His primary areas of investigation include Genetics, Genome-wide association study, Internal medicine, Single-nucleotide polymorphism and Endocrinology. His Alcohol dependence research extends to Genetics, which is thematically connected. His study in Genome-wide association study is interdisciplinary in nature, drawing from both Meta-analysis, Lipid metabolism, Cholesterol and Medical genetics.
In the field of Internal medicine, his study on Body mass index and Obesity overlaps with subjects such as Transmembrane transporter activity and Kidney development. The various areas that John Whitfield examines in his Single-nucleotide polymorphism study include Urate transport, Genetic variation and SLC22A12. His Endocrinology research includes themes of Serum iron, Heart failure, Cardiology and Polymorphism.
His main research concerns Genetics, Internal medicine, Endocrinology, Genome-wide association study and Alcohol. His Single-nucleotide polymorphism, Quantitative trait locus, Allele, Genetic association and Locus study are his primary interests in Genetics. Internal medicine is closely attributed to Carbohydrate deficient transferrin in his study.
He is studying Cholesterol, which is a component of Endocrinology. He works in the field of Alcohol, namely Alcohol dependence. His Alcohol dependence study frequently involves adjacent topics like Psychiatry.
John Whitfield mainly focuses on Genome-wide association study, Genetics, Internal medicine, Genetic association and Single-nucleotide polymorphism. His work deals with themes such as Alcohol dependence, Schizophrenia, Psychiatry, Bioinformatics and Disease, which intersect with Genome-wide association study. As part of one scientific family, he deals mainly with the area of Genetics, narrowing it down to issues related to the Meta-analysis, and often Genome.
His Internal medicine research incorporates elements of Alcohol and Endocrinology. His study in the field of Cholesterol also crosses realms of Mendelian randomization, Fractional anisotropy and White matter. His studies in Genetic association integrate themes in fields like Transferrin, Kidney disease, Renal function, Demography and Kidney.
John Whitfield mostly deals with Genome-wide association study, Genetics, Genetic association, Single-nucleotide polymorphism and Internal medicine. By researching both Genome-wide association study and Mendelian randomization, John Whitfield produces research that crosses academic boundaries. In most of his Genetics studies, his work intersects topics such as Body mass index.
His studies deal with areas such as Transferrin, Genetic epidemiology, Kidney disease and Renal function as well as Genetic association. His studies in Single-nucleotide polymorphism integrate themes in fields like Transferrin receptor, Genetic variation, Hemochromatosis and Locus. His study connects Endocrinology and Internal medicine.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich;Kiran Musunuru;Albert V. Smith;Andrew C. Edmondson.
Nature (2010)
Discovery and refinement of loci associated with lipid levels
Cristen J. Willer;Ellen M. Schmidt;Sebanti Sengupta;Gina M. Peloso;Gina M. Peloso;Gina M. Peloso.
Nature Genetics (2013)
Genetic and environmental contributions to alcohol dependence risk in a national twin sample: consistency of findings in women and men.
A. C. Heath;K. K. Bucholz;P. A. F. Madden;S. H. Dinwiddie.
Psychological Medicine (1997)
Gamma Glutamyl Transferase
J. B. Whitfield.
Critical Reviews in Clinical Laboratory Sciences (2001)
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
Yurii S Aulchenko;Samuli Ripatti;Ida Lindqvist;Dorret Boomsma.
Nature Genetics (2009)
Common variants associated with plasma triglycerides and risk for coronary artery disease
Ron Do;Cristen J. Willer;Ellen M. Schmidt;Sebanti Sengupta.
Nature Genetics (2013)
Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations
Melanie Kolz;Toby Johnson;Toby Johnson;Toby Johnson;Serena Sanna;Alexander Teumer.
PLOS Genetics (2009)
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
Anna Köttgen;Anna Köttgen;Eva Albrecht;Alexander Teumer;Veronique Vitart.
Nature Genetics (2013)
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Mengzhen Liu;Yu Jiang;Robbee Wedow;Yue Li;Yue Li.
Nature Genetics (2019)
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.
John C Chambers;John C Chambers;John C Chambers;Weihua Zhang;Weihua Zhang;Joban S. Sehmi;Joban S. Sehmi;Xinzhong Li.
Nature Genetics (2011)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
QIMR Berghofer Medical Research Institute
University of Queensland
Washington University in St. Louis
Vrije Universiteit Amsterdam
Washington University in St. Louis
Vrije Universiteit Amsterdam
King's College London
National Institutes of Health
University of Tartu
Guy's and St Thomas' NHS Foundation Trust
University of Amsterdam
University of Auckland
University of New South Wales
École Polytechnique Fédérale de Lausanne
National Taiwan University
University of Helsinki
University of Padua
Loyola University Chicago
Université Paris Cité
University of Arizona
University of Oxford
KU Leuven
Université Paris Cité
Boston University
Universität Hamburg
University of Colorado Boulder