Jonathan L Haines

发表

Jonathan L Haines, J. Haines, 2016, Current protocols in human genetics.

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality

Dana C Crawford, Yuki Bradford, Mariza de Andrade, 2011, Genetic epidemiology.

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.

Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network

Gerard Tromp, Dana C Crawford, Helena Kuivaniemi, 2015, Genetic epidemiology.

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.

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

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

A prevalence‐based association test for case‐control studies

Chun Li, Jacquelaine Bartlett, Scott M. Williams, 2008, Genetic epidemiology.

Assessing the accuracy of observer-reported ancestry in a biorepository linked to electronic medical records

Joshua C Denny, Dan M Roden, Dana C Crawford, 2010, Genetics in Medicine.

Automated extraction of clinical traits of multiple sclerosis in electronic medical records

Joshua C Denny, William S Bush, Subramaniam Sriram, 2013, Journal of the American Medical Informatics Association : JAMIA.

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

Tin Aung, Paul Mitchell, Ching-Yu Cheng, 2013, 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.

Genetics, statistics and human disease: analytical retooling for complexity.

Jonathan L Haines, Jason H. Moore, J. Haines, 2004, Trends in genetics : TIG.

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.

GATA2 Is Associated with Familial Early-Onset Coronary Artery Disease

Elizabeth R Hauser, Tianyuan Wang, Pascal J Goldschmidt-Clermont, 2006, PLoS genetics.

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.

Inverse association of female hormone replacement therapy with age-related macular degeneration and interactions with ARMS2 polymorphisms.

Stephen G Schwartz, Paul Gallins, Anita Agarwal, 2010, Investigative ophthalmology & visual science.

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.

Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

Chun Li, Lan Jiang, Jonathan L Haines, 2005, BMC Medical Genetics.

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.

Mitochondrial haplogroups and peripheral neuropathy during antiretroviral therapy: an adult AIDS clinical trials group study

Marshall Summar, Marylyn D Ritchie, Robert W Shafer, 2005, AIDS.

Quality Control for the Illumina HumanExome BeadChip

Robert P Igo, Janey L Wiggs, Jonathan L Haines, 2016, Current protocols in 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.

Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium

Gerard Tromp, Peggy L Peissig, Marylyn D Ritchie, 2016, PLoS genetics.

The use of animal models in the study of complex disease: all else is never equal or why do so many human studies fail to replicate animal findings?

Scott M. Williams, Scott M Williams, Jonathan L Haines, 2004, BioEssays : news and reviews in molecular, cellular and developmental biology.

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.

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA.

Stephanie Gogarten, Wendy Brodeur, Andrew Crenshaw, 2011, Human molecular 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.

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 between apolipoprotein E genotype and Alzheimer disease in African American subjects.

Robert C Green, David Bachman, L Adrienne Cupples, 2002, Archives of neurology.

Association study of Parkin gene polymorphisms with idiopathic Parkinson disease.

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

Genetic variants associated with optic nerve vertical cup-to-disc ratio are risk factors for primary open angle glaucoma in a US Caucasian population.

Louis R Pasquale, Janey L Wiggs, Jonathan L Haines, 2011, Investigative ophthalmology & visual science.

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.