(Q33375794)

26 July 2017

title

Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson disease (English)

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26 July 2017

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whole genome sequencing

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Balaji S Srinivasan

1

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26 July 2017

Jaleh Doostzadeh

2

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26 July 2017

Farnaz Absalan

3

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26 July 2017

Sharareh Mohandessi

4

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26 July 2017

Roxana Jalili

5

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26 July 2017

Saharnaz Bigdeli

6

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26 July 2017

Justin Wang

7

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26 July 2017

Jaydev Mahadevan

8

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26 July 2017

Caroline L G Lee

9

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26 July 2017

Ronald W Davis

10

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26 July 2017

J William Langston

11

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26 July 2017

Mostafa Ronaghi

12

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26 July 2017

publication date

1 February 2009

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26 July 2017

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26 July 2017

volume

30

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26 July 2017

issue

2

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26 July 2017

page(s)

228-238

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Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays

26 July 2017

cites work

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21 June 2018

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Molecular inversion probe assay

21 June 2018

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Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies

21 June 2018

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Genome partitioning of genetic variation for height from 11,214 sibling pairs

21 June 2018

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Parkinson disease, 10 years after its genetic revolution: multiple clues to a complex disorder

21 June 2018

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21 June 2018

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A genomic pathway approach to a complex disease: axon guidance and Parkinson disease

21 June 2018

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Common genetic variants account for differences in gene expression among ethnic groups

21 June 2018

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21 June 2018

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Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study

21 June 2018

1 reference

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Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

21 June 2018

1 reference

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The roles of intracellular protein-degradation pathways in neurodegeneration

21 June 2018

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A gene-centric approach to genome-wide association studies

21 June 2018

1 reference

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Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease

21 June 2018

1 reference

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Considerations for genomewide association studies in Parkinson disease

21 June 2018

1 reference

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Methodological improvements of pyrosequencing technology

21 June 2018

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

21 June 2018

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Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles

21 June 2018

1 reference

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ROCR: visualizing classifier performance in R

21 June 2018

1 reference

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Haploview: analysis and visualization of LD and haplotype maps

21 June 2018

1 reference

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Limitations of the odds ratio in gauging the performance of a diagnostic, prognostic, or screening marker

21 June 2018

1 reference

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Mutant genes responsible for Parkinson's disease

21 June 2018

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A Bayesian Networks Approach for Predicting Protein-Protein Interactions from Genomic Data

21 June 2018

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Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene 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=2793088

Multiplexed genotyping with sequence-tagged molecular inversion probes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2793088

Association of homozygous 7048G7049 variant in the intron six of Nurr1 gene 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=2793088

A sequencing method based on real-time pyrophosphate

21 June 2018

1 reference

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A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2793088

No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2793088

Microarray reality checks in the context of a complex disease

31 October 2018

1 reference

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A common NURR1 polymorphism associated with Parkinson disease and diffuse Lewy body disease.

31 October 2018

1 reference

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Variations in the monoamine oxidase B (MAOB) gene are associated with Parkinson's disease.

31 October 2018

1 reference

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Hardy–Weinberg equilibrium in genetic association studies: an empirical evaluation of reporting, deviations and power

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2793088

31 October 2018

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12 December 2020

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12 December 2020

A probabilistic functional network of yeast genes

1 reference

PubMed

12 December 2020

Detection of genotyping errors and pseudo-SNPs via deviations from Hardy-Weinberg equilibrium

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PubMed

12 December 2020

Parkinson's disease genetics: a complex disease comes to the clinic

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PubMed

12 December 2020

Estimating the Dimension of a Model

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Crossref

https://api.crossref.org/works/10.1002%2FHUMU.20840

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1002/HUMU.20840

1 reference

26 July 2017

1 reference

26 July 2017

1 reference