Wendy L. McArdle mainly investigates Genetics, Genome-wide association study, Single-nucleotide polymorphism, Genetic association and Locus. Her studies in Genetics integrate themes in fields like Body mass index, Menarche and Case-control study. Wendy L. McArdle has researched Genome-wide association study in several fields, including Linkage disequilibrium, Immunology, Allele, Allele frequency and Disease.
Her Allele frequency research includes themes of Population stratification, Human genetics and CDKN2BAS. Specifically, her work in Single-nucleotide polymorphism is concerned with the study of SNP. Her study looks at the relationship between Locus and topics such as Genetic variation, which overlap with Minor allele frequency.
Her primary areas of investigation include Genetics, Genome-wide association study, Single-nucleotide polymorphism, Genetic association and Immunology. Her study in Locus, Methylation, Allele, Gene and Candidate gene falls within the category of Genetics. Her Genome-wide association study study combines topics in areas such as Polymorphism, Meta-analysis, Internal medicine, Heritability and Genetic architecture.
Her Single-nucleotide polymorphism study also includes
Her scientific interests lie mostly in Genetics, Association, Biobank, Genetic variants and Folic acid. She integrates Genetics and Trait in her studies. Wendy L. McArdle usually deals with Biobank and limits it to topics linked to Schizophrenia and Genome-wide association study.
The concepts of her Genome-wide association study study are interwoven with issues in Immune system, Asthma and Immunology. Her studies deal with areas such as Offspring, University hospital and Family medicine as well as Folic acid. Her research investigates the connection with Family medicine and areas like Pregnancy which intersect with concerns in Depression, Mental health, Clinical psychology, Anxiety and Cognition.
Wendy L. McArdle mostly deals with Folic acid, Family medicine, Research centre, Folic acid supplementation and University hospital. She regularly links together related areas like Prenatal Exposure Delayed Effects in her Folic acid studies. Her biological study spans a wide range of topics, including Offspring and Pregnancy.
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.
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
Paul R. Burton;David G. Clayton;Lon R. Cardon;Nick Craddock.
Nature (2007)
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 studies of body mass index yield new insights for obesity biology
Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice.
Faculty of Health; Institute of Health and Biomedical Innovation (2015)
Genome-wide association study identifies eight loci associated with blood pressure
Christopher Newton-Cheh;Christopher Newton-Cheh;Toby Johnson;Toby Johnson;Vesela Gateva;Martin D. Tobin.
Nature Genetics (2009)
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
Miles Parkes;Jeffrey C Barrett;Natalie J Prescott;Mark Tremelling.
Nature Genetics (2007)
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
Paul R Burton;David G Clayton;Lon R Cardon;Nick Craddock.
Nature Genetics (2007)
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
Philip L De Jager;Philip L De Jager;Xiaoming Jia;Joanne Wang;Paul I W de Bakker.
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)
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Nick Craddock;Matthew E. Hurles;Niall Cardin;Richard D. Pearson.
Nature (2010)
Newly identified genetic risk variants for celiac disease related to the immune response
Karen A Hunt;Alexandra Zhernakova;Graham Turner;Graham A R Heap.
Nature Genetics (2008)
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:
St George's, University of London
Harvard University
Erasmus University Rotterdam
Erasmus University Rotterdam
King's College London
Helmholtz Zentrum München
University of Bristol
University of Cambridge
Imperial College London
University of Cambridge
Peking University
Microsoft (United States)
University of Helsinki
Spanish National Research Council
University of California, Berkeley
Tohoku University
Griffith University
University of Toronto
The University of Texas Health Science Center at San Antonio
McMaster University
University of Arizona
China University of Geosciences
Northwestern University
Boston University
University Medical Center Groningen
University of Toronto