David‐Alexandre Trégouët

Author

Also Known As

A J Swift, Alan R. Shuldiner, Alex P. Reiner, Alun Evans, Andreas Ziegler, Andrew D. Johnson, Anke Tönjes, Ben Wright, Christopher Kabrhel, D A Tregouet

467

Publications

33K

Citations

H-Index

158

Concepts

All Affiliations

Inserm Sorbonne Université Fondation pour l’innovation en Cadiométabolisme et Nutrition Bordeaux Population Health Université Paris Cité

About

David‐Alexandre Trégouët is an author at Inserm specializing in medicine, genetics, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	38	59	7.6K
2	Public Health	26	33	5.2K
3	Health Sciences	4	4	170
4	Engineering	3	3	494
5	Natural Sciences	1	1	10

David‐Alexandre Trégouët

184

Publications

19.1K

Citations

H-Index

Page 1

	Year	Citations
Genomewide Association Analysis of Coronary Artery Disease Nilesh J. Samani, Jeanette Erdmann, Alistair S. Hall, New England Journal of Medicine	2007	2K
Large-scale association analysis identifies new risk loci for coronary artery disease Panos Deloukas, Stavroula Kanoni, Christina Willenborg, Nature Genetics Genome-wide Association StudyLarge-scale Association AnalysisEpidemiologyCardiovascular EpidemiologyCardiovascular Disease	2012	1.7K
DNA methylation and body-mass index: a genome-wide analysis Katherine Dick, Christopher P. Nelson, Loukia Tsaprouni, The Lancet Epigenetic ChangeGeneticsDna MethylationEpigenomicsGenomics	2014	785
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture Sonja I. Berndt, Stefan Gustafsson, Reedik Mägi, Nature Genetics Genome-wide Association StudyGenetic AnalysisGenotype-phenotype AssociationMedicineGenetics	2013	676
Genetics and Beyond – The Transcriptome of Human Monocytes and Disease Susceptibility Tanja Zeller, Philipp S. Wild, Silke Szymczak, PLoS ONE	2010	599
Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation Josine L. Min, Gibran Hemani, Eilís Hannon, Nature Genetics BiologyChromatinGenetic EffectsGenome StudyEpigenetic Change	2021	500
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease David‐Alexandre Trégouët, Inke R. König, Jeanette Erdmann, Nature Genetics Genome-wide Association StudyAllelic VariantGenetic DeterminantRisk LocusCardiovascular Disease	2009	473
A Novel Channelopathy in Pulmonary Arterial Hypertension Lijiang Ma, Danilo Roman‐Campos, Eric D. Austin, New England Journal of Medicine	2013	456
EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension Mélanie Eyries, David Montani, Barbara Girerd, Nature Genetics Pulmonary Arterial HypertensionPulmonary CirculationGeneticsPathologyEif2ak4 Mutations	2013	445
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy Eric Villard, Claire Perret, Françoise Gary, European Heart Journal	2011	347

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