Camille Leroy - Concepedia

Author

Camille Leroy

Inserm

Also Known As

C. Leroy, CAMILLE LEROY, Camille Leroy, Gaëlle Jouanjan, James Gibbs, Leroy, Camille

Publications

371

Citations

H-Index

Concepts

All Affiliations

Inserm Centre Hospitalier Universitaire de Reims Université de Reims Champagne-Ardenne Assistance Publique – Hôpitaux de Paris Hôpital Robert-Debré

About

Camille Leroy is an author at Inserm specializing in medicine, health sciences, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	252
2	Health Sciences	2	2	96
3	Endocrinology	1	1	47
4	Molecular Biology	1	1	25
5	Molecular Genetics	1	1	25

Camille Leroy

Publications

351

Citations

H-Index

Page 1

	Year	Citations
The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients Camille Leroy, Emilie Landais, Sylvain Briault, European Journal of Human Genetics Clinical DisordersNew PatientsGenetic DisorderMedicine2Q37-deletion Syndrome	2012	131
Bipolar affective disorder and early dementia onset in a male patient with SHANK3 deletion Ksenija Vucurovic, Emilie Landais, Cécile Delahaigue, European Journal of Medical Genetics Bipolar Affective DisorderHealth SciencesPsychiatryDementiaDepression	2012	49
Early-onset obesity and paternal 2pter deletion encompassing the ACP1, TMEM18, and MYT1L genes Martine Doco‐Fenzy, Camille Leroy, Anouck Schneider, European Journal of Human Genetics ObesityMetabolic SyndromeMyt1l GenesEarly-onset ObesityMetabolic Disorder	2013	47
Fetal phenotype associated with the 22q11 deletion A Noël, Fanny Pelluard, Anne‐Lise Delezoide, American Journal of Medical Genetics Part A	2014	47
De novo deletion of <i>TBL1XR1</i> in a child with non‐specific developmental delay supports its implication in intellectual disability Anne‐Claude Tabet, Camille Leroy, Céline Dupont, American Journal of Medical Genetics Part A	2014	32
Xq25 duplication: the crucial role of the <i><scp>STAG2</scp></i> gene in this novel human cohesinopathy Camille Leroy, Marie‐Line Jacquemont, Bérénice Doray, Clinical Genetics Array CghGeneticsGenetic EpidemiologyGenomic MechanismPathology	2015	25
Foveal Hypoplasia Grading in 95 Cases of Congenital Aniridia: Correlation to Phenotype and PAX6 Genotype Alejandra Daruich, Matthieu P. Robert, Camille Leroy, American Journal of Ophthalmology	2021	20

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