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Human Genomics|February 26, 2025
Causal effects of education, intelligence, and income on COVID-19: evidence from a Mendelian randomization studyYuqing Song, Ancha Baranova, Hongbao Cao, et al.
Human Genomics|February 21, 2025
Analysis of genotypic distribution and rare variants of patients with α/β-thalassemia screened in one hospital in Beijing, ChinaHan Zhang, Ziran Wang, Zhuo Yang, et al.
Human Genomics|January 17, 2025
The interplay of sex and genotype in disease associations: a comprehensive network analysis in the UK BiobankVivek Sriram, Jakob Woerner, Yong-Yeol Ahn, et al.
Human Genomics|January 6, 2025
Uncovering potential causal genes for undiagnosed congenital anomalies using an in-house pipeline for trio-based whole-genome sequencingJeong-Min Kim, Hye-Won Cho, Dong Mun Shin, et al.
Human Genomics|March 12, 2025
Establishing a European wastewater pathogen monitoring network employing aviation samples: a proof of conceptRobert Morfino, Bernd Manfred Gawlik, Simona Tavazzi, et al.
Human Genomics|September 3, 2024
The T-cell repertoire of Spanish patients with COVID-19 as a strategy to link T-cell characteristics to the severity of the diseaseFernando Marín-Benesiu, Lucia Chica-Redecillas, Verónica Arenas-Rodríguez, et al.
Human Genomics|August 28, 2024
Variant Impact Predictor database (VIPdb), version 2: trends from three decades of genetic variant impact predictorsYu-Jen Lin, Arul S Menon, Zhiqiang Hu, et al.
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.
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