Janan Mohamad

Janan Mohamad

UNVERIFIED PROFILE

Are you Janan Mohamad?   Register this Author

Register author
Janan Mohamad

Janan Mohamad

Publications by authors named "Janan Mohamad"

Are you Janan Mohamad?   Register this Author

6Publications

224Reads

28Profile Views

Variant in Central Centrifugal Cicatricial Alopecia.

N Engl J Med 2019 02 13;380(9):833-841. Epub 2019 Feb 13.

From the Department of Dermatology (L.M., O.S., A.P., M.P., E.W., L.S., V.B., J.M., E.S.) and the Institute of Pathology (A.G.), Tel Aviv Medical Center, the Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine (L.M., A.P., J.M., E.S.), and the Department of Cell and Developmental Biology (O.I., T.R., N.S.), Tel Aviv University, Tel Aviv, and the Schulich Faculty of Chemistry, Technion, Haifa (N.A.) - all in Israel; the Institute of Human Genetics, University of Bonn, School of Medicine and University Hospital Bonn, Bonn, Germany (M.-T.R., R.C.B.); L'Unité Différenciation Epitheliale et Autoimmunité Rhumatoïde (UDEAR), INSERM, Université Paul Sabatier, Université de Toulouse Midi-Pyrénées, Toulouse, France (M.-C.M., M.S.); the Department of Dermatology, Wake Forest Baptist Medical Center, Winston-Salem, NC (L.U., A.M.); and the Dermatology Department, Nelson R. Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa (N.C.D).

View Article

Download full-text PDF

Source
http://www.nejm.org/doi/10.1056/NEJMoa1816614
Publisher Site
http://dx.doi.org/10.1056/NEJMoa1816614DOI Listing
February 2019

Loss-of-function mutations in caspase recruitment domain-containing protein 14 (CARD14) are associated with a severe variant of atopic dermatitis.

J Allergy Clin Immunol 2019 Jan 21;143(1):173-181.e10. Epub 2018 Sep 21.

Department of Dermatology, Tel Aviv Medical Center, Tel Aviv, Israel; Department of Human Molecular Genetics and Biochemistry, Tel Aviv University, Tel Aviv, Israel. Electronic address:

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S00916749183134
Publisher Site
http://dx.doi.org/10.1016/j.jaci.2018.09.002DOI Listing
January 2019

Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A.

J Invest Dermatol 2018 08 27;138(8):1736-1743. Epub 2018 Jun 27.

Department of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel; Department of Human Molecular Genetics & Biochemistry, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jid.2018.04.032DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056331PMC
August 2018

SAM syndrome is characterized by extensive phenotypic heterogeneity.

Exp Dermatol 2018 07;27(7):787-790

Department of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/exd.13551DOI Listing
July 2018

ARCI7 Revisited and Repositioned.

J Invest Dermatol 2017 04 21;137(4):970-972. Epub 2016 Dec 21.

Department of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel; Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jid.2016.12.008DOI Listing
April 2017

Loss-of-Function Mutations in SERPINB8 Linked to Exfoliative Ichthyosis with Impaired Mechanical Stability of Intercellular Adhesions.

Am J Hum Genet 2016 08 28;99(2):430-6. Epub 2016 Jul 28.

Centre for Cell Biology and Cutaneous Research, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, UK. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ajhg.2016.06.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974070PMC
August 2016