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Human Genomics|April 3, 2024
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous populationNejat Mahdieh, Morteza Heidari, Zahra Rezaei, et al.Human Genomics|February 7, 2024
Gene expression analysis reveals diabetes-related gene signaturesM I Farrim, A Gomes, D Milenkovic, et al.Human Genomics|February 3, 2024
Polymorphisms in transcription factor binding sites and enhancer regions and pancreatic ductal adenocarcinoma riskPelin Ünal, Ye Lu, Bas Bueno-de-Mesquita, et al.Human Genomics|January 30, 2024
Congenital septal defects in Karachi, Pakistan: an update of mutational screening by high-resolution melting (HRM) analysis of MTHFR C677TSyed Irtiza Ali, Obaid Yusuf Khan, Nadir Naveed, et al.Human Genomics|January 31, 2024
The effectiveness of expanded carrier screening based on next-generation sequencing for severe monogenic genetic diseasesXue Zhang, Qian Chen, Junnan Li, et al.Human Genomics|February 7, 2024
Protein-protein interaction network-based integration of GWAS and functional data for blood pressure regulation analysisEvridiki-Pandora G Tsare, Maria I Klapa, Nicholas K MoschonasHuman Genomics|February 2, 2024
Solanidine is a sensitive and specific dietary biomarker for CYP2D6 activityJohanna I Kiiski, Mikko Neuvonen, Mika Kurkela, et al.Human Genomics|May 22, 2024
Polygenic risk score predicting susceptibility and outcome of benign prostatic hyperplasia in the Han ChineseSheng-Chun Hung, Li-Wen Chang, Tzu-Hung Hsiao, et al.Human Genomics|May 24, 2024
Critical insights on "Association of the C allele of rs479200 in the EGLN1 gene with COVID‑19 severity in Indian population: a novel finding"Nimita Deora, Priya Agrohi, Prashant K Mallick, et al.Human Genomics|May 10, 2024
Development, validation and application of single molecule molecular inversion probe based novel integrated genetic screening method for 29 common lysosomal storage disorders in IndiaHarsh Sheth, Aadhira Nair, Riddhi Bhavsar, et al.Pageof 111