Výsledky vyhledávání - Hélène Choquet
- Zobrazuji výsledky 1 - 20 z 37
- Přejít na další stránku
-
1
Molecular Basis of Obesity: Current Status and Future Prospects Autor Hélène Choquet, David Meyre
Vydáno 2011Artigo -
2
Genetics of Obesity: What have we Learned? Autor Hélène Choquet, David Meyre
Vydáno 2011Artigo -
3
Genomic insights into early-onset obesity Autor Hélène Choquet, David Meyre
Vydáno 2010Artigo -
4
-
5
-
6
-
7
The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies Autor Stéphane Cauchi, Kevin T. Nead, Hélène Choquet, Fritz Horber, Natascha Potoczna, Beverley Balkau, Michel Marre, G. Charpentier, Philippe Froguel, David Meyre
Vydáno 2008Artigo -
8
-
9
-
10
-
11
Association of Cardiovascular Risk Factors with Disease Severity in Cerebral Cavernous Malformation Type 1 Subjects with the Common Hispanic Mutation Autor Hélène Choquet, Jeffrey Nelson, Ludmila Pawlikowska, Charles E. McCulloch, Amy Akers, Beth Baca, Yasir Khan, Blaine L. Hart, Leslie Morrison, Helen Kim
Vydáno 2013Artigo -
12
Polymorphisms in Inflammatory and Immune Response Genes Associated with Cerebral Cavernous Malformation Type 1 Severity Autor Hélène Choquet, Ludmila Pawlikowska, Jeffrey Nelson, Charles E. McCulloch, Amy Akers, Beth Baca, Yasir Khan, Blaine L. Hart, Leslie Morrison, Helen Kim
Vydáno 2014Artigo -
13
-
14
Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1 Autor Hélène Choquet, Eliana Trapani, Luca Goitre, Lorenza Trabalzini, Amy Akers, Marco Maria Fontanella, Blaine L. Hart, Leslie Morrison, Ludmila Pawlikowska, Helen Kim, Saverio Francesco Retta
Vydáno 2016Artigo -
15
Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study Autor Eric Jorgenson, Khanh K. Thai, Thomas J. Hoffmann, Lori C. Sakoda, Mark Kvale, Yambazi Banda, Cathy Schaefer, Neil Risch, Jennifer R. Mertens, Constance Weisner, Hélène Choquet
Vydáno 2017Artigo -
16
A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure Autor Hélène Choquet, Khanh K. Thai, Jie Yin, Thomas J. Hoffmann, Mark Kvale, Yambazi Banda, Catherine Schaefer, Neil Risch, K. Saidas Nair, Ronald B. Melles, Eric Jorgenson
Vydáno 2017Artigo -
17
Transcription Factor <i>TCF7L2</i> Genetic Study in the French Population Autor Stéphane Cauchi, Stephen Eyre, Christian Dina, Hélène Choquet, Chantal Samson, Sophie Gallina, Beverley Balkau, G. Charpentier, François Pattou, Volodymyr Stetsyuk, Raphaël Scharfmann, Bart Staels, Gema Frühbeck, Philippe Froguel
Vydáno 2006Artigo -
18
A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects Autor Hélène Choquet, Ronald B. Melles, Deepti Anand, Jie Yin, Gabriel Cuéllar-Partida, Wei Wang, Thomas J. Hoffmann, K. Saidas Nair, Pirro G. Hysi, Salil A. Lachke, Eric Jorgenson
Vydáno 2021Revisão -
19
Visual Impairment, Eye Conditions, and Diagnoses of Neurodegeneration and Dementia Autor Erin L. Ferguson, Mary Thoma, Peter T. Buto, Jingxuan Wang, M. Maria Glymour, Thomas J. Hoffmann, Hélène Choquet, Shea J. Andrews, Kristine Yaffe, Kaitlin B. Casaletto, Willa D. Brenowitz
Vydáno 2024Artigo -
20
Effects of <i>TCF7L2</i> Polymorphisms on Obesity in European Populations Autor Stéphane Cauchi, Hélène Choquet, Ruth Gutiérrez‐Aguilar, Frédéric Capel, Katrine Grau, Christine Proença, Christian Dina, Alex Duval, Beverley Balkau, Michel Marre, Natascha Potoczna, Dominique Langin, Fritz Horber, Grith Lykke Sørensen, G. Charpentier, Stephen Eyre, Philippe Froguel
Vydáno 2008Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Genotype
Medicine
Single-nucleotide polymorphism
Genome-wide association study
Genetic association
Internal medicine
Endocrinology
Computational biology
Bioinformatics
Population
Disease
Environmental health
Biobank
Genetic architecture
Glaucoma
Heritability
Neuroscience
Obesity
Ophthalmology
Quantitative trait locus
Genetic variants
Missing heritability problem
Pathology
Allele
Diabetes mellitus
Evolutionary biology
Genome