Identification of genetic modifiers of age-at-onset for familial Parkinson's disease (Q30833988)

21 August 2017

Identification of genetic modifiers of age-at-onset for familial Parkinson's disease (English)

1 reference

21 August 2017

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11

Beate Ritz

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21 August 2017

8

Zbigniew K Wszolek

1 reference

21 August 2017

2

Owen A Ross

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21 August 2017

14

Stewart A Factor

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21 August 2017

9

Peter A Silburn

1 reference

21 August 2017

George D Mellick

10

1 reference

ORCID Public Data File 2021

Joanna Siuda

6

object named as

Joanna Siuda

1 reference

21 August 2017

13

Cyrus P Zabetian

1 reference

21 August 2017

7

Timothy Lynch

1 reference

21 August 2017

Erin M Hill-Burns

1

1 reference

21 August 2017

William T Wissemann

3

1 reference

21 August 2017

Alexandra I Soto-Ortolaza

4

1 reference

21 August 2017

Sepideh Zareparsi

5

1 reference

21 August 2017

Clemens R Scherzer

12

1 reference

21 August 2017

Patrick J Breheny

15

1 reference

21 August 2017

Haydeh Payami

16

1 reference

21 August 2017

11 July 2016

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21 August 2017

Human Molecular Genetics

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21 August 2017

25

1 reference

21 August 2017

17

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21 August 2017

3849-3862

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Strategies for Imputing and Analyzing Rare Variants in Association Studies

21 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Genetic risk and age in Parkinson's disease: Continuum not stratum

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Genetic variability in the regulation of gene expression in ten regions of the human brain

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Identification of a novel Parkinson's disease locus via stratified genome-wide association study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Predicting the risk of rheumatoid arthritis and its age of onset through modelling genetic risk variants with smoking

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Unrecognized vitamin D3 deficiency is common in Parkinson disease: Harvard Biomarker Study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

A genetic basis for the variable effect of smoking/nicotine on Parkinson's disease.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Genome-wide association study of the age of onset of childhood asthma

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Analysis of high accuracy, quantitative proteomics data in the MaxQB database

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Combinatorial patterning of chromatin regulators uncovered by genome-wide location analysis in human cells

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

VPS35 mutations in Parkinson disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

LocusZoom: regional visualization of genome-wide association scan results

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

ProbABEL package for genome-wide association analysis of imputed data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

The heritability of risk and age at onset of Parkinson's disease after accounting for known genetic risk factors

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Pathological roles of MAPK signaling pathways in human diseases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Parkinson's disease and cancer risk: a systematic review and meta-analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Somatic mutations of the Parkinson's disease-associated gene PARK2 in glioblastoma and other human malignancies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

SCAN: SNP and copy number annotation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Dopamine transporter genetic variants and pesticides in Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Visualizing disease associations: graphic analysis of frequency distributions as a function of age using moving average plots (MAP) with application to Alzheimer's and Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Parkinson's disease and residential exposure to maneb and paraquat from agricultural applications in the central valley of California

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Complex segregation analysis of Parkinson's disease: The Mayo Clinic Family Study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Haploview: analysis and visualization of LD and haplotype maps

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Molecular cloning and expression regulation of PRG-3, a new member of the plasticity-related gene family

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

alpha-Synuclein locus triplication causes Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Parkin, a gene implicated in autosomal recessive juvenile parkinsonism, is a candidate tumor suppressor gene on chromosome 6q25-q27

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Segregation analysis of Parkinson disease revealing evidence for a major causative gene.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Prediction of the coding sequences of unidentified human genes. VI. The coding sequences of 80 new genes (KIAA0201-KIAA0280) deduced by analysis of cDNA clones from cell line KG-1 and brain

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Anatomy and physiology of glutamate in the CNS.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216611

Segregation analysis of Parkinson disease.

21 June 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW206

Impact of Parkinson's disease risk loci on age at onset

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW206

Apolipoprotein E genotype and Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW206

Shrinkage methods enhanced the accuracy of parameter estimation using Cox models with small number of events

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW206

Loss of expression of tropomyosin-1, a novel class II tumor suppressor that induces anoikis, in primary breast tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW206

Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW206

Combined effects of smoking, coffee, and NSAIDs on Parkinson's disease risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW206

Exploring gene-environment interactions in Parkinson’s disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW206

Heterozygousparkinpoint mutations are as common in control subjects as in Parkinson's patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW206

Cumulative genetic risk and age at onset in Parkinson's disease

21 January 2018

1 reference

12 December 2020

Increased risk of Parkinson's disease in parents and siblings of patients

1 reference

12 December 2020

Avoiding infinite estimates of time-dependent effects in small-sample survival studies

1 reference

12 December 2020

SnapShot: Genetics of Parkinson's disease

1 reference

12 December 2020

Identifiers

DOI

10.1093/HMG/DDW206

1 reference

21 August 2017

1 reference

21 August 2017

PubMed publication ID

27402877

1 reference