Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease (Q24531223)

4 July 2017

Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease (English)

1 reference

4 July 2017

1 reference

7

1 reference

Margaret A. Pericak-Vance

4 July 2017

6

object named as

Margaret A Pericak-Vance

0 references

Sofia A. Oliveira

1

object named as

Sofia A Oliveira

1 reference

4 July 2017

Yi-Ju Li

2

0 references

Stephan Züchner

4

object named as

Stephan Zuchner

1 reference

4 July 2017

Maher A Noureddine

3

1 reference

4 July 2017

Xuejun Qin

5

1 reference

4 July 2017

language of work or name

English

0 references

publication date

28 June 2005

1 reference

American Journal of Human Genetics

4 July 2017

1 reference

4 July 2017

77

1 reference

4 July 2017

2

1 reference

4 July 2017

252-264

1 reference

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

4 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

The kappa B transcriptional enhancer motif and signal sequences of V(D)J recombination are targets for the zinc finger protein HIVEP3/KRC: a site selection amplification binding study

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

A mammalian homolog of Drosophila schnurri, KRC, regulates TNF receptor-driven responses and interacts with TRAF2

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Developmental changes of eukaryotic initiation factor 2B subunits in rat hippocampus

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Multipoint quantitative-trait linkage analysis in general pedigrees

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Polymorphisms in glutathione S-transferase omega-1 and AD, vascular dementia, and stroke

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Family-based tests for associating haplotypes with general phenotype data: application to asthma genetics

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Age at onset in two common neurodegenerative diseases is genetically controlled

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

A test for linkage and association in general pedigrees: the pedigree disequilibrium test

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Removing the sampling restrictions from family-based tests of association for a quantitative-trait locus

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

A general test of association for quantitative traits in nuclear families

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Dopamine systems in human immunodeficiency virus-associated dementia.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Sequence variation in the proximity of IDE may impact age at onset of both Parkinson disease and Alzheimer disease.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Implementing a unified approach to family-based tests of association.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Embryonic lethal abnormal visual RNA-binding proteins involved in growth, differentiation, and posttranscriptional gene expression

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Exact tests for association between alleles at arbitrary numbers of loci

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Expression profiling of substantia nigra in Parkinson disease, progressive supranuclear palsy, and frontotemporal dementia with parkinsonism.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Apolipoprotein E controls the risk and age at onset of Parkinson disease

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

A haplotype at the PARK3 locus influences onset age for Parkinson's disease: the GenePD study

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Genotype‐based association test for general pedigrees: The genotype‐PDT

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Glutathione s-transferase omega 1-1 is a target of cytokine release inhibitory drugs and may be responsible for their effect on interleukin-1beta posttranslational processing

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

A susceptibility gene for late-onset idiopathic Parkinson's disease

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Complete genomic screen in Parkinson disease: evidence for multiple genes.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224528

Deletions in the Parkin gene and genetic heterogeneity in a Greek family with early onset Parkinson's disease

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15986317

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

GOLD--graphical overview of linkage disequilibrium

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15986317

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The Unified Parkinson's Disease Rating Scale (UPDRS): status and recommendations

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F432588

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1086/432588

1 reference

OpenCitations bibliographic resource ID

4 July 2017

2392080

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

4 July 2017

1 reference