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Human Genomics|January 24, 2009
Association tests and software for copy number variant dataVincent PlagnolHuman Genomics|November 1, 2022
Copy number variant analysis for syndromic congenital heart disease in the Chinese populationPing Li, Weicheng Chen, Mengru Li, et al.Human Genomics|September 27, 2022
Circular RNA hsa_circ_0000915 promotes propranolol resistance of hemangioma stem cells in infantile haemangiomasHongrang Chen, Yongsheng LiHuman Genomics|November 4, 2022
Integrated proteomic and metabolomic modules identified as biomarkers of mortality in the Atherosclerosis Risk in Communities study and the African American Study of Kidney Disease and HypertensionLinda Zhou, Aditya Surapaneni, Eugene P Rhee, et al.Human Genomics|November 28, 2023
MmisAT and MmisP: an efficient and accurate suite of variant analysis toolkit for primary mitochondrial diseasesShuangshuang Huang, Zhaoyu Wu, Tong Wang, et al.Human Genomics|November 26, 2023
Targeted sequencing of high-density SNPs provides an enhanced tool for forensic applications and genetic landscape exploration in Chinese Korean ethnic groupQiong Lan, Yifeng Lin, Xi Wang, et al.Human Genomics|December 19, 2023
SPP1 is associated with adverse prognosis and predicts immunotherapy efficacy in penile cancerYuantao Zou, Xingliang Tan, Gangjun Yuan, et al.Human Genomics|December 19, 2023
The Human Genome Organisation (HUGO) and a vision for Ecogenomics: the Ecological Genome ProjectBenjamin Capps, Ruth Chadwick, Zohar Lederman, et al.Human Genomics|March 27, 2024
Paternal aging impacts expression and epigenetic markers as early as the first embryonic tissue lineage differentiationMichelle M Denomme, Blair R McCallie, Mary E Haywood, et al.Human Genomics|February 27, 2024
Combining full-length gene assay and SpliceAI to interpret the splicing impact of all possible SPINK1 coding variantsHao Wu, Jin-Huan Lin, Xin-Ying Tang, et al.Pageof 112