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Human Genomics|November 6, 2024
Best practices for germline variant and DNA methylation analysis of second- and third-generation sequencing dataFerdinando Bonfiglio, Andrea Legati, Vito Alessandro Lasorsa, et al.
Human Genomics|November 19, 2024
Analysis of public perceptions on the use of artificial intelligence in genomic medicineJack E Harrison, Fiona Lynch, Zornitza Stark, et al.
Human Genomics|November 4, 2024
Drosophila Toxicogenomics: genetic variation and sexual dimorphism in susceptibility to 4-MethylimidazoleKatelynne M Collins, Elisabeth Howansky, Sarah C Macon-Foley, et al.
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-Gieske
Human 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.
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