Françoise Gary

Publications by Year

Research Areas

Gestational Diabetes Research and Management, Cardiovascular Effects of Exercise, Diabetes Management and Research, Pregnancy and preeclampsia studies, Genetic and phenotypic traits in livestock

Most-Cited Works

• → Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy(1999)1,339 cited
• → A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome(1997)881 cited
• → A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy(2011)347 cited
• → Organization and Sequence of Human Cardiac Myosin Binding Protein C Gene (MYBPC3) and Identification of Mutations Predicted to Produce Truncated Proteins in Familial Hypertrophic Cardiomyopathy(1997)302 cited
• → A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy(2013)172 cited
• → Mutation in the Human Acetylcholinesterase-Associated Collagen Gene, COLQ, Is Responsible for Congenital Myasthenic Syndrome with End-Plate Acetylcholinesterase Deficiency (Type Ic)(1998)160 cited
• → Mineralocorticoid receptor mutations are the principal cause of renal type 1 pseudohypoaldosteronism(2006)88 cited
• Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy.(1999)
• → Poor Reliability and Poor Adherence to Self-Monitoring of Blood Glucose Are Common in Women With Gestational Diabetes Mellitus and May Be Associated With Poor Pregnancy Outcomes(2017)77 cited
• → Double heterozygosity for mutations in the β-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy(1999)68 cited