In Vitro Fertilization May Increase the Risk of Beckwith-Wiedemann Syndrome Related to the Abnormal Imprinting of the KCNQ1OT Gene

Christine Gicquel, Véronique Gaston, Jacqueline Mandelbaum, +3

The American Journal of Human Genetics

InfertilityDevelopmental BiologyFertilityGenetic DisorderGenetics +8

Molecular markers and long-term recurrences in a large cohort of patients with sporadic adrenocortical tumors.

Christine Gicquel, Xavier Bertagna, Véronique Gaston, +10

PubMed

Cancer PathologyMolecular MarkersPathologyTumor BiologySporadic Adrenocortical Tumors +15

Structural and Functional Abnormalities at 11p15 Are Associated with the Malignant Phenotype in Sporadic Adrenocortical Tumors: Study on a Series of 82 Tumors¹

Christine Gicquel, Marie‐Laure Raffin‐Sanson, Véronique Gaston, +6

The Journal of Clinical Endocrinology & Metabolism

Paternal AlleleGeneticsPathologyTumor BiologySporadic Adrenocortical Tumors +17

Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome

Éric Bieth, Sanaa Eddiry, Véronique Gaston, +10

European Journal of Human Genetics

Mendelian DisorderGenetic DisorderGeneticsPathogenesisPathology +8

Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith–Wiedemann syndrome

Véronique Gaston, Yves Le Bouc, V. Soupre, +6

European Journal of Human Genetics

H19 GenesEpigenetic RegulationMedicineGeneticsGenetic Disorder +8

Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens

Olivier Patat, A. Pagin, Aurore Siegfried, +12

The American Journal of Human Genetics

Signal TransductionDevelopmental BiologyG Protein-coupled ReceptorGenetic DisorderGenetics +4

Autocrine role of IGF-II in proliferation of human adrenocortical carcinoma NCI H295R cell line

Armelle Logié, Nathalie Boulle, Véronique Gaston, +4

Journal of Molecular Endocrinology

Autocrine RoleGrowth HormoneCancer GrowthPathologyFibroblast Growth Factor +8

<i>CFTR</i>-France, a national relational patient database for sharing genetic and phenotypic data associated with rare<i>CFTR</i>variants

Mireille Claustres, C. Thèze, Marie des Georges, +22

Human Mutation

GeneticsDatabasesGenetic EpidemiologyPathologyDisease Gene Identification +20

A Case Report in Favor of a Multistep Adrenocortical Tumorigenesis

Marie‐Hélène Bernard, Stan B. Sidhu, Nicole Berger, +6

The Journal of Clinical Endocrinology & Metabolism

Neuro-oncologyAdrenal GlandHealth SciencesTumor HeterogeneityAdrenal Health +11

Mutations in <i>WNT10A</i> are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia

Julie Plaisancié, Isabelle Bailleul‐Forestier, Véronique Gaston, +19

American Journal of Medical Genetics Part A

Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderMedicine +11