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LGI1 gene

Known as: IB1099, Leucine-Rich, Glioma Inactivated 1 Gene, LEUCINE-RICH GENE, GLIOMA-INACTIVATED, 1 
This gene plays a role in neural cell function and is involved in the suppression of brain cancer.
National Institutes of Health

Related topics

Related topics

5 relations
Congenital EpilepsyInhibition of Cancer Cell GrowthLGI1 protein, humanMalignant Glioma

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LGI1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2016
Highly Cited
2016
Immunoadsorption therapy in autoimmune encephalitides
Objective: It was hypothesized that in encephalitides with autoantibodies directed to CNS surface antigens an antibody-removing… 
Review
2016
Review
2016
Autoimmune Encephalopathies and Dementias
Purpose of Review:This article describes the methods of diagnosis and management of autoimmune encephalopathies and dementias… 
Highly Cited
2008
Highly Cited
2008
Penetrance of LGI1 mutations in autosomal dominant partial epilepsy with auditory features
Background: Assessment of the penetrance of disease-causing mutations is extremely important for developing clinical applications… 
Review
2007
Review
2007
Pelvic tenderness is not limited to the prostate in chronic prostatitis/chronic pelvic pain syndrome (CPPS) type IIIA and IIIB: comparison of men with and without CP/CPPS
BackgroundWe wished to determine if there were differences in pelvic and non-pelvic tenderness between men with chronic… 
Highly Cited
2005
Highly Cited
2005
Abnormal Phonologic Processing in Familial Lateral Temporal Lobe Epilepsy Due to a New LGI1 Mutation
Summary:  Purpose: Autosomal dominant lateral temporal lobe epilepsy (ADLTLE) is a rare familial epilepsy with onset in… 
Highly Cited
2004
Highly Cited
2004
LGI1 mutations in autosomal dominant partial epilepsy with auditory features
Objectives: Mutations in LGI1 cause autosomal dominant partial epilepsy with auditory features (ADPEAF), a form of familial… 
Highly Cited
2004
Highly Cited
2004
LGI1 mutations in temporal lobe epilepsies
Background and Objectives: A number of familial temporal lobe epilepsies (TLE) have been recently recognized. Mutations in LGI1… 
Highly Cited
2004
Highly Cited
2004
A de novo LGI1 mutation in sporadic partial epilepsy with auditory features
Review
2003
Review
2003
Channelopathies as a genetic cause of epilepsy.
Purpose of reviewThis review describes the significant number of new gene associations with epilepsy syndromes that have emerged… 
Review
2002
Review
2002
The novel EPTP repeat defines a superfamily of proteins implicated in epileptic disorders.
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