Next-Generation Sequencing For Gene and Pathway Discovery and Analysis in Autism Spectrum Disorders

Guiqing Cai; Joseph D. Buxbaum

doi:10.1016/B978-0-12-391924-3.00011-9

Next-Generation Sequencing For Gene and Pathway Discovery and Analysis in Autism Spectrum Disorders

Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review

1 Scopus citations

Original language	English
Title of host publication	The Neuroscience of Autism Spectrum Disorders
Publisher	Elsevier
Pages	169-177
Number of pages	9
ISBN (Electronic)	9780123919243
DOIs	https://doi.org/10.1016/B978-0-12-391924-3.00011-9
State	Published - 1 Jan 2012

Access to Document

10.1016/B978-0-12-391924-3.00011-9

Cite this

@inbook{d5d66c7e2f964afba6a2a9a197ec3ec1,

title = "Next-Generation Sequencing For Gene and Pathway Discovery and Analysis in Autism Spectrum Disorders",

author = "Guiqing Cai and Buxbaum, {Joseph D.}",

note = "Funding Information: Additional whole-exome projects include those led by researchers at the Hospital for Sick Children at Toronto, which aims to create whole-exome sequences for a cohort of 1,000 Canadian patients ( Walker et al., 2011 ). Meanwhile, the UK10K project is currently performing whole-exome sequencing of about 600 ASD subjects ( http://www.uk10k.org/goals.html ). Supported by a NIMH Grand Opportunity grant, the Broad Institute and Harvard Medical School are also conducting a study of whole-exome and eventually whole- genome sequencing of Middle Eastern patients with a recessive form of autism whose parents share a common ancestry. ",

year = "2012",

month = jan,

day = "1",

doi = "10.1016/B978-0-12-391924-3.00011-9",

language = "English",

pages = "169--177",

booktitle = "The Neuroscience of Autism Spectrum Disorders",

publisher = "Elsevier",

address = "Netherlands",

}

TY - CHAP

T1 - Next-Generation Sequencing For Gene and Pathway Discovery and Analysis in Autism Spectrum Disorders

AU - Cai, Guiqing

AU - Buxbaum, Joseph D.

N1 - Funding Information: Additional whole-exome projects include those led by researchers at the Hospital for Sick Children at Toronto, which aims to create whole-exome sequences for a cohort of 1,000 Canadian patients ( Walker et al., 2011 ). Meanwhile, the UK10K project is currently performing whole-exome sequencing of about 600 ASD subjects ( http://www.uk10k.org/goals.html ). Supported by a NIMH Grand Opportunity grant, the Broad Institute and Harvard Medical School are also conducting a study of whole-exome and eventually whole- genome sequencing of Middle Eastern patients with a recessive form of autism whose parents share a common ancestry.

PY - 2012/1/1

Y1 - 2012/1/1

UR - http://www.scopus.com/inward/record.url?scp=85149544295&partnerID=8YFLogxK

U2 - 10.1016/B978-0-12-391924-3.00011-9

DO - 10.1016/B978-0-12-391924-3.00011-9

M3 - Chapter

AN - SCOPUS:84882679345

SP - 169

EP - 177

BT - The Neuroscience of Autism Spectrum Disorders

PB - Elsevier

ER -