Researchclopedia

Research Researchers Institutions Topics Submit About

Command Palette

Search for a command to run...

Researchclopedia

Research Researchers Institutions About

© 2026 Researchclopedia. Powered by OpenAlex under CC0 license.

Elisabeth Stögmann | Researchclopedia

Back to researchers

Elisabeth Stögmann

Medical University of Vienna ORCID

122

Works

18,342

Citations

30

h-index

54

i10-index

Research Topics

Dementia and Cognitive Impairment Research Alzheimer's disease research and treatments Genetic Associations and Epidemiology

Affiliations

University of Dundee2023–2023

Vienna General Hospital2002–2008

Klinik Hietzing2009–2009

Institute of Human Genetics2006–2006

Schizophrenia Society of Ontario2022–2022

Top Works

Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A

Dalia Kasperavičiūtė,Claudia B. Catarino,et al.

2013196 citations

Genomics and Rare Diseases

Epilepsy research and treatment

Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy

Fritz Zimprich,Raute Sunder‐Plaßmann,et al.

2004168 citations

A functional polymorphism in the prodynorphin gene promotor is associated with temporal lobe epilepsy

Elisabeth Stögmann,Alexander Zimprich,et al.

2002109 citations

Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2

Elisabeth Stögmann,Eva M. Reinthaler,et al.

201384 citations

Clinical Seizure Lateralization in Frontal Lobe Epilepsy

Silvia Bonelli,Stefanie Lurger,et al.

200777 citations

Idiopathic generalized epilepsy phenotypes associated with different <i>EFHC1</i> mutations

Elisabeth Stögmann,Peter Lichtner,et al.

200670 citations

Activities of Daily Living and Depressive Symptoms in Patients with Subjective Cognitive Decline, Mild Cognitive Impairment, and Alzheimer’s Disease

Elisabeth Stögmann,Doris Moser,et al.

201570 citations

[Sex differences in Alzheimer's disease].

Reinhold Schmidt,Eva Kienbacher,et al.

200869 citations

A novel mutation in the VCP gene (G157R) in a german family with inclusion‐body myopathy with paget disease of bone and frontotemporal dementia

Atbin Djamshidian,Jochen Schaefer,et al.

200962 citations