Michel Vekemans - Concepedia

Author

Michel Vekemans

Also Known As

F Is4, Gary Shaw, J Siffroi, John Rogers, M J Vekemans, M Vekemans, M. J. J. Vekemans, M. VEKEMANS, M. Vekemans, Marilyn Silva

405

Publications

17.1K

Citations

H-Index

176

Concepts

All Affiliations

Hôpital Necker-Enfants Malades Inserm Université Paris Cité Assistance Publique – Hôpitaux de Paris Délégation Paris 5

About

Michel Vekemans is an author at Hôpital Necker-Enfants Malades specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	51	95	10.7K
2	Public Health	14	16	564
3	Social Sciences	4	4	666
4	Natural Sciences	3	3	520
5	Health Sciences	2	2	121

Michel Vekemans

165

Publications

14.5K

Citations

H-Index

Page 1

	Year	Citations
Isolation by Size of Epithelial Tumor Cells Giovanna Vona, Abdelmajid Sabile, Malek Louha, American Journal Of Pathology Epithelial Tumor CellsBiological MicroenvironmentsMedicineCell BiologyCancer Research	2000	1.1K
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome Jeanne Amiel, Béatrice Laudier, Tania Attié‐Bitach, Nature Genetics Genetic DisorderGeneticsInherited Metabolic DiseaseHypoxia (Medicine)Pediatrics	2003	850
splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3 Douglas J. Epstein, Michel Vekemans, Philippe Gros Cell Paired HomeodomainKnockout MouseDevelopmental BiologySomatic VariantMouse Neural Tube	1991	660
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome Marion Delous, Lekbir Baala, Rémi Salomon, Nature Genetics Cerebello-oculo-renal SyndromeCiliary Gene Rpgrip1lDevelopmental BiologyGenetic DisorderMeckel Syndrome	2007	489
Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence Sabina Benko, Judy Fantes, Jeanne Amiel, Nature Genetics Sequence MotifComparative GenomicsGeneticsMedicineSequence Analysis	2009	433
SHOX mutations in dyschondrosteosis (Leri-Weill syndrome) Valérie Belin, Véronica Cusin, Géraldine Viot, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsHistopathologyPathology	1998	356
Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans Loïc de Pontual, Evelyn Yao, Patrick Callier, Nature Genetics Developmental BiologyGrowth DefectsHuman GrowthMedicineGenetics	2011	306
Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes Enza Maria Valente, Clare V. Logan, Soumaya Mougou-Zerelli, Nature Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsMolecular Genetics	2010	281
Pleiotropic Effects of CEP290 (NPHP6) Mutations Extend to Meckel Syndrome Lekbir Baala, Sophie Audollent, Jelena Martinović, The American Journal of Human Genetics Mendelian DisorderDisease MechanismGenetic DisorderMeckel SyndromeGenetics	2007	280
Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain Marc Abitbol, Christian Ménini, Anne‐Lise Delezoide, Nature Genetics Developmental BiologyBrain StructureDevelopmental Cognitive NeuroscienceNeuroanatomyMedicine	1993	275

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