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Chang-En Yu

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Lynn Bekris; Martin R Farlow; Doug R Galasko; Jeffrey A Kaye; James B Leverenz; Gail Li; Franziska Lutz; Steve Millard; Joseph F Quinn; Debby W Tsuang; Chang-En Yu; Elaine R Peskind
Tau phosphorylation pathway genes and cerebrospinal fluid tau levels in Alzheimer's disease.
Lynn Bekris; Martin R Farlow; Douglas R Galasko; Jeffrey A Kaye; James B Leverenz; Gail Li; Franziska Lutz; Thomas J Montine; Elaine R Peskind; Joseph F Quinn; Debby W Tsuang; Chang-En Yu
ADAM10 expression and promoter haplotype in Alzheimer's disease.
Sulgi Kim; Lesley Leong; Steven P Millard; Allen Radant; Debby W Tsuang; Dorcas Dobie; Chang-En Yu; Ellen M Wijsman
Inheritance model introduces differential bias in CNV calls between parents and offspring.

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2012: Lynn Bekris; Martin R Farlow; Doug R Galasko; Jeffrey A Kaye; James B Leverenz; Gail Li; Franziska Lutz; Steve Millard; Joseph F Quinn; Debby W Tsuang; Chang-En Yu; Elaine R Peskind
Tau phosphorylation pathway genes and cerebrospinal fluid tau levels in Alzheimer's disease.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012;159B(7):874-83.
2012: Lynn Bekris; Martin R Farlow; Douglas R Galasko; Jeffrey A Kaye; James B Leverenz; Gail Li; Franziska Lutz; Thomas J Montine; Elaine R Peskind; Joseph F Quinn; Debby W Tsuang; Chang-En Yu
ADAM10 expression and promoter haplotype in Alzheimer's disease.
Neurobiology of aging 2012;33(9):2229.e1-2229.e9.
2012: Sulgi Kim; Lesley Leong; Steven P Millard; Allen Radant; Debby W Tsuang; Dorcas Dobie; Chang-En Yu; Ellen M Wijsman
Inheritance model introduces differential bias in CNV calls between parents and offspring.
Genetic epidemiology 2012;36(5):488-98.
2012: James S Meabon; Kole D Meeker; David V Pow; Ian R Sweet; G Stennis Watson; Chang-En Yu; Lynn Bekris; Robert K Fujimura; Aven Lee; David G Cook
Differential expression of the glutamate transporter GLT-1 in pancreas.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2012;60(2):139-51.
2012: Lynn Bekris; Franziska Lutz; Chang-En Yu
Functional analysis of APOE locus genetic variation implicates regional enhancers in the regulation of both TOMM40 and APOE.
Journal of human genetics 2012;57(1):18-25.
2011: O Korvatska; Annette Estes; Jeffrey Munson; Geraldine Dawson; L M Bekris; R Kohen; Chang-En Yu; Gerard D Schellenberg; Wendy H Raskind
Mutations in the TSGA14 gene in families with autism spectrum disorders.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011;156B(3):303-11.
2011: Lynn Bekris; N M Galloway; S Millard; David J Lockhart; Ge Li; Douglas Galasko; Martin R Farlow; Christopher M Clark; Joseph F Quinn; Jeffrey A Kaye; Gerard D Schellenberg; James B Leverenz; Peter Seubert; Debby W Tsuang; Elaine Peskind; Chang-En Yu
Amyloid precursor protein (APP) processing genes and cerebrospinal fluid APP cleavage product levels in Alzheimer's disease.
Neurobiology of aging 2011;32(3):556.e13-23.
2010: Lynn M Bekris; Chang-En Yu; Thomas D Bird; Debby W Tsuang
Genetics of Alzheimer disease.
Journal of geriatric psychiatry and neurology 2010;23(4):213-27.
2010: Elizabeth E Marchani; Thomas D Bird; Ellen J Steinbart; Elisabeth Rosenthal; Chang-En Yu; Gerard D Schellenberg; Ellen M Wijsman
Evidence for three loci modifying age-at-onset of Alzheimer's disease in early-onset PSEN2 families.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010;153B(5):1031-41.
2010: Chang-En Yu; Elizabeth Marchani; Georg Nikisch; Ulrich Müller; Dagmar Nolte; Andreas Hertel; Ellen M Wijsman; Thomas D Bird
The N141I mutation in PSEN2: implications for the quintessential case of Alzheimer disease.
Archives of neurology 2010;67(5):631-3.
2010: Lynn M Bekris; Nichole M Galloway; Thomas J Montine; Gerard D Schellenberg; Chang-En Yu
APOE mRNA and protein expression in postmortem brain are modulated by an extended haplotype structure.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010;153B(2):409-17.
2010: Chang-En Yu; Thomas D Bird; Lynn M Bekris; Thomas J Montine; James B Leverenz; Ellen Steinbart; Nichole M Galloway; Howard Feldman; Randall L Woltjer; Carol A Miller; Elisabeth McCarty Wood; Murray Grossman; Leo McCluskey; Christopher M Clark; Manuela Neumann; Adrian Danek; Douglas Galasko; Steven E Arnold; Alice Chen-Plotkin; Anna Karydas; Bruce L Miller; John Q Trojanowski; Virginia M-Y Lee; Gerard D Schellenberg; Vivianna M Van Deerlin
The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration.
Archives of neurology 2010;67(2):161-70.
2010: Debby W Tsuang; Steven P Millard; Benjamin Ely; Peter Chi; Kenneth Wang; Wendy H Raskind; Sulgi Kim; Zoran Brkanac; Chang-En Yu
The effect of algorithms on copy number variant detection.
PloS one 2010;5(12):e14456.
2009: Dale R Nyholt; Chang-En Yu; Peter M Visscher
On Jim Watson's APOE status: genetic information is hard to hide.
European journal of human genetics : EJHG 2009;17(2):147-9.
2009: Ge Li; Elaine Peskind; Steven P Millard; Peter Chi; Izabela Sokal; Chang-En Yu; Lynn M Bekris; Murray A Raskind; Douglas Galasko; Thomas J Montine
Cerebrospinal fluid concentration of brain-derived neurotrophic factor and cognitive function in non-demented subjects.
PloS one 2009;4(5):e5424.
2008: Matthew J Winton; Vivianna M Van Deerlin; Linda K Kwong; Wuxing Yuan; Elisabeth McCarty Wood; Chang-En Yu; Gerard D Schellenberg; Rosa Rademakers; Richard Caselli; Anna Karydas; John Q Trojanowski; Bruce L Miller; Virginia M-Y Lee
A90V TDP-43 variant results in the aberrant localization of TDP-43 in vitro.
FEBS letters 2008;582(15):2252-6.
2008: Vivianna M Van Deerlin; James B Leverenz; Lynn M Bekris; Thomas D Bird; Wuxing Yuan; Lauren B Elman; Dana Clay; Elisabeth McCarty Wood; Alice S Chen-Plotkin; Maria Martinez-Lage; Ellen Steinbart; Leo McCluskey; Murray Grossman; Manuela Neumann; I-Lin Wu; Wei-Shiung Yang; Robert Kalb; Douglas Galasko; Thomas J Montine; John Q Trojanowski; Virginia M-Y Lee; Gerard D Schellenberg; Chang-En Yu
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis.
Lancet neurology 2008;7(5):409-16.
2008: Lynn M Bekris; Steven P Millard; Nichole M Galloway; Simona Vuletic; John J Albers; Ge Li; Douglas Galasko; Charles DeCarli; Martin R Farlow; Chris M Clark; Joseph F Quinn; Jeffrey A Kaye; Gerard D Schellenberg; Debby W Tsuang; Elaine Peskind; Chang-En Yu
Multiple SNPs within and surrounding the apolipoprotein E gene influence cerebrospinal fluid apolipoprotein E protein levels.
Journal of Alzheimer's disease : JAD 2008;13(3):255-66.
2007: Rosa Rademakers; Matt Baker; Jennifer Gass; Jennifer Adamson; Edward D Huey; Parastoo Momeni; Salvatore Spina; Giovanni Coppola; Anna M Karydas; Heather Stewart; Nancy Johnson; Ging-Yuek Hsiung; Brendan Kelley; Karen Kuntz; Ellen Steinbart; Elisabeth McCarty Wood; Chang-En Yu; Keith A Josephs; Eric Sorenson; Kyle B Womack; Sandra Weintraub; Stuart M Pickering-Brown; Peter R Schofield; William S Brooks; Vivianna M Van Deerlin; Julie Snowden; Christopher M Clark; Andrew Kertesz; Kevin Boylan; Bernardino Ghetti; David Neary; Gerard D Schellenberg; Thomas Beach; Marek-Marsel Mesulam; D M A Mann; Jordan Grafman; Ian R Mackenzie; Howard Feldman; Thomas D Bird; Ronald C. Petersen; David S. Knopman; Bradley Boeve; Daniel Geschwind; Bruce L Miller; Zbigniew K Wszolek; Carol F Lippa; Eileen H Bigio; dennis dickson; Neill Graff-Radford; Michael Hutton
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.
Lancet neurology 2007;6(10):857-68.
2007: Chang-En Yu; Howard Seltman; Elaine Peskind; Nichole Galloway; Peter X Zhou; Elisabeth Rosenthal; Ellen M Wijsman; Debby W Tsuang; Bernie Devlin; Gerard D Schellenberg
Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association.
Genomics 2007;89(6):655-65.
2007: James B Leverenz; Chang-En Yu; Thomas J Montine; Ellen J Steinbart; L M Bekris; Cyrus Zabetian; L K Kwong; Virginia M-Y Lee; Gerard D Schellenberg; Thomas D Bird
A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology.
Brain : a journal of neurology 2007;130(Pt 5):1360-74.
2007: Peter Szatmari; Andrew D Paterson; Lonnie Zwaigenbaum; Wendy Roberts; Jessica Brian; Xiao-Qing Liu; John B Vincent; Jennifer L Skaug; Ann P Thompson; Lili Senman; Lars Feuk; Cheng Qian; Susan E Bryson; Marshall B Jones; Christian R Marshall; Stephen W Scherer; Veronica J Vieland; Christopher Bartlett; La Vonne Mangin; Rhinda Goedken; Alberto Segre; Margaret Pericak-Vance; Michael Cuccaro; John Gilbert; Harry H Wright; Ruth K Abramson; Catalina Betancur; Thomas Bourgeron; Christopher Gillberg; Marion Leboyer; Joseph Buxbaum; Kenneth L Davis; Eric Hollander; Jeremy Silverman; Joachim Hallmayer; Linda Lotspeich; James S Sutcliffe; Jonathan L Haines; Susan E Folstein; Joseph Piven; Thomas H Wassink; Val Sheffield; Daniel Geschwind; Maja Bucan; W Ted Brown; Rita M Cantor; John N Constantino; T Conrad Gilliam; Martha Herbert; Clara Lajonchere; David Ledbetter; Christa Lese Martin; Janet Miller; Stan Nelson; Carol A Samango-Sprouse; Sarah J Spence; Sate Matthew; Rudolph E Tanzi; Hilary Coon; Geraldine Dawson; Bernie Devlin; Annette Estes; Pamela Flodman; Lambertus Klei; William M McMahon; Nancy J Minshew; Jeffrey Munson; Elena Korvatska; Patricia M Rodier; Gerard D Schellenberg; Moyra Smith; M Anne Spence; Chris Stodgell; Ping Guo Tepper; Ellen M Wijsman; Chang-En Yu; Bernadette Rogé; Carine Mantoulan; Kerstin Wittemeyer; Annemarie Poustka; Bärbel Felder; Sabine M Klauck; Claudia Schuster; Fritz Poustka; Sven Bölte; Sabine Feineis-Matthews; Evelyn Herbrecht; Gabi Schmötzer; John Tsiantis; Katerina Papanikolaou; Elena Maestrini; Elena Bacchelli; Francesca Blasi; Simona Carone; Claudio Toma; Herman Van Engeland; Maretha de Jonge; Chantal Kemner; Frederieke Koop; Frederike Koop; Marjolein Langemeijer; Marjolijn Langemeijer; Channa Hijmans; Channa Hijimans; Wouter G Staal; Gillian Baird; Patrick Bolton; Michael L Rutter; Emma Weisblatt; Jonathan Green; Catherine Aldred; Julie-Anne Wilkinson; Andrew Pickles; Ann Le Couteur; Tom Berney; Helen McConachie; Anthony J Bailey; Kostas Francis; Gemma Honeyman; Aislinn Hutchinson; Jeremy R Parr; Simon Wallace; Anthony P Monaco; Gabrielle Barnby; Kazuhiro Kobayashi; Janine A Lamb; Ines Sousa; Nuala Sykes; Edwin H Cook; Stephen J Guter; Bennett L Leventhal; Jeff Salt; Catherine Lord; Christina Corsello; Vanessa Hus; Daniel E Weeks; Fred Volkmar; Maïté Tauber; Eric Fombonne; Andy Shih; Kacie J Meyer
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Nature genetics 2007;39(3):319-28.
2007: Purnima Desai Sundar; Chang-En Yu; Weiva Sieh; Ellen J Steinbart; Ralph M Garruto; Kiyomitsu Oyanagi; Ulla-Katrina Craig; Thomas D Bird; Ellen M Wijsman; Douglas Galasko; Gerard D Schellenberg
Two sites in the MAPT region confer genetic risk for Guam ALS/PDC and dementia.
Human molecular genetics 2007;16(3):295-306.
2007: Weiva Sieh; Chang-En Yu; Thomas D Bird; Gerard D Schellenberg; Ellen M Wijsman
Accounting for linkage disequilibrium among markers in linkage analysis: impact of haplotype frequency estimation and molecular haplotypes for a gene in a candidate region for Alzheimer's disease.
Human heredity 2007;63(1):26-34.
2007: Denise M Kay; Dawn Moran; Lina Moses; Parvoneh Poorkaj-Navas; Cyrus Zabetian; John G Nutt; Stewart A Factor; Chang-En Yu; Jennifer S Montimurro; Robert G Keefe; Gerard D Schellenberg; Haydeh Payami
Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients.
Annals of neurology 2007;61(1):47-54.
2006: Gerard D Schellenberg; Geraldine Dawson; Yun Ju Sung; Annette Estes; Jeffrey Munson; E Rosenthal; J Rothstein; Pamela Flodman; Moyra Smith; Hilary Coon; L Leong; Chang-En Yu; Stodgell Christopher; Patricia M Rodier; M Anne Spence; Nancy J Minshew; William M McMahon; Ellen M Wijsman
Evidence for multiple loci from a genome scan of autism kindreds.
Molecular psychiatry 2006;11(11):1049-60, 979.
2004: Chang-En Yu; Bernie Devlin; Nichole Galloway; Elaine Loomis; Gerard D Schellenberg
ADLAPH: A molecular haplotyping method based on allele-discriminating long-range PCR.
Genomics 2004;84(3):600-12.
2004: Ellen M Wijsman; E Warwick Daw; Chang-En Yu; Haydeh Payami; Ellen J Steinbart; David Nochlin; Erin M Conlon; Thomas D Bird; Gerard D Schellenberg
Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2.
American journal of human genetics 2004;75(3):398-409.
2003: Andrew D Skol; Keith A Young; Debby W Tsuang; Stephen Faraone; Susan L Haverstock; Stephen F Bingham; Sarita Prabhudesai; Felicitas Mena; Aerath Sri Kumar Menon; Chang-En Yu; Paul Rundell; John Pepple; F Sauter; Charlene Baldwin; David Weiss; Joseph F Collins; Tim Keith; Michael Boehnke; Gerard D Schellenberg; Ming T Tsuang
Modest evidence for linkage and possible confirmation of association between NOTCH4 and schizophrenia in a large Veterans Affairs Cooperative Study sample.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;118B(1):8-15.
2002: Razia Sultana; Chang-En Yu; Jun Yu; Jeffrey Munson; Donghui Chen; Wenhui Hua; Annette Estes; Fanny Cortes; Flora de la Barra; Dongmei Yu; Syed T Haider; Barbara J Trask; Eric Green; Wendy H Raskind; Christine M Disteche; Ellen M Wijsman; Geraldine Dawson; Daniel R Storm; Gerard D Schellenberg; Enrique C Villacres
Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins.
Genomics 2002;80(2):129-34.
2002: Chang-En Yu; Geraldine Dawson; Jeffrey Munson; Ian D'Souza; Julie Osterling; Annette Estes; Anne-Louise Leutenegger; Pamela Flodman; Moyra Smith; Wendy H Raskind; M Anne Spence; William M McMahon; Ellen M Wijsman; Gerard D Schellenberg
Presence of large deletions in kindreds with autism.
American journal of human genetics 2002;71(1):100-15.
2000: Gil Blander; N Zalle; Juan Fernando Martinez Leal; RL Bar-Or; Chang-En Yu; Moshe Oren
The Werner syndrome protein contributes to induction of p53 by DNA damage.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2000;14(14):2138-40.
1999: Gil Blander; Jonathan Kipnis; Juan Fernando Martinez Leal; Chang-En Yu; Gerard D Schellenberg; Moshe Oren
Physical and functional interaction between p53 and the Werner's syndrome protein.
The Journal of biological chemistry 1999;274(41):29463-9.
1999: Elisa A Spillare; Ana I Robles; Xin Wei Wang; Jiang Cheng Shen; Chang-En Yu; Gerard D Schellenberg; Curtis C Harris
p53-mediated apoptosis is attenuated in Werner syndrome cells.
Genes & development 1999;13(11):1355-60.
1998: James B Leverenz; Chang-En Yu; Gerard D Schellenberg
Aging-associated neuropathology in Werner syndrome.
Acta neuropathologica 1998;96(4):421-4.
1998: Fuki M Hisama; Oshima Junko; Chang-En Yu; Y H Fu; J Mulligan; Sherman M Weissman; Gerard D Schellenberg
Comparison of methods for identifying transcription units and transcription map of the Werner syndrome gene region.
Genomics 1998;52(3):352-7.
1998: V Sharma; Parvoneh Poorkaj-Navas; Fuki M Hisama; L Bonnycastle; Chang-En Yu; H Massa; Barbara J Trask; Kevin Clancy; D Patterson; Sherman M Weissman; Gerard D Schellenberg
An expression map from human chromosome 14q24.3.
Genomics 1998;47(2):314-8.
1997: Chang-En Yu; Oshima Junko; Ellen M Wijsman; Jun Nakura; T Miki; C Piussan; S Matthews; Y H Fu; J Mulligan; George M Martin; Gerard D Schellenberg
Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.
American journal of human genetics 1997;60(2):330-41.
1996: Oshima Junko; Chang-En Yu; C Piussan; G Klein; J Jabkowski; S Balci; T Miki; Jun Nakura; T Ogihara; J Ells; M Smith; M I Melaragno; M Fraccaro; Susi Scappaticci; J Matthews; S Ouais; A Jarzebowicz; Gerard D Schellenberg; George M Martin
Homozygous and compound heterozygous mutations at the Werner syndrome locus.
Human molecular genetics 1996;5(12):1909-13.
1996: Walter A Kukull; Gerard D Schellenberg; James D Bowen; Wayne C McCormick; Chang-En Yu; Linda Teri; J D Thompson; Ellen S O'Meara; Eric B Larson
Apolipoprotein E in Alzheimer's disease risk and case detection: a case-control study.
Journal of clinical epidemiology 1996;49(10):1143-8.
1996: Jun Nakura; T Miki; L Ye; Noriaki Mitsuda; Y Zhao; K Kihara; Chang-En Yu; Oshima Junko; Ken-Ichiro Fukuchi; Ellen M Wijsman; Gerard D Schellenberg; George M Martin; S i Murano; Katsuyuki Hashimoto; Y Fujiwara; Toshio Ogihara
Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis.
Genomics 1996;36(1):130-41.
1996: Chang-En Yu; Oshima Junko; Fuki M Hisama; S Matthews; Barbara J Trask; Gerard D Schellenberg
A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21.
Genomics 1996;35(3):431-40.
1996: Katrina Goddard; Chang-En Yu; Oshima Junko; T Miki; Jun Nakura; C Piussan; George M Martin; Gerard D Schellenberg; Ellen M Wijsman
Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers.
American journal of human genetics 1996;58(6):1286-302.
1996: Chang-En Yu; Oshima Junko; Y H Fu; Ellen M Wijsman; Fuki M Hisama; R Alisch; S Matthews; Jun Nakura; T Miki; S Ouais; George M Martin; J Mulligan; Gerard D Schellenberg
Positional cloning of the Werner's syndrome gene.
Science (New York, N.Y.) 1996;272(5259):258-62.
1996: Haydeh Payami; Sepideh Zareparsi; K R Montee; Gary Sexton; Jeffrey A Kaye; Thomas D Bird; Chang-En Yu; Ellen M Wijsman; L L Heston; M Litt; Gerard D Schellenberg
Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in women.
American journal of human genetics 1996;58(4):803-11.
1995: Ephrat Levy-Lahad; Wilma Wasco; Parvoneh Poorkaj-Navas; Donna M Romano; Oshima Junko; Warren H Pettingell; Chang-En Yu; P D Jondro; S D Schmidt; K Wang
Candidate gene for the chromosome 1 familial Alzheimer's disease locus.
Science (New York, N.Y.) 1995;269(5226):973-7.
1995: Gail P Jarvik; Ellen M Wijsman; Walter A Kukull; Gerard D Schellenberg; Chang-En Yu; Eric B Larson
Interactions of apolipoprotein E genotype, total cholesterol level, age, and sex in prediction of Alzheimer's disease: a case-control study.
Neurology 1995;45(6):1092-6.
1995: Hugh Hendrie; Kathleen S Hall; Siu Hui; Frederick W Unverzagt; Chang-En Yu; Debomoy K Lahiri; Amrik Sahota; Martin R Farlow; B Musick; C A Class
Apolipoprotein E genotypes and Alzheimer's disease in a community study of elderly African Americans.
Annals of neurology 1995;37(1):118-20.
1994: Jun Nakura; Ellen M Wijsman; T Miki; Kouzin Kamino; Chang-En Yu; Oshima Junko; Ken-Ichiro Fukuchi; J L Weber; C Piussan; M I Melaragno
Homozygosity mapping of the Werner syndrome locus (WRN).
Genomics 1994;23(3):600-8.
1994: L L Bonnycastle; Chang-En Yu; C R Hunt; Barbara J Trask; Kevin Clancy; J L Weber; D Patterson; Gerard D Schellenberg
Cloning, sequencing, and mapping of the human chromosome 14 heat shock protein gene (HSPA2).
Genomics 1994;23(1):85-93.
1994: Oshima Junko; Chang-En Yu; M Boehnke; J L Weber; S Edelhoff; M J Wagner; Dan E Wells; S Wood; Christine M Disteche; George M Martin
Integrated mapping analysis of the Werner syndrome region of chromosome 8.
Genomics 1994;23(1):100-13.
1994: Chang-En Yu; Oshima Junko; Katrina Goddard; T Miki; Jun Nakura; T Ogihara; Martin Poot; H Hoehn; M Fraccaro; C Piussan
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndrome.
American journal of human genetics 1994;55(2):356-64.
1994: Haydeh Payami; K R Montee; Jeffrey A Kaye; Thomas D Bird; Chang-En Yu; Ellen M Wijsman; Gerard D Schellenberg
Alzheimer's disease, apolipoprotein E4, and gender.
JAMA : the journal of the American Medical Association 1994;271(17):1316-7.
1994: M Chang; G C Burmer; J Sweasy; Lawrence A Loeb; S Edelhoff; Christine M Disteche; Chang-En Yu; L Anderson; Oshima Junko; Jun Nakura
Evidence against DNA polymerase beta as a candidate gene for Werner syndrome.
Human genetics 1994;93(5):507-12.
1994: M Sapru; J Gu; X Gu; D Smith; Chang-En Yu; D Wells; M Wagner
A panel of radiation hybrids for human chromosome 8.
Genomics 1994;21(1):208-16.
1994: Chang-En Yu; Haydeh Payami; J M Olson; M Boehnke; Ellen M Wijsman; H T Orr; Walter A Kukull; Katrina Goddard; EJ Nemens; J A White
The apolipoprotein E/CI/CII gene cluster and late-onset Alzheimer disease.
American journal of human genetics 1994;54(4):631-42.
1994: Chang-En Yu; L Anderson; Oshima Junko; Gerard D Schellenberg
Dinucleotide repeat polymorphisms at the GSR gene.
Human molecular genetics 1994;3(1):212.
1994: Chang-En Yu; L Anderson; Oshima Junko; Gerard D Schellenberg
Dinucleotide repeat polymorphism at the FGFR1 gene.
Human molecular genetics 1994;3(1):212.
1994: Chang-En Yu; L Anderson; Oshima Junko; Gerard D Schellenberg
Dinucleotide repeat polymorphism at the D8S131 locus.
Human molecular genetics 1994;3(1):211.
1993: L L Bonnycastle; Chang-En Yu; Ellen M Wijsman; H T Orr; D Patterson; Kevin Clancy; Katrina Goddard; M E Alonso; EJ Nemens; J A White
The c-fos gene and early-onset familial Alzheimer's disease.
Neuroscience letters 1993;160(1):33-6.
1993: Michael S Chaussee; D Gerlach; Chang-En Yu; Joseph J Ferretti
Inactivation of the streptococcal erythrogenic toxin B gene (speB) in Streptococcus pyogenes.
Infection and immunity 1993;61(9):3719-23.
1991: Chang-En Yu; Joseph J Ferretti
Molecular characterization of new group A streptococcal bacteriophages containing the gene for streptococcal erythrogenic toxin A (speA).
Molecular & general genetics : MGG 1991;231(1):161-8.
1991: Chang-En Yu; Joseph J Ferretti
Frequency of the erythrogenic toxin B and C genes (speB and speC) among clinical isolates of group A streptococci.
Infection and immunity 1991;59(1):211-5.
1989: Chang-En Yu; Joseph J Ferretti
Molecular epidemiologic analysis of the type A streptococcal exotoxin (erythrogenic toxin) gene (speA) in clinical Streptococcus pyogenes strains.
Infection and immunity 1989;57(12):3715-9.