Whole-exome sequencing and neurite outgrowth analysis in autism spectrum disorder-Reference-Cited by-同舟云学术

Whole-exome sequencing and neurite outgrowth analysis in autism spectrum disorder

Published:2015-11-19 Issue:3 Volume:61 Page:199-206
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Hashimoto Ryota^ORCID,Nakazawa Takanobu,Tsurusaki Yoshinori,Yasuda Yuka,Nagayasu Kazuki,Matsumura Kensuke,Kawashima Hitoshi,Yamamori Hidenaga,Fujimoto Michiko,Ohi Kazutaka,Umeda-Yano Satomi,Fukunaga Masaki,Fujino Haruo,Kasai Atsushi,Hayata-Takano Atsuko,Shintani Norihito^ORCID,Takeda Masatoshi,Matsumoto Naomichi,Hashimoto Hitoshi

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/jhg2015141.pdf

Reference38 articles.

1. Iossifov, I., O'Roak, B. J., Sanders, S. J., Ronemus, M., Krumm, N., Levy, D. et al. The contribution of de novo coding mutations to autism spectrum disorder. Nature 515, 216–221 (2014).

2. De Rubeis, S., He, X., Goldberg, A. P., Poultney, C. S., Samocha, K., Ercument Cicek, A. et al. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature 515, 209–215 (2014).

3. Iossifov, I., Ronemus, M., Levy, D., Wang, Z., Hakker, I., Rosenbaum, J. et al. De novo gene disruptions in children on the autistic spectrum. Neuron 74, 285–299 (2012).

4. Krumm, N., O'Roak, B. J., Shendure, J. & Eichler, E. E. A de novo convergence of autism genetics and molecular neuroscience. Trends Neurosci. 37, 95–105 (2014).

5. Malhotra, D. & Sebat, J. CNVs: harbingers of a rare variant revolution in psychiatric genetics. Cell 148, 1223–1241 (2012).

Cited by 80 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Getting smart – Deciphering the neuronal functions of protein kinase D;Biochimica et Biophysica Acta (BBA) - Molecular Cell Research;2024-10

2. Analysis of human neuronal cells carrying ASTN2 deletion associated with psychiatric disorders;Translational Psychiatry;2024-06-03

3. sFlt-1 impairs neurite growth and neuronal differentiation in SH-SY5Y cells and human neurons;Bioscience Reports;2024-05

4. ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes;Journal of Medical Genetics;2024-03-20

5. Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability;The American Journal of Human Genetics;2024-03