Colleen M Cebulla, MD, PhD

College

College of Medicine

Department/Division

Ophthalmology

Academic Title

Assoc Professor

Research Program

Molecular Biology and Cancer Genetics

Research Interest

Cancer, Melanoma, Retinoblastoma, Retinal Detachment, Inflammation, Down Syndrome, Endometrial Cancer

In addition to seeing patients, Dr. Cebulla is actively engaged in both basic and clinical. The focus of Dr. Cebulla's lab is translational research on retinal detachments and uveal melanoma. Also, a collaborative group with Dr. Cebulla, Dr. Mohammed Abdel-Rahman and Dr. Frederick Davidorf has identified that over 10% of patients with uveal melanoma have a heritable cancer syndrome. They are working hard to identify the genes responsible for increased cancer in the family and have identified a new cancer syndrome due to mutation in the BAP1 gene. They are currently involved in understanding factors which influence survival with metastatic disease and on targeted therapy for melanoma.

Education and Background

Office Location

5020 OSU Eye & Ear Institute

915 Olentangy River Road, Columbus, Ohio 43212

614-652-2600

614-652-2610

cebulla.1@osu.edu

Publications

Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma.

Robertson AG, Shih J, Yau C, Gibb EA, Oba J, Mungall KL, Hess JM, Uzunangelov V, Walter V, Danilova L, Lichtenberg TM, Kucherlapati M, Kimes PK, Tang M, Penson A, Babur O, Akbani R, Bristow CA, Hoadley KA, Iype L, Chang MT, TCGA Research Network, Cherniack AD, Benz C, Mills GB, Verhaak RGW, Griewank KG, Felau I, Zenklusen JC, Gershenwald JE, Schoenfield L, Lazar AJ, Abdel-Rahman MH, Roman-Roman S, Stern MH, Cebulla CM, Williams MD, Jager MJ, Coupland SE, Esmaeli B, Kandoth C, Woodman SE

Cancer Cell 32 204-220.e15 08/14/2017
The chick eye in vision research: An excellent model for the study of ocular disease.

Wisely CE, Sayed JA, Tamez H, Zelinka C, Abdel-Rahman MH, Fischer AJ, Cebulla CM

Prog Retin Eye Res in press 06/28/2017
Germline BAP1 alterations in familial uveal melanoma.

Rai K, Pilarski R, Boru G, Rehman M, Saqr AH, Massengill JB, Singh A, Marino MJ, Davidorf FH, Cebulla CM, Abdel-Rahman M, Rai K, Pilarski R, Boru G, Rehman M, Saqr AH, Massengill JB, Singh A, Marino MJ, Davidorf FH, Cebulla CM, H Abdel-Rahman M

Genes Chromosomes Cancer 56 168-174 02/01/2017
Germline BAP1 alterations in familial uveal melanoma.

Rai K, Pilarski R, Boru G, Rehman M, Saqr AH, Massengill JB, Singh A, Marino MJ, Davidorf FH, Cebulla CM, Abdel-Rahman M, Rai K, Pilarski R, Boru G, Rehman M, Saqr AH, Massengill JB, Singh A, Marino MJ, Davidorf FH, Cebulla CM, H Abdel-Rahman M

Genes Chromosomes Cancer 56 168-174 02/01/2017
Breaking bad news: A communication competency for ophthalmology training programs.

Hilkert SM, Cebulla CM, Jain SG, Pfeil SA, Benes SC, Robbins SL

Surv Ophthalmol 61 791-798 11/01/2016
Genetic markers of pigmentation are novel risk loci for uveal melanoma.

Ferguson R, Vogelsang M, Ucisik-Akkaya E, Rai K, Pilarski R, Martinez CN, Rendleman J, Kazlow E, Nagdimov K, Osman I, Klein RJ, Davidorf FH, Cebulla CM, Abdel-Rahman MH, Kirchhoff T

Sci Rep 6 31191 08/08/2016
Uveal Melanoma Mimicking Advanced Coats' Disease in a Young Patient.

Gupta N, Terrell W, Schoenfield L, Kirsch C, Cebulla CM

Ocul Oncol Pathol 2 140-3 04/01/2016
Germline BAP1 mutations misreported as somatic based on tumor-only testing.

Abdel-Rahman MH, Rai K, Pilarski R, Davidorf FH, Cebulla CM

Fam Cancer 15 327-30 04/01/2016
Comprehensive review of BAP1 tumor predisposition syndrome with report of two new cases.

Rai K, Pilarski R, Cebulla CM, Abdel-Rahman MH

Clin Genet 89 285-94 03/01/2016
Multimodal Imaging and Clinicopathologic Correlation in Primary Uveal Lymphoma.

Erickson B, Mantopoulos D, Schoenfield L, Cebulla CM

Case Rep Ophthalmol 7 39-43 01/01/2016
Long-term visual acuity outcomes in patients with uveal melanoma treated with 125I episcleral OSU-Nag plaque brachytherapy.

Wisely CE, Hadziahmetovic M, Reem RE, Hade EM, Nag S, Davidorf FH, Martin D, Cebulla CM

Brachytherapy 15 12-22 01/01/2016
Bilateral optic neuropathy following bite from brown recluse spider (Loxosceles reclusa).

Mantopoulos D, Hendershot AJ, Cebulla CM, Hirsh DK

Cutan Ocul Toxicol 35 168-72 01/01/2016
Activation of glucocorticoid receptors in Müller glia is protective to retinal neurons and suppresses microglial reactivity.

Gallina D, Zelinka CP, Cebulla C, Fischer AJ, Gallina D, Zelinka CP, Cebulla CM, Fischer AJ

Exp Neurol 273 114-25 11/01/2015
Activation of glucocorticoid receptors in Müller glia is protective to retinal neurons and suppresses microglial reactivity.

Gallina D, Zelinka CP, Cebulla C, Fischer AJ, Gallina D, Zelinka CP, Cebulla CM, Fischer AJ

Exp Neurol 273 114-25 11/01/2015
Dislocated Crystalline Lens Mimicking Metastatic Endometrial Cancer.

Park S, Shah N, Cebulla CM

JAMA Ophthalmol 133 e151336 09/01/2015
Bilateral Choroidopathy and Serous Retinal Detachments During Ipilimumab Treatment for Cutaneous Melanoma.

Mantopoulos D, Kendra KL, Letson AD, Cebulla CM

JAMA Ophthalmol 133 965-7 08/01/2015
Analysis of BAP1 Germline Gene Mutation in Young Uveal Melanoma Patients.

Cebulla CM, Binkley EM, Pilarski R, Massengill JB, Rai K, Liebner DA, Marino MJ, Singh AD, Abdel-Rahman MH

Ophthalmic Genet 36 126-31 06/01/2015
A case of vogt-koyanagi-harada syndrome with persistent dyspnea secondary to laryngeal edema.

Mantopoulos D, deSilva BW, Cebulla CM

Case Rep Ophthalmol 5 361-4 09/01/2014
Ocular melanoma and the BAP1 hereditary cancer syndrome: implications for the dermatologist.

Martorano LM, Winkelmann RR, Cebulla CM, Abdel-Rahman MH, Campbell SM

Int J Dermatol 53 657-63 06/01/2014
Retinal MMP-12, MMP-13, TIMP-1, and TIMP-2 expression in murine experimental retinal detachment.

Kim B, Abdel-Rahman MH, Wang T, Pouly S, Mahmoud AM, Cebulla CM

Invest Ophthalmol Vis Sci 55 2031-40 04/01/2014
Expanding the clinical phenotype of hereditary BAP1 cancer predisposition syndrome, reporting three new cases.

Pilarski R, Cebulla CM, Massengill JB, Rai K, Rich T, Strong L, McGillivray B, Asrat MJ, Davidorf FH, Abdel-Rahman MH

Genes Chromosomes Cancer 53 177-82 02/01/2014
Charles Bonnet syndrome and Terson's syndrome: good news from bad news.

Lubow M, Cebulla CM

Graefes Arch Clin Exp Ophthalmol 251 2257 09/01/2013

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Colleen M Cebulla, MD, PhD

College

Department/Division

Academic Title

Research Program

Research Interest

Education and Background

Office Location

Publications

Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma.

The chick eye in vision research: An excellent model for the study of ocular disease.

Germline BAP1 alterations in familial uveal melanoma.

Germline BAP1 alterations in familial uveal melanoma.

Breaking bad news: A communication competency for ophthalmology training programs.

Genetic markers of pigmentation are novel risk loci for uveal melanoma.

Uveal Melanoma Mimicking Advanced Coats' Disease in a Young Patient.

Germline BAP1 mutations misreported as somatic based on tumor-only testing.

Comprehensive review of BAP1 tumor predisposition syndrome with report of two new cases.

Multimodal Imaging and Clinicopathologic Correlation in Primary Uveal Lymphoma.

Long-term visual acuity outcomes in patients with uveal melanoma treated with 125I episcleral OSU-Nag plaque brachytherapy.

Bilateral optic neuropathy following bite from brown recluse spider (Loxosceles reclusa).

Activation of glucocorticoid receptors in Müller glia is protective to retinal neurons and suppresses microglial reactivity.

Activation of glucocorticoid receptors in Müller glia is protective to retinal neurons and suppresses microglial reactivity.

Dislocated Crystalline Lens Mimicking Metastatic Endometrial Cancer.

Bilateral Choroidopathy and Serous Retinal Detachments During Ipilimumab Treatment for Cutaneous Melanoma.

Analysis of BAP1 Germline Gene Mutation in Young Uveal Melanoma Patients.

A case of vogt-koyanagi-harada syndrome with persistent dyspnea secondary to laryngeal edema.

Ocular melanoma and the BAP1 hereditary cancer syndrome: implications for the dermatologist.

Retinal MMP-12, MMP-13, TIMP-1, and TIMP-2 expression in murine experimental retinal detachment.

Expanding the clinical phenotype of hereditary BAP1 cancer predisposition syndrome, reporting three new cases.

Charles Bonnet syndrome and Terson's syndrome: good news from bad news.

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Colleen M Cebulla, MD, PhD

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