Varret, Mathilde

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

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TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome

National Heart, L., Boileau, C., Guo, D.-C., Hanna, N., Regalado, E. S., Detaint, D., Gong, L., Varret, M., Prakash, S. K., Li, A. H., et al. (2012) · Nature Genetics

Connective tissue disorders researchAortic Disease and Treatment Approaches

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APOE gene variants in primary dyslipidemia

Khalil, Y. A., Rabès, J.-P., Boileau, C., & Varret, M. (2021) · Atherosclerosis

Lipoproteins and Cardiovascular HealthLipid metabolism and disorders

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Description of a Large Family with Autosomal Dominant Hypercholesterolemia Associated with the APOE p.Leu167del Mutation

Marduel, M., Ouguerram, K., Serre, V., Bonnefont-Rousselot, D., Marques-Pinheiro, A., Erik Berge, K., Devillers, M., Luc, G., Lecerf, J.-M., Tosolini, L., et al. (2013) · Human Mutation

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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

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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

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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

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APOE Molecular Spectrum in a French Cohort with Primary Dyslipidemia

Abou Khalil, Y., Marmontel, O., Ferrières, J., Paillard, F., Yelnik, C., Carreau, V., Charrière, S., Bruckert, E., Gallo, A., Giral, P., et al. (2022) · International Journal of Molecular Sciences

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Additive Effect of APOE Rare Variants on the Phenotype of Familial Hypercholesterolemia

Marmontel, O., Abou-Khalil, Y., Bluteau, O., Cariou, B., Carreau, V., Charrière, S., Divry, E., Gallo, A., Moulin, P., Paillard, F., et al. (2023) · Arteriosclerosis, Thrombosis, and Vascular Biology

Lipoproteins and Cardiovascular HealthLipid metabolism and disorders

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