586 Publications
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| 586 Publications from Scopus |
This is a list of publications by this researcher, listed chronologically starting with the most recent first. New publications appear in this list weekly. The source of publications and 'cited by' data for this application is Scopus.
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1.
2013Louis R. Pasquale; Stephanie J. Loomis; Jae H. Kang; Brian L. Yaspan; Wael Abdrabou; Donald L. Budenz; Teresa C. Chen; Elizabeth Delbono; David S. Friedman; Douglas Gaasterland; et al.
American Journal of Ophthalmology. 2013;155(2):342-353.e5.0 -
2.
2013Rosalyn Lang; Vinaya A. Kelkar; Jennifer R. Byrd; Christopher L. Edwards; Margaret Pericak-Vance; Goldie S. Byrd
Journal of Public Health Management and Practice. 2013;19(2):110-118.0 -
3.
2013Martin A. Kohli; Krista John-Williams; Ruchita Rajbhandary; Adam Naj; Patrice Whitehead; Kara Hamilton; Regina M. Carney; Clinton Wright; Elizabeth Crocco; Harry E. Gwirtzman; et al.
Repeat expansions in the C9ORF72 gene contribute to Alzheimer's disease in Caucasians
Neurobiology of Aging. 2013;34(5):1519.e5-1519.e12.0 -
4.
2013Patrick Holton; Mina Ryten; Michael Nalls; Daniah Trabzuni; Michael E. Weale; Dena Hernandez; Helen Crehan; J. Raphael Gibbs; Richard Mayeux; Jonathan L. Haines; et al.
Initial Assessment of the Pathogenic Mechanisms of the Recently Identified Alzheimer Risk Loci
Annals of Human Genetics. 2013;77(2):85-105.0 -
5.
2013Evadnie Rampersaud; Lubov Nathanson; Jeffrey Farmer; Karyn Meshbane; Richard L. Belton; Amy Dressen; Michael Cuccaro; Anthony Musto; Sylvia Daunert; Sapna Deo; et al.
Genomic Signatures of a Global Fitness Index in a Multi-Ethnic Cohort of Women
Annals of Human Genetics. 2013;77(2):147-157.0 -
6.
2013Akinori Miyashita; Asako Koike; Gyungah Jun; Li-San Wang; Satoshi Takahashi; Etsuro Matsubara; Takeshi Kawarabayashi; Mikio Shoji; Naoki Tomita; Hiroyuki Arai; et al.
PLoS ONE. 2013;8(4).0 -
7.
2013Carlos Cruchaga; John S.K. Kauwe; Oscar Harari; Sheng Chih Jin; Yefei Cai; Celeste M. Karch; Bruno A. Benitez; Amanda T. Jeng; Tara Skorupa; David Carrell; et al.
GWAS of Cerebrospinal Fluid Tau Levels Identifies Risk Variants for Alzheimer's Disease
Neuron. 2013.0 -
8.
2013Lars G. Fritsche; Wei Chen; Matthew Schu; Brian L. Yaspan; Yi Yu; Gudmar Thorleifsson; Donald J. Zack; Satoshi Arakawa; Valentina Cipriani; Stephan Ripke; et al.
Seven new loci associated with age-related macular degeneration
Nature Genetics. 2013;45(4):433-439.0 -
9.
2013Christiane Reitz; Gyungah Jun; Adam Naj; Ruchita Rajbhandary; Badri Narayan Vardarajan; Li-San Wang; Otto Valladares; Chiao-Feng Lin; Eric B. Larson; Neill R. Graff-Radford; et al.
JAMA - Journal of the American Medical Association. 2013;309(14):1483-1492.2 -
10.
2013Athena Hadjixenofontos; Michael A. Schmidt; Patrice L. Whitehead; Ioanna Konidari; Dale J. Hedges; Harry H. Wright; Ruth K. Abramson; Ramkumar Menon; Scott M. Williams; Michael L. Cuccaro; et al.
Evaluating Mitochondrial DNA Variation in Autism Spectrum Disorders
Annals of Human Genetics. 2013;77(1):9-21.0 -
11.
2012Guiqing Cai; Gil Atzmon; Adam C. Naj; Gary W. Beecham; Nir Barzilai; Jonathan L. Haines; Mary Sano; Margaret Pericak-Vance; Joseph D. Buxbaum
Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer Disease
Neurobiology of Aging. 2012;33(2):416-417.e3.2 -
12.
2012Gaofeng Wang; William K. Scott; Patrice Whitehead; Brenda L. Court; Jaclyn L. Kovach; Stephen G. Schwartz; Anita Agarwal; Sander Dubovy; Jonathan L. Haines; Margaret A. Pericak-Vance
A novel ARMS2 splice variant is identified in human retina
Experimental Eye Research. 2012;94(1):187-191.2 -
13.
2012Monique D. Courtenay; John R. Gilbert; Lan Jiang; Anna C. Cummings; Paul J. Gallins; Laura Caywood; Lori Reinhart-Mercer; Denise Fuzzell; Claire Knebusch; Renee Laux; et al.
Mitochondrial Haplogroup X is associated with successful aging in the Amish
Human Genetics. 2012;131(2):201-208.0 -
14.
2012Brooke A. DeRosa; Jessica M. Van Baaren; Gaurav K. Dubey; Joycelyn M. Lee; Michael L. Cuccaro; Jeffery M. Vance; Margaret A. Pericak-Vance; Derek M. Dykxhoorn
Neuroscience Letters. 2012;516(1):9-14.4 -
15.
2012Janey L. Wiggs; Brian L. Yaspan; Michael A. Hauser; Jae H. Kang; R. Rand Allingham; Lana M. Olson; Wael Abdrabou; Bao J. Fan; Dan Y. Wang; Wendy Brodeur; et al.
PLoS Genetics. 2012;8(4).9 -
16.
2012Jillian P. Casey; Tiago Magalhaes; Judith M. Conroy; Regina Regan; Naisha Shah; Richard Anney; Denis C. Shields; Brett S. Abrahams; Joana Almeida; Elena Bacchelli; et al.
Human Genetics. 2012;131(4):565-579.11 -
17.
2012Dale J. Hedges; Kara L. Hamilton-Nelson; Stephanie J. Sacharow; Laura Nations; Gary W. Beecham; Zhanna M. Kozhekbaeva; Brittany L. Butler; Holly N. Cukier; Patrice L. Whitehead; Deqiong Ma; et al.
Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci
Molecular Autism. 2012;3(1).2 -
18.
2012M.I. Kamboh; F.Y. Demirci; X. Wang; R.L. Minster; M.M. Carrasquillo; V.S. Pankratz; S.G. Younkin; A.J. Saykin; G. Jun; C. Baldwin; et al.
Genome-wide association study of Alzheimer's disease
Translational Psychiatry. 2012;2.2 -
19.
2012Liyong Wang; Kenju Hara; Jessica M. Van Baaren; Justin C. Price; Gary W. Beecham; Paul J. Gallins; Patrice L. Whitehead; Gaofeng Wang; Chunrong Lu; Michael A. Slifer; et al.
Vitamin D receptor and Alzheimer's disease: A genetic and functional study
Neurobiology of Aging. 2012;33(8):e1-e9.1 -
20.
2012Gladys Montenegro; Adriana P. Rebelo; James Connell; Rachel Allison; Carla Babalini; Michela D'Aloia; Pasqua Montieri; Rebecca Schüle; Hiroyuki Ishiura; Justin Price; et al.
Journal of Clinical Investigation. 2012;122(2):538-544.16 -
21.
2012Digna R.Velez Edwards; John R. Gilbert; James E. Hicks; Jamie L. Myers; Lan Jiang; Anna C. Cummings; Shengru Guo; Paul J. Gallins; Ioanna Konidari; Laura Caywood; et al.
Linkage and association of successful aging to the 6q25 region in large Amish kindreds
Age. 2012:1-11.0 -
22.
2012Mariet Allen; Fanggeng Zou; High Seng Chai; Curtis S. Younkin; Julia Crook; V. Shane Pankratz; Minerva M. Carrasquillo; Christopher N. Rowley; Asha A. Nair; Sumit Middha; et al.
Novel late-onset Alzheimer disease loci variants associate with brain gene expression
Neurology. 2012;79(3):221-228.5 -
23.
2012Megan Ulmer; Jun Li; Brian L. Yaspan; Ayse Bilge Ozel; Julia E. Richards; Sayoko E. Moroi; Felicia Hawthorne; Donald L. Budenz; David S. Friedman; Douglas Gaasterland; et al.
Investigative Ophthalmology and Visual Science. 2012;53(8):4468-4474.3 -
24.
2012Fanggeng Zou; High Seng Chai; Curtis S. Younkin; Mariet Allen; Julia Crook; V. Shane Pankratz; Minerva M. Carrasquillo; Christopher N. Rowley; Asha A. Nair; Sumit Middha; et al.
Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants
PLoS Genetics. 2012;8(6).3 -
25.
2012Janey L. Wiggs; Michael A. Hauser; Wael Abdrabou; Robert Rand Allingham; Donald L. Budenz; Elizabeth DelBono; David S. Friedman; Jae H. Kang; Douglas Gaasterland; Terry Gaasterland; et al.
Journal of Glaucoma. 2012.2 -
26.
2012Michael L. Cuccaro; Roberto F. Tuchman; Kara L. Hamilton; Harry H. Wright; Ruth K. Abramson; Jonathan L. Haines; John R. Gilbert; Margaret Pericak-Vance
Journal of Autism and Developmental Disorders. 2012;42(8):1630-1641.1 -
27.
2012Giovanni Coppola; Subashchandrabose Chinnathambi; Jason JiYong Lee; Beth A. Dombroski; Matt C. Baker; Alexandra I. Soto-ortolaza; Suzee E. Lee; Eric Klein; Alden Y. Huang; Renee Sears; et al.
Human Molecular Genetics. 2012;21(15):3500-3512.3 -
28.
2012Anthony J. Griswold; Deqiong Ma; Holly N. Cukier; Laura D. Nations; Mike A. Schmidt; Ren-Hua Chung; James M. Jaworski; Daria Salyakina; Ioanna Konidari; Patrice L. Whitehead; et al.
Human Molecular Genetics. 2012;21(15):3513-3523.10 -
29.
2012Anna C. Cummings; Lan Jiang; Digna R. Velez Edwards; Jacob L. Mccauley; Renee Laux; Lynne L. Mcfarland; Denise Fuzzell; Clare Knebusch; Laura Caywood; Lori Reinhart-Mercer; et al.
Annals of Human Genetics. 2012;76(5):342-351.1 -
30.
2012Stephen G. Schwartz; Anita Agarwal; Jaclyn L. Kovach; Paul J. Gallins; William Cade; Eric A. Postel; Gaofeng Wang; Juan Ayala-Haedo; Kylee M. Spencer; Jonathan L. Haines; et al.
The ARMS2 A69S variant and bilateral advanced age-related macular degeneration
Retina. 2012;32(8):1486-1491.0 -
31.
2012Gyungah Jun; Badri N. Vardarajan; Jacqueline Buros; Chang-En Yu; Michele V. Hawk; Beth A. Dombroski; Paul K. Crane; Eric B. Larson; Richard Mayeux; Jonathan L. Haines; et al.
Comprehensive search for Alzheimer disease susceptibility loci in the APOE region
Archives of Neurology. 2012;69(10):1270-1279.6 -
32.
2012Nathalie C. Schnetz-Boutaud; Joshua Hoffman; Jared E. Coe; Deborah G. Murdock; Margaret A. Pericak-Vance; Jonathan L. Haines
Annals of Human Genetics. 2012;76(6):448-453.1 -
33.
2012Richard Anney; Lambertus Klei; Dalila Pinto; Joana Almeida; Elena Bacchelli; Gillian Baird; Nadia Bolshakova; Sven Bölte; Patrick F. Bolton; Thomas Bourgeron; et al.
Individual common variants exert weak effects on the risk for autism spectrum disorderspi
Human Molecular Genetics. 2012;21(21):4781-4792.4 -
34.
2012Zhao-Jun Liu; Yurong Tan; Gary W. Beecham; David M. Seo; Runxia Tian; Yan Li; Roberto I. Vazquez-Padron; Margaret Pericak-Vance; Jeffery M. Vance; Pascal J. Goldschmidt-Clermont; et al.
Atherosclerosis. 2012;225(2):296-303.0 -
35.
2012David C. Whitcomb; Jessica LaRusch; Alyssa M. Krasinskas; Lambertus Klei; Jill P. Smith; Randall E. Brand; John P. Neoptolemos; Markus M. Lerch; Matt Tector; Bimaljit S. Sandhu; et al.
Nature Genetics. 2012;44(12):1349-1354.0 -
36.
2012Thomas L Ortel; Craig S Kitchens; Doruk Erkan; Leonardo R Brandão; Susan Hahn; Andra H James; Roshni Kulkarni; Marilyn J Manco-Johnson; Margaret Pericak-Vance; Jeffery Vance
Clinical causes and treatment of the thrombotic storm
Expert Review of Hematology. 2012;5(6):553-559.0 -
37.
2012Holly N. Cukier; Joycelyn M. Lee; Deqiong Ma; Juan I. Young; Vera Mayo; Brittany L. Butler; Sandhya S. Ramsook; Joseph A. Rantus; Alexander J. Abrams; Patrice L. Whitehead; et al.
Autism Research. 2012;5(6):385-397.0 -
38.
2011Ren-Hua Chung; Deqiong Ma; Kai Wang; Dale J. Hedges; James M. Jaworski; John R. Gilbert; Michael L. Cuccaro; Harry H. Wright; Ruth K. Abramson; Ioanna Konidari; et al.
Molecular Autism. 2011;2(1).2 -
39.
2011Kylee L. Spencer; Lana M. Olson; Nathalie Schnetz-Boutaud; Paul Gallins; Anita Agarwal; Alessandro Iannaccone; Stephen B. Kritchevsky; Melissa Garcia; Michael A. Nalls; Anne B. Newman; et al.
PLoS ONE. 2011;6(3).7 -
40.
2011Anna C. Cummings; Stephen L. Lee; Jacob L. Mccauley; Lan Jiang; Amy Crunk; Lynne L. Mcfarland; Paul J. Gallins; Denise Fuzzell; Clare Knebusch; Charles E. Jackson; et al.
A Genome-Wide Linkage Screen in the Amish with Parkinson Disease Points to Chromosome 6
Annals of Human Genetics. 2011;75(3):351-358.0 -
41.
2011Holly N. Cukier; Daria Salyakina; Sarah F. Blankstein; Joycelyn L. Robinson; Stephanie Sacharow; Deqiong Ma; Harry H. Wright; Ruth K. Abramson; Ramkumar Menon; Scott M. Williams; et al.
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 2011;156(4):493-501.4 -
42.
2011Adam C. Naj; Gyungah Jun; Gary W. Beecham; Li-San Wang; Badri Narayan Vardarajan; Jacqueline Buros; Paul J. Gallins; Joseph D. Buxbaum; Gail P. Jarvik; Paul K. Crane; et al.
Nature Genetics. 2011;43(5):436-443.189 -
43.
2011Brian L. Yaspan; William S. Bush; Eric S. Torstenson; Deqiong Ma; Margaret A. Pericak-Vance; Marylyn D. Ritchie; James S. Sutcliffe; Jonathan L. Haines
Genetic analysis of biological pathway data through genomic randomization
Human Genetics. 2011;129(5):563-571.10 -
44.
2011D.S. Mccorquodale; U. Ozomaro; J. Huang; G. Montenegro; A. Kushman; L. Citrigno; J. Price; F. Speziani; M.A. Pericak-Vance; S. Züchner
Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia
Clinical Genetics. 2011;79(6):523-530.5 -
45.
2011Dale J. Hedges; Toumy Guettouche; Shan Yang; Guney Bademci; Ashley Diaz; Ashley Andersen; William F. Hulme; Sara Linker; Arpit Mehta; Yvonne J. K. Edwards; et al.
Comparison of three targeted enrichment strategies on the Solid sequencing platform
PLoS ONE. 2011;6(4).17 -
46.
2011Kylee L. Spencer; Lana M. Olson; Nathalie Schnetz-Boutaud; Paul Gallins; Gaofeng Wang; William K. Scott; Anita Agarwal; Johanna Jakobsdottir; Yvette Conley; Daniel E. Weeks; et al.
Investigative Ophthalmology and Visual Science. 2011;52(3):1748-1754.2 -
47.
2011Anthony J. Griswold; Deqiong Ma; Stephanie J. Sacharow; Joycelyn L. Robinson; James M. Jaworski; Harry H. Wright; Ruth K. Abramson; Helle Lybæk; Nina Øyen; Michael L. Cuccaro; et al.
A de novo 1.5Mb microdeletion on chromosome 14q23.2-23.3 in a patient with autism and spherocytosis
Autism Research. 2011;4(3):221-227.2 -
48.
2011Digna R. Velez Edwards; John R. Gilbert; Lan Jiang; Paul J. Gallins; Laura Caywood; Marilyn Creason; Denise Fuzzell; Clare Knebusch; Charles E. Jackson; Margaret A. Pericak-Vance; et al.
Successful Aging Shows Linkage to Chromosomes 6, 7, and 14 in the Amish
Annals of Human Genetics. 2011;75(4):516-528.3 -
49.
2011John P. Hussman; Ren-Hua Chung; Anthony J. Griswold; James M. Jaworski; Daria Salyakina; Deqiong Ma; Ioanna Konidari; Patrice L. Whitehead; Jeffery M. Vance; Eden R. Martin; et al.
Molecular Autism. 2011;2(1).12 -
50.
2011Stephen Sawcer; Garrett Hellenthal; Matti Pirinen; Chris C.A. Spencer; Nikolaos A. Patsopoulos; Loukas Moutsianas; Alexander Dilthey; Zhan Su; Colin Freeman; Sarah E. Hunt; et al.
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Nature. 2011;476(7359):214-219.247 -
51.
2011Rebecca L. Zuvich; William S. Bush; Jacob L. McCauley; Ashley H. Beecham; Philip L. De Jager; Adrian J. Ivinson; Alastair Compston; David A. Hafler; Stephen L. Hauser; Stephen J. Sawcer; et al.
Human Molecular Genetics. 2011;20(17):3517-3524.12 -
52.
2011Goldie S. Byrd; Christopher L. Edwards; Vinaya A. Kelkar; Ruth G. Phillips; Jennifer R. Byrd; Dora Som Pim-Pong; Takiyah D. Starks; Ashleigh L. Taylor; Raechel E. Mckinley; Yi-Ju Li; et al.
Journal of the National Medical Association. 2011;103(6):480-487.4 -
53.
2011Han-Xiang Deng; Wenjie Chen; Seong-Tshool Hong; Kym M. Boycott; George H. Gorrie; Nailah Siddique; Yi Yang; Faisal Fecto; Yong Shi; Hong Zhai; et al.
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
Nature. 2011;477(7363):211-215.119 -
54.
2011Daria Salyakina; Holly N. Cukier; Joycelyn M. Lee; Stephanie Sacharow; Laura D. Nations; Deqiong Ma; James M. Jaworski; Ioanna Konidari; Patrice L. Whitehead; Harry H. Wright; et al.
PLoS ONE. 2011;6(10).7 -
55.
2011Christiane Reitz; Rong Cheng; Ekaterina Rogaeva; Joseph H. Lee; Shinya Tokuhiro; Fanggeng Zou; Karolien Bettens; Kristel Sleegers; Eng King Tan; Ryo Kimura; et al.
Meta-analysis of the association between variants in SORL1 and Alzheimer disease
Archives of Neurology. 2011;68(1):99-106.35 -
56.
2011Christiane Reitz; Shinya Tokuhiro; Lorraine N. Clark; Christopher Conrad; Jean-Paul Vonsattel; Lili-Naz Hazrati; András Palotás; Raphael Lantigua; Martin Medrano; Ivonne Z. Jiménez-Velázquez; et al.
Annals of Neurology. 2011;69(1):47-64.24 -
57.
2011Stephan Züchner; Julia Dallman; Rong Wen; Gary Beecham; Adam Naj; Amjad Farooq; Martin A. Kohli; Patrice L. Whitehead; William Hulme; Ioanna Konidari; et al.
Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa
American Journal of Human Genetics. 2011;88(2):201-206.32 -
58.
2011Richard Sherva; Clinton T. Baldwin; Rivka Inzelberg; Badri Vardarajan; L. Adrienne Cupples; Kathryn Lunetta; Abdalla Bowirrat; Adam Naj; Margaret Pericak-Vance; Robert P. Friedland; et al.
Journal of Alzheimer's Disease. 2011;23(2):349-359.4 -
59.
2011Yvonne J. K. Edwards; Gary W. Beecham; William K. Scott; Sawsan Khuri; Guney Bademci; Demet Tekin; Eden R. Martin; Zhijie Jiang; Deborah C. Mash; Jarlath ffrench-Mullen; et al.
PLoS ONE. 2011;6(2).5 -
60.
2011Craig S. Kitchens; Doruk Erkan; Leonardo R. Brando; Susan Hahn; Andra H. James; Roshni Kulkarni; Margaret Pericak-Vance; Jeffery Vance; Thomas L. Ortel
American Journal of Medicine. 2011;124(4):290-296.3 -
61.
2010Pascal J. Goldschmidt-Clermont; David M. Seo; Liyong Wang; Gary W. Beecham; Zhao-Jun Liu; Roberto I. Vazquez-Padron; Chunming Dong; Joshua M. Hare; Michael S. Kapiloff; Nanette H. Bishopric; et al.
Inflammation, stem cells and atherosclerosis genetics
Current Opinion in Molecular Therapeutics. 2010;12(6):712-723.5 -
62.
2010Martha P. Montgomery; Freya Kamel; Margaret A. Pericak-Vance; Jonathan L. Haines; Eric A. Postel; Anita Agarwal; Marie Richards; William K. Scott; Silke Schmidt
Overall diet quality and age-related macular degeneration
Ophthalmic Epidemiology. 2010;17(1):58-65.3 -
63.
2010D.Q. Ma; R. Rabionet; I. Konidari; J. Jaworski; H.N. Cukier; H.H. Wright; R.K. Abramson; J.R. Gilbert; M.L. Cuccaro; et al.
Association and gene-gene interaction of SLC6A4 and ITGB3 in autism
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 2010;153(2):477-483.9 -
64.
2010Dalila Pinto; Alistair T. Pagnamenta; Lambertus Klei; Richard Anney; Daniele Merico; Regina Regan; Judith Conroy; Tiago R. Magalhaes; Catarina Correia; Brett S. Abrahams; et al.
Functional impact of global rare copy number variation in autism spectrum disorders
Nature. 2010;466(7304):368-372.377 -
65.
2010Holly N. Cukier; Raquel Rabionet; Ioanna Konidari; Melissa Y. Rayner-Evans; Mary L. Baltos; Harry H. Wright; Ruth K. Abramson; Eden R. Martin; Michael L. Cuccaro; et al.
Novel variants identified in methyl-CpG-binding domain genes in autistic individuals
Neurogenetics. 2010;11(3):291-303.11 -
66.
2010F. Esposito; N.A. Patsopoulos; S. Cepok; I. Kockum; V. Leppä; D.R. Booth; R.N. Heard; G.J. Stewart; M. Cox; R.J. Scott; et al.
IL12A, MPHOSPH9/CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci
Genes and Immunity. 2010;11(5):397-405.20 -
67.
2010Farren B. S. Briggs; Benjamin A. Goldstein; Jacob L. McCauley; Rebecca L. Zuvich; Philip L. De Jager; John D. Rioux; Adrian J. Ivinson; Alastair Compston; David A. Hafler; Stephen L. Hauser; et al.
Variation within DNA repair pathway genes and risk of multiple sclerosis
American Journal of Epidemiology. 2010;172(2):217-224.9 -
68.
2010Bruce A.C. Cree; John D. Rioux; Jacob L. McCauley; F.D.Gourraud Pierre-Antoine; Philippe Goyette; Joseph McElroy; Philip de Jager; Adam Santaniello; Timothy J. Vyse; et al.
PLoS ONE. 2010;5(6).14 -
69.
2010Carol A. Christianson; Karen Potter Powell; Susan Estabrooks Hahn; Deborah Bartz; Tiese Roxbury; Susan H. Blanton; Jeffery M. Vance; Margaret Pericak-Vance; Joseph Telfair; Vincent C. Henrich
Genetics in Medicine. 2010;12(9):587-593.2 -
70.
2010Richard Anney; Lambertus Klei; Dalila Pinto; Regina Regan; Judith Conroy; Tiago R. Magalhaes; Catarina Correia; Brett S. Abrahams; Nuala Sykes; Alistair T. Pagnamenta; et al.
A genome-wide scan for common alleles affecting risk for autism
Human Molecular Genetics. 2010;19(20):4072-4082.91 -
71.
2010Farren B.S. Briggs; Selena E. Bartlett; Benjamin A. Goldstein; Joanne Wang; Jacob L. McCauley; Rebecca L. Zuvich; Philip L. de jager; John D. Rioux; Adrian J. Ivinson; Alastair Compston; et al.
Human Molecular Genetics. 2010;19(21):4286-4295.7 -
72.
2010Gyungah Jun; Adam C. Naj; Gary W. Beecham; Li-San Wang; Jacqueline Buros; Paul J. Gallins; Joseph D. Buxbaum; Nilufer Ertekin-Taner; M. Daniele Fallin; Robert Friedland; et al.
Archives of Neurology. 2010;67(12):1473-1484.84 -
73.
2010Adam C. Naj; Gary W. Beecham; Eden R. Martin; Paul J. Gallins; Eric H. Powell; Ioanna Konidari; Patrice L. Whitehead; Guiqing Cai; Vahram Haroutunian; William K. Scott; et al.
PLoS Genetics. 2010;6(9).35 -
74.
2010Gary W. Beecham; Adam C. Naj; John R. Gilbert; Jonathan L. Haines; Joseph D. Buxbaum; Margaret A. Pericak-Vance
PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility
Psychiatric Genetics. 2010;20(6):321-324.6 -
75.
2010Gaofeng Wang; William K. Scott; Jonathan L. Haines; Margaret A. Pericak-Vance
Genotype at polymorphism rs11200638 and HTRA1 expression level
Archives of Ophthalmology. 2010;128(11):1491-1493.2 -
76.
2010M. Ban; J.L. McCauley; R. Zuvich; A. Baker; L. Bergamaschi; M. Cox; A. Kemppinen; S. D'Alfonso; F.R. Guerini; J. Lechner-Scott; et al.
Genes and Immunity. 2010;11(8):660-664.8 -
77.
2010Jean-Charles Lambert; Kristel Sleegers; Antonio González-Pérez; Martin Ingelsson; Gary W. Beecham; Mikko Hiltunen; Onofre Combarros; Maria J. Bullido; Nathalie Brouwers; Karolien Bettens; et al.
Journal of Alzheimer's Disease. 2010;22(1):247-255.13 -
78.
2010The International Multiple Sclerosis Genetics Consortium (IMSGC)
Evidence for Polygenic Susceptibility to Multiple Sclerosis-The Shape of Things to Come
American Journal of Human Genetics. 2010;86(4):621-625.47 -
79.
2010Todd L. Edwards; William K. Scott; Cherylyn Almonte; Amber Burt; Eric H. Powell; Gary W. Beecham; Liyong Wang; Stephan Züchner; Ioanna Konidari; Gaofeng Wang; et al.
Annals of Human Genetics. 2010;74(2):97-109.104 -
80.
2010Digna R. Velez Edwards; Paul Gallins; Monica Polk; Juan Ayala-Haedo; Stephen G. Schwartz; Jaclyn L. Kovach; Kylee Spencer; Gaofeng Wang; Anita Agarwal; Eric A. Postel; et al.
Investigative Ophthalmology and Visual Science. 2010;51(4):1873-1879.5 -
81.
2010Rebecca L. Zuvich; Jacob L. McCauley; Jorge R. Oksenberg; Stephen J. Sawcer; Philip L. De Jager; Cristin Aubin; Anne H. Cross; Laura Piccio; Neelum T. Aggarwal; Denis Evans; et al.
Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility
Human Genetics. 2010;127(5):525-535.23 -
82.
2010Gaofeng Wang; Kylee L. Spencer; William K. Scott; Patrice Whitehead; Brenda L. Court; Juan Ayala-Haedo; Ping Mayo; Stephen G. Schwartz; Jaclyn L. Kovach; Paul Gallins; et al.
Analysis of the indel at the ARMS2 3′UTR in age-related macular degeneration
Human Genetics. 2010;127(5):595-602.14 -
83.
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1999Kamel Ben Othmane; Ellen Johnson; Marisa Menold; Felicia L. Graham; Mongi Ben Hamida; Osamu Hasegawa; Allison D. Rogala; Akio Ohnishi; Margaret Pericak-Vance; Faycal Hentati; et al.
Genomics. 1999;62(3):344-349.52 -
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1999Monica A. De La Paz; Vanessa K. Guy; Suzanne Abou-Donia; Ruth Heinis; Bekki Bracken; Jeffery M. Vance; John R. Gilbert; J. Donald M. Gass; Jonathan L. Haines; et al.
Analysis of the Stargardt disease gene (ABCR) in age-related macular degeneration
Ophthalmology. 1999;106(8):1531-1536.68 -
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1999A. Ashley-Koch; C.M. Wolpert; M.M. Menold; L. Zaeem; S. Basu; S.L. Donnelly; S.A. Ravan; C.M. Powell; M.B. Qumsiyeh; A.S. Aylsworth; et al.
Genetic studies of autistic disorder and chromosome 7
Genomics. 1999;61(3):227-236.141 -
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1999Peter J. Conlon; Kelvin Lynn; Michelle P. Winn; L. Darryl Quarles; Mary Lou Bembe; Margaret Pericak-Vance; Marcy Speer; David N. Howell
Spectrum of disease in familial focal and segmental glomerulosclerosis
Kidney International. 1999;56(5):1863-1871.35 -
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1999C.M. Hulette; M.A. Pericak-Vance; A.D. Roses; D.E. Schmechel; L.H. Yamaoka; P.C. Gaskell; K.A. Welsh-Bohmer; R.A. Crowther; M.G. Spillantini
Journal of Neuropathology and Experimental Neurology. 1999;58(8):859-866.42 -
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1999Eric Seboun; Jorge R. Oksenberg; Antony Rombos; Koishiro Usuku; Donald E. Goodkin; Robin R. Lincoln; Michael Wong; D. Pham-Dinh; O. Boesplug-Tanguy; R. Carsique; et al.
Linkage analysis of candidate myelin genes in familial multiple sclerosis
Neurogenetics. 1999;2(3):155-162.19 -
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1999Marcy C. Speer; J. Nye; D. McLone; G. Worley; E.C. Melvin; K.D. Viles; A. Franklin; C. Drake; J. Mackey; T.M. George; et al.
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1999Gary W. Small; William K. Scott; Scott Komo; Larry H. Yamaoka; Lindsay A. Farrer; Sanford H. Auerbach; Ann M. Saunders; Allen D. Roses; Jonathan L. Haines; Margaret A. Pericak-Vance
No association between the HLA-A2 allele and Alzheimer disease
Neurogenetics. 1999;2(3):177-182.14 -
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1999W.K. Scott; L.H. Yamaoka; J.M. Stajich; B.L. Scott; J.M. Vance; A.D. Roses; M.A. Pericak-Vance; R.L. Watts; M. Nance; J. Hubble; et al.
The α-synuclein gene is not a major risk factor in familial Parkinson disease [2]
Neurogenetics. 1999;2(3):191-192.15 -
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1999Michelle P. Winn; Peter J. Conlon; Kelvin L. Lynn; David N. Howell; Deborah A. Gross; Allison R. Rogala; Anne H. Smith; Felicia L. Graham; MaryLou Bembe; L. Daryl Quarles; et al.
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Kidney International. 1999;55(4):1241-1246.38 -
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1999E.A. Rogaeva; S. Premkumar; J. Grubber; L. Serneels; W.K. Scott; T. Kawarai; Y. Song; D.M. Hill; S.M. Abou-Donia; E.R. Martin; et al.
An α-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease [5] (multiple letters)
Nature Genetics. 1999;22(1):19-22.90 -
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1999Gary W. Small; Stephen T. Chen; Scott Komo; Linda Ercoli; Susan Bookheimer; Karen Miller; Helen Lavretsky; Sanjaya Saxena; Andrea Kaplan; Deborah Dorsey; et al.
Memory self-appraisal in middle-aged and older adults with the apolipoprotein E-4 allele
American Journal of Psychiatry. 1999;156(7):1035-1038.52 -
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1999Marcy C. Speer; Jeffery M. Vance; Janet M. Grubber; Felicia Lennon Graham; Jeffrey M. Stajich; Kristi D. Viles; Allison Rogala; Robert McMichael; Jerry Chutkow; et al.
Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7
American Journal of Human Genetics. 1999;64(2):556-562.54 -
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1999Michelle P. Winn; Peter J. Conlon; Kelvin L. Lynn; David N. Howell; Brandon D. Slotterbeck; Anne H. Smith; Felicia L. Graham; Marylou Bembe; L. Daryl Quarles; Margaret A. Pericak-Vance; et al.
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1999Ludwine M. Messiaen; Tom Callens; Kyle J. Roux; Geert R. Mortier; Anne De Paepe; Marc Abramowicz; Margaret A. Pericak-Vance; Jeffery M. Vance; Margaret R. Wallace
Genetics in Medicine. 1999;1(6):248-253.14 -
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1999J.L. Haines; M.A. Pericak-Vance
Genetics of multiple sclerosis.
Current directions in autoimmunity. 1999;1:273-288.1 -
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1999Janet M. Grubber; Ann M. Saunders; Alison R. Crane-Gatherum; William K. Scott; Eden R. Martin; Carol S. Haynes; P.M. Conneally; Gary W. Small; Allen D. Roses; et al.
Neuroscience Letters. 1999;269(2):115-119.23 -
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1999W.K. Scott; J.M. Grubber; S.M. Abou-Donia; T.D. Church; A.M. Saunders; A.D. Roses; M.A. Pericak-Vance; P.M. Conneally; G.W. Small; J.L. Haines
Further evidence linking late-onset Alzheimer disease with chromosome 12 [3] (multiple letters)
Journal of the American Medical Association. 1999;281(6):513-514.24 -
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1999Jennifer L. Anderson; Mehmood Khan; William S. David; Zohreh Mahdavi; Frank Q. Nuttall; Elizabeth Krech; Sandra G. West; Jeffery M. Vance; Margaret A. Pericak-Vance; Martha A. Nance
Confirmation of linkage of hereditary partial lipodystrophy to chromosome 1q21-22
American Journal of Medical Genetics. 1999;82(2):161-165.27 -
354.
1999Lewis O. Maddox; Marisa M. Menold; Meredyth P. Bass; Allison R. Rogala; Margaret A. Pericak-Vance; Jeffery M. Vance; John R. Gilbert
Autistic disorder and chromosome 15q11-q13: Construction and analysis of a BAC/PAC contig
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1999K.W. Small; N. Udar; S. Yelchits; R. Klein; C. Garcia; G. Gallardo; B. Puech; V. Puech; D. Saperstein; J. Lim; et al.
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1999B. Fontaine; I. Cournu; I. Arnaud; M.-C. Babron; S. Eichenbaum-Voline; J.R. Oksenberg; M.A. Pericak-Vance; J.L. Haines; G. Semama; et al.
Chromosome 17q22-q24 and multiple sclerosis genetic susceptibility
Genes and Immunity. 1999;1(2):149-150.6 -
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1998Te-Cheng Pan; Rui-Zhu Zhang; Margaret A. Pericak-Vance; Rup Tandan; Timothy Fries; Jeffrey M. Stajich; Kristi Viles; Jeffery M. Vance; Mon-Li Chu; et al.
Human Molecular Genetics. 1998;7(5):807-812.61 -
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1998Jonathan L. Haines; Henry A. Terwedow; Katie Burgess; Margaret A. Pericak-Vance; Jackie B. Rimmler; Eden R. Martin; Jorge R. Oksenberg; Robin Lincoln; David Y. Zhang; Diosdado R. Banatao; et al.
Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity
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1998Marcy C. Speer; Jeffery M. Vance; Felicia Lennon-Graham; Jeffrey M. Stajich; Kristi D. Viles; James M. Gilchrist; Vincenzo Nigro; Robert McMichael; Jerry G. Chutkow; Lucia Bartoloni; et al.
Exclusion of identified LGMD 1 loci from four dominant limb-girdle muscular dystrophy families
Human Heredity. 1998;48(4):179-184.3 -
360.
1998R.R. Allingham; J.L. Wiggs; K.F. Damji; L. Herndon; J. Youn; D.A. Tallett; K.H. Jones; E.A. Del Bono; M. Reardon; et al.
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1998Lindsay A. Farrer; Carmela R. Abraham; Jonathan L. Haines; Ekaterina A. Rogaeva; Youqiang Song; Walker T. McGraw; Nicholas Brindle; Smita Premkumar; William K. Scott; Larry H. Yamaoka; et al.
Association between bleomycin hydrolase and Alzheimer's disease in Caucasians
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1998Marisa M. Menold; Menachem Sadeh; Felicia Lennon; Ilan Blatt; Yochanan Goldhammer; Larry H. Yamaoka; Jeffery M. Vance; Margaret A. Pericak-Vance
Evidence for genetic heterogeneity supports clinical differences in congenital myasthenic syndromes
Human Heredity. 1998;48(6):325-332.4 -
363.
1998M.A. Nance; W.A. Raabe; H. Midani; E.H. Kolodny; W.S. David; L. Megna; M.A. Pericak-Vance; J.L. Haines
Clinical heterogeneity of familial spastic paraplegia linked to chromosome 2p21
Human Heredity. 1998;48(3):169-178.10 -
364.
1998Catherine T. Falk; James M. Gilchrist; Margaret A. Pericak-Vance; Marcy C. Speer
American Journal of Human Genetics. 1998;62(4):941-949.9 -
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1998K.F. Damji; C.J. Gallione; R.R. Allingham; B. Slotterbeck; A.E. Guttmacher; K.A. Pasyk; J.M. Vance; M.A. Pericak-Vance; M.C. Speer; et al.
Human Genetics. 1998;102(2):207-212.5 -
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1998M.A. Pericak-Vance; M.L. Bass; L.H. Yamaoka; P.C. Gaskell; W.K. Scott; H.A. Terwedow; M.M. Menold; P.M. Conneally; G.W. Small; A.M. Saunders; et al.
Complete genomic screen in late-onset familial Alzheimer's disease
Neurobiology of Aging. 1998;19(SUPPL. 1):S39-S42.40 -
367.
1998Ning-Pu Liu; Jennifer Baldwin; Felicia Lennon; Jeffrey M. Stajich; Eugene J.-M. A. Thonar; Margaret A. Pericak-Vance; Gordon K. Klintworth; Jeffery M. Vance
Coexistence of macular corneal dystrophy types I and II in a single sibship
British Journal of Ophthalmology. 1998;82(3):241-244.16 -
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1998William K. Scott; Larry H. Yamaoka; Meredyth P. Bass; P. Craig Gaskell; P. Michael Conneally; Gary W. Small; Lindsay A. Farrer; Sanford A. Auerbach; Ann M. Saunders; et al.
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369.
1998Teepu Siddique; Margaret A. Pericak-Vance; Janice Caliendo; Seong-Tshool Hong; W.-Y. Hung; Jocelyn Kaplan; Diane McKenna-Yasek; Jackie B. Rimmler; Peter Sapp; Ann M. Saunders; et al.
Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis
Neurogenetics. 1998;1(3):213-216.28 -
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1998J.R. Gilbert; V. Guy; A. Kumar; C. Wolpert; R. Kandt; A. Aylesworth; A.D. Roses; M.A. Pericak-Vance
Mutation and polymorphism analysis in the tuberous sclerosis 2 (TSC2) gene
Neurogenetics. 1998;1(4):267-272.15 -
371.
1998N.-P. Liu; J. Baldwin; F. Jonasson; S. Dew-Knight; J.M. Stajich; F. Lennon; M.A. Pericak-Vance; G.K. Klintworth; J.M. Vance
American Journal of Human Genetics. 1998;63(3):912-917.19 -
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1998J.L. Wiggs; R.R. Allingham; D. Vollrath; K.H. Jones; M. De la Paz; J. Kern; K. Patterson; V.L. Babb; E.A. Del Bono; et al.
American Journal of Human Genetics. 1998;63(5):1549-1552.118 -
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1998Lucia Bartoloni; Stephen K. Horrigan; Kristi D. Viles; James M. Gilchrist; Jeffery M. Stajich; Jeffery M. Vance; Larry H. Yamaoka; Margaret A. Pericak-Vance; Carol A. Westbrook; et al.
Genomics. 1998;54(2):250-255.17 -
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1998Kamel Ben Othmane; Julie M. Rochelle; Mongi Ben Hamida; Brandon Slotterbeck; Nagesh Rao; Faycal Hentati; Margaret A. Pericak-Vance; Jeffery M. Vance
Fine localization of the CMT4A locus using a PAC contig and haplotype analysis
Neurogenetics. 1998;2(1):18-23.9 -
375.
1998Afif Hentati; Karim Ouahchi; Margaret A. Pericak-Vance; Deepak Nijhawan; Arsalan Ahmad; Yi Yang; Jackie Rimmler; Wu-Yen Hung; Beate Schlotter; Akhtar Ahmed; et al.
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1998Meredyth P. Bass; Larry H. Yamaoka; William K. Scott; P. Craig Gaskell; Kathleen A. Welsh-Bohmer; Allen D. Roses; Ann M. Saunders; Jonathan L. Haines; Margaret A. Pericak-Vance
Neuroscience Letters. 1998;250(2):79-82.3 -
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1998E.S. Martin; S.E. Martin; D.S. Borgaonkar; M.A. Pericak-Vance; J.L. Haines
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Journal of the American Medical Association. 1998;279(6):433.4 -
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1998C. Lavedan; S. Buchholtz; G. Auburger; R.L. Albin; A. Athanassiadou; J. Blancato; J.A. Burguera; R.E. Ferrell; V. Kostic; E. Leroy; et al.
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1998R. Rand Allingham; Janey L. Wiggs; Monica A. De La Paz; Doug Vollrath; Deidre A. Tallett; Bob Broomer; Katherine H. Jones; Elizabeth A. Del Bono; Jeremy Kern; et al.
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1998M.C. Speer; J.M. Gilchrist; J.M. Stajich; P.C. Gaskell; G.A. Westbrook; S.K. Horrigan; L. Bartoloni; L.H. Yamaoka; W.K. Scott; et al.
Evidence for anticipation in autosomal dominant limb-girdle muscular dystrophy
Journal of Medical Genetics. 1998;35(4):305-308.8 -
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1998Takeshi Ikeuchi; Kazuhiro Sanpei; Hiroki Takano; Hidenao Sasaki; Kunio Tashiro; Géraldine Cancel; Alexis Brice; Thomas D. Bird; Gerry D. Schellenberg; et al.
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17q
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1997S. Povey; J. Attwood; B. Chadwick; J. Frezal; J.L. Haines; M. Knowles; D.J. Kwiatkowski; O.I. Olopade; S. Slaugenhaupt; N.K. Spurr; et al.
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1997Justin P. Rubio; Adrian Danek; Caroline Stone; Richard Chalmers; Nicholas Wood; Christine Verellen; Xavier Ferrer; Alessandro Malandrini; Gian M. Fabrizi; Michela Manfredi; et al.
Chorea-acanthocytosis: Genetic linkage to chromosome 9q21
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1997W.K. Scott; A.M. Saunders; P.C. Gaskell; P.A. Locke; J.H. Growdon; L.A. Farrer; S.A. Auerbach; A.D. Roses; J.L. Haines; M.A. Pericak-Vance
Apolipoprotein E ε2 does not increase risk of early-onset sporadic Alzheimer's disease
Annals of Neurology. 1997;42(3):376-378.14 -
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1997Gary W. Small; Ernest P. Noble; Steven S. Matsuyama; Lissy F. Jarvik; Scott Komo; Andrea Kaplan; Terry Ritchie; Meredyth L. Pritchard; Ann M. Saunders; P. Michael Conneally; et al.
D 2 dopamine receptor A1 allele in Alzheimer disease and aging
Archives of Neurology. 1997;54(3):281-285.6 -
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1997M.A. De La Paz; M.A. Pericak-Vance; J.L. Haines; J.M. Seddon
Phenotypic heterogeneity in families with age-related macular degeneration
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1997Margaret A. Pericak-Vance; Meredyth P. Bass; Larry H. Yamaoka; Perry C. Gaskell; William K. Scott; Henry A. Terwedow; Marissa M. Menold; P. Michael Conneally; Gary W. Small; Jeffery M. Vance; et al.
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1997Jeffrey M. Stajich; James M. Gilchrist; Felicia Lennon; Arnold Lee; Larry Yamaoka; Barbara Rosi; Perry C. Gaskell; Meredyth Pritchard; Lauren Donald; Allen D. Roses; et al.
Neuromuscular Disorders. 1997;7(SUPPL. 1):S75-S81.7 -
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1997W.K. Scott; J.M. Stajich; L.H. Yamaoka; M.C. Speer; J.M. Vance; A.D. Roses; M.A. Pericak-Vance; M.H. Polymeropoulos
Genetic complexity and Parkinson's disease
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1997Lindsay A. Farrer; L. Adrienne Cupples; Jonathan L. Haines; Bradley Hyman; Walter A. Kukull; Richard Mayeux; Richard H. Myers; Margaret A. Pericak-Vance; Neil Risch; et al.
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1997David N. Messina; Marcy C. Speer; Margaret A. Pericak-Vance; Elizabeth M. McNally
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1997M.I. Kamboh; C.E. Aston; R.E. Ferrell; S.T. Dekosky; J.L. Haines; W.K. Scott; M.A. Pericak-Vance
Re: Genetic effect of α1-antichymotrypsin on the risk of Alzheimer disease
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1997W.K. Scott; L.H. Yamaoka; P.A. Locke; B.L. Rosi; P.C. Gaskell; A.M. Saunders; P.M. Conneally; G.W. Small; L.A. Farrer; et al.
Genetic Epidemiology. 1997;14(3):307-315.25 -
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1997Monica A. De La Paz; Margaret A. Pericak-Vance; Felicia Lennon; Jonathan L. Haines; Johanna M. Seddon
Exclusion of TIMP3 as a candidate locus in age-related macular degeneration
Investigative Ophthalmology and Visual Science. 1997;38(6):1060-1065.69 -
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1997Tony Juneja; Margaret A. Pericak-Vance; Nigel G. Laing; Sundeep Dave; Teepu Siddique
Neurology. 1997;48(1):55-57.101 -
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1997A. Kumar; R.S. Kandt; C. Wolpert; A.D. Roses; M.A. Pericak-Vance; J.R. Gilbert
A novel splice site mutation (156 + 1G → A) in the TSC2 gene
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1997W.K. Scott; M.A. Pericak-Vance; J.L. Haines; D.A. Bell; J.A. Taylor; A.D. Long; M.N. Grote; C.H. Langley; B. Muller-Myhsok; L. Abel; et al.
Genetic analysis of complex diseases
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1997William K. Scott; P. Craig Gaskell; Felicia Lennon; Chantelle M. Wolpert; Marisa M. Menold; Arthur S. Aylsworth; Carolyn Warner; Carolyn D. Farrell; Rose-Mary N. Boustany; Susan G. Albright; et al.
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1997Marcy C. Speer; Margaret A. Pericak-Vance; Jeffrey M. Stajich; Jennifer Sarrica; Matthew Jordan; Allen D. Roses; Jeffery M. Vance; John R. Gilbert
Further exclusion of FSHD1B from the telomeric region of 10q
Neurogenetics. 1997;1(2):151-152.2 -
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1997Margaret A. Pericak-Vance; Marcy C. Speer; Felicia Lennon; Sandra G. West; Marisa M. Menold; Jeffrey M. Stajich; Chanteile M. Wolpert; Brandon D. Slotterbeck; Masaaki Saito; Richard W. Tim; et al.
Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity
Neurogenetics. 1997;1(2):89-93.18 -
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1997William K. Scott; Marcy C. Speer; Suzanne M. Leal; Linda M. Brzustowicz; Carol S. Haynes; Margaret A. Pericak-Vance
False positive rates in a genomic screen for complex quantitative traits
Genetic Epidemiology. 1997;14(6):891-896.1 -
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1997S. Povey; J. Attvvood; B. Chadwick; J. Frezal; J.L. Haines; M. Knowles; D.J. Kwiatkowski; O.I. Olopade; S. Slaugenhaupt; N.K. Spurr; et al.
Report on the 1996 International chromosome 9 workshop
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1997J.S. Andersen; R.R. Allingham; E. Stefansson; M. Loftsdottir; T. Sverisson; E. Thorgeirsson; F. Jonasson; P. Price; J. Hamilton; K. Damji; et al.
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1996J.L. Haines; M. Ter-Minassian; A. Bazyk; J.F. Gusella; D.J. Kim; H. Terwedow; M.A. Pericak-Vance; J.B. Rimmler; C.S. Haynes; A.D. Roses; et al.
Nature Genetics. 1996;13(4):469-471.538 -
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1996J.L. Wiggs; K.F. Damji; J.L. Haines; M.A. Pericak-Vance; R.R. Allingham
The distinction between juvenile and adult-onset primary open-angle glaucoma [4]
American Journal of Human Genetics. 1996;58(1):243-244.18 -
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1996J.L. Haines; M.L. Pritchard; A.M. Saunders; J.M. Schildkraut; J.H. Growdon; P.C. Gaskell; L.A. Farrer; S.A. Auerbach; J.F. Gusella; P.A. Locke; et al.
No genetic effect of α1-antichymotrypsin in Alzheimer disease
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1996M.A. Pericak-Vance; C.C. Johnson; J.B. Rimmler; A.M. Saunders; L.C. Robinson; E.G. D'Hondt; C.E. Jackson; J.L. Haines
Alzheimer's disease and apolipoprotein E-4 allele in an Amish population
Annals of Neurology. 1996;39(6):700-704.34 -
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1996Karim F. Damji; R. Rand Allingham; Stephen C. Pollock; Kent Small; Karen E. Lewis; Jeffrey M. Stajich; Larry H. Yamaoka; Jeffery M. Vance; Margaret A. Pericak-Vance
Archives of Neurology. 1996;53(4):338-344.44 -
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1996A.D. Roses; G. Einstein; J. Gilbert; M. Goedert; S.-H. Han; D. Huang; C. Hulette; E. Masliah; M.A. Pericak-Vance; et al.
Annals of the New York Academy of Sciences. 1996;777:146-157.32 -
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1996Kent W. Small; Stephen C. Pollock; Jeffrey M. Vance; Jeff M. Stajich; Margaret Pericak-Vance
Ocular motility in North Carolina autosomal dominant ataxia
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1996J.M. Vance; M.C. Speer; J.M. Stajich; S. West; C. Wolpert; P. Gaskell; F. Lennon; R.M. Tim; M. Rozear; K.B. Othmane; et al.
American Journal of Human Genetics. 1996;59(1):258-262.33 -
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1996Jeffery M. Vance; Fridbert Jonasson; Felicia Lennon; Jennifer Sarrica; Karim F. Damji; Jennifer Stauffer; Margaret A. Pericak-Vance; Gordon K. Klintworth
Linkage of a gene for macular corneal dystrophy to chromosome 16
American Journal of Human Genetics. 1996;58(4):757-762.66 -
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1996W.K. Scott; A.D. Roses; J.L. Haines; M.A. Pericak-Vance; J. Perez-Tur; F. Wavrant-de Vrieze; J.C. Lambert; M.-C. Chartier-Harlin
Presenilin-1 polymorphism and Alzheimer's disease [17]
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1996M.L. Pritchard; A.M. Saunders; P.C. Gaskell; G.W. Small; P.M. Conneally; B. Rosi; L.H. Yamaoka; A.D. Roses; J.L. Haines; et al.
Neuroscience Letters. 1996;209(2):105-108.29 -
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1996D.W. Johnson; J.N. Berg; M.A. Baldwin; C.J. Gallione; I. Marondel; S.J. Yoon -; T.T. Stenzel; M. Speer; M.A. Pericak-Vance; A. Diamond; et al.
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1996W.K. Scott; J.H. Growdon; A.D. Roses; J.L. Haines; M.A. Pericak-Vance
Presenilin-1 polymorphism and Alzheimer's disease.
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1996Kaoru Okuizumi; Osamu Onodera; Koji Seki; Hajime Tanaka; Yoshio Namba; Kazuhiko Ikeda; Ann M. Saunders; Margaret A. Pericak-Vance; Allen D. Roses; Shoji Tsuji
Annals of Neurology. 1996;40(2):251-254.34 -
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1996Yu Xia; H.A. De Rohan Suva; Barbara L. Rosi; Larry H. Yamaoka; Jacqueline B. Rimmler; Margaret A. Pericak-Vance; Allen D. Roses; Xiaohua Chen; Eliezer Masliah; Richard Deteresa; et al.
Genetic studies in Alzheimer's disease with an NACP/α-synuclein polymorphism
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1996Kazuo Isozumi; Robert DeLong; Jocelyn Kaplan; Han-Xiang Deng; Zafar Iqbal; Wu-Yen Hung; Kirk C. Wilhelmsen; Afif Hentati; Margaret A. Pericak-Vance; Teepu Siddique
Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31
Human Molecular Genetics. 1996;5(9):1377-1382.51 -
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1996J.K. Fink; T. Heiman-Patterson; T. Bird; F. Cambi; M.-P. Dubé; D.A. Figlewicz; J.L. Haines; A. Hentati; M.A. Pericak-Vance; W. Raskind; et al.
Hereditary spastic paraplegia: Advances in genetic research
Neurology. 1996;46(6):1507-1514.136 -
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1996Marcy C. Speer; Rup Tandan; P. Nagesh Rao; Timothy Fries; Jeffrey M. Stajich; Pieter A. Bolhuis; G. Joost Jöbsis; Jeffery M. Vance; Kristi D. Viles; Karen Sheffield; et al.
Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37
Human Molecular Genetics. 1996;5(7):1043-1046.35 -
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1996Jonathan L. Haines; Meredyth L. Pritchard; Ann M. Saunders; Joellen M. Schildkraut; John H. Growdon; Peter C. Gaskell; Lindsay A. Farrer; Sanford A. Auerbach; James F. Gusella; Patricia A. Locke; et al.
No association between α1-antichymotrypsin and familial Alzheimer's disease
Annals of the New York Academy of Sciences. 1996;802:35-41.9 -
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1996Gary W. Small; Scott Komo; Asenath La Rue; Sanjaya Saxena; Michael E. Phelps; John C. Mazziotta; Ann M. Saunders; Jonathan L. Haines; Margaret A. Pericak-Vance; et al.
Early detection of Alzheimer's disease by combining apolipoprotein E and neuroimaging
Annals of the New York Academy of Sciences. 1996;802:70-78.47 -
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1996J.L. Wiggs; R.R. Allingham; E.A. DelBono; M. Reardon; M. Ter-minassian; K.F. Damji; J. Youn; K.H. Jones; M.A. Pericak-Vance; et al.
The juvenile glaucoma gene on 1q21-q31 is not associated with Primary Open Angle Glaucoma (POAG)
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1996J.M. Seddon; M. Pericak-Vance; J. Haines; J. Rimmler; H.A. De La Paz
Genetic linkage analysis of the TIMP3 locus in age-related macular degeneration
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426.
1996A.M. Saunders; C. Hulette; K.A. Welsh-Bohmer; D.E. Schmechel; B. Crain; J.R. Burke; M.J. Alberts; W.J. Strittmatter; J.C.S. Breitner; C. Rosenberg; et al.
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1996Jeffrey M. Stajich; James M. Gilchrist; Felicia Lennon; Arnold Lee; Larry Yamaoka; Barbara Helms; Perry C. Gaskell; Lauren Donald; Allen D. Roses; Jeffrey M. Vance; et al.
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13
Annals of Neurology. 1996;40(5):801-804.14 -
428.
1996Larry H. Yamaoka; Kathleen A. Welsh-Bohmer; Christine M. Hulette; P. Craig Gaskell Jr.; Michael Murray; Jackie L. Rimmler; Barbara Rosi Helms; Marc Guerra; Allen D. Roses; et al.
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1996R.R. Allingham; J.L. Wiggs; K.F. Damji; J. Youn; D.A. Tallett; K.H. Jones; E.A. Del Bono; M. Reardon; M. Ter-minassian; et al.
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1996K.F. Damji; J.M. Vance; F. Jonasson; F. Lennon; J. Sarrica; J. Stauffer; M.A. Pericak-Vance; G.K. Klintworth
Linkage of a gene for macular corneal dystrophy to chromosome 16
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431.
1996M.A. De La Paz; M. Pericak-Vance; J. Haines; J.M. Seddon
Phenotypic heterogeneity in families with age-related macular degeneration
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1995M.C. Speer; J.M. Gilchrist; J.G. Chutkow; R. McMichael; C.A. Westbrook; J.M. Stajich; E.M. Jorgenson; P.C. Gaskell; B.L. Rosi; et al.
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1995A.D. Roses; A.M. Saunders; M.A. Alberts; W.J. Strittmatter; D. Schmechel; E. Gorder; M.A. Pericak-Vance; T. Pirttila; T. Lehtimaki; T. Nikkari; et al.
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1995M.A. Pericak-Vance; A.E. Bale; J.L. Haines; D.J. Kwiatkowski; A. Pilz; S. Slaugenhaupt; J.A. White; J.H. Edwards; D. Marchuk; O.I. Olopades; et al.
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1995Y. Nakagawa; T. Kitamoto; H. Furukawa; K. Ogomori; J. Tateishi; I. Zerr; M. Helmhold; T. Weber; A.D. Roses; A.M. Saunders; et al.
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1995E.H. Corder; A.M. Saunders; W.J. Strittmatter; D.E. Schmechel; P.C. Gaskell Jr.; A.D. Roses; M.A. Pericak-Vance; G.W. Small; J.L. Haines; et al.
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1995M.A. Pericak-Vance; J.L. Haines
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1995A. Kumar; R.S. Kandt; C. Wolpert; A.D. Roses; M.A. Perikac-Vance; J.R. Gilbert
Mutation analysis of the TSC2 gene in an African-American family
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1995K.W. Small; M. Stalvey; L. Fisher; L. Mullen; C. Dickel; K. Beadles; R. Reimer; A. Lessner; K. Lewis; M.A. Pericak-Vance
Blepharophimosis syndrome is linked to chromosome 3q
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1995C.J. Gallione; K.A. Pasyk; L.M. Boon; F. Lennon; D.W. Johnson; E.A. Helmboid; D.S. Markel; M. Vikkula; J.B. Mulliken; M.L. Warman; et al.
A gene for familial venous malformations maps to chromosome 9p in a second large kindred
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1995G.W. Small; J.C. Mazziotta; M.T. Collins; L.R. Baxter; M.E. Phelps; M.A. Mandelkern; A. Kaplan; A. La Rue; C.F. Adamson; L. Chang; et al.
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1995E.H. Corder; A.M. Saunders; M.A. Pericak-Vance; A.D. Roses; J.E. Riggs; R.W. Keefover
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1995M.A. Pericak-Vance; D.F. Barker; J. Bergoffen; P. Chance; S. Cochrane; N. Dahl; M.-C. Exler; P.R. Fain; N.D. Fairweather; K. Fischbeck; et al.
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1995M.C. Speer; H.M. Kingston; R.-M.N. Boustany; P.C. Gaskell; L.C. Robinson; F. Lennon; C.M. Wolpert; L.H. Yamaoka; S.G. Kahler; E.L. Hogan; et al.
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American Journal of Medical Genetics - Neuropsychiatric Genetics. 1995;60(4):307-311.2 -
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1995E.H. Corder; A.M. Saunders; W.J. Strittmatter; D.E. Schmechel; P.C. Gaskell Jr.; J.B. Rimmler; P.A. Locke; P.M. Conneally; K.E. Schmader; et al.
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1995K.B. Othmane; D. Loeb; R. Hayworth-Hodgte; F. Hentati; N. Rao; A.D. Roses; M.B. Hamida; M.A. Pericak-Vance; J.M. Vance
Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A
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1995A. Kumar; C. Wolpert; R.S. Kandt; J. Segal; J. Pufky; A.D. Roses; M.A. Pericak-Vance; J.R. Gilbert
A de novo frame-shift mutation in the tuberin gene
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1995K.B. Othmane; M.C. Speer; J. Stauffer; S. Blel; L. Middleton; B.C. Hamida; A. Etribi; D. Loeb; F. Hentati; et al.
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1995J.R. Gilbert; M.C. Speer; J. Stajich; R. Clancy; K. Lewis; H. Qiu; L. Yamaoka; A. Kumar; J. Vance; C. Stewart; et al.
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1995John C.S. Breitner; Kathleen A. Welsh; Michael J. Helms; Perry C. Gaskell; Barbara A. Gau; Allen D. Roses; Margaret A. Pericak-Vance; Ann M. Saunders
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1995A.D. Roses; A.M. Saunders; E.H. Corder; M.A. Pericak-Vance; S.H. Han; G. Einstein; C. Hulette; D.E. Schmechel; M. Holsti; D. Huang
Arzneimittel-Forschung/Drug Research. 1995;45(3 A):413-417.20 -
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1995A.D. Roses; A.M. Saunders; W.J. Strittmatter; D.E. Schmechel; M.A. Pericak-Vance; B. Hyman
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1995M.C. Speer; L.H. Yamaoka; J. Stajich; K. Lewis; M.A. Pericak-Vance; R. Stacy; R. Tandan; T.J. Fries
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1994J. Attwood; M. Chiano; A. Collins; H. Donis-Keller; N. Dracopoli; J. Fountain; C. Falk; D. Goudie; J. Gusella; J. Haines; et al.
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1994L.H. Yamaoka; C.A. Westbrook; M.C. Speer; J.M. Gilchrist; E.W. Jabs; E.G. Schweins; J.M. Stajich; P.C. Gaskell; A.D. Roses; et al.
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1994Seol-Heui Han; Gillian Einstein; Karl H. Weisgraber; Warren J. Strittmatter; Ann M. Saunders; Margaret Pericak-Vance; Allen D. Roses; Donald E. Schmechel
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1994A.D. Roses; M.A. Pericak-Vance; A.M. Saunders; D. Schmechel; D. Goldgaber; W. Strittmatter
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1994S.-H. Han; C. Hulette; A.M. Saunders; G. Einstein; M. Pericak-Vance; W.J. Strittmatter; A.D. Roses; D.E. Schmechel
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1994Deborah B. Loeb; Margaret A. Pericak-Vance; Jeffrey M. Stajich; Jeffery M. Vance
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1994David Y. Huang; Michel Goedert; Ross Jakes; Karl H. Weisgraber; Craig C. Garner; Ann M. Saunders; Margaret A. Pericak-Vance; Donald E. Schmechel; Allen D. Roses; et al.
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1994W.J. Strittmatter; A.M. Saunders; M. Goedert; K.H. Weisgraber; L.M. Dong -; R. Jakes; D.Y. Huang; M. Pericak-Vance; D. Schmechel; et al.
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1994Afif Hentati; Margaret A. Pericak-Vance; Felicia Lennon; Brad Wasserman; Faycal Hentati; Tony Juneja; Misha H. Angrist; Wu-Yen Hung; Rose-Mary Boustany; Saeed Bohlega; et al.
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1994J.R. Burke; T. Ikeuchi; R. Koide; S. Tsuji; M. Yamada; M.A. Pericak-Vance; J.M. Vance
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1994A. Hentati; M.A. Pericak-Vance; W.-Y. Hung; S. Belal; N. Laing; R.-M. Boustany; F. Hentati; M. Ben Hamida; T. Siddique
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1994James R. Burke; Martha S. Wingfield; Karen E. Lewis; Allen D. Roses; James E. Lee; Christine Hulette; Margaret A. Pericak-Vance; Jeffery M. Vance
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1994K.A. McAllister; K.M. Grogg; D.W. Johnson; C.J. Gallione; M.A. Baldwin; C.E. Jackson; E.A. Helmbold; D.S. Markel; W.C. McKinnon; J. Murrell; et al.
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1994C. Merette; L.M. Brzustowicz; R.J. Daniels; K.E. Davies; T.C. Gilliam; J. Melki; A. Munnich; M.A. Pericak-Vance; T. Siddique; B. Voosen; et al.
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1994W.J. Strittmatter; K.H. Weisgraber; M. Goedert; A.M. Saunders; D. Huang; E.H. Corder; L.-M. Dong; R. Jakes; M.J. Alberts; J.R. Gilbert; et al.
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1994P. St George-Hyslop; D. Crapper McLachlan; T. Tuda; E. Rogaev; H. Karlinsky; C.F. Lippa; D. Pollen; M.A. Pericak-Vance; E.H. Corder; et al.
Alzheimer's disease and possible gene interaction
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1994A.D. Roses; W.J. Strittmatter; M.A. Pericak-Vance; E.H. Corder; A.M. Saunders; D.E. Schmechel
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1994K.A. McAllister; F. Lennon; B. Bowles-Biesecker; W.C. McKinnon; E.A. Helmbold; D.S. Markel; C.E. Jackson; A.E. Guttmacher; M.A. Pericak-Vance; et al.
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1993E.H. Corder; A.M. Saunders; W.J. Strittmatter; D.E. Schmechel; P.C. Gaskell; G.W. Small; A.D. Roses; J.L. Haines; M.A. Pericak-Vance
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1993B. Weiffenbach; J. Dubois; D. Storvick; R. Tawil; S.J. Jacobsen; J. Gilbert; C. Wijmenga; J.R. Mendell; S. Winokur; M.R. Altherr; et al.
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1993M.J. Econs; P.R. Fain; M. Norman; M.C. Speer; M.A. Pericak-Vance; P.A. Becker; D.F. Barker; A. Taylor; M.K. Drezner
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1993A.M. Saunders; W.J. Strittmatter; D. Schmechel; P.H. St. George-Hyslop; M.A. Pericak-Vance; S.H. Joo; B.L. Rosi; J.F. Gusella; D.R. Crapper-MacLachlan; et al.
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1993A.M. Saunders; K. Schmader; J.C.S. Breitner; M.D. Benson; W.T. Brown; L. Goldfarb; D. Goldgaber; M.G. Manwaring; M.H. Szymanski; N. McCown; et al.
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1993W.J. Strittmatter; A.M. Saunders; D. Schmechel; M. Pericak-Vance; J. Enghild; G.S. Salvesen; A.D. Roses
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1993H.-X. Deng; A. Hentati; J.A. Tainer; Z. Iqbal; A. Cayabyab; W.-Y. Hung; E.D. Getzoff; P. Hu; B. Herzfeldt; R.P. Roos; et al.
Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase
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1993J.R. Gilbert; J.M. Stajich; S. Wall; S.C. Carter; H. Qiu; J.M. Vance; C.S. Stewart; M.C. Speer; J. Pufky; L.H. Yamaoka; et al.
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American Journal of Human Genetics. 1993;53(2):401-408.46 -
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1993K. Ben Othmane; F. Hentati; F. Lennon; C. Ben Hamida; S. Blel; A.D. Roses; M.A. Pericak-Vance; M. Ben Hamida; J.M. Vance
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q
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1993J. Bergoffen; J. Trofatter; M.A. Pericak-Vance; J.L. Haines; P.F. Chance; K.H. Fischbeck
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1993M.A. Pericak-Vance; P.H. St. George-Hyslop; P.C. Gaskell Jr.; J. Growdon; B.J. Crain; C. Hulette; J.F. Gusella; L. Yamaoka; R.E. Tanzi; et al.
Linkage analysis in familial Alzheimer disease: Description of the Duke and Boston data sets
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1993W.J. Strittmatter; K.H. Weisgraber; D.Y. Huang; L.-M. Dong; G.S. Salvesen; M. Pericak-Vance; D. Schmechel; A.M. Saunders; D. Goldgaber; et al.
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1992G.W. Padberg; C. Wijmenga; M. Upadhyaya; B. Weiffenbach; O.F. Brouwer; J. Murray; M. Pericak-Vance; P. Lunt; R.R. Frants; P.S. Harper; et al.
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1992H.H. Ropers; M.A. Pericak-Vance; A.V. Carrano
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1992A.I. McClatchey; P. Van den Bergh; M.A. Pericak-Vance; W. Raskind; C. Verellen; D. McKenna-Yasek; K. Rao; J.L. Haines; T. Bird; R.H. Brown Jr.; et al.
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1992M.C. Speer; C.S. Haynes; M.A. Paricak-Vance
Segregation analysis in cutaneous malignant melanoma/dysplastic nevus syndrome families
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1992J.R. Gilbert; J.M. Stajich; M.C. Speer; J.M. Vance; C.S. Stewart; L.H. Yamaoka; F. Samson; M. Fardeau; T.G. Potter; et al.
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1992H.H. Ropers; M.A. Pericak-Vance; M.J. Siciliano; H.W. Mohrenweiser
Report of the second international workshop on human chromosome 19 mapping
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1992Marcy C. Speer; Larry H. Yamaoka; James H. Gilchrist; C.P. Gaskell; Jeffrey M. Stajich; Jeffery M. Vance; Alexey Kazantsev; Anselmo A. Lastra; Carol S. Haynes; Jacques S. Beckmann; et al.
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1992M. Sarfarazi; C. Wijmenga; M. Upadhyaya; B. Weiffenbach; C. Hyser; K. Mathews; J. Murray; J. Gilbert; M. Pericak-Vance; P. Lunt; et al.
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1992K.W. Small; J.L. Weber; A. Roses; F. Lennon; J.M. Vance; M.A. Pericak-Vance
North Carolina macular dystrophy is assigned to chromosome 6
Genomics. 1992;13(3):681-685.47 -
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1992M.J. Econs; D.F. Barker; M.C. Speer; M.A. Pericak-Vance; P.R. Fain; M.K. Drezner
Multilocus mapping of the X-linked hypophosphatemic rickets gene
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1992C. Pritchard; N. Zhu; J. Zuo; L. Bull; M.A. Pericak-Vance; J.M. Vance; A.D. Roses; A. Milatovich; U. Francke; D.R. Cox; et al.
Recombination of 4p16 DNA markers in an unusual family with Huntington disease
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1992L.J. Loprest; M.A. Pericak-Vance; J. Stajich; P.C. Gaskell; A.M. Lucas; F. Lennon; L.H. Yamaoka; A.D. Roses; J.M. Vance
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1992A.I. McClatchey; J. Trofatter; D. McKenna-Yasek; W. Raskind; T. Bird; M. Pericak- Vance; J. Gilchrist; K. Arahata; D. Radosavljevic; H.G. Worthen; et al.
American Journal of Human Genetics. 1992;50(5):896-901.22 -
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1992R.S. Kandt; J.L. Haines; M. Smith; H. Northrup; R.J.M. Gardner; M.P. Short; K. Dumars; E.S. Roach; S. Steingold; S. Wall; et al.
Nature Genetics. 1992;2(1):37-41.164 -
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1992Kamel Ben Othmane; Mongi Ben Hamida; Margaret A. Pericak-Vance; Christiane Ben Hamida; Samir Blel; Susan C. Carter; Anne M. Bowcock; Konstantin Petruhkin; T. Conrad Gilliam; et al.
Nature Genetics. 1992;2(4):315-317.104 -
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1992P. St George-Hyslop; J. Haines; E. Rogaev; M. Mortilla; G. Vaula; M. Pericak-Vance; J.-F. Foncin; M. Montesi; A. Bruni; S. Sorbi; et al.
Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14
Nature Genetics. 1992;2(4):330-334.204 -
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1992J.R. Sampson; L.A.J. Janssen; L.A. Sandkuijl; J. Amos; H. Bovey; J. Haines; D. Kwiatkowski; P. Short; P. Brook-Carter; J.M. Connor; et al.
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1991M.A. Pericak-Vance; J.L. Bebout; P.C. Gaskell Jr.; L.H. Yamaoka; W.-Y. Hung; M.J. Alberts; A.P. Walker; R.J. Bartlett; C.A. Haynes; K.A. Welsh; et al.
Linkage studies in familial Alzheimer disease: Evidence for chromosome 19 linkage
American Journal of Human Genetics. 1991;48(6):1034-1050.325 -
507.
1991N.G. Laing; A.P. Walker; P.A. Akkari; D.C. Chandler; M.G. Layton; M.E. Mears; T. Yamada; R.J. Bartlett; M.A. Pericak-Vance; W.-Y. Hung; et al.
Prenatal Diagnosis. 1991;11(1):63-67.0 -
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1991R.S. Kandt; P.M. Conneally; P.M. Connor; J.L. Haines; M. Pericak-Vance; M. Smith
Panel discussion II: Linkage studies in tuberous sclerosis. Current status and future prospects
Annals of the New York Academy of Sciences. 1991;615:316-318.0 -
509.
1991M.J. Alberts; M.A. Pericak-Vance; V. Royal; J. Bebout; P. Gaskell; J. Thomas; W.-Y. Hung; C. Clark; N. Earl; A.D. Roses
Genetic linkage analysis of nerve growth factor (beta) in familial Alzheimer's disease
Annals of Neurology. 1991;30(2):216-219.1 -
510.
1991V. Royal; M.J. Alberts; M.A. Pericak-Vance; G. Finocchiaro; J. Bebout; L. Yamaoka; W.-Y. Hung; P.C. Gaskell; A.D. Roses
RsaI RFLP for electron transport flavoprotein-beta(ETFB)
Nucleic Acids Research. 1991;19(14):4021.0 -
511.
1991J.L. Haines; J. Amos; J. Attwood; N.T. Bech-Hansen; M. Burley; P.M. Conneally; J.M. Connor; R. Fahsold; P. Flodman; A. Fryer; et al.
Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative dataset
Annals of the New York Academy of Sciences. 1991;615:256-264.13 -
512.
1991R.S. Kandt; M.A. Pericak-Vance; W.-Y. Hung; R.J.M. Gardner; P.E. Crossen; M.D. Nellist; M.C. Speer; A.D. Roses
Linkage studies in tuberous sclerosis. Chromosome 9?, 11?, or maybe 14!
Annals of the New York Academy of Sciences. 1991;615:284-297.2 -
513.
1991K.W. Small; J.L. Weber; W.-Y. Hung; J. Vance; A. Roses; M. Pericak-Vance
Short communication. North Carolina macular dystrophy: Exclusion map using RFLPs and microsatellites
Genomics. 1991;11(3):763-766.2 -
514.
1991J.M. Vance; D. Barker; L.H. Yamaoka; J.M. Stajich; L. Loprest; W.-Y. Hung; K. Fischbeck; A.D. Roses; M.A. Pericak-Vance
Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2
Genomics. 1991;9(4):623-628.27 -
515.
1991S.L. Secore; A.P. Walker; M.H. Herbstreith; T. Siddique; A.J. Jeffers; T.R. DeShields; M.C. Speer; M.A. Pericak-Vance; W.A. Golembieski; D.I. Smith; et al.
Nucleic Acids Research. 1991;19(22):6349.0 -
516.
1991Gerard D. Schellenberg; Margaret A. Pericak-Vance; Ellen M. Wijsman; Deborah K. Moore; Perry C. Gaskell Jr.; Larry A. Yamaoka; Jacqueline L. Bebout; Leojean Anderson; Kathleen A. Welsh; Christopher M. Clark; et al.
Linkage analysis of familial Alzheimer disease, using chromosome 21 markers
American Journal of Human Genetics. 1991;48(3):563-583.14 -
517.
1991M.J. Alberts; R.S. Kandt; M.A. Pericak-Vance; J. Bebout; M.C. Speer; S. Siddique t.; L. Yamaoka; W.-Y. Hung; P.C. Gaskell; A.D. Roses
Mspl RFLP for microtubule associated protein-2 (MAP2)
Nucleic Acids Research. 1991;19(4):960.0 -
518.
1991M.C. Speer; D. Goldgaber; L.G. Goldfarb; A.D. Roses; M.A. Pericak-Vance
Genomics. 1991;9(2):366-368.8 -
519.
1991A. Goate; M.-C. Chartier-Harlin; M. Mullan; J. Brown; F. Crawford; L. Fidani; L. Giuffra; A. Haynes; N. Irving; et al.
Nature. 1991;349(6311):704-706.1933 -
520.
1991H.H. Ropers; M.A. Pericak-Vance
Report of the committee on the genetic constitution of chromosome 19
Cytogenetics and Cell Genetics. 1991;58(1-2):751-784.5 -
521.
1991T. Siddique; P. Hu; A. Hentati; G. Deng; W.Y. Hung; M.G. McInnis; A.C. Warren; J. Rimmler; S. Antonarakis; M.A. Pericak-Vance
A molecular genetic approach to amyotrophic lateral sclerosis.
International journal of neurology. 1991;25-26:60-69.0 -
522.
1991Teepu Siddique; Denise A. Figlewicz; Margaret A. Pericak-Vance; Jonathan L. Haines; Guy Rouleau; Anita J. Jeffers; Peter Sapp; Wu-Yen Hung; Jacqueline Bebout; Diane Mckenna-Yasek; et al.
New England Journal of Medicine. 1991;324(20):1381-1384.185 -
523.
1990M.J. Econs; M.A. Pericak-Vance; H. Betz; R.J. Bartlett; M.C. Speer; M.K. Drezner
The human glycine receptor: A new probe that is linked to the X-linked hypophosphatemic rickets gene
Genomics. 1990;7(3):439-441.6 -
524.
1990M.A. Pericak-Vance; J.L. Bebout; L.A. Yamaoka; P.C. Gaskell Jr.; W.-Y. Hung; M.J. Alberts; C.M. Clark; C.S. Haynes; K.A. Welsh; N.L. Earl; et al.
Molecular biology and genetics of Alzheimer's disease: proceedings of the International Symposium on Dementia: Molecular Biology and Genetics of Alzheimer's Disease. ICS884. 1990:215-228.1 -
525.
1990A.D. Roses; M.A. Pericak-Vance; C.M. Clark; J.R. Gilbert; L.H. Yamaoka; C.S. Haynes; M.C. Speer; P.C. Gaskell; W.Y. Hung; et al.
Linkage studies of late-onset familial Alzheimer's disease.
Advances in neurology. 1990;51:185-196.2 -
526.
1990L.H. Yamaoka; M.A. Pericak-Vance; M.C. Speer; P.C. Gaskell Jr.; J. Stajich; C. Haynes; W.-Y. Hung; C. Laberge; M.-C. Thibault; J. Mathieu; et al.
Tight linkage of creatine kinase (CKMM) to myotonic dystrophy on chromosome 19
Neurology. 1990;40(2):222-226.3 -
527.
1990A.P. Walker; F.S. Collins; T. Siddique; L.H. Yamaoka; M.H. Herbstreith; M.A. Pericak-Vance; S.L. Secore; W.-Y. Hung; A.M. Goate; J.A. Hardy; et al.
D21S194, a jump clone from D21S16
Nucleic Acids Research. 1990;18(7):1931.0 -
528.
1990J.M. Vance; K.W. Small; M.A. Jones; J.M. Stajich; L.H. Yamaoka; A.D. Roses; W.-Y. Hung; M.A. Pericak-Vance
Confirmation of linkage in von Hippel-Lindau disease
Genomics. 1990;6(3):565-567.7 -
529.
1990M.C. Speer; M.A. Pericak-Vance; L. Yamaoka; W.-Y. Hung; A. Ashley; J.M. Stajich; A.D. Roses
Presymptomatic and prenatal diagnosis in myotonic dystrophy by genetic linkage studies
Neurology. 1990;40(4):671-676.1 -
530.
1990H.H. Ropers; M.A. Pericak-Vance
Report of the committee on the genetic constitution of chromosome 19
Cytogenetics and Cell Genetics. 1990;55(1-4):218-228.1 -
531.
1989M. Sarfarazi; M. Upadhyaya; G. Padberg; M. Pericak-Vance; T. Siddique; G. Lucotte; P. Lunt
An exclusion map for facioscapulohumeral (Landouzy-Dejerine) disease
Journal of Medical Genetics. 1989;26(8):481-484.1 -
532.
1989R.S. Kandt; M.A. Pericak-Vance; W.-Y. Hung; R.J.M. Gardner; M. Nellist; K. Phillips; K. Warner; M.C. Speer; P.E. Crossen; et al.
Absence of linkage of ABO blood group locus to familial tuberous sclerosis
Experimental Neurology. 1989;104(3):223-228.4 -
533.
1989M.M. Le Beau; D. Ryan Jr.; M.A. Pericak-Vance
Report of the committee on the genetic constitution of chromosomes 18 and 19.
Cytogenetics and Cell Genetics. 1989;51(1-4):338-357.2 -
534.
1989T. Siddique; M.A. Pericak-Vance; B.R. Brooks; R.P. Roos; W.-Y. Hung; J.P. Antel; T.L. Munsat; K. Phillips; K. Warner; M. Speer; et al.
Linkage analysis in familial amyotrophic lateral sclerosis
Neurology. 1989;39(7):919-925.32 -
535.
1989N.G. Laing; T. Siddique; R. Bartlett; L.H. Yamaoka; W.-Y. Hung; M.A. Pericak-Vance; A.D. Roses
Duchenne muscular dystrophy: Detection of deletion carriers by spectrophotometric densitometry
Clinical Genetics. 1989;35(6):393-398.1 -
536.
1989T. Siddique; H. Roper; M.A. Pericak-Vance; J. Shaw; K.L. Warner; W.Y. Hung; K.L. Phillips; P. Lunt; W.J.K. Cumming; A.D. Roses
Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral disease
Journal of Medical Genetics. 1989;26(8):487-489.1 -
537.
1989A. McConkie-Rosell; Y.-T. Chen; D. Harris; M.C. Speer; M.A. Pericak-Vance; J.-H. Ding; W.E. Highsmith Jr.; M. Knowles; S.G. Kahler
Mild cystic fibrosis linked to chromosome 7q22 markers with an uncommon haplotype
Annals of Internal Medicine. 1989;111(10):797-801.2 -
538.
1989S.R. Diehl; M. Boehnke; R.P. Erickson; L.M. Ploughman; K.A. Seiler; J.L. Lieberman; H.B. Clarke; M.A. Bruce; E.K. Schorry; et al.
American Journal of Human Genetics. 1989;44(1):33-37.0 -
539.
1989J.M. Vance; M.A. Pericak-Vance; L.H. Yamaoka; M.C. Speer; G.O.D. Rosenwasser; K. Small; P.C. Gaskell Jr.; W.-Y. Hung; M.J. Alberts; et al.
Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type 1
American Journal of Human Genetics. 1989;44(1):25-29.1 -
540.
1989R.C. Griggs; D.S. Wood; R.T. Moxley III; T. Ashizawa; H. Epstein; J.F. Hejtmancik; M.B. Perryman; R. Bartlett; J. Gilbert; J. Lee; et al.
Criteria for establishing the validity of genetic recombination in myotonic dystrophy
Neurology. 1989;39(3):420-421.27 -
541.
1989J.M. Vance; G.A. Nicholson; L.H. Yamaoka; J. Stajich; C.S. Stewart; M.C. Speer; W.-Y. Hung; A.D. Roses; D. Barker; et al.
Linkage of Charcot-Marie-Tooth type 1a to chromosome 17
Experimental Neurology. 1989;104(2):186-189.62 -
542.
1989A.P. Walker; R.J. Bartlett; N.G. Laing; J. Koh; S.L. Secore; M.C. Speer; M.A. Pericak-Vance; W.-Y. Hung; L.H. Yamaoka; et al.
Inherited deletion at Duchenne dystrophy locus in normal male
Lancet. 1989;1(8636):496.7 -
543.
1989B.R. Seizinger; G.E. Farmer; J.L. Haines; L.J. Ozelius; K. Anderson; B.R. Korf; D.M. Parry; M.A. Pericak-Vance; J.J. Mulvihill; A. Menon; et al.
Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1)
American Journal of Human Genetics. 1989;44(1):30-32.1 -
544.
1989A.D. Roses; M.A. Pericak-Vance; L. Yamaoka; C. Haynes; M. Speer; P. Gaskell; W.Y. Hung; C.M. Clark; A. Heyman; et al.
Linkage studies in familial Alzheimer's disease.
Progress in clinical and biological research. 1989;317:201-215.3 -
545.
1989M.C. Speer; S.L. Sherman; C.S. Haynes; M.A. Pericak-Vance
Mapping strategies for multiple linked markers.
Progress in clinical and biological research. 1989;329:75-80.0 -
546.
1989D.V. Dawson; A.D. Roses; M.A. Pericak-Vance; E.B. Kaplan; R.C. Elston; C.S. Haynes; P.C. Gaskell Jr.; A. Heyman; C.M. Clark; et al.
Sib-pair linkage analysis in late onset Alzheimer's disease.
Progress in clinical and biological research. 1989;317:223-228.0 -
547.
1988M.C. Speer; M.A. Pericak-Vance; L.H. Yamaoka; J. Koh; Wu-Yen Hung; P.C. Gaskell Jr.; J.M. Vance; R.J. Bartlett; A.D. Roses
Prenatal diagnosis using deletion studies in Duchenne muscular dystrophy
Prenatal Diagnosis. 1988;8(6):427-437.1 -
548.
1988A.D. Roses; M.A. Pericak-Vance; R.J. Bartlett; L.H. Yamaoka; J.E. Lee; J. Koh; J.C. Chen; J.R. Gilbert; D.A. Ross; M.H. Herbstreith; et al.
Australian Paediatric Journal. 1988;24(SUPPL. 1):66-69.0 -
549.
1988T. Siddique; R. Bartlett; M. Pericak-Vance; L. Yamaoka; J. Koh; J. Chen; W.-Y. Hung; R. Kandt; A.D. Roses
Update on the molecular genetics of Duchenne muscular dystrophy
Australian Paediatric Journal. 1988;24(SUPPL. 1):9-14.0 -
550.
1988M.A. Pericak-Vance; W.Y. Hung; L. Yamaoka; C. Haynes; R.J. Bartlett; J.M. Vance; J. Lee; T. Siddique; P.C. Gaskell; et al.
Systematic gene mapping man: Data management considerations
Australian Paediatric Journal. 1988;24(SUPPL. 1):87-89.0 -
551.
1988R.J. Bartlett; M.A. Pericak-Vance; J. Koh; L.H. Yamaoka; J.C. Chen; W.-Y. Hung; M.C. Speer; M.C. Wapenaar; G.J.B. Van Ommen; E. Bakker; et al.
Duchenne muscular dystrophy: High frequency of deletions
Neurology. 1988;38(1):1-4.2 -
552.
1988J.M. Gilchrist; M. Pericak-Vance; L. Silverman; A.D. Roses
Clinical and genetic investigation in autosomal dominant limb-girdle muscular dystrophy
Neurology. 1988;38(1):5-9.51 -
553.
1988M.A. Pericak-Vance; L.H. Yamaoka; C.S. Haynes; M.C. Speer; J.L. Haines; P.C. Gaskell; W.-Y. Hung; C.M. Clark; A.L. Heyman; J.A. Trofatter; et al.
Genetic linkage studies in Alzheimer's disease families
Experimental Neurology. 1988;102(3):271-279.37 -
554.
1988M. LeBeau; M. Pericak-Vance
Report of the committee on the genetic constitution of chromosomes 18 and 19
Cytogenetics and Cell Genetics. 1988;49(1-3):99-101.0 -
555.
1988A.P. Walker; R.J. Bartlett; L.H. Yamaoka; S.L. Secore; J.E. Lee; J. Gilbert; M. Herbstreith; M.A. Pericak-Vance; W.-Y. Hung; A.D. Roses
A Bgl II polymorphism detected by LDR152 [D19S19]
Nucleic Acids Research. 1988;16(18):9063.0 -
556.
1988A.D. Roses; M.A. Pericak-Vance; R.J. Bartlett; L.H. Yamaoka; J.E. Lee; J. Koh; J.C. Chen; J.R. Gilbert; D.A. Ross; et al.
Myotonic dystrophy: update on progress to define the gene.
Australian Paediatric Journal. 1988;24 Suppl 1:66-69.0 -
557.
1987E.D. Shields; D.A. Russell; M.A. Pericak-Vance
Genetic epidemiology of the susceptibility to leprosy
Journal of Clinical Investigation. 1987;79(4):1139-1143.41 -
558.
1987J.T. Lanman Jr.; M.A. Pericak-Vance; R.J. Bartlett; J.C. Chen; L. Yamaoka; J. Koh; M.C. Speer; W.-Y. Hung; A.D. Roses
Familial inheritance of a DXS164 deletion mutation from a heterozygous female
American Journal of Human Genetics. 1987;41(2):138-144.0 -
559.
1987S.R. Diehl; M. Boehnke; F.S. Collins; R.P. Erickson; I.J. Karolyi; L.M. Ploughman; M.A. Pericak-Vance; A.S. Aylsworth; A.D. Roses
Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8
Journal of Medical Genetics. 1987;24(9):532-534.0 -
560.
1987M.P. Rozear; M.A. Pericak-Vance; K. Fischbeck; J.M. Stajich; P.C. Gaskell Jr.; D.A. Krendel; D.G. Graham; D.V. Dawson; A.D. Roses
Hereditary motor and sensory neuropathy, X-linked: A half century follow-up
Neurology. 1987;37(9):1460-1465.64 -
561.
1987M.A. Pericak-Vance; L.H. Yamaoka; J.M. Vance; A.S. Aylsworth; G.O.D. Rossenwasser; P.C. Gaskell Jr.; M.J. Alberts; W.-Y. Hung; C. Haynes; et al.
Linkage studies in peripheral neurofibromatosis
Journal of Medical Genetics. 1987;24(9):530-532.0 -
562.
1987R.J. Bartlett; M.A. Pericak-Vance; J.T. Lanman Jr.; A.P. Killam; J.R. Gilbert; J.M. Stajick; J.C. Chen; T. Siddique; R.S. Kandt; M. Sirotkin-Roses
Prenatal detection of an inherited Duchenne muscular dystrophy deletion allele.
Neurology. 1987;37(2):355-356.1 -
563.
1987R.J. Bartlett; M.A. Pericak-Vance; L. Yamaoka; J. Gilbert; M. Herbstreith; W.Y. Hung; J.E. Lee; T. Mohandas; G. Bruns; C. Laberge
A new probe for the diagnosis of myotonic muscular dystrophy
Science. 1987;235(4796):1648-1650.3 -
564.
1987M.A. Pericak-Vance; L.H. Yamaoka; J.M. Vance; K. Small; G.O.D. Rosenwasser; P.C. Gaskell Jr.; W.-Y. Hung; M.J. Alberts; C.S. Haynes; et al.
Genetic linkage studies of chromosome 17 RFLPs in von Recklinghausen neurofibromatosis (NF1)
Genomics. 1987;1(4):349-352.1 -
565.
1987J.M. Vance; M.A. Pericak-Vance; M.H. Bowman; C.S. Payne; L. Fredane; T. Siddique; A.D. Roses; E.W. Massey
Chorea-acanthocytosis: A report of three new families and implications for genetic counselling
American Journal of Medical Genetics. 1987;28(2):403-410.15 -
566.
1987B.R. Seizinger; G.A. Rouleau; A.H. Lane; G. Farmer; L.J. Ozelius; J.L. Haines; D.M. Parry; B.R. Korf; M.A. Pericak-Vance; A.G. Faryniarz; et al.
Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17
Genomics. 1987;1(4):346-348.10 -
567.
1987J. Koh; M.A. Pericak-Vance; L.H. Yamaoka; W.-Y. Hung; R.G. Worton; J.E. Lee; R.S. Kandt; R.J. Bartlett; M.C. Speer; et al.
Inherited deletion at Duchenne dystrophy locus in normal male
Lancet. 1987;2(8568):1154-1155.1 -
568.
1987B.R. Seizinger; G.A. Rouleau; L.J. Ozelius; A.H. Lane; A.G. Faryniarz; M.V. Chao; S. Huson; B.R. Korf; D.M. Parry; M.A. Pericak-Vance; et al.
Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene
Cell. 1987;49(5):589-594.75 -
569.
1986K.H. Fischbeck; N. ar-Rushdi; M. Pericak-Vance; M. Rozear; A.D. Roses; J.P. Fryns
X-linked neuropathy: Gene localization with DNA probes
Annals of Neurology. 1986;20(4):527-532.41 -
570.
1986G.E. Moore; A.D. Roses; M.A. Pericak-Vance; W.E. Garrett Jr.; F.H. Schachat
Promiscuous expression of myosin in myotonic dystrophy
Muscle and Nerve. 1986;9(4):355-363.3 -
571.
1986R.A. Coleman; J.M. Stajich; V.W. Pact; M.A. Pericak-Vance
The ischemic exercise test in normal adults and in patients with weakness and cramps
Muscle and Nerve. 1986;9(3):216-221.15 -
572.
1986A.D. Roses; M.A. Pericak-Vance; L.H. Yamaoka; M.H. Herbstreith; R.J. Bartlett; T. Siddique; W.Y. Hung; D.A. Ross; T.K. Mohandas; et al.
A new tightly linked DNA probe for myotonic dystrophy.
Neurology. 1986;36(8):1146.0 -
573.
1986M.A. Pericak-Vance; D.A. Meyers; J.F. Gusella
Genetic analysis workshop IV: Huntington Disease linkage analysis, data description
Genetic Epidemiology. 1986;3(SUPPL. 1):193-196.0 -
574.
1986M.A. Pericak-Vance; D.A. Meyers
Genetic analysis workshop IV: Huntington Disease linkage analysis summary
Genetic Epidemiology. 1986;3(SUPPL. 1):197-209.0 -
575.
1986C. Haynes; M. Pericak-Vance; D. Dawson
Analysis of Huntington Disease linkage and age-of-onset distributions
Genetic Epidemiology. 1986;3(SUPPL. 1):235-239.5 -
576.
1986M.A. Pericak-Vance; L.H. Yamaoka; R.I.F. Assinder; W.Y. Hung; R.J. Bartlett; J.M. Stajich; P.C. Gaskell; D.A. Ross; S. Sherman; G.H. Fey
Tight linkage of apolipoprotein C2 to myotonic dystrophy on chromosome 19
Neurology. 1986;36(11):1418-1423.0 -
577.
1986A.D. Roses; M.A. Pericak-Vance; D.A. Ross; L. Yamaoka; R.J. Bartlett
RFLPS at the D19S19 locus of human chromosome 19 linked to myotonic dystrophy (DM)
Nucleic Acids Research. 1986;14(13):5569.0 -
578.
1985A.P. Monaco; C.J. Bertelson; W. Middlesworth; C.A. Colletti; J. Aldridge; K.H. Fischbeck; R. Bartlett; M.A. Pericak-Vance; A.D. Roses; L.M. Kunkel
Nature. 1985;316(6031):842-845.49 -
579.
1985M.A. Pericak-Vance; J.M. Vance; R.C. Elston; K.K. Namboodiri; T.A. Fogle
Segregation and linkage analysis of α-N-acetyl-D-glucosaminidase (NAG) levels in a black family
American Journal of Medical Genetics. 1985;20(2):295-306.4 -
580.
1985L.H. Yamaoka; R.J. Bartlett; D.A. Ross; G.H. Fey; D.H. Ledbetter; G. Bruns; M.A. Pericak-Vance; M.H. Herbstreith; A.D. Roses
Journal of Neurogenetics. 1985;2(6):403-412.0 -
581.
1983A.D. Roses; M.A. Pericak-Vance; L.H. Yamaoka; E. Stubblefield; J. Stajich; J.M. Vance; M.J. Roses; D.B. Carter
Recombinant DNA strategies in genetic neurological diseases
Muscle and Nerve. 1983;6(5):339-355.0 -
582.
1983P. Hudgson; M.W. McAdams; M.A. Pericak-Vance; T.M. Edwards; A.D. Roses
Effect of sera from myasthenia gravis patients on acetylcholine receptors in myotube cultures
Journal of the Neurological Sciences. 1983;59(1):37-45.1 -
583.
1983M.A. Pericak Vance; R.C. Elston; P.M. Conneally; D.V. Dawson
Age-of-onset heterogeneity in Huntington disease families
American Journal of Medical Genetics. 1983;14(1):49-59.1 -
584.
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