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Matthew W State

Showing results (101-110 of 123) with videos related to

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Nature|April 13, 2012
De novo mutations revealed by whole-exome sequencing are strongly associated with autismStephan J Sanders, Michael T Murtha, Abha R Gupta, et al.
Cell Reports|April 9, 2020
Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal CortexDonna M Werling, Sirisha Pochareddy, Jinmyung Choi, et al.
Science (New York, N.Y.)|December 15, 2018
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorderJoon-Yong An, Kevin Lin, Lingxue Zhu, et al.
Cell|July 28, 2018
The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric DisordersA Jeremy Willsey, Montana T Morris, Sheng Wang, et al.
Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Cell|January 26, 2020
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of AutismF Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, et al.
Science (New York, N.Y.)|November 25, 2017
Molecular and cellular reorganization of neural circuits in the human lineageAndré M M Sousa, Ying Zhu, Mary Ann Raghanti, et al.
Nature|November 4, 2014
The contribution of de novo coding mutations to autism spectrum disorderIvan Iossifov, Brian J O'Roak, Stephan J Sanders, et al.
Science (New York, N.Y.)|January 26, 2013
Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMOVictoria E Clark, E Zeynep Erson-Omay, Akdes Serin, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
A foundational atlas of autism protein interactions reveals molecular convergenceBelinda Wang, Rasika Vartak, Yefim Zaltsman, et al.
Pageof 13

Showing results (101-110 of 123) with videos related to

Sort By:
Pageof 13
Nature|April 13, 2012
De novo mutations revealed by whole-exome sequencing are strongly associated with autismStephan J Sanders, Michael T Murtha, Abha R Gupta, et al.
Cell Reports|April 9, 2020
Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal CortexDonna M Werling, Sirisha Pochareddy, Jinmyung Choi, et al.
Science (New York, N.Y.)|December 15, 2018
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorderJoon-Yong An, Kevin Lin, Lingxue Zhu, et al.
Cell|July 28, 2018
The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric DisordersA Jeremy Willsey, Montana T Morris, Sheng Wang, et al.
Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Cell|January 26, 2020
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of AutismF Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, et al.
Science (New York, N.Y.)|November 25, 2017
Molecular and cellular reorganization of neural circuits in the human lineageAndré M M Sousa, Ying Zhu, Mary Ann Raghanti, et al.
Nature|November 4, 2014
The contribution of de novo coding mutations to autism spectrum disorderIvan Iossifov, Brian J O'Roak, Stephan J Sanders, et al.
Science (New York, N.Y.)|January 26, 2013
Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMOVictoria E Clark, E Zeynep Erson-Omay, Akdes Serin, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
A foundational atlas of autism protein interactions reveals molecular convergenceBelinda Wang, Rasika Vartak, Yefim Zaltsman, et al.
Pageof 13