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Tychele N Turner

Showing results (31-40 of 65) with videos related to

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Nature Genetics|May 12, 2015
Excess of rare, inherited truncating mutations in autismNiklas Krumm, Tychele N Turner, Carl Baker, et al.
Cell Genomics|March 12, 2025
Proteome-wide assessment of differential missense variant clustering in neurodevelopmental disorders and cancerJeffrey K Ng, Yilin Chen, Titilope M Akinwe, et al.
Genetics|April 6, 2022
Ancestry adjustment improves genome-wide estimates of regional intoleranceTristan J Hayeck, Nicholas Stong, Evan Baugh, et al.
Cell|October 3, 2017
Genomic Patterns of De Novo Mutation in Simplex AutismTychele N Turner, Bradley P Coe, Diane E Dickel, et al.
Biology Open|October 13, 2025
Generation and characterization of a knockout mouse of an enhancer of EBF3Emily Cordova Hurtado, Janine M Wotton, Alexander Gulka, et al.
Biological Psychiatry|September 19, 2019
Clinical Phenotypes of Carriers of Mutations in CHD8 or Its Conserved Target GenesJennifer S Beighley, Caitlin M Hudac, Anne B Arnett, et al.
JAMA Psychiatry|April 17, 2024
Examining Sex Differences in Autism HeritabilitySven Sandin, Benjamin H K Yip, Weiyao Yin, et al.
HGG Advances|January 20, 2022
From karyotypes to precision genomics in 9p deletion and duplication syndromesEleanor I Sams, Jeffrey K Ng, Victoria Tate, et al.
Human Molecular Genetics|September 15, 2023
A common single nucleotide variant in the cytokine receptor-like factor-3 (CRLF3) gene causes neuronal deficits in human and mouse cellsAnna F Wilson, Rasha Barakat, Rui Mu, et al.
Biorxiv : the Preprint Server for Biology|January 20, 2025
Generation and Characterization of a Knockout Mouse of an Enhancer of <i>EBF3</i>Emily Cordova Hurtado, Janine M Wotton, Alexander Gulka, et al.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
Nature Genetics|May 12, 2015
Excess of rare, inherited truncating mutations in autismNiklas Krumm, Tychele N Turner, Carl Baker, et al.
Cell Genomics|March 12, 2025
Proteome-wide assessment of differential missense variant clustering in neurodevelopmental disorders and cancerJeffrey K Ng, Yilin Chen, Titilope M Akinwe, et al.
Genetics|April 6, 2022
Ancestry adjustment improves genome-wide estimates of regional intoleranceTristan J Hayeck, Nicholas Stong, Evan Baugh, et al.
Cell|October 3, 2017
Genomic Patterns of De Novo Mutation in Simplex AutismTychele N Turner, Bradley P Coe, Diane E Dickel, et al.
Biology Open|October 13, 2025
Generation and characterization of a knockout mouse of an enhancer of EBF3Emily Cordova Hurtado, Janine M Wotton, Alexander Gulka, et al.
Biological Psychiatry|September 19, 2019
Clinical Phenotypes of Carriers of Mutations in CHD8 or Its Conserved Target GenesJennifer S Beighley, Caitlin M Hudac, Anne B Arnett, et al.
JAMA Psychiatry|April 17, 2024
Examining Sex Differences in Autism HeritabilitySven Sandin, Benjamin H K Yip, Weiyao Yin, et al.
HGG Advances|January 20, 2022
From karyotypes to precision genomics in 9p deletion and duplication syndromesEleanor I Sams, Jeffrey K Ng, Victoria Tate, et al.
Human Molecular Genetics|September 15, 2023
A common single nucleotide variant in the cytokine receptor-like factor-3 (CRLF3) gene causes neuronal deficits in human and mouse cellsAnna F Wilson, Rasha Barakat, Rui Mu, et al.
Biorxiv : the Preprint Server for Biology|January 20, 2025
Generation and Characterization of a Knockout Mouse of an Enhancer of <i>EBF3</i>Emily Cordova Hurtado, Janine M Wotton, Alexander Gulka, et al.
Pageof 7