Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease (Q34591257)

3 August 2017

Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease (English)

1 reference

3 August 2017

13

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Enza Maria Valente

33

Christine Van Broeckhoven

Enza Maria Valente

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52

Christine Van Broeckhoven

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Ilse Gijselinck

5

Ilse Gijselinck

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Kristel Sleegers

3

Kristel Sleegers

1 reference

3 August 2017

Sebastiaan Engelborghs

48

Sebastiaan Engelborghs

1 reference

3 August 2017

Gaëtan Garraux

42

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George D. Mellick

George D Mellick

24

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Aldo Quattrone

Aldo Quattrone

36

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Suzanne Lesage

12

Suzanne Lesage

1 reference

3 August 2017

Aline Verstraeten

2

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Ekaterina Rogaeva

19

Ekaterina Rogaeva

1 reference

3 August 2017

18

Zbigniew K Wszolek

1 reference

3 August 2017

28

Nobutaka Hattori

1 reference

3 August 2017

22

Christine Klein

1 reference

3 August 2017

21

Anthony E Lang

1 reference

3 August 2017

17

Owen A Ross

1 reference

3 August 2017

30

Eng-King Tan

1 reference

3 August 2017

25

Peter A Silburn

1 reference

3 August 2017

11

Rejko Krüger

1 reference

3 August 2017

35

Grazia Annesi

1 reference

3 August 2017

38

Laura Brighina

1 reference

3 August 2017

Georgios M Hadjigeorgiou

26

Georgios M Hadjigeorgiou

1 reference

3 August 2017

27

Efthimios Dardiotis

1 reference

3 August 2017

46

Grzegorz Opala

1 reference

3 August 2017

49

Peter Paul De Deyn

1 reference

3 August 2017

51

Marc Cruts

1 reference

3 August 2017

50

Patrick Cras

1 reference

3 August 2017

8

Ellen Corsmit

1 reference

3 August 2017

4

Eline Wauters

1 reference

3 August 2017

Demetrius M. Maraganore

47

Demetrius M Maraganore

1 reference

3 August 2017

29

Kotaro Ogaki

1 reference

3 August 2017

40

Andreas Puschmann

1 reference

Magdalena Boczarska-Jedynak

3 August 2017

45

Magdalena Boczarska-Jedynak

1 reference

3 August 2017

37

Carlo Ferrarese

1 reference

3 August 2017

Jessie Theuns

1

1 reference

3 August 2017

Stefanie Smolders

6

1 reference

3 August 2017

David Crosiers

7

1 reference

3 August 2017

Ellen Elinck

9

1 reference

3 August 2017

Manu Sharma

10

1 reference

3 August 2017

Sun Ju Chung

14

1 reference

3 August 2017

Mi-Jung Kim

15

1 reference

3 August 2017

Young Jin Kim

16

1 reference

3 August 2017

Zhengrui Xi

20

1 reference

3 August 2017

Anne Weissbach

23

1 reference

3 August 2017

Yi Zhao

31

1 reference

3 August 2017

Jan Aasly

32

1 reference

3 August 2017

Simona Petrucci

34

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3 August 2017

Angela Deutschländer

39

1 reference

3 August 2017

Christer Nilsson

41

1 reference

3 August 2017

Mark S LeDoux

43

1 reference

3 August 2017

Ronald F Pfeiffer

44

1 reference

3 August 2017

GEO-PD Consortium

53

1 reference

3 August 2017

language of work or name

English

0 references

publication date

17 October 2014

1 reference

3 August 2017

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3 August 2017

83

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3 August 2017

1906-1913

1 reference

3 August 2017

21

1 reference

Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease

3 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

C9ORF72 expansions, parkinsonism, and Parkinson disease: a clinicopathologic study.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Current insights into the C9orf72 repeat expansion diseases of the FTLD/ALS spectrum

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

C9orf72 repeat expansions are a rare genetic cause of parkinsonism

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Parkinson disease is not associated with C9ORF72 repeat expansions

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Analysis of the C9orf72 repeat in Parkinson's disease, essential tremor and restless legs syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Screening for C9orf72 repeat expansions in parkinsonian syndromes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Frontotemporal dementia in a Brazilian kindred with the c9orf72 mutation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Investigation of c9orf72 in 4 neurodegenerative disorders

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Large C9orf72 repeat expansions are not a common cause of Parkinson's disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Characterization of a family with c9FTD/ALS associated with the GGGGCC repeat expansion in C9ORF72.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Improved accuracy of clinical diagnosis of Lewy body Parkinson's disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Incidence and distribution of parkinsonism in Olmsted County, Minnesota, 1976-1990.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Diagnostic criteria for Parkinson disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Parkinsonism: onset, progression, and mortality

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Meta-analysis in clinical trials

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Investigation of C9orf72 repeat expansions in Parkinson's disease

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

No GGGGCC-hexanucleotide repeat expansion in C9ORF72 in parkinsonism patients in Sweden

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4248456

Research diagnostic criteria for Parkinson's disease

9 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25326098

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1212/WNL.0000000000001012

1 reference

3 August 2017

1 reference

3 August 2017

1 reference