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Human genomics

Showing results (211-220 of 1,251) with videos related to

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Human Genomics|January 8, 2026
Molecular mechanisms and therapeutic strategies for the recurrent F9 (c.520 + 13 A > G) variant in hemophilia BHuayang Zhang, Chong Wang, Meixiu Gu, et al.
Human Genomics|March 1, 2023
Global distribution of functionally important CYP2C9 alleles and their inferred metabolic consequencesYitian Zhou, Lenka Nevosadová, Erik Eliasson, et al.
Human Genomics|March 1, 2023
Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritanceValerie Jacquemin, Nassim Versbraegen, Sarah Duerinckx, et al.
Human Genomics|March 21, 2023
Biallelic variants in NOS3 and GUCY1A3, the two major genes of the nitric oxide pathway, cause moyamoya cerebral angiopathyStéphanie Guey, Dominique Hervé, Manoëlle Kossorotoff, et al.
Human Genomics|February 1, 2023
Genome-wide allele and haplotype-sharing patterns suggested one unique Hmong-Mein-related lineage and biological adaptation history in Southwest ChinaGuanglin He, Jiawen Wang, Lin Yang, et al.
Human Genomics|February 11, 2023
Integrated analysis of RNA methylation regulators crosstalk and immune infiltration for predictive and personalized therapy of diabetic nephropathyJia Li, Dongwei Liu, Jingjing Ren, et al.
Human Genomics|July 3, 2025
Shared genetic architecture between stroke and blood lipids: a large-scale genome-wide cross-trait analysisWenya Bai, Guilin Zhou, Huan Jiang, et al.
Human Genomics|December 10, 2025
Recurrent somatic copy number alterations in resected cerebral cavernous malformationsAndrew K Ressler, Evon Debose-Scarlett, Amanda Fuenzalida, et al.
Human Genomics|December 6, 2025
Genome-wide methylation profiles of primary and matched distant metastasis: insights from the Dutch Early-Stage melanoma (D-ESMEL) studyJasper Ouwerkerk, Thamila Kerkour, Antien Mooyaart, et al.
Human Genomics|December 5, 2025
Data visiting governance: a conceptual frameworkDonrich Thaldar
Pageof 126

Showing results (211-220 of 1,251) with videos related to

Sort By:
Pageof 126
Human Genomics|January 8, 2026
Molecular mechanisms and therapeutic strategies for the recurrent F9 (c.520 + 13 A > G) variant in hemophilia BHuayang Zhang, Chong Wang, Meixiu Gu, et al.
Human Genomics|March 1, 2023
Global distribution of functionally important CYP2C9 alleles and their inferred metabolic consequencesYitian Zhou, Lenka Nevosadová, Erik Eliasson, et al.
Human Genomics|March 1, 2023
Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritanceValerie Jacquemin, Nassim Versbraegen, Sarah Duerinckx, et al.
Human Genomics|March 21, 2023
Biallelic variants in NOS3 and GUCY1A3, the two major genes of the nitric oxide pathway, cause moyamoya cerebral angiopathyStéphanie Guey, Dominique Hervé, Manoëlle Kossorotoff, et al.
Human Genomics|February 1, 2023
Genome-wide allele and haplotype-sharing patterns suggested one unique Hmong-Mein-related lineage and biological adaptation history in Southwest ChinaGuanglin He, Jiawen Wang, Lin Yang, et al.
Human Genomics|February 11, 2023
Integrated analysis of RNA methylation regulators crosstalk and immune infiltration for predictive and personalized therapy of diabetic nephropathyJia Li, Dongwei Liu, Jingjing Ren, et al.
Human Genomics|July 3, 2025
Shared genetic architecture between stroke and blood lipids: a large-scale genome-wide cross-trait analysisWenya Bai, Guilin Zhou, Huan Jiang, et al.
Human Genomics|December 10, 2025
Recurrent somatic copy number alterations in resected cerebral cavernous malformationsAndrew K Ressler, Evon Debose-Scarlett, Amanda Fuenzalida, et al.
Human Genomics|December 6, 2025
Genome-wide methylation profiles of primary and matched distant metastasis: insights from the Dutch Early-Stage melanoma (D-ESMEL) studyJasper Ouwerkerk, Thamila Kerkour, Antien Mooyaart, et al.
Human Genomics|December 5, 2025
Data visiting governance: a conceptual frameworkDonrich Thaldar
Pageof 126