Chrystel Leroy
Paris, 75014, France
Last Updated: 09/26/2026
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Found 10 publications
Geographic information in the French national health data system: Key challenges for territorial health studies.
Journal: Journal of epidemiology and population health
Published: January 05, 2026
Evaluation of a saliva molecular point of care for the detection of SARS-CoV-2 in ambulatory care.
Journal: Scientific reports
Published: July 13, 2021
Accuracy of saliva and nasopharyngeal sampling for detection of SARS-CoV-2 in community screening: a multicentric cohort study.
Journal: European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology
Published: May 31, 2021
Phenotypic Variability in a Family with Acrodysostosis Type 2 Caused by a Novel PDE4D Mutation Affecting the Serine Target of Protein Kinase-A Phosphorylation.
Journal: Journal of clinical research in pediatric endocrinology
Published: May 19, 2017
The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.
Journal: The Journal of clinical endocrinology and metabolism
Published: August 01, 2014
Neurofibromatosis type 1 molecular diagnosis: what can NGS do for you when you have a large gene with loss of function mutations?
Journal: European journal of human genetics : EJHG
Published: February 21, 2014
Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients.
Journal: European journal of endocrinology
Published: September 14, 2013
Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness.
Journal: American journal of human genetics
Published: November 30, 2012
Custom oligonucleotide array-based CGH: a reliable diagnostic tool for detection of exonic copy-number changes in multiple targeted genes.
Journal: European journal of human genetics : EJHG
Published: August 06, 2012
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.
Journal: PLoS genetics
Published: March 08, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026