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Nature Medicine
|
January 27, 2015
Whole-genome sequencing of quartet families with autism spectrum disorder
Ryan K C Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, et al.
Nature
|
July 28, 2020
Genome-wide detection of tandem DNA repeats that are expanded in autism
Brett Trost, Worrawat Engchuan, Charlotte M Nguyen, et al.
Brain : a Journal of Neurology
|
July 28, 2025
Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatonia
Harsha Murthy, Ny Hoang, Jamie C Stark, et al.
NPJ Genomic Medicine
|
October 12, 2019
A large data resource of genomic copy number variation across neurodevelopmental disorders
Mehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.
Nature
|
May 13, 2026
An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autism
Clarrisa A Bradley, Sangyoon Y Ko, Meng Tian, et al.
Nature Neuroscience
|
March 7, 2017
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
Ryan K C Yuen, Daniele Merico, Matt Bookman, et al.
American Journal of Human Genetics
|
April 28, 2021
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature
Dmitrijs Rots, Eric Chater-Diehl, Alexander J M Dingemans, et al.
Cell
|
November 11, 2022
Genomic architecture of autism from comprehensive whole-genome sequence annotation
Brett Trost, Bhooma Thiruvahindrapuram, Ada J S Chan, et al.
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Showing results (21-30 of 28) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 28 results.
Nature Medicine
|
January 27, 2015
Whole-genome sequencing of quartet families with autism spectrum disorder
Ryan K C Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, et al.
Nature
|
July 28, 2020
Genome-wide detection of tandem DNA repeats that are expanded in autism
Brett Trost, Worrawat Engchuan, Charlotte M Nguyen, et al.
Brain : a Journal of Neurology
|
July 28, 2025
Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatonia
Harsha Murthy, Ny Hoang, Jamie C Stark, et al.
NPJ Genomic Medicine
|
October 12, 2019
A large data resource of genomic copy number variation across neurodevelopmental disorders
Mehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.
Nature
|
May 13, 2026
An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autism
Clarrisa A Bradley, Sangyoon Y Ko, Meng Tian, et al.
Nature Neuroscience
|
March 7, 2017
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
Ryan K C Yuen, Daniele Merico, Matt Bookman, et al.
American Journal of Human Genetics
|
April 28, 2021
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature
Dmitrijs Rots, Eric Chater-Diehl, Alexander J M Dingemans, et al.
Cell
|
November 11, 2022
Genomic architecture of autism from comprehensive whole-genome sequence annotation
Brett Trost, Bhooma Thiruvahindrapuram, Ada J S Chan, et al.
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