Yvonne Weber - Concepedia

Author

Yvonne Weber

Hertie Institute for Clinical Brain Research ORCID

Also Known As

Andreas van Baalen, Christian M Korff, Felicitas Becker, Ilona Krey, Jason D. Heaney, Julie Vogt, Nick Watts, Ryan G Wagner, Weber, Yvonne, Weber, Yvonne G

286

Publications

13.6K

Citations

H-Index

128

Concepts

All Affiliations

Hertie Institute for Clinical Brain Research University of Tübingen Christian-Albrechts-Universität zu Kiel University of Cologne Universität Ulm

About

Yvonne Weber is an author at Hertie Institute for Clinical Brain Research specializing in medicine, neuroscience, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	29	42	5.5K
2	Social Sciences	19	20	2.5K
3	Public Health	6	6	312
4	Natural Sciences	3	3	800
5	Health Sciences	2	2	381

Yvonne Weber

109

Publications

11.1K

Citations

H-Index

Page 1

	Year	Citations
Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery Ingmar Blümcke, Roberto Spreafico, Gerrit Haaker, New England Journal of Medicine	2017	876
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy Heather C. Mefford, Andrew J. Sharp, Michel Guipponi, Nature Genetics Neurobiology Of DiseasePsychiatric GeneticsNeurologyMicrodeletions Increase RiskNeuropathology	2009	553
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
Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies Carolien G. F. de Kovel, Holger Trucks, Heather C. Mefford, Brain	2009	447
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
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak Yvonne Weber, Alexander Storch, Thomas V. Wuttke, Journal of Clinical Investigation Electrolyte DisorderGlut1 MutationsPathologyPathophysiologyCellular Physiology	2008	354
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1 Arvid Suls, Peter Dedeken, Karolien Goffin, Brain Neurological DisorderGlucose UptakeSocial SciencesGenetic AnalysisParoxysmal Exercise-induced Dyskinesia	2008	340
Targeted next generation sequencing as a diagnostic tool in epileptic disorders Johannes R. Lemke, Erik Riesch, Tim Scheurenbrand, Epilepsia	2012	321
De novo variants in neurodevelopmental disorders with epilepsy Henrike Heyne, Tarjinder Singh, Hannah Stamberger, Nature Genetics Neurodevelopmental DisordersGenetic DisorderNeurologyNeuroscienceAbnormal Development	2018	306
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott, The American Journal of Human Genetics Allelic VariantUltra-rare Genetic VariationWhole-exome Sequencing StudyGeneticsGenetic Disorder	2019	298

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