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Human Genomics|April 22, 2017
Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia veraElina A M Hirvonen, Esa Pitkänen, Kari Hemminki, et al.Human Genomics|November 20, 2016
A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive diseaseElisa Napolitano Ferreira, Bruna Durães Figueiredo Barros, Jorge Estefano de Souza, et al.Human Genomics|November 23, 2016
Transcriptome analysis reveals manifold mechanisms of cyst development in ADPKDRita M C de Almeida, Sherry G Clendenon, William G Richards, et al.Human Genomics|February 27, 2014
Forced swim test induces divergent global transcriptomic alterations in the hippocampus of high versus low novelty-seeker ratsPothitos M Pitychoutis, Despina Sanoudou, Margarita Papandreou, et al.Human Genomics|August 30, 2019
Three miRNAs cooperate with host genes involved in human cardiovascular diseaseYan Zhu, Jingjing Xie, Hong SunHuman Genomics|August 25, 2019
Diversity of ATM gene variants: a population-based genome data analysis for precision medicineHisanori Fukunaga, Yasuyuki Taki, Kevin M PriseHuman Genomics|May 11, 2015
Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfectaKatre Maasalu, Tiit Nikopensius, Sulev Kõks, et al.Human Genomics|May 1, 2015
Comparative sequence- and structure-inspired drug design for PilF protein of Neisseria meningitidisAbijeet Singh Mehta, Kirti Snigdha, M Sharada Potukuchi, et al.Human Genomics|August 30, 2025
Multi-omics signature of healthy versus unhealthy lifestyles reveals associations with diseasesGrace Fu, Blake R Rushing, Lee Graves, et al.Human Genomics|August 30, 2025
DNA methylation in adaptation to high-altitude environments and pathogenesis of related diseasesXingkai Zhang, Yuxi Yang, Qinghai ShiPageof 112