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HGG Advances|July 21, 2022
Erratum: Discovery of a neuromuscular syndrome caused by biallelic variants in <i>ASCC3</i>Divya Nair, Dong Li, Hannah Erdogan, et al.HGG Advances|January 20, 2022
Discovery of a neuromuscular syndrome caused by biallelic variants in <i>ASCC3</i>Divya Nair, Dong Li, Hannah Erdogan, et al.Biorxiv : the Preprint Server for Biology|May 25, 2026
A novel mouse model of rare neurodevelopmental disorder, TBCK SyndromeAshley J Melendez-Perez, Emily L Durham, Dana E Layo-Carris, et al.Nature Cardiovascular Research|January 6, 2026
Pathogenetic mechanisms of muscle-specific ribosomes in dilated cardiomyopathyMichael R Murphy, Mythily Ganapathi, Esther R Rotlevi, et al.Life (Basel, Switzerland)|January 28, 2026
Coliform Load and Antimicrobial Resistance in Ghana's Seafood Processing Effluent (2021-2024): Evidence of Operational Improvement and Persistent AMR RiskEbenezer Worlanyo Wallace-Dickson, Meldon Ansah-Koi Agyarkwa, Nana Ama Browne Klutse, et al.European Journal of Human Genetics : EJHG|June 3, 2020
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndromeTheodore G Drivas, Dong Li, Divya Nair, et al.Science Advances|December 3, 2020
Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patientsLaura Bryant, Dong Li, Samuel G Cox, et al.Pageof 10