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Human genomics

Showing results (531-540 of 1,110) with videos related to

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Human Genomics|January 24, 2009
Novel variants of major drug-metabolising enzyme genes in diverse African populations and their predicted functional effectsAlice Matimba, Jurgen Del-Favero, Christine Van Broeckhoven, et al.
Human Genomics|May 31, 2019
Statement on bioinformatics and capturing the benefits of genome sequencing for societyBenjamin Capps, Ruth Chadwick, Yann Joly, et al.
Human Genomics|April 12, 2019
The significance of trisomy 7 mosaicism in noninvasive prenatal screeningYiming Qi, Jiexia Yang, Yaping Hou, et al.
Human Genomics|July 28, 2016
A comparative study of k-spectrum-based error correction methods for next-generation sequencing data analysisIsaac Akogwu, Nan Wang, Chaoyang Zhang, et al.
Human Genomics|August 23, 2025
Increasing pathogenic germline variant diagnosis rates in precision medicine: current best practices and future opportunitiesSonam Dukda, Manoharan Kumar, Andrew Calcino, et al.
Human Genomics|June 25, 2015
SIRT1 affects DNA methylation of polycomb group protein target genes, a hotspot of the epigenetic shift observed in ageingLuisa A Wakeling, Laura J Ions, Suzanne M Escolme, et al.
Human Genomics|June 14, 2015
Is the genomic translational pipeline being disrupted?Marc S Williams
Human Genomics|March 11, 2018
2-deoxy-2-[18]fluoro-D-glucose PET/CT (18FDG PET/CT) may not be a viable biomarker in Pompe diseaseU Plöckinger, V Prasad, A Ziagaki, et al.
Human Genomics|March 2, 2018
A hypomorphic inherited pathogenic variant in DDX3X causes male intellectual disability with additional neurodevelopmental and neurodegenerative featuresGeorgios Kellaris, Kamal Khan, Shahid M Baig, et al.
Human Genomics|November 16, 2017
Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadismAbdulaziz Alsemari, Banan Al-Younes, Ewa Goljan, et al.
Pageof 111

Showing results (531-540 of 1,110) with videos related to

Sort By:
Pageof 111
Human Genomics|January 24, 2009
Novel variants of major drug-metabolising enzyme genes in diverse African populations and their predicted functional effectsAlice Matimba, Jurgen Del-Favero, Christine Van Broeckhoven, et al.
Human Genomics|May 31, 2019
Statement on bioinformatics and capturing the benefits of genome sequencing for societyBenjamin Capps, Ruth Chadwick, Yann Joly, et al.
Human Genomics|April 12, 2019
The significance of trisomy 7 mosaicism in noninvasive prenatal screeningYiming Qi, Jiexia Yang, Yaping Hou, et al.
Human Genomics|July 28, 2016
A comparative study of k-spectrum-based error correction methods for next-generation sequencing data analysisIsaac Akogwu, Nan Wang, Chaoyang Zhang, et al.
Human Genomics|August 23, 2025
Increasing pathogenic germline variant diagnosis rates in precision medicine: current best practices and future opportunitiesSonam Dukda, Manoharan Kumar, Andrew Calcino, et al.
Human Genomics|June 25, 2015
SIRT1 affects DNA methylation of polycomb group protein target genes, a hotspot of the epigenetic shift observed in ageingLuisa A Wakeling, Laura J Ions, Suzanne M Escolme, et al.
Human Genomics|June 14, 2015
Is the genomic translational pipeline being disrupted?Marc S Williams
Human Genomics|March 11, 2018
2-deoxy-2-[18]fluoro-D-glucose PET/CT (18FDG PET/CT) may not be a viable biomarker in Pompe diseaseU Plöckinger, V Prasad, A Ziagaki, et al.
Human Genomics|March 2, 2018
A hypomorphic inherited pathogenic variant in DDX3X causes male intellectual disability with additional neurodevelopmental and neurodegenerative featuresGeorgios Kellaris, Kamal Khan, Shahid M Baig, et al.
Human Genomics|November 16, 2017
Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadismAbdulaziz Alsemari, Banan Al-Younes, Ewa Goljan, et al.
Pageof 111