(Q48256432)

10 February 2018

title

EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohorts (English)

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10 February 2018

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9

Thomas Gasser

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10 February 2018

8

Daniela Berg

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10 February 2018

ORCID Public Data File 2021

Christine Klein

7

Christine Klein

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10 February 2018

1

Huttenlocher J

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10 February 2018

Rejko Krüger

2

Krüger R

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10 February 2018

P. Capetian

3

Capetian P

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10 February 2018

Kathrin Brockmann

5

Brockmann K

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10 February 2018

Ilona Csoti

6

Csoti I

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10 February 2018

Michael Bonin

10

Bonin M

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10 February 2018

Olaf Riess

11

Riess O

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10 February 2018

Peter Bauer

12

Bauer P

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10 February 2018

Katja Lohmann

4

Lohmann K

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10 February 2018

language of work or name

English

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publication date

3 November 2014

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10 February 2018

Journal of Medical Genetics

published in

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10 February 2018

volume

52

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10 February 2018

issue

1

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10 February 2018

page(s)

37-41

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10 February 2018

Genetic characteristics of leucine-rich repeat kinase 2 (LRRK2) associated Parkinson's disease

cites work

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Diagnostic criteria for Parkinson disease

21 January 2018

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Milestones in PD genetics

21 January 2018

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Translation initiator EIF4G1 mutations in familial Parkinson disease

21 January 2018

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Study of the genetic variability in a Parkinson's Disease gene: EIF4G1

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease

21 January 2018

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Designing the national resident assessment instrument for nursing homes.

21 January 2018

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Protection of privacy by third-party encryption in genetic research in Iceland

21 January 2018

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Detection of sharing by descent, long-range phasing and haplotype imputation

21 January 2018

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

A novel endonuclease IV post-PCR genotyping system

21 January 2018

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A rare variant in MYH6 is associated with high risk of sick sinus syndrome

21 January 2018

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Identification of low-frequency variants associated with gout and serum uric acid levels

21 January 2018

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SIFT: Predicting amino acid changes that affect protein function

21 January 2018

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A method and server for predicting damaging missense mutations

21 January 2018

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Analysis of EIF4G1 in ethnic Chinese

21 January 2018

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EIF4G1 Ala502Val and Arg1205His variants in Chinese patients with Parkinson disease.

21 January 2018

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Sequence variants in eukaryotic translation initiation factor 4-gamma (eIF4G1) are associated with Lewy body dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

eIF4GI links nutrient sensing by mTOR to cell proliferation and inhibition of autophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Translation initiation factor eIF4G-1 binds to eIF3 through the eIF3e subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Oxidative stress in Parkinson's disease: a mechanism of pathogenic and therapeutic significance

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

VPS35 Asp620Asn and EIF4G1 Arg1205His mutations are rare in Parkinson disease from southwest China

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

The importance of rare DNA variation in neurologic disease: cautionary tale

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Role of mendelian genes in "sporadic" Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

Familial Aggregation of Parkinson's Disease in Iceland

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2014-102570

10.1136/JMEDGENET-2014-102570

21 January 2018

Identifiers

DOI

1 reference

10 February 2018

release_syelm56gcbbw7hd36xvljn7hty

Fatcat ID

0 references

1 reference

10 February 2018