Virginie Grybek
Reims, France
Last Updated: 09/26/2026
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Found 11 publications
Genetic and Epigenetic Defects at the GNAS Locus Lead to Distinct Patterns of Skeletal Growth but Similar Early-Onset Obesity.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: January 02, 2018
Clinical and genetic characteristics of xeroderma pigmentosum in Nepal.
Journal: Journal of the European Academy of Dermatology and Venereology : JEADV
Published: July 05, 2017
LRP1 expression in colon cancer predicts clinical outcome.
Journal: Oncotarget
Published: May 11, 2017
The Prevalence of GNAS Deficiency-Related Diseases in a Large Cohort of Patients Characterized by the EuroPHP Network.
Journal: The Journal of clinical endocrinology and metabolism
Published: July 19, 2016
From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network.
Journal: European journal of endocrinology
Published: February 08, 2016
European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA study.
Journal: European journal of human genetics : EJHG
Published: March 13, 2015
Loss of methylation at GNAS exon A/B is associated with increased intrauterine growth.
Journal: The Journal of clinical endocrinology and metabolism
Published: January 21, 2015
Lessons from McCune-Albright syndrome-associated intraductal papillary mucinous neoplasms: : GNAS-activating mutations in pancreatic carcinogenesis.
Journal: JAMA surgery
Published: June 06, 2014
European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA study.
Journal: European journal of human genetics : EJHG
Published: March 10, 2014
Methylation and transcripts expression at the imprinted GNAS locus in human embryonic and induced pluripotent stem cells and their derivatives.
Journal: Stem cell reports
Published: February 21, 2014
Analysis of AP2S1, a calcium-sensing receptor regulator, in familial and sporadic isolated hypoparathyroidism.
Journal: The Journal of clinical endocrinology and metabolism
Published: January 16, 2014
Showing 1-11 of 11
Last Updated: 09/26/2026