(Q31132884)

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Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor (English)

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

amyotrophic lateral sclerosis

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author name string

Özgün Uyan

1

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Özgür Ömür

2

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Zeynep Sena Ağım

3

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Aslıhan Özoğuz

4

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Hong Li

5

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Yeşim Parman

6

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Feza Deymeer

7

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Piraye Oflazer

8

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Filiz Koç

9

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Ersin Tan

10

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Hilmi Özçelik

11

1 reference

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18 August 2017

A Nazlı Başak

12

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18 August 2017

language of work or name

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publication date

26 August 2013

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Europe PubMed Central

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18 August 2017

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Europe PubMed Central

PMC publication ID

18 August 2017

8

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18 August 2017

8

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

e72381

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

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Creative Commons Attribution 4.0 International

26 August 2013

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April 2022 Public Data File from Crossref

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0 references

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1 reference

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28 July 2018

EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans

1 reference

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28 July 2018

ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population

1 reference

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Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis

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Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

1 reference

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High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

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28 July 2018

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis

1 reference

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28 July 2018

Analysis of genome-wide copy number variation in Irish and Dutch ALS populations

1 reference

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28 July 2018

Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen

1 reference

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28 July 2018

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

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28 July 2018

ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study

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Molecular biology of amyotrophic lateral sclerosis: insights from genetics

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28 July 2018

Detection of large-scale variation in the human genome

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28 July 2018

The human genome browser at UCSC

1 reference

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28 July 2018

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

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28 July 2018

The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci

1 reference

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21 January 2018

A large genome scan for rare CNVs in amyotrophic lateral sclerosis

1 reference

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21 January 2018

Genomic copy number variations in three Southeast Asian populations

1 reference

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Integrating common and rare genetic variation in diverse human populations

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Origins and functional impact of copy number variation in the human genome

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A genome-wide association study of sporadic ALS in a homogenous Irish population.

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Interstitial deletion 11(p11.12p11.2) and analphoid marker formation results in inherited Potocki-Shaffer syndrome.

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Identifiers

10.1371/JOURNAL.PONE.0072381

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

2013PLoSO...872381U

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

ResearchGate publication ID

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