Elias I Traboulsi (Elias Traboulsi, E Traboulsi)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 12

Top Venues

Ophthalmic genetics

Proceedings of the National Academy of Sciences of the United States of America

Journal of binocular vision and ocular motility

Cleveland Clinic Foundation

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

Affiliation History

Cleveland Clinic Foundation Jul 01 1997

United States

Vice-Chair for Education :: Cole Eye Institute

Publications

Jesse L Berry, Elias I Traboulsi, Francis L Munier
A. Linn Murphree, MD: the Mississippi man who conquered retinoblastoma and changed the fate of patients and their families. Ophthalmic genetics 43 (6) (2023)
Jesse L Berry, Elias I Traboulsi, Francis L Munier
A. Linn Murphree, MD: the Mississippi man who conquered retinoblastoma and changed the fate of patients and their families. Ophthalmic genetics 43 (6) (2023)
Reem Amine, Elias I Traboulsi
Indications for Systemic and Genetic Testing in Patients with Congenital Cataracts. Journal of binocular vision and ocular motility 73 (4) (2023)
Sruthi Arepalli, Meghan J M DeBenedictis, Alex Yuan, Elias I Traboulsi
Severe retinal complications in Knobloch Syndrome - Three siblings without clinically apparent occipital defects and a review of the literature. Ophthalmic genetics (2022)
Matthew W Russell, Justin C Muste, Kanika Seth, Madhukar Kumar, Collin A Rich, Rishi P Singh, Elias I Traboulsi
Functional imaging of mitochondria in genetically confirmed retinal dystrophies using flavoprotein fluorescence. Ophthalmic genetics (2022)
Bernd Wissinger, Britta Baumann, Elena Buena-Atienza, Zeinab Ravesh, Artur V Cideciyan, Katarina Stingl, Isabelle Audo, Isabelle Meunier, Béatrice Bocquet, Elias I Traboulsi, Alison J Hardcastle, Jessica C Gardner, Michel Michaelides, Kari E Branham, Thomas Rosenberg, Sten Andreasson, Hélène Dollfus, David Birch, Andrea L Vincent, Loreto Martorell, Jaume Catala, Ulrich Kellner, Klaus Rüther, Birgit Lorenz, Markus N Preising, Emanuela Manfredini, Yuri A Zarate, Raymon Vijzelaar, Eberhart Zrenner, Samuel G Jacobson, Susanne Kohl
The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy. Proceedings of the National Academy of Sciences of the United States of America 119 (27) (2022)
H Al-Hindi, M Z Chauhan, R Sanders, H Samarah, Meghan J M DeBenedictis, Elias I Traboulsi, S H Uwaydat
TULP1 related retinal dystrophy: report of rare and novel variants with a previously undescribed phenotype in two cases. Ophthalmic genetics (2021)
Razek Georges Coussa, Elliott H Sohn, Ian C Han, Sumit Parikh, Elias I Traboulsi
Mitochondrial DNA A3243G variant-associated retinopathy: a meta-analysis of the clinical course of visual acuity and correlation with systemic manifestations. Ophthalmic genetics 42 (4) (2021)
Matthew S Elitt, Joan E Tamburro, Rocio T Moran, Elias I Traboulsi
Cutis marmorata telangiectatica congenita: a focus on its diagnosis, ophthalmic anomalies, and possible etiologic factors. Ophthalmic genetics 41 (2) (2020)
Madeline Williamson, Elias I Traboulsi, Meghan J M DeBenedictis
Investigation of CEP290 genotype-phenotype correlations in a patient with retinitis pigmentosa, infertility, end-stage renal disease, and a novel mutation. Ophthalmic genetics 41 (2) (2020)
Razek Georges Coussa, Yue Zhao, Meghan J M DeBenedictis, Allison Babiuch, Jonathan Sears, Elias I Traboulsi
Novel mutation in CTNNB1 causes familial exudative vitreoretinopathy (FEVR) and microcephaly: case report and review of the literature. Ophthalmic genetics 41 (1) (2020)
Yue Zhao, Razek Georges Coussa, Meghan J M DeBenedictis, Elias I Traboulsi
Retinal dystrophy associated with a Kizuna (KIZ) mutation and a predominantly macular phenotype. Ophthalmic genetics 40 (5) (2019)

Elias I Traboulsi.css-eqlu8i{font-size:small;padding-left:4px;} (Elias Traboulsi, E Traboulsi)

Publication Activity (10 Years)

Top Topics

Top Venues

Elias I Traboulsi (Elias Traboulsi, E Traboulsi)