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C Yuen

Showing results (351-360 of 369) with videos related to

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Molecular Psychiatry|May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersO Mercati, G Huguet, A Danckaert, et al.
American Journal of Human Genetics|July 16, 2013
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencingYong-hui Jiang, Ryan K C Yuen, Xin Jin, et al.
NAR Molecular Medicine|December 13, 2024
<i>C9orf72</i> repeat expansion creates the unstable folate-sensitive fragile site FRA9AMila Mirceta, Monika H M Schmidt, Natalie Shum, et al.
G3 (Bethesda, Md.)|January 15, 2017
<i>De Novo</i> Genome and Transcriptome Assembly of the Canadian Beaver (<i>Castor canadensis</i>)Si Lok, Tara A Paton, Zhuozhi Wang, et al.
Nature|July 28, 2020
Genome-wide detection of tandem DNA repeats that are expanded in autismBrett Trost, Worrawat Engchuan, Charlotte M Nguyen, et al.
Biorxiv : the Preprint Server for Biology|November 21, 2024
<i>C9orf72</i> expansion creates the unstable folate-sensitive fragile site FRA9AMila Mirceta, Monika H M Schmidt, Natalie Shum, et al.
Psychiatric Genetics|September 9, 2016
Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16-20 October 2015Gwyneth Zai, Bonnie Alberry, Janine Arloth, et al.
NPJ Genomic Medicine|August 16, 2016
Genome-wide characteristics of <i>de novo</i> mutations in autismRyan K C Yuen, Daniele Merico, Hongzhi Cao, et al.
Brain : a Journal of Neurology|July 22, 2019
Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain sizeDiana Le Duc, Cecilia Giulivi, Susan M Hiatt, et al.
The New England Journal of Medicine|April 11, 2019
Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in <i>GLS</i>André B P van Kuilenburg, Maja Tarailo-Graovac, Phillip A Richmond, et al.
Pageof 37

Showing results (351-360 of 369) with videos related to

Sort By:
Pageof 37
Molecular Psychiatry|May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersO Mercati, G Huguet, A Danckaert, et al.
American Journal of Human Genetics|July 16, 2013
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencingYong-hui Jiang, Ryan K C Yuen, Xin Jin, et al.
NAR Molecular Medicine|December 13, 2024
<i>C9orf72</i> repeat expansion creates the unstable folate-sensitive fragile site FRA9AMila Mirceta, Monika H M Schmidt, Natalie Shum, et al.
G3 (Bethesda, Md.)|January 15, 2017
<i>De Novo</i> Genome and Transcriptome Assembly of the Canadian Beaver (<i>Castor canadensis</i>)Si Lok, Tara A Paton, Zhuozhi Wang, et al.
Nature|July 28, 2020
Genome-wide detection of tandem DNA repeats that are expanded in autismBrett Trost, Worrawat Engchuan, Charlotte M Nguyen, et al.
Biorxiv : the Preprint Server for Biology|November 21, 2024
<i>C9orf72</i> expansion creates the unstable folate-sensitive fragile site FRA9AMila Mirceta, Monika H M Schmidt, Natalie Shum, et al.
Psychiatric Genetics|September 9, 2016
Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16-20 October 2015Gwyneth Zai, Bonnie Alberry, Janine Arloth, et al.
NPJ Genomic Medicine|August 16, 2016
Genome-wide characteristics of <i>de novo</i> mutations in autismRyan K C Yuen, Daniele Merico, Hongzhi Cao, et al.
Brain : a Journal of Neurology|July 22, 2019
Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain sizeDiana Le Duc, Cecilia Giulivi, Susan M Hiatt, et al.
The New England Journal of Medicine|April 11, 2019
Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in <i>GLS</i>André B P van Kuilenburg, Maja Tarailo-Graovac, Phillip A Richmond, et al.
Pageof 37