Klaus Zerres - Concepedia

Author

Klaus Zerres

Also Known As

C. Altehoefer, Elke Wühl, Florian Lang, K ZERRES, K Zerres, K. ZERRES, K. Zerres, KLAUS ZERRES, Klaus P. Zerres, Klaus Zerres

871

Publications

22.7K

Citations

H-Index

277

Concepts

All Affiliations

RWTH Aachen University University of Bonn Institute of Human Genetics Universitätsklinikum Aachen University of Cologne

About

Klaus Zerres is an author at RWTH Aachen University specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	53	139	11.2K
2	Health Sciences	11	11	471
3	Arts	1	1	19
4	Education	1	1	29
5	Language Studies	1	1	28

Klaus Zerres

255

Publications

19.9K

Citations

H-Index

Page 1

	Year	Citations
Germ-Line Mutations in Nonsyndromic Pheochromocytoma Hartmut P.H. Neumann, Birke Bausch, Sarah R. McWhinney, New England Journal of Medicine	2002	1.4K
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3 Linda M. Brzustowicz, Thomas Lehner, Lucio H. Castilla, Nature Developmental BiologyGenetic DisorderGeneticsMolecular GeneticsMedical Genetics	1990	617
Natural History in Proximal Spinal Muscular Atrophy Klaus Zerres Archives of Neurology	1995	541
PKHD1, the Polycystic Kidney and Hepatic Disease 1 Gene, Encodes a Novel Large Protein Containing Multiple Immunoglobulin-Like Plexin-Transcription–Factor Domains and Parallel Beta-Helix 1 Repeats Luiz F. Onuchic, Laszlo Furu, Yasuyuki Nagasawa, The American Journal of Human Genetics Signaling PathwayAutoimmune DiseaseDisease MechanismKidney ResearchLiver Physiology	2002	506
Quantitative Analysis of Survival Motor Neuron Copies: Identification of Subtle SMN1 Mutations in Patients with Spinal Muscular Atrophy, Genotype-Phenotype Correlation, and Implications for Genetic Counseling Brunhilde Wirth, Micaela A. Godoy Herz, A Wetter, The American Journal of Human Genetics Rare DiseasesGenetic DisorderGeneticsNeuromotor DisordersGenetic Epidemiology	1999	361
Mutations in the gene encoding immunoglobulin μ-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1 Katja Grohmann, Markus Schuelke, Alexander Diers, Nature Genetics Transcriptional RegulationImmunogeneticsAutoimmune DiseaseDisease PathophysiologyMedicine	2001	341
Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD) Carsten Bergmann, Jan Senderek, Ellen Windelen, Kidney International Pkhd1 MutationsUrologyRenal DiseaseMendelian DisorderGenetic Disorder	2005	341
Loss of Nephrocystin-3 Function Can Cause Embryonic Lethality, Meckel-Gruber-like Syndrome, Situs Inversus, and Renal-Hepatic-Pancreatic Dysplasia Carsten Bergmann, Manfred Fliegauf, Nadina Ortiz Brüchle, The American Journal of Human Genetics Meckel-gruber-like SyndromeDevelopmental BiologyRenal-hepatic-pancreatic DysplasiaPathologyMorphogenesis	2008	328
Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals Eric Hahnen, Randolf Forkert, Christine Marke, Human Molecular Genetics	1995	286
A collaborative study on the natural history of childhood and juvenile onset proximal spinal muscular atrophy (type II and III SMA): 569 patients Klaus Zerres, Sabine Rudnik‐Schöneborn, Eric Forrest, Journal of the Neurological Sciences Neuromusculoskeletal DisorderSpinal DisorderNatural HistoryPediatricsCollaborative Study	1997	282

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