B Wittwer - Concepedia

Author

B Wittwer

Also Known As

B Wittwer, B. Bernhard Wittwer, B. Wittwer, Bärbel Wittwer

Publications

883

Citations

H-Index

Concepts

All Affiliations

B Wittwer is an author at University of Münster specializing in genetics, medicine, and gene expression.

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	782
2	Molecular Genetics	2	2	548
3	Natural Sciences	1	1	479
4	Molecular Biology	1	1	479
5	Pathology	1	1	234

B Wittwer

Publications

865

Citations

H-Index

Page 1

	Year	Citations
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3) A Meindl, Katherine L. Dry, Karin A. Herrmann, Nature Genetics Exchange FactorRcc1 GuanineNatural SciencesGeneticsGenomic Mechanism	1996	479
Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III H.‐J. Lüdecke, Jörg Schaper, Peter Meinecke, The American Journal of Human Genetics Genetic DisorderGeneticsGenetic EpidemiologyPathologyPhenotypic Spectrum	2001	234
Opitz G/BBB Syndrome in Xp22: Mutations in the MID1 Gene Cluster in the Carboxy-Terminal Domain Karin Gaudenz, Erich Roessler, Nandita Quaderi, The American Journal of Human Genetics Developmental AnomalyOpitz G/bbb SyndromeDevelopmental BiologyMendelian DisorderGenetic Disorder	1998	69
A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa Alfons Meindl, Maria Raquel Santos Carvalho, Klaus M. Herrmann, Human Molecular Genetics	1995	57
Clinical presentation and mutation identification in the NBS1 gene in a boy with Nijmegen breakage syndrome Saskia Kleier, Martin Herrmann, B Wittwer, Clinical Genetics	2000	14
New X-linked mental retardation syndrome with the gene mapped tentatively in Xp22.3 B Wittwer, Renate Kircheisen, Jutta Leutelt, American Journal of Medical Genetics	1996	12

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