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Journal Abstract Search

236 related items for PubMed ID: 23625158

  • 1. Peripheral blood gene expression signature differentiates children with autism from unaffected siblings.
    Kong SW, Shimizu-Motohashi Y, Campbell MG, Lee IH, Collins CD, Brewster SJ, Holm IA, Rappaport L, Kohane IS, Kunkel LM.
    Neurogenetics; 2013 May; 14(2):143-52. PubMed ID: 23625158
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  • 2. A prospective study of autistic-like traits in unaffected siblings of probands with autism spectrum disorder.
    Georgiades S, Szatmari P, Zwaigenbaum L, Bryson S, Brian J, Roberts W, Smith I, Vaillancourt T, Roncadin C, Garon N.
    JAMA Psychiatry; 2013 Jan; 70(1):42-8. PubMed ID: 22945359
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  • 4. De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
    Sanders SJ, Murtha MT, Gupta AR, Murdoch JD, Raubeson MJ, Willsey AJ, Ercan-Sencicek AG, DiLullo NM, Parikshak NN, Stein JL, Walker MF, Ober GT, Teran NA, Song Y, El-Fishawy P, Murtha RC, Choi M, Overton JD, Bjornson RD, Carriero NJ, Meyer KA, Bilguvar K, Mane SM, Sestan N, Lifton RP, Günel M, Roeder K, Geschwind DH, Devlin B, State MW.
    Nature; 2012 Apr 04; 485(7397):237-41. PubMed ID: 22495306
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  • 6. Risk of Psychiatric and Neurodevelopmental Disorders Among Siblings of Probands With Autism Spectrum Disorders.
    Jokiranta-Olkoniemi E, Cheslack-Postava K, Sucksdorff D, Suominen A, Gyllenberg D, Chudal R, Leivonen S, Gissler M, Brown AS, Sourander A.
    JAMA Psychiatry; 2016 Jun 01; 73(6):622-9. PubMed ID: 27145529
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  • 7. Whole Brain White Matter Tract Deviation and Idiosyncrasy From Normative Development in Autism and ADHD and Unaffected Siblings Link With Dimensions of Psychopathology and Cognition.
    Tung YH, Lin HY, Chen CL, Shang CY, Yang LY, Hsu YC, Tseng WI, Gau SS.
    Am J Psychiatry; 2021 Aug 01; 178(8):730-743. PubMed ID: 33726525
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  • 13. Measuring shared variants in cohorts of discordant siblings with applications to autism.
    Ye K, Iossifov I, Levy D, Yamrom B, Buja A, Krieger AM, Wigler M.
    Proc Natl Acad Sci U S A; 2017 Jul 03; 114(27):7073-7076. PubMed ID: 28630308
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  • 17. Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
    Pizzo L, Jensen M, Polyak A, Rosenfeld JA, Mannik K, Krishnan A, McCready E, Pichon O, Le Caignec C, Van Dijck A, Pope K, Voorhoeve E, Yoon J, Stankiewicz P, Cheung SW, Pazuchanics D, Huber E, Kumar V, Kember RL, Mari F, Curró A, Castiglia L, Galesi O, Avola E, Mattina T, Fichera M, Mandarà L, Vincent M, Nizon M, Mercier S, Bénéteau C, Blesson S, Martin-Coignard D, Mosca-Boidron AL, Caberg JH, Bucan M, Zeesman S, Nowaczyk MJM, Lefebvre M, Faivre L, Callier P, Skinner C, Keren B, Perrine C, Prontera P, Marle N, Renieri A, Reymond A, Kooy RF, Isidor B, Schwartz C, Romano C, Sistermans E, Amor DJ, Andrieux J, Girirajan S.
    Genet Med; 2019 Apr 03; 21(4):816-825. PubMed ID: 30190612
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  • 18. Cellular and molecular characterization of multiplex autism in human induced pluripotent stem cell-derived neurons.
    Lewis EMA, Meganathan K, Baldridge D, Gontarz P, Zhang B, Bonni A, Constantino JN, Kroll KL.
    Mol Autism; 2019 Apr 03; 10():51. PubMed ID: 31893020
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