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Human Genomics|October 6, 2018
Identification of gross deletions in FBN1 gene by MLPAHang Yang, Yanyun Ma, Mingyao Luo, et al.Human Genomics|September 26, 2021
Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 lociChris M Pappas, Moussa A Zouache, Stacie Matthews, et al.Human Genomics|May 10, 2023
Genetic basis of STEM occupational choice and regional economic performance: a UK biobank genome-wide association studyChen Zhu, Qiran Zhao, Jianbo He, et al.Human Genomics|May 15, 2023
Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni familiesMaria Asaad, Mona Mahfood, Abdullah Al Mutery, et al.Human Genomics|May 3, 2023
Twist exome capture allows for lower average sequence coverage in clinical exome sequencingBurcu Yaldiz, Erdi Kucuk, Juliet Hampstead, et al.Human Genomics|April 25, 2023
Genome-wide analysis toward the epigenetic aetiology of myelodysplastic syndrome disease progression and pharmacoepigenomic basis of hypomethylating agents drug treatment responseStavroula Siamoglou, Ruben Boers, Maria Koromina, et al.Human Genomics|April 21, 2021
An ensemble of the iCluster method to analyze longitudinal lncRNA expression data for psoriasis patientsSuyan Tian, Chi WangHuman Genomics|August 14, 2025
Spatial transcriptomics and scRNA-seq: decoding tumor complexity and constructing prognostic models in colorectal cancerWei Song, Yatao Wang, Min Zhou, et al.Human Genomics|August 7, 2025
TRP channels in hepatocellular carcinoma: integrative Mendelian randomization and multi-omics analyses highlight MCOLN3/TRPV4 as candidate dual-effect biomarkersZhe Xu, Chong Pang, Xundi XuHuman Genomics|November 13, 2025
Fetal fractions mediate the association between total cell-free DNA and preeclampsia risk in a non-invasive prenatal testing cohortBin Zhang, Xusheng Chen, Sijie Xi, et al.Pageof 112