Finished sequence and assembly of the DUF1220-rich 1q21 region using a haploid human genome-Reference-Cited by-同舟云学术

Finished sequence and assembly of the DUF1220-rich 1q21 region using a haploid human genome

Published:2014-05-20 Issue:1 Volume:15 Page:
ISSN:1471-2164
Container-title:BMC Genomics
language:en
Short-container-title:BMC Genomics

Author:

O’Bleness Majesta,Searles Veronica B,Dickens C Michael,Astling David,Albracht Derek,Mak Angel C Y,Lai Yvonne Y Y,Lin Chin,Chu Catherine,Graves Tina,Kwok Pui-Yan,Wilson Richard K,Sikela James M

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Biotechnology

Link

https://link.springer.com/content/pdf/10.1186/1471-2164-15-387.pdf

Reference28 articles.

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3. Davis JM, Searles VB, Anderson N, Keeney J, Dumas L, Sikela JM: DUF1220 dosage is linearly associated with increasing severity of the three primary symptoms of autism. PLoS Genet. 2014, 10 (3): e1004241-10.1371/journal.pgen.1004241. doi:10.1371/journal.pgen.1004241

4. Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Bryson SE, Carson AR, Casallo G, Casey J, Chung BH, Cochrane L, Corsello C, et al: Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 2010, 466: 368-372. 10.1038/nature09146.

5. International Schizophrenia Consortium: Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature. 2008, 455: 178-179. 10.1038/455178a.

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