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Stephan J Sanders

Showing results (131-140 of 154) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|December 3, 2025
Common and rare variant genetic contributions in African Americans with autismMatilde Cirnigliaro, Jennifer K Lowe, Alexander O Flynn-Carroll, et al.
Biorxiv : the Preprint Server for Biology|September 18, 2025
Human-specific features of the cerebellum and ZP2-regulated synapse developmentSuel-Kee Kim, Adriana Cherskov, Aastha Sindhwani, et al.
American Journal of Human Genetics|August 18, 2023
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomaliesChelsea Lowther, Elise Valkanas, Jessica L Giordano, et al.
Nature Genetics|October 10, 2017
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probandsSheng Chih Jin, Jason Homsy, Samir Zaidi, 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.
Cell|March 12, 2026
Human-specific features of the cerebellum and ZP2-regulated synapse developmentSuel-Kee Kim, Adriana Cherskov, Aastha Sindhwani, et al.
Nature Genetics|April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorderDonna M Werling, Harrison Brand, Joon-Yong An, et al.
Science (New York, N.Y.)|December 15, 2018
Integrative functional genomic analysis of human brain development and neuropsychiatric risksMingfeng Li, Gabriel Santpere, Yuka Imamura Kawasawa, et al.
Nature|May 14, 2013
De novo mutations in histone-modifying genes in congenital heart diseaseSamir Zaidi, Murim Choi, Hiroko Wakimoto, et al.
Neuron|January 29, 2013
Using whole-exome sequencing to identify inherited causes of autismTimothy W Yu, Maria H Chahrour, Michael E Coulter, et al.
Pageof 16

Showing results (131-140 of 154) with videos related to

Sort By:
Pageof 16
Medrxiv : the Preprint Server for Health Sciences|December 3, 2025
Common and rare variant genetic contributions in African Americans with autismMatilde Cirnigliaro, Jennifer K Lowe, Alexander O Flynn-Carroll, et al.
Biorxiv : the Preprint Server for Biology|September 18, 2025
Human-specific features of the cerebellum and ZP2-regulated synapse developmentSuel-Kee Kim, Adriana Cherskov, Aastha Sindhwani, et al.
American Journal of Human Genetics|August 18, 2023
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomaliesChelsea Lowther, Elise Valkanas, Jessica L Giordano, et al.
Nature Genetics|October 10, 2017
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probandsSheng Chih Jin, Jason Homsy, Samir Zaidi, 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.
Cell|March 12, 2026
Human-specific features of the cerebellum and ZP2-regulated synapse developmentSuel-Kee Kim, Adriana Cherskov, Aastha Sindhwani, et al.
Nature Genetics|April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorderDonna M Werling, Harrison Brand, Joon-Yong An, et al.
Science (New York, N.Y.)|December 15, 2018
Integrative functional genomic analysis of human brain development and neuropsychiatric risksMingfeng Li, Gabriel Santpere, Yuka Imamura Kawasawa, et al.
Nature|May 14, 2013
De novo mutations in histone-modifying genes in congenital heart diseaseSamir Zaidi, Murim Choi, Hiroko Wakimoto, et al.
Neuron|January 29, 2013
Using whole-exome sequencing to identify inherited causes of autismTimothy W Yu, Maria H Chahrour, Michael E Coulter, et al.
Pageof 16