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The British Journal of Nutrition|October 9, 2010
Metabolic imprinting, programming and epigenetics - a review of present priorities and future opportunitiesBryan Hanley, Jean Dijane, Mary Fewtrell, et al.
Human Mutation|August 10, 2004
Genotype-phenotype correlation in von Hippel-Lindau families with renal lesionsCatherine Gallou, Dominique Chauveau, Stéphane Richard, et al.
European Journal of Human Genetics : EJHG|June 24, 2010
A fourth locus for autosomal dominant hypercholesterolemia maps at 16q22.1Alice Marques-Pinheiro, Marie Marduel, Jean-Pierre Rabès, et al.
Plos One|January 5, 2011
Sex- and diet-specific changes of imprinted gene expression and DNA methylation in mouse placenta under a high-fat dietCatherine Gallou-Kabani, Anne Gabory, Jörg Tost, et al.
Nutrients|May 1, 2019
Effect of Maternal Obesity and Preconceptional Weight Loss on Male and Female Offspring Metabolism and Olfactory Performance in MicePolina E Panchenko, Marie-Christine Lacroix, Mélanie Jouin, et al.
Plos One|November 13, 2012
Maternal diets trigger sex-specific divergent trajectories of gene expression and epigenetic systems in mouse placentaAnne Gabory, Laure Ferry, Isabelle Fajardy, et al.
Clinical Chemistry and Laboratory Medicine|July 10, 2007
Third Santorini conference pharmacogenomics workshop report: "Pharmacogenomics at the crossroads: what else than good science will be needed for the field to become part of Personalized Medicine?"Adrián Llerena, Gerd Michel, Elise Jeannesson, et al.
Human Mutation|September 11, 2008
Identification of 23 TGFBR2 and 6 TGFBR1 gene mutations and genotype-phenotype investigations in 457 patients with Marfan syndrome type I and II, Loeys-Dietz syndrome and related disordersChantal Stheneur, Gwenaëlle Collod-Béroud, Laurence Faivre, et al.
European Journal of Pediatrics|January 26, 2002
Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 casesPascale de Lonlay, Jean-Christophe Fournet, Guy Touati, et al.
Human Mutation|August 26, 2003
Update of the UMD-FBN1 mutation database and creation of an FBN1 polymorphism databaseGwenaëlle Collod-Béroud, Saga Le Bourdelles, Lesley Ades, et al.
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