Selective ablation of cochlear hair cells promotes engraftment of human embryonic stem cell-derived progenitors in the mouse organ of Corti

por Takeda, Hiroki, Dondzillo, Anna, Randall, Jessica A., Gubbels, Samuel P.
Publicado 2021

Presigmoid Approach to Dumbbell Trigeminal Schwannoma

por Kunigelis, Katherine E., Craig, Daniel, Yang, Alexander, Gubbels, Samuel, Youssef, A. Samy
Publicado 2018

Novel candidate genes for cholesteatoma in chronic otitis media

por Lee, Nam K., Cass, Stephen P., Gubbels, Samuel P., Gomez, Helen Z., Scholes, Melissa A., Jenkins, Herman A., Santos-Cortez, Regie Lyn P.
Publicado 2023

Rare Coding Variants in Patients with Non-Syndromic Vestibular Dysfunction

por Sumalde, Angelo Augusto M., Scholes, Melissa A., Kalmanson, Olivia A., Terhune, Elizabeth A., Frejo, Lidia, Wethey, Cambria I., Roman-Naranjo, Pablo, Carry, Patrick M., Gubbels, Samuel P., Lopez-Escamez, Jose A., Hadley-Miller, Nancy, Santos-Cortez, Regie Lyn P.
Publicado 2023

Identification of Novel Genes and Biological Pathways That Overlap in Infectious and Nonallergic Diseases of the Upper and Lower Airways Using Network Analyses

por Baschal, Erin E., Larson, Eric D., Bootpetch Roberts, Tori C., Pathak, Shivani, Frank, Gretchen, Handley, Elyse, Dinwiddie, Jordyn, Moloney, Molly, Yoon, Patricia J., Gubbels, Samuel P., Scholes, Melissa A., Cass, Stephen P., Jenkins, Herman A., Frank, Daniel N., Yang, Ivana V., Schwartz, David A., Ramakrishnan, Vijay R., Santos-Cortez, Regie Lyn P.
Publicado 2020

The FUT2 Variant c.461G>A (p.Trp154*) Is Associated With Differentially Expressed Genes and Nasopharyngeal Microbiota Shifts in Patients With Otitis Media

por Elling, Christina L., Scholes, Melissa A., Streubel, Sven-Olrik, Larson, Eric D., Wine, Todd M., Bootpetch, Tori C., Yoon, Patricia J., Kofonow, Jennifer M., Gubbels, Samuel P., Cass, Stephen P., Robertson, Charles E., Jenkins, Herman A., Prager, Jeremy D., Frank, Daniel N., Chan, Kenny H., Friedman, Norman R., Ryan, Allen F., Santos-Cortez, Regie Lyn P.
Publicado 2022

Multi-omic studies on missense PLG variants in families with otitis media

por Bootpetch, Tori C., Hafrén, Lena, Elling, Christina L., Baschal, Erin E., Manichaikul, Ani W., Pine, Harold S., Szeremeta, Wasyl, Scholes, Melissa A., Cass, Stephen P., Larson, Eric D., Chan, Kenny H., Ishaq, Rafaqat, Prager, Jeremy D., Shaikh, Rehan S., Gubbels, Samuel P., Yousaf, Ayesha, Wine, Todd M., Bamshad, Michael J., Yoon, Patricia J., Jenkins, Herman A., Nickerson, Deborah A., Streubel, Sven-Olrik, Friedman, Norman R., Frank, Daniel N., Einarsdottir, Elisabet, Kere, Juha, Riazuddin, Saima, Daly, Kathleen A., Leal, Suzanne M., Ryan, Allen F., Mattila, Petri S., Ahmed, Zubair M., Sale, Michele M., Chonmaitree, Tasnee, Santos-Cortez, Regie Lyn P.
Publicado 2020