A. Onipinla

发表

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Simon C. Potter, P. Donnelly, C. Spencer, 2007, Nature.

Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls

Jake K. Byrnes, Tomas W. Fitzgerald, P. Donnelly, 2010, Nature.

Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls

Jake K. Byrnes, Tomas W. Fitzgerald, Renwick, 2010 .

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

Simon C. Potter, David M. Evans, P. Donnelly, 2007, Nature Genetics.

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

Judy H. Cho, John P. Ferguson, G. Wainrib, 2019, Scientific Reports.

Polymorphisms in the WNK1 Gene Are Associated with Blood Pressure Variation and Urinary Potassium Excretion

P. Elliott, R. Collins, N. Samani, 2009, PloS one.

PLoS medicine Volume: 5 ISSN: 1549-1676 ISO Abbreviation: PLoS Med. Publication Date: 2008 Oct

Patricia B. Munroe, Richard Dobson, Mark J. Caulfield, 2008 .

Contrasting associations between aldosterone synthase gene polymorphisms and essential hypertension in blacks and in whites

A. Onipinla, Yanbin Dong, Haidong Zhu, 2003, Journal of hypertension.

Blood pressure loci identified with a gene-centric array.

Jean Tichet, Tom R. Gaunt, Jackie A Cooper, 2011, American journal of human genetics.

Molecular variants of the sodium/hydrogen exchanger type 3 gene and essential hypertension

A. Onipinla, Yanbin Dong, Haidong Zhu, 2004, Journal of hypertension.

Relationship between the M235T and G(-6)A polymorphisms of the angiotensinogen gene

A. Onipinla, G. Sagnella, G. MacGregor, 1999, Journal of Human Hypertension.

Targeting 160 Candidate Genes for Blood Pressure Regulation with a Genome-Wide Genotyping Array

Christian Gieger, Thomas Meitinger, Nilesh Samani, 2009, PloS one.

Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations

Christian Gieger, Thomas Meitinger, Nilesh Samani, 2009, Human molecular genetics.

A population study of ethnic variations in the angiotensin-converting enzyme I/D polymorphism: relationships with gender, hypertension and impaired glucose metabolism.

A. Onipinla, D. Cook, F. Cappuccio, 1999, Journal of hypertension.

SLC2A9 Is a High-Capacity Urate Transporter in Humans

P. Elliott, N. Samani, Morris J. Brown, 2008, PLoS medicine.

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

Judy H. Cho, John P. Ferguson, G. Wainrib, 2019, Scientific Reports.

Title : Polymorphisms in the WNK 1 Gene Are Associated with Blood Pressure Variation and Urinary Potassium Excretion

P. Elliott, R. Collins, N. Samani, 2009 .

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height.

Tom R. Gaunt, Tom S. Price, Joseph T. Glessner, 2011, American journal of human genetics.

Increased Support for Linkage of a Novel Locus on Chromosome 5q13 for Essential Hypertension in the British Genetics of Hypertension Study

N. Samani, J. Webster, Morris J. Brown, 2006, Hypertension.

Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension.

D. Clayton, N. Samani, J. Webster, 2006, American journal of human genetics.

Differences between disease‐associated endoplasmic reticulum aminopeptidase 1 (ERAP1) isoforms in cellular expression, interactions with tumour necrosis factor receptor 1 (TNF‐R1) and regulation by cytokines

P. Munroe, A. Onipinla, M. Caulfield, 2015, Clinical and experimental immunology.

Recent advances in the identification of genes for human hypertension

P. Munroe, A. Onipinla, M. Caulfield, 2005, Expert review of cardiovascular therapy.

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.

P. Donnelly, C. Spencer, A. Silman, 2007, Nature genetics.

Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

Simon C. Potter, C. Spencer, A. Silman, 2007, Nature.

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

Lisa, Husam, John P. Ferguson, 2023 .