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Human Genomics|August 15, 2024
Assessing the contribution of genes involved in monogenic bone disorders to the etiology of atypical femoral fracturesNatalia Garcia-Giralt, Diana Ovejero, Daniel Grinberg, et al.Human Genomics|June 24, 2024
Elucidating the role of liver enzymes as markers and regulators in ovarian cancer: a synergistic approach using Mendelian randomization, single-cell analysis, and clinical evidenceYinxing Zhu, Min Jiang, Zihan Gu, et al.Human Genomics|June 13, 2024
Next-generation sequencing profiling of miRNAs in individuals with 22q11.2 deletion syndrome revealed altered expression of miR-185-5pAnelisa Gollo Dantas, Beatriz Carvalho Nunes, Natália Nunes, et al.Human Genomics|June 17, 2024
Application of mendelian randomization in ocular diseases: a reviewXiran Zhang, Weichen Yuan, Jun Xu, et al.Human Genomics|October 23, 2023
Transcriptome driven discovery of novel candidate genes for human neurological disorders in the telomer-to-telomer genome assembly eraClemens Falker-GieskeHuman Genomics|March 21, 2024
Hemorrhoidal disease and its genetic association with depression, bipolar disorder, anxiety disorders, and schizophrenia: a bidirectional mendelian randomization studyZhiguang Huang, Jian Huang, Chun Kai Leung, et al.Human Genomics|March 25, 2024
Clinical spectrum of Transthyretin amyloidogenic mutations among diverse population originsAntonella De Lillo, Gita A Pathak, Aislinn Low, et al.Human Genomics|March 23, 2024
Structural rearrangements as a recurrent pathogenic mechanism for SETBP1 haploinsufficiencyV Alesi, S Genovese, M C Roberti, et al.Human Genomics|April 2, 2024
Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association studyEunyoung Choi, Jaeseung Song, Yubin Lee, et al.Human Genomics|April 2, 2024
Profiling the role of m6A effectors in the regulation of pluripotent reprogrammingWenjun Wang, Lei Zhou, Hui Li, et al.Pageof 111