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Jonathan Haines

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.

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Pericak-Vance Margaret A; Haines Jonathan L
Beyond proof of principle: new genes for Alzheimer's disease through collaboration.
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.

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All Publications

2009: Pericak-Vance Margaret A; Haines Jonathan L
Beyond proof of principle: new genes for Alzheimer's disease through collaboration.
Lancet neurology 2009;8(11):977-9.
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: Huang Yifan; Trentham-Dietz Amy; García-Closas Montserrat; Newcomb Polly A; Titus-Ernstoff Linda; Hampton John M; Chanock Stephen J; Haines Jonathan L; Egan Kathleen M
Association of CYP1B1 haplotypes and breast cancer risk in Caucasian women.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2009;18(4):1321-3.
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: Zheng Wei; Long Jirong; Gao Yu-Tang; Li Chun; Zheng Ying; Xiang Yong-Bin; Wen Wanqing; Levy Shawn; Deming Sandra L; Haines Jonathan L; Gu Kai; Fair Alecia Malin; Cai Qiuyin; Lu Wei; Shu Xiao-Ou
Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1.
Nature genetics 2009;41(3):324-8.
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: Srinivasan Balaji S; Chen Jinbo; Cheng Cheng; Conti David; Duan Shiwei; Fridley Brooke L; Gu Xiangjun; Haines Jonathan L; Jorgenson Eric; Kraja Aldi; Lasky-Su Jessica; Li Lang; Rodin Andrei; Wang Dai; Province Mike; Ritchie Marylyn D
Methods for analysis in pharmacogenomics: lessons from the Pharmacogenetics Research Network Analysis Group.
Pharmacogenomics 2009;10(2):243-51.
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: 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: Ryckman Kelli K; Jiang Lan; Li Chun; Bartlett Jacquelaine; Haines Jonathan L; Williams Scott M
A prevalence-based association test for case-control studies.
Genetic epidemiology 2008;32(7):600-5.
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: Lee S L; Murdock D G; McCauley J L; Bradford Y; Crunk A; McFarland L; Jiang L; Wang T; Schnetz-Boutaud N; Haines J L
A genome-wide scan in an Amish pedigree with parkinsonism.
Annals of human genetics 2008;72(Pt 5):621-9.
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: Darbar Dawood; Kannankeril Prince J; Donahue Brian S; Kucera Gayle; Stubblefield Tanya; Haines Jonathan L; George Alfred L; Roden Dan M
Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.
Circulation 2008;117(15):1927-35.
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: Darbar Dawood; Hardy Amanda; Haines Jonathan L; Roden Dan M
Prolonged signal-averaged P-wave duration as an intermediate phenotype for familial atrial fibrillation.
Journal of the American College of Cardiology 2008;51(11):1083-9.
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: Shibao Cyndya; Garland Emily M; Gamboa Alfredo; Vnencak-Jones Cindy L; Van Woeltz M; Haines Jonathan L; Yu Chang; Biaggioni Italo
PRNP M129V homozygosity in multiple system atrophy vs. Parkinson's disease.
Clinical autonomic research : official journal of the Clinical Autonomic Research Society 2008;18(1):13-9.
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: Fan Bao Jian; Chen Teresa; Grosskreutz Cynthia; Pasquale Louis; Rhee Douglas; DelBono Elizabeth; Haines Jonathan L; Wiggs Janey L
Lack of association of polymorphisms in homocysteine metabolism genes with pseudoexfoliation syndrome and glaucoma.
Molecular vision 2008;14():2484-91.
2008: Sud A; Del Bono E A; Haines J L; Wiggs J L
Fine mapping of the GLC1K juvenile primary open-angle glaucoma locus and exclusion of candidate genes.
Molecular vision 2008;14():1319-26.
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.
2008: Fan Bao Jian; Pasquale Louis; Grosskreutz Cynthia L; Rhee Douglas; Chen Teresa; DeAngelis Margaret M; Kim Ivana; del Bono Elizabeth; Miller Joan W; Li Tiansen; Haines Jonathan L; Wiggs Janey L
DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S. clinic-based population with broad ethnic diversity.
BMC medical genetics 2008;9():5.
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: 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: Liang Xueying; Trentham-Dietz Amy; Titus-Ernstoff Linda; Newcomb Polly A; Welch Rober A; Hutchinson Amy A; Hampton John M; Sutcliffe Cara B; Haines Jonathan L; Egan Kathleen M
Whole-genome amplification of oral rinse self-collected DNA in a population-based case-control study of breast cancer.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2007;16(8):1610-4.
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: 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: Sprague Brian L; Trentham-Dietz Amy; Garcia-Closas Montserrat; Newcomb Polly A; Titus-Ernstoff Linda; Hampton John M; Chanock Stephen J; Haines Jonathan L; Egan Kathleen M
Genetic variation in TP53 and risk of breast cancer in a population-based case control study.
Carcinogenesis 2007;28(8):1680-6.
2007: Williams Scott M; Canter Jeffrey A; Crawford Dana C; Moore Jason H; Ritchie Marylyn D; Haines Jonathan L
Problems with genome-wide association studies.
Science (New York, N.Y.) 2007;316(5833):1840-2.
2007: Hedera P; Blair M A; Andermann E; Andermann F; D'Agostino D; Taylor K A; Chahine L; Pandolfo M; Bradford Y; Haines J L; Abou-Khalil B
Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.
Neurology 2007;68(24):2107-12.
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: 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: 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: Abou-Khalil B; Krei L; Lazenby B; Harris P A; Haines J L; Hedera P
Familial genetic predisposition, epilepsy localization and antecedent febrile seizures.
Epilepsy research 2007;73(1):104-10.
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: Shah S H; Kraus W E; Crossman D C; Granger C B; Haines J L; Jones C J H; Mooser V; Huang L; Haynes C; Dowdy E; Vega G L; Grundy S M; Vance J M; Hauser E R
Serum lipids in the GENECARD study of coronary artery disease identify quantitative trait loci and phenotypic subsets on chromosomes 3q and 5q.
Annals of human genetics 2006;70(Pt 6):738-48.
2006: Hedera Peter; Ma Shaochun; Blair Marcia A; Taylor Kelly A; Hamati Aline; Bradford Yuki; Abou-Khalil Bassel; Haines Jonathan L
Identification of a novel locus for febrile seizures and epilepsy on chromosome 21q22.
Epilepsia 2006;47(10):1622-8.
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: Ritchie Marylyn D; Haas David W; Motsinger Alison A; Donahue John P; Erdem Huso; Raffanti Stephen; Rebeiro Peter; George Alfred L; Kim Richard B; Haines Jonathan L; Sterling Timothy R
Drug transporter and metabolizing enzyme gene variants and nonnucleoside reverse-transcriptase inhibitor hepatotoxicity.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2006;43(6):779-82.
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: Ma Shaochun; Davis Thomas L; Blair Marcia A; Fang John Y; Bradford Yuki; Haines Jonathan L; Hedera Peter
Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?
Movement disorders : official journal of the Movement Disorder Society 2006;21(9):1368-74.
2006: Connelly Jessica J; Wang Tianyuan; Cox Julie E; Haynes Carol; Wang Liyong; Shah Svati H; Crosslin David R; Hale A Brent; Nelson Sarah; Crossman David C; Granger Christopher B; Haines Jonathan L; Jones Christopher J H; Vance Jeffery M; Goldschmidt-Clermont Pascal J; Kraus William E; Hauser Elizabeth R; Gregory Simon G
GATA2 is associated with familial early-onset coronary artery disease.
PLoS genetics 2006;2(8):e139.
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: 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: Kallianpur Asha R; Hulgan Todd; Canter Jeffrey A; Ritchie Marylyn D; Haines Jonathan L; Robbins Gregory K; Shafer Robert W; Clifford David B; Haas David W
Hemochromatosis (HFE) gene mutations and peripheral neuropathy during antiretroviral therapy.
AIDS (London, England) 2006;20(11):1503-13.
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: 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: 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: 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: Ma Shaochun; Abou-Khalil Bassel; Blair Marcia A; Sutcliffe James S; Haines Jonathan L; Hedera Peter
Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizures.
Neuroscience letters 2006;394(1):74-8.
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: Thornton-Wells Tricia A; Moore Jason H; Haines Jonathan L
Dissecting trait heterogeneity: a comparison of three clustering methods applied to genotypic data.
BMC bioinformatics 2006;7():204.
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: 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: Hulgan Todd; Haas David W; Haines Jonathan L; Ritchie Marylyn D; Robbins Gregory K; Shafer Robert W; Clifford David B; Kallianpur Asha R; Summar Marshall; Canter Jeffrey A
Mitochondrial haplogroups and peripheral neuropathy during antiretroviral therapy: an adult AIDS clinical trials group study.
AIDS (London, England) 2005;19(13):1341-9.
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: 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: 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: Kallianpur A R; Hall L D; Yadav M; Byrne D W; Speroff T; Dittus R S; Haines J L; Christman B W; Summar M L
The hemochromatosis C282Y allele: a risk factor for hepatic veno-occlusive disease after hematopoietic stem cell transplantation.
Bone marrow transplantation 2005;35(12):1155-64.
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: 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: Ma Shaochun; Abou-Khalil Bassel; Sutcliffe James S; Haines Jonathan L; Hedera Peter
The GABBR1 locus and the G1465A variant is not associated with temporal lobe epilepsy preceded by febrile seizures.
BMC medical genetics 2005;6():13.
2005: Canter Jeffrey A; Eshaghian Alex; Fessel Joshua; Summar Marshall L; Roberts L Jackson; Morrow Jason D; Sligh James E; Haines Jonathan L
Degree of heteroplasmy reflects oxidant damage in a large family with the mitochondrial DNA A8344G mutation.
Free radical biology & medicine 2005;38(5):678-83.
2005: McCauley Jacob L; Li Chun; Jiang Lan; Olson Lana M; Crockett Genea; Gainer Kimberly; Folstein Susan E; Haines Jonathan L; Sutcliffe James S
Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates.
BMC medical genetics 2005;6():1.
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.
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: Thornton-Wells Tricia A; Moore Jason H; Haines Jonathan L
Genetics, statistics and human disease: analytical retooling for complexity.
Trends in genetics : TIG 2004;20(12):640-7.
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: McCauley Jacob L; Olson Lana M; Delahanty Ryan; Amin Taneem; Nurmi Erika L; Organ Edward L; Jacobs Michelle M; Folstein Susan E; Haines Jonathan L; Sutcliffe James S
A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;131B(1):51-9.
2004: Hedera Peter; Fenichel Gerald M; Blair Marcia; Haines Jonathan L
Novel mutation in the SPG3A gene in an African American family with an early onset of hereditary spastic paraplegia.
Archives of neurology 2004;61(10):1600-3.
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: 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: Wiggs J L; Lynch S; Ynagi G; Maselli M; Auguste J; Del Bono E A; Olson L M; Haines J L
A genomewide scan identifies novel early-onset primary open-angle glaucoma loci on 9q22 and 20p12.
American journal of human genetics 2004;74(6):1314-20.
2004: Hutcheson Holli B; Olson Lana M; Bradford Yuki; Folstein Susan E; Santangelo Susan L; Sutcliffe James S; Haines Jonathan L
Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes.
BMC medical genetics 2004;5():12.
2004: McCauley J L; Olson L M; Dowd M; Amin T; Steele A; Blakely R D; Folstein S E; Haines J L; Sutcliffe J S
Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;127B(1):104-12.
2004: Hedera Peter; Abou-Khalil Bassel; Crunk Amy E; Taylor Kelly A; Haines Jonathan L; Sutcliffe James S
Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene.
Epilepsia 2004;45(3):218-22.
2004: Kallianpur Asha R; Hall Lynn D; Yadav Meeta; Christman Brian W; Dittus Robert S; Haines Jonathan L; Parl Fritz F; Summar Marshall L
Increased prevalence of the HFE C282Y hemochromatosis allele in women with breast cancer.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2004;13(2):205-12.
2004: Williams Scott M; Haines Jonathan L; Moore Jason H
The use of animal models in the study of complex disease: all else is never equal or why do so many human studies fail to replicate animal findings?
BioEssays : news and reviews in molecular, cellular and developmental biology 2004;26(2):170-9.
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: Sena D F; Finzi S; Rodgers K; Del Bono E; Haines J L; Wiggs J L
Founder mutations of CYP1B1 gene in patients with congenital glaucoma from the United States and Brazil.
Journal of medical genetics 2004;41(1):e6.
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.
2004: Haines Jonathan; Camarata Stephen
Examination of candidate genes in language disorder: a model of genetic association for treatment studies.
Mental retardation and developmental disabilities research reviews 2004;10(3):208-17.
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: 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: Haas David W; Wilkinson Grant R; Kuritzkes Daniel R; Richman Douglas D; Nicotera Janet; Mahon Laura F; Sutcliffe Cara; Siminski Sue; Andersen Janet; Coughlin Kristine; Clayton Ellen W; Haines Jonathan; Marshak Ann; Saag Michael; Lawrence Jody; Gustavson Jeffrey; Anne Bennett Jo; Christensen Rolf; Matula Margaret A; Wood Alastair J J;
A multi-investigator/institutional DNA bank for AIDS-related human genetic studies: AACTG Protocol A5128.
HIV clinical trials 2003;4(5):287-300.
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: 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: Nurmi Erika L; Dowd Michael; Tadevosyan-Leyfer Ovsanna; Haines Jonathan L; Folstein Susan E; Sutcliffe James S
Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13.
Journal of the American Academy of Child and Adolescent Psychiatry 2003;42(7):856-63.
2003: Nurmi E L; Amin T; Olson L M; Jacobs M M; McCauley J L; Lam A Y; Organ E L; Folstein S E; Haines J L; Sutcliffe J S
Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.
Molecular psychiatry 2003;8(6):624-34, 570.
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: Thornton Tricia A; Haines Jonathan L
PowerTrim: An automated decision support algorithm for preprocessing family-based genetic data.
American journal of human genetics 2003;72(5):1280-1.
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: 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: Hutcheson Holli B; Bradford Y; Folstein S E; Gardiner M B; Santangelo S L; Sutcliffe J S; Haines J L
Defining the autism minimum candidate gene region on chromosome 7.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;117B(1):90-6.
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: Spiekerkoetter Ute; Eeds Angela; Yue Zou; Haines Jonathan; Strauss Arnold W; Summar Marshall
Uniparental disomy of chromosome 2 resulting in lethal trifunctional protein deficiency due to homozygous alpha-subunit mutations.
Human mutation 2002;20(6):447-51.
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: Thomas Alan Q; Lane Kirk; Phillips John; Prince Melissa; Markin Cheryl; Speer Marcy; Schwartz David A; Gaddipati Radhika; Marney Annis; Johnson Joyce; Roberts Richard; Haines Jonathan; Stahlman Mildred; Loyd James E
Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred.
American journal of respiratory and critical care medicine 2002;165(9):1322-8.
2002: Graff-Radford Neill R; Green Robert C; Go Rodney C P; Hutton Michael L; Edeki Timi; Bachman David; Adamson Jennifer L; Griffith Patrick; Willis Floyd B; Williams Mary; Hipps Yvonne; Haines Jonathan L; Cupples L Adrienne; Farrer Lindsay A
Association between apolipoprotein E genotype and Alzheimer disease in African American subjects.
Archives of neurology 2002;59(4):594-600.
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: 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: Gao Hanlin; Boustany Rose-Mary N; Espinola Janice A; Cotman Susan L; Srinidhi Lakshmi; Antonellis Kristen Auger; Gillis Tammy; Qin Xuebin; Liu Shumei; Donahue Leah R; Bronson Roderick T; Faust Jerry R; Stout Derek; Haines Jonathan L; Lerner Terry J; MacDonald Marcy E
Mutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouse.
American journal of human genetics 2002;70(2):324-35.
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.
2001: Abou-Khalil B; Ge Q; Desai R; Ryther R; Bazyk A; Bailey R; Haines J L; Sutcliffe J S; George A L
Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation.
Neurology 2001;57(12):2265-72.
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: 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: 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: Bradford Y; Haines J; Hutcheson H; Gardiner M; Braun T; Sheffield V; Cassavant T; Huang W; Wang K; Vieland V; Folstein S; Santangelo S; Piven J
Incorporating language phenotypes strengthens evidence of linkage to autism.
American journal of medical genetics 2001;105(6):539-47.
2001: Wassink T H; Piven J; Vieland V J; Huang J; Swiderski R E; Pietila J; Braun T; Beck G; Folstein S E; Haines J L; Sheffield V C
Evidence supporting WNT2 as an autism susceptibility gene.
American journal of medical genetics 2001;105(5):406-13.
2001: Pearson D L; Dawling S; Walsh W F; Haines J L; Christman B W; Bazyk A; Scott N; Summar M L
Neonatal pulmonary hypertension--urea-cycle intermediates, nitric oxide production, and carbamoyl-phosphate synthetase function.
The New England journal of medicine 2001;344(24):1832-8.
2001: Tiller G E; Hannig V L; Dozier D; Carrel L; Trevarthen K C; Wilcox W R; Mundlos S; Haines J L; Gedeon A K; Gecz J
A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda.
American journal of human genetics 2001;68(6):1398-407.
2001: Haines J L
Genetic linkage reference maps: access to Internet-based resources.
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2001;Appendix 5():Appendix 5.
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.
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: Kunst C B; Messer L; Gordon J; Haines J; Patterson D
Genetic mapping of a mouse modifier gene that can prevent ALS onset.
Genomics 2000;70(2):181-9.
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: Xie H G; Stein C M; Kim R B; Gainer J V; Sofowora G; Dishy V; Brown N J; Goree R E; Haines J L; Wood A J
Human beta2-adrenergic receptor polymorphisms: no association with essential hypertension in black or white Americans.
Clinical pharmacology and therapeutics 2000;67(6):670-5.
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: Guo Z; Cupples L A; Kurz A; Auerbach S H; Volicer L; Chui H; Green R C; Sadovnick A D; Duara R; DeCarli C; Johnson K; Go R C; Growdon J H; Haines J L; Kukull W A; Farrer L A
Head injury and the risk of AD in the MIRAGE study.
Neurology 2000;54(6):1316-23.
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.
1999: Barrett S; Beck J C; Bernier R; Bisson E; Braun T A; Casavant T L; Childress D; Folstein S E; Garcia M; Gardiner M B; Gilman S; Haines J L; Hopkins K; Landa R; Meyer N H; Mullane J A; Nishimura D Y; Palmer P; Piven J; Purdy J; Santangelo S L; Searby C; Sheffield V; Singleton J; Slager S
An autosomal genomic screen for autism. Collaborative linkage study of autism.
American journal of medical genetics 1999;88(6):609-15.
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: 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: Xie H G; Stein C M; Kim R B; Xiao Z S; He N; Zhou H H; Gainer J V; Brown N J; Haines J L; Wood A J
Frequency of functionally important beta-2 adrenoceptor polymorphisms varies markedly among African-American, Caucasian and Chinese individuals.
Pharmacogenetics 1999;9(4):511-6.
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: 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: Bejaoui K; McKenna-Yasek D; Hosler B A; Burns-Deater E; Deater L M; O'Neill G; Haines J L; Brown R H
Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22.
Neurology 1999;52(3):510-5.
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: Haines J L; Pericak-Vance M A
Genetics of multiple sclerosis.
Current directions in autoimmunity 1999;1():273-88.
1999: Garcia M E; Haines J L
Hunting genetic diseases: exploring a multistage approach to identifying disease loci.
Genetic epidemiology 1999;17 Suppl 1():S557-62.
1998: Hosler B A; Sapp P C; Berger R; O'Neill G; Bejaoui K; Hamida M B; Hentati F; Chin W; McKenna-Yasek D; Haines J L; Patterson D; Horvitz H R; Brown R H; Day C B
Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33.
Neurogenetics 1998;2(1):34-42.
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: 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: McKenna M J; Kristiansen A G; Bartley M L; Rogus J J; Haines J L
Association of COL1A1 and otosclerosis: evidence for a shared genetic etiology with mild osteogenesis imperfecta.
The American journal of otology 1998;19(5):604-10.
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: 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: Kwiatkowska J; Jozwiak S; Hall F; Henske E P; Haines J L; McNamara P; Braiser J; Wigowska-Sowinska J; Kasprzyk-Obara J; Short M P; Kwiatkowski D J
Comprehensive mutational analysis of the TSC1 gene: observations on frequency of mutation, associated features, and nonpenetrance.
Annals of human genetics 1998;62(Pt 4):277-85.
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: 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: Haines J L; Boustany R M; Alroy J; Auger K J; Shook K S; Terwedow H; Lerner T J
Chromosomal localization of two genes underlying late-infantile neuronal ceroid lipofuscinosis.
Neurogenetics 1998;1(3):217-22.
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: 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: 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: 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: Humphrey D; Kwiatkowska J; Henske E P; Haines J L; Halley D; van Slegtenhorst M; Kwiatkowski D J
Cloning and evaluation of RALGDS as a candidate for the tuberous sclerosis gene TSC1.
Annals of human genetics 1997;61(Pt 4):299-305.
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: Andersen J S; Pralea A M; DelBono E A; Haines J L; Gorin M B; Schuman J S; Mattox C G; Wiggs J L
A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-q36.
Archives of ophthalmology 1997;115(3):384-8.
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: Blacker D; Haines J L; Rodes L; Terwedow H; Go R C; Harrell L E; Perry R T; Bassett S S; Chase G; Meyers D; Albert M S; Tanzi R
ApoE-4 and age at onset of Alzheimer's disease: the NIMH genetics initiative.
Neurology 1997;48(1):139-47.
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.
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: McKenna M J; Kristiansen A G; Haines J
Polymerase chain reaction amplification of a measles virus sequence from human temporal bone sections with active otosclerosis.
The American journal of otology 1996;17(6):827-30.
1996: Rao V S; Cupples A; van Duijn C M; Kurz A; Green R C; Chui H; Duara R; Auerbach S A; Volicer L; Wells J; van Broeckhoven C; Growdon J H; Haines J L; Farrer L A
Evidence for major gene inheritance of Alzheimer disease in families of patients with and without apolipoprotein E epsilon 4.
American journal of human genetics 1996;59(3):664-75.
1996: Phillips J C; del Bono E A; Haines J L; Pralea A M; Cohen J S; Greff L J; Wiggs J L
A second locus for Rieger syndrome maps to chromosome 13q14.
American journal of human genetics 1996;59(3):613-9.
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: 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: 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: 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: Wilson P J; Ramesh V; Kristiansen A; Bove C; Jozwiak S; Kwiatkowski D J; Short M P; Haines J L
Novel mutations detected in the TSC2 gene from both sporadic and familial TSC patients.
Human molecular genetics 1996;5(2):249-56.
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: Pericak-Vance M A; Haines J L
Genetic susceptibility to Alzheimer disease.
Trends in genetics : TIG 1995;11(12):504-8.
1995: Haines J L; Boustany R M; Worster T; Ter-Minassian M; Jondro P; Lerner T J
Genome-wide search for CLN2, the gene causing late-infantile neuronal ceroid-lipofuscinosis (LNCL).
American journal of medical genetics 1995;57(2):344-7.
1995: Lerner T J; D'Arigo K L; Haines J L; Doggett N A; Taschner P E; de Vos N; Buckler A J
Isolation of genes from the Batten candidate region using exon amplification. Batten Disease Consortium.
American journal of medical genetics 1995;57(2):320-3.
1995: Xu L; Sterner C; Maheshwar M M; Wilson P J; Nellist M; Short P M; Haines J L; Sampson J R; Ramesh V
Alternative splicing of the tuberous sclerosis 2 (TSC2) gene in human and mouse tissues.
Genomics 1995;27(3):475-80.
1995: Paglinauan C; Haines J L; Del Bono E A; Schuman J; Stawski S; Wiggs J L
Exclusion of chromosome 1q21-q31 from linkage to three pedigrees affected by the pigment-dispersion syndrome.
American journal of human genetics 1995;56(5):1240-3.
1995: Bejaoui K; Hirabayashi K; Hentati F; Haines J L; Ben Hamida C; Belal S; Miller R G; McKenna-Yasek D; Weissenbach J; Rowland L P
Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14.
Neurology 1995;45(4):768-72.
1995: Short M P; Richardson E P; Haines J L; Kwiatkowski D J
Clinical, neuropathological and genetic aspects of the tuberous sclerosis complex.
Brain pathology (Zurich, Switzerland) 1995;5(2):173-9.
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: Henske E P; Short M P; Jozwiak S; Bovey C M; Ramlakhan S; Haines J L; Kwiatkowski D J
Identification of VAV2 on 9q34 and its exclusion as the tuberous sclerosis gene TSC1.
Annals of human genetics 1995;59(Pt 1):25-37.
1995: Blumenfeld A; Lucente D E; Trofatter J A; Lerner T; Slaugenhaupt S A; Liebert C B; Monahan M; Haines J L; Gusella J F; Breakefield X O; Parysek L M
Peripherin gene is linked to keratin 18 gene on human chromosome 12.
Somatic cell and molecular genetics 1995;21(1):83-8.
1995: Rogus J J; Haines J L
Evaluation of screening strategies to detect an oligogenic disease.
Genetic epidemiology 1995;12(6):665-9.
1995: Locke P A; Conneally P M; Tanzi R E; Gusella J F; Haines J L
Apolipoprotein E4 allele and Alzheimer disease: examination of allelic association and effect on age at onset in both early- and late-onset cases.
Genetic epidemiology 1995;12(1):83-92.
1994: Gregor P; Gaston S M; Yang X; O'Regan J P; Rosen D R; Tanzi R E; Patterson D; Haines J L; Horvitz H R; Uhl G R
Genetic and physical mapping of the GLUR5 glutamate receptor gene on human chromosome 21.
Human genetics 1994;94(5):565-70.
1994: Yan W L; Lerner T J; Haines J L; Gusella J F
Sequence analysis and mapping of a novel human mitochondrial ATP synthase subunit 9 cDNA (ATP5G3).
Genomics 1994;24(2):375-7.
1994: Schultz E A; Callen D F; Doggett N A; Haines J L; Lerner T J
Microsatellite repeat polymorphism at the D16S366 locus.
Human molecular genetics 1994;3(9):1713.
1994: Kim S K; Haines J L; Berson E L; Dryja T P
Nonallelic heterogeneity in autosomal dominant retinitis pigmentosa with incomplete penetrance.
Genomics 1994;22(3):659-660.
1994: Tsuda T; Lopez R; Rogaeva E A; Freedman M; Rogaev E; Drachman D; Pollen D; Haines J; Liang Y; McLachlan D R
Are the associations between Alzheimer's disease and polymorphisms in the apolipoprotein E and the apolipoprotein CII genes due to linkage disequilibrium?
Annals of neurology 1994;36(1):97-100.
1994: St George-Hyslop P; Rogaeva E; Huterer J; Tsuda T; Santos J; Haines J L; Schlumpf K; Rogaev E I; Liang Y; McLachlan D R
Machado-Joseph disease in pedigrees of Azorean descent is linked to chromosome 14.
American journal of human genetics 1994;55(1):120-5.
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: Povey S; Armour J; Farndon P; Haines J L; Knowles M; Olopade F; Pilz A; White J A; Kwiatkowski D J
Report and abstracts of the Third International Workshop on Chromosome 9. Cambridge, United Kingdom, 9-11 April, 1994.
Annals of human genetics 1994;58(Pt 3):177-250.
1994: Figlewicz D A; McInnis M G; Goto J; Haines J L; Warren A C; Krizus A; Khodr N; Brown R H; McKenna-Yasek D; Antonarakis S E
Identification of flanking markers for the familial amyotrophic lateral sclerosis gene ALS1 on chromosome 21.
Journal of the neurological sciences 1994;124 Suppl():90-5.
1994: Mitchison H M; Taschner P E; O'Rawe A M; de Vos N; Phillips H A; Thompson A D; Kozman H M; Haines J L; Schlumpf K; D'Arigo K
Genetic mapping of the Batten disease locus (CLN3) to the interval D16S288-D16S383 by analysis of haplotypes and allelic association.
Genomics 1994;22(2):465-8.
1994: Wiggs J L; Haines J L; Paglinauan C; Fine A; Sporn C; Lou D
Genetic linkage of autosomal dominant juvenile glaucoma to 1q21-q31 in three affected pedigrees.
Genomics 1994;21(2):299-303.
1994: Rosen D R; Sapp P; O'Regan J; McKenna-Yasek D; Schlumpf K S; Haines J L; Gusella J F; Horvitz H R; Brown R H
Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers.
American journal of medical genetics 1994;51(1):61-9.
1994: Lerner T J; Boustany R M; MacCormack K; Gleitsman J; Schlumpf K; Breakefield X O; Gusella J F; Haines J L
Linkage disequilibrium between the juvenile neuronal ceroid lipofuscinosis gene and marker loci on chromosome 16p 12.1.
American journal of human genetics 1994;54(1):88-94.
1994: Robberecht W; Sapp P; Viaene M K; Rosen D; McKenna-Yasek D; Haines J; Horvitz R; Theys P; Brown R
Cu/Zn superoxide dismutase activity in familial and sporadic amyotrophic lateral sclerosis.
Journal of neurochemistry 1994;62(1):384-7.
1994: Attwood J; Chiano M; Collins A; Donis-Keller H; Dracopoli N; Fountain J; Falk C; Goudie D; Gusella J; Haines J
CEPH consortium Map of chromosome 9.
Genomics 1994;19(2):203-14.
1993: Kwiatkowski D J; Dib C; Slaugenhaupt S A; Povey S; Gusella J F; Haines J L
An index marker map of chromosome 9 provides strong evidence for positive interference.
American journal of human genetics 1993;53(6):1279-88.
1993: Rogaev E I; Lukiw W J; Vaula G; Haines J L; Rogaeva E A; Tsuda T; Alexandrova N; Liang Y; Mortilla M; Amaducci L
Analysis of the c-FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial Alzheimer's disease.
Neurology 1993;43(11):2275-9.
1993: Henske E P; Ozelius L; Gusella J F; Haines J L; Kwiatkowski D J
A high-resolution linkage map of human 9q34.1.
Genomics 1993;17(3):587-91.
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: Blumenfeld A; Slaugenhaupt S A; Axelrod F B; Lucente D E; Maayan C; Liebert C B; Ozelius L J; Trofatter J A; Haines J L; Breakefield X O
Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis.
Nature genetics 1993;4(2):160-4.
1993: Gregor P; Reeves R H; Jabs E W; Yang X; Dackowski W; Rochelle J M; Brown R H; Haines J L; O'Hara B F; Uhl G R
Chromosomal localization of glutamate receptor genes: relationship to familial amyotrophic lateral sclerosis and other neurological disorders of mice and humans.
Proceedings of the National Academy of Sciences of the United States of America 1993;90(7):3053-7.
1993: Goto J; Figlewicz D A; Haines J L; Brown R H; Khodr N; Rouleau G A
The glycinamide ribonucleotide transformylase (GART) gene is not responsible for familial amyotrophic lateral sclerosis.
Neuromuscular disorders : NMD 1993;3(2):157-60.
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: Yan W; Boustany R M; Konradi C; Ozelius L; Lerner T; Trofatter J A; Julier C; Breakefield X O; Gusella J F; Haines J L
Localization of juvenile, but not late-infantile, neuronal ceroid lipofuscinosis on chromosome 16.
American journal of human genetics 1993;52(1):89-95.
1993: Locke P A; MacDonald M E; Srinidhi J; Gilliam T C; Tanzi R E; Conneally P M; Wexler N S; Haines J L; Gusella J F
A genetic linkage map of the chromosome 4 short arm.
Somatic cell and molecular genetics 1993;19(1):95-101.
1993: Blumenfeld A; Axelrod F B; Trofatter J A; Maayan C; Lucente D E; Slaugenhaupt S A; Liebert C B; Ozelius L J; Haines J L; Breakefield X O
Exclusion of familial dysautonomia from more than 60% of the genome.
Journal of medical genetics 1993;30(1):47-52.
1993: Kwiatkowski D J; Armour J; Bale A E; Fountain J W; Goudie D; Haines J L; Knowles M A; Pilz A; Slaugenhaupt S; Povey S
Report and abstracts of the Second International Workshop on Human Chromosome 9 Mapping 1993.
Cytogenetics and cell genetics 1993;64(2):93-121.
1993: Haines J L; Guillemette W; Rosen D; Brown R; Donaldson D; Patterson D
A genetic linkage map of chromosome 21: a look at meiotic phenomena.
Progress in clinical and biological research 1993;384():51-61.
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: Grafton S T; Mazziotta J C; Pahl J J; St George-Hyslop P; Haines J L; Gusella J; Hoffman J M; Baxter L R; Phelps M E
Serial changes of cerebral glucose metabolism and caudate size in persons at risk for Huntington's disease.
Archives of neurology 1992;49(11):1161-7.
1992: Ozelius L J; Kwiatkowski D J; Schuback D E; Breakefield X O; Wexler N S; Gusella J F; Haines J L
A genetic linkage map of human chromosome 9q.
Genomics 1992;14(3):715-20.
1992: Donaldson D H; Rosen D R; O'Regan J; Sapp P C; Horvitz H R; Gusella J F; Haines J L; Pestka S; Jung V; Nusbaum C
Two independent dinucleotide repeat polymorphisms at the D21S235 locus (21q22.1).
Human molecular genetics 1992;1(8):651.
1992: Haines J L
Chromlook: an interactive program for error detection and mapping in reference linkage data.
Genomics 1992;14(2):517-9.
1992: Rosen D R; Sapp P C; O'Regan J; Horvitz H R; Donaldson D H; Nussbaum C; Gusella J F; Haines J L; Pestka S; Jung V
Dinucleotide repeat polymorphisms (D21S223 and D21S224) at 21q22.1.
Human molecular genetics 1992;1(7):547.
1992: Narod S A; Parry D M; Parboosingh J; Lenoir G M; Ruttledge M; Fischer G; Eldridge R; Martuza R L; Frontali M; Haines J
Neurofibromatosis type 2 appears to be a genetically homogeneous disease.
American journal of human genetics 1992;51(3):486-96.
1992: Trofatter J A; Sytsma M L; Gusella J F; Haines J L
Dinucleotide repeat polymorphism at the topoisomerase (DNA) I pseudogene 2 (TOPIP2).
Human molecular genetics 1992;1(6):455.
1992: Kandt R S; Haines J L; Smith M; Northrup H; Gardner R J; Short M P; Dumars K; Roach E S; Steingold S; Wall S
Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease.
Nature genetics 1992;2(1):37-41.
1992: Tanzi R E; Vaula G; Romano D M; Mortilla M; Huang T L; Tupler R G; Wasco W; Hyman B T; Haines J L; Jenkins B J
Assessment of amyloid beta-protein precursor gene mutations in a large set of familial and sporadic Alzheimer disease cases.
American journal of human genetics 1992;51(2):273-82.
1992: Karlinsky H; Vaula G; Haines J L; Ridgley J; Bergeron C; Mortilla M; Tupler R G; Percy M E; Robitaille Y; Noldy N E
Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the beta-amyloid precursor protein gene.
Neurology 1992;42(8):1445-53.
1992: Ionasescu V V; Trofatter J; Haines J L; Ionasescu R; Searby C
Mapping of the gene for X-linked dominant Charcot-Marie-Tooth neuropathy.
Neurology 1992;42(4):903-8.
1992: Ionasescu V V; Trofatter J; Haines J L; Ionasescu R; Searby C
Charcot-Marie-Tooth neuropathy related to chromosome 1.
American journal of medical genetics 1992;42(5):728-32.
1992: Ionasescu V V; Trofatter J; Haines J L; Summers A M; Ionasescu R; Searby C
X-linked recessive Charcot-Marie-Tooth neuropathy: clinical and genetic study.
Muscle & nerve 1992;15(3):368-73.
1992: Tanzi R E; Watkins P C; Stewart G D; Wexler N S; Gusella J F; Haines J L
A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and age.
American journal of human genetics 1992;50(3):551-8.
1992: Haines J L; Yan W L; Boustany R M; Jewell A; Julier C; Breakefield X O; Gusella J F
Linkage analysis in juvenile neuronal ceroid lipofuscinosis.
American journal of medical genetics 1992;42(4):542-5.
1992: Baxter L R; Mazziotta J C; Pahl J J; Grafton S T; St George-Hyslop P; Haines J L; Gusella J F; Szuba M P; Selin C E; Guze B H
Psychiatric, genetic, and positron emission tomographic evaluation of persons at risk for Huntington's disease.
Archives of general psychiatry 1992;49(2):148-54.
1992: Kwiatkowski D J; Henske E P; Weimer K; Ozelius L; Gusella J F; Haines J
Construction of a GT polymorphism map of human 9q.
Genomics 1992;12(2):229-40.
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: Haines J L; Trofatter J A
Genetic linkage and affected pedigree member analysis in malignant melanoma.
Cytogenetics and cell genetics 1992;59(2-3):206-7.
1992: Haines J L; Trofatter J A; Tanzi R E; Watkins P; Wexler N S; Conneally P M; Gusella J F
Chromosome 21 genetic linkage data set based on the Venezuelan reference pedigree.
Cytogenetics and cell genetics 1992;59(2-3):88-9.
1991: Haines J L; Short M P; Kwiatkowski D J; Jewell A; Andermann E; Bejjani B; Yang C H; Gusella J F; Amos J A
Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity.
American journal of human genetics 1991;49(4):764-72.
1991: Haines J L
The genetics of Alzheimer disease--a teasing problem.
American journal of human genetics 1991;48(6):1021-5.
1991: Ionasescu V V; Trofatter J; Haines J L; Summers A M; Ionasescu R; Searby C
Heterogeneity in X-linked recessive Charcot-Marie-Tooth neuropathy.
American journal of human genetics 1991;48(6):1075-83.
1991: Trofatter J A; Gusella J F; Haines J L
Dinucleotide repeat polymorphism at the debrisoquine 4-hydroxylase (CYP2D) locus.
Nucleic acids research 1991;19(10):2802.
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: Janssen L A; Povey S; Attwood J; Sandkuyl L A; Lindhout D; Flodman P; Smith M; Sampson J R; Haines J L; Merkens E C
A comparative study on genetic heterogeneity in tuberous sclerosis: evidence for one gene on 9q34 and a second gene on 11q22-23.
Annals of the New York Academy of Sciences 1991;615():306-15.
1991: Brown R H; Horvitz H R; Rouleau G A; McKenna-Yasek D; Beard C; Sapp P; Haines J L; Gusella J F; Figlewicz D A
Gene linkage in familial amyotrophic lateral sclerosis: a progress report.
Advances in neurology 1991;56():215-26.
1991: Fontaine B; Trofatter J; Rouleau G A; Khurana T S; Haines J; Brown R; Gusella J F
Different gene loci for hyperkalemic and hypokalemic periodic paralysis.
Neuromuscular disorders : NMD 1991;1(4):235-8.
1991: Haines J L; Amos J; Attwood J; Bech-Hansen N T; Burley M; Conneally P M; Connor J M; Fahsold R; Flodman P; Fryer A
Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative dataset.
Annals of the New York Academy of Sciences 1991;615():256-64.
1991: Short M P; Haines J; Jewell A; Bejjani B; Yang C H; Wyandt H; MacFarlane H; Andermann E; Kwiatkowski D; Amos J
Clinical findings and linkage studies in familial tuberous sclerosis.
Annals of the New York Academy of Sciences 1991;615():380-1.
1990: Fontaine B; Khurana T S; Hoffman E P; Bruns G A; Haines J L; Trofatter J A; Hanson M P; Rich J; McFarlane H; Yasek D M
Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene.
Science (New York, N.Y.) 1990;250(4983):1000-2.
1990: Grafton S T; Mazziotta J C; Pahl J J; St George-Hyslop P; Haines J L; Gusella J; Hoffman J M; Baxter L R; Phelps M E
A comparison of neurological, metabolic, structural, and genetic evaluations in persons at risk for Huntington's disease.
Annals of neurology 1990;28(5):614-21.
1990: St George-Hyslop P H; Haines J L; Farrer L A; Polinsky R; Van Broeckhoven C; Goate A; McLachlan D R; Orr H; Bruni A C; Sorbi S
Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. FAD Collaborative Study Group.
Nature 1990;347(6289):194-7.
1990: Haines J L; Ozelius L J; McFarlane H; Menon A; Tzall S; Martiniuk F; Hirschhorn R; Gusella J F
A genetic linkage map of chromosome 17.
Genomics 1990;8(1):1-6.
1990: Rouleau G A; Bazanowski A; Gusella J F; Haines J L
A genetic map of chromosome 1: comparison of different data sets and linkage programs.
Genomics 1990;7(3):313-8.
1990: Kastelein J J; Haines J L; Hayden M R
The gene causing familial hypoalphalipoproteinemia is not caused by a defect in the apo AI-CIII-AIV gene cluster in a Spanish family.
Human genetics 1990;84(5):396-400.
1990: Rouleau G A; Seizinger B R; Wertelecki W; Haines J L; Superneau D W; Martuza R L; Gusella J F
Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.
American journal of human genetics 1990;46(2):323-8.
1990: Tanzi R E; Haines J L; Gusella J F
Detailed genetic linkage map of human chromosome 21: patterns of recombination according to age and sex.
Progress in clinical and biological research 1990;360():15-26.
1989: St George-Hyslop P H; Haines J L; Polinsky R J; Tanzi R E; Farrer L; Myers R H; Gusella J F
Molecular genetics of familial Alzheimer's disease.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 1989;16(4 Suppl):465-7.
1989: Sims K B; Ozelius L; Corey T; Rinehart W B; Liberfarb R; Haines J; Chen W J; Norio R; Sankila E; de la Chapelle A
Norrie disease gene is distinct from the monoamine oxidase genes.
American journal of human genetics 1989;45(3):424-34.
1989: St George-Hyslop P H; Myers R H; Haines J L; Farrer L A; Tanzi R E; Abe K; James M F; Conneally P M; Polinsky R J; Gusella J F
Familial Alzheimer's disease: progress and problems.
Neurobiology of aging 1989;10(5):417-25.
1989: MacDonald M E; Cheng S V; Zimmer M; Haines J L; Poustka A; Allitto B; Smith B; Whaley W L; Romano D M; Jagadeesh J
Clustering of multiallele DNA markers near the Huntington's disease gene.
The Journal of clinical investigation 1989;84(3):1013-6.
1989: MacDonald M E; Haines J L; Zimmer M; Cheng S V; Youngman S; Whaley W L; Wexler N; Bucan M; Allitto B A; Smith B
Recombination events suggest potential sites for the Huntington's disease gene.
Neuron 1989;3(2):183-90.
1989: Conneally P M; Haines J L; Tanzi R E; Wexler N S; Penchaszadeh G K; Harper P S; Folstein S E; Cassiman J J; Myers R H; Young A B
Huntington disease: no evidence for locus heterogeneity.
Genomics 1989;5(2):304-8.
1989: Menon A G; Ledbetter D H; Rich D C; Seizinger B R; Rouleau G A; Michels V F; Schmidt M A; Dewald G; DallaTorre C M; Haines J L
Characterization of a translocation within the von Recklinghausen neurofibromatosis region of chromosome 17.
Genomics 1989;5(2):245-9.
1989: Cheng S V; Martin G R; Nadeau J H; Haines J L; Bucan M; Kozak C A; MacDonald M E; Lockyer J L; Ledley F D; Woo S L
Synteny on mouse chromosome 5 of homologs for human DNA loci linked to the Huntington disease gene.
Genomics 1989;4(3):419-26.
1989: Robbins C; Theilmann J; Youngman S; Haines J; Altherr M J; Harper P S; Payne C; Junker A; Wasmuth J; Hayden M R
Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90.
American journal of human genetics 1989;44(3):422-5.
1989: Rouleau G A; Haines J L; Bazanowski A; Colella-Crowley A; Trofatter J A; Wexler N S; Conneally P M; Gusella J F
A genetic linkage map of the long arm of human chromosome 22.
Genomics 1989;4(1):1-6.
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: St George-Hyslop P H; Tanzi R E; Haines J L; Polinsky R J; Farrer L; Myers R H; Gusella J F
Molecular genetics of familial Alzheimer's disease.
European neurology 1989;29 Suppl 3():25-7.
1989: Haines J L; Farrer L A; Myers R H
Linkage map of anonymous loci near the CF gene.
Progress in clinical and biological research 1989;329():29-34.
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: Whaley W L; Michiels F; MacDonald M E; Romano D; Zimmer M; Smith B; Leavitt J; Bucan M; Haines J L; Gilliam T C
Mapping of D4S98/S114/S113 confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4.
Nucleic acids research 1988;16(24):11769-80.
1988: Hayden M R; Robbins C; Allard D; Haines J; Fox S; Wasmuth J; Fahy M; Bloch M
Improved predictive testing for Huntington disease by using three linked DNA markers.
American journal of human genetics 1988;43(5):689-94.
1988: Wertelecki W; Rouleau G A; Superneau D W; Forehand L W; Williams J P; Haines J L; Gusella J F
Neurofibromatosis 2: clinical and DNA linkage studies of a large kindred.
The New England journal of medicine 1988;319(5):278-83.
1988: Tanzi R E; Haines J L; Watkins P C; Stewart G D; Wallace M R; Hallewell R; Wong C; Wexler N S; Conneally P M; Gusella J F
Genetic linkage map of human chromosome 21.
Genomics 1988;3(2):129-36.
1988: Cheng S V; Nadeau J H; Tanzi R E; Watkins P C; Jagadesh J; Taylor B A; Haines J L; Sacchi N; Gusella J F
Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17.
Proceedings of the National Academy of Sciences of the United States of America 1988;85(16):6032-6.
1988: Ozelius L; Hsu Y P; Bruns G; Powell J F; Chen S; Weyler W; Utterback M; Zucker D; Haines J; Trofatter J A
Human monoamine oxidase gene (MAOA): chromosome position (Xp21-p11) and DNA polymorphism.
Genomics 1988;3(1):53-8.
1988: Wasmuth J J; Hewitt J; Smith B; Allard D; Haines J L; Skarecky D; Partlow E; Hayden M R
A highly polymorphic locus very tightly linked to the Huntington's disease gene.
Nature 1988;332(6166):734-6.
1988: Seizinger B R; Rouleau G A; Ozelius L J; Lane A H; Farmer G E; Lamiell J M; Haines J; Yuen J W; Collins D; Majoor-Krakauer D
Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma.
Nature 1988;332(6161):268-9.
1988: Hayden M R; Hewitt J; Wasmuth J J; Kastelein J J; Langlois S; Conneally M; Haines J; Smith B; Hilbert C; Allard D
A polymorphic DNA marker that represents a conserved expressed sequence in the region of the Huntington disease gene.
American journal of human genetics 1988;42(1):125-31.
1988: Haines J L; Ozelius L; St George-Hyslop P; Wexler N S; Gusella J F; Conneally P M
Partial linkage map of chromosome 13q in the region of the Wilson disease and retinoblastoma genes.
Genetic epidemiology 1988;5(6):375-80.
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: Gilliam T C; Bucan M; MacDonald M E; Zimmer M; Haines J L; Cheng S V; Pohl T M; Meyers R H; Whaley W L; Allitto B A
A DNA segment encoding two genes very tightly linked to Huntington's disease.
Science (New York, N.Y.) 1987;238(4829):950-2.
1987: Rouleau G A; Wertelecki W; Haines J L; Hobbs W J; Trofatter J A; Seizinger B R; Martuza R L; Superneau D W; Conneally P M; Gusella J F
Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22.
Nature 1987;329(6136):246-8.
1987: Tanzi R E; St George-Hyslop P H; Haines J L; Polinsky R J; Nee L; Foncin J F; Neve R L; McClatchey A I; Conneally P M; Gusella J F
The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid beta-protein gene.
Nature 1987;329(6135):156-7.
1987: Gilliam T C; Tanzi R E; Haines J L; Bonner T I; Faryniarz A G; Hobbs W J; MacDonald M E; Cheng S V; Folstein S E; Conneally P M
Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomere.
Cell 1987;50(4):565-71.
1987: Dlouhy S R; Christian J C; Haines J L; Conneally P M; Hodes M E
Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter.
Human genetics 1987;75(2):136-9.
1987: St George-Hyslop P H; Tanzi R E; Polinsky R J; Haines J L; Nee L; Watkins P C; Myers R H; Feldman R G; Pollen D; Drachman D
The genetic defect causing familial Alzheimer's disease maps on chromosome 21.
Science (New York, N.Y.) 1987;235(4791):885-90.
1987: St George-Hyslop P; Polinsky R; Haines J; Nee L; Tanzi R; Conneally P; Growdon J; Myers R; Pollen D; Drachman D
Search for the familial Alzheimer's disease gene.
Journal of neural transmission. Supplementum 1987;24():13-21.
1986: Pettenati M J; Haines J L; Higgins R R; Wappner R S; Palmer C G; Weaver D D
Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature.
Human genetics 1986;74(2):143-54.
1986: Haines J L; Panter S S; Rich S S; Eaton J W; Tsai M Y; Anderson V E
Reduced plasma haptoglobin and urinary taurine in familial seizures identified through the multisib strategy.
American journal of medical genetics 1986;24(4):723-34.
1986: Trofatter J A; Haines J L; Conneally P M
LIPIN: an interactive data entry and management program for LIPED.
American journal of human genetics 1986;39(1):147-8.
1986: Baehner R L; Kunkel L M; Monaco A P; Haines J L; Conneally P M; Palmer C; Heerema N; Orkin S H
DNA linkage analysis of X chromosome-linked chronic granulomatous disease.
Proceedings of the National Academy of Sciences of the United States of America 1986;83(10):3398-401.
1986: Haines J L; Trofatter J A
Multipoint linkage analysis of spinocerebellar ataxia and markers on chromosome 6.
Genetic epidemiology 1986;3(6):399-405.
1986: Haines J L; Conneally P M
Causes of death in Huntington disease as reported on death certificates.
Genetic epidemiology 1986;3(6):417-23.
1986: Gusella J F; Gilliam T C; Tanzi R E; MacDonald M E; Cheng S V; Wallace M; Haines J; Conneally P M; Wexler N S
Molecular genetics of Huntington's disease.
Cold Spring Harbor symposia on quantitative biology 1986;51 Pt 1():359-64.
1986: Haines J L; Yount E A; Conneally P M
Analysis of Huntington disease linkage to G8.
Genetic epidemiology. Supplement 1986;1():223-8.
1985: Haines J L; Rich S S; Tsai M Y; Anderson V E
Altered amino acid levels in multiply affected sibships with seizures.
Epilepsia 1985;26(6):642-8.
1985: Panter S S; Sadrzadeh S M; Hallaway P E; Haines J L; Anderson V E; Eaton J W
Hypohaptoglobinemia associated with familial epilepsy.
The Journal of experimental medicine 1985;161(4):748-54.
1985: Farrer L A; Haines J L; Yount E A
Automating data manipulation for genetic analysis using a data base management system.
Human heredity 1985;35(5):296-301.
1984: Haines J L; Schut L J; Weitkamp L R; Thayer M; Anderson V E
Spinocerebellar ataxia in a large kindred: age at onset, reproduction, and genetic linkage studies.
Neurology 1984;34(12):1542-8.
1981: Haines J; Schumm W; Kennedy C E
Child guidance as perceived by foster parents and social workers --a research note.
Child welfare 1981;60(10):703-8.

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