Anne Claude Tabet - Concepedia

Author

Anne Claude Tabet

Hôpital Robert-Debré

Also Known As

A Tabet, A. C. Tabet, A. Tabet, A.C. Tabet, Ann Swillen, Anne C. Tabet, Anne Claude Tabet, Tabet A, Tabet, Anne Claude

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

Hôpital Robert-Debré Inserm Assistance Publique – Hôpitaux de Paris Centre Hospitalier Intercommunal de Poissy Université Paris Cité

About

Anne Claude Tabet is an author at Hôpital Robert-Debré specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	175
2	Molecular Genetics	3	3	106
3	Neurology	3	3	65
4	Public Health	2	2	53
5	Social Sciences	1	1	30

Anne Claude Tabet

Publications

593

Citations

H-Index

Page 1

	Year	Citations
Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies Francesca Romana Grati, D. Molina Gomes, José Carlos Ferreira, Prenatal Diagnosis	2015	303
16p13.11 microduplication in 45 new patients: refined clinical significance and genotype–phenotype correlations Laïla El Khattabi, Solveig Heide, Jean‐Hubert Caberg, Journal of Medical Genetics	2018	93
Chromosome 22q13.3 deletion syndrome with a de novo interstitial 22q13.3 cryptic deletion disrupting SHANK3 Annick Toutain, A. Aboura, Céline Dupont, European Journal of Medical Genetics Gene Deletion DataCryptic DeletionGenetic DisorderGeneticsPathology	2009	57
Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder Xénia Latypova, Marie Vincent, Alice Mollé, The American Journal of Human Genetics Neurodevelopmental DisordersSyndromic AutismPsychiatric GeneticsAutismNeurology	2021	30
Cytogenetic analysis of trophoblasts by comparative genomic hybridization in embryo‐fetal development anomalies Anne Claude Tabet, A. Aboura, M C Dauge, Prenatal Diagnosis FertilityCytogeneticsGeneticsComparative Genomic HybridizationGenomics	2001	27
Molecular characterization of 39 <i>de novo</i><scp>sSMC</scp>: contribution to prognosis and genetic counselling, a prospective study Nathalie Marle, Danielle Martinet, Azzedine Aboura, Clinical Genetics CytogeneticsGeneticsGenetic EpidemiologyPathologyMolecular Genetics	2013	26
Prenatal phenotype of Williams–Beuren syndrome and of the reciprocal duplication syndrome Livia Marcato, Licia Turolla, Eva Pompilii, Clinical Case Reports Neurological DisorderGeneticsWilliams-beuren SyndromeMolecular GeneticsCopy Losses/gains	2014	23
Application of a new molecular technique for the genetic evaluation of products of conception Francesca Romana Grati, D. Molina Gomes, Devika Ganesamoorthy, Prenatal Diagnosis	2012	22
Further delineation of BCAP31-linked intellectual disability: description of 17 new families with LoF and missense variants Sandra Whalen, Marie Shaw, Cyril Mignot, European Journal of Human Genetics Down SyndromeIntellectual ImpairmentNew FamiliesGenetic DisorderDisability	2021	12

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