Search Results - Stephanie Ware

P259: Characterization of 297 NICU patients with congenital anomalies evaluated with genome sequencing by Tejasvi Kakani, Caroline Parker, Benjamin Helm, Samardeep Gurudatta, Lindsey Helvaty, Liesbeth Vossaert, Matthew Durbin, Theodore Wilson, Stephanie Ware, Kristen Suhrie

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P171: Yield of different genomic testing approaches in infants with congenital heart disease by Gabrielle Geddes, Erin Conboy, Sara Fitzgerald-Butt, Benjamin Helm, Evan-Jacob Garcia, Laura Haneline, Riad Lutfi, Larry Markham, Melinda Markham, Kelly Schmit, Kayleigh Swaggart, Stephanie Ware

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Zic3 enables bimodal regulation of tyrosine hydroxylase expression in olfactory bulb and midbrain-derived neurons by Smitha Bhaskar, Jeevan Gowda, Akshay Hegde, Surya Chandra Rao Thumu, Shreetama Banerjee, Helen M Bellchambers, Narendrakumar Ramanan, Paloma Merchan Sala, Kenneth Campbell, Stephanie Ware, Jyothi Prasanna, Anujith Kumar

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P535: The undiagnosed rare disease clinic program of Indiana University: Lessons learned from the first 100 patients enrolled (Phase-I pilot) by Khurram Liaqat, Francesco Vetrini, Erin Conboy, Kayla Treat, Lili Mantcheva, Marco Abreu, Tae-Hwi Schwantes-An, Kevin Booth, Reynold Ly, Amy Breman, Marwan Tayeh, Benjamin Helm, Brett Graham, Stephanie Ware

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P626: Enhancing ultra-rare disease diagnoses through multi-omics integration and multi-site collaboration in the Indiana University Undiagnosed Rare Disease Clinic (URDC) cohort by Khurram Liaqat, Kayla Treat, Lili Mantcheva, Marco Abreu, Tae-Hwi Schwantes-An, Kevin Booth, Marwan Tayeh, Summan Thahiem, Benjamin Helm, Brett Graham, Patrick Gillespie, Stephanie Ware, Erin Conboy, Francesco Vetrini

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