Cole Eye Institute
Cleveland Clinic
Cleveland, OH
Ophthalmology
Dr. Elias I. Traboulsi, MD
Elias Traboulsi is an expert in the field of Ophthalmology. He over the years received 43 awards: "America's Top Doctors", "Adolf Franceschetti Lectureship", "Merit Award, Center for Child Neurology", "Distinguished Alumnus Visiting Professorship", "Sam and Maria Miller Master Educator Award", "Scholarship in Teaching Award", "Richard G. Richard MD Memorial Lectureship", "Great Ormond Street Hospital Gold Medal Visiting Professor", "Theresa M. and Wayne M. Caygill, MD Lectureship", "Honorary Membership", "Inaugural Joseph Calhoun MD Memorial Lectureship", "5th Kathryn L. Ober Lectureship", "Marshall M. Parks Lectureship", "William B. Scott Lectureship", "35th Victor G. Simpson Lectureship", "Teacher of the Year", "Northern Ohio Live", "Ollendorff Lectureship", "Johnson Lectureship", "Senior Honor Award", "Honorary member", "Georgia Knights Templar Educational Trust Lecturer", "Elected to the American Ophthalmological Society", "Recipient of the Sandy and Tom Trudell Award for the Study of Retinal Degenerative Disease", "Castle Connolly Americas Top Doctors", "Honor Award", "Cleveland Clinic Foundation International Center Physician-of-the-Year Award", "Inaugural Martha Leffler Lincoln Lectureship in Pediatric Ophthalmology", "John-Pratt Johnson Lectureship in Pediatric Ophthalmology", "Robb-Petersen Lectureship in Pediatric Ophthalmology", "Clinician-Scientist Award", "Faculty Recognition Award", "L. Harrell Pierce Wilmer Resident Teaching Award", "First Camille Matta Visiting Professor and Lecturer", "Recognition Award for Outstanding Dedication and Leadership", "Fellowship Award", "Marshall M. Parks Fellowship Award", "Recognition Award", "Research Award", "Physicians Recognition Award", "Alpha Omega Alpha Honor Medical Society Member", "Top MD" and "Fellow (FAAO)". Elias Traboulsi is a published doctor and has 98 publications published. The lastest was: 'Molecular biology and genetics of embryonic eyelid development.' Elias Traboulsi accepts Medicare.
Publications
- The Use of a Mobile Van for School Vision Screening: Results of 63 841 Evaluations.
- Molecular biology and genetics of embryonic eyelid development.
- Corneal Deformation Response and Ocular Geometry: A Noninvasive Diagnostic Strategy in Marfan Syndrome.
- Histopathological comparison of Eyes from patients with autosomal recessive retinitis pigmentosa caused by novel EYS mutations.
- The effects of surgical factors on postoperative Astigmatism in patients enrolled in the Infant Aphakia Treatment Study (IATS).
- Outcomes of Strabismus Surgery with or without Trainee Participation as Surgeon.
- Surgical management of lens subluxation in Marfan Syndrome.
- Sequencing Analysis of the ATOH7 Gene in Individuals with Optic Nerve Hypoplasia.
- Severe Neutropenia Presenting With Candida Albicans Eyelid Abscess in a 1-Year-Old Child.
- Retinal Dystrophy with Intraretinal Cystoid Spaces Associated with Mutations in the Crumbs Homologue (CRB1) gene.
- Predictors of visual acuity and genotype-phenotype correlates in a cohort of patients with Stargardt disease.
- Non-selective assembly of fibrillin-1 and fibrillin-2 in the rodent ocular zonule and in cultured cells: Implications for Marfan Syndrome.
- Identification of Three ABCA4 Sequence Variations Exclusive to African American Patients in a Cohort of Patients With Stargardt Disease.
- Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing.
- Congenital abnormalities of the Optic nerve: from gene mutation to clinical expression.
- Neonatal stroke and progressive leukoencephalopathy in a child with an ACTA2 mutation.
- Childhood retinal dystrophies: what's in a name?
- Visual Acuity Changes in Patients With Leber Congenital Amaurosis and Mutations in CEP290.
- Comparison of inferior oblique myectomy to recession for the treatment of superior oblique palsy.
- Cost of intraocular lens versus contact lens treatment after unilateral congenital Cataract surgery: retrospective analysis at age 1 year.
- Autosomal Dominant Retinitis Pigmentosa Secondary to Pre-mRNA Splicing-Factor Gene PRPF31 (RP11): Review of Disease Mechanism and Report of a Family with a Novel 3-Bas...
- Ocular manifestations of the autoinflammatory Syndromes.
- Axial elongation following Cataract surgery during the first year of life in the infant Aphakia Treatment Study.
- Evaluation of choroidal thickness in retinitis pigmentosa using enhanced depth imaging Optical coherence tomography.
- Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal Degeneration.
- Pigmented and depigmented lesions of the ocular fundus.
- The infant aphakia treatment study contact lens experience: one-year outcomes.
- Adherence to occlusion therapy in the first six months of follow-up and visual acuity among participants in the Infant Aphakia Treatment Study (IATS).
- Tuberous Sclerosis Complex: Genotype/Phenotype Correlation of Retinal Findings.
- Predictors of adherence to occlusion therapy 3 months after Cataract extraction in the Infant Aphakia Treatment Study.
- Unilateral rectus muscle recession in the treatment of Duane syndrome.
- Building an innovative model for personalized healthcare.
- Ophthalmologic abnormalities in Mowat-Wilson Syndrome and a mutation in ZEB2.
- Predictability of intraocular lens calculation and early refractive status: the Infant Aphakia Treatment Study.
- Choroideremia: Effect of age on visual acuity in patients and female carriers.
- Choroideremia: A review of general findings and pathogenesis.
- ADAMTSL4, a secreted glycoprotein widely distributed in the eye, binds fibrillin-1 microfibrils and accelerates microfibril biogenesis.
- Efficacy of the intraoperative relaxed muscle positioning technique in thyroid eye disease and analysis of cases requiring reoperation.
- Oculodentodigital dysplasia: new ocular findings and a novel connexin 43 mutation.
- ADAMTS10 Protein Interacts with Fibrillin-1 and Promotes Its Deposition in Extracellular Matrix of Cultured Fibroblasts.
- Performance of patients with deficient stereoacuity on the Eyesi microsurgical simulator.
- BBS genotype-phenotype assessment of a multiethnic patient cohort calls for a revision of the disease definition.
- Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken Syndrome.
- Duane syndrome in the setting of chromosomal duplications.
- Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosa.
- Periocular granuloma annulare in four children.
- Xerophthalmia and Intracranial Hypertension in an Autistic Child with Vitamin A Deficiency.
- Unilateral megalopapilla and contralateral Optic nerve hypoplasia: a case report and review of the literature.
- Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance.
- Leber congenital amaurosis: clinical correlations with genotypes, gene therapy trials update, and future directions.
- Maculopathy Due to Cobalamin C (cb1C) Disease in an Amish Child.
- Orbital cyst: prenatal diagnosis.
- Morning glory disk anomaly--more than meets the eye.
- Lacrimal sac compression, not massage.
- Sequence alterations in RX in patients with microphthalmia, anophthalmia, and Coloboma.
- Novel ABCA4 compound heterozygous mutations cause severe progressive autosomal recessive cone-rod dystrophy presenting as Stargardt disease.
- Functional analysis of an ADAMTS10 signal peptide mutation in Weill-Marchesani Syndrome demonstrates a long-range effect on secretion of the full-length enzyme.
- Use of Tegaderm for postoperative eye dressing in children.
- Descemet stripping automated endothelial keratoplasty in a 2-year-old child.
- The value of keratometry and central Corneal thickness measurements in the clinical diagnosis of Marfan syndrome.
- Aniridia with preserved visual function: a report of four cases with no mutations in PAX6.
- The use of microarray technology in deciphering the cause of genetic eye diseases: LOXL1 and exfoliation Syndrome.
- Hypermetropia and Esotropia in myotonic dystrophy.
- CNGA3 mutations in two United Arab Emirates families with achromatopsia.
- Vision First, a program to detect and treat eye diseases in young children: the first four years.
- Syndrome of myelinated retinal nerve fibers, myopia, and amblyopia: a review.
- Cohen Syndrome: report of nine cases and review of the literature, with emphasis on ophthalmic features.
- Malignant melanoma of the conjunctiva in children: a review of the international literature 1965-2006.
- Molecular genetics for the pediatric ophthalmologist.
- Acute idiopathic frosted branch angiitis.
- Congenital cranial dysinnervation Disorders and more.
- Novel mutations in FRMD7 in X-linked congenital nystagmus. Mutation in brief #963. Online.
- Bilateral Macular lesions in a 10-year-old girl.
- Introducing a new computer-based test for the clinical evaluation of color discrimination.
- Intraoperative relaxed muscle positioning technique for strabismus repair in thyroid eye disease.
- Intracranial vascular anomalies in patients with morning glory disk anomaly.
- Ocular abnormalities in mice lacking the Ski proto-oncogene.
- Heterozygous and homozygous mutations in PITX3 in a large Lebanese family with posterior polar Cataracts and neurodevelopmental abnormalities.
- Optic atrophy and sensorineural hearing loss in a family caused by an R445H OPA1 mutation.
- SOX2 mutation causes anophthalmia, hearing loss, and brain anomalies.
- Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein.
- The challenges and surprises of studying the genetics of age-related Macular degeneration.
- Identifying photoreceptors in Blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success.
- Ocular manifestations of familial adenomatous polyposis (Gardner Syndrome).
- Polychromasia capsulare (multicolored capsule): report of three families.
- Prevalence of psychosocial disturbances in children with nonorganic visual loss.
- Delineation of Cohen Syndrome following a large-scale genotype-phenotype screen.
- Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).
- Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis.
- Brown Syndrome associated with velocardiofacial Syndrome.
- Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2.
- Classification and surgical management of patients with familial and sporadic forms of congenital fibrosis of the extraocular muscles.
- Thirty-year follow-up of a patient with leber congenital amaurosis and novel RPE65 mutations.
- Congenital abnormalities of cranial nerve development: overview, molecular mechanisms, and further evidence of heterogeneity and complexity of Syndromes with congenita...
- Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).
- A novel PHOX2A/ARIX mutation in an Iranian family with congenital fibrosis of extraocular muscles type 2 (CFEOM2).
- Ophthalmologic findings in patients with nonsyndromic plagiocephaly.
Schools
American University Of Beirut Faculty Of Medicine
American University Beirut Hospital
Georgetown University Hospital
Chldns Hospital
Johns Hopkins Hospital
Procedures Preformed
- Anterior Vitrectomy
- Cataract Removal Surgery
- Conjunctivoplasty
- Excision of Chalazion
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Conditions Treated
- Acquired Coloboma
- Age-Related Macular Degeneration
- Alternating Hyperphoria
- Anterior Ischemic Optic Neuropathy
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Doctors Specialties
- Clinical Genetics
- Ophthalmology
Accepted Insurances
- Aetna HMO
- Choice Plus POS II
- Pathway X Tiered Hosp/Ind Direct Access OH
- Anthem Blue Cross Blue Shield HMO
- Anthem Blue Cross Blue Shield PPO
- Assurant Health
- Blue Card PPO
- Blue Cross Blue Shield of Illinois PPO
- CareSource
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- Open Access Plus
- Cofinity PPO
- Commercial Insurance Company
- CoreSource
- Coventry Health Care
- EBS-RMSCO
- First Health (Coventry Health Care) PPO
- Frontpath Health Coalition
- Golden Rule
- GEHA
- Health Alliance
- Medicare Advantage PFFS
- HealthPartners
- HealthSmart
- Choice Care PPO
- Kaiser Permanente
- Medicaid
- Medical Mutual of Ohio POS
- Medicare MCR
- Meritain Health
- Molina
- MultiPlan PPO
- PHCS Network PPO
- Mutual of Omaha
- Paramount
- Tricare
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
- United Healthcare
- Univera Healthcare
- UPMC Health Plan
- WellCare
- Wells Fargo Insurance
Awards
- America's Top Doctors
- Adolf Franceschetti Lectureship
- Merit Award, Center for Child Neurology
- Distinguished Alumnus Visiting Professorship
- Sam and Maria Miller Master Educator Award
- Scholarship in Teaching Award
- Richard G. Richard MD Memorial Lectureship
- Great Ormond Street Hospital Gold Medal Visiting Professor
- Theresa M. and Wayne M. Caygill, MD Lectureship
- Honorary Membership
- Inaugural Joseph Calhoun MD Memorial Lectureship
- 5th Kathryn L. Ober Lectureship
- Marshall M. Parks Lectureship
- William B. Scott Lectureship
- 35th Victor G. Simpson Lectureship
- Teacher of the Year
- Northern Ohio Live
- Ollendorff Lectureship
- Johnson Lectureship
- Senior Honor Award
- Honorary member
- Georgia Knights Templar Educational Trust Lecturer
- Elected to the American Ophthalmological Society
- Recipient of the Sandy and Tom Trudell Award for the Study of Retinal Degenerative Disease
- Castle Connolly America’s Top Doctors
- Honor Award
- Cleveland Clinic Foundation International Center “Physician-of-the-Year†Award
- Inaugural Martha Leffler Lincoln Lectureship in Pediatric Ophthalmology
- John-Pratt Johnson Lectureship in Pediatric Ophthalmology
- Robb-Petersen Lectureship in Pediatric Ophthalmology
- Clinician-Scientist Award
- Faculty Recognition Award
- L. Harrell Pierce Wilmer Resident Teaching Award
- First Camille Matta Visiting Professor and Lecturer
- Recognition Award for Outstanding Dedication and Leadership
- Fellowship Award
- Marshall M. Parks Fellowship Award
- Recognition Award
- Research Award
- Physician’s Recognition Award
- Alpha Omega Alpha Honor Medical Society Member
- Top MD
- Fellow (FAAO)
Education
-
Children's National Medical Center - George Washington University
-
Georgetown University Hospital
-
Johns Hopkins University
-
American University of Beirut Faculty of Medicine
Hospital
-
Cleveland Clinic
Drug Facts
| NPI NUMBER |
|
1669414132 |
| NPPES Provider LastName |
|
TRABOULSI |
| NPPES Provider FirstName |
|
ELIAS |
| NPPES Provider ZIPCode |
|
441950001 |
| NPPES Provider State |
|
OH |
| Specialty Description |
|
Ophthalmology |
| Total Claim Count |
|
15.0 |
| Distinct Opioid Count |
|
0.0 |
| Opioid Claim Count |
|
0.0 |
| Percent Opioid Claims |
|
0.0 |
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Medicare Facts
| National Provider Identifier [NPI] |
1669414132 |
| Last Name Of The Provider |
TRABOULSI |
| First Name Of The Provider |
ELIAS |
| View All |
|
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