Work

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

Year: 2006

Type: article

Study design: Observational Study

Source: Human Molecular Genetics

DOI: 10.1093/hmg/ddl436

Authors: Javier Simon-Sanchez, Sonja Scholz, Hon-Chung Fung, Mar Matarin, Dena Hernandez, J. Raphael Gibbs, Angela Britton, Fabienne Wavrant de Vrieze, Elizabeth Peckham, Katrina Gwinn-Hardy, Anthony Crawley, Judith C. Keen, Josefina Nash, Digamber Borgaonkar, John Hardy, Andrew Singleton

Institutions: Consejo Superior de Investigaciones Científicas, Instituto de Biomedicina de Valencia, Chang Gung University, Chang Gung Memorial Hospital, University College London, National Institute on Aging, National Institutes of Health, National Institute of Neurological Disorders and Stroke, Coriell Institute For Medical Research

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Parkinson's UK, National Institutes of Health, National Institute on Aging, National Institute of Neurological Disorders and Stroke

Award: G3327757157

OpenAlex ID: W2160854895

FWCI: 16.61

Cites: 19

Cited by: 229

Related to: 10