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Human Genomics|April 2, 2023
Allelic phenotype prediction of phenylketonuria based on the machine learning methodYang Fang, Jinshuang Gao, Yaqing Guo, et al.Human Genomics|March 29, 2023
In silico prioritisation of microRNA-associated common variants in multiple sclerosisIfeolutembi A Fashina, Claire E McCoy, Simon J FurneyHuman Genomics|April 13, 2021
Targeted exome sequencing identifies mutational landscape in a cohort of 1500 Chinese patients with non-small cell lung carcinoma (NSCLC)Ya-Jun Zhou, Wei Zheng, Qing-Hua Zeng, et al.Human Genomics|July 2, 2014
Ranking non-synonymous single nucleotide polymorphisms based on disease conceptsHashem A Shihab, Julian Gough, Matthew Mort, et al.Human Genomics|July 1, 2020
Novel biallelic loss-of-function variants in CEP290 cause Joubert syndrome in two siblingsXiang Wang, Zhu Zhang, Xueguang Zhang, et al.Human Genomics|April 18, 2015
Evaluation of copy number variation and gene expression in neurofibromatosis type-1-associated malignant peripheral nerve sheath tumoursLaura E Thomas, Jincy Winston, Ellie Rad, et al.Human Genomics|May 18, 2023
Genetic mutations in HER2-positive breast cancer: possible association with response to trastuzumab therapyNermine H Zakaria, Doaa Hashad, Marwa H Saied, et al.Human Genomics|November 20, 2012
6th Golden Helix Pharmacogenomics Day: pharmacogenomics and individualized therapyMaja Stojiljkovic, Amira Fazlagic, Lidija Dokmanovic-Krivokapic, et al.Human Genomics|November 20, 2012
Collaborative software for traditional and translational researchAri E Berman, William K Barnett, Sean D MooneyHuman Genomics|November 20, 2012
An emerging role for microRNAs in NF1 tumorigenesisAshni Sedani, David N Cooper, Meena UpadhyayaPageof 112