A common genetic variant in the Neurexin family member CNTNAP2 is related to language but not communication skills in youth with Autism Spectrum Disorder.

Autor: Arutiunian V; Center for Child Health, Behavior and Development, Seattle Children's Research Institute, Seattle, Washington, USA., Santhosh M; Center for Child Health, Behavior and Development, Seattle Children's Research Institute, Seattle, Washington, USA., Neuhaus E; Center for Child Health, Behavior and Development, Seattle Children's Research Institute, Seattle, Washington, USA.; Department of Psychiatry and Behavioral Science, University of Washington, Seattle, Washington, USA., Sullivan CAW; Department of Pediatrics, Yale School of Medicine, New Haven, Connecticut, USA., Bernier RA; Department of Psychiatry and Behavioral Science, University of Washington, Seattle, Washington, USA., Bookheimer SY; Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.; Center for Autism Research and Treatment, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA., Dapretto M; Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.; Center for Autism Research and Treatment, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA., Geschwind DH; Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.; Center for Autism Research and Treatment, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.; Department of Neurology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.; Department of Human Genetics, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA., Jack A; Department of Psychology, George Mason University, Fairfax, Virginia, USA., McPartland JC; Yale Child Study Center, Yale School of Medicine, New Haven, Connecticut, USA., Van Horn JD; Department of Psychology, University of Virginia, Charlottesville, Virginia, USA.; School of Data Science, University of Virginia, Charlottesville, Virginia, USA., Pelphrey KA; Department of Neurology, School of Medicine, University of Virginia, Virginia, USA., Gupta AR; Department of Pediatrics, Yale School of Medicine, New Haven, Connecticut, USA.; Yale Child Study Center, Yale School of Medicine, New Haven, Connecticut, USA.; Department of Neuroscience, Yale School of Medicine, New Haven, Connecticut, USA., Webb SJ; Center for Child Health, Behavior and Development, Seattle Children's Research Institute, Seattle, Washington, USA.; Department of Psychiatry and Behavioral Science, University of Washington, Seattle, Washington, USA.

Publikováno v: Autism research : official journal of the International Society for Autism Research [Autism Res] 2024 Jul 10. Date of Electronic Publication: 2024 Jul 10.

Association of genetic variants with autism spectrum disorder in Japanese children revealed by targeted sequencing.

Autor: Yuka Shiota, Tomoaki Nishiyama, Shigeru Yokoyama, Yuko Yoshimura, Chiaki Hasegawa, Sanae Tanaka, Sumie Iwasaki, Mitsuru Kikuchi

Publikováno v: Frontiers in Genetics; 2024, p1-13, 13p

Modelling adult neurogenesis in the aging rodent hippocampus: a midlife crisis.

Autor: Arellano, Jon I., Rakic, Pasko

Publikováno v: Frontiers in Neuroscience; 2024, p1-16, 16p

Alzheimer‐like tau accumulation in dentate gyrus mossy cells induces spatial cognitive deficits by disrupting multiple memory‐related signaling and inhibiting local neural circuit.

Autor: Li, Shihong¹ (AUTHOR), Zhou, Qiuzhi¹ (AUTHOR), Liu, Enjie² (AUTHOR) liuenjie01@163.com, Du, Huiyun³ (AUTHOR), Yu, Nana¹ (AUTHOR), Yu, Haitao¹ (AUTHOR), Wang, Weijin¹ (AUTHOR), Li, Mengzhu¹ (AUTHOR), Weng, Ying¹ (AUTHOR), Gao, Yang¹ (AUTHOR), Pi, Guilin¹ (AUTHOR), Wang, Xin¹ (AUTHOR), Ke, Dan¹ (AUTHOR), Wang, Jian‐Zhi^1,4 (AUTHOR) wangjz@mail.hust.edu.cn

Publikováno v: Aging Cell. May2022, Vol. 21 Issue 5, p1-15. 15p.

Genetic Insights: Examining CNTNAP2 rs7794745 Gene Polymorphism and Its Impact on ABLLS Assessment in Middle Euphrates Children in Iraq with Autism Spectrum Disorder.

Autor: AL-Safar, Safaa R. M., AL-Zubaidy, Haydar F. S., Alwaidh, Roaa Hameed

Publikováno v: MSystems; Mar2024, Vol. 9 Issue 3, p93-97, 5p