M. C. Hors‐Cayla - Concepedia

Author

M. C. Hors‐Cayla

Also Known As

HORS-CAYLA, M.C., M C Hors-Cayla, M C Hors-cayla, M. C. HORS‐CAYLA, M. C. Hors-Cayla, M. C. Hors‐Cayla, M. Hors-Cayla, M.-C. Hors-Cayla, M.C. Hors-Cayla, Marie-Claude Hors-Cayla

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

Inserm Hôpital des Enfants Hôpital Necker-Enfants Malades Château de Longchamp Centre National de la Recherche Scientifique

About

M. C. Hors‐Cayla is an author at Inserm specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	28	1.3K
2	Natural Sciences	6	6	165
3	Biochemistry	3	3	80
4	Biology	2	2	56
5	Engineering	1	1	26

M. C. Hors‐Cayla

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Mapping of the gene for anti-Müllerian hormone to the short arm of human chromosome 19 Odile Cohen‐Haguenauer, Jean‐Yves Picard, Marie‐Geneviève Mattéi, Cytogenetic and Genome Research Human Chromosome 19CytogeneticsGeneticsMolecular GeneticsReproductive Biology	1987	208
The gene for incontinentia pigmenti is assigned to Xq28 A. Sefiani, Laurent Abel, S. Heuertz, Genomics Genetic DisorderMedicineGeneticsPathologyGene Characterization	1989	115
Alport syndrome and diffuse leiomyomatosis: Deletions in the 5′ end of the COL4A5 collagen gene Corinne Antignac, Jing Zhou, Marek Sanak, Kidney International FibrosisSurgical PathologyDiffuse LeiomyomatosisPathologyGeneral Pathology	1992	98
The Gene for Bazex-Dupré-Christol Syndrome Maps to Chromosome Xq P. Vabres, Didier Lacombe, Linda G. Rabinowitz, Journal of Investigative Dermatology CytogeneticsGenetic DisorderGeneticsMolecular GeneticsChromosomal Rearrangement	1995	92
Deletions in the COL4A5 collagen gene in X-linked Alport syndrome. Characterization of the pathological transcripts in nonrenal cells and correlation with disease expression. Corinne Antignac, Bertrand Knebelmann, Laurent Drouot, Journal of Clinical Investigation GeneticsRenal PathologyGenetic EpidemiologyPathologyAlpha 5	1994	88
The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28 A. Smahl, Christel Hydén‐Granskog, Borut Peterlin, Human Molecular Genetics	1994	72
Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome I. Oberlé, Giovanna Camerino, C. Kloepfer, Human Genetics ChromatinX-linked SequencesDevelopmental BiologySomatic VariantCell Division	1986	70
A New DNA Marker Tightly Linked to the Fragile X Locus ( <i>FRAXA</i> ) G K Suthers, David F. Callen, V.J. Hyland, Science GeneticsGenomic MechanismMolecular BiologyMolecular GeneticsDisease Gene Identification	1989	61
Cattle gene mapping by somatic cell hybridization study of 17 enzyme markers S. Heuertz, M. C. Hors‐Cayla Cytogenetic and Genome Research GeneticsMolecular GeneticsGenomicsBovine Enzyme MarkersAnimal Genetics	1981	51
Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers A. Sefiani, Ridha Mrad, Louise R. Simard, Human Genetics UrologyGeneticsMolecular GeneticsDermatologyMedicine	1991	46

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