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Human genomics

Showing results (761-770 of 1,110) with videos related to

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Human Genomics|April 23, 2024
GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tractXuanjin Du, Chunyan Wang, Jialu Liu, et al.
Human Genomics|February 4, 2026
Extrachromosomal DNA drives molecular and clinical heterogeneity in hepatocellular carcinoma: a multi-omics analysis and prognostic model developmentKai Huang, Guangquan Zhang, Shuai Hu, et al.
Human Genomics|February 15, 2026
From enrichment to interpretation: PS4-driven reclassification in Taiwanese inherited retinal degenerationYu-Shu Huang, Chien-Yu Lin, Yu-An Chen, et al.
Human Genomics|December 10, 2025
Genetic screening for hearing loss of 38,589 neonates with follow-up in South ChinaXia Gu, Runzhong Huang, Jie Xie, et al.
Human Genomics|December 26, 2024
Integrating single-cell RNA-seq and bulk RNA-seq to construct a neutrophil prognostic model for predicting prognosis and immune response in oral squamous cell carcinomaJinhang Wang, Zifeng Cui, Qiwen Song, et al.
Human Genomics|January 14, 2025
High clinical utility of long-read sequencing for precise diagnosis of congenital adrenal hyperplasia in 322 probandsYunpeng Wang, Gaohui Zhu, Danhua Li, et al.
Human Genomics|February 6, 2025
Sideroflexin family genes were dysregulated and associated with tumor progression in prostate cancersHua Huang, Huibo Lian, Wang Liu, et al.
Human Genomics|December 8, 2023
Whole mitogenome sequencing uncovers a relation between mitochondrial heteroplasmy and leprosy severityFelipe Gouvea de Souza, Moisés Batista da Silva, Gilderlanio S de Araújo, et al.
Human Genomics|December 8, 2023
Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese familiesXiuqin Bao, Danqing Qin, Jicheng Wang, et al.
Human Genomics|January 4, 2024
The diversity and clinical implications of genetic variants influencing clopidogrel bioactivation and response in the Emirati populationLubna Q Khasawneh, Habiba Alsafar, Hiba Alblooshi, et al.
Pageof 111

Showing results (761-770 of 1,110) with videos related to

Sort By:
Pageof 111
Human Genomics|April 23, 2024
GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tractXuanjin Du, Chunyan Wang, Jialu Liu, et al.
Human Genomics|February 4, 2026
Extrachromosomal DNA drives molecular and clinical heterogeneity in hepatocellular carcinoma: a multi-omics analysis and prognostic model developmentKai Huang, Guangquan Zhang, Shuai Hu, et al.
Human Genomics|February 15, 2026
From enrichment to interpretation: PS4-driven reclassification in Taiwanese inherited retinal degenerationYu-Shu Huang, Chien-Yu Lin, Yu-An Chen, et al.
Human Genomics|December 10, 2025
Genetic screening for hearing loss of 38,589 neonates with follow-up in South ChinaXia Gu, Runzhong Huang, Jie Xie, et al.
Human Genomics|December 26, 2024
Integrating single-cell RNA-seq and bulk RNA-seq to construct a neutrophil prognostic model for predicting prognosis and immune response in oral squamous cell carcinomaJinhang Wang, Zifeng Cui, Qiwen Song, et al.
Human Genomics|January 14, 2025
High clinical utility of long-read sequencing for precise diagnosis of congenital adrenal hyperplasia in 322 probandsYunpeng Wang, Gaohui Zhu, Danhua Li, et al.
Human Genomics|February 6, 2025
Sideroflexin family genes were dysregulated and associated with tumor progression in prostate cancersHua Huang, Huibo Lian, Wang Liu, et al.
Human Genomics|December 8, 2023
Whole mitogenome sequencing uncovers a relation between mitochondrial heteroplasmy and leprosy severityFelipe Gouvea de Souza, Moisés Batista da Silva, Gilderlanio S de Araújo, et al.
Human Genomics|December 8, 2023
Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese familiesXiuqin Bao, Danqing Qin, Jicheng Wang, et al.
Human Genomics|January 4, 2024
The diversity and clinical implications of genetic variants influencing clopidogrel bioactivation and response in the Emirati populationLubna Q Khasawneh, Habiba Alsafar, Hiba Alblooshi, et al.
Pageof 111