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Michael C Sierant

Showing results (1-10 of 8) with videos related to

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Genomics & Informatics|January 3, 2019
Single-Cell Ssequencing in Cancer: Recent Applications to Immunogenomics and Multi-omics ToolsMichael C Sierant, Jungmin Choi
American Journal of Human Genetics|April 25, 2026
Benchmarking genetic birth prevalence estimates against newborn screening dataMichael C Sierant, Nicholas Knoblauch, Evan Witt, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2025
Recessive genetic contribution to congenital heart disease in 5,424 probandsWeilai Dong, Sheng Chih Jin, Michael C Sierant, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 24, 2025
Genomic analysis of 11,555 probands identifies 60 dominant congenital heart disease genesMichael C Sierant, Sheng Chih Jin, Kaya Bilguvar, et al.
Iscience|October 21, 2020
Exome Sequencing Implicates Impaired GABA Signaling and Neuronal Ion Transport in Trigeminal NeuralgiaWeilai Dong, Sheng Chih Jin, August Allocco, 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 Medicine|October 20, 2020
Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalusSheng Chih Jin, Weilai Dong, Adam J Kundishora, et al.
Nature Genetics|September 29, 2020
Mutations disrupting neuritogenesis genes confer risk for cerebral palsySheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Genomics & Informatics|January 3, 2019
Single-Cell Ssequencing in Cancer: Recent Applications to Immunogenomics and Multi-omics ToolsMichael C Sierant, Jungmin Choi
American Journal of Human Genetics|April 25, 2026
Benchmarking genetic birth prevalence estimates against newborn screening dataMichael C Sierant, Nicholas Knoblauch, Evan Witt, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2025
Recessive genetic contribution to congenital heart disease in 5,424 probandsWeilai Dong, Sheng Chih Jin, Michael C Sierant, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 24, 2025
Genomic analysis of 11,555 probands identifies 60 dominant congenital heart disease genesMichael C Sierant, Sheng Chih Jin, Kaya Bilguvar, et al.
Iscience|October 21, 2020
Exome Sequencing Implicates Impaired GABA Signaling and Neuronal Ion Transport in Trigeminal NeuralgiaWeilai Dong, Sheng Chih Jin, August Allocco, 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 Medicine|October 20, 2020
Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalusSheng Chih Jin, Weilai Dong, Adam J Kundishora, et al.
Nature Genetics|September 29, 2020
Mutations disrupting neuritogenesis genes confer risk for cerebral palsySheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari, et al.
Pageof 1