Gavin R Oliver

Publication Activity (10 Years)

Years Active: 2019-2021
Publications (10 Years): 5

Top Topics

Top Venues

Molecular genetics & genomic medicine

Journal of medical Internet research

This page only lists publications with an associated author ORCID identifier.

Publications

Saranya Sankaranarayanan, Jagadheshwar Balan, Jesse R Walsh, Yanhong Wu, Sara Minnich, Amy L Piazza, Collin Osborne, Gavin R Oliver, Jessica Lesko, Kathy L Bates, Kia Khezeli, Darci R Block, Margaret A DiGuardo, Justin Kreuter, John C O'Horo, John Kalantari, Eric W Klee, Mohamed E Salama, Benjamin R Kipp, William George Morice, Garrett Jenkinson
COVID-19 Mortality Prediction From Deep Learning in a Large Multistate Electronic Health Record and Laboratory Information System Data Set: Algorithm Development and Validation. Journal of medical Internet research 23 (9) (2021)
Gavin R Oliver, Sofia Marcano-Bonilla, Jonathan Quist, Ezequiel J Tolosa, Eriko Iguchi, Amy A Swanson, Nicole L Hoppman, Tanya Schwab, Ashley Sigafoos, Naresh Prodduturi, Jesse S Voss, Shannon M Knight, Jin Zhang, Numrah Fadra, Raul Urrutia, Michael Zimmerman, Jan B Egan, Anthony G Bilyeu, Jin Jen, Ema Veras, Rema'a Al-Safi, Matthew Block, Sarah Kerr, Martin E Fernandez-Zapico, John K Schoolmeester, Eric W Klee
LPCAT1-TERT fusions are uniquely recurrent in epithelioid trophoblastic tumors and positively regulate cell growth. PloS one 16 (5) (2021)
Joel A Morales-Rosado, Erica L Macke, Margot A Cousin, Gavin R Oliver, Radhika Dhamija, Eric W Klee
Interpretation challenges of novel dual-class missense and splice-impacting variant in POLR3A-related late-onset hereditary spastic ataxia. Molecular genetics & genomic medicine 8 (9) (2020)
Gavin R Oliver, Xiaojia Tang, Laura E Schultz-Rogers, Noemi Vidal-Folch, W Garrett Jenkinson, Tanya L Schwab, Krutika Gaonkar, Margot A Cousin, Asha Nair, Shubham Basu, Pritha Chanana, Devin Oglesbee, Eric W Klee
A tailored approach to fusion transcript identification increases diagnosis of rare inherited disease. PloS one 14 (10) (2019)
Gavin R Oliver, Patrick R Blackburn, Marissa S Ellingson, Erin Conboy, Filippo Pinto E Vairo, Matthew Webley, Erik Thorland, Matthew Ferber, Els Van Hul, Ilse M van der Werf, Wim Wuyts, Dusica Babovic-Vuksanovic, Eric W Klee
RNA-Seq detects a SAMD12-EXT1 fusion transcript and leads to the discovery of an EXT1 deletion in a child with multiple osteochondromas. Molecular genetics & genomic medicine 7 (3) (2019)