Do I have an ethical dilemma?

por Levin, Alex V.
Publicado 2010

Evaluation of Spoken Dialogue Technology for Real-Time Health Data Collection

por Levin, Esther, Levin, Alex
Publicado 2006

Genetics for the ophthalmologist

por Sadagopan, Karthikeyan A., Capasso, Jenina, Levin, Alex V.
Publicado 2012

Spontaneously resolving macular cyst in an infant

por Ganesh, Anuradha, Khalighi, Misha, Hammersmith, Kristin, Levin, Alex V.
Publicado 2013

Efficient Moment-Based Inference of Admixture Parameters and Sources of Gene Flow

por Lipson, Mark, Loh, Po-Ru, Levin, Alex, Reich, David, Patterson, Nick, Berger, Bonnie
Publicado 2013

How genetics works? An illustrative case report

por Khetan, Vikas, Zanolli, Mario, Capasso, Jenina, Refice, Nanette Zale, Neeley, Kimberley, Levin, Alex V
Publicado 2016

A global sampling approach to designing and reengineering RNA secondary structures

por Levin, Alex, Lis, Mieszko, Ponty, Yann, O’Donnell, Charles W., Devadas, Srinivas, Berger, Bonnie, Waldispühl, Jérôme
Publicado 2012

Autoimmune retinopathy associated with systemic lupus erythematosus: A diagnostic dilemma

por Wuthisiri, Wadakarn, Lai, Yu-Hung, Capasso, Jenina, Blidner, Martin, Salz, David, Kruger, Erik, Levin, Alex V
Publicado 2017

Genetic testing: Getting it right

por Paredes, Diego I., Haefeli, Lorena M., Okoye, Onochie, Capasso, Jenina E., Wyman, Celeste, Khetan, Vikas, Levin, Alex V.
Publicado 2023

Organophosphate retinopathy

por Pham, Hang, Lingao, Michelle D., Ganesh, Anuradha, Capasso, Jenina E., Keep, Rosanne, Sadagopan, Karthikeyan A., Levin, Alex V.
Publicado 2016

Resident immune cells of the avascular lens: Mediators of the injury and fibrotic response of the lens

por Menko, A. Sue, DeDreu, JodiRae, Logan, Caitlin M., Paulson, Heather, Levin, Alex V., Walker, Janice L.
Publicado 2021

Changes in nascent chromatin structure regulate activation of the pro-fibrotic transcriptome and myofibroblast emergence in organ fibrosis

por Basta, Morgan D., Petruk, Svetlana, Summer, Ross, Rosenbloom, Joel, Wermuth, Peter J., Macarak, Edward, Levin, Alex V., Mazo, Alexander, Walker, Janice L.
Publicado 2023

Deep Learning Approach for Differentiating Etiologies of Pediatric Retinal Hemorrhages: A Multicenter Study

por Khosravi, Pooya, Huck, Nolan A., Shahraki, Kourosh, Hunter, Stephen C., Danza, Clifford Neil, Kim, So Young, Forbes, Brian J., Dai, Shuan, Levin, Alex V., Binenbaum, Gil, Chang, Peter D., Suh, Donny W.
Publicado 2023

Spectrum of PEX1 and PEX6 variants in Heimler syndrome

por Smith, Claire E L, Poulter, James A, Levin, Alex V, Capasso, Jenina E, Price, Susan, Ben-Yosef, Tamar, Sharony, Reuven, Newman, William G, Shore, Roger C, Brookes, Steven J, Mighell, Alan J, Inglehearn, Chris F
Publicado 2016

Severe Familial Exudative Vitreoretinopathy, Congenital Hearing Loss, and Developmental Delay in a Child With Biallelic Variants in FZD4

por van der Ende, Sarah R., Meyers, Benjamin S., Capasso, Jenina E., Sasongko, Mario, Yonekawa, Yoshihiro, Pihlblad, Matthew, Huey, Jennifer, Bedoukian, Emma C., Krantz, Ian D., Ngo, Michael H., McMaster, Christopher R., Levin, Alex V., Robitaille, Johane M.
Publicado 2022

Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders

por Reis, Linda M, Sorokina, Elena A, Dudakova, Lubica, Moravikova, Jana, Skalicka, Pavlina, Malinka, Frantisek, Seese, Sarah E, Thompson, Samuel, Bardakjian, Tanya, Capasso, Jenina, Allen, William, Glaser, Tom, Levin, Alex V, Schneider, Adele, Khan, Ayesha, Liskova, Petra, Semina, Elena V
Publicado 2021

Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach

por Petersen-Jones, Simon M., Occelli, Laurence M., Winkler, Paige A., Lee, Winston, Sparrow, Janet R., Tsukikawa, Mai, Boye, Sanford L., Chiodo, Vince, Capasso, Jenina E., Becirovic, Elvir, Schön, Christian, Seeliger, Mathias W., Levin, Alex V., Michalakis, Stylianos, Hauswirth, William W., Tsang, Stephen H.
Publicado 2017

Eight previously unidentified mutations found in the OA1 ocular albinism gene

por Mayeur, Hélène, Roche, Olivier, Vêtu, Christelle, Jaliffa, Carolina, Marchant, Dominique, Dollfus, Hélène, Bonneau, Dominique, Munier, Francis L, Schorderet, Daniel F, Levin, Alex V, Héon, Elise, Sutherland, Joanne, Lacombe, Didier, Said, Edith, Mezer, Eedy, Kaplan, Josseline, Dufier, Jean-Louis, Marsac, Cécile, Menasche, Maurice, Abitbol, Marc
Publicado 2006

Axenfeld-Rieger syndrome: more than meets the eye

por Reis, Linda M., Maheshwari, Mohit, Capasso, Jenina, Atilla, Huban, Dudakova, Lubica, Thompson, Samuel, Zitano, Lia, Lay-Son, Guillermo, Lowry, R. Brian, Black, Jennifer, Lee, Joseph, Shue, Ann, Kremlikova Pourova, Radka, Vaneckova, Manuela, Skalicka, Pavlina, Jedlickova, Jana, Trkova, Marie, Williams, Bradley, Richard, Gabriele, Bachman, Kristine, Seeley, Andrea H., Costakos, Deborah, Glaser, Thomas M, Levin, Alex V., Liskova, Petra, Murray, Jeffrey C., Semina, Elena V.
Publicado 2023

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