D-Index & Metrics Best Publications
Genetics
UK
2023

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
Medicine D-index 106 Citations 64,525 893 World Ranking 3737 National Ranking 374
Genetics D-index 101 Citations 60,484 686 World Ranking 445 National Ranking 69

Research.com Recognitions

Awards & Achievements

2023 - Research.com Genetics in United Kingdom Leader Award

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Internal medicine
  • Disease

His primary scientific interests are in Genetics, Genome-wide association study, Single-nucleotide polymorphism, Genetic association and Immunology. His study in Genome-wide association study is interdisciplinary in nature, drawing from both Internal medicine, Disease, Inflammatory bowel disease, Bioinformatics and Locus. His Disease study combines topics in areas such as Human genetics and Candidate gene.

His Single-nucleotide polymorphism research includes themes of Bone density, Osteoporosis, Gene interaction and Polymorphism. Matthew A. Brown has researched Genetic association in several fields, including Quantitative trait locus, Blood pressure, Linkage disequilibrium and Methylenetetrahydrofolate reductase. His study looks at the relationship between Immunology and topics such as Case-control study, which overlap with Asthma.

His most cited work include:

  • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (7922 citations)
  • Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (1970 citations)
  • Five years of GWAS discovery (1767 citations)

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

Matthew A. Brown mostly deals with Genetics, Ankylosing spondylitis, Internal medicine, Immunology and Single-nucleotide polymorphism. His Genetics study is mostly concerned with Genome-wide association study, Genetic association, Genetic predisposition, Allele frequency and Haplotype. Matthew A. Brown interconnects Odds ratio, Locus and Bioinformatics in the investigation of issues within Genome-wide association study.

His Ankylosing spondylitis study incorporates themes from Physical therapy, Disease, Pathology and Major histocompatibility complex. His work carried out in the field of Internal medicine brings together such families of science as Gastroenterology, Endocrinology and Oncology. His Genotyping research extends to Single-nucleotide polymorphism, which is thematically connected.

He most often published in these fields:

  • Genetics (40.20%)
  • Ankylosing spondylitis (29.21%)
  • Internal medicine (30.41%)

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

  • Internal medicine (30.41%)
  • Disease (12.57%)
  • Genetics (40.20%)

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

Internal medicine, Disease, Genetics, Immunology and Genome-wide association study are his primary areas of study. His Internal medicine research is multidisciplinary, incorporating elements of Endocrinology and Oncology. His study in Genetic predisposition, Gene, Genotyping and Imputation is carried out as part of his Genetics studies.

Matthew A. Brown has included themes like Microbiome, Allele and Genotype in his Immunology study. His study with Genome-wide association study involves better knowledge in Single-nucleotide polymorphism. The study incorporates disciplines such as Prospective cohort study and Radiography in addition to Ankylosing spondylitis.

Between 2017 and 2021, his most popular works were:

  • Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (328 citations)
  • Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans (77 citations)
  • Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans (77 citations)

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

  • Gene
  • Internal medicine
  • Disease

Matthew A. Brown spends much of his time researching Immunology, Genome-wide association study, Single-nucleotide polymorphism, Genetics and Disease. His Immunology research incorporates elements of Microbiome and Allele. His biological study spans a wide range of topics, including Genetic association and Genotype.

The concepts of his Genome-wide association study study are interwoven with issues in Schizophrenia, Bipolar disorder, Medical genetics, Locus and Age of onset. His work deals with themes such as Internal medicine, Genetic predisposition and Heritability, which intersect with Single-nucleotide polymorphism. His Disease research includes themes of Ankylosing spondylitis, Bioinformatics and Serology.

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

Five years of GWAS discovery

Peter M. Visscher;Peter M. Visscher;Matthew A. Brown;Mark I. McCarthy;Mark I. McCarthy;Jian Yang.
American Journal of Human Genetics (2012)

2678 Citations

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Stephen Sawcer;Garrett Hellenthal;Matti Pirinen;Chris C. A. Spencer.
Nature (2011)

2667 Citations

Genome-wide association study identifies five new schizophrenia loci

Stephan Ripke;Alan R. Sanders;Kenneth S. Kendler;Douglas F. Levinson.
Nature Genetics (2011)

2508 Citations

10 Years of GWAS Discovery: Biology, Function, and Translation

Peter M. Visscher;Naomi R. Wray;Qian Zhang;Pamela Sklar.
American Journal of Human Genetics (2017)

2477 Citations

Genetics of rheumatoid arthritis contributes to biology and drug discovery

Yukinori Okada;Yukinori Okada;Di Wu;Di Wu;Di Wu;Gosia Trynka;Gosia Trynka;Towfique Raj;Towfique Raj.
Nature (2014)

2009 Citations

Correction: Corrigendum: Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis

John Bowes;Ashley Budu-Aggrey;Ulrike Huffmeier;Steffen Uebe.
Nature Communications (2015)

1393 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

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

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

Eileen M Shore;Meiqi Xu;George J Feldman;David A Fenstermacher.
Nature Genetics (2006)

1153 Citations

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