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Page 1
Assessing Postnatal Mortality in Smith-Lemli-Opitz Syndrome.
Selvaraman A, Rahhal S, Bianconi S, Furnary T, Porter FD. Selvaraman A, et al. Among authors: furnary t. Am J Med Genet A. 2024 Sep 13:e63875. doi: 10.1002/ajmg.a.63875. Online ahead of print. Am J Med Genet A. 2024. PMID: 39271956
An AI-powered patient triage platform for future viral outbreaks using COVID-19 as a disease model.
Charkoftaki G, Aalizadeh R, Santos-Neto A, Tan WY, Davidson EA, Nikolopoulou V, Wang Y, Thompson B, Furnary T, Chen Y, Wunder EA, Coppi A, Schulz W, Iwasaki A, Pierce RW, Cruz CSD, Desir GV, Kaminski N, Farhadian S, Veselkov K, Datta R, Campbell M, Thomaidis NS, Ko AI; Yale IMPACT Study Team; Thompson DC, Vasiliou V. Charkoftaki G, et al. Among authors: furnary t. Hum Genomics. 2023 Aug 29;17(1):80. doi: 10.1186/s40246-023-00521-4. Hum Genomics. 2023. PMID: 37641126 Free PMC article.
Endocrine pancreas-specific Gclc gene deletion causes a severe diabetes phenotype.
Davidson EA, Chen Y, Singh S, Orlicky DJ, Thompson B, Wang Y, Charkoftaki G, Furnary TA, Cardone RL, Kibbey RG, Shearn CT, Nebert DW, Thompson DC, Vasiliou V. Davidson EA, et al. Among authors: furnary ta. bioRxiv [Preprint]. 2023 Jun 26:2023.06.13.544855. doi: 10.1101/2023.06.13.544855. bioRxiv. 2023. PMID: 37398356 Free PMC article. Preprint.