Christian Kubisch - Concepedia

Author

Christian Kubisch

Also Known As

Alexander E. Volk, C Kubisch, C. Kubisch, C., Kubisch, Capra, Valeria, Christian Kubisch, Hisama, Fuki M., Junko Oshima, Kubisch Christian, Kubisch, C.

325

Publications

22.1K

Citations

H-Index

187

Concepts

All Affiliations

Universität Hamburg University Medical Center Hamburg-Eppendorf Universität Ulm University of Cologne University of Bonn

About

Christian Kubisch is an author at Universität Hamburg specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	45	82	10.7K
2	Arts	6	6	383
3	Health Sciences	6	6	486
4	Natural Sciences	5	5	269
5	Engineering	4	4	221

Christian Kubisch

172

Publications

17.6K

Citations

H-Index

Page 1

	Year	Citations
Analysis of shared heritability in common disorders of the brain Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Science Brain FunctionPsychiatric DisordersGeneticsGenetic EpidemiologyNeuropsychiatry	2018	2K
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase Alfredo Ramı́rez, André Heimbach, Jan Gründemann, Nature Genetics Alzheimer's DiseaseP-type AtpaseHereditary ParkinsonismParkinson DiseaseGenetics	2006	1.2K
A Potassium Channel Mutation in Neonatal Human Epilepsy Christian Biervert, Björn C. Schroeder, Christian Kubisch, Science	1998	1.1K
KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness Christian Kubisch, Björn C. Schroeder, Thomas Friedrich, Cell	1999	862
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene Alfons Meindl, Heide Hellebrand, Constanze Wiek, Nature Genetics Breast OncologySomatic VariantCancer PathologyOvarian Cancer PedigreesGenetics	2010	727
Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy Björn C. Schroeder, Christian Kubisch, Valentin Stein, Nature Hyperpolarization (Biology)NeurophysiologyPhysiologyIon ChannelsModerate Loss	1998	524
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D Hanno J. Bolz, Benigna von Brederlow, Alfredo Ramı́rez, Nature Genetics Genetic DisorderGeneticsPathogenesisPathologyNew Member	2001	493
Genome-wide association study reveals three susceptibility loci for common migraine in the general population Daniel I. Chasman, Markus Schürks, Verneri Anttila, Nature Genetics Genome-wide Association StudyCluster HeadacheGenotype-phenotype AssociationGeneticsGenetic Epidemiology	2011	420
KCNQ5, a Novel Potassium Channel Broadly Expressed in Brain, Mediates M-type Currents Björn C. Schroeder, Mirko Hechenberger, Frank Weinreich, Journal of Biological Chemistry	2000	390
Genome-wide association analysis identifies susceptibility loci for migraine without aura Tobias Freilinger, Verneri Anttila, Boukje de Vries, Nature Genetics Genome-wide Association StudyCluster HeadacheNeurogenomicsGeneticsGenetic Epidemiology	2012	339

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