(Q29417095)

English

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

16 April 2017

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. (English)

1 reference

Europe PubMed Central

16 April 2017

Parkinson's disease

1 reference

based on heuristic

inferred from title

42

1 reference

Europe PubMed Central

16 April 2017

23

0 references

24

0 references

Cordelia Langford

32

0 references

Leena Peltonen-Palotie

40

0 references

17

0 references

Christopher G. Mathew

35

0 references

Vincent Plagnol

4

0 references

Hannah Blackburn

12

0 references

26

0 references

object named as

Sarah Hunt

30

0 references

object named as

Huw R Morris

50

0 references

object named as

Elvira Bramon

14

0 references

object named as

Matti Pirinen

41

0 references

object named as

Aiden Corvin

21

0 references

Kailash Phatechand Bhatia

object named as

Kailash Bhatia

11

0 references

Richard C Trembath

object named as

Richard C Trembath

47

0 references

Janusz A. Jankowski

object named as

Janusz Jankowski

31

0 references

Nicholas W. Wood

object named as

Nicholas W Wood

52

0 references

Roger A. Barker

object named as

Roger A Barker

9

0 references

Karen E Morrison

object named as

Karen E Morrison

37

0 references

object named as

Carl E Clarke

20

0 references

object named as

Mark I McCarthy

36

0 references

Andrew John Lees

33

object named as

Andrew J Lees

1 reference

Europe PubMed Central

16 April 2017

Wellcome Trust Case Control Consortium 2

2

object named as

Wellcome Trust Case Control Consortium 2

1 reference

Europe PubMed Central

16 April 2017

John Anthony Hardy

28

object named as

John Hardy

1 reference

Europe PubMed Central

16 April 2017

Coro Paisán-Ruíz

7

object named as

Coro Paisan-Ruiz

0 references

51

object named as

Peter Donnelly

1 reference

Europe PubMed Central

16 April 2017

Patrick F. Chinnery

19

object named as

Patrick F Chinnery

1 reference

Europe PubMed Central

16 April 2017

22

object named as

Nicholas Craddock

1 reference

Europe PubMed Central

16 April 2017

29

object named as

Gavin Hudson

1 reference

Europe PubMed Central

16 April 2017

author name string

UK Parkinson's Disease Consortium

1

1 reference

Europe PubMed Central

16 April 2017

Chris C A Spencer

3

1 reference

Europe PubMed Central

16 April 2017

Amy Strange

5

1 reference

Europe PubMed Central

16 April 2017

Michelle Gardner

6

1 reference

Europe PubMed Central

16 April 2017

Gavin Band

8

1 reference

Europe PubMed Central

16 April 2017

Celine Bellenguez

10

1 reference

Europe PubMed Central

16 April 2017

Jennie M Blackwell

13

1 reference

Europe PubMed Central

16 April 2017

Martin A Brown

15

1 reference

Europe PubMed Central

16 April 2017

Matthew A Brown

16

1 reference

Europe PubMed Central

16 April 2017

Juan-Pablo Casas

18

1 reference

Europe PubMed Central

16 April 2017

Jonathan Evans

25

1 reference

Europe PubMed Central

16 April 2017

Emma Gray

27

1 reference

Europe PubMed Central

16 April 2017

Hugh S Markus

34

1 reference

Europe PubMed Central

16 April 2017

Colin N A Palmer

38

1 reference

Europe PubMed Central

16 April 2017

Justin P Pearson

39

1 reference

Europe PubMed Central

16 April 2017

Simon Potter

43

1 reference

Europe PubMed Central

16 April 2017

Anna Rautanen

44

1 reference

Europe PubMed Central

16 April 2017

Stephen J Sawcer

45

1 reference

Europe PubMed Central

16 April 2017

Zhan Su

46

1 reference

Europe PubMed Central

16 April 2017

Ananth C Viswanathan

48

1 reference

Europe PubMed Central

16 April 2017

Nigel W Williams

49

1 reference

Europe PubMed Central

16 April 2017

publication date

2 November 2010

1 reference

Europe PubMed Central

16 April 2017

number of pages

9

0 references

Human Molecular Genetics

1 reference

Europe PubMed Central

16 April 2017

20

1 reference

Europe PubMed Central

16 April 2017

2

1 reference

Europe PubMed Central

16 April 2017

345-353

1 reference

Europe PubMed Central

16 April 2017

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

18 April 2017

The distribution and most recent common ancestor of the 17q21 inversion in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

18 April 2017

Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

18 April 2017

Genome-wide association study reveals genetic risk underlying Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

18 April 2017

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

18 April 2017

Evolutionary toggling of the MAPT 17q21.31 inversion region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

18 April 2017

PLINK: a tool set for whole-genome association and population-based linkage analyses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

18 April 2017

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

18 April 2017

Principal components analysis corrects for stratification in genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

18 April 2017

A common LRRK2 mutation in idiopathic Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

18 April 2017

alpha-Synuclein locus triplication causes Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

18 April 2017

A new multipoint method for genome-wide association studies by imputation of genotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

18 April 2017

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

18 April 2017

A common inversion under selection in Europeans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

18 April 2017

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

18 April 2017

Detecting gene-gene interactions that underlie human diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

3 June 2018

A genotype calling algorithm for the Illumina BeadArray platform

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

3 June 2018

The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

3 June 2018

Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

3 June 2018

Multiple regions of alpha-synuclein are associated with Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

3 June 2018

LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ469

21 January 2018

The structure of the tau haplotype in controls and in progressive supranuclear palsy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ469

21 January 2018

Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ469

21 January 2018

Different MAPT haplotypes are associated with Parkinson's disease and progressive supranuclear palsy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3005904

26 November 2018

The tau H2 haplotype is almost exclusively Caucasian in origin

1 reference

https://pubmed.ncbi.nlm.nih.gov/21044948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of MAPT haplotype-tagging SNPs with sporadic Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21044948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region

1 reference

https://pubmed.ncbi.nlm.nih.gov/21044948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/HMG/DDQ469

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q29417095&oldid=2121031573"