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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.
Human Genomics|September 6, 2023
Generation and characterization of a zebrafish knockout model of abcb4, a homolog of the human multidrug efflux transporter P-glycoproteinJinhee Park, Hyosung Kim, Leen Alabdalla, et al.
Human Genomics|September 1, 2023
Genetics in ophthalmology: molecular blueprints of retinoblastomaLeon Marković, Anja Bukovac, Ana Maria Varošanec, et al.
Human Genomics|August 17, 2023
Next-generation sequencing analysis of the molecular spectrum of thalassemia in Southern Jiangxi, ChinaTong Yang, Xuemei Luo, Yanqiu Liu, et al.
Human Genomics|January 10, 2024
A novel upregulated hsa_circ_0032746 regulates the oncogenesis of esophageal squamous cell carcinoma by regulating miR-4270/MCM3 axisSachin Mulmi Shrestha, Xin Fang, Hui Ye, et al.
Human Genomics|December 15, 2023
Mitochondrial DNA copy number variation across three generations: a possible biomarker for assessing perinatal outcomesHisanori Fukunaga, Atsuko Ikeda
Human Genomics|December 15, 2023
LINE-1 global DNA methylation, iron homeostasis genes, sex and age in sudden sensorineural hearing loss (SSNHL)Veronica Tisato, Alessandro Castiglione, Andrea Ciorba, et al.
Human Genomics|November 23, 2023
Dispersed DNA variants underlie hearing loss in South Florida's minority populationLéShon Peart, Joanna Gonzalez, Dayna Morel Swols, et al.
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