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Markus Wolff | Researchclopedia

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Markus Wolff

Swiss Epilepsy Center ORCID

132

Works

7,223

Citations

38

h-index

66

i10-index

Research Topics

Epilepsy research and treatment Genetics and Neurodevelopmental Disorders Genomics and Rare Diseases

Affiliations

Université Claude Bernard Lyon 11987–1987

Boston Children's Hospital2007–2007

University of Potsdam2008–2010

University of Southern Denmark2015–2015

School of the Art Institute of Chicago2016–2016

Top Works

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

Markus Wolff,Katrine M. Johannesen,et al.

2017567 citations

Pharmacological Effects and Toxicity Studies

Neuroscience and Neuropharmacology Research

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

Johannes R. Lemke,Dennis Lal,et al.

2013437 citations

Targeted next generation sequencing as a diagnostic tool in epileptic disorders

Johannes R. Lemke,Erik Riesch,et al.

2012322 citations

<i>STXBP1</i> encephalopathy

Hannah Stamberger,Marina Nikanorova,et al.

2016310 citations

Severe Myoclonic Epilepsy of Infants (Dravet Syndrome): Natural History and Neuropsychological Findings

Markus Wolff,Catherine Cassé‐Perrot,et al.

2006305 citations

The phenotypic spectrum of <i>SCN8A</i> encephalopathy

Jan Larsen,Gemma L. Carvill,et al.

2015283 citations

In utero antiepileptic drug exposure

Kimford J. Meador,Gus A. Baker,et al.

2006276 citations

De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

EuroEPINOMICS RES,Steffen Syrbe,et al.

2015270 citations

Mutations of DEPDC5 cause autosomal dominant focal epilepsies

Saeko Ishida,Fabienne Picard,et al.

2013255 citations