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L Howe

Showing results (801-810 of 822) with videos related to

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NPJ Genomic Medicine|October 12, 2019
A large data resource of genomic copy number variation across neurodevelopmental disordersMehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.
JAMA Surgery|December 20, 2018
Association Between 6-Week Postdischarge Risk Classification and 12-Month Outcomes After Orthopedic TraumaRenan C Castillo, Yanjie Huang, Daniel Scharfstein, et al.
Nature Genetics|March 30, 2024
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsyDarcy L Fehlings, Mehdi Zarrei, Worrawat Engchuan, et al.
Nucleic Acids Research|November 7, 2019
Ensembl 2020Andrew D Yates, Premanand Achuthan, Wasiu Akanni, et al.
Nature|May 13, 2026
An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autismClarrisa A Bradley, Sangyoon Y Ko, Meng Tian, et al.
Nucleic Acids Research|November 2, 2020
Ensembl 2021Kevin L Howe, Premanand Achuthan, James Allen, et al.
Human Molecular Genetics|January 2, 2014
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypesAnath C Lionel, Kristiina Tammimies, Andrea K Vaags, et al.
Nature Neuroscience|March 7, 2017
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorderRyan K C Yuen, Daniele Merico, Matt Bookman, et al.
Nucleic Acids Research|November 18, 2021
Ensembl 2022Fiona Cunningham, James E Allen, Jamie Allen, et al.
Nucleic Acids Research|November 1, 2022
Ensembl 2023Fergal J Martin, M Ridwan Amode, Alisha Aneja, et al.
Pageof 83

Showing results (801-810 of 822) with videos related to

Sort By:
Pageof 83
NPJ Genomic Medicine|October 12, 2019
A large data resource of genomic copy number variation across neurodevelopmental disordersMehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.
JAMA Surgery|December 20, 2018
Association Between 6-Week Postdischarge Risk Classification and 12-Month Outcomes After Orthopedic TraumaRenan C Castillo, Yanjie Huang, Daniel Scharfstein, et al.
Nature Genetics|March 30, 2024
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsyDarcy L Fehlings, Mehdi Zarrei, Worrawat Engchuan, et al.
Nucleic Acids Research|November 7, 2019
Ensembl 2020Andrew D Yates, Premanand Achuthan, Wasiu Akanni, et al.
Nature|May 13, 2026
An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autismClarrisa A Bradley, Sangyoon Y Ko, Meng Tian, et al.
Nucleic Acids Research|November 2, 2020
Ensembl 2021Kevin L Howe, Premanand Achuthan, James Allen, et al.
Human Molecular Genetics|January 2, 2014
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypesAnath C Lionel, Kristiina Tammimies, Andrea K Vaags, et al.
Nature Neuroscience|March 7, 2017
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorderRyan K C Yuen, Daniele Merico, Matt Bookman, et al.
Nucleic Acids Research|November 18, 2021
Ensembl 2022Fiona Cunningham, James E Allen, Jamie Allen, et al.
Nucleic Acids Research|November 1, 2022
Ensembl 2023Fergal J Martin, M Ridwan Amode, Alisha Aneja, et al.
Pageof 83