K. Parnell

发表

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 .

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.

Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

P. Donnelly, C. Spencer, C. Freeman, 2010 .

Type 2 diabetes TCF7L2 risk genotypes alter birth weight: a study of 24,053 individuals.

M. Jarvelin, M. McCarthy, D. Strachan, 2007, American journal of human genetics.

HLA-DQA1–HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants

M. Tremelling, M. Parkes, C. Lees, 2014, 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.

A common variation in deiodinase 1 gene DIO1 is associated with the relative levels of free thyroxine and triiodothyronine.

D. Hernandez, D. Melzer, A. Singleton, 2008, The Journal of clinical endocrinology and metabolism.

Genetic and microbial factors modulating the ubiquitin proteasome system in inflammatory bowel disease

C. Wijmenga, T. Ahmad, P. Rutgeerts, 2013, Gut.

Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

Simon C. Potter, P. Donnelly, C. Spencer, 2009, Nature Genetics.

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

Lisa, Husam, John P. Ferguson, 2023 .

The transcription factor 7‐like 2 (TCF7L2) gene is associated with Type 2 diabetes in UK community‐based cases, but the risk allele frequency is reduced compared with UK cases selected for genetic studies

B. Shields, B. Knight, K. Parnell, 2007, Diabetic medicine : a journal of the British Diabetic Association.

A common variation in deiodinase 1 gene DIO1 is associated with the relative levels of free thyroxine and triiodothyronine.

D. Hernandez, D. Melzer, A. Singleton, 2008, The Journal of clinical endocrinology and metabolism.