User profiles for F. Zimprich

Fritz Zimprich

Medical University of Vienna
Verified email at meduniwien.ac.at
Cited by 22943

The clinical impact of pharmacogenetics on the treatment of epilepsy

W Löscher, U Klotz, F Zimprich, D Schmidt - Epilepsia, 2009 - Wiley Online Library
Drug treatment of epilepsy is characterized by unpredictability of efficacy, adverse drug
reactions, and optimal doses in individual patients, which, at least in part, is a consequence of …

[HTML][HTML] Clinical features, pathogenesis, and treatment of myasthenia gravis: a supplement to the Guidelines of the German Neurological Society

…, B Schalke, C Schneider-Gold, F Zimprich… - Journal of …, 2016 - Springer
Myasthenia gravis (MG) is an autoimmune antibody-mediated disorder of neuromuscular
synaptic transmission. The clinical hallmark of MG consists of fluctuating fatigability and …

Biological insights from 108 schizophrenia-associated genetic loci

…, BK Wormley, H Simon Xi, CC Zai, X Zheng, F Zimprich… - Nature, 2014 - nature.com
Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of
alleles, including common alleles of small effect that might be detected by genome-wide …

[PDF][PDF] A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease

…, R Kralovics, A Peters, F Zimprich… - The American Journal of …, 2011 - cell.com
To identify rare causal variants in late-onset Parkinson disease (PD), we investigated an
Austrian family with 16 affected individuals by exome sequencing. We found a missense …

15q13. 3 microdeletions increase risk of idiopathic generalized epilepsy

…, PS Reif, F Rosenow, Y Weber, H Lerche, F Zimprich… - Nature …, 2009 - nature.com
We identified 15q13.3 microdeletions encompassing the CHRNA7 gene in 12 of 1,223
individuals with idiopathic generalized epilepsy (IGE), which were not detected in 3,699 controls (…

Recurrent microdeletions at 15q11. 2 and 16p13. 11 predispose to idiopathic generalized epilepsies

…, MEM Swinkels, YG Weber, I Unterberger, F Zimprich… - Brain, 2010 - academic.oup.com
Idiopathic generalized epilepsies account for 30% of all epilepsies. Despite a predominant
genetic aetiology, the genetic factors predisposing to idiopathic generalized epilepsies …

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

…, U Stephani, I Helbig, H Lerche, F Zimprich… - Nature …, 2013 - nature.com
Idiopathic focal epilepsy (IFE) with rolandic spikes is the most common childhood epilepsy,
comprising a phenotypic spectrum from rolandic epilepsy (also benign epilepsy with …

The demyelinating potential of antibodies to myelin oligodendrocyte glycoprotein is related to their ability to fix complement.

SJ Piddlesden, H Lassmann, F Zimprich… - The American journal …, 1993 - ncbi.nlm.nih.gov
A panel of 13 monoclonal antibodies (mAbs) has been raised to the central nervous system-specific
glycoprotein, myelin oligodendrocyte glycoprotein; five of these mAbs recognize a …

[HTML][HTML] Genetic structure of Europeans: a view from the North–East

M Nelis, T Esko, R Mägi, F Zimprich, A Zimprich… - PloS one, 2009 - journals.plos.org
… Pair-wise F st values between samples were calculated using EIGENSOFT. F st values …
In our study, F st was found to correlate considerably with geographic distances (r 2 = 0.382, …

Complement genes contribute sex-biased vulnerability in diverse disorders

…, JQ Wu, HS Xi, CC Zai, X Zheng, F Zimprich… - Nature, 2020 - nature.com
Many common illnesses, for reasons that have not been identified, differentially affect men
and women. For instance, the autoimmune diseases systemic lupus erythematosus (SLE) and …