A. Britton

发表

Neural network-derived electrocardiographic features have prognostic significance and important phenotypic and genotypic associations

D. O’Regan, J. Waks, K. Hnatkova, 2023, medRxiv.

Cross-Sectional Exploration of Plasma Biomarkers of Alzheimer’s Disease in Down Syndrome: Early Data from the Longitudinal Investigation for Enhancing Down Syndrome Research (LIFE-DSR) Study

Sarah J. Hart, H. D. Rosas, D. Airey, 2021, Journal of clinical medicine.

Genotype, haplotype and copy-number variation in worldwide human populations

Zachary A. Szpiech, Sonja W. Scholz, D. Hernandez, 2008, Nature.

The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans

Jun S. Liu, Ellen T. Gelfand, Ayellet V. Segrè, 2015, Science.

Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseases

Andrew B. Nobel, Fred A. Wright, Ivan Rusyn, 2015, Scientific Reports.

Genome-Wide Association Study of White Blood Cell Count in 16,388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT)

Yusuke Nakamura, Yukinori Okada, David Couper, 2011, PLoS genetics.

A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)

Mark I. McCarthy, Luigi Ferrucci, Kara Stevens, 2008, PLoS genetics.

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.

Sonja W. Scholz, S. Bandinelli, D. Hernandez, 2009, Human molecular genetics.

Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data

Sonja W. Scholz, Adriano Chiò, Gabriele Mora, 2007, The Lancet Neurology.

A Novel Approach to High-Quality Postmortem Tissue Procurement: The GTEx Project

Ellen T. Gelfand, Ayellet V. Segrè, Latarsha J. Carithers, 2015, Biopreservation and biobanking.

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals.

Sonja W. Scholz, John Hardy, Mar Matarin, 2007, Human molecular genetics.

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release

Sonja W. Scholz, Scott Silliman, Carl D Langefeld, 2007, The Lancet Neurology.

Corrigendum: Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseases

Ellen T. Gelfand, Ayellet V. Segrè, Casandra A. Trowbridge, 2016, Scientific Reports.

Genome-Wide Association of Body Fat Distribution in African Ancestry Populations Suggests New Loci

Mary K. Wojczynski, Charles Kooperberg, Lewis H. Kuller, 2013, PLoS genetics.

A Meta-Analysis Identifies New Loci Associated with Body Mass index in Individuals of African Ancestry

Xiaofeng Zhu, Olufunmilayo I. Olopade, Alex P. Reiner, 2013, Nature Genetics.

Identification, Replication, and Fine-Mapping of Loci Associated with Adult Height in Individuals of African Ancestry

Gary K. Chen, Cameron D. Palmer, J. Witte, 2011, PLoS genetics.

Meta-analysis of loci associated with age at natural menopause in African-American women.

Gary K. Chen, Kathleen F. Kerr, Jeanette S. Andrews, 2014, Human molecular genetics.

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

Sonja W. Scholz, D. Hernandez, A. Singleton, 2006, The Lancet Neurology.

Genomewide SNP assay reveals mutations underlying Parkinson disease

Sonja W. Scholz, D. Hernandez, A. Singleton, 2008, Human mutation.

Genome-wide association study of age at menarche in African-American women.

Gary K. Chen, C. Carlson, E. Demerath, 2013, Human molecular genetics.

A feasibility study demonstrating that independence, quality of life, and adaptive behavioral skills can improve in children with Down syndrome after using assistive technology

Kaylin White, James Hendrix, A. Britton, 2023, PloS one.

Analysis of Nigerians with Apparently Sporadic Parkinson Disease for Mutations in LRRK2, PRKN and ATXN3

A. Singleton, J. Hardy, R. Akinyemi, 2008, PloS one.

Comprehensive Screening of a North American Parkinson’s Disease Cohort for LRRK2 Mutation

Janel O. Johnson, A. Singleton, R. Nussbaum, 2007, Neurodegenerative Diseases.

Structural genomic variation in ischemic stroke

Sonja W. Scholz, D. Hernandez, A. Singleton, 2008, Neurogenetics.

Correction: Identification, Replication, and Fine-Mapping of Loci Associated with Adult Height in Individuals of African Ancestry

Gary K. Chen, Sanjay R. Patel, Cameron D. Palmer, 2011, PLoS Genetics.

Candidate Gene Polymorphisms for Ischemic Stroke

A. Singleton, J. Hardy, S. Chanock, 2009, Stroke.

Genome-wide association study of age at menarche in African-American women.

Gary K. Chen, Kathleen F. Kerr, C. Carlson, 2013, Human molecular genetics.

A Meta-Analysis Identifies New Loci Associated with Body Mass index in Individuals of African Ancestry

Gary K. Chen, Scott M. Williams, Nicholette D. Palmer, 2013, Nature Genetics.