Nadège Bondurand - Concepedia

Author

Nadège Bondurand

Inserm ORCID

Also Known As

Asma Chaoui, Bondurand, N, Christiane Zweier, N. Bondurand, Nadege Bondurand, Nadège Bondurand, Nadége Bondurand

Publications

5.2K

Citations

H-Index

Concepts

All Affiliations

Inserm Université Paris-Est Créteil Assistance Publique – Hôpitaux de Paris Université Paris Cité Centre National de la Recherche Scientifique

About

Nadège Bondurand is an author at Inserm specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	23	2.4K
2	Social Sciences	3	3	187
3	Health Sciences	2	2	215
4	Natural Sciences	2	2	178
5	Public Health	1	1	29

Nadège Bondurand

Publications

4.1K

Citations

H-Index

Page 1

	Year	Citations
SOX10 mutations in patients with Waardenburg-Hirschsprung disease Véronique Pingault, Nadège Bondurand, Kirsten Kuhlbrodt, Nature Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsPathogenesis	1998	817
Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome Nadège Bondurand Human Molecular Genetics	2000	455
Mutation of the Sry-related <i>Sox10</i> gene in <i>Dominant megacolon</i> , a mouse model for human Hirschsprung disease Beate Herbarth, Véronique Pingault, Nadège Bondurand, Proceedings of the National Academy of Sciences	1998	356
Deletions at the SOX10 Gene Locus Cause Waardenburg Syndrome Types 2 and 4 Nadège Bondurand, Florence Dastot‐Le Moal, Laure Stanchina, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyMolecular Genetics	2007	256
Neuron and glia generating progenitors of the mammalian enteric nervous system isolated from foetal and postnatal gut cultures Nadège Bondurand, Dipa Natarajan, Nikhil Thapar, Development	2003	214
Human Connexin 32, a gap junction protein altered in the X-linked form of Charcot-Marie-Tooth disease, is directly regulated by the transcription factor SOX10 Nadège Bondurand Human Molecular Genetics	2001	208
Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness Véronique Pingault, Virginie Bodereau, Viviane Baral, The American Journal of Human Genetics	2013	195
Maintenance of mammalian enteric nervous system progenitors by SOX10 and endothelin 3 signalling Nadège Bondurand, Dipa Natarajan, Amanda Barlow, Development Glial BiologyTranscriptional Regulator Sox10Cellular PhysiologyNeuroregenerationEpendyma	2006	166
Functional Analysis of Sox10 Mutations Found in Human Waardenburg-Hirschsprung Patients Kirsten Kuhlbrodt, Claudia Schmidt, Elisabeth Sock, Journal of Biological Chemistry Sox10 StructureGeneticsMolecular BiologyMolecular GeneticsDisease Gene Identification	1998	139
Interactions between Sox10, Edn3 and Ednrb during enteric nervous system and melanocyte development Laure Stanchina, Viviane Baral, Fabienne Robert, Developmental Biology Developmental BiologyCell SignalingNeuroscienceMolecular NeurobiologyNervous System	2006	136

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