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Human Genomics|July 1, 2026
Analysis of whole-exome sequencing data from nearly 10,000 Iranian individuals: identification of recessive mitochondrial disease variants and proposal of a population-specific carrier screening panelMohadeseh Fathi, Parvaneh Karimzadeh, Farzad Ahmadabadi, et al.Human Genomics|July 18, 2026
Decoding dry eye disease based on bioinformatics and in vitro experimental: the role of immune responses and natural product interventionXi Long, Guicheng Liu, Pei Liu, et al.Human Genomics|March 20, 2021
Genetic-variant hotspots and hotspot clusters in the human genome facilitating adaptation while increasing instabilityXi Long, Hong XueHuman Genomics|November 22, 2018
Trans-activation-based risk assessment of BRCA1 BRCT variants with unknown clinical significanceJonas Langerud, Elisabeth Jarhelle, Marijke Van Ghelue, et al.Human Genomics|February 17, 2019
Considerations for the use of Cre recombinase for conditional gene deletion in the mouse lensPhuong T Lam, Stephanie L Padula, Thanh V Hoang, et al.Human Genomics|November 15, 2018
Perceptions of students in health and molecular life sciences regarding pharmacogenomics and personalized medicineLejla Mahmutovic, Betul Akcesme, Camil Durakovic, et al.Human Genomics|February 24, 2019
vi-HMM: a novel HMM-based method for sequence variant identification in short-read dataMan Tang, Mohammad Shabbir Hasan, Hongxiao Zhu, et al.Human Genomics|August 29, 2019
Translating pharmacogenomics into clinical decisions: do not let the perfect be the enemy of the goodKristi Krebs, Lili MilaniHuman Genomics|January 29, 2021
Genetic risk factors for autoimmune hepatitis: implications for phenotypic heterogeneity and biomarkers for drug responseTakashi Higuchi, Shomi Oka, Hiroshi Furukawa, et al.Human Genomics|December 14, 2021
Estimating prevalence of human traits among populations from polygenic risk scoresBritney E Graham, Brian Plotkin, Louis Muglia, et al.Pageof 112