IDEAS home Printed from https://ideas.repec.org/a/plo/pone00/0112399.html
   My bibliography  Save this article

Protein Interaction Networks Reveal Novel Autism Risk Genes within GWAS Statistical Noise

Author

Listed:
  • Catarina Correia
  • Guiomar Oliveira
  • Astrid M Vicente

Abstract

Genome-wide association studies (GWAS) for Autism Spectrum Disorder (ASD) thus far met limited success in the identification of common risk variants, consistent with the notion that variants with small individual effects cannot be detected individually in single SNP analysis. To further capture disease risk gene information from ASD association studies, we applied a network-based strategy to the Autism Genome Project (AGP) and the Autism Genetics Resource Exchange GWAS datasets, combining family-based association data with Human Protein-Protein interaction (PPI) data. Our analysis showed that autism-associated proteins at higher than conventional levels of significance (P

Suggested Citation

  • Catarina Correia & Guiomar Oliveira & Astrid M Vicente, 2014. "Protein Interaction Networks Reveal Novel Autism Risk Genes within GWAS Statistical Noise," PLOS ONE, Public Library of Science, vol. 9(11), pages 1-11, November.
  • Handle: RePEc:plo:pone00:0112399
    DOI: 10.1371/journal.pone.0112399
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0112399
    Download Restriction: no

    File URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0112399&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pone.0112399?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Stephan J. Sanders & Michael T. Murtha & Abha R. Gupta & John D. Murdoch & Melanie J. Raubeson & A. Jeremy Willsey & A. Gulhan Ercan-Sencicek & Nicholas M. DiLullo & Neelroop N. Parikshak & Jason L. S, 2012. "De novo mutations revealed by whole-exome sequencing are strongly associated with autism," Nature, Nature, vol. 485(7397), pages 237-241, May.
    2. Dalila Pinto & Alistair T. Pagnamenta & Lambertus Klei & Richard Anney & Daniele Merico & Regina Regan & Judith Conroy & Tiago R. Magalhaes & Catarina Correia & Brett S. Abrahams & Joana Almeida & Ele, 2010. "Functional impact of global rare copy number variation in autism spectrum disorders," Nature, Nature, vol. 466(7304), pages 368-372, July.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Sheng Wang & Belinda Wang & Vanessa Drury & Sam Drake & Nawei Sun & Hasan Alkhairo & Juan Arbelaez & Clif Duhn & Vanessa H. Bal & Kate Langley & Joanna Martin & Pieter J. Hoekstra & Andrea Dietrich & , 2023. "Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD," Nature Communications, Nature, vol. 14(1), pages 1-18, December.
    2. Hiroshi Yasuda & Toyoharu Tsutsui, 2013. "Assessment of Infantile Mineral Imbalances in Autism Spectrum Disorders (ASDs)," IJERPH, MDPI, vol. 10(11), pages 1-17, November.
    3. Yudong Gao & Daichi Shonai & Matthew Trn & Jieqing Zhao & Erik J. Soderblom & S. Alexandra Garcia-Moreno & Charles A. Gersbach & William C. Wetsel & Geraldine Dawson & Dmitry Velmeshev & Yong-hui Jian, 2024. "Proximity analysis of native proteomes reveals phenotypic modifiers in a mouse model of autism and related neurodevelopmental conditions," Nature Communications, Nature, vol. 15(1), pages 1-18, December.
    4. Svetlana Frenkel & Charles N Bernstein & Michael Sargent & Qin Kuang & Wenxin Jiang & John Wei & Bhooma Thiruvahindrapuram & Elizabeth Spriggs & Stephen W Scherer & Pingzhao Hu, 2019. "Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease," PLOS ONE, Public Library of Science, vol. 14(6), pages 1-16, June.
    5. Frantisek Honti & Stephen Meader & Caleb Webber, 2014. "Unbiased Functional Clustering of Gene Variants with a Phenotypic-Linkage Network," PLOS Computational Biology, Public Library of Science, vol. 10(8), pages 1-7, August.
    6. Jingfen Lan & Ziheng Liao & A. K. Alvi Haque & Qiang Yu & Kun Xie & Yang Guo, 2024. "CNVbd: A Method for Copy Number Variation Detection and Boundary Search," Mathematics, MDPI, vol. 12(3), pages 1-15, January.
    7. Andrew K MacLeod & Gail Davies & Antony Payton & Albert Tenesa & Sarah E Harris & David Liewald & Xiayi Ke & Michelle Luciano & Lorna M Lopez & Alan J Gow & Janie Corley & Paul Redmond & Geraldine McN, 2012. "Genetic Copy Number Variation and General Cognitive Ability," PLOS ONE, Public Library of Science, vol. 7(12), pages 1-9, December.
    8. Mathilde André & Nicolas Brucato & Georgi Hudjasov & Vasili Pankratov & Danat Yermakovich & Francesco Montinaro & Rita Kreevan & Jason Kariwiga & John Muke & Anne Boland & Jean-François Deleuze & Vinc, 2024. "Positive selection in the genomes of two Papua New Guinean populations at distinct altitude levels," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
    9. Noor B. Almandil & Deem N. Alkuroud & Sayed AbdulAzeez & Abdulla AlSulaiman & Abdelhamid Elaissari & J. Francis Borgio, 2019. "Environmental and Genetic Factors in Autism Spectrum Disorders: Special Emphasis on Data from Arabian Studies," IJERPH, MDPI, vol. 16(4), pages 1-16, February.
    10. Tetsushi Sadakata & Yo Shinoda & Akira Sato & Hirotoshi Iguchi & Chiaki Ishii & Makoto Matsuo & Ryosuke Yamaga & Teiichi Furuichi, 2013. "Mouse Models of Mutations and Variations in Autism Spectrum Disorder-Associated Genes: Mice Expressing Caps2/Cadps2 Copy Number and Alternative Splicing Variants," IJERPH, MDPI, vol. 10(12), pages 1-19, November.
    11. Xin He & Stephan J Sanders & Li Liu & Silvia De Rubeis & Elaine T Lim & James S Sutcliffe & Gerard D Schellenberg & Richard A Gibbs & Mark J Daly & Joseph D Buxbaum & Matthew W State & Bernie Devlin &, 2013. "Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes," PLOS Genetics, Public Library of Science, vol. 9(8), pages 1-12, August.
    12. Chang Hoon Cho & Ilana Vasilisa Deyneko & Dylann Cordova-Martinez & Juan Vazquez & Anne S. Maguire & Jenny R. Diaz & Abigail U. Carbonell & Jaafar O. Tindi & Min-Hui Cui & Roman Fleysher & Sophie Molh, 2023. "ANKS1B encoded AIDA-1 regulates social behaviors by controlling oligodendrocyte function," Nature Communications, Nature, vol. 14(1), pages 1-20, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pone00:0112399. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: plosone (email available below). General contact details of provider: https://journals.plos.org/plosone/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.