Considerations for genomewide association studies in Parkinson disease.

American journal of human genetics ·Vol. 78 ·No. 6 ·2006-06-00 ·Pages 1081-2

Myers RH

Abstract

暂无摘要

MeSH Terms

Genetic Linkage Genome, Human/genetics Humans Parkinson Disease/epidemiology,genetics

Authors & Affiliations

1 authors, click to expand affiliations / ORCID

Myers Richard H

References (9)

9 references, click to expand

Genomewide association, Parkinson disease, and PARK10.
Am J Hum Genet. 2006 Jun;78(6):1084-8; author reply 1092-4 PMID: 16685661
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
Neuron. 2004 Nov 18;44(4):601-7 PMID: 15541309
High-resolution whole-genome association study of Parkinson disease.
Am J Hum Genet. 2005 Nov;77(5):685-93 PMID: 16252231
Parkinson's disease: piecing together a genetic jigsaw.
Brain. 2003 Aug;126(Pt 8):1722-33 PMID: 12805097
No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.
Am J Hum Genet. 2006 Jun;78(6):1088-90; author reply 1092-4 PMID: 16685662
Segregation analysis of Parkinson disease revealing evidence for a major causative gene.
Am J Med Genet. 2002 May 1;109(3):191-7 PMID: 11977177
A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.
Am J Hum Genet. 2006 Jun;78(6):1090-2; author reply 1092-4 PMID: 16685663
Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease.
Am J Hum Genet. 2006 Jun;78(6):1082-4; author reply 1092-4 PMID: 16685660
Blood is thicker than water: the strengths of family-based case-control studies.
Neurology. 2005 Feb 8;64(3):408-9 PMID: 15699365

Article Info

Journal

American journal of human genetics

Abbr.

Am J Hum Genet

ISSN

0002-9297

DOI

Published

2006-06-00

Pages

1081-2

Language

English

Region

United States

NLM ID

0370475

PMCID

PMC1474090

Subset

Corrections

CommentOn

PMID: 16685660

CommentOn

PMID: 16685661

CommentOn

PMID: 16685662

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