O. Vérier‐Mine

Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness

Véronique Pingault, Virginie Bodereau, Viviane Baral et al. · The American Journal of Human Genetics · 2013 · 197 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Is pregnancy a risk factor for microvascular complications? The EURODIAB Prospective Complications Study

O. Vérier‐Mine, Nish Chaturvedi, David J. Webb et al. · Diabetic Medicine · 2005 · 124 citations

Public Health, Endocrinology, Maternal Health +12

Is mild gestational hyperglycaemia associated with maternal and neonatal complications? The Diagest Study

A. Vambergue, M C Nuttens, O. Vérier‐Mine et al. · Diabetic Medicine · 2000 · 101 citations

Public Health, Maternal Health, Obstetrics +17

The Prevalence of<i>CHD7</i>Missense Versus Truncating Mutations Is Higher in Patients With Kallmann Syndrome Than in Typical CHARGE Patients

Séverine Marcos, Julie Sarfati, Chrystel Leroy et al. · The Journal of Clinical Endocrinology & Metabolism · 2014 · 86 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Practical implementation, education and interpretation guidelines for continuous glucose monitoring: A French position statement

Sophie Borot, P.‐Y. Benhamou, Catherine Atlan et al. · Diabetes & Metabolism · 2017 · 69 citations

Medicine, Endocrinology, Medical Education +15