Sequencing of selected chromatin remodelling genes reveals increased burden of rare missense variants in ASD patients from the Japanese population-Reference-Cited by-同舟云学术

Sequencing of selected chromatin remodelling genes reveals increased burden of rare missense variants in ASD patients from the Japanese population

Published:2022-02-17 Issue:2 Volume:34 Page:154-167
ISSN:0954-0261
Container-title:International Review of Psychiatry
language:en
Short-container-title:International Review of Psychiatry

Author:

Lo Tzuyao¹,Kushima Itaru¹²,Aleksic Branko¹,Kato Hidekazu¹,Nawa Yoshihiro¹,Hayashi Yu¹,Otgonbayar Gantsooj¹,Kimura Hiroki¹,Arioka Yuko¹²³,Mori Daisuke¹⁴,Ozaki Norio¹

Affiliation:

1. Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan

2. Medical Genomics Center, Nagoya University Hospital, Nagoya, Japan

3. Center for Advanced Medicine and Clinical Research, Nagoya University Hospital, Nagoya, Japan

4. Brain and Mind Research Center, Nagoya University, Nagoya, Japan

Funder

Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT) and the Ministry of Health, Labour and Welfare of Japan; the Japan Agency for Medical Research and Development

the Japan Society for the Promotion of Science

Uehara Memorial Foundation

SENSHIN Medical Research Foundation.

Publisher

Informa UK Limited

Subject

Psychiatry and Mental health

Link

https://www.tandfonline.com/doi/pdf/10.1080/09540261.2022.2072193

Reference72 articles.

1. A method and server for predicting damaging missense mutations

2. mSWI/SNF (BAF) Complexes Are Indispensable for the Neurogenesis and Development of Embryonic Olfactory Epithelium