Hélène Blanché - Concepedia

Author

Hélène Blanché

Also Known As

Blanche H, Blanche, H., Blanche, Helene, Blanché, Hélène, Debabrata Mukhopadhyay, Fabrice Carrat, Frédéric Blond, Fumihiko Matsuda, H Blanche, H Blanché

181

Publications

21.9K

Citations

H-Index

137

Concepts

All Affiliations

Fondation Jean Dausset-CEPH Inserm Centre National de la Recherche Scientifique Sorbonne Université Université Paris Cité

About

Hélène Blanché is an author at Fondation Jean Dausset-CEPH specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	31	41	8.2K
2	Public Health	12	13	3K
3	Natural Sciences	6	6	415
4	Biology	4	4	286
5	Health Sciences	2	2	326

Hélène Blanché

Publications

14.8K

Citations

H-Index

Page 1

	Year	Citations
The complete genome sequence of a Neanderthal from the Altai Mountains Kay Prüfer, Fernando Racimo, Nick Patterson, Nature	2013	2.3K
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants Lars G. Fritsche, Wilmar Igl, Jessica N. Cooke Bailey, Nature Genetics Genome-wide Association StudyOcular DiseaseOphthalmologyGeneticsAge-related Diseases	2015	1.6K
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25 Rayjean J. Hung, James McKay, Valérie Gaborieau, Nature Tobacco ControlLung Cancer MapsNicotineMolecular BiologyCancer Genomics	2008	1.3K
Insights into human genetic variation and population history from 929 diverse genomes Anders Bergström, Shane McCarthy, Ruoyun Hui, Science	2020	1K
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24 Brent W. Zanke, Celia M.T. Greenwood, Jagadish Rangrej, Nature Genetics Genome-wide Association StudyGenome-wide AssociationGeneticsColorectal CancerPathology	2007	727
Association of <i>FOXO3A</i> variation with human longevity confirmed in German centenarians Friederike Flachsbart, Amke Caliebe, Rabea Kleindorp, Proceedings of the National Academy of Sciences	2009	567
A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma Corine Bertolotto, Fabienne Lesueur, Sandy Giuliano, Nature Somatic VariantGeneticsMelanomaRenal CarcinomaPathology	2011	513
Paraoxonase polymorphism Met-Leu54 is associated with modified serum concentrations of the enzyme. A possible link between the paraoxonase gene and increased risk of cardiovascular disease in diabetes. M C Garin, Richard W. James, Philippe Dussoix, Journal of Clinical Investigation GeneticsGenetic EpidemiologyHuman PolymorphismOxidative StressMetabolic Syndrome	1997	476
Predisposing Gene for Early-Onset Prostate Cancer, Localized on Chromosome 1q42.2-43 Philippe Berthon, Antoine Valéri, Annick Cohen-Akenine, The American Journal of Human Genetics ChromatinUrologyEarly-onset Prostate CancerGeneticsProstatic Disease	1998	362
Gln-Arg192 polymorphism of paraoxonase and coronary heart disease in type 2 diabetes Juan Carlos Ruiz, Alfredo Morabia, Hélène Blanché, The Lancet Metabolic SyndromeGenetic DeterminantCardiovascular DiseaseDiabetesGenetic Epidemiology	1995	342

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