Gene therapy for inherited retinal diseases

por Nuzbrokh, Yan, Ragi, Sara D., Tsang, Stephen H.
Publicado 2021

Epidemiology and Survival of Kaposi’s Sarcoma by Race in the United States: A Surveillance, Epidemiology, and End Results Database Analysis

por Ragi, Sara D, Moseley, Isabelle, Ouellette, Samantha, Rao, Babar
Publicado 2022

Tinea versicolour in underrepresented groups: An All of Us database analysis

por Moseley, Isabelle, Ragi, Sara D., Ouellette, Samantha, Rao, Babar
Publicado 2022

Treatment-Emergent Adverse Events in Gene Therapy Trials for Inherited Retinal Diseases: A Narrative Review

por Nuzbrokh, Yan, Kassotis, Alexis S., Ragi, Sara D., Jauregui, Ruben, Tsang, Stephen H.
Publicado 2020

Evaluation of hair regrowth after minoxidil and dutasteride tattooing in men with androgenetic alopecia

por Ragi, Sara D., Ghanian, Soha, Rogers, Nicole, Peterson, Danielle M., Johnson, Luke S., Wambier, Carlos G.
Publicado 2023

Sequential multiple retinal vein occlusions and transient ischemic attack in MTHFR polymorphism and protein S deficiency

por Cho, Ahra, Ragi, Sara D., Oh, Jin Kyun, Lima de Carvalho, Jose Ronaldo, Ryu, Joseph, Yang, Ber‐Yuh, Tsang, Stephen H.
Publicado 2020

Compound heterozygous novel frameshift variants in the PROM1 gene result in Leber congenital amaurosis

por Ragi, Sara D., Lima de Carvalho, Jose Ronaldo, Tanaka, Akemi J., Park, Karen Sophia, Mahajan, Vinit B., Maumenee, Irene H., Tsang, Stephen H.
Publicado 2019

Novel mutations in the 3-box motif of the BACK domain of KLHL7 associated with nonsyndromic autosomal dominant retinitis pigmentosa

por Oh, Jin Kyun, Lima de Carvalho, Jose Ronaldo, Sun, Young Joo, Ragi, Sara, Yang, Jing, Levi, Sarah R., Ryu, Joseph, Bassuk, Alexander G., Mahajan, Vinit B., Tsang, Stephen H.
Publicado 2019

Clinical exome sequencing for inherited retinal degenerations at a tertiary care center

por Ganapathi, Mythily, Thomas-Wilson, Amanda, Buchovecky, Christie, Dharmadhikari, Avinash, Barua, Subit, Lee, Winston, Ruan, Merry Z. C., Soucy, Megan, Ragi, Sara, Tanaka, Joy, Clark, Lorraine N., Naini, Ali B., Liao, Jun, Mansukhani, Mahesh, Tsang, Stephen, Jobanputra, Vaidehi
Publicado 2022

Compound heterozygous inheritance of two novel COQ2 variants results in familial coenzyme Q deficiency

por Abdelhakim, Aliaa H., Dharmadhikari, Avinash V., Ragi, Sara D., de Carvalho, Jose Ronaldo Lima, Xu, Christine L., Thomas, Amanda L., Buchovecky, Christie M., Mansukhani, Mahesh M., Naini, Ali B., Liao, Jun, Jobanputra, Vaidehi, Maumenee, Irene H., Tsang, Stephen H.
Publicado 2020

CNGB1‐related rod‐cone dystrophy: A mutation review and update

por Nassisi, Marco, Smirnov, Vasily M., Solis Hernandez, Cyntia, Mohand‐Saïd, Saddek, Condroyer, Christel, Antonio, Aline, Kühlewein, Laura, Kempf, Melanie, Kohl, Susanne, Wissinger, Bernd, Nasser, Fadi, Ragi, Sara D., Wang, Nan‐Kai, Sparrow, Janet R., Greenstein, Vivienne C., Michalakis, Stylianos, Mahroo, Omar A., Ba‐Abbad, Rola, Michaelides, Michel, Webster, Andrew R., Degli Esposti, Simona, Saffren, Brooke, Capasso, Jenina, Levin, Alex, Hauswirth, William W., Dhaenens, Claire‐Marie, Defoort‐Dhellemmes, Sabine, Tsang, Stephen H., Zrenner, Eberhart, Sahel, Jose‐Alain, Petersen‐Jones, Simon M., Zeitz, Christina, Audo, Isabelle
Publicado 2021