A family study ofDRD3rs6280, SLC1A2rs3794087 andMAPTrs1052553 variants in essential tremor

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(2018)   MOVEMENT DISORDERS

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(2016)   EUROPEAN JOURNAL OF NEUROLOGY

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(2016)   EUROPEAN JOURNAL OF NEUROLOGY

Missense mutations inTENM4, a regulator of axon guidance and central myelination, cause essential tremor

(2015) Hyun Hor et al.   HUMAN MOLECULAR GENETICS

Genetics of essential tremor: Meta-analysis and review

(2014) G. Kuhlenbaumer et al.   NEUROLOGY

Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease

(2014) Hilal Unal Gulsuner et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Update on genetics of essential tremor

(2013) F. J. Jiménez-Jiménez et al.   ACTA NEUROLOGICA SCANDINAVICA

The microtubule associated protein tau H1 haplotype and risk of essential tremor

(2013) L. N. Clark et al.   EUROPEAN JOURNAL OF NEUROLOGY

Identification of FUS p.R377W in essential tremor

(2013) A. Rajput et al.   EUROPEAN JOURNAL OF NEUROLOGY

Fused in Sarcoma (FUS) gene mutations are not a frequent cause of essential tremor in Europeans

(2013) S. Ortega-Cubero et al.   NEUROBIOLOGY OF AGING

Genetic analysis of the fused in sarcoma gene in Chinese Han patients with essential tremor

(2013) Wen Zheng et al.   NEUROBIOLOGY OF AGING

SLC1A2 variant associated with essential tremor but not Parkinson disease in Chinese subjects

(2013) E.-K. Tan et al.   NEUROLOGY

Identification of a novel risk variant in the FUS gene in essential tremor

(2013) Y.-R. Wu et al.   NEUROLOGY

FUS in familial essential tremor – The search for common causes is still on

(2013) Peter Hedera et al.   PARKINSONISM & RELATED DISORDERS

Investigating the role of FUS exonic variants in Essential Tremor

(2013) Catherine Labbé et al.   PARKINSONISM & RELATED DISORDERS

No association of the SLC1A2 rs3794087 allele with risk for essential tremor in the Spanish population

(2013) Elena García-Martín et al.   Pharmacogenetics and Genomics

Research Highlights: Highlights from the latest articles in essential tremor biomarkers and pharmacogenomics

(2013) José AG Agúndez et al.   PHARMACOGENOMICS

SLC1A2 Variant Is Associated with Essential Tremor in Taiwanese Population

(2013) Shao-wen Yu et al.   PLoS One

Dopamine receptor D3 (DRD3) gene rs6280 variant and risk for restless legs syndrome

(2013) Félix Javier Jiménez-Jiménez et al.   SLEEP MEDICINE

Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor

(2012) Nancy D. Merner et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor

(2012) S. Thier et al.   NEUROLOGY

H1-MAPT and the Risk for Familial Essential Tremor

(2012) Elena García-Martín et al.   PLoS One

Revisiting the relationship between essential tremor and Parkinson's disease

(2011) R. Fekete et al.   MOVEMENT DISORDERS

Association between Essential Tremor and Other Neurodegenerative Diseases: What Is the Epidemiological Evidence?

(2011) Hiral LaRoia et al.   NEUROEPIDEMIOLOGY

MAPT H1 haplotype is a risk factor for essential tremor and multiple system atrophy

(2011) C. Vilarino-Guell et al.   NEUROLOGY

Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patients

(2008) Delia Lorenz et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Reappraisal of the role of the DRD3 gene in essential tremor

(2008) Marcia A. Blair et al.   PARKINSONISM & RELATED DISORDERS