Wadih M Zein (Brian P Brooks)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 7

Top Topics

Diabetic Retinopathy

Intellectual Disability

High Throughput

Top Venues

Genetics in medicine : official journal of the American College of Medical Genetics

Ophthalmic genetics

The British journal of ophthalmology

Eye (London, England)

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

Publications

Rabia Faridi, Rizwan Yousaf, Shoujun Gu, Sayaka Inagaki, Amy E Turriff, Keith Pelstring, Bin Guan, Amelia Naik, Andrew J Griffith, Samuel Mawuli Adadey, Elvis Twumasi Aboagye, Gordon Akanzuwine Awandare, Robert J Morell, Ekaterini Tsilou, Amanda G Noyes, Laura Anne Goodell Sulmonte, Ambroise Wonkam, Isabelle Schrauwen, Regie Lyn P Santos-Cortez, Hela Azaiez, Carmen C Brewer, Sheikh Riazuddin, Robert B Hufnagel, Michael Hoa, Wadih M Zein, J Karl de Dios, Thomas B Friedman
Variants of LRP2, encoding a multifunctional cell-surface endocytic receptor, associated with hearing loss and retinal dystrophy. Clinical genetics (2023)
Laryssa A Huryn, Taylor Flaherty, Rosalie Nolen, Lev Prasov, Wadih M Zein, Catherine A Cukras, Sharon Osgood, Neelam Raja, Mark D Levin, Susan Vitale, Brian P Brooks, Robert B Hufnagel, Beth A Kozel
Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome. The British journal of ophthalmology (2022)
Volha V Malechka, Catherine A Cukras, Emily Y Chew, Yuri V Sergeev, Delphine Blain, Brett G Jeffrey, Ehsan Ullah, Robert B Hufnagel, Brian P Brooks, Laryssa A Huryn, Wadih M Zein
Clinical Phenotypes of CDHR1 -Associated Retinal Dystrophies. Genes 13 (5) (2022)
Joanne Li, Nancy Aguilera, Tao Liu, Andrew J Bower, John P Giannini, Catherine Cukras, Tiarnan D L Keenan, Emily Chew, Brian P Brooks, Wadih M Zein, Laryssa A Huryn, Robert B Hufnagel, Johnny Tam
Structural integrity of retinal pigment epithelial cells in eyes with age-related scattered hypofluorescent spots on late phase indocyanine green angiography (ASHS-LIA). Eye (London, England) (2022)
Rosalie M Nolen, Robert B Hufnagel, Thomas B Friedman, Amy E Turriff, Carmen C Brewer, Christopher K Zalewski, Kelly A King, Talah T Wafa, Andrew J Griffith, Brian P Brooks, Wadih M Zein
Atypical and ultra-rare Usher syndrome: a review. Ophthalmic genetics 41 (5) (2020)
Thierry Vilboux, Daniel A Doherty, Ian A Glass, Melissa A Parisi, Ian G Phelps, Andrew R Cullinane, Wadih Zein, Wadih M Zein, Theo Heller, Ariane G Soldatos, Neal L Oden, Deniz Yildirimli, Meghana Vemulapalli, James C Mullikin, null Nisc Comparative Sequencing Program, May Christine V Malicdan, William A Gahl, Meral Gunay-Aygun
Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single center. Genetics in medicine : official journal of the American College of Medical Genetics 19 (8) (2017)
Christina Lam, Carlos Ferreira, Donna Krasnewich, Camilo Toro, Lea Latham, Wadih M Zein, Tanya Lehky, Carmen Brewer, Eva H Baker, Audrey Thurm, Cristan A Farmer, Sergio D Rosenzweig, Jonathan J Lyons, John M Schreiber, Andrea Gropman, Shilpa Lingala, Marc G Ghany, Beth Solomon, Ellen F Macnamara, Mariska Davids, Constantine A Stratakis, Virginia Kimonis, William A Gahl, Lynne Wolfe
Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation. Genetics in medicine : official journal of the American College of Medical Genetics 19 (2) (2016)