Search Results - "Aitman, Tim J"
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α1-A680T Variant in GUCY1A3 as a Candidate Conferring Protection From Pulmonary Hypertension Among Kyrgyz Highlanders
Published in Circulation. Cardiovascular genetics (01-12-2014)“…BACKGROUND—Human variation in susceptibility to hypoxia-induced pulmonary hypertension is well recognized. High-altitude residents who do not develop pulmonary…”
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FCGR3B copy number variation is associated with systemic lupus erythematosus risk in Afro-Caribbeans
Published in Rheumatology (Oxford, England) (01-07-2011)“…Objectives. To evaluate FCGR3B copy number variation (CNV) in African and European populations and to determine if FCGR3B copy number is associated with SLE…”
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Genetic basis of transcriptome differences between the founder strains of the rat HXB/BXH recombinant inbred panel
Published in Genome biology (27-04-2012)“…BACKGROUND: With the advent of next generation sequencing it has become possible to detect genomic variation on a large scale. However, predicting which…”
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Ancient DNA at the edge of the world: Continental immigration and the persistence of Neolithic male lineages in Bronze Age Orkney
Published in Proceedings of the National Academy of Sciences - PNAS (22-02-2022)“…Raw sequencing reads of ancient samples produced for this study have been deposited in the European Nucleotide Archive under accession no. PRJEB46830. Modern…”
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Combined sequence-based and genetic mapping analysis of complex traits in outbred rats
Published in Nature genetics (01-07-2013)“…The Rat Genome Sequencing and Mapping Consortium reports a combined sequence-based and genetic mapping analysis of 160 phenotypes in an outbred rat…”
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Genomes and phenomes of a population of outbred rats and its progenitors
Published in Scientific data (01-01-2014)“…Finding genetic variants that contribute to phenotypic variation is one of the main challenges of modern genetics. We used an outbred population of rats…”
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Association of variation in Fcgamma receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples
Published in Annals of the rheumatic diseases (01-09-2010)“…There is increasing evidence that variation in gene copy number (CN) influences clinical phenotype. The low-affinity Fcgamma receptor 3B (FCGR3B) located in…”
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