner L L; Cree B A C; Barcellos L F; Pericak-Vance M A; Schmidt S; Gregory S; Hauser S L; Haines J L; Oksenberg J R; Ritchie M D
Multifactor dimensionality reduction reveals gene-gene interactions associated with multiple sclerosis susceptibility in African Americans.
Genes and immunity 2006;7(4):310-5.
2006: Burwick R M; Ramsay P P; Haines J L; Hauser S L; Oksenberg J R; Pericak-Vance M A; Schmidt S; Compston A; Sawcer S; Cittadella R; Savettieri G; Quattrone A; Polman C H; Uitdehaag B M J; Zwemmer J N P; Hawkins C P; Ollier W E R; Weatherby S; Enzinger C; Fazekas F; Schmidt H; Schmidt R; Hillert J; Masterman T; Hogh P; Niino M; Kikuchi S; Maciel P; Santos M; Rio M E; Kwiecinski H; Zakrzewska-Pniewska B; Evangelou N; Palace J; Barcellos L F
APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers.
Neurology 2006;66(9):1373-83.
2006: Ashley-Koch A E; Mei H; Jaworski J; Ma D Q; Ritchie M D; Menold M M; Delong G R; Abramson R K; Wright H H; Hussman J P; Cuccaro M L; Gilbert J R; Martin E R; Pericak-Vance M A
An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder.
Annals of human genetics 2006;70(Pt 3):281-92.
2006: Rabionet Raquel; McCauley Jacob L; Jaworski James M; Ashley-Koch Allison E; Martin Eden R; Sutcliffe James S; Haines Jonathan L; DeLong G Robert; Abramson Ruth K; Wright Harry H; Cuccaro Michael L; Gilbert John R; Pericak-Vance Margaret A
Lack of association between autism and SLC25A12.
The American journal of psychiatry 2006;163(5):929-31.
2006: Schmidt Silke; Hauser Michael A; Scott William K; Postel Eric A; Agarwal Anita; Gallins Paul; Wong Frank; Chen Yu Sarah; Spencer Kylee; Schnetz-Boutaud Nathalie; Haines Jonathan L; Pericak-Vance Margaret A
Cigarette smoking strongly modifies the association of LOC387715 and age-related macular degeneration.
American journal of human genetics 2006;78(5):852-64.
2006: Züchner Stephan; Kail Melanie E; Nance Martha A; Gaskell Perry C; Svenson Ingrid K; Marchuk Douglas A; Pericak-Vance Margaret A; Ashley-Koch Allison E
A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12.
Neurogenetics 2006;7(2):127-9.
2006: Slifer M A; Martin E R; Bronson P G; Browning-Large C; Doraiswamy P M; Welsh-Bohmer K A; Gilbert J R; Haines J L; Pericak-Vance M A
Lack of association between UBQLN1 and Alzheimer disease.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(3):208-13.
2006: Pillai Sreekumar G; Chiano Mathias N; White Nicola J; Speer Marcy; Barnes Kathleen C; Carlsen Karin; Gerritsen Jorrit; Helms Peter; Lenney Warren; Silverman Michael; Sly Peter; Sundy John; Tsanakas John; von Berg Andrea; Whyte Moira; Varsani Shela; Skelding Paul; Hauser Michael; Vance Jeffery; Pericak-Vance Margaret; Burns Daniel K; Middleton Lefkos T; Brewster Shyama R; Anderson Wayne H; Riley John H
A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p.
European journal of human genetics : EJHG 2006;14(3):307-16.
2006: Hahs Daniel W; McCauley Jacob L; Crunk Amy E; McFarland Lynne L; Gaskell Perry C; Jiang Lan; Slifer Susan H; Vance Jeffery M; Scott William K; Welsh-Bohmer Kathleen A; Johnson Stephanie R; Jackson Charles E; Pericak-Vance Margaret A; Haines Jonathan L
A genome-wide linkage analysis of dementia in the Amish.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(2):160-6.
2006: Liang X; Schnetz-Boutaud N; Kenealy S J; Jiang L; Bartlett J; Lynch B; Gaskell P C; Gwirtsman H; McFarland L; Bembe M L; Bronson P; Gilbert J R; Martin E R; Pericak-Vance M A; Haines J L
Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus.
Molecular psychiatry 2006;11(3):280-5.
2006: Xu Pu-Ting; Li Yi-Ju; Qin Xue-Jun; Scherzer Clemens R; Xu Hong; Schmechel Donald E; Hulette Christine M; Ervin John; Gullans Steven R; Haines Jonathan; Pericak-Vance Margaret A; Gilbert John R
Differences in apolipoprotein E3/3 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease.
Neurobiology of disease 2006;21(2):256-75.
2006: Haines Jonathan L; Schnetz-Boutaud Nathalie; Schmidt Silke; Scott William K; Agarwal Anita; Postel Eric A; Olson Lana; Kenealy Shannon J; Hauser Michael; Gilbert John R; Pericak-Vance Margaret A
Functional candidate genes in age-related macular degeneration: significant association with VEGF, VLDLR, and LRP6.
Investigative ophthalmology & visual science 2006;47(1):329-35.
2006: Kenealy S J; Herrel L A; Bradford Y; Schnetz-Boutaud N; Oksenberg J R; Hauser S L; Barcellos L F; Schmidt S; Gregory S G; Pericak-Vance M A; Haines J L
Examination of seven candidate regions for multiple sclerosis: strong evidence of linkage to chromosome 1q44.
Genes and immunity 2006;7(1):73-6.
2006: Li Yi-Ju; Xu Puting; Qin Xuejun; Schmechel Donald E; Hulette Christine M; Haines Jonathan L; Pericak-Vance Margaret A; Gilbert John R
A comparative analysis of the information content in long and short SAGE libraries.
BMC bioinformatics 2006;7():504.
2006: Challa Pratap; Hauser Michael Arthur; Luna Coralia Catalina; Freedman Sharon Fridovich; Pericak-Vance Margaret; Yang Jun; McDonald Marie Theresa; Allingham R Rand
Juvenile bilateral lens dislocation and glaucoma associated with a novel mutation in the fibrillin 1 gene.
Molecular vision 2006;12():1009-15.
2006: McCauley Jacob L; Hahs Daniel W; Jiang Lan; Scott William K; Welsh-Bohmer Kathleen A; Jackson Charles E; Vance Jeffery M; Pericak-Vance Margaret A; Haines Jonathan L
Combinatorial Mismatch Scan (CMS) for loci associated with dementia in the Amish.
BMC medical genetics 2006;7():19.
2005: Xu Hong; Gregory Simon G; Hauser Elizabeth R; Stenger Judith E; Pericak-Vance Margaret A; Vance Jeffery M; Züchner Stephan; Hauser Michael A
SNPselector: a web tool for selecting SNPs for genetic association studies.
Bioinformatics (Oxford, England) 2005;21(22):4181-6.
2005: Martin E R; Bronson P G; Li Y-J; Wall N; Chung R-H; Schmechel D E; Small G; Xu P-T; Bartlett J; Schnetz-Boutaud N; Haines J L; Gilbert J R; Pericak-Vance M A
Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease.
Journal of medical genetics 2005;42(10):787-92.
2005: van der Walt Joelle M; Scott William K; Slifer Susan; Gaskell P C; Martin Eden R; Welsh-Bohmer Kathleen; Creason Marilyn; Crunk Amy; Fuzzell Denise; McFarland Lynne; Kroner Charles C; Jackson C E; Haines Jonathan L; Pericak-Vance Margaret A
Maternal lineages and Alzheimer disease risk in the Old Order Amish.
Human genetics 2005;118(1):115-22.
2005: Sawcer Stephen; Ban Maria; Maranian Mel; Yeo Tai Wai; Compston Alastair; Kirby Andrew; Daly Mark J; De Jager Philip L; Walsh Emily; Lander Eric S; Rioux John D; Hafler David A; Ivinson Adrian; Rimmler Jacqueline; Gregory Simon G; Schmidt Silke; Pericak-Vance Margaret A; Akesson Eva; Hillert Jan; Datta Pameli; Oturai Annette; Ryder Lars P; Harbo Hanne F; Spurkland Anne; Myhr Kjell-Morten; Laaksonen Mikko; Booth David; Heard Robert; Stewart Graeme; Lincoln Robin; Barcellos Lisa F; Hauser Stephen L; Oksenberg Jorge R; Kenealy Shannon J; Haines Jonathan L;
A high-density screen for linkage in multiple sclerosis.
American journal of human genetics 2005;77(3):454-67.
2005: Ma D Q; Whitehead P L; Menold M M; Martin E R; Ashley-Koch A E; Mei H; Ritchie M D; Delong G R; Abramson R K; Wright H H; Cuccaro M L; Hussman J P; Gilbert J R; Pericak-Vance M A
Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism.
American journal of human genetics 2005;77(3):377-88.
2005: Svenson Ingrid K; Kloos Mark T; Jacon Amy; Gallione Carol; Horton April C; Pericak-Vance Margaret A; Ehlers Michael D; Marchuk Douglas A
Subcellular localization of spastin: implications for the pathogenesis of hereditary spastic paraplegia.
Neurogenetics 2005;6(3):135-41.
2005: Fisher Sheila A; Abecasis Goncalo R; Yashar Beverly M; Zareparsi Sepideh; Swaroop Anand; Iyengar Sudha K; Klein Barbara E K; Klein Ronald; Lee Kristine E; Majewski Jacek; Schultz Dennis W; Klein Michael L; Seddon Johanna M; Santangelo Susan L; Weeks Daniel E; Conley Yvette P; Mah Tammy S; Schmidt Silke; Haines Jonathan L; Pericak-Vance Margaret A; Gorin Michael B; Schulz Heidi L; Pardi Fabio; Lewis Cathryn M; Weber Bernhard H F
Meta-analysis of genome scans of age-related macular degeneration.
Human molecular genetics 2005;14(15):2257-64.
2005: Oliveira Sofia A; Li Yi-Ju; Noureddine Maher A; Zuchner Stephan; Qin Xuejun; Pericak-Vance Margaret A; Vance Jeffery M
Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.
American journal of human genetics 2005;77(2):252-64.
2005: Slifer Michael A; Martin Eden R; Haines Jonathan L; Pericak-Vance Margaret A
The ubiquilin 1 gene and Alzheimer's disease.
The New England journal of medicine 2005;352(26):2752-3; author reply 2752-3.
2005: Allingham R Rand; Wiggs Janey L; Hauser Elizabeth R; Larocque-Abramson Karen R; Santiago-Turla Cecilia; Broomer Bob; Del Bono Elizabeth A; Graham Felicia L; Haines Jonathan L; Pericak-Vance Margaret A; Hauser Michael A
Early adult-onset POAG linked to 15q11-13 using ordered subset analysis.
Investigative ophthalmology & visual science 2005;46(6):2002-5.
2005: Winn Michelle P; Conlon Peter J; Lynn Kelvin L; Farrington Merry Kay; Creazzo Tony; Hawkins April F; Daskalakis Nikki; Kwan Shu Ying; Ebersviller Seth; Burchette James L; Pericak-Vance Margaret A; Howell David N; Vance Jeffery M; Rosenberg Paul B
A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis.
Science (New York, N.Y.) 2005;308(5729):1801-4.
2005: Noureddine Maher A; Qin Xue-Jun; Oliveira Sofia A; Skelly Tara J; van der Walt Joelle; Hauser Michael A; Pericak-Vance Margaret A; Vance Jeffery M; Li Yi-Ju
Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease.
Human genetics 2005;117(1):27-33.
2005: Skaar D A; Shao Y; Haines J L; Stenger J E; Jaworski J; Martin E R; DeLong G R; Moore J H; McCauley J L; Sutcliffe J S; Ashley-Koch A E; Cuccaro M L; Folstein S E; Gilbert J R; Pericak-Vance M A
Analysis of the RELN gene as a genetic risk factor for autism.
Molecular psychiatry 2005;10(6):563-71.
2005: Postel Eric A; Agarwal Anita; Schmidt Silke; Fan Yu-Ti R; Scott William K; Gilbert John R; Haines Jonathan L; Pericak-Vance Margaret A
Comparing age-related macular degeneration phenotype in probands from singleton and multiplex families.
American journal of ophthalmology 2005;139(5):820-5.
2005: Ashley-Koch A E; Shao Y; Rimmler J B; Gaskell P C; Welsh-Bohmer K A; Jackson C E; Scott W K; Haines J L; Pericak-Vance M A
An autosomal genomic screen for dementia in an extended Amish family.
Neuroscience letters 2005;379(3):199-204.
2005: Ma D Q; Jaworski J; Menold M M; Donnelly S; Abramson R K; Wright H H; Delong G R; Gilbert J R; Pericak-Vance M A; Cuccaro Michael L
Ordered-subset analysis of savant skills in autism for 15q11-q13.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;135B(1):38-41.
2005: Haines Jonathan L; Hauser Michael A; Schmidt Silke; Scott William K; Olson Lana M; Gallins Paul; Spencer Kylee L; Kwan Shu Ying; Noureddine Maher; Gilbert John R; Schnetz-Boutaud Nathalie; Agarwal Anita; Postel Eric A; Pericak-Vance Margaret A
Complement factor H variant increases the risk of age-related macular degeneration.
Science (New York, N.Y.) 2005;308(5720):419-21.
2005: Züchner Stephan; Noureddine Maher; Kennerson Marina; Verhoeven Kristien; Claeys Kristl; De Jonghe Peter; Merory John; Oliveira Sofia A; Speer Marcy C; Stenger Judith E; Walizada Gina; Zhu Danqing; Pericak-Vance Margaret A; Nicholson Garth; Timmerman Vincent; Vance Jeffery M
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.
Nature genetics 2005;37(3):289-94.
2005: Schmidt Silke; Haines Jonathan L; Postel Eric A; Agarwal Anita; Kwan Shu Ying; Gilbert John R; Pericak-Vance Margaret A; Scott William K
Joint effects of smoking history and APOE genotypes in age-related macular degeneration.
Molecular vision 2005;11():941-9.
2005: Abramson R K; Ravan S A; Wright H H; Wieduwilt K; Wolpert C M; Donnelly S A; Pericak-Vance M A; Cuccaro M L
The relationship between restrictive and repetitive behaviors in individuals with autism and obsessive compulsive symptoms in parents.
Child psychiatry and human development 2005;36(2):155-65.
2005: Boyles Abee L; Scott William K; Martin Eden R; Schmidt Silke; Li Yi-Ju; Ashley-Koch Allison; Bass Meredyth P; Schmidt Michael; Pericak-Vance Margaret A; Speer Marcy C; Hauser Elizabeth R
Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.
Human heredity 2005;59(4):220-7.
2005: Stenger Judith E; Xu Hong; Haynes Carol; Hauser Elizabeth R; Pericak-Vance Margaret; Goldschmidt-Clermont Pascal J; Vance Jeffery M
Statistical Viewer: a tool to upload and integrate linkage and association data as plots displayed within the Ensembl genome browser.
BMC bioinformatics 2005;6():95.
2004: Li Yi-Ju; Pericak-Vance Margaret A; Haines Jonathan L; Siddique Nailah; McKenna-Yasek Diane; Hung Wu-Yen; Sapp Peter; Allen Coy I; Chen Wenjie; Hosler Betsy; Saunders Ann M; Dellefave Lisa M; Brown Robert H; Siddique Teepu
Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis.
Neurogenetics 2004;5(4):209-13.
2004: Cree B A C; Khan O; Bourdette D; Goodin D S; Cohen J A; Marrie R A; Glidden D; Weinstock-Guttman B; Reich D; Patterson N; Haines J L; Pericak-Vance M; DeLoa C; Oksenberg J R; Hauser S L
Clinical characteristics of African Americans vs Caucasian Americans with multiple sclerosis.
Neurology 2004;63(11):2039-45.
2004: Rabionet Raquel; Jaworski James M; Ashley-Koch Allison E; Martin Eden R; Sutcliffe James S; Haines Jonathan L; Delong G Robert; Abramson Ruth K; Wright Harry H; Cuccaro Michael L; Gilbert John R; Pericak-Vance Margaret A
Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes.
Neuroscience letters 2004;372(3):209-14.
2004: Kenealy S J; Babron M-C; Bradford Y; Schnetz-Boutaud N; Haines J L; Rimmler J B; Schmidt S; Pericak-Vance M A; Barcellos L F; Lincoln R R; Oksenberg J R; Hauser S L; Clanet M; Brassat D; Edan G; Yaouanq J; Semana G; Cournu-Rebeix I; Lyon-Caen O; Fontaine B;
A second-generation genomic screen for multiple sclerosis.
American journal of human genetics 2004;75(6):1070-8.
2004: Nicodemus Kristin K; Stenger Judith E; Schmechel Donald E; Welsh-Bohmer Kathleen A; Saunders Ann M; Roses Allen D; Gilbert John R; Vance Jeffery M; Haines Jonathan L; Pericak-Vance Margaret A; Martin Eden R
Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease.
Neurogenetics 2004;5(4):201-8.
2004: Oliveira Sofia A; Scott William K; Zhang Fengyu; Stajich Jeffrey M; Fujiwara Kenichiro; Hauser Michael; Scott Burton L; Pericak-Vance Margaret A; Vance Jeffery M; Martin Eden R
Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype.
Neurogenetics 2004;5(3):147-55.
2004: Hauser Elizabeth R; Crossman David C; Granger Christopher B; Haines Jonathan L; Jones Christopher J H; Mooser Vincent; McAdam Brendan; Winkelmann Bernhard R; Wiseman Alan H; Muhlestein J Brent; Bartel Alan G; Dennis Charles A; Dowdy Elaine; Estabrooks Susan; Eggleston Karen; Francis Sheila; Roche Kath; Clevenger Paula W; Huang Liling; Pedersen Bonnie; Shah Svati; Schmidt Silke; Haynes Carol; West Sandra; Asper Donny; Booze Michael; Sharma Sanjay; Sundseth Scott; Middleton Lefkos; Roses Allen D; Hauser Michael A; Vance Jeffery M; Pericak-Vance Margaret A; Kraus William E
A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.
American journal of human genetics 2004;75(3):436-47.
2004: Svenson Ingrid K; Kloos Mark T; Gaskell P Craig; Nance Martha A; Garbern James Y; Hisanaga Shin-ichi; Pericak-Vance Margaret A; Ashley-Koch Allison E; Marchuk Douglas A
Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations.
Neurogenetics 2004;5(3):157-64.
2004: Sawcer Stephen J; Maranian Mel; Singlehurst Sara; Yeo TaiWai; Compston Alastair; Daly Mark J; De Jager Philip L; Gabriel Stacey; Hafler David A; Ivinson Adrian J; Lander Eric S; Rioux John D; Walsh Emily; Gregory Simon G; Schmidt Silke; Pericak-Vance Margaret A; Barcellos Lisa; Hauser Stephen L; Oksenberg Jorge R; Kenealy Shannon J; Haines Jonathan L
Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping.
Human molecular genetics 2004;13(17):1943-9.
2004: Weeks Daniel E; Conley Yvette P; Tsai Hui-Ju; Mah Tammy S; Schmidt Silke; Postel Eric A; Agarwal Anita; Haines Jonathan L; Pericak-Vance Margaret A; Rosenfeld Philip J; Paul T Otis; Eller Andrew W; Morse Lawrence S; Dailey J P; Ferrell Robert E; Gorin Michael B
Age-related maculopathy: a genomewide scan with continued evidence of susceptibility loci within the 1q31, 10q26, and 17q25 regions.
American journal of human genetics 2004;75(2):174-89.
2004: Schmidt Silke; Scott William K; Postel Eric A; Agarwal Anita; Hauser Elizabeth R; De La Paz Monica A; Gilbert John R; Weeks Daniel E; Gorin Michael B; Haines Jonathan L; Pericak-Vance Margaret A
Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12.
BMC genetics 2004;5():18.
2004: van der Walt Joelle M; Dementieva Yulia A; Martin Eden R; Scott William K; Nicodemus Kristin K; Kroner Charles C; Welsh-Bohmer Kathleen A; Saunders Ann M; Roses Allen D; Small Gary W; Schmechel Donald E; Murali Doraiswamy P; Gilbert John R; Haines Jonathan L; Vance Jeffery M; Pericak-Vance Margaret A
Analysis of European mitochondrial haplogroups with Alzheimer disease risk.
Neuroscience letters 2004;365(1):28-32.
2004: Li Y J; Hauser M A; Scott W K; Martin E R; Booze M W; Qin X J; Walter J W; Nance M A; Hubble J P; Koller W C; Pahwa R; Stern M B; Hiner B C; Jankovic J; Goetz C G; Small G W; Mastaglia F; Haines J L; Pericak-Vance M A; Vance J M
Apolipoprotein E controls the risk and age at onset of Parkinson disease.
Neurology 2004;62(11):2005-9.
2004: Barcellos Lisa F; Begovich Ann B; Reynolds Rebecca L; Caillier Stacy J; Brassat David; Schmidt Silke; Grams Sarah E; Walker Karen; Steiner Lori L; Cree Bruce A C; Stillman Althea; Lincoln Robin R; Pericak-Vance Margaret A; Haines Jonathan L; Erlich Henry A; Hauser Stephen L; Oksenberg Jorge R
Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis.
Annals of neurology 2004;55(6):793-800.
2004: van der Walt Joelle M; Noureddine Maher A; Kittappa Raja; Hauser Michael A; Scott William K; McKay Ron; Zhang Fengyu; Stajich Jeffrey M; Fujiwara Kenichiro; Scott Burton L; Pericak-Vance Margaret A; Vance Jeffery M; Martin Eden R
Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease.
American journal of human genetics 2004;74(6):1121-7.
2004: Züchner Stephan; Mersiyanova Irina V; Muglia Maria; Bissar-Tadmouri Nisrine; Rochelle Julie; Dadali Elena L; Zappia Mario; Nelis Eva; Patitucci Alessandra; Senderek Jan; Parman Yesim; Evgrafov Oleg; Jonghe Peter De; Takahashi Yuji; Tsuji Shoij; Pericak-Vance Margaret A; Quattrone Aldo; Battaloglu Esra; Polyakov Alexander V; Timmerman Vincent; Schröder J Michael; Vance Jeffery M;
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.
Nature genetics 2004;36(5):449-51.
2004: Raiford K L; Shao Y; Allen I C; Martin E R; Menold M M; Wright H H; Abramson R K; Worley G; DeLong G R; Vance J M; Cuccaro M L; Gilbert J R; Pericak-Vance M A
No association between the APOE gene and autism.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;125B(1):57-60.
2004: Pericak-Vance Margaret A; Rimmler Jackie B; Haines Jonathan L; Garcia Melissa E; Oksenberg Jorge R; Barcellos Lisa F; Lincoln Robin; Hauser Stephen L; Cournu-Rebeix Isabelle; Azoulay-Cayla Ariele; Lyon-Caen Olivier; Fontaine Bertrand; Duhamel Emmanuelle; Coppin Helene; Brassat David; Roth Marie-Paule; Clanet Michel; Alizadeh Mehdi; Yaouanq Jacqueline; Quelvennec Erwann; Semana Gilbert; Edan Gilles; Babron Marie-Claude; Genin Emmanuelle; Clerget-Darpoux Francoise
Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study.
Neurogenetics 2004;5(1):45-8.
2004: Kenealy Shannon J; Schmidt Silke; Agarwal Anita; Postel Eric A; De La Paz Monica A; Pericak-Vance Margaret A; Haines Jonathan L
Linkage analysis for age-related macular degeneration supports a gene on chromosome 10q26.
Molecular vision 2004;10():57-61.
2004: Oksenberg Jorge R; Barcellos Lisa F; Cree Bruce A C; Baranzini Sergio E; Bugawan Teodorica L; Khan Omar; Lincoln Robin R; Swerdlin Amy; Mignot Emmanuel; Lin Ling; Goodin Douglas; Erlich Henry A; Schmidt Silke; Thomson Glenys; Reich David E; Pericak-Vance Margaret A; Haines Jonathan L; Hauser Stephen L
Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans.
American journal of human genetics 2004;74(1):160-7.
2003: Li Yi-Ju; Oliveira Sofia A; Xu Puting; Martin Eden R; Stenger Judith E; Scherzer Clemens R; Hauser Michael A; Scott William K; Small Gary W; Nance Martha A; Watts Ray L; Hubble Jean P; Koller William C; Pahwa Rajesh; Stern Mathew B; Hiner Bradley C; Jankovic Joseph; Goetz Christopher G; Mastaglia Frank; Middleton Lefkos T; Roses Allen D; Saunders Ann M; Schmechel Donald E; Gullans Steven R; Haines Jonathan L; Gilbert John R; Vance Jeffery M; Pericak-Vance Margaret A; Hulette Christine; Welsh-Bohmer Kathleen A
Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease.
Human molecular genetics 2003;12(24):3259-67.
2003: Scott William K; Hauser Elizabeth R; Schmechel Donald E; Welsh-Bohmer Kathleen A; Small Gary W; Roses Allen D; Saunders Ann M; Gilbert John R; Vance Jeffery M; Haines Jonathan L; Pericak-Vance Margaret A
Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22.
American journal of human genetics 2003;73(5):1041-51.
2003: Martin E R; Bass M P; Gilbert J R; Pericak-Vance M A; Hauser E R
Genotype-based association test for general pedigrees: the genotype-PDT.
Genetic epidemiology 2003;25(3):203-13.
2003: Kenealy Shannon J; Pericak-Vance Margaret A; Haines Jonathan L
The genetic epidemiology of multiple sclerosis.
Journal of neuroimmunology 2003;143(1-2):7-12.
2003: Wiggs Janey L; Auguste Josette; Allingham R Rand; Flor Jason D; Pericak-Vance Margaret A; Rogers Kathryn; LaRocque Karen R; Graham Felicia L; Broomer Bob; Del Bono Elizabeth; Haines Jonathan L; Hauser Michael
Lack of association of mutations in optineurin with disease in patients with adult-onset primary open-angle glaucoma.
Archives of ophthalmology 2003;121(8):1181-3.
2003: Oliveira Sofia A; Martin Eden R; Scott William K; Nicodemus Kristin K; Small Gary W; Schmechel Donald E; Doraiswamy P Murali; Roses Allen D; Saunders Ann M; Gilbert John R; Haines Jonathan L; Vance Jeffery M; Pericak-Vance Margaret A
The Q7R Saitohin gene polymorphism is not associated with Alzheimer disease.
Neuroscience letters 2003;347(3):143-6.
2003: Sapp Peter C; Hosler Betsy A; McKenna-Yasek Diane; Chin Wendy; Gann Amity; Genise Hilary; Gorenstein Julie; Huang Michael; Sailer Wen; Scheffler Meg; Valesky Marianne; Haines Jonathan L; Pericak-Vance Margaret; Siddique Teepu; Horvitz H Robert; Brown Robert H
Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosis.
American journal of human genetics 2003;73(2):397-403.
2003: Matise Tara C; Sachidanandam Ravi; Clark Andrew G; Kruglyak Leonid; Wijsman Ellen; Kakol Jerzy; Buyske Steven; Chui Buena; Cohen Patrick; de Toma Claudia; Ehm Margaret; Glanowski Stephen; He Chunsheng; Heil Jeremy; Markianos Kyriacos; McMullen Ivy; Pericak-Vance Margaret A; Silbergleit Arkadiy; Stein Lincoln; Wagner Michael; Wilson Alexander F; Winick Jeffrey D; Winn-Deen Emily S; Yamashiro Carl T; Cann Howard M; Lai Eric; Holden Arthur L
A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set.
American journal of human genetics 2003;73(2):271-84.
2003: Oliveira Sofia A; Scott William K; Nance Martha A; Watts Ray L; Hubble Jean P; Koller William C; Lyons Kelly E; Pahwa Rajesh; Stern Matthew B; Hiner Bradley C; Jankovic Joseph; Ondo William G; Allen Fred H; Scott Burton L; Goetz Christopher G; Small Gary W; Mastaglia Frank L; Stajich Jeffrey M; Zhang Fengyu; Booze Michael W; Reaves Joshua A; Middleton Lefkos T; Haines Jonathan L; Pericak-Vance Margaret A; Vance Jeffery M; Martin Eden R
Association study of Parkin gene polymorphisms with idiopathic Parkinson disease.
Archives of neurology 2003;60(7):975-80.
2003: Schmidt Silke; Postel Eric A; Agarwal Anita; Allen I Coy; Walters Shaune N; De la Paz Monica A; Scott William K; Haines Jonathan L; Pericak-Vance Margaret A; Gilbert John R
Detailed analysis of allelic variation in the ABCA4 gene in age-related maculopathy.
Investigative ophthalmology & visual science 2003;44(7):2868-75.
2003: Caillier S; Barcellos L F; Baranzini S E; Swerdlin A; Lincoln R R; Steinman L; Martin E; Haines J L; Pericak-Vance M; Hauser S L; Oksenberg J R;
Osteopontin polymorphisms and disease course in multiple sclerosis.
Genes and immunity 2003;4(4):312-5.
2003: Oliveira Sofia A; Scott William K; Martin Eden R; Nance Martha A; Watts Ray L; Hubble Jean P; Koller William C; Pahwa Rajesh; Stern Matthew B; Hiner Bradley C; Ondo William G; Allen Fred H; Scott Burton L; Goetz Christopher G; Small Gary W; Mastaglia Frank; Stajich Jeffrey M; Zhang Fengyu; Booze Michael W; Winn Michelle P; Middleton Lefkos T; Haines Jonathan L; Pericak-Vance Margaret A; Vance Jeffery M
Parkin mutations and susceptibility alleles in late-onset Parkinson's disease.
Annals of neurology 2003;53(5):624-9.
2003: Trembath Yuri; Rosenberg Carolyn; Ervin John F; Schmechel Donald E; Gaskell Perry; Pericak-Vance Margaret; Vance Jeffery; Hulette Christine M
Lewy body pathology is a frequent co-pathology in familial Alzheimer's disease.
Acta neuropathologica 2003;105(5):484-8.
2003: van der Walt J M; Martin E R; Scott W K; Zhang F; Nance M A; Watts R L; Hubble J P; Haines J L; Koller W C; Lyons K; Pahwa R; Stern M B; Colcher A; Hiner B C; Jankovic J; Ondo W G; Allen F H; Goetz C G; Small G W; Mastaglia F; Roses A D; Stajich J M; Booze M W; Fujiwara K; Gibson R A; Middleton L T; Scott B L; Pericak-Vance M A; Vance J M
Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson's disease.
Neurology 2003;60(7):1189-91.
2003: Hauser Elizabeth R; Mooser Vincent; Crossman David C; Haines Jonathan L; Jones Christopher H; Winkelmann Bernhard R; Schmidt Silke; Scott William K; Roses Allen D; Pericak-Vance Margaret A; Granger Christopher B; Kraus William E;
Design of the Genetics of Early Onset Cardiovascular Disease (GENECARD) study.
American heart journal 2003;145(4):602-13.
2003: van der Walt Joelle M; Nicodemus Kristin K; Martin Eden R; Scott William K; Nance Martha A; Watts Ray L; Hubble Jean P; Haines Jonathan L; Koller William C; Lyons Kelly; Pahwa Rajesh; Stern Matthew B; Colcher Amy; Hiner Bradley C; Jankovic Joseph; Ondo William G; Allen Fred H; Goetz Christopher G; Small Gary W; Mastaglia Frank; Stajich Jeffrey M; McLaurin Adam C; Middleton Lefkos T; Scott Burton L; Schmechel Donald E; Pericak-Vance Margaret A; Vance Jeffery M
Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease.
American journal of human genetics 2003;72(4):804-11.
2003: Carney Regina M; Wolpert Chantelle M; Ravan Sarah A; Shahbazian Mona; Ashley-Koch Allison; Cuccaro Michael L; Vance Jeffery M; Pericak-Vance Margaret A
Identification of MeCP2 mutations in a series of females with autistic disorder.
Pediatric neurology 2003;28(3):205-11.
2003: Shao Yujun; Cuccaro M L; Hauser E R; Raiford K L; Menold M M; Wolpert C M; Ravan S A; Elston L; Decena K; Donnelly S L; Abramson R K; Wright H H; DeLong G R; Gilbert J R; Pericak-Vance M A
Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.
American journal of human genetics 2003;72(3):539-48.
2003: Barcellos L F; Oksenberg J R; Begovich A B; Martin E R; Schmidt S; Vittinghoff E; Goodin D S; Pelletier D; Lincoln R R; Bucher P; Swerdlin A; Pericak-Vance M A; Haines J L; Hauser S L;
HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course.
American journal of human genetics 2003;72(3):710-6.
2003: Cuccaro Michael L; Shao Yujun; Bass Meredyth P; Abramson Ruth K; Ravan Sarah A; Wright Harry H; Wolpert Chantelle M; Donnelly Shannon L; Pericak-Vance Margaret A
Behavioral comparisons in autistic individuals from multiplex and singleton families.
Journal of autism and developmental disorders 2003;33(1):87-91.
2003: Cuccaro Michael L; Shao Yujan; Grubber Janet; Slifer Michael; Wolpert Chantelle M; Donnelly Shannon L; Abramson Ruth K; Ravan Sarah A; Wright Harry H; DeLong G Robert; Pericak-Vance Margaret A
Factor analysis of restricted and repetitive behaviors in autism using the Autism Diagnostic Interview-R.
Child psychiatry and human development 2003;34(1):3-17.
2002: Schmidt Silke; Klaver Caroline; Saunders Ann; Postel Eric; De La Paz Monica; Agarwal Anita; Small Kent; Udar Nitin; Ong John; Chalukya Meenal; Nesburn Anthony; Kenney Cristina; Domurath Ruth; Hogan Molly; Mah Tammy; Conley Yvette; Ferrell Robert; Weeks Daniel; de Jong Paulus T V M; van Duijn Cornelia; Haines Jonathan; Pericak-Vance Margaret; Gorin Michael
A pooled case-control study of the apolipoprotein E (APOE) gene in age-related maculopathy.
Ophthalmic genetics 2002;23(4):209-23.
2002: Hauser Michael A; Conde Cecilia B; Kowaljow Valeria; Zeppa Guillermo; Taratuto Ana L; Torian Udana M; Vance Jeffery; Pericak-Vance Margaret A; Speer Marcy C; Rosa Alberto L
myotilin Mutation found in second pedigree with LGMD1A.
American journal of human genetics 2002;71(6):1428-32.
2002: Reid Evan; Kloos Mark; Ashley-Koch Allison; Hughes Lori; Bevan Simon; Svenson Ingrid K; Graham Felicia Lennon; Gaskell Perry C; Dearlove Andrew; Pericak-Vance Margaret A; Rubinsztein David C; Marchuk Douglas A
A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10).
American journal of human genetics 2002;71(5):1189-94.
2002: Speer Marcy C; Graham Felicia Lennon; Bonner Erin; Collier Keva; Stajich Jeffrey M; Gaskell Perry C; Pericak-Vance Margaret A; Vance Jeffery M
Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432.
Neurogenetics 2002;4(2):83-5.
2002: Challa P; Herndon L W; Hauser M A; Broomer B W; Pericak-Vance M A; Ababio-Danso Ben; Allingham R R
Prevalence of myocilin mutations in adults with primary open-angle glaucoma in Ghana, West Africa.
Journal of glaucoma 2002;11(5):416-20.
2002: Scott William K; Vance Jeffery M; Haines Jonathan L; Pericak-Vance Margaret A
Linkage of Parkinsonism and Alzheimer's disease with Lewy body pathology to chromosome 12.
Annals of neurology 2002;52(4):524; author reply 524.
2002: Haines Jonathan L; Bradford Yuki; Garcia Melissa E; Reed Allison D; Neumeister Elizabeth; Pericak-Vance Margaret A; Rimmler Jacqueline B; Menold Marissa M; Martin Eden R; Oksenberg Jorge R; Barcellos Lisa F; Lincoln Robin; Hauser Stephen L;
Multiple susceptibility loci for multiple sclerosis.
Human molecular genetics 2002;11(19):2251-6.
2002: Venkatesh C P; Pillai V S; Raghunath A; Prakash V S; Vathsala R; Pericak-Vance Margaret A; Kumar A
Clinical phenotype and linkage analysis of the congenital fibrosis of the extraocular muscles in an Indian family.
Molecular vision 2002;8():294-7.
2002: Neary John J; Conlon Peter J; Croke David; Dorman Anthony; Keogan Mary; Zhang Feng Yu; Vance Jeffery M; Pericak-Vance Margaret A; Scott William K; Winn Michelle P
Linkage of a gene causing familial membranoproliferative glomerulonephritis type III to chromosome 1.
Journal of the American Society of Nephrology : JASN 2002;13(8):2052-7.
2002: Li Yi-Ju; Scott William K; Hedges Dale J; Zhang Fengyu; Gaskell P Craig; Nance Martha A; Watts Ray L; Hubble Jean P; Koller William C; Pahwa Rajesh; Stern Matthew B; Hiner Bradley C; Jankovic Joseph; Allen Fred A; Goetz Christopher G; Mastaglia Frank; Stajich Jeffrey M; Gibson Rachel A; Middleton Lefkos T; Saunders Ann M; Scott Burton L; Small Gary W; Nicodemus Kristin K; Reed Allison D; Schmechel Donald E; Welsh-Bohmer Kathleen A; Conneally P Michael; Roses Allen D; Gilbert John R; Vance Jeffery M; Haines Jonathan L; Pericak-Vance Margaret A
Age at onset in two common neurodegenerative diseases is genetically controlled.
American journal of human genetics 2002;70(4):985-93.
2002: Shao Yujun; Raiford Kimberly L; Wolpert Chantelle M; Cope Heidi A; Ravan Sarah A; Ashley-Koch Allison A; Abramson Ruth K; Wright Harry H; DeLong Robert G; Gilbert John R; Cuccaro Michael L; Pericak-Vance Margaret A
Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder.
American journal of human genetics 2002;70(4):1058-61.
2002: Schmidt Silke; Barcellos Lisa F; DeSombre Karen; Rimmler Jacqueline B; Lincoln Robin R; Bucher Patricia; Saunders Ann M; Lai Eric; Martin Eden R; Vance Jeffery M; Oksenberg Jorge R; Hauser Stephen L; Pericak-Vance Margaret A; Haines Jonathan L;
Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis.
American journal of human genetics 2002;70(3):708-17.
2002: McCoy Pinky A; Shao Yujun; Wolpert Chantelle M; Donnelly Shannon L; Ashley-Koch Allison; Abel Heidi L; Ravan Sarah A; Abramson Ruth K; Wright Harry H; DeLong G Robert; Cuccaro Michael L; Gilbert John R; Pericak-Vance Margaret A
No association between the WNT2 gene and autistic disorder.
American journal of medical genetics 2002;114(1):106-9.
2002: Shao Yujun; Wolpert Chantelle M; Raiford Kimberly L; Menold Marisa M; Donnelly Shannon L; Ravan Sarah A; Bass Meredyth P; McClain Cate; von Wendt Lennart; Vance Jeffery M; Abramson Ruth H; Wright Harry H; Ashley-Koch Allison; Gilbert John R; DeLong Robert G; Cuccaro Michael L; Pericak-Vance Margaret A
Genomic screen and follow-up analysis for autistic disorder.
American journal of medical genetics 2002;114(1):99-105.
2002: Barcellos L F; Oksenberg J R; Green A J; Bucher P; Rimmler J B; Schmidt S; Garcia M E; Lincoln R R; Pericak-Vance M A; Haines J L; Hauser S L;
Genetic basis for clinical expression in multiple sclerosis.
Brain : a journal of neurology 2002;125(Pt 1):150-8.
2002: Baxter Rachel V; Ben Othmane Kamel; Rochelle Julie M; Stajich Jason E; Hulette Christine; Dew-Knight Susan; Hentati Faycal; Ben Hamida Mongi; Bel S; Stenger Judy E; Gilbert John R; Pericak-Vance Margaret A; Vance Jeffery M
Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21.
Nature genetics 2002;30(1):21-2.
2001: Jones K W; Ehm M G; Pericak-Vance M A; Haines J L; Boyd P R; Peroutka S J
Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus.
Genomics 2001;78(3):150-4.
2001: Svenson I K; Ashley-Koch A E; Pericak-Vance M A; Marchuk D A
A second leaky splice-site mutation in the spastin gene.
American journal of human genetics 2001;69(6):1407-9.
2001: Martin E R; Scott W K; Nance M A; Watts R L; Hubble J P; Koller W C; Lyons K; Pahwa R; Stern M B; Colcher A; Hiner B C; Jankovic J; Ondo W G; Allen F H; Goetz C G; Small G W; Masterman D; Mastaglia F; Laing N G; Stajich J M; Ribble R C; Booze M W; Rogala A; Hauser M A; Zhang F; Gibson R A; Middleton L T; Roses A D; Haines J L; Scott B L; Pericak-Vance M A; Vance J M
Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease.
JAMA : the journal of the American Medical Association 2001;286(18):2245-50.
2001: Scott W K; Nance M A; Watts R L; Hubble J P; Koller W C; Lyons K; Pahwa R; Stern M B; Colcher A; Hiner B C; Jankovic J; Ondo W G; Allen F H; Goetz C G; Small G W; Masterman D; Mastaglia F; Laing N G; Stajich J M; Slotterbeck B; Booze M W; Ribble R C; Rampersaud E; West S G; Gibson R A; Middleton L T; Roses A D; Haines J L; Scott B L; Vance J M; Pericak-Vance M A
Complete genomic screen in Parkinson disease: evidence for multiple genes.
JAMA : the journal of the American Medical Association 2001;286(18):2239-44.
2001: Pericak-Vance M A; Rimmler J B; Martin E R; Haines J L; Garcia M E; Oksenberg J R; Barcellos L F; Lincoln R; Goodkin D E; Hauser S L
Linkage and association analysis of chromosome 19q13 in multiple sclerosis.
Neurogenetics 2001;3(4):195-201.
2001: Yang Y; Hentati A; Deng H X; Dabbagh O; Sasaki T; Hirano M; Hung W Y; Ouahchi K; Yan J; Azim A C; Cole N; Gascon G; Yagmour A; Ben-Hamida M; Pericak-Vance M; Hentati F; Siddique T
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.
Nature genetics 2001;29(2):160-5.
2001: Nurmi E L; Bradford Y; Chen Y; Hall J; Arnone B; Gardiner M B; Hutcheson H B; Gilbert J R; Pericak-Vance M A; Copeland-Yates S A; Michaelis R C; Wassink T H; Santangelo S L; Sheffield V C; Piven J; Folstein S E; Haines J L; Sutcliffe J S
Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families.
Genomics 2001;77(1-2):105-13.
2001: Barcellos L F; Caillier S; Dragone L; Elder M; Vittinghoff E; Bucher P; Lincoln R R; Pericak-Vance M; Haines J L; Weiss A; Hauser S L; Oksenberg J R
PTPRC (CD45) is not associated with the development of multiple sclerosis in U.S. patients.
Nature genetics 2001;29(1):23-4.
2001: Rampoldi L; Dobson-Stone C; Rubio J P; Danek A; Chalmers R M; Wood N W; Verellen C; Ferrer X; Malandrini A; Fabrizi G M; Brown R; Vance J; Pericak-Vance M; Rudolf G; Carrè S; Alonso E; Manfredi M; Németh A H; Monaco A P
A conserved sorting-associated protein is mutant in chorea-acanthocytosis.
Nature genetics 2001;28(2):119-20.
2001: Pericak-Vance M A
Overview of linkage analysis in complex traits.
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2001;Chapter 1():Unit 1.9.
2001: Pericak-Vance M A
Analysis of genetic linkage data for Mendelian traits.
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2001;Chapter 1():Unit 1.4.
2001: Green A J; Barcellos L F; Rimmler J B; Garcia M E; Caillier S; Lincoln R R; Bucher P; Pericak-Vance M A; Haines J L; Hauser S L; Oksenberg J R;
Sequence variation in the transforming growth factor-beta1 (TGFB1) gene and multiple sclerosis susceptibility.
Journal of neuroimmunology 2001;116(1):116-24.
2001: Svenson I K; Ashley-Koch A E; Gaskell P C; Riney T J; Cumming W J; Kingston H M; Hogan E L; Boustany R M; Vance J M; Nance M A; Pericak-Vance M A; Marchuk D A
Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia.
American journal of human genetics 2001;68(5):1077-85.
2001: Wolpert C M; Donnelly S L; Cuccaro M L; Hedges D J; Poole C P; Wright H H; Gilbert J R; Pericak-Vance M A
De novo partial duplication of chromosome 7p in a male with autistic disorder.
American journal of medical genetics 2001;105(3):222-5.
2001: Ashley-Koch A; Bonner E R; Gaskell P C; West S G; Tim R; Wolpert C M; Jones R; Farrell C D; Nance M; Svenson I K; Marchuk D A; Boustany R M; Vance J M; Scott W K; Pericak-Vance M A
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.
Neurogenetics 2001;3(2):91-7.
2001: Allingham R R; Seo B; Rampersaud E; Bembe M; Challa P; Liu N; Parrish T; Karolak L; Gilbert J; Pericak-Vance M A; Klintworth G K; Vance J M
A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis.
American journal of human genetics 2001;68(2):491-4.
2001: Menold M M; Shao Y; Wolpert C M; Donnelly S L; Raiford K L; Martin E R; Ravan S A; Abramson R K; Wright H H; Delong G R; Cuccaro M L; Pericak-Vance M A; Gilbert J R
Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder.
Journal of neurogenetics 2001;15(3-4):245-59.
2001: Schmidt S; Shao Y; Hauser E R; Slifer S H; Martin E R; Scott W K; Speer M C; Pericak-Vance M A
Life after the screen: making sense of many P-values.
Genetic epidemiology 2001;21 Suppl 1():S546-51.
2000: Schmidt S; Saunders A M; De La Paz MA; Postel E A; Heinis R M; Agarwal A; Scott W K; Gilbert J R; McDowell J G; Bazyk A; Gass J D; Haines J L; Pericak-Vance M A
Association of the apolipoprotein E gene with age-related macular degeneration: possible effect modification by family history, age, and gender.
Molecular vision 2000;6():287-93.
2000: Pericak-Vance M A; Grubber J; Bailey L R; Hedges D; West S; Santoro L; Kemmerer B; Hall J L; Saunders A M; Roses A D; Small G W; Scott W K; Conneally P M; Vance J M; Haines J L
Identification of novel genes in late-onset Alzheimer's disease.
Experimental gerontology 2000;35(9-10):1343-52.
2000: Hosler B A; Siddique T; Sapp P C; Sailor W; Huang M C; Hossain A; Daube J R; Nance M; Fan C; Kaplan J; Hung W Y; McKenna-Yasek D; Haines J L; Pericak-Vance M A; Horvitz H R; Brown R H
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22.
JAMA : the journal of the American Medical Association 2000;284(13):1664-9.
2000: Hauser E R; Pericak-Vance M A
Genetic analysis for common complex disease.
American heart journal 2000;140(4):S36-44.
2000: Hauser M A; Horrigan S K; Salmikangas P; Torian U M; Viles K D; Dancel R; Tim R W; Taivainen A; Bartoloni L; Gilchrist J M; Stajich J M; Gaskell P C; Gilbert J R; Vance J M; Pericak-Vance M A; Carpen O; Westbrook C A; Speer M C
Myotilin is mutated in limb girdle muscular dystrophy 1A.
Human molecular genetics 2000;9(14):2141-7.
2000: Rosenberg C K; Pericak-Vance M A; Saunders A M; Gilbert J R; Gaskell P C; Hulette C M
Lewy body and Alzheimer pathology in a family with the amyloid-beta precursor protein APP717 gene mutation.
Acta neuropathologica 2000;100(2):145-52.
2000: Bookheimer S Y; Strojwas M H; Cohen M S; Saunders A M; Pericak-Vance M A; Mazziotta J C; Small G W
Patterns of brain activation in people at risk for Alzheimer's disease.
The New England journal of medicine 2000;343(7):450-6.
2000: Martin E R; Lai E H; Gilbert J R; Rogala A R; Afshari A J; Riley J; Finch K L; Stevens J F; Livak K J; Slotterbeck B D; Slifer S H; Warren L L; Conneally P M; Schmechel D E; Purvis I; Pericak-Vance M A; Roses A D; Vance J M
SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease.
American journal of human genetics 2000;67(2):383-94.
2000: Liao H X; Montefiori D C; Patel D D; Lee D M; Scott W K; Pericak-Vance M; Haynes B F
Linkage of the CCR5 Delta 32 mutation with a functional polymorphism of CD45RA.
Journal of immunology (Baltimore, Md. : 1950) 2000;165(1):148-57.
2000: Wolpert C M; Menold M M; Bass M P; Qumsiyeh M B; Donnelly S L; Ravan S A; Vance J M; Gilbert J R; Abramson R K; Wright H H; Cuccaro M L; Pericak-Vance M A
Three probands with autistic disorder and isodicentric chromosome 15.
American journal of medical genetics 2000;96(3):365-72.
2000: Donnelly S L; Wolpert C M; Menold M M; Bass M P; Gilbert J R; Cuccaro M L; Delong G R; Pericak-Vance M A
Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome.
American journal of medical genetics 2000;96(3):312-6.
2000: Nance M A; Nuttall F Q; Econs M J; Lyles K W; Viles K D; Vance J M; Pericak-Vance M A; Speer M C
Heterogeneity in Paget disease of the bone.
American journal of medical genetics 2000;92(5):303-7.
2000: Small G W; Ercoli L M; Silverman D H; Huang S C; Komo S; Bookheimer S Y; Lavretsky H; Miller K; Siddarth P; Rasgon N L; Mazziotta J C; Saxena S; Wu H M; Mega M S; Cummings J L; Saunders A M; Pericak-Vance M A; Roses A D; Barrio J R; Phelps M E
Cerebral metabolic and cognitive decline in persons at genetic risk for Alzheimer's disease.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(11):6037-42.
2000: Gilbert J R; Kumar A; Newey S; Rao N; Ioannou P; Qiu H; Lin D; Xu P; Pettenati M J; Pericak-Vance M A
Physical and cDNA mapping in the DBH region of human chromosome 9q34.
Human heredity 2000;50(3):151-7.
2000: Barcellos L F; Schito A M; Rimmler J B; Vittinghoff E; Shih A; Lincoln R; Callier S; Elkins M K; Goodkin D E; Haines J L; Pericak-Vance M A; Hauser S L; Oksenberg J R
CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis. Multiple Sclerosis Genetics Group.
Immunogenetics 2000;51(4-5):281-8.
2000: Wiggs J L; Allingham R R; Hossain A; Kern J; Auguste J; DelBono E A; Broomer B; Graham F L; Hauser M; Pericak-Vance M; Haines J L
Genome-wide scan for adult onset primary open angle glaucoma.
Human molecular genetics 2000;9(7):1109-17.
2000: Bass M P; Menold M M; Wolpert C M; Donnelly S L; Ravan S A; Hauser E R; Maddox L O; Vance J M; Abramson R K; Wright H H; Gilbert J R; Cuccaro M L; DeLong G R; Pericak-Vance M A
Genetic studies in autistic disorder and chromosome 15.
Neurogenetics 2000;2(4):219-26.
2000: Scott W K; Grubber J M; Conneally P M; Small G W; Hulette C M; Rosenberg C K; Saunders A M; Roses A D; Haines J L; Pericak-Vance M A
Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: potential genetic and phenotypic heterogeneity.
American journal of human genetics 2000;66(3):922-32.
2000: Wolpert C; Pericak-Vance M A; Abramson R K; Wright H H; Cuccaro M L
Autistic symptoms among children and young adults with isodicentric chromosome 15.
American journal of medical genetics 2000;96(1):128-9.
2000: Martin E R; Menold M M; Wolpert C M; Bass M P; Donnelly S L; Ravan S A; Zimmerman A; Gilbert J R; Vance J M; Maddox L O; Wright H H; Abramson R K; DeLong G R; Cuccaro M L; Pericak-Vance M A
Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.
American journal of medical genetics 2000;96(1):43-8.
2000: Melvin E C; George T M; Worley G; Franklin A; Mackey J; Viles K; Shah N; Drake C R; Enterline D S; McLone D; Nye J; Oakes W J; McLaughlin C; Walker M L; Peterson P; Brei T; Buran C; Aben J; Ohm B; Bermans I; Qumsiyeh M; Vance J; Pericak-Vance M A; Speer M C
Genetic studies in neural tube defects. NTD Collaborative Group.
Pediatric neurosurgery 2000;32(1):1-9.
2000: Martin E R; Gilbert J R; Lai E H; Riley J; Rogala A R; Slotterbeck B D; Sipe C A; Grubber J M; Warren L L; Conneally P M; Saunders A M; Schmechel D E; Purvis I; Pericak-Vance M A; Roses A D; Vance J M
Analysis of association at single nucleotide polymorphisms in the APOE region.
Genomics 2000;63(1):7-12.
1999: Othmane K B; Johnson E; Menold M; Graham F L; Hamida M B; Hasegawa O; Rogala A D; Ohnishi A; Pericak-Vance M; Hentati F; Vance J M
Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15.
Genomics 1999;62(3):344-9.
1999: Maddox L O; Menold M M; Bass M P; Rogala A R; Pericak-Vance M A; Vance J M; Gilbert J R
Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig.
Genomics 1999;62(3):325-31.
1999: Small K W; Udar N; Yelchits S; Klein R; Garcia C; Gallardo G; Puech B; Puech V; Saperstein D; Lim J; Haller J; Flaxel C; Kelsell R; Hunt D; Evans K; Lennon F; Pericak-Vance M
North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysis.
Molecular vision 1999;5():38.
1999: Fontaine B; Cournu I; Arnaud I; Babron M C; Eichenbaum-Voline S; Oksenberg J R; Pericak-Vance M A; Haines J L; Semama G; Liblau R; Lyon-Caen O; Clerget-Darpoux F; Clanet M; Hauser S L
Chromosome 17q22-q24 and multiple sclerosis genetic susceptibility. American-French Multiple Sclerosis Genetic Group.
Genes and immunity 1999;1(2):149-50.
1999: Conlon P J; Lynn K; Winn M P; Quarles L D; Bembe M L; Pericak-Vance M; Speer M; Howell D N
Spectrum of disease in familial focal and segmental glomerulosclerosis.
Kidney international 1999;56(5):1863-71.
1999: Ashley-Koch A; Wolpert C M; Menold M M; Zaeem L; Basu S; Donnelly S L; Ravan S A; Powell C M; Qumsiyeh M B; Aylsworth A S; Vance J M; Gilbert J R; Wright H H; Abramson R K; DeLong G R; Cuccaro M L; Pericak-Vance M A
Genetic studies of autistic disorder and chromosome 7.
Genomics 1999;61(3):227-36.
1999: Messiaen L M; Callens T; Roux K J; Mortier G R; De Paepe A; Abramowicz M; Pericak-Vance M A; Vance J M; Wallace M R
Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicing.
Genetics in medicine : official journal of the American College of Medical Genetics 1999;1(6):248-53.
1999: Scott W K; Yamaoka L H; Stajich J M; Scott B L; Vance J M; Roses A D; Pericak-Vance M A; Watts R L; Nance M; Hubble J; Koller W; Stern M B; Colcher A; Allen F H; Hiner B C; Jankovic J; Ondo W; Laing N G; Mastaglia F; Goetz C; Pappert E; Small G W; Masterman D; Haines J L; Davies T L
The alpha-synuclein gene is not a major risk factor in familial Parkinson disease.
Neurogenetics 1999;2(3):191-2.
1999: Small G W; Scott W K; Komo S; Yamaoka L H; Farrer L A; Auerbach S H; Saunders A M; Roses A D; Haines J L; Pericak-Vance M A
No association between the HLA-A2 allele and Alzheimer disease.
Neurogenetics 1999;2(3):177-82.
1999: Seboun E; Oksenberg J R; Rombos A; Usuku K; Goodkin D E; Lincoln R R; Wong M; Pham-Dinh D; Boesplug-Tanguy O; Carsique R; Fitoussi R; Gartioux C; Reyes C; Ribierre F; Faure S; Fizames C; Gyapay G; Weissenbach J; Dautigny A; Rimmler J B; Garcia M E; Pericak-Vance M A; Haines J L; Hauser S L
Linkage analysis of candidate myelin genes in familial multiple sclerosis.
Neurogenetics 1999;2(3):155-62.
1999: Hulette C M; Pericak-Vance M A; Roses A D; Schmechel D E; Yamaoka L H; Gaskell P C; Welsh-Bohmer K A; Crowther R A; Spillantini M G
Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke Family 1684.
Journal of neuropathology and experimental neurology 1999;58(8):859-66.
1999: De La Paz M A; Guy V K; Abou-Donia S; Heinis R; Bracken B; Vance J M; Gilbert J R; Gass J D; Haines J L; Pericak-Vance M A
Analysis of the Stargardt disease gene (ABCR) in age-related macular degeneration.
Ophthalmology 1999;106(8):1531-6.
1999: Grubber J M; Saunders A M; Crane-Gatherum A R; Scott W K; Martin E R; Haynes C S; Conneally P M; Small G W; Roses A D; Haines J L; Pericak-Vance M A
Analysis of association between Alzheimer disease and the K variant of butyrylcholinesterase (BCHE-K).
Neuroscience letters 1999;269(2):115-9.
1999: Small G W; Chen S T; Komo S; Ercoli L; Bookheimer S; Miller K; Lavretsky H; Saxena S; Kaplan A; Dorsey D; Scott W K; Saunders A M; Haines J L; Roses A D; Pericak-Vance M A
Memory self-appraisal in middle-aged and older adults with the apolipoprotein E-4 allele.
The American journal of psychiatry 1999;156(7):1035-8.
1999: Winn M P; Conlon P J; Lynn K L; Howell D N; Slotterbeck B D; Smith A H; Graham F L; Bembe M; Quarles L D; Pericak-Vance M A; Vance J M
Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity.
Genomics 1999;58(2):113-20.
1999: Rogaeva E A; Premkumar S; Grubber J; Serneels L; Scott W K; Kawarai T; Song Y; Hill D L; Abou-Donia S M; Martin E R; Vance J J; Yu G; Orlacchio A; Pei Y; Nishimura M; Supala A; Roberge B; Saunders A M; Roses A D; Schmechel D; Crane-Gatherum A; Sorbi S; Bruni A; Small G W; Conneally P M; Haines J L; Van Leuven F; St George-Hyslop P H; Farrer L A; Pericak-Vance M A
An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease.
Nature genetics 1999;22(1):19-22.
1999: Winn M P; Conlon P J; Lynn K L; Howell D N; Gross D A; Rogala A R; Smith A H; Graham F L; Bembe M; Quarles L D; Pericak-Vance M A; Vance J M
Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis. International Collaborative Group for the Study of Familial Focal Segmental Glomerulosclerosis.
Kidney international 1999;55(4):1241-6.
1999: Scott W K; Grubber J M; Abou-Donia S M; Church T D; Saunders A M; Roses A D; Pericak-Vance M A; Conneally P M; Small G W; Haines J L
Further evidence linking late-onset Alzheimer disease with chromosome 12.
JAMA : the journal of the American Medical Association 1999;281(6):513-4.
1999: Speer M C; Vance J M; Grubber J M; Lennon Graham F; Stajich J M; Viles K D; Rogala A; McMichael R; Chutkow J; Goldsmith C; Tim R W; Pericak-Vance M A
Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7.
American journal of human genetics 1999;64(2):556-62.
1999: Anderson J L; Khan M; David W S; Mahdavi Z; Nuttall F Q; Krech E; West S G; Vance J M; Pericak-Vance M A; Nance M A
Confirmation of linkage of hereditary partial lipodystrophy to chromosome 1q21-22.
American journal of medical genetics 1999;82(2):161-5.
1999: Haines J L; Pericak-Vance M A
Genetics of multiple sclerosis.
Current directions in autoimmunity 1999;1():273-88.
1999: Anderson J L; Hauser E R; Martin E R; Scott W K; Ashley-Koch A; Kim K J; Monks S A; Haynes C S; Speer M C; Pericak-Vance M A
Complete genomic screen for disease susceptibility loci in nuclear families.
Genetic epidemiology 1999;17 Suppl 1():S473-8.
1998: Lavedan C; Buchholtz S; Auburger G; Albin R L; Athanassiadou A; Blancato J; Burguera J A; Ferrell R E; Kostic V; Leroy E; Leube B; Mota-Vieira L; Papapetropoulos T; Pericak-Vance M A; Pinkus J; Scott W K; Ulm G; Vasconcelos J; Vilchez J J; Nussbaum R L; Polymeropoulos M H
Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease.
DNA research : an international journal for rapid publication of reports on genes and genomes 1998;5(6):401-2.
1998: Hentati A; Ouahchi K; Pericak-Vance M A; Nijhawan D; Ahmad A; Yang Y; Rimmler J; Hung W; Schlotter B; Ahmed A; Ben Hamida M; Hentati F; Siddique T
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers.
Neurogenetics 1998;2(1):55-60.
1998: Ben Othmane K; Rochelle J M; Ben Hamida M; Slotterbeck B; Rao N; Hentati F; Pericak-Vance M A; Vance J M
Fine localization of the CMT4A locus using a PAC contig and haplotype analysis.
Neurogenetics 1998;2(1):18-23.
1998: Bartoloni L; Horrigan S K; Viles K D; Gilchrist J M; Stajich J M; Vance J M; Yamaoka L H; Pericak-Vance M A; Westbrook C A; Speer M C
Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31.
Genomics 1998;54(2):250-5.
1998: Farrer L A; Abraham C R; Haines J L; Rogaeva E A; Song Y; McGraw W T; Brindle N; Premkumar S; Scott W K; Yamaoka L H; Saunders A M; Roses A D; Auerbach S A; Sorbi S; Duara R; Pericak-Vance M A; St George-Hyslop P H
Association between bleomycin hydrolase and Alzheimer's disease in caucasians.
Annals of neurology 1998;44(5):808-11.
1998: Menold M M; Sadeh M; Lennon F; Blatt I; Goldhammer Y; Yamaoka L H; Vance J M; Pericak-Vance M A
Evidence for genetic heterogeneity supports clinical differences in congenital myasthenic syndromes.
Human heredity 1998;48(6):325-32.
1998: Allingham R R; Wiggs J L; De La Paz M A; Vollrath D; Tallett D A; Broomer B; Jones K H; Del Bono E A; Kern J; Patterson K; Haines J L; Pericak-Vance M A
Gln368STOP myocilin mutation in families with late-onset primary open-angle glaucoma.
Investigative ophthalmology & visual science 1998;39(12):2288-95.
1998: Wiggs J L; Allingham R R; Vollrath D; Jones K H; De La Paz M; Kern J; Patterson K; Babb V L; Del Bono E A; Broomer B W; Pericak-Vance M A; Haines J L
Prevalence of mutations in TIGR/Myocilin in patients with adult and juvenile primary open-angle glaucoma.
American journal of human genetics 1998;63(5):1549-52.
1998: Allingham R R; Wiggs J L; Damji K F; Herndon L; Youn J; Tallett D A; Jones K H; Del Bono E A; Reardon M; Haines J L; Pericak-Vance M A
Adult-onset primary open angle glaucoma does not localize to chromosome 2cen-q13 in North American families.
Human heredity 1998;48(5):251-5.
1998: Liu N P; Baldwin J; Jonasson F; Dew-Knight S; Stajich J M; Lennon F; Pericak-Vance M A; Klintworth G K; Vance J M
Haplotype analysis in Icelandic families defines a minimal interval for the macular corneal dystrophy type I gene.
American journal of human genetics 1998;63(3):912-7.
1998: Gilbert J R; Guy V; Kumar A; Wolpert C; Kandt R; Aylesworth A; Roses A D; Pericak-Vance M A
Mutation and polymorphism analysis in the tuberous sclerosis 2 (TSC2) gene.
Neurogenetics 1998;1(4):267-72.
1998: Haines J L; Terwedow H A; Burgess K; Pericak-Vance M A; Rimmler J B; Martin E R; Oksenberg J R; Lincoln R; Zhang D Y; Banatao D R; Gatto N; Goodkin D E; Hauser S L
Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group.
Human molecular genetics 1998;7(8):1229-34.
1998: Bass M P; Yamaoka L H; Scott W K; Gaskell P C; Welsh-Bohmer K A; Roses A D; Saunders A M; Haines J L; Pericak-Vance M A
No association of alpha1-antichymotrypsin flanking region polymorphism and Alzheimer disease risk in early- and late-onset Alzheimer disease patients.
Neuroscience letters 1998;250(2):79-82.
1998: Speer M C; Vance J M; Lennon-Graham F; Stajich J M; Viles K D; Gilchrist J M; Nigro V; McMichael R; Chutkow J G; Bartoloni L; Horrigan S K; Westbrook C A; Pericak-Vance M A
Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families.
Human heredity 1998;48(4):179-84.
1998: Nance M A; Raabe W A; Midani H; Kolodny E H; David W S; Megna L; Pericak-Vance M A; Haines J L
Clinical heterogeneity of familial spastic paraplegia linked to chromosome 2p21.
Human heredity 1998;48(3):169-78.
1998: Pan T C; Zhang R Z; Pericak-Vance M A; Tandan R; Fries T; Stajich J M; Viles K; Vance J M; Chu M L; Speer M C
Missense mutation in a von Willebrand factor type A domain of the alpha 3(VI) collagen gene (COL6A3) in a family with Bethlem myopathy.
Human molecular genetics 1998;7(5):807-12.
1998: Speer M C; Gilchrist J M; Stajich J M; Gaskell P C; Westbrook C A; Horrigan S K; Bartoloni L; Yamaoka L H; Scott W K; Pericak-Vance M A
Evidence for anticipation in autosomal dominant limb-girdle muscular dystrophy.
Journal of medical genetics 1998;35(4):305-8.
1998: Ikeuchi T; Sanpei K; Takano H; Sasaki H; Tashiro K; Cancel G; Brice A; Bird T D; Schellenberg G D; Pericak-Vance M A; Welsh-Bohmer K A; Clark L N; Wilhelmsen K; Tsuji S
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17q.
Genomics 1998;49(2):321-6.
1998: Falk C T; Gilchrist J M; Pericak-Vance M A; Speer M C
Using neural networks as an aid in the determination of disease status: comparison of clinical diagnosis to neural-network predictions in a pedigree with autosomal dominant limb-girdle muscular dystrophy.
American journal of human genetics 1998;62(4):941-9.
1998: Siddique T; Pericak-Vance M A; Caliendo J; Hong S T; Hung W Y; Kaplan J; McKenna-Yasek D; Rimmler J B; Sapp P; Saunders A M; Scott W K; Siddique N; Haines J L; Brown R H
Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis.
Neurogenetics 1998;1(3):213-6.
1998: Scott W K; Yamaoka L H; Bass M P; Gaskell P C; Conneally P M; Small G W; Farrer L A; Auerbach S A; Saunders A M; Roses A D; Haines J L; Pericak-Vance M A
No genetic association between the LRP receptor and sporadic or late-onset familial Alzheimer disease.
Neurogenetics 1998;1(3):179-83.
1998: Liu N P; Baldwin J; Lennon F; Stajich J M; Thonar E J; Pericak-Vance M A; Klintworth G K; Vance J M
Coexistence of macular corneal dystrophy types I and II in a single sibship.
The British journal of ophthalmology 1998;82(3):241-4.
1998: Damji K F; Gallione C J; Allingham R R; Slotterbeck B; Guttmacher A E; Pasyk K A; Vance J M; Pericak-Vance M A; Speer M C; Marchuk D A
Quantitative DNA pooling to increase the efficiency of linkage analysis in autosomal dominant disease.
Human genetics 1998;102(2):207-12.
1998: Pericak-Vance M A; Bass M L; Yamaoka L H; Gaskell P C; Scott W K; Terwedow H A; Menold M M; Conneally P M; Small G W; Saunders A M; Roses A D; Haines J L
Complete genomic screen in late-onset familial Alzheimer's disease.
Neurobiology of aging 1998;19(1 Suppl):S39-42.
1997: Stajich J M; Gilchrist J M; Lennon F; Lee A; Yamaoka L; Rosi B; Gaskell P C; Pritchard M; Donald L; Roses A D; Vance J M; Pericak-Vance M A
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation.
Neuromuscular disorders : NMD 1997;7 Suppl 1():S75-81.
1997: Messina D N; Speer M C; Pericak-Vance M A; McNally E M
Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23.
American journal of human genetics 1997;61(4):909-17.
1997: Rubio J P; Danek A; Stone C; Chalmers R; Wood N; Verellen C; Ferrer X; Malandrini A; Fabrizi G M; Manfredi M; Vance J; Pericak-Vance M; Brown R; Rudolf G; Picard F; Alonso E; Brin M; Németh A H; Farrall M; Monaco A P
Chorea-acanthocytosis: genetic linkage to chromosome 9q21.
American journal of human genetics 1997;61(4):899-908.
1997: Farrer L A; Cupples L A; Haines J L; Hyman B; Kukull W A; Mayeux R; Myers R H; Pericak-Vance M A; Risch N; van Duijn C M
Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium.
JAMA : the journal of the American Medical Association 1997;278(16):1349-56.
1997: Pericak-Vance M A; Bass M P; Yamaoka L H; Gaskell P C; Scott W K; Terwedow H A; Menold M M; Conneally P M; Small G W; Vance J M; Saunders A M; Roses A D; Haines J L
Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12.
JAMA : the journal of the American Medical Association 1997;278(15):1237-41.
1997: Speer M C; Pericak-Vance M A; Stajich J M; Sarrica J; Jordan M; Roses A D; Vance J M; Gilbert J R
Further exclusion of FSHD1B from the telomeric region of 10q.
Neurogenetics 1997;1(2):151-2.
1997: Scott W K; Gaskell P C; Lennon F; Wolpert C M; Menold M M; Aylsworth A S; Warner C; Farrell C D; Boustany R M; Albright S G; Boyd E; Kingston H M; Cumming W J; Vance J M; Pericak-Vance M A
Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia.
Neurogenetics 1997;1(2):95-102.
1997: Pericak-Vance M A; Speer M C; Lennon F; West S G; Menold M M; Stajich J M; Wolpert C M; Slotterbeck B D; Saito M; Tim R W; Rozear M P; Middleton L T; Tsuji S; Vance J M
Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity.
Neurogenetics 1997;1(2):89-93.
1997: De la Paz M A; Pericak-Vance M A; Haines J L; Seddon J M
Phenotypic heterogeneity in families with age-related macular degeneration.
American journal of ophthalmology 1997;124(3):331-43.
1997: Scott W K; Saunders A M; Gaskell P C; Locke P A; Growdon J H; Farrer L A; Auerbach S A; Roses A D; Haines J L; Pericak-Vance M A
Apolipoprotein E epsilon2 does not increase risk of early-onset sporadic Alzheimer's disease.
Annals of neurology 1997;42(3):376-8.
1997: Scott W K; Staijich J M; Yamaoka L H; Speer M C; Vance J M; Roses A D; Pericak-Vance M A
Genetic complexity and Parkinson's disease. Deane Laboratory Parkinson Disease Research Group.
Science (New York, N.Y.) 1997;277(5324):387-8; author reply 389.
1997: Povey S; Attwood J; Chadwick B; Frezal J; Haines J L; Knowles M; Kwiatkowski D J; Olopade O I; Slaugenhaupt S; Spurr N K; Smith M; Steel K; White J A; Pericak-Vance M A
Report on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4-6, 1996.
Annals of human genetics 1997;61(Pt 3):183-206.
1997: De La Paz M A; Pericak-Vance M A; Lennon F; Haines J L; Seddon J M
Exclusion of TIMP3 as a candidate locus in age-related macular degeneration.
Investigative ophthalmology & visual science 1997;38(6):1060-5.
1997: Small G W; Noble E P; Matsuyama S S; Jarvik L F; Komo S; Kaplan A; Ritchie T; Pritchard M L; Saunders A M; Conneally P M; Roses A D; Haines J L; Pericak-Vance M A
D2 dopamine receptor A1 allele in Alzheimer disease and aging.
Archives of neurology 1997;54(3):281-5.
1997: Scott W K; Pericak-Vance M A; Haines J L
Genetic analysis of complex diseases.
Science (New York, N.Y.) 1997;275(5304):1327; author reply 1329-30.
1997: Raskind W H; Pericak-Vance M A; Lennon F; Wolff J; Lipe H P; Bird T D
Familial spastic paraparesis: evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2.
American journal of medical genetics 1997;74(1):26-36.
1997: Juneja T; Pericak-Vance M A; Laing N G; Dave S; Siddique T
Prognosis in familial amyotrophic lateral sclerosis: progression and survival in patients with glu100gly and ala4val mutations in Cu,Zn superoxide dismutase.
Neurology 1997;48(1):55-7.
1997: Scott W K; Speer M C; Leal S M; Brzustowicz L M; Haynes C S; Pericak-Vance M A
False positive rates in a genomic screen for complex quantitative traits.
Genetic epidemiology 1997;14(6):891-6.
1997: Scott W K; Yamaoka L H; Locke P A; Rosi B L; Gaskell P C; Saunders A M; Conneally P M; Small G W; Farrer L A; Growdon J H; Roses A D; Pericak-Vance M A; Haines J L
No association or linkage between an intronic polymorphism of presenilin-1 and sporadic or late-onset familial Alzheimer disease.
Genetic epidemiology 1997;14(3):307-15.
1997: Kumar A; Kandt R S; Wolpert C; Roses A D; Pericak-Vance M A; Gilbert J R
A novel splice site mutation (156 + 1G-->A) in the TSC2 gene.
Human mutation 1997;9(1):64-5.
1996: Small G W; Komo S; La Rue A; Saxena S; Phelps M E; Mazziotta J C; Saunders A M; Haines J L; Pericak-Vance M A; Roses A D
Early detection of Alzheimer's disease by combining apolipoprotein E and neuroimaging.
Annals of the New York Academy of Sciences 1996;802():70-8.
1996: Haines J L; Pritchard M L; Saunders A M; Schildkraut J M; Growdon J H; Gaskell P C; Farrer L A; Auerbach S A; Gusella J F; Locke P A; Rosi B L; Yamaoka L; Small G W; Conneally P M; Roses A D; Pericak-Vance M
No association between alpha 1-antichymotrypsin and familial Alzheimer's disease.
Annals of the New York Academy of Sciences 1996;802():35-41.
1996: Yamaoka L H; Welsh-Bohmer K A; Hulette C M; Gaskell P C; Murray M; Rimmler J L; Helms B R; Guerra M; Roses A D; Schmechel D E; Pericak-Vance M A
Linkage of frontotemporal dementia to chromosome 17: clinical and neuropathological characterization of phenotype.
American journal of human genetics 1996;59(6):1306-12.
1996: Stajich J M; Gilchrist J M; Lennon F; Lee A; Yamaoka L; Helms B; Gaskell P C; Donald L; Roses A D; Vance J M; Pericak-Vance M A
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13.
Annals of neurology 1996;40(5):801-4.
1996: Isozumi K; DeLong R; Kaplan J; Deng H X; Iqbal Z; Hung W Y; Wilhelmsen K C; Hentati A; Pericak-Vance M A; Siddique T
Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31.
Human molecular genetics 1996;5(9):1377-82.
1996: Okuizumi K; Onodera O; Seki K; Tanaka H; Namba Y; Ikeda K; Saunders A M; Pericak-Vance M A; Roses A D; Tsuji S
Lack of association of very low density lipoprotein receptor gene polymorphism with Caucasian Alzheimer's disease.
Annals of neurology 1996;40(2):251-4.
1996: Xia Y; Rohan de Silva H A; Rosi B L; Yamaoka L H; Rimmler J B; Pericak-Vance M A; Roses A D; Chen X; Masliah E; DeTeresa R; Iwai A; Sundsmo M; Thomas R G; Hofstetter C R; Gregory E; Hansen L A; Katzman R; Thal L J; Saitoh T
Genetic studies in Alzheimer's disease with an NACP/alpha-synuclein polymorphism.
Annals of neurology 1996;40(2):207-15.
1996: Haines J L; Ter-Minassian M; Bazyk A; Gusella J F; Kim D J; Terwedow H; Pericak-Vance M A; Rimmler J B; Haynes C S; Roses A D; Lee A; Shaner B; Menold M; Seboun E; Fitoussi R P; Gartioux C; Reyes C; Ribierre F; Gyapay G; Weissenbach J; Hauser S L; Goodkin D E; Lincoln R; Usuku K; Oksenberg J R
A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group.
Nature genetics 1996;13(4):469-71.
1996: Speer M C; Tandan R; Rao P N; Fries T; Stajich J M; Bolhuis P A; Jöbsis G J; Vance J M; Viles K D; Sheffield K; James C; Kahler S G; Pettenati M; Gilbert J R; Denton P H; Yamaoka L H; Pericak-Vance M A
Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37.
Human molecular genetics 1996;5(7):1043-6.
1996: Small K W; Pollock S C; Vance J M; Stajich J M; Pericak-Vance M
Ocular motility in North Carolina autosomal dominant ataxia.
Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society 1996;16(2):91-5.
1996: Scott W K; Roses A D; Haines J L; Pericak-Vance M A
Presenilin-1 polymorphism and Alzheimer's disease.
Lancet 1996;347(9014):1560.
1996: Pericak-Vance M A; Johnson C C; Rimmler J B; Saunders A M; Robinson L C; D'Hondt E G; Jackson C E; Haines J L
Alzheimer's disease and apolipoprotein E-4 allele in an Amish population.
Annals of neurology 1996;39(6):700-4.
1996: Fink J K; Heiman-Patterson T; Bird T; Cambi F; Dubé M P; Figlewicz D A; Fink J K; Haines J L; Heiman-Patterson T; Hentati A; Pericak-Vance M A; Raskind W; Rouleau G A; Siddique T
Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group.
Neurology 1996;46(6):1507-14.
1996: Johnson D W; Berg J N; Baldwin M A; Gallione C J; Marondel I; Yoon S J; Stenzel T T; Speer M; Pericak-Vance M A; Diamond A; Guttmacher A E; Jackson C E; Attisano L; Kucherlapati R; Porteous M E; Marchuk D A
Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.
Nature genetics 1996;13(2):189-95.
1996: Pritchard M L; Saunders A M; Gaskell P C; Small G W; Conneally P M; Rosi B; Yamaoka L H; Roses A D; Haines J L; Pericak-Vance M A
No association between very low density lipoprotein receptor (VLDL-R) and Alzheimer disease in American Caucasians.
Neuroscience letters 1996;209(2):105-8.
1996: Damji K F; Allingham R R; Pollock S C; Small K; Lewis K E; Stajich J M; Yamaoka L H; Vance J M; Pericak-Vance M A
Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias.
Archives of neurology 1996;53(4):338-44.
1996: Vance J M; Jonasson F; Lennon F; Sarrica J; Damji K F; Stauffer J; Pericak-Vance M A; Klintworth G K
Linkage of a gene for macular corneal dystrophy to chromosome 16.
American journal of human genetics 1996;58(4):757-62.
1996: Haines J L; Pritchard M L; Saunders A M; Schildkraut J M; Growdon J H; Gaskell P C; Farrer L A; Auerbach S A; Gusella J F; Locke P A; Rosi B L; Yamaoka L; Small G W; Conneally P M; Roses A D; Pericak-Vance M A
No genetic effect of alpha1-antichymotrypsin in Alzheimer disease.
Genomics 1996;33(1):53-6.
1996: Scott W K; Growdon J H; Roses A D; Haines J L; Pericak-Vance M A
Presenilin-1 polymorphism and Alzheimer's disease.
Lancet 1996;347(9009):1186-7.
1996: Roses A D; Einstein G; Gilbert J; Goedert M; Han S H; Huang D; Hulette C; Masliah E; Pericak-Vance M A; Saunders A M; Schmechel D E; Strittmatter W J; Weisgraber K H; Xi P T
Morphological, biochemical, and genetic support for an apolipoprotein E effect on microtubular metabolism.
Annals of the New York Academy of Sciences 1996;777():146-57.
1996: Wiggs J L; Damji K F; Haines J L; Pericak-Vance M A; Allingham R R
The distinction between juvenile and adult-onset primary open-angle glaucoma.
American journal of human genetics 1996;58(1):243-4.
1995: Kumar A; Kandt R S; Wolpert C; Roses A D; Pericak-Vance M A; Gilbert J R
Mutation analysis of the TSC2 gene in an African-American family.
Human molecular genetics 1995;4(12):2295-8.
1995: Pericak-Vance M A; Haines J L
Genetic susceptibility to Alzheimer disease.
Trends in genetics : TIG 1995;11(12):504-8.
1995: Speer M C; Yamaoka L H; Stajich J; Lewis K; Pericak-Vance M A; Stacy R; Tandan R; Fries T J
Bethlem myopathy is not allelic to limb-girdle muscular dystrophy type 1A.
American journal of medical genetics 1995;58(2):197-8.
1995: Kumar A; Wolpert C; Kandt R S; Segal J; Pufky J; Roses A D; Pericak-Vance M A; Gilbert J R
A de novo frame-shift mutation in the tuberin gene.
Human molecular genetics 1995;4(8):1471-2.
1995: Breitner J C; Welsh K A; Helms M J; Gaskell P C; Gau B A; Roses A D; Pericak-Vance M A; Saunders A M
Delayed onset of Alzheimer's disease with nonsteroidal anti-inflammatory and histamine H2 blocking drugs.
Neurobiology of aging 1995;16(4):523-30.
1995: Othmane K B; Loeb D; Hayworth-Hodgte R; Hentati F; Rao N; Roses A D; Ben Hamida M; Pericak-Vance M A; Vance J M
Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A.
Genomics 1995;28(2):286-90.
1995: Corder E H; Saunders A M; Pericak-Vance M A; Roses A D
There is a pathologic relationship between ApoE-epsilon 4 and Alzheimer's disease.
Archives of neurology 1995;52(7):650-1.
1995: Pericak-Vance M A; Barker D F; Bergoffen J A; Chance P; Cochrane S; Dahl N; Exler M C; Fain P R; Fairweather N D; Fischbeck K
Consortium fine localization of X-linked Charcot-Marie-Tooth disease (CMTX1): additional support that connexin32 is the defect in CMTX1.
Human heredity 1995;45(3):121-8.
1995: Small K W; Stalvey M; Fisher L; Mullen L; Dickel C; Beadles K; Reimer R; Lessner A; Lewis K; Pericak-Vance M A
Blepharophimosis syndrome is linked to chromosome 3q.
Human molecular genetics 1995;4(3):443-8.
1995: Roses A D; Saunders A M; Corder E H; Pericak-Vance M A; Han S H; Einstein G; Hulette C; Schmechel D E; Holsti M; Huang D
Influence of the susceptibility genes apolipoprotein E-epsilon 4 and apolipoprotein E-epsilon 2 on the rate of disease expressivity of late-onset Alzheimer's disease.
Arzneimittel-Forschung 1995;45(3A):413-7.
1995: Roses A D; Saunders A M; Alberts M A; Strittmatter W J; Schmechel D; Gorder E; Pericak-Vance M A
Apolipoprotein E E4 allele and risk of dementia.
JAMA : the journal of the American Medical Association 1995;273(5):374-5; author reply 375-6.
1995: Corder E H; Saunders A M; Strittmatter W J; Schmechel D E; Gaskell P C; Roses A D; Pericak-Vance M A; Small G W; Haines J L
The apolipoprotein E E4 allele and sex-specific risk of Alzheimer's disease.
JAMA : the journal of the American Medical Association 1995;273(5):373-4.
1995: Roses A D; Saunders A M; Strittmatter W J; Schmechel D E; Pericak-Vance M A; Hyman B
Apolipoprotein E in Creutzfeldt-Jacob disease.
Lancet 1995;345(8941):69.
1994: Burke J R; Ikeuchi T; Koide R; Tsuji S; Yamada M; Pericak-Vance M A; Vance J M
Dentatorubral-pallidoluysian atrophy and Haw River syndrome.
Lancet 1994;344(8938):1711-2.
1994: McAllister K A; Lennon F; Bowles-Biesecker B; McKinnon W C; Helmbold E A; Markel D S; Jackson C E; Guttmacher A E; Pericak-Vance M A; Marchuk D A
Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype.
Journal of medical genetics 1994;31(12):927-32.
1994: Strittmatter W J; Saunders A M; Goedert M; Weisgraber K H; Dong L M; Jakes R; Huang D Y; Pericak-Vance M; Schmechel D; Roses A D
Isoform-specific interactions of apolipoprotein E with microtubule-associated protein tau: implications for Alzheimer disease.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(23):11183-6.
1994: Huang D Y; Goedert M; Jakes R; Weisgraber K H; Garner C C; Saunders A M; Pericak-Vance M A; Schmechel D E; Roses A D; Strittmatter W J
Isoform-specific interactions of apolipoprotein E with the microtubule-associated protein MAP2c: implications for Alzheimer's disease.
Neuroscience letters 1994;182(1):55-8.
1994: Hentati A; Pericak-Vance M A; Lennon F; Wasserman B; Hentati F; Juneja T; Angrist M H; Hung W Y; Boustany R M; Bohlega S
Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers.
Human molecular genetics 1994;3(10):1867-71.
1994: Han S H; Einstein G; Weisgraber K H; Strittmatter W J; Saunders A M; Pericak-Vance M; Roses A D; Schmechel D E
Apolipoprotein E is localized to the cytoplasm of human cortical neurons: a light and electron microscopic study.
Journal of neuropathology and experimental neurology 1994;53(5):535-44.
1994: Yamaoka L H; Westbrook C A; Speer M C; Gilchrist J M; Jabs E W; Schweins E G; Stajich J M; Gaskell P C; Roses A D; Pericak-Vance M A
Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9.
Neuromuscular disorders : NMD 1994;4(5-6):471-5.
1994: Loeb D B; Pericak-Vance M A; Stajich J M; Vance J M
A novel mutation in the von Hippel-Lindau gene.
Human molecular genetics 1994;3(8):1423-4.
1994: Hentati A; Pericak-Vance M A; Hung W Y; Belal S; Laing N; Boustany R M; Hentati F; Ben Hamida M; Siddique T
Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.
Human molecular genetics 1994;3(8):1263-7.
1994: Burke J R; Wingfield M S; Lewis K E; Roses A D; Lee J E; Hulette C; Pericak-Vance M A; Vance J M
The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family.
Nature genetics 1994;7(4):521-4.
1994: Han S H; Hulette C; Saunders A M; Einstein G; Pericak-Vance M; Strittmatter W J; Roses A D; Schmechel D E
Apolipoprotein E is present in hippocampal neurons without neurofibrillary tangles in Alzheimer's disease and in age-matched controls.
Experimental neurology 1994;128(1):13-26.
1994: Hentati A; Bejaoui K; Pericak-Vance M A; Hentati F; Speer M C; Hung W Y; Figlewicz D A; Haines J; Rimmler J; Ben Hamida C
Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.
Nature genetics 1994;7(3):425-8.
1994: Roses A D; Strittmatter W J; Pericak-Vance M A; Corder E H; Saunders A M; Schmechel D E
Clinical application of apolipoprotein E genotyping to Alzheimer's disease.
Lancet 1994;343(8912):1564-5.
1994: Mérette C; Brzustowicz L M; Daniels R J; Davies K E; Gilliam T C; Melki J; Munnich A; Pericak-Vance M A; Siddique T; Voosen B
An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy.
Genomics 1994;21(1):27-33.
1994: Roses A D; Pericak-Vance M A; Saunders A M; Schmechel D; Goldgaber D; Strittmatter W
Complex genetic disease: can genetic strategies in Alzheimer's disease and new genetic mechanisms be applied to epilepsy?
Epilepsia 1994;35 Suppl 1():S20-8.
1993: Schmechel D E; Saunders A M; Strittmatter W J; Crain B J; Hulette C M; Joo S H; Pericak-Vance M A; Goldgaber D; Roses A D
Increased amyloid beta-peptide deposition in cerebral cortex as a consequence of apolipoprotein E genotype in late-onset Alzheimer disease.
Proceedings of the National Academy of Sciences of the United States of America 1993;90(20):9649-53.
1993: Ben Othmane K; Hentati F; Lennon F; Ben Hamida C; Blel S; Roses A D; Pericak-Vance M A; Ben Hamida M; Vance J M
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.
Human molecular genetics 1993;2(10):1625-8.
1993: Strittmatter W J; Weisgraber K H; Huang D Y; Dong L M; Salvesen G S; Pericak-Vance M; Schmechel D; Saunders A M; Goldgaber D; Roses A D
Binding of human apolipoprotein E to synthetic amyloid beta peptide: isoform-specific effects and implications for late-onset Alzheimer disease.
Proceedings of the National Academy of Sciences of the United States of America 1993;90(17):8098-102.
1993: Econs M J; Fain P R; Norman M; Speer M C; Pericak-Vance M A; Becker P A; Barker D F; Taylor A; Drezner M K
Flanking markers define the X-linked hypophosphatemic rickets gene locus.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 1993;8(9):1149-52.
1993: Ben Othmane K; Middleton L T; Loprest L J; Wilkinson K M; Lennon F; Rozear M P; Stajich J M; Gaskell P C; Roses A D; Pericak-Vance M A
Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity.
Genomics 1993;17(2):370-5.
1993: Saunders A M; Strittmatter W J; Schmechel D; George-Hyslop P H; Pericak-Vance M A; Joo S H; Rosi B L; Gusella J F; Crapper-MacLachlan D R; Alberts M J
Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease.
Neurology 1993;43(8):1467-72.
1993: Corder E H; Saunders A M; Strittmatter W J; Schmechel D E; Gaskell P C; Small G W; Roses A D; Haines J L; Pericak-Vance M A
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families.
Science (New York, N.Y.) 1993;261(5123):921-3.
1993: Pericak-Vance M A; Nunes K J; Whisenant E; Loeb D B; Small K W; Stajich J M; Rimmler J B; Yamaoka L H; Smith D I; Drabkin H A
Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26.
Journal of medical genetics 1993;30(6):487-91.
1993: Strittmatter W J; Saunders A M; Schmechel D; Pericak-Vance M; Enghild J; Salvesen G S; Roses A D
Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease.
Proceedings of the National Academy of Sciences of the United States of America 1993;90(5):1977-81.
1993: Bergoffen J; Trofatter J; Pericak-Vance M A; Haines J L; Chance P F; Fischbeck K H
Linkage localization of X-linked Charcot-Marie-Tooth disease.
American journal of human genetics 1993;52(2):312-8.
1993: Pericak-Vance M A; St George-Hyslop P H; Gaskell P C; Growdon J; Crain B J; Hulette C; Gusella J F; Yamaoka L; Tanzi R E; Roses A D
Linkage analysis in familial Alzheimer disease: description of the Duke and Boston data sets.
Genetic epidemiology 1993;10(6):361-4.
1992: St George-Hyslop P; Haines J; Rogaev E; Mortilla M; Vaula G; Pericak-Vance M; Foncin J F; Montesi M; Bruni A; Sorbi S
Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14.
Nature genetics 1992;2(4):330-4.
1992: Ben Othmane K; Ben Hamida M; Pericak-Vance M A; Ben Hamida C; Blel S; Carter S C; Bowcock A M; Petruhkin K; Gilliam T C; Roses A D
Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.
Nature genetics 1992;2(4):315-7.
1992: Sarfarazi M; Wijmenga C; Upadhyaya M; Weiffenbach B; Hyser C; Mathews K; Murray J; Gilbert J; Pericak-Vance M; Lunt P
Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium.
American journal of human genetics 1992;51(2):396-403.
1992: Small K W; Weber J L; Roses A; Lennon F; Vance J M; Pericak-Vance M A
North Carolina macular dystrophy is assigned to chromosome 6.
Genomics 1992;13(3):681-5.
1992: Econs M J; Barker D F; Speer M C; Pericak-Vance M A; Fain P R; Drezner M K
Multilocus mapping of the X-linked hypophosphatemic rickets gene.
The Journal of clinical endocrinology and metabolism 1992;75(1):201-6.
1992: Pritchard C; Zhu N; Zuo J; Bull L; Pericak-Vance M A; Vance J M; Roses A D; Milatovich A; Francke U; Cox D R
Recombination of 4p16 DNA markers in an unusual family with Huntington disease.
American journal of human genetics 1992;50(6):1218-30.
1992: McClatchey A I; Trofatter J; McKenna-Yasek D; Raskind W; Bird T; Pericak-Vance M; Gilchrist J; Arahata K; Radosavljevic D; Worthen H G
Dinucleotide repeat polymorphisms at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenita.
American journal of human genetics 1992;50(5):896-901.
1992: Loprest L J; Pericak-Vance M A; Stajich J; Gaskell P C; Lucas A M; Lennon F; Yamaoka L H; Roses A D; Vance J M
Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entities.
Neurology 1992;42(3 Pt 1):597-601.
1992: McClatchey A I; Van den Bergh P; Pericak-Vance M A; Raskind W; Verellen C; McKenna-Yasek D; Rao K; Haines J L; Bird T; Brown R H
Temperature-sensitive mutations in the III-IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita.
Cell 1992;68(4):769-74.
1992: Speer M C; Haynes C S; Pericak-Vance M A
Segregation analysis in cutaneous malignant melanoma/dysplastic nevus syndrome families.
Cytogenetics and cell genetics 1992;59(2-3):225-7.
1992: Ropers H H; Pericak-Vance M A; Carrano A V
Report of the Second International Workshop on Human Chromosome 19 mapping 1992.
Cytogenetics and cell genetics 1992;60(2):87-95.
1991: Secore S L; Walker A P; Herbstreith M H; Siddique T; Jeffers A J; DeShields T R; Speer M C; Pericak-Vance M A; Golembieski W A; Smith D I
A StuI polymorphism on chromosome 3p14.1-14.2 (D3S622) defined by two polymorphic StuI sites 2.4 kb apart.
Nucleic acids research 1991;19(22):6349.
1991: Small K W; Weber J L; Hung W Y; Vance J; Roses A; Pericak-Vance M
North Carolina macular dystrophy: exclusion map using RFLPs and microsatellites.
Genomics 1991;11(3):763-6.
1991: Alberts M J; Pericak-Vance M A; Royal V; Bebout J; Gaskell P; Thomas J; Hung W Y; Clark C; Earl N; Roses A D
Genetic linkage analysis of nerve growth factor (beta) in familial Alzheimer's disease.
Annals of neurology 1991;30(2):216-9.
1991: Royal V; Alberts M J; Pericak-Vance M A; Finocchiaro G; Bebout J; Yamaoka L; Hung W Y; Gaskell P C; Roses A D
RsaI RFLP for electron transport flavoprotein-beta(ETFB).
Nucleic acids research 1991;19(14):4021.
1991: Pericak-Vance M A; Bebout J L; Gaskell P C; Yamaoka L H; Hung W Y; Alberts M J; Walker A P; Bartlett R J; Haynes C A; Welsh K A
Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage.
American journal of human genetics 1991;48(6):1034-50.
1991: Siddique T; Figlewicz D A; Pericak-Vance M A; Haines J L; Rouleau G; Jeffers A J; Sapp P; Hung W Y; Bebout J; McKenna-Yasek D
Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity.
The New England journal of medicine 1991;324(20):1381-4.
1991: Vance J M; Barker D; Yamaoka L H; Stajich J M; Loprest L; Hung W Y; Fischbeck K; Roses A D; Pericak-Vance M A
Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2.
Genomics 1991;9(4):623-8.
1991: Schellenberg G D; Pericak-Vance M A; Wijsman E M; Moore D K; Gaskell P C; Yamaoka L A; Bebout J L; Anderson L; Welsh K A; Clark C M
Linkage analysis of familial Alzheimer disease, using chromosome 21 markers.
American journal of human genetics 1991;48(3):563-83.
1991: Alberts M J; Kandt R S; Pericak-Vance M A; Bebout J; Speer M C; Siddique T S; Yamaoka L; Hung W Y; Gaskell P C; Roses A D
MspI RFLP for microtubule associated protein-2 (MAP2).
Nucleic acids research 1991;19(4):960.
1991: Speer M C; Goldgaber D; Goldfarb L G; Roses A D; Pericak-Vance M A
Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pter.
Genomics 1991;9(2):366-8.
1991: Laing N G; Walker A P; Akkari P A; Chandler D C; Layton M G; Mears M E; Yamada T; Bartlett R J; Pericak-Vance M A; Hung W Y
Identification of Duchenne muscular dystrophy genomic probe P20 constant Taql fragment corresponding to the EcoRV and Mspl polymorphisms.
Prenatal diagnosis 1991;11(1):63-7.
1991: Siddique T; Hu P; Hentati A; Deng G; Hung W Y; McInnis M G; Warren A C; Rimmler J; Antonarakis S; Pericak-Vance M A
A molecular genetic approach to amyotrophic lateral sclerosis.
International journal of neurology 1991;25-26():60-9.
1991: Kandt R S; Pericak-Vance M A; Hung W Y; Gardner R J; Crossen P E; Nellist M D; Speer M C; Roses A D
Linkage studies in tuberous sclerosis. Chromosome 9?, 11?, or maybe 14!
Annals of the New York Academy of Sciences 1991;615():284-97.
1990: Econs M J; Pericak-Vance M A; Betz H; Bartlett R J; Speer M C; Drezner M K
The human glycine receptor: a new probe that is linked to the X-linked hypophosphatemic rickets gene.
Genomics 1990;7(3):439-41.
1990: Speer M C; Pericak-Vance M A; Yamaoka L; Hung W Y; Ashley A; Stajich J M; Roses A D
Presymptomatic and prenatal diagnosis in myotonic dystrophy by genetic linkage studies.
Neurology 1990;40(4):671-6.
1990: Walker A P; Collins F S; Siddique T; Yamaoka L H; Herbstreith M H; Pericak-Vance M A; Secore S L; Hung W Y; Goate A M; Hardy J A
D21S194, a jump clone from D21S16.
Nucleic acids research 1990;18(7):1931.
1990: Vance J M; Small K W; Jones M A; Stajich J M; Yamaoka L H; Roses A D; Hung W Y; Pericak-Vance M A
Confirmation of linkage in von Hippel-Lindau disease.
Genomics 1990;6(3):565-7.
1990: Yamaoka L H; Pericak-Vance M A; Speer M C; Gaskell P C; Stajich J; Haynes C; Hung W Y; Laberge C; Thibault M C; Mathieu J
Tight linkage of creatine kinase (CKMM) to myotonic dystrophy on chromosome 19.
Neurology 1990;40(2):222-6.
1990: Roses A D; Pericak-Vance M A; Clark C M; Gilbert J R; Yamaoka L H; Haynes C S; Speer M C; Gaskell P C; Hung W Y; Trofatter J A
Linkage studies of late-onset familial Alzheimer's disease.
Advances in neurology 1990;51():185-96.
1990: Ropers H H; Pericak-Vance M A
Report of the committee on the genetic constitution of chromosome 19.
Cytogenetics and cell genetics 1990;55(1-4):218-28.
1989: McConkie-Rosell A; Chen Y T; Harris D; Speer M C; Pericak-Vance M A; Ding J H; Highsmith W E; Knowles M; Kahler S G
Mild cystic fibrosis linked to chromosome 7q22 markers with an uncommon haplotype.
Annals of internal medicine 1989;111(10):797-801.
1989: Sarfarazi M; Upadhyaya M; Padberg G; Pericak-Vance M; Siddique T; Lucotte G; Lunt P
An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease.
Journal of medical genetics 1989;26(8):481-4.
1989: Siddique T; Roper H; Pericak-Vance M A; Shaw J; Warner K L; Hung W Y; Phillips K L; Lunt P; Cumming W J; Roses A D
Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral disease.
Journal of medical genetics 1989;26(8):487-9.
1989: Siddique T; Pericak-Vance M A; Brooks B R; Roos R P; Hung W Y; Antel J P; Munsat T L; Phillips K; Warner K; Speer M
Linkage analysis in familial amyotrophic lateral sclerosis.
Neurology 1989;39(7):919-25.
1989: Laing N G; Siddique T; Bartlett R; Yamaoka L H; Hung W Y; Pericak-Vance M A; Roses A D
Duchenne muscular dystrophy: detection of deletion carriers by spectrophotometric densitometry.
Clinical genetics 1989;35(6):393-8.
1989: Kandt R S; Pericak-Vance M A; Hung W Y; Gardner R J; Nellist M; Phillips K; Warner K; Speer M C; Crossen P E; Laing N G
Absence of linkage of ABO blood group locus to familial tuberous sclerosis.
Experimental neurology 1989;104(3):223-8.
1989: Vance J M; Nicholson G A; Yamaoka L H; Stajich J; Stewart C S; Speer M C; Hung W Y; Roses A D; Barker D; Pericak-Vance M A
Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17.
Experimental neurology 1989;104(2):186-9.
1989: Bartlett R J; Walker A P; Laing N G; Koh J; Secore S L; Speer M C; Pericak-Vance M; Hung W Y; Yamaoka L H; Siddique T
Inherited deletion at Duchenne dystrophy locus in normal male.
Lancet 1989;1(8636):496-7.
1989: Diehl S R; Boehnke M; Erickson R P; Ploughman L M; Seiler K A; Lieberman J L; Clarke H B; Bruce M A; Schorry E K; Pericak-Vance M
A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) gene.
American journal of human genetics 1989;44(1):33-7.
1989: Seizinger B R; Farmer G E; Haines J L; Ozelius L J; Anderson K; Korf B R; Parry D M; Pericak-Vance M A; Mulvihill J J; Menon A
Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1).
American journal of human genetics 1989;44(1):30-2.
1989: Vance J M; Pericak-Vance M A; Yamaoka L H; Speer M C; Rosenwasser G O; Small K; Gaskell P C; Hung W Y; Alberts M J; Haynes C S
Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type I.
American journal of human genetics 1989;44(1):25-9.
1989: Le Beau M M; Ryan D; Pericak-Vance M A
Report of the committee on the genetic constitution of chromosomes 18 and 19.
Cytogenetics and cell genetics 1989;51(1-4):338-57.
1989: Speer M C; Sherman S L; Haynes C S; Pericak-Vance M A
Mapping strategies for multiple linked markers.
Progress in clinical and biological research 1989;329():75-80.
1989: Dawson D V; Roses A D; Pericak-Vance M A; Kaplan E B; Elston R C; Haynes C S; Gaskell P C; Heyman A; Clark C M; Earl N L
Sib-pair linkage analysis in late onset Alzheimer's disease.
Progress in clinical and biological research 1989;317():223-8.
1989: Roses A D; Pericak-Vance M A; Yamaoka L; Haynes C; Speer M; Gaskell P; Hung W Y; Clark C M; Heyman A; Trofatter J
Linkage studies in familial Alzheimer's disease.
Progress in clinical and biological research 1989;317():201-15.
1988: Pericak-Vance M A; Yamaoka L H; Haynes C S; Speer M C; Haines J L; Gaskell P C; Hung W Y; Clark C M; Heyman A L; Trofatter J A
Genetic linkage studies in Alzheimer's disease families.
Experimental neurology 1988;102(3):271-9.
1988: Walker A P; Bartlett R J; Yamaoka L H; Secore S L; Lee J E; Gilbert J; Herbstreith M; Pericak-Vance M A; Hung W Y; Roses A D
A Bgl II polymorphism detected by LDR152 [D19S19].
Nucleic acids research 1988;16(18):9063.
1988: Speer M C; Pericak-Vance M A; Yamaoka L H; Koh J; Hung W Y; Gaskell P C; Vance J M; Bartlett R J; Roses A D
Prenatal diagnosis using deletion studies in Duchenne muscular dystrophy.
Prenatal diagnosis 1988;8(6):427-37.
1988: Gilchrist J M; Pericak-Vance M; Silverman L; Roses A D
Clinical and genetic investigation in autosomal dominant limb-girdle muscular dystrophy.
Neurology 1988;38(1):5-9.
1988: Bartlett R J; Pericak-Vance M A; Koh J; Yamaoka L H; Chen J C; Hung W Y; Speer M C; Wapenaar M C; Van Ommen G J; Bakker E
Duchenne muscular dystrophy: high frequency of deletions.
Neurology 1988;38(1):1-4.
1988: LeBeau M; Pericak-Vance M
Report of the committee on the genetic constitution of chromosomes 18 and 19.
Cytogenetics and cell genetics 1988;49(1-3):99-101.
1988: Siddique T; Bartlett R; Pericak-Vance M; Yamaoka L; Koh J; Chen J; Hung W Y; Kandt R; Roses A D
Update on the molecular genetics of Duchenne muscular dystrophy.
Australian paediatric journal 1988;24 Suppl 1():9-14.
1988: Roses A D; Pericak-Vance M A; Bartlett R J; Yamaoka L H; Lee J E; Koh J; Chen J C; Gilbert J R; Ross D A; Herbstreith M H
Myotonic dystrophy: update on progress to define the gene.
Australian paediatric journal 1988;24 Suppl 1():66-9.
1988: Pericak-Vance M A; Hung W Y; Yamaoka L; Haynes C; Bartlett R J; Vance J M; Lee J; Siddique T; Gaskell P C; Stajich J
Systematic gene mapping in man: data management considerations.
Australian paediatric journal 1988;24 Suppl 1():87-9.
1987: Pericak-Vance M A; Yamaoka L H; Vance J M; Small K; Rosenwasser G O; Gaskell P C; Hung W Y; Alberts M J; Haynes C S; Speer M C
Genetic linkage studies of chromosome 17 RFLPs in von Recklinghausen neurofibromatosis (NF1).
Genomics 1987;1(4):349-52.
1987: Seizinger B R; Rouleau G A; Lane A H; Farmer G; Ozelius L J; Haines J L; Parry D M; Korf B R; Pericak-Vance M A; Faryniarz A G
Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17.
Genomics 1987;1(4):346-8.
1987: Koh J; Bartlett R J; Pericak-Vance M A; Speer M C; Yamaoka L H; Phillips K; Hung W Y; Ray P N; Worton R G; Gilbert J R
Inherited deletion at Duchenne dystrophy locus in normal male.
Lancet 1987;2(8568):1154-5.
1987: Vance J M; Pericak-Vance M A; Bowman M H; Payne C S; Fredane L; Siddique T; Roses A D; Massey E W
Chorea-acanthocytosis: a report of three new families and implications for genetic counselling.
American journal of medical genetics 1987;28(2):403-10.
1987: Rozear M P; Pericak-Vance M A; Fischbeck K; Stajich J M; Gaskell P C; Krendel D A; Graham D G; Dawson D V; Roses A D
Hereditary motor and sensory neuropathy, X-linked: a half century follow-up.
Neurology 1987;37(9):1460-5.
1987: Diehl S R; Boehnke M; Collins F S; Erickson R P; Karolyi I J; Ploughman L M; Pericak-Vance M A; Aylsworth A S; Roses A D
Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8.
Journal of medical genetics 1987;24(9):532-4.
1987: Pericak-Vance M A; Yamaoka L H; Vance J M; Aylsworth A S; Rossenwasser G O; Gaskell P C; Alberts M J; Hung W Y; Haynes C; Roses A D
Linkage studies in peripheral neurofibromatosis.
Journal of medical genetics 1987;24(9):530-2.
1987: Lanman J T; Pericak-Vance M A; Bartlett R J; Chen J C; Yamaoka L; Koh J; Speer M C; Hung W Y; Roses A D
Familial inheritance of a DXS164 deletion mutation from a heterozygous female.
American journal of human genetics 1987;41(2):138-44.
1987: Seizinger B R; Rouleau G A; Ozelius L J; Lane A H; Faryniarz A G; Chao M V; Huson S; Korf B R; Parry D M; Pericak-Vance M A
Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene.
Cell 1987;49(5):589-94.
1987: Shields E D; Russell D A; Pericak-Vance M A
Genetic epidemiology of the susceptibility to leprosy.
The Journal of clinical investigation 1987;79(4):1139-43.
1987: Bartlett R J; Pericak-Vance M A; Yamaoka L; Gilbert J; Herbstreith M; Hung W Y; Lee J E; Mohandas T; Bruns G; Laberge C
A new probe for the diagnosis of myotonic muscular dystrophy.
Science (New York, N.Y.) 1987;235(4796):1648-50.
1987: Bartlett R J; Pericak-Vance M A; Lanman J T; Killam A P; Gilbert J R; Stajick J M; Chen J C; Siddique T; Kandt R S; Sirotkin-Roses M
Prenatal detection of an inherited Duchenne muscular dystrophy deletion allele.
Neurology 1987;37(2):355-6.
1986: Pericak-Vance M A; Yamaoka L H; Assinder R I; Hung W Y; Bartlett R J; Stajich J M; Gaskell P C; Ross D A; Sherman S; Fey G H
Tight linkage of apolipoprotein C2 to myotonic dystrophy on chromosome 19.
Neurology 1986;36(11):1418-23.
1986: Fischbeck K H; ar-Rushdi N; Pericak-Vance M; Rozear M; Roses A D; Fryns J P
X-linked neuropathy: gene localization with DNA probes.
Annals of neurology 1986;20(4):527-32.
1986: Roses A D; Pericak-Vance M A; Yamaoka L H; Herbstreith M H; Bartlett R J; Siddique T; Hung W Y; Ross D A; Mohandas T K; Bruns G
A new tightly linked DNA probe for myotonic dystrophy.
Neurology 1986;36(8):1146.
1986: Roses A D; Pericak-Vance M A; Ross D A; Yamaoka L; Bartlett R J
RFLPs at the D19S19 locus of human chromosome 19 linked to myotonic dystrophy (DM).
Nucleic acids research 1986;14(13):5569.
1986: Kunkel L M; Hejtmancik J F; Caskey C T; Speer A; Monaco A P; Middlesworth W; Colletti C A; Bertelson C; Müller U; Bresnan M; Shapiro F; Tantravahi U; Speer J; Latt S A; Bartlett R; Pericak-Vance M A; Roses A D; Thompson M W; Ray P N; Worton R G; Fischbeck K H; Gallano P; Coulon M; Duros C; Boue J; Junien C; Chelly J; Hamard G; Jeanpierre M; Lambert M; Kaplan J C; Emery A; Dorkins H; McGlade S; Davies K E; Boehm C; Arveiler B; Lemaire C; Morgan G J; Denton M J; Amos J; Bobrow M; Benham F; Boswinkel E; Cole C; Dubowitz V; Hart K; Hodgson S; Johnson L; Walker A; Roncuzzi L; Ferlini A; Nobile C; Romeo G; Wilcox D E; Affara N A; Ferguson-Smith M A; Lindolf M; Kaariainen H; de la Chapelle A; Ionasescu V; Searby C; Ionasescu R; Bakker E; van Ommen G J; Pearson P L; Greenberg C R; Hamerton J L; Wrogemann K; Doherty R A; Polakowska R; Hyser C; Quirk S; Thomas N; Harper J F; Darras B T; Francke U
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
Nature 1986;322(6074):73-7.
1986: Moore G E; Roses A D; Pericak-Vance M A; Garrett W E; Schachat F H
Promiscuous expression of myosin in myotonic dystrophy.
Muscle & nerve 1986;9(4):355-63.
1986: Coleman R A; Stajich J M; Pact V W; Pericak-Vance M A
The ischemic exercise test in normal adults and in patients with weakness and cramps.
Muscle & nerve 1986;9(3):216-21.
1986: Pericak-Vance M A; Meyers D A
Genetic analysis workshop IV: Huntington disease linkage analysis summary.
Genetic epidemiology. Supplement 1986;1():197-209.
1986: Pericak-Vance M A; Meyers D A; Gusella J F; Folstein S E; Conneally P M
Genetic analysis workshop IV: Huntington disease linkage analysis, data description.
Genetic epidemiology. Supplement 1986;1():193-6.
1986: Haynes C; Pericak-Vance M; Dawson D
Analysis of Huntington disease linkage and age-of-onset distributions.
Genetic epidemiology. Supplement 1986;1():235-9.
1985: Yamaoka L H; Bartlett R J; Ross D A; Fey G H; Ledbetter D H; Bruns G; Pericak-Vance M A; Herbstreith M H; Roses A D
Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophy.
Journal of neurogenetics 1985;2(6):403-12.
1985: Monaco A P; Bertelson C J; Middlesworth W; Colletti C A; Aldridge J; Fischbeck K H; Bartlett R; Pericak-Vance M A; Roses A D; Kunkel L M
Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment.
Nature 1985;316(6031):842-5.
1985: Pericak-Vance M A; Vance J M; Elston R C; Namboodiri K K; Fogle T A
Segregation and linkage analysis of alpha-N-acetyl-D-glucosaminidase (NAG) levels in a black family.
American journal of medical genetics 1985;20(2):295-306.
1983: Roses A D; Pericak-Vance M A; Yamaoka L H; Stubblefield E; Stajich J; Vance J M; Roses M J; Carter D B
Recombinant DNA strategies in genetic neurological diseases.
Muscle & nerve 1983;6(5):339-55.
1983: Hudgson P; McAdams M W; Pericak-Vance M A; Edwards T M; Roses A D
Effect of sera from myasthenia gravis patients on acetylcholine receptors in myotube cultures.
Journal of the neurological sciences 1983;59(1):37-45.
1983: Pericak-Vance M A; Elston R C; Conneally P M; Dawson D V
Age-of-onset heterogeneity in Huntington disease families.
American journal of medical genetics 1983;14(1):49-59.
1981: Vance J M; Conneally P M; Wappner R S; Yu P L; Brandt I K; Pericak-Vance M A
Carrier detection in Sanfilippo syndrome type B: report of six families.
Clinical genetics 1981;20(2):135-40.
1980: Vance J M; Pericak-Vance M A; Elston R C; Conneally P M; Namboodiri K K; Wappner R S; Yu P L
Evidence of genetic variation for alpha-N-acetyl-D-glucosaminidase in black and white populations: a new polymorphism.
American journal of medical genetics 1980;7(2):131-40.
1978: Pericak-Vance M A; Conneally P M; Merritt A D; Roos R; Norton J A; Vance J M
Genetic linkage studies in Huntington disease.
Cytogenetics and cell genetics 1978;22(1-6):640-5.

Sign-in to see more

Sign-in free and Explore the Exciting World of BiomedExperts:

NetworkView

Margaret Pericak-Vance

Research Profile (preview)

Concepts & Ideas

Procedures

Physiology

Disorders

Genes & Molecular Sequences

Chemicals & Drugs

Network (preview)

Publications

Sign in free and see...

Visualized networks:

GeoTargeted Searches:

Research Profiles:

Geonetwork of Margaret Pericak-Vance (preview)

All Publications