Varaico: Literature-Extracted Genetic Variants

Gene:HS1BP3
Variant:p.S89G
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HS1BP3

NM_022460.4:p.S89G

Associated Papers

Genetic Risk Factors for Essential Tremor: A Review.

Siokas V et al.

Tremor and Other Hyperkinetic Movements (new York, N.y.), 2020

[Essential tremor: genetic update].

Deng H et al.

Expert Reviews in Molecular Medicine, 2019

Whole-exome sequencing for variant discovery in blepharospasm.

Tian J et al.

Molecular Genetics & Genomic Medicine, 2018

Linkage of familial essential tremor to chromosome 5q35.

Hicks JE et al.

Movement Disorders : Official Journal of the Movement Disorder Society, 2016

Genetic analysis of the leucine-rich repeat and lg domain containing Nogo receptor-interacting protein 1 gene in essential tremor.

Liang H et al.

Journal of Molecular Neuroscience : Mn, 2013

Genetics of essential tremor.

Jasinska-Myga B et al.

Parkinsonism & Related Disorders, 2012

Heritable essential tremor-idiopathic normal pressure hydrocephalus (ETINPH).

Zhang J et al.

American Journal of Medical Genetics. Part A, 2008

Genetics of essential tremor.

Deng H et al.

Brain : a Journal of Neurology, 2007

A family with Parkinson disease, essential tremor, bell palsy, and parkin mutations.

Deng H et al.

Archives of Neurology, 2007

Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23.

Shatunov A et al.

Brain : a Journal of Neurology, 2006

Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?

Ma S et al.

Movement Disorders : Official Journal of the Movement Disorder Society, 2006

A functional variant of the dopamine D3 receptor is associated with risk and age-at-onset of essential tremor.

Jeanneteau F et al.

Proceedings of the National Academy of Sciences of the United States of America, 2006

HS1-BP3 gene variant is common in familial essential tremor.

Higgins JJ et al.

Movement Disorders : Official Journal of the Movement Disorder Society, 2006

Extended study of A265G variant of HS1BP3 in essential tremor and Parkinson disease.

Deng H et al.

Neurology, 2005

A variant in the HS1-BP3 gene is associated with familial essential tremor.

Higgins JJ et al.

Neurology, 2005

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."