Zohra Rahmani - Concepedia

Author

Zohra Rahmani

Centre National de la Recherche Scientifique

Also Known As

Z Rahmani, Z. Rahmani, Zohra Rahmani

Publications

Citations

H-Index

Concepts

All Affiliations

Centre National de la Recherche Scientifique Hôpital Necker-Enfants Malades Institut Necker Enfants Malades University of Colorado Health Inserm

About

Zohra Rahmani is an author at Centre National de la Recherche Scientifique specializing in medicine, molecular genetics, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	14	8.1K
2	Cell Biology	6	6	233
3	Cellular Physiology	2	2	109
4	Natural Sciences	1	1	15
5	Social Sciences	1	1	23

Zohra Rahmani

Publications

Citations

H-Index

Page 1

	Year	Citations
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis D.R. Rosen, Teepu Siddique, David T. Patterson, Nature Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurological DisorderGeneticsMolecular Biology	1993	7K
Molecular Mapping of Twenty-Four Features of Down Syndrome on Chromosome 21 Jean Maurice Delabar, Didier Theophile, Zohra Rahmani, European Journal of Human Genetics Down SyndromeChromatinDevelopmental BiologyMendelian DisorderMolecular Mapping	1993	444
Hepatitis B Virus X Protein Colocalizes to Mitochondria with a Human Voltage-Dependent Anion Channel, HVDAC3, and Alters Its Transmembrane Potential Zohra Rahmani, Kyung-Won Huh, Robert S. Lasher, Journal of Virology	2000	309
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome. Zohra Rahmani, Jean‐Louis Blouin, N. Créau-Goldberg, Proceedings of the National Academy of Sciences Down SyndromeChromatinD21s55 RegionPartial DuplicationDevelopmental Biology	1989	260
aPKC‐mediated phosphorylation regulates asymmetric membrane localization of the cell fate determinant Numb Christian A. Smith, Kimberly Lau, Zohra Rahmani, The EMBO Journal	2007	228
A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis D.R. Rosen, Allen C. Bowling, David Patterson, Human Molecular Genetics	1994	155
Mapping of the down syndrome phenotype on chromosome 21 at the molecular level Pierre‐Marie Sinet, Didier Theophile, Zohra Rahmani, Biomedicine & Pharmacotherapy Down SyndromeDevelopmental BiologyGenetic DisorderGeneticsMolecular Level	1994	99
DYRK1A Enhances the Mitogen-activated Protein Kinase Cascade in PC12 Cells by Forming a Complex with Ras, B-Raf, and MEK1 Paul A. Kelly, Zohra Rahmani Molecular Biology of the Cell Pc12 CellsSignal TransductionDevelopmental BiologyDown Syndrome PatientsRegulated Kinase 1A	2005	82
Isolation of a novel human voltage-dependent anion channel gene Zohra Rahmani, C Maunoury, Aleem Siddiqui European Journal of Human Genetics ChannelopathiesMolecular PhysiologySignal TransductionHyperpolarization (Biology)Genetics	1998	64
Separating the spindle, checkpoint, and timer functions of BubR1 Zohra Rahmani, Mary E. Gagou, Christophe Lefebvre, The Journal of Cell Biology Developmental BiologyCell DivisionTimer FunctionsTiming AnalysisSpindle Function	2009	57

Page 1