Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.

Autor: Cukier HN, Dueker ND, Slifer SH, Lee JM, Whitehead PL, Lalanne E, Leyva N, Konidari I, Gentry RC, Hulme WF, Booven DV, Mayo V, Hofmann NK, Schmidt MA, Martin ER, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA; John P, Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, 1501 NW 10th Avenue, BRB-314 (M860), Miami, FL, USA. mpericak@med.miami.edu.

Publikováno v: Molecular autism [Mol Autism] 2014 Jan 10; Vol. 5 (1), pp. 1. Date of Electronic Publication: 2014 Jan 10.

Tomosyn affects dense core vesicle composition but not exocytosis in mammalian neurons.

Autor: Subkhangulova, Aygul, Gonzalez-Lozano, Miguel A., Groffen, Alexander J. A ., van Weering, Jan R. T., Smit, August B., Toonen, Ruud F., Verhage, Matthijs

Publikováno v: eLife; 9/11/2023, p1-30, 30p

Regulation of Neural Circuit Development by Cadherin-11 Provides Implications for Autism.

Autor: Frei, Jeannine A., Niescier, Robert F., Bridi, Morgan S., Durens, Madel, Nestor, Jonathan E., Kilander, Michaela B. C., Xiaobing Yuan, Dykxhoorn, Derek M., Nestor, Michael W., Shiyong Huang, Blatt, Gene J., Yu-Chih Lin

Publikováno v: eNeuro; Jul/Aug2021, Vol. 8 Issue 4, p1-25, 25p

Neurodevelopmental Perspectives on Wnt Signaling in Psychiatry.

Autor: Mulligan, Kimberly A., Cheyette, Benjamin N. R.

Publikováno v: Molecular Neuropsychiatry; Feb2017, Vol. 2 Issue 4, p219-246, 28p

The contribution of protein intrinsic disorder to understand the role of genetic variants uncovered by autism spectrum disorders exome studies.

Autor: Schuch, Jaqueline Bohrer, Paixão‐Côrtes, Vanessa Rodrigues, Friedrich, Deise C., Tovo‐Rodrigues, Luciana

Publikováno v: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics; Apr2016, Vol. 171B Issue 3, p479-491, 13p