Margaret A Pericak-Vance

发表

Association of CAV1/CAV2 genomic variants with primary open-angle glaucoma overall and by gender and pattern of visual field loss.

Robert N Weinreb, Peter Kraft, Terry Gaasterland, 2014, Ophthalmology.

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Eden R Martin, Seth Love, Brian Lawlor, 2019, Nature Genetics.

No gene is an island: the flip-flop phenomenon.

Eden R Martin, M. Pericak-Vance, E. Martin, 2007, American journal of human genetics.

Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease.

Eden R Martin, John R Gilbert, Jonathan L Haines, 2009, American journal of human genetics.

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease

Danqing Zhu, Stephan Züchner, M. Pericak-Vance, 2005, Nature Genetics.

Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis.

Pablo Villoslada, Xavier Montalban, Antonio Uccelli, 2006, Human molecular genetics.

Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease.

Eden R Martin, Kenichiro Fujiwara, Fengyu Zhang, 2004, American journal of human genetics.

Interleukin 7 receptor α chain ( IL7R ) shows allelic and functional association with multiple sclerosis

Silke Schmidt, Stephen J Sawcer, Stephen L Hauser, 2007, Nature Genetics.

Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals.

Stephen J Sawcer, Stephen L Hauser, Alastair Compston, 2010, Human molecular genetics.

CDKN2B-AS1 genotype-glaucoma feature correlations in primary open-angle glaucoma patients from the United States.

Robert N Weinreb, Terry Gaasterland, Gadi Wollstein, 2013, American journal of ophthalmology.

A second major histocompatibility complex susceptibility locus for multiple sclerosis

Stephan Beck, Roger Horton, Stephen L Hauser, 2007, Annals of neurology.

Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans.

Silke Schmidt, Emmanuel Mignot, Stephen L Hauser, 2004, American journal of human genetics.

A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.

Silke Schmidt, Lefkos Middleton, Vincent Mooser, 2004, American journal of human genetics.

Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12

Silke Schmidt, Daniel E Weeks, Michael B Gorin, 2004, BMC Genetics.

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Thomas Bourgeron, Alberto Segre, Alberto Maria Segre, 2007, Nature Genetics.

Lack of association between autism and SLC25A12.

Eden R Martin, John R Gilbert, Jonathan L Haines, 2006, The American journal of psychiatry.

Meta-analysis of the association between variants in SORL1 and Alzheimer disease.

Sandro Sorbi, Masatoshi Takeda, Eng King Tan, 2011, Archives of neurology.

Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come.

William S Bush, Stephen J Sawcer, Jorge R Oksenberg, 2010, American journal of human genetics.

Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open angle glaucoma

Robert N Weinreb, Peter Kraft, Terry Gaasterland, 2015, Nature Genetics.

Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders

Eden R Martin, Derek Van Booven, Susan H Slifer, 2014, Molecular Autism.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Jianxin Shi, Susmita Datta, Aribert Rothenberger, 2013, Nature Genetics.

Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci

Ludwig Kappos, Paul M Matthews, Stephen J Sawcer, 2009, Nature Genetics.

Integrated whole transcriptome and DNA methylation analysis identifies gene networks specific to late-onset Alzheimer's disease.

Eden Martin, Deborah C Mash, J. Gilbert, 2015, Journal of Alzheimer's disease : JAD.

Confronting complexity in late‐onset Alzheimer disease: application of two‐stage analysis approach addressing heterogeneity and epistasis

Eden R Martin, Jonathan L Haines, J. Haines, 2008, Genetic epidemiology.

Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci

Kara L Hamilton-Nelson, Stephen L Hauser, Jorge R Oksenberg, 2012, Molecular Autism.

Genome‐Wide Association and Linkage Study in the Amish Detects a Novel Candidate Late‐Onset Alzheimer Disease Gene

Lan Jiang, John R Gilbert, Jonathan L Haines, 2012, Annals of human genetics.

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1

Carl D Langefeld, Aleksey Shatunov, Gabriele Mora, 2013, Neurobiology of Aging.

Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways.

Eden R Martin, Scott M. Williams, Scott M Williams, 2012, Human molecular genetics.

Age at onset in two common neurodegenerative diseases is genetically controlled.

Rajesh Pahwa, Fengyu Zhang, Kristin K Nicodemus, 2002, American journal of human genetics.

Complement factor H increases risk for atrophic age-related macular degeneration.

Silke Schmidt, Paul Gallins, Anita Agarwal, 2006, Ophthalmology.

Comprehensive search for Alzheimer disease susceptibility loci in the APOE region.

Paul K Crane, Richard Mayeux, Kathryn L Lunetta, 2012, Archives of neurology.

A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set.

Jeremy Heil, Leonid Kruglyak, Alexander F Wilson, 2003, American journal of human genetics.

Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease.

Eden R Martin, Rajesh Pahwa, Clemens R Scherzer, 2003, Human molecular genetics.

Association study of Parkin gene polymorphisms with idiopathic Parkinson disease.

Eden R Martin, Rajesh Pahwa, Fengyu Zhang, 2003, Archives of neurology.

The Expanding Role of MBD Genes in Autism: Identification of a MECP2 Duplication and Novel Alterations in MBD5, MBD6, and SETDB1

Juan I. Young, John R Gilbert, Jonathan L Haines, 2012, Autism research : official journal of the International Society for Autism Research.

Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans.

Oscar L Lopez, David A Bennett, Robert C Green, 2013, JAMA.

Variation within DNA repair pathway genes and risk of multiple sclerosis.

Stephen J Sawcer, Stephen L Hauser, Alastair Compston, 2010, American journal of epidemiology.