Parkinson disease loci in the mid-western Amish (Q28943294)

5

object named as

D. R. Velez Edwards

1 reference

14 March 2017

M. F. Davis

1

1 reference

14 March 2017

A. C. Cummings

2

1 reference

14 March 2017

L. N. D'Aoust

3

1 reference

14 March 2017

L. Jiang

4

1 reference

14 March 2017

R. Laux

6

1 reference

14 March 2017

L. Reinhart-Mercer

7

1 reference

14 March 2017

D. Fuzzell

8

1 reference

14 March 2017

W. K. Scott

9

1 reference

14 March 2017

M. A. Pericak-Vance

10

1 reference

14 March 2017

S. L. Lee

11

1 reference

14 March 2017

J. L. Haines

https://scigraph.springernature.com/pub.10.1007/s00439-013-1316-1

12

1 reference

14 March 2017

1 November 2013

1 reference

14 March 2017

1 reference

14 March 2017

132

1 reference

14 March 2017

1213–1221

1 reference

14 March 2017

11

1 reference

14 March 2017

0 references

cites work

Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Genetics of Parkinson's disease

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

A two-stage meta-analysis identifies several new loci for Parkinson's disease

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Smoking, caffeine, and nonsteroidal anti-inflammatory drugs in families with Parkinson disease

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

High-resolution whole-genome association study of Parkinson disease.

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Genetics meets environment: evaluating gene-environment interactions in neurologic diseases

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

A genome-wide linkage screen in the Amish with Parkinson disease points to chromosome 6

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Loss-of-function mutations in RAB18 cause Warburg micro syndrome.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

A genome-wide scan in an Amish pedigree with parkinsonism

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Pesticide exposure and risk of Parkinson's disease: a family-based case-control study

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Case-control association testing with related individuals: a more powerful quasi-likelihood score test

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Meta analysis of whole-genome linkage scans with data uncertainty: an application to Parkinson's disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Occupational and environmental risk factors for Parkinson's disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Anabaptist genealogy database

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Incidence of Parkinson's disease: variation by age, gender, and race/ethnicity

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Age at onset in two common neurodegenerative diseases is genetically controlled

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Diagnostic criteria for Parkinson disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3797866

Evaluating power and type 1 error in large pedigree analyses of binary traits

3 June 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1316-1

Validation of a short Orientation-Memory-Concentration Test of cognitive impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1316-1

Clinical and genetic evaluation of 8 Polish families with levodopa-responsive parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1316-1

An approach for cutting large and complex pedigrees for linkage analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1316-1

An evaluation of the performance of HapMap SNP data in a Shanghai Chinese population: analyses of allele frequency, linkage disequilibrium pattern and tagging SNPs transferability on chromosome 1q21-q25

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1316-1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1316-1

A genome wide linkage disequilibrium screen in Parkinson’s disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1316-1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1316-1

Chromosome 5 and Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1316-1

Case-control study of the ?-synuclein interacting protein gene and Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1316-1

Parkinsonism: onset, progression, and mortality. 1967

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23793441

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

HaploPainter: a tool for drawing pedigrees with complex haplotypes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23793441

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic association study of synphilin-1 in idiopathic Parkinson's disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23793441