Categoría: ORIGINAL ARTICLE
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Genetic variations in CYP2A6, CYP2E1, GSTM1, GSTT1 genes and the risk of Nasopharyngeal carcinoma in North African population
Annals of Human Genetics, EarlyView.
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Causal effect of severe and non‐severe malaria on dyslipidemia in African Ancestry individuals: A Mendelian randomization study
Annals of Human Genetics, EarlyView.
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The prevalence and linkage disequilibrium of 21 genetic variations related to thrombophilia, folate cycle, and hypertension in reproductive age women of Rostov region (Russia)
Annals of Human Genetics, Volume 88, Issue 2, Page 171-181, March 2024.
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Clinical application of prospective whole‐exome sequencing in the diagnosis of genetic disease: Experience of a regional disease center in South Korea
Annals of Human Genetics, Volume 88, Issue 2, Page 101-112, March 2024.
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The effect of TRIM5 variants on the susceptibility to HIV‐1 infection and disease progression in the Polish population
Annals of Human Genetics, Volume 88, Issue 2, Page 154-170, March 2024.
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Low‐pass whole genome sequencing is a reliable and cost‐effective approach for copy number variant analysis in the clinical setting
Annals of Human Genetics, Volume 88, Issue 2, Page 113-125, March 2024.
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Association of blood lipid profiles and asthma: A bidirectional two‐sample Mendelian randomization study
Annals of Human Genetics, EarlyView.
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ABCA1 variant rs9282541 is associated with metabolic syndrome in Maya children
Annals of Human Genetics, EarlyView.
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Investigation of the association between the Toll‐like receptor 1 rs4833095 variation and gastric adenocarcinoma recurrence
Annals of Human Genetics, EarlyView.