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Human Genomics|August 10, 2021
A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variantsMaria-Theodora Pandi, Maria Koromina, Iordanis Tsafaridis, et al.Human Genomics|February 14, 2023
Genetic association of PRKCD and CARD9 polymorphisms with Vogt-Koyanagi-Harada disease in the Chinese Han populationChunya Zhou, Shiya Cai, Yuhong Xie, et al.Human Genomics|November 30, 2016
Head-and-neck squamous cell carcinoma risk in smokers: no association detected between phenotype and AHR, CYP1A1, CYP1A2, or CYP1B1 genotypeLucia F Jorge-Nebert, Ge Zhang, Keith M Wilson, et al.Human Genomics|October 30, 2016
Navigating the dynamic landscape of long noncoding RNA and protein-coding gene annotations in GENCODESaakshi Jalali, Shrey Gandhi, Vinod ScariaHuman Genomics|March 5, 2017
Genetic determinants of clinical heterogeneity of the coronary artery disease in the population of Hyderabad, IndiaRayabarapu Pranavchand, Arramraju Sreenivas Kumar, Battini Mohan ReddyHuman Genomics|November 25, 2016
Targeted next generation sequencing identifies novel NOTCH3 gene mutations in CADASIL diagnostics patientsNeven Maksemous, Robert A Smith, Larisa M Haupt, et al.Human Genomics|October 22, 2022
Nidogen-1 could play a role in diabetic kidney disease development in type 2 diabetes: a genome-wide association meta-analysisAhmed Khattab, Ali TorkamaniHuman Genomics|February 9, 2021
Pathogenic convergence of CNVs in genes functionally associated to a severe neuromotor developmental delay syndromeJuan L García-Hernández, Luis A Corchete, Íñigo Marcos-Alcalde, et al.Human Genomics|February 11, 2021
The Human Genome Organisation (HUGO) and the 2020 COVID-19 pandemicBenjamin Capps, Yann Joly, John Mulvihill, et al.Pageof 112