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Frontiers in Genetics|September 7, 2023
Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHDClaudia Strafella, Valerio Caputo, Sara Bortolani, et al.
Frontiers in Genetics|September 8, 2023
PSF toolkit: an R package for pathway curation and topology-aware analysisSiras Hakobyan, Ani Stepanyan, Lilit Nersisyan, et al.
Frontiers in Genetics|August 25, 2023
Natural selection shapes the evolution of SARS-CoV-2 Omicron in BangladeshMohammad Tanbir Habib, Saikt Rahman, Mokibul Hassan Afrad, et al.
Frontiers in Genetics|August 24, 2023
Case report: Progressive pulmonary artery hypertension in a case of megalencephaly-capillary malformation syndromeYuri Yoh, Tadashi Shiohama, Tomoko Uchida, et al.
Frontiers in Genetics|August 24, 2023
Microbiota composition and its impact on DNA methylation in colorectal cancerMelva Gutierrez-Angulo, Maria de la Luz Ayala-Madrigal, Jose Miguel Moreno-Ortiz, et al.
Frontiers in Genetics|August 24, 2023
Long-term safety and dose escalation of intracerebroventricular CLN5 gene therapy in sheep supports clinical translation for CLN5 Batten diseaseNadia L Mitchell, Samantha J Murray, Martin P Wellby, et al.
Frontiers in Genetics|August 28, 2023
Prognostic effect of lncRNA BBOX1-AS1 in malignancies: a meta-analysisGuangyao Lin, Yongzhou Wang, Li Deng, et al.
Frontiers in Genetics|August 21, 2023
HMG-boxes, ribosomopathies and neurodegenerative diseaseTom Moss, Mark S LeDoux, Colyn Crane-Robinson
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