Author details

Full Name

G M Lathrop

Affiliation

ORCID

Career Start Year

1982

Papers

331

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
34172473	Genetically increased circulating FUT3 level leads to reduced risk of idiopathic pulmonary fibrosis: a Mendelian randomisation study.	Eur Respir J	2022
33350870	Estimating cell-type-specific DNA methylation effects in heterogeneous cellular populations.	Epigenomics	2021
32675199	The undiagnosed disease burden associated with alpha-1 antitrypsin deficiency genotypes.	Eur Respir J	2020
32341527	Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.	Nat Genet	2020
31127295	A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure.	Hum Mol Genet	2019
30605491	The influence of obesity-related factors in the etiology of renal cell carcinoma-A mendelian randomization study.	PLoS Med	2019
30582441	Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.	Circ Res	2019
29853305	Corrigendum re "Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma" [Eur Urol 2017;72:747-54].	Eur Urol	2018
28797570	Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma.	Eur Urol	2017
26657656	Aristolochic acid exposure in Romania and implications for renal cell carcinoma.	Br J Cancer	2016
25077817	Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions.	Int J Cancer	2015
25707804	An epigenome-wide association study of total serum immunoglobulin E concentration.	Nature	2015
26237428	Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.	Nat Genet	2015
25182136	Fine mapping of eight psoriasis susceptibility loci.	Eur J Hum Genet	2015
25231748	The effect on melanoma risk of genes previously associated with telomere length.	J Natl Cancer Inst	2014
25351205	Variation in genomic landscape of clear cell renal cell carcinoma across Europe.	Nat Commun	2014
23708191	Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.	Nat Genet	2013
23937567	Quantitative variation in plasma angiotensin-I converting enzyme activity shows allelic heterogeneity in the ABO blood group locus.	Annals of Human Genetics	2013
23886662	A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis.	Hum Mol Genet	2013
23876493	Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls.	Circ Cardiovasc Genet	2013
23345460	A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines.	Genome Res	2013
23297363	Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.	Hum Mol Genet	2013
23455637	A variant in FTO shows association with melanoma risk not due to BMI.	Nat Genet	2013
23455636	Seven new loci associated with age-related macular degeneration.	Nat Genet	2013
22238593	A genome-wide association search for type 2 diabetes genes in African Americans.	PLoS One	2012
22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	PLoS Genet	2012
22581228	A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.	Nat Genet	2012
22006220	Integrating pathway analysis and genetics of gene expression for genome-wide association study of basal cell carcinoma.	Hum Genet	2012
21734403	Coordinated conditional simulation with SLINK and SUP of many markers linked or associated to a trait in large pedigrees.	Hum Hered	2011
21983787	Genome-wide association study identifies three new melanoma susceptibility loci.	Nat Genet	2011
20360734	Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.	Nature	2010
20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Nature	2010
20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Nat Genet	2010
21060786	Infantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11.	PLoS ONE	2010
20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Nat Genet	2010
19060906	Common variants at 30 loci contribute to polygenic dyslipidemia.	Nat Genet	2009
19557161	Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution.	PLoS Genet	2009
19169254	Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.	Nat Genet	2009
19578364	Genome-wide association study identifies three loci associated with melanoma risk.	Nat Genet	2009
19430483	Genome-wide association study identifies eight loci associated with blood pressure.	Nat Genet	2009
19347040	Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion.	PLoS One	2009
18443594	SNP and haplotype mapping for genetic analysis in the rat.	Nat Genet	2008
18193043	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	Nat Genet	2008
18842065	SLC2A9 is a high-capacity urate transporter in humans.	PLoS Med	2008
18179892	Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.	Am J Hum Genet	2008
17720924	Genetic and haplotypic structure in 14 European and African cattle breeds.	Genetics	2007
17611496	Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma.	Nature	2007
17873877	A genome-wide association study of global gene expression.	Nat Genet	2007
16826522	Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension.	Am J Hum Genet	2006
16543358	Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension.	Hum Mol Genet	2006