G. Mark Lathrop
Affiliations: | Wellcome Trust Center for Human Genetics | University of Oxford, Oxford, United Kingdom |
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"G. Lathrop"Children
Sign in to add traineeGustavo Turecki | grad student | (Neurotree) | |
Joseph Douglas Terwilliger | post-doc | 1994-1996 | Oxford |
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Publications
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Landi MT, Bishop DT, MacGregor S, et al. (2020) Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Nature Genetics |
Page DJ, Miossec MJ, Williams SG, et al. (2018) Whole Exome Sequencing Reveals the Major Genetic Contributors to Non-Syndromic Tetralogy of Fallot. Circulation Research |
Machiela MJ, Hofmann JN, Carreras-Torres R, et al. (2018) Corrigendum re "Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma" [Eur Urol 2017;72:747-54]. European Urology |
Law MH, Bishop DT, Lee JE, et al. (2015) Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Nature Genetics |
Liang L, Willis-Owen SA, Laprise C, et al. (2015) An epigenome-wide association study of total serum immunoglobulin E concentration. Nature. 520: 670-4 |
Barrett JH, Taylor JC, Bright C, et al. (2015) Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions. International Journal of Cancer. Journal International Du Cancer. 136: 1351-60 |
Scelo G, Riazalhosseini Y, Greger L, et al. (2014) Variation in genomic landscape of clear cell renal cell carcinoma across Europe. Nature Communications. 5: 5135 |
Terao C, Bayoumi N, McKenzie CA, et al. (2013) Quantitative variation in plasma angiotensin-I converting enzyme activity shows allelic heterogeneity in the ABO blood group locus. Annals of Human Genetics. 77: 465-71 |
Weidinger S, Willis-Owen SA, Kamatani Y, et al. (2013) A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis. Human Molecular Genetics. 22: 4841-56 |
Mamasoula C, Prentice RR, Pierscionek T, et al. (2013) Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls. Circulation. Cardiovascular Genetics. 6: 347-53 |