Mazen Kurban - Concepedia

Author

Mazen Kurban

American University of Beirut Medical Center ORCID

Also Known As

Firas Kreidieh, Kurban M, M Kurban, M. Kurban, MAZEN KURBAN, Madeline S.L. Ho, Mazen Kurban, Mazen S. Kurban, Mazen Samir Kurban, Minawar Kurban

234

Publications

3.3K

Citations

H-Index

Concepts

All Affiliations

American University of Beirut Medical Center American University of Beirut Columbia University Niigata University Advanced Dermatology

About

Mazen Kurban is an author at American University of Beirut Medical Center specializing in medicine, pathology, and dermatology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	17	469
2	Allergy	2	2	32
3	Health Sciences	1	1	10
4	Anatomy	1	1	11
5	Biology	1	1	18

Mazen Kurban

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture Yutaka Shimomura, Muhammad Wajid, Lynn Petukhova, The American Journal of Human Genetics Skin DevelopmentHuman Hair TextureGeneticsKeratin 74Dermatology	2010	98
Plasmacytoid dendritic cells in alopecia areata: missing link? Jihane Abou Rahal, Mazen Kurban, Abdul‐Ghani Kibbi, Journal of the European Academy of Dermatology and Venereology	2014	70
Trps1 and Its Target Gene Sox9 Regulate Epithelial Proliferation in the Developing Hair Follicle and Are Associated with Hypertrichosis Katherine A. Fantauzzo, Mazen Kurban, Brynn Levy, PLoS Genetics	2012	69
Mutations in the Cholesterol Transporter Gene ABCA5 Are Associated with Excessive Hair Overgrowth Gina M. DeStefano, Mazen Kurban, Kwame Anyane‐Yeboa, PLoS Genetics	2014	59
Whole-exome sequencing in a single proband reveals a mutation in the CHST8 gene in autosomal recessive peeling skin syndrome Rita Cabral, Mazen Kurban, Muhammad Wajid, Genomics Chst8 GeneSkin DevelopmentGenetic DisorderWhole-exome SequencingGenetics	2012	57
Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis Gina M. DeStefano, Katherine A. Fantauzzo, Lynn Petukhova, Proceedings of the National Academy of Sciences	2013	55
Acrodermatitis Continua of Hallopeau Is a Clinical Phenotype of DITRA: Evidence that It Is a Variant of Pustular Psoriasis Ossama Abbas, Salam Itani, Samer Ghosn, Dermatology	2013	53
Hereditary Leukonychia, or Porcelain Nails, Resulting from Mutations in PLCD1 Maija Kiuru, Mazen Kurban, Munenari Itoh, The American Journal of Human Genetics Genetic DisorderGeneticsPathologyPorcelain NailsMolecular Genetics	2011	51
Mutations in <i>SDR9C7</i> gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosis Yohya Shigehara, Shujiro Okuda, Georges Nemer, Human Molecular Genetics	2016	50
Mutations in SDR9C7 gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosis Yohya Shigehara, Shujiro Okuda, Georges Nemer, Journal of Dermatological Science Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseMolecular Biology	2017	47

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