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Human Genomics|November 16, 2023
The hospital Israelita Albert Einstein standards for constitutional sequence variants classification: version 2023Caio Robledo D'Angioli Costa Quaio, José Ricardo Magliocco Ceroni, Michele Araújo Pereira, et al.Human Genomics|July 17, 2023
Landscape of germline pathogenic variants in patients with dual primary breast and lung cancerNing-Yuan Lee, Melissa Hum, Sabna Zihara, et al.Human Genomics|July 20, 2023
Characterizing the polygenic architecture of complex traits in populations of East Asian and European descentAntonella De Lillo, Frank R Wendt, Gita A Pathak, et al.Human Genomics|July 7, 2023
The impact of ABCB1, CYP3A4/5 and ABCG2 gene polymorphisms on rivaroxaban trough concentrations and bleeding events in patients with non-valvular atrial fibrillationTingting Wu, Shuyi Wu, Li Li, et al.Human Genomics|July 7, 2023
Monitoring SARS-CoV-2 variants in wastewater of Dhaka City, Bangladesh: approach to complement public health surveillance systemsRehnuma Haque, Mohammad Enayet Hossain, Mojnu Miah, et al.Human Genomics|July 7, 2023
Phenotypic variability to medication management: an update on fragile X syndromeNasser A Elhawary, Imad A AlJahdali, Iman S Abumansour, et al.Human Genomics|July 7, 2023
Alzheimer's disease: using gene/protein network machine learning for molecule discovery in olive oilLuís Rita, Natalie R Neumann, Ivan Laponogov, et al.Human Genomics|August 16, 2023
Determining the utility of diagnostic genomics: a conceptual frameworkAndrew Mallett, Zornitza Stark, Zoe Fehlberg, et al.Human Genomics|August 8, 2023
The application of long-read sequencing in clinical settingsJosephine B Oehler, Helen Wright, Zornitza Stark, et al.Human Genomics|September 5, 2023
RUN(X) out of blood: emerging RUNX1 functions beyond hematopoiesis and links to Down syndromeEsteban J Rozen, Christopher D Ozeroff, Mary Ann AllenPageof 112