Cédric Le Caignec - Concepedia

Author

Cédric Le Caignec

Also Known As

C Le Caignec, C. Le Caignec, C.L. Caignec, Caignec, Cedric Le, Caignec, Cédric Le, Callewaert, Bert, Cdric Le Caignec, Cedric Le Caignec, Cedric Le caignec, Cedric Le Caignec

190

Publications

10.4K

Citations

H-Index

169

Concepts

All Affiliations

Inserm Génétique Médicale & Génomique Fonctionelle Centre Hospitalier Universitaire de Nantes Institut du Thorax Centre National de la Recherche Scientifique

About

Cédric Le Caignec is an author at Inserm specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	38	59	6.3K
2	Natural Sciences	5	5	331
3	Arts	2	2	245
4	Health Sciences	2	2	72
5	Engineering	1	1	138

Cédric Le Caignec

103

Publications

9.4K

Citations

H-Index

Page 1

	Year	Citations
Chromosome instability is common in human cleavage-stage embryos Evelyne Vanneste, Thierry Voet, Cédric Le Caignec, Nature Medicine ChromatinChromosome InstabilityChromosome DynamicsDevelopmental BiologyCytogenetics	2009	888
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2 Robin Walters, Sébastien Jacquemont, Armand Valsesia, Nature ObesityMetabolic SyndromeChildhood ObesityDevelopmental BiologyMetabolic Disorder	2010	554
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Nature Gene DosageGeneticsHuman PolymorphismMolecular GeneticsChromosome 16P11.2	2011	474
SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome Vincent Probst, Arthur A.M. Wilde, Julien Barc, Circulation Cardiovascular Genetics	2009	315
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities Debra D’Angelo, Sébastien Lebon, Qixuan Chen, JAMA Psychiatry	2015	290
Whole-genome multiple displacement amplification from single cells Claudia Spits, Cédric Le Caignec, Martine De Rycke, Nature Protocols Single Cell SequencingMedicineSingle CellsSingle-cell GenomicsTranscriptomics Technology	2006	284
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families Virpi Leppä, Stephanie N. Kravitz, Joris Andrieux, The American Journal of Human Genetics Rare InheritedGenetic DisorderGeneticsMolecular GeneticsAsd Risk	2016	228
Mutations in MAP3K1 Cause 46,XY Disorders of Sex Development and Implicate a Common Signal Transduction Pathway in Human Testis Determination Alexander Pearlman, Johnny Loke, Cédric Le Caignec, The American Journal of Human Genetics SpermatogenesisHuman Testis DeterminationDevelopmental BiologySex DeterminationGenetic Disorder	2010	220
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants Lucilla Pizzo, Matthew Jensen, Andrew Polyak, Genetics in Medicine	2018	218
Single-cell chromosomal imbalances detection by array CGH Cédric Le Caignec, Claudia Spits, Karen Sermon, Nucleic Acids Research Array CghGenetic TestingCytogeneticsGeneticsPathology	2006	204

Page 1