الدكتور مازن قربان | جامعة حمد بن خليفة
Hamad Bin Khalifa University

أعضاء هيئة التدريس

الدكتور مازن قربان

الدكتور مازن قربان (PhD)


أستاذ مساعد
كلية العلوم الصحية والحيوية

السيرة الذاتية

Dr. Mazen Kurban is a Dermatologist and American Board Certified in Clinical Molecular Genetics.

He obtained a degree in dermatology from the American University of Beirut (AUB) Medical Center. He then obtained his Clinical and Molecular Geneticist degree from Columbia University Medical Center, New York.

Dr. Kurban has more than 150 publications in peer-reviewed journals with more than 10 years’ experience of dealing with clinical dermatology patients at AUB.

 


الاهتمامات البحثية

  • Genodermatoses and Related Skin Diseases
  • Skin Cancer
  • Stem Cells

الخبرات

Clinical expertise in skin diseases as well as genetic diseases.

  • Clinical, basic and translational research in the field of Dermatology

المؤهلات العلمية

MD

American University of Beirut

2004
  • Dermatology

    American University of Beirut

    2008
  • Clinical Molecular Genetics

    Columbia University, New York, USA

    2011

المؤلفات المختارة

  • El-Hachem N, Eid E, Nemer G, Dbaibo G, Abbas O, Rubeiz N, Zeineldine S, Matar GM, Bikorimana JP, Shammaa R, Haibe-Kains B, Kurban M*, Rafei M.

    Integrative Transcriptome Analyses Empower The Anti-Covid-19 Drug Arsenal. Iscience. 2020, vol.23, no.11, pp-101697.

    2020
  • Nemer G, El-Hachem N, Eid E, Hamie L, Bardawil T, Khalil S, El-Rassy I, Safi R, Khalil A, Abbas O, Shimomura Y, Kurban M*.

    A Novel Traf3ip2 Variant Causing Familial Scarring Alopecia With Mixed Features Of Discoid Lupus Erythematosus And Folliculitis Decalvans. Clinical Genetics. 2020, vol.98, no.2, pp-116-125.

    2020
  • Hamie L, Eid E, Abbas O, Safi R, Nammour T, Tamim H, Makki M, Stephan C, Hasbani D, Wehbe H, Ghaoui N, Hawa M, Nasser N, Eid A, Kibbi AG, Kurban M*.

    Supar, A Potential Inflammatory Mediator In Psoriasis Pathogenesis. Clinical And Experimental Pharmacology & Physiology. 2020.

    2020
  • Safi R, Malek E, Nemer G, Sayed R, Eid E, Khalil S, Nasser N, Abbas O, Mohsen-Kanson T, Kurban M*.

    Comparative Characterization Of Sun Exposed And Sun Protected Skin-Derived Mesenchymal-Like Stem Cells In Variegate Porphyria And Healthy Individuals. Photodermatology, Photoimmunology & Photomedicine. 2020.

    2020
  • El Sabeh M, Kassir MF, Ghanem P, Saifi O, El Hadi D, Khalifeh Y, Ekkawi AR, Ghabach M, Chaaya M, Nemer G, Abbas O, Kurban M*.

    Consanguinity Rates Among Syrian Refugees In Lebanon: A Study On Genetic Awareness. Journal Of Biosocial Science. 2020, pp-1-11.

    2020
  • Khalil S, Eid E, Hamieh L, Bardawil T, Moujaes Z, Khalil W, Abbas O, Kurban M.

    Genodermatoses With Teeth Abnormalities. Oral Diseases. 2020.

    2020
  • Safi R, Mohsen-Kanson T, Nemer G, Dekmak B, Rubeiz N, El-Sabban M, Nassar D, Eid A, Abbas O, Kibbi AG, Kurban M*.

    Loss Of Ferrochelatase Is Protective Against Colon Cancer Cells: Ferrochelatase A Possible Regulator Of The Long Noncoding Rna H19. Journal Of Gastrointestinal Oncology. 2019, vol.10, no.5, pp-859-868.

    2019
  • Khalil S, Bardawil T, Saade S, Chedraoui A, Ramadan N, Hasbani DJ, Abbas O, Nemer G, Rubeiz N, Kurban M*.

    Use Of Topical Glycolic Acid Plus A Lovastatin-Cholesterol Combination Cream For The Treatment Of Autosomal Recessive Congenital Ichthyoses. Jama Dermatology. 2018, vol.154, no.11, pp-1320-1323.

    2018
  • Bergqvist C, Kadara H, Hamie L, Nemer G, Safi R, Karouni M, Marrouche N, Abbas O, Hasbani DJ, Kibbi AG, Nassar D, Shimomura Y, Kurban M*.

    Slurp-1 Is Mutated In Mal De Meleda, A Potential Molecular Signature For Melanoma And A Putative Squamous Lineage Tumor Suppressor Gene. International Journal Of Dermatology. 2018, vol.57, no.2, pp-162-170.

    2018
  • Kadara H, Nemer G, Safi R, Rebeiz N, Daou L, Delbani D, Btadini W, Abbas O, Tofaili M, Bitar F, Kibbi AG, Shimomura Y, Kurban M*.

    Erythropoietic Protoporphyria A Clinical And Molecular Study From Lebanon: Ferrochelatase A Potential Tumor Suppressor Gene In Colon Cancer. Clinical Genetics. 2017, vol.92, no.5, pp-495-502.

    2017