Intake of flavonoids and risk of dementia

Daniel Commenges, Virginie Scotet, S. Renaud, +3

European Journal of Epidemiology

Association of rare chymotrypsinogen C (CTRC) gene variations in patients with idiopathic chronic pancreatitis

Emmanuelle Masson, Jian‐Min Chen, Virginie Scotet, +2

Human Genetics

Pancreatic Fluid CollectionImmunologyGastroenterologyPathologyIdiopathic Chronic Pancreatitis +4

HAMP as a modifier gene that increases the phenotypic expression of the HFE pC282Y homozygous genotype

Sandrine Jacolot, Gérald Le Gac, Virginie Scotet, +3

Blood

Determination of the relative contribution of three genes–the cystic fibrosis transmembrane conductance regulator gene, the cationic trypsinogen gene, and the pancreatic secretory trypsin inhibitor gene–to the etiology of idiopathic chronic pancreatitis

Marie‐Pierre Audrézet, Jian‐Min Chen, Cédric Le Maréchal, +6

European Journal of Human Genetics

Molecular PhysiologyDisease MechanismImmunologyGastroenterologyPathology +6

Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis

Virginie Scotet, Marc De Braekeleer, Michel Roussey, +15

The Lancet

Early DiagnosisNeonatal ScreeningNewborn ScreeningNeonatologyDiagnosis +6

Hereditary Hemochromatosis: Effect of Excessive Alcohol Consumption on Disease Expression in Patients Homozygous for the C282Y Mutation

Virginie Scotet

American Journal of Epidemiology

Hereditary HemochromatosisMetabolic DisorderIron MetabolismGeneticsGenetic Epidemiology +23

Early onset hereditary hemochromatosis resulting from a novel <i>TFR2</i> gene nonsense mutation (R105X) in two siblings of north French descent

Gérald Le Gac, F. Mons, Sandrine Jacolot, +3

British Journal of Haematology

Evidence of association between GDF5 polymorphisms and congenital dislocation of the hip in a Caucasian population

Karen Rouault, Virginie Scotet, Sandrine Autret, +6

Osteoarthritis and Cartilage

GeneticsGenetic EpidemiologyHuman PolymorphismCongenital DislocationMedical Genetics +4

Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis

Aurore Carré, Mireille Castanet, Sylvia Sura‐Trueba, +8

Human Genetics

Developmental BiologyFoxe1 Alanine StretchGenetic DisorderGeneticsGenetic Susceptibility +6

Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis

Marie de Tayrac, Marie‐Paule Roth, Anne‐Marie Jouanolle, +12

Journal of Hepatology

Heme HomeostasisIron MetabolismGeneticsGenetic EpidemiologyPathology +9