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 and Molecular Biology D-index 101 Citations 35,284 232 World Ranking 415 National Ranking 54
Medicine D-index 96 Citations 35,480 245 World Ranking 4403 National Ranking 416

Research.com Recognitions

Awards & Achievements

2016 - Member of Academia Europaea

Fellow of The Academy of Medical Sciences, United Kingdom

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Mutation
  • Genetics

Richard C. Trembath mostly deals with Genetics, Genome-wide association study, Immunology, BMPR2 and Internal medicine. His research combines Psoriasis and Genetics. His Genome-wide association study study incorporates themes from Odds ratio, Disease, Inflammatory bowel disease, Case-control study and Genetic association.

His Immunology research integrates issues from Inflammatory arthritis, HLA-B27 and Allele. Richard C. Trembath combines subjects such as Transforming growth factor beta, Pulmonary hypertension and Frameshift mutation with his study of BMPR2. His work in Internal medicine addresses subjects such as Endocrinology, which are connected to disciplines such as Bone morphogenetic protein receptor, Right ventricular hypertrophy and Pulmonary artery.

His most cited work include:

  • Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (1970 citations)
  • Heterozygous germline mutations in BMPR2 , encoding a TGF-β receptor, cause familial primary pulmonary hypertension (1186 citations)
  • A Genome-Wide Association Study Identifies New Psoriasis Susceptibility Loci and an Interaction Between HLA-C and ERAP1 (768 citations)

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

His primary areas of study are Genetics, Psoriasis, Gene, Internal medicine and Immunology. His Locus, Allele, Mutation, Genome-wide association study and Single-nucleotide polymorphism investigations are all subjects of Genetics research. His Locus research is multidisciplinary, incorporating perspectives in Genetic linkage and Haplotype.

The concepts of his Mutation study are interwoven with issues in BMPR2 and Molecular biology. His Genome-wide association study research includes themes of Schizophrenia, Disease, Genetic predisposition and Genetic association. In his research on the topic of Internal medicine, Bone morphogenetic protein is strongly related with Endocrinology.

He most often published in these fields:

  • Genetics (56.00%)
  • Psoriasis (19.20%)
  • Gene (20.80%)

What were the highlights of his more recent work (between 2016-2021)?

  • Genetics (56.00%)
  • Genome-wide association study (11.80%)
  • Disease (7.20%)

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

Richard C. Trembath spends much of his time researching Genetics, Genome-wide association study, Disease, Internal medicine and Gene. Richard C. Trembath regularly ties together related areas like Age of onset in his Genetics studies. His studies in Genome-wide association study integrate themes in fields like Schizophrenia, Genetic predisposition, Immunology, Genetic association and Locus.

He usually deals with Immunology and limits it to topics linked to Receptor and Psoriasis treatment. His Pulmonary hypertension, Odds ratio and Pulmonary embolism study in the realm of Internal medicine connects with subjects such as In patient. His work carried out in the field of Gene brings together such families of science as Drug development and Computational biology.

Between 2016 and 2021, his most popular works were:

  • Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (328 citations)
  • Identification of rare sequence variation underlying heritable pulmonary arterial hypertension. (136 citations)
  • Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants (106 citations)

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

  • Gene
  • Mutation
  • Internal medicine

Richard C. Trembath mainly investigates Genome-wide association study, Genetics, Genetic variation, Genetic association and Gene. His Genome-wide association study research is multidisciplinary, incorporating elements of Schizophrenia, Keratoconus, Mendelian Randomization Analysis, Quantitative trait locus and Candidate gene. As part of his studies on Genetics, Richard C. Trembath frequently links adjacent subjects like Age of onset.

His Genetic variation study combines topics in areas such as Immunology and Immune system. His Immunology research incorporates elements of Cell activation and Kidney transplantation. His study in Genetic association is interdisciplinary in nature, drawing from both Odds ratio, Genotyping, Oncology and Locus.

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

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)

2262 Citations

Heterozygous germline mutations in BMPR2 , encoding a TGF-β receptor, cause familial primary pulmonary hypertension

Kirk B. Lane;Rajiv D. Machado;Michael W. Pauciulo;Jennifer R. Thomson.
Nature Genetics (2000)

1398 Citations

A Genome-Wide Association Study Identifies New Psoriasis Susceptibility Loci and an Interaction Between HLA-C and ERAP1

Amy Strange;Francesca Capon;Chris C A Spencer.
Nature Genetics (2010)

841 Citations

Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta family.

Jennifer R Thomson;Rajiv D Machado;Michael W Pauciulo;Neil V Morgan.
Journal of Medical Genetics (2000)

789 Citations

Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia

Richard Trembath;J R Thomson;Rajiv Machado;N Morgan.
The New England Journal of Medicine (2001)

778 Citations

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

DM Evans;A Dilthey;M Pirinen;T Zayats.
Scopus (2011)

764 Citations

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

Lam C. Tsoi;Sarah L. Spain;Sarah L. Spain;Jo Knight;Eva Ellinghaus;Eva Ellinghaus.
Nature Genetics (2012)

749 Citations

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

D M Evans;Spencer Cca.;J J Pointon;Z Su.
Nature Genetics (2011)

737 Citations

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

Sue Shackleton;David J. Lloyd;Stephen N.J. Jackson;Richard Evans.
Nature Genetics (2000)

728 Citations

Genetics and genomics of pulmonary arterial hypertension

Florent Soubrier;Wendy K. Chung;Rajiv Machado;Ekkehard Grünig.
Journal of the American College of Cardiology (2009)

658 Citations

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