Commonly used genomic arrays may lose information due to imperfect coverage of discovered variants f...
Commonly used genomic arrays may lose information due to imperfect coverage of discovered variants for autism spectrum disorder
About this item
Full title
Author / Creator
Yao, Michael , Daniels, Jason , Grosvenor, Luke , Morrill, Valerie , Feinberg, Jason I. , Bakulski, Kelly M. , Piven, Joseph , Hazlett, Heather C. , Shen, Mark D. , Newschaffer, Craig , Lyall, Kristen , Schmidt, Rebecca J. , Hertz-Picciotto, Irva , Croen, Lisa A. , Fallin, M. Daniele , Ladd-Acosta, Christine , Volk, Heather and Benke, Kelly
Publisher
England: BioMed Central Ltd
Journal title
Language
English
Formats
Publication information
Publisher
England: BioMed Central Ltd
Subjects
More information
Scope and Contents
Contents
Common genetic variation has been shown to account for a large proportion of ASD heritability. Polygenic scores generated for autism spectrum disorder (ASD-PGS) using the most recent discovery data, however, explain less variance than expected, despite reporting significant associations with ASD and other ASD-related traits. Here, we investigate th...
Alternative Titles
Full title
Commonly used genomic arrays may lose information due to imperfect coverage of discovered variants for autism spectrum disorder
Authors, Artists and Contributors
Author / Creator
Daniels, Jason
Grosvenor, Luke
Morrill, Valerie
Feinberg, Jason I.
Bakulski, Kelly M.
Piven, Joseph
Hazlett, Heather C.
Shen, Mark D.
Newschaffer, Craig
Lyall, Kristen
Schmidt, Rebecca J.
Hertz-Picciotto, Irva
Croen, Lisa A.
Fallin, M. Daniele
Ladd-Acosta, Christine
Volk, Heather
Benke, Kelly
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_065b3e24ae6742c08b0d1d741348b431
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_065b3e24ae6742c08b0d1d741348b431
Other Identifiers
ISSN
1866-1955,1866-1947
E-ISSN
1866-1955
DOI
10.1186/s11689-024-09571-8
