Novel Insights Into the Etiology of Diabetes From Genome-Wide Association Studies

Por Palmer, Colin N.A.
Publicado em 2009

The peroxisome proliferator activated receptor δ is required for the differentiation of THP-1 monocytic cells by phorbol ester

Por Vosper, Helen, Khoudoli, Guennadi A, Palmer, Colin NA
Publicado em 2003

Effect of Serotonin Transporter 5HTTLPR Polymorphism on Gastrointestinal Intolerance to Metformin: A GoDARTS Study

Por Dujic, Tanja, Zhou, Kaixin, Tavendale, Roger, Palmer, Colin N.A., Pearson, Ewan R.
Publicado no Diabetes Care (2016)

Association of Organic Cation Transporter 1 with Intolerance to Metformin in Type 2 Diabetes: A GoDARTS Study

Por Dujic, Tanja, Zhou, Kaixin, Donnelly, Louise A, Tavendale, Roger, Palmer, Colin NA, Pearson, Ewan R
Publicado no Diabetes (2014)

Utility of Population-Level DNA Sequence Data in the Diagnosis of Hereditary Endocrine Disease

Por Newey, Paul J., Berg, Jonathan N., Zhou, Kaixin, Palmer, Colin N.A., Thakker, Rajesh V.
Publicado no J Endocr Soc (2017)

Association of common variation in the PPARA gene with incident myocardial infarction in individuals with type 2 diabetes: A Go-DARTS study

Por Doney, Alex SF, Fischer, Bettina, Lee, Simon P, Morris, Andrew D, Leese, Graham, Palmer, Colin NA
Publicado em 2005

The FTO Gene is Associated with an Atherogenic Lipid Profile and Myocardial Infarction in Patients with Type 2 Diabetes: A Go-DARTS study

Por Doney, Alex SF, Dannfald, Jennifer, Kimber, Charlotte H, Donnelly, Louise A, Pearson, Ewan, Morris, Andrew D., Palmer, Colin NA
Publicado em 2009

Clinical and genetic determinants of progression of type 2 diabetes: A DIRECT Study

Por Zhou, Kaixin, Donnelly, Louise A, Morris, Andrew D, Franks, Paul W, Jennison, Chris, Palmer, Colin NA, Pearson, Ewan R
Publicado em 2013

A Genome-wide Association Study Provides Evidence of Sex-specific Involvement of Chr1p35.1 (ZSCAN20-TLR12P) and Chr8p23.1 (HMGB1P46) With Diabetic Neuropathic Pain

Por Meng, Weihua, Deshmukh, Harshal A., Donnelly, Louise A., Torrance, Nicola, Colhoun, Helen M., Palmer, Colin N.A., Smith, Blair H.
Publicado no EBioMedicine (2015)

Glycemic Exposure and Blood Pressure Influencing Progression and Remission of Diabetic Retinopathy: A longitudinal cohort study in GoDARTS

Por Liu, Yiyuan, Wang, Minghui, Morris, Andrew D., Doney, Alex S.F., Leese, Graham P., Pearson, Ewan R., Palmer, Colin N.A.
Publicado em 2013

Male preponderance in early diagnosed type 2 diabetes is associated with the ARE insertion/deletion polymorphism in the <it>PPP1R3A </it>locus

Por Leese Graham, Boyle Douglas I, Cohen Patricia TW, Cecil Joanne E, Fischer Bettina, Doney Alex SF, Morris Andrew D, Palmer Colin NA
Publicado em 2003-06-01

Male preponderance in early diagnosed type 2 diabetes is associated with the ARE insertion/deletion polymorphism in the PPP1R3A locus

Por Doney, Alex SF, Fischer, Bettina, Cecil, Joanne E, Cohen, Patricia TW, Boyle, Douglas I, Leese, Graham, Morris, Andrew D, Palmer, Colin NA
Publicado em 2003

Haplotype analysis of the PPARγ Pro12Ala and C1431T variants reveals opposing associations with body weight

Por Doney, Alex, Fischer, Bettina, Frew, David, Cumming, Alastair, Flavell, David M, World, Michael, Montgomery, Hugh E, Boyle, Douglas, Morris, Andrew, Palmer, Colin NA
Publicado em 2002

Assessing the Combined Impact of 18 Common Genetic Variants of Modest Effect Sizes on Type 2 Diabetes Risk

Por Lango, Hana, Palmer, Colin N.A., Morris, Andrew D., Zeggini, Eleftheria, Hattersley, Andrew T., McCarthy, Mark I., Frayling, Timothy M., Weedon, Michael N.
Publicado em 2008

Combined Effect of Inflammatory Gene Polymorphisms and the Risk of Ischemic Stroke in a Prospective Cohort of Subjects With Type 2 Diabetes: A Go-DARTS Study

Por Palmer, Colin N.A., Kimber, Charlotte H., Doney, Alex S.F., Proia, Anna S., Morris, Andrew D., Gaetani, Eleonora, Quarta, Miriam, Smith, Roy C., Pola, Roberto
Publicado em 2010

Genetic variants predicting left ventricular hypertrophy in a diabetic population: a Go-DARTS study including meta-analysis

Por Parry, Helen M, Donnelly, Louise A, Van Zuydam, Natalie, Doney, Alexander SF, Elder, Douglas HJ, Morris, Andrew D, Struthers, Alan D, Palmer, Colin NA, Lang, Chim C
Publicado em 2013

Gene-Environment Interaction in the Onset of Eczema in Infancy: Filaggrin Loss-of-Function Mutations Enhanced by Neonatal Cat Exposure

Por Bisgaard, Hans, Simpson, Angela, Palmer, Colin N.A, Bønnelykke, Klaus, Mclean, Irwin, Mukhopadhyay, Somnath, Pipper, Christian B, Halkjaer, Liselotte B, Lipworth, Brian, Hankinson, Jenny, Woodcock, Ashley, Custovic, Adnan
Publicado em 2008

Genetic Variation in Kruppel like Factor 15 Is Associated with Left Ventricular Hypertrophy in Patients with Type 2 Diabetes: Discovery and Replication Cohorts

Por Patel, Sheila K., Wai, Bryan, Lang, Chim C., Levin, Daniel, Palmer, Colin N.A., Parry, Helen M., Velkoska, Elena, Harrap, Stephen B., Srivastava, Piyush M., Burrell, Louise M.
Publicado no EBioMedicine (2017)

Both High and Low HbA1c Predict Incident Heart Failure in Type 2 Diabetes Mellitus

Por Parry, Helen M., Deshmukh, Harshal, Levin, Daniel, Van Zuydam, Natalie, Elder, Douglas H.J., Morris, Andrew D., Struthers, Allan D., Palmer, Colin N.A., Doney, Alex S.F., Lang, Chim C.
Publicado no Circ Heart Fail (2015)

Reduced-Function SLC22A1 Polymorphisms Encoding Organic Cation Transporter 1 and Glycemic Response to Metformin: A GoDARTS Study

Por Zhou, Kaixin, Donnelly, Louise A., Kimber, Charlotte H., Donnan, Peter T., Doney, Alex S.F., Leese, Graham, Hattersley, Andrew T., McCarthy, Mark I., Morris, Andrew D., Palmer, Colin N.A., Pearson, Ewan R.
Publicado em 2009