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Tychele N Turner

Showing results (51-60 of 65) with videos related to

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Cell|July 22, 2025
Human-specific gene expansions contribute to brain evolutionDaniela C Soto, José M Uribe-Salazar, Gulhan Kaya, et al.
Biorxiv : the Preprint Server for Biology|October 10, 2024
Gene expansions contributing to human brain evolutionDaniela C Soto, José M Uribe-Salazar, Gulhan Kaya, et al.
American Journal of Human Genetics|January 11, 2016
Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNATychele N Turner, Fereydoun Hormozdiari, Michael H Duyzend, et al.
Nature|March 26, 2015
Loss of δ-catenin function in severe autismTychele N Turner, Kamal Sharma, Edwin C Oh, et al.
Nature Communications|November 9, 2016
De novo genic mutations among a Chinese autism spectrum disorder cohortTianyun Wang, Hui Guo, Bo Xiong, et al.
Nature Genetics|August 18, 2022
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genesXueya Zhou, Pamela Feliciano, Chang Shu, et al.
American Journal of Human Genetics|December 22, 2020
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
Human Genomics|July 14, 2021
Coding and noncoding variants in EBF3 are involved in HADDS and simplex autismEvin M Padhi, Tristan J Hayeck, Zhang Cheng, et al.
Nature Neuroscience|June 20, 2017
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domainsMadeleine R Geisheker, Gabriel Heymann, Tianyun Wang, et al.
Nature Genetics|February 14, 2017
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biasesHolly A F Stessman, Bo Xiong, Bradley P Coe, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
Cell|July 22, 2025
Human-specific gene expansions contribute to brain evolutionDaniela C Soto, José M Uribe-Salazar, Gulhan Kaya, et al.
Biorxiv : the Preprint Server for Biology|October 10, 2024
Gene expansions contributing to human brain evolutionDaniela C Soto, José M Uribe-Salazar, Gulhan Kaya, et al.
American Journal of Human Genetics|January 11, 2016
Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNATychele N Turner, Fereydoun Hormozdiari, Michael H Duyzend, et al.
Nature|March 26, 2015
Loss of δ-catenin function in severe autismTychele N Turner, Kamal Sharma, Edwin C Oh, et al.
Nature Communications|November 9, 2016
De novo genic mutations among a Chinese autism spectrum disorder cohortTianyun Wang, Hui Guo, Bo Xiong, et al.
Nature Genetics|August 18, 2022
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genesXueya Zhou, Pamela Feliciano, Chang Shu, et al.
American Journal of Human Genetics|December 22, 2020
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
Human Genomics|July 14, 2021
Coding and noncoding variants in EBF3 are involved in HADDS and simplex autismEvin M Padhi, Tristan J Hayeck, Zhang Cheng, et al.
Nature Neuroscience|June 20, 2017
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domainsMadeleine R Geisheker, Gabriel Heymann, Tianyun Wang, et al.
Nature Genetics|February 14, 2017
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biasesHolly A F Stessman, Bo Xiong, Bradley P Coe, et al.
Pageof 7