Markus Wolff - Concepedia

Author

Markus Wolff

University Children's Hospital Tübingen ORCID

Also Known As

M Wolff, M. C. Wolff, M. WOLFF, M. Wolff, MARK S. WOLFF, Markus Wolff, Max T. Wolff, Saskia Biskup, Stefan Wolking, Steven M. Wolf

134

Publications

7.1K

Citations

H-Index

Concepts

All Affiliations

University Children's Hospital Tübingen University of Tübingen Diakonie Kork Schön Klinik Vogtareuth Hertie Institute for Clinical Brain Research

About

Markus Wolff is an author at University Children's Hospital Tübingen specializing in medicine, neurology, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	20	2.1K
2	Health Sciences	6	6	528
3	Education	1	1	23
4	Engineering	1	1	15
5	Natural Sciences	1	1	493

Markus Wolff

Publications

5.8K

Citations

H-Index

Page 1

	Year	Citations
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders Markus Wolff, Katrine M. Johannesen, Ulrike B. S. Hedrich, Brain	2017	558
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies Bassel Abou‐Khalil, Pauls Auce, Andreja Avberšek, Nature Communications Epilepsy TherapiesGeneticsGenetic EpidemiologyMolecular GeneticsMonogenic Epilepsy Genes	2018	493
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes Johannes R. Lemke, Dennis Lal, Eva M. Reinthaler, Nature Genetics Neurobiology Of DiseaseNeurophysiologyGeneticsRolandic SpikesClinical Neuroscience	2013	436
Targeted next generation sequencing as a diagnostic tool in epileptic disorders Johannes R. Lemke, Erik Riesch, Tim Scheurenbrand, Epilepsia	2012	321
Severe Myoclonic Epilepsy of Infants (Dravet Syndrome): Natural History and Neuropsychological Findings Markus Wolff, Catherine Cassé‐Perrot, Charlotte Dravet Epilepsia	2006	305
The phenotypic spectrum of <i>SCN8A</i> encephalopathy Jan Larsen, Gemma L. Carvill, Elena Gardella, Neurology	2015	282
In utero antiepileptic drug exposure Kimford J. Meador, Gus A. Baker, Richard H. Finnell, Neurology	2006	275
Mutations of DEPDC5 cause autosomal dominant focal epilepsies Saeko Ishida, Fabienne Picard, Gabrielle Rudolf, Nature Genetics MedicineGeneticsNeurogeneticsGenetic Disorder	2013	253
<i>GRIN2B</i> encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects Konrad Platzer, Hongjie Yuan, Hannah M. Schutz, Journal of Medical Genetics	2017	249
The landscape of epilepsy-related GATOR1 variants Sara Baldassari, Fabienne Picard, Nienke E. Verbeek, Genetics in Medicine	2018	236

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