Martin Häusler - Concepedia

Author

Martin Häusler

Also Known As

Garen Haryanyan, Gerhard Kluger, Häusler, M., Häusler, Martin, Häusler, Martin Georg, Ingo Helbig, M HAUSLER, M HÄUSLER, M Häusler, M. G. Häusler

195

Publications

Citations

H-Index

182

Concepts

All Affiliations

RWTH Aachen University Universitätsklinikum Aachen Innsbruck Medical University Ludwig-Maximilians-Universität München University Medical Center Freiburg

About

Martin Häusler is an author at RWTH Aachen University specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	43	2.4K
2	Social Sciences	8	8	293
3	Health Sciences	3	3	75
4	Public Health	3	3	158
5	Engineering	1	1	10

Martin Häusler

Publications

4.5K

Citations

H-Index

Page 1

	Year	Citations
Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in <i>KCNJ10</i> Ute I. Scholl, Murim Choi, Tiewen Liu, Proceedings of the National Academy of Sciences Clinical DisordersMendelian DisorderGenetic DisorderGeneticsPathogenesis	2009	484
Clinical and neuroradiological differences of paediatric acute disseminating encephalomyelitis with and without antibodies to the myelin oligodendrocyte glycoprotein Matthias Baumann, Kamil Şahin, Christian Lechner, Journal of Neurology Neurosurgery & Psychiatry	2014	310
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
Febrile infection–related epilepsy syndrome (FIRES): A nonencephalitic encephalopathy in childhood Andreas van Baalen, Martin Häusler, Rainer Boor, Epilepsia	2010	229
Rituximab Treatment and Long-term Outcome of Patients With Autoimmune Encephalitis Franziska Thaler, Luise Zimmermann, Stefan Kammermeier, Neurology Neuroimmunology & Neuroinflammation	2021	158
Molecular characterization of folate receptor 1 mutations delineates cerebral folate transport deficiency Marcel Grapp, Isabell Anna Just, Tarja Linnankivi, Brain Brain DevelopmentGeneticsDisease Gene IdentificationSocial SciencesClinical Genetics	2012	126
Neurological complications of acute and persistent Epstein‐Barr virus infection in paediatric patients Martin Häusler, Vincent T. Ramaekers, Martin Doenges, Journal of Medical Virology	2002	119
Antibodies to MOG and AQP4 in children with neuromyelitis optica and limited forms of the disease Christian Lechner, Matthias Baumann, Eva-Maria Hennes, Journal of Neurology Neurosurgery & Psychiatry	2015	117
Clinical, serological and genetic predictors of response to immunotherapy in anti-IgLON5 disease Thomas Grüter, Franziska E. Möllers, Anja Tietz, Brain ImmunohematologySystemic DiseasesImmunodeficienciesImmunologyGenetic Epidemiology	2022	103
Reduced folate transport to the CNS in female Rett patients V. Ramaekers, Steen Ingemann Hansen, Jan Holm, Neurology	2003	95

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