(Q38107504)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23682623%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

title

Update on genetics of essential tremor (English)

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1 March 2020

3

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1 March 2020

Oswaldo Lorenzo Betancor

4

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1 March 2020

Pau Pastor

5

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1 March 2020

José Agundez

6

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1 March 2020

author name string

F J Jiménez-Jiménez

1

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1 March 2020

H Alonso-Navarro

2

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1 March 2020

language of work or name

English

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publication date

18 May 2013

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Acta Neurologica Scandinavica

1 March 2020

published in

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1 March 2020

volume

128

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1 March 2020

issue

6

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1 March 2020

page(s)

359-371

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Etiology of essential tremor: should we be searching for environmental causes?

1 March 2020

cites work

1 reference

Elevation of blood beta-carboline alkaloids in essential tremor

21 January 2018

1 reference

Environmental risk factors for essential tremor

21 January 2018

1 reference

Clinical manifestations of essential tremor

21 January 2018

1 reference

Essential tremor in Papua, New Guinea

21 January 2018

1 reference

Essential tremor in Rochester, Minnesota: a 45-year study

21 January 2018

1 reference

Hereditary neurodegenerative disorders in Nigerian Africans

21 January 2018

1 reference

Essential tremor: clinical correlates in 350 patients

21 January 2018

1 reference

Prevalence of essential tremor: a door-to-door survey in Terrasini, Sicily. Sicilian Neuro-Epidemiologic Study Group.

21 January 2018

1 reference

Prevalence of essential tremor in three elderly populations of central Spain

21 January 2018

1 reference

Essential tremor: phenotypic expression in a clinical cohort

21 January 2018

1 reference

Validity of family history data on essential tremor

21 January 2018

1 reference

Validity of family history in essential tremor

21 January 2018

1 reference

A study of hereditary essential tremor

21 January 2018

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Prevalence of asymptomatic tremor in relatives of patients with essential tremor

21 January 2018

1 reference

OBSERVATIONS ON ESSENTIAL (HEREDOFAMILIAL) TREMOR

21 January 2018

1 reference

How familial is familial tremor? The genetic epidemiology of essential tremor

21 January 2018

1 reference

Familial essential tremor in 4 kindreds. Prospects for genetic mapping

21 January 2018

1 reference

Genetic heterogeneity in autosomal dominant essential tremor

21 January 2018

1 reference

Genetics of essential tremor

21 January 2018

1 reference

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

21 January 2018

1 reference

Increased tremor severity in bilineal essential tremor: a report of two families

21 January 2018

1 reference

Phenocopies in families with essential tremor and restless legs syndrome challenge Mendelian laws. Epigenetics might provide answers

21 January 2018

1 reference

Study of possible factors associated with age of onset in essential tremor

21 January 2018

1 reference

High concordance for essential tremor in monozygotic twins of old age.

21 January 2018

1 reference

Orthostatic tremor in monozygotic twins

21 January 2018

1 reference

Familial orthostatic tremor: an additional report in siblings

21 January 2018

1 reference

Mapping of a familial essential tremor gene, FET1, to chromosome 3q13

21 January 2018

1 reference

A gene (ETM) for essential tremor maps to chromosome 2p22-p25.

21 January 2018

1 reference

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

21 January 2018

1 reference

Further evidence of genetic heterogeneity in familial essential tremor

21 January 2018

1 reference

Linkage exclusion in Italian families with hereditary essential tremor

21 January 2018

1 reference

Linkage with the Ser9Gly DRD3 polymorphism in essential tremor families

21 January 2018

1 reference

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

21 January 2018

1 reference

Dopamine receptor D3 (DRD3) genotype and allelic variants and risk for essential tremor.

21 January 2018

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DRD3 variant and risk of essential tremor

21 January 2018

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Reappraisal of the role of the DRD3 gene in essential tremor

21 January 2018

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DRD3 Ser9Gly variant is not associated with essential tremor in a series of Italian patients.

21 January 2018

1 reference

Case-control study of patients with essential tremor in Latvia

21 January 2018

1 reference

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

21 January 2018

1 reference

Integrated physical map of the human essential tremor gene region (ETM2) on chromosome 2p24.3-p24.2.

21 January 2018

1 reference

Haplotype analysis at the ETM2 locus in a Singaporean sample with familial essential tremor.

21 January 2018

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

21 January 2018

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HS1-BP3 gene variant is common in familial essential tremor

21 January 2018

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

21 January 2018

1 reference

Frequent sequence variation at the ETM2 locus and its association with sporadic essential tremor in Korea

21 January 2018

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

21 January 2018

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

21 January 2018

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LINGO-1 negatively regulates myelination by oligodendrocytes

21 January 2018

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Inhibition of the leucine-rich repeat protein LINGO-1 enhances survival, structure, and function of dopaminergic neurons in Parkinson's disease models

21 January 2018

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Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

21 January 2018

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Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

21 January 2018

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LINGO1 variant increases risk of familial essential tremor

21 January 2018

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LINGO1 rs9652490 is associated with essential tremor and Parkinson disease

21 January 2018

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LINGO1 polymorphisms are associated with essential tremor in Europeans

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Analysis of Lingo1 variant in sporadic and familial essential tremor among Asians

21 January 2018

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Lack of association of LINGO1 rs9652490 and rs11856808 SNPs with familial essential tremor.

21 January 2018

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LINGO1 variants in the French-Canadian population

21 January 2018

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Screening of 10 SNPs of LINGO1 gene in patients with essential tremor in the Latvian population

21 January 2018

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LINGO1 and risk for essential tremor: results of a meta-analysis of rs9652490 and rs11856808.

21 January 2018

1 reference

No gene is an island: the flip-flop phenomenon

21 January 2018

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Lingo2 variants associated with essential tremor and Parkinson's disease

21 January 2018

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Role of excitatory amino acid transporter-2 (EAAT2) and glutamate in neurodegeneration: opportunities for developing novel therapeutics.

21 January 2018

1 reference

A miRNA signature in leukocytes from sporadic amyotrophic lateral sclerosis.

21 January 2018

1 reference

Revisiting the relationship between essential tremor and Parkinson's disease

21 January 2018

1 reference

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

21 January 2018

1 reference

Genetic variants of α-synuclein are not associated with essential tremor

21 January 2018

1 reference

Mutational analysis of parkin gene by denaturing high-performance liquid chromatography (DHPLC) in essential tremor.

21 January 2018

1 reference

The LRRK2 I2012T, G2019S and I2020T mutations are not common in patients with essential tremor

21 January 2018

1 reference

Essential tremor and the common LRRK2 G2385R variant

21 January 2018

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Common mutations in the LRRK2 exon 41 are not responsible for essential tremor in Italian patients

21 January 2018

1 reference

Mutations in the Parkinson's disease genes, Leucine Rich Repeat Kinase 2 (LRRK2) and Glucocerebrosidase (GBA), are not associated with essential tremor

21 January 2018

1 reference

Genetic association study of glucocerebrosidase gene L444P mutation in essential tremor and multiple system atrophy in mainland China

21 January 2018

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

21 January 2018

1 reference

H1-MAPT and the risk for familial essential tremor

21 January 2018

1 reference

The nonsynonymous Thr105Ile polymorphism of the histamine N-methyltransferase is associated to the risk of developing essential tremor

21 January 2018

1 reference

Histamine N-methyltransferase Thr105Ile is not associated with Parkinson's disease or essential tremor

21 January 2018

1 reference

Association of the C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene in patients with essential tremor in Turkey

21 January 2018

1 reference

CYP2C19 polymorphism and risk for essential tremor

21 January 2018

1 reference

Changes at the CYP2C locus and disruption of CYP2C8/9 linkage disequilibrium in patients with essential tremor

21 January 2018

1 reference

Paraoxonase 1 (PON1) polymorphisms and risk for essential tremor

21 January 2018

1 reference

Genetic essential tremor in gamma-aminobutyric acidA receptor alpha1 subunit knockout mice.

21 January 2018

1 reference

Genetic analysis of the GABRA1 gene in patients with essential tremor

21 January 2018

1 reference

Gamma-aminobutyric acid (GABA) receptor rho (GABRR) polymorphisms and risk for essential tremor

21 January 2018

1 reference

Gamma-aminobutyric acid GABRA4, GABRE, and GABRQ receptor polymorphisms and risk for essential tremor

21 January 2018

1 reference

GABA(A) receptor- and GABA transporter polymorphisms and risk for essential tremor

21 January 2018

1 reference

Interaction between blood lead concentration and delta-amino-levulinic acid dehydratase gene polymorphisms increases the odds of essential tremor

21 January 2018

1 reference

Genetic analysis of SCA 2 and 3 repeat expansions in essential tremor and atypical Parkinsonism

21 January 2018

1 reference

The fragile X premutation presenting as essential tremor

21 January 2018

1 reference

Fragile X premutation presenting as essential tremor

21 January 2018

1 reference

Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort

21 January 2018

1 reference

Screen for expanded FMR1 alleles in patients with essential tremor

21 January 2018

1 reference

No evidence of association between CAG expansions and essential tremor in a large cohort of Italian patients

21 January 2018

1 reference

Evaluation of SCN8A as a candidate gene for autosomal dominant essential tremor

21 January 2018

1 reference

Exome sequencing identifies FUS mutations as a cause of essential tremor

21 January 2018

1 reference

Genetic analysis of the FUS/TLS gene in essential tremor

21 January 2018

1 reference

Correlates of functional disability in essential tremor

21 January 2018

1 reference

Familial essential tremor and idiopathic torsion dystonia are different genetic entities

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/ANE.12148

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23682623%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

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