2016 - Member of Academia Europaea
Fellow of The Academy of Medical Sciences, United Kingdom
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 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.
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.
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.
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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)
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)
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)
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)
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)
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)
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)
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)
LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.
Sue Shackleton;David J. Lloyd;Stephen N.J. Jackson;Richard Evans.
Nature Genetics (2000)
Genetics and genomics of pulmonary arterial hypertension
Florent Soubrier;Wendy K. Chung;Rajiv Machado;Ekkehard Grünig.
Journal of the American College of Cardiology (2009)
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