Junien, Claudine

Mutations in PCSK9 cause autosomal dominant hypercholesterolemia

Abifadel, M., Varret, M., Rabès, J.-P., Allard, D., Ouguerram, K., Devillers, M., Cruaud, C., Benjannet, S., Wickham, L., Erlich, D., et al. (2003) · Nature Genetics

Lipoproteins and Cardiovascular HealthLipid metabolism and disorders

Cited by 2,985

Placental contribution to the origins of sexual dimorphism in health and diseases: sex chromosomes and epigenetics

Gabory, A., Roseboom, T. J., Moore, T., Moore, L. G., & Junien, C. (2013) · Biology of Sex Differences

Birth, Development, and HealthGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Cited by 344

Placental contribution to nutritional programming of health and diseases: epigenetics and sexual dimorphism

Tarrade, A., Panchenko, P., Junien, C., & Gabory, A. (2015) · Journal of Experimental Biology

Birth, Development, and HealthPregnancy and preeclampsia studies

Cited by 251

Sex- and Diet-Specific Changes of Imprinted Gene Expression and DNA Methylation in Mouse Placenta under a High-Fat Diet

Gallou-Kabani, C., Gabory, A., Tost, J., Karimi, M., Mayeur, S., Lesage, J., Boudadi, E., Gross, M.-S., Taurelle, J., Vigé, A., et al. (2010) · PLoS ONE

Genetic Syndromes and ImprintingBirth, Development, and Health

Cited by 229

Maternal Diets Trigger Sex-Specific Divergent Trajectories of Gene Expression and Epigenetic Systems in Mouse Placenta

Gabory, A., Ferry, L., Fajardy, I., Jouneau, L., Gothié, J.-D., Vigé, A., Fleur, C., Mayeur, S., Gallou-Kabani, C., Gross, M.-S., et al. (2012) · PLoS ONE

Birth, Development, and HealthGenetic Syndromes and Imprinting

Cited by 204

Molecular spectrum of autosomal dominant hypercholesterolemia in France

Marduel, M., Carrié, A., Sassolas, A., Devillers, M., Carreau, V., Di Filippo, M., Erlich, D., Abifadel, M., Marques-Pinheiro, A., Munnich, A., et al. (2010) · Human Mutation

Lipoproteins and Cardiovascular HealthLipid metabolism and disorders

Cited by 115

The molecular basis of familial hypercholesterolemia in Lebanon: Spectrum of LDLR mutations and role of PCSK9 as a modifier gene

Abifadel, M., Rabès, J.-P., Jambart, S., Halaby, G., Gannagé-Yared, M.-H., Sarkis, A., Beaino, G., Varret, M., Salem, N., Corbani, S., et al. (2009) · Human Mutation

Lipoproteins and Cardiovascular HealthLipid metabolism and disorders

Cited by 99

Maternal obesity programs increased leptin gene expression in rat male offspring via epigenetic modifications in a depot-specific manner

Lecoutre, S., Oger, F., Pourpe, C., Butruille, L., Marousez, L., Dickes-Coopman, A., Laborie, C., Guinez, C., Lesage, J., Vieau, D., et al. (2017) · Molecular Metabolism

Birth, Development, and HealthEpigenetics and DNA Methylation

Cited by 49

A fourth locus for autosomal dominant hypercholesterolemia maps at 16q22.1

The French Research Network on ADH, Marques-Pinheiro, A., Marduel, M., Rabès, J.-P., Devillers, M., Villéger, L., Allard, D., Weissenbach, J., Guerin, M., Zair, Y., et al. (2010) · European Journal of Human Genetics

Lipoproteins and Cardiovascular HealthGenetic Associations and Epidemiology

Cited by 38