Steffen Syrbe - Concepedia

Author

Steffen Syrbe

Also Known As

EuroEPINOMICS RES, Fatme Seval Ismail, Jolanda H Schieving, Justina Dargvainiene, KCNA3 study group, Klarissa Hanja Stürner, Kurt-Wolfram Sühs, S Syrbe, S. Syrbe, Steffen Syrbe

198

Publications

5.2K

Citations

H-Index

115

Concepts

All Affiliations

Heidelberg University University Hospital Heidelberg University Hospital Leipzig Leipzig University Diakonie Kork

About

Steffen Syrbe is an author at Heidelberg University specializing in medicine, neurology, and pediatrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	23	1.1K
2	Social Sciences	8	8	610
3	Education	5	5	172
4	Public Health	2	2	61
5	Health Sciences	1	1	29

Steffen Syrbe

Publications

3.3K

Citations

H-Index

Page 1

	Year	Citations
Delineating the <i>GRIN1</i> phenotypic spectrum Johannes R. Lemke, Kirsten Geider, Katherine L. Helbig, Neurology	2016	202
Benign infantile seizures and paroxysmal dyskinesia caused by an <i>SCN8A</i> mutation Elena Gardella, Felicitas Becker, Rikke S. Møller, Annals of Neurology	2015	187
Clinical spectrum and genotype–phenotype associations of KCNA2-related encephalopathies Silvia Masnada, Ulrike B. S. Hedrich, Elena Gardella, Brain	2017	158
Children with multiphasic disseminated encephalomyelitis and antibodies to the myelin oligodendrocyte glycoprotein (MOG): Extending the spectrum of MOG antibody positive diseases Matthias Baumann, Eva-Maria Hennes, Kathrin Schanda, Multiple Sclerosis Journal	2016	157
The gain of function <i>SCN1A</i> disorder spectrum: novel epilepsy phenotypes and therapeutic implications Andreas Brunklaus, Tobias Brünger, Tony Feng, Brain Neurological DisorderScn1a Variants ClusterTherapeutic ImplicationsSynaptic SignalingEpilepsy	2022	137
Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age – a multicenter retrospective study Afshin Saffari, Ines Brösse, Adelheid Wiemer‐Kruel, Orphanet Journal of Rare Diseases	2019	124
Assessing the landscape of <i>STXBP1</i>-related disorders in 534 individuals Julie Xian, Shridhar Parthasarathy, Sarah M. Ruggiero, Brain	2021	111
Neurodevelopmental Disorders Caused by De Novo Variants in <i>KCNB1 </i>Genotypes and Phenotypes Carolien G. F. de Kovel, Steffen Syrbe, Eva H. Brilstra, JAMA Neurology	2017	103
Germline AGO2 mutations impair RNA interference and human neurological development Davor Lessel, Daniela M. Zeitler, Margot R.F. Reijnders, Nature Communications	2020	97
Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy Steffen Syrbe, Frederike L. Harms, Elena Parrini, Brain NeurogenomicsBrain DevelopmentNeurological DisorderGeneticsNeurochemical Biomarkers	2017	96

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