D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics D-index 84 Citations 50,132 146 World Ranking 840 National Ranking 124

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Genetics
  • Internal medicine

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 most cited work include:

  • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (7922 citations)
  • Discovery and refinement of loci associated with lipid levels (1814 citations)
  • Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (1134 citations)

What are the main themes of her work throughout her whole career to date?

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

  • Haplotype which is related to area like Allele frequency,
  • Genetic model which is related to area like Fibrinogen and Endocrinology. Her Genetic association research incorporates themes from Genetic marker and Genetic predisposition. Her study in Immunology is interdisciplinary in nature, drawing from both Disease, Genotype and Case-control study.

She most often published in these fields:

  • Genetics (57.98%)
  • Genome-wide association study (47.90%)
  • Single-nucleotide polymorphism (26.05%)

What were the highlights of her more recent work (between 2017-2021)?

  • Genetics (57.98%)
  • Association (1.68%)
  • Biobank (2.52%)

In recent papers she was focusing on the following fields of study:

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.

Between 2017 and 2021, her most popular works were:

  • Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks (203 citations)
  • Cohort Profile: Pregnancy And Childhood Epigenetics (PACE) Consortium (58 citations)
  • The long-term impact of folic acid in pregnancy on offspring DNA methylation: Follow-up of the Aberdeen folic acid supplementation trial (AFAST) (26 citations)

In her most recent research, the most cited papers focused on:

  • Gene
  • Internal medicine
  • Genetics

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.

Best Publications

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)

8473 Citations

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)

2398 Citations

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)

1689 Citations

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)

1383 Citations

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)

1370 Citations

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)

1329 Citations

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)

927 Citations

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)

896 Citations

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)

871 Citations

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)

810 Citations

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