Genetic analysis of theFUS/TLSgene in essential tremor

Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor

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

Linking LINGO1 to essential tremor

(2010) Eng-King Tan   EUROPEAN JOURNAL OF HUMAN GENETICS

Replication of the LINGO1 gene association with essential tremor in a North American population

(2010) Lorraine N Clark et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

How common is the most common adult movement disorder? Update on the worldwide prevalence of essential tremor

(2010) Elan D. Louis et al.   MOVEMENT DISORDERS

LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease

(2010) Carles Vilariño-Güell et al.   NEUROGENETICS

Genetic contribution of FUS to frontotemporal lobar degeneration

(2010) T. Van Langenhove et al.   NEUROLOGY

Screening for two SNPs of LINGO1 gene in patients with essential tremor or sporadic Parkinson's disease in Chinese population

(2010) Xing Zuo et al.   NEUROSCIENCE LETTERS

Recent advances in the genetics of amyotrophic lateral sclerosis

(2009) Paul N. Valdmanis et al.   Current Neurology and Neuroscience Reports

Role of LINGO1 polymorphisms in Parkinson's disease

(2009) Dietrich Haubenberger et al.   MOVEMENT DISORDERS

Variant in the sequence of the LINGO1 gene confers risk of essential tremor

(2009) Hreinn Stefansson et al.   NATURE GENETICS

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

(2009) Prateek Kumar et al.   Nature Protocols

Prevalence of Essential Tremor in a Multiethnic, Community-Based Study in Northern Manhattan, New York, N.Y.

(2009) Elan D. Louis et al.   NEUROEPIDEMIOLOGY

LINGO1 VARIANT INCREASES RISK OF FAMILIAL ESSENTIAL TREMOR

(2009) E. -K. Tan et al.   NEUROLOGY

Essential tremor is associated with dementia: Prospective population-based study in New York

(2009) S. P. Thawani et al.   NEUROLOGY

Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6

(2009) C. Vance et al.   SCIENCE

Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

(2009) T. J. Kwiatkowski et al.   SCIENCE