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Human Genomics|June 5, 2024
Deep learning-based pathway-centric approach to characterize recurrent hepatocellular carcinoma after liver transplantationJeffrey To, Soumita Ghosh, Xun Zhao, et al.
Human Genomics|November 15, 2023
Identification of genetic loci jointly influencing COVID-19 and coronary heart diseasesSiyue Wang, Hexiang Peng, Feng Chen, et al.
Human Genomics|October 5, 2023
Decoding cell-type contributions to the cfRNA transcriptomic landscape of liver cancerAram Safrastyan, Christian Höner Zu Siederdissen, Damian Wollny
Human Genomics|October 6, 2023
Epigenomic signature of major congenital heart defects in newborns with Down syndromeJulia S Mouat, Shaobo Li, Swe Swe Myint, et al.
Human Genomics|October 5, 2023
Revealing parental mosaicism: the hidden answer to the recurrence of apparent de novo variantsMianne Lee, Adrian C Y Lui, Joshua C K Chan, et al.
Human Genomics|October 3, 2023
Whole-exome sequencing reveals candidate high-risk susceptibility genes for endometriosisSusanna Nousiainen, Outi Kuismin, Siiri Reinikka, et al.
Human Genomics|September 22, 2023
ANXA1 is identified as a key gene associated with high risk and T cell infiltration in primary sclerosing cholangitisJian Zhang, Huiwen Wang, Jinqing Liu, et al.
Human Genomics|September 26, 2023
The causal relationship between COVID-19 and seventeen common digestive diseases: a two-sample, multivariable Mendelian randomization studyZhiqi Wang, Huanyu Zhou, Shurui Zhang, et al.
Human Genomics|October 3, 2023
Mendelian randomization analysis reveals fresh fruit intake as a protective factor for urolithiasisYiwei Lin, Cheng Zhou, Yuqing Wu, et al.
Human Genomics|September 16, 2024
Whole-exome sequencing to identify causative variants in juvenile sudden cardiac deathMartina Modena, Alberto Giannoni, Alberto Aimo, et al.
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