G. Mark Lathrop

Affiliations: 
Wellcome Trust Center for Human Genetics University of Oxford, Oxford, United Kingdom 
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"G. Lathrop"

Children

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Gustavo 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
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