Works by Mohamad, Janan

Results: 11

Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population.

Published in:

Experimental Dermatology, 2021, v. 30, n. 9, p. 1290, doi. 10.1111/exd.14345

By:

Mohamad, Janan;
Samuelov, Liat;
Malchin, Natalia;
Rabinowitz, Tom;
Assaf, Sari;
Malki, Liron;
Malovitski, Kiril;
Israeli, Shirli;
Grafi‐Cohen, Meital;
Bitterman‐Deutsch, Ora;
Molho‐Pessach, Vered;
Cohen‐Barak, Eran;
Bach, Gideon;
Garty, Ben Zion;
Bergman, Reuven;
Harel, Avikam;
Nanda, Arti;
Lestringant, Giles G.;
McGrath, John;
Shalev, Stavit

Publication type:

Article

Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis.

Published in:

Experimental Dermatology, 2020, v. 29, n. 8, p. 742, doi. 10.1111/exd.14140

By:

Mohamad, Janan;
Nanda, Arti;
Pavlovsky, Mor;
Peled, Alon;
Malchin, Natalia;
Malovitski, Kiril;
Pramanik, Rashida;
Weissglas‐Volkov, Daphna;
Shomron, Noam;
McGrath, John;
Sprecher, Eli;
Sarig, Ofer

Publication type:

Article

SAM syndrome is characterized by extensive phenotypic heterogeneity.

Published in:

Experimental Dermatology, 2018, v. 27, n. 7, p. 787, doi. 10.1111/exd.13551

By:

Taiber, Shahar;
Samuelov, Liat;
Mohamad, Janan;
Barak, Eran Cohen;
Sarig, Ofer;
Shalev, Stavit Allon;
Lestringant, Gilles;
Sprecher, Eli

Publication type:

Article

Cutaneous and Developmental Effects of CARD14 Overexpression in Zebrafish.

Published in:

Biomedicines, 2022, v. 10, n. 12, p. 3192, doi. 10.3390/biomedicines10123192

By:

Baniel, Avital;
Ziv, Limor;
Ben-Moshe, Zohar;
Sarig, Ofer;
Mohamad, Janan;
Peled, Alon;
Rechavi, Gideon;
Gothilf, Yoav;
Sprecher, Eli

Publication type:

Article

Defective cathepsin Z affects EGFR expression and causes autosomal dominant palmoplantar keratoderma.

Published in:

British Journal of Dermatology, 2023, v. 189, n. 3, p. 302, doi. 10.1093/bjd/ljad167

By:

Malovitski, Kiril;
Sarig, Ofer;
Feller, Yarden;
Bergson, Shir;
Assaf, Sari;
Mohamad, Janan;
Pavlovsky, Mor;
Giladi, Moshe;
Sprecher, Eli

Publication type:

Article

A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes.

Published in:

British Journal of Dermatology, 2022, v. 187, n. 5, p. 773, doi. 10.1111/bjd.21766

By:

Mohamad, Janan;
Sarig, Ofer;
Beattie, Paula;
Malovitski, Kiril;
Assaf, Sari;
O'Toole, Edel;
Schwartz, Janice;
Evans, Holly;
Samuelov, Liat;
Sprecher, Eli

Publication type:

Article

Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa.

Published in:

Pediatric Dermatology, 2023, v. 40, n. 6, p. 1021, doi. 10.1111/pde.15440

By:

Bergson, Shir;
Daniely, Daniel;
Bomze, David;
Mohamad, Janan;
Malovitski, Kiril;
Meijers, Odile;
Briskin, Valeria;
Bihari, Ofer;
Malchin, Natalia;
Israeli, Shirli;
Mashiah, Jacob;
Falik‐Zaccai, Tzipora;
Avitan‐Hersh, Emily;
Eskin‐Schwartz, Marina;
Allon‐Shalev, Stavit;
Sarig, Ofer;
Sprecher, Eli;
Samuelov, Liat

Publication type:

Article

Epidermolytic epidermal nevus caused by a somatic mutation in KRT2.

Published in:

Pediatric Dermatology, 2021, v. 38, n. 2, p. 538, doi. 10.1111/pde.14529

By:

Mohamad, Janan;
Samuelov, Liat;
Assaf, Sari;
Vodo, Dan;
Sarig, Ofer;
Sprecher, Eli

Publication type:

Article

Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4.

Published in:

American Journal of Medical Genetics. Part A, 2023, v. 191, n. 12, p. 2806, doi. 10.1002/ajmg.a.63408

By:

Peled, Alon;
Sarig, Ofer;
Mohamad, Janan;
Eskin‐Schwartz, Marina;
Vodo, Dan;
Bochner, Ron;
Malchin, Natalya;
Isakov, Ofer;
Shomron, Noam;
Fainberg, Gilad;
Bertolini, Marta;
Paus, Ralf;
Sprecher, Eli

Publication type:

Article

Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1.

Published in:

American Journal of Medical Genetics. Part A, 2022, v. 188, n. 10, p. 2879, doi. 10.1002/ajmg.a.62924

By:

Mohamad, Janan;
Samuelov, Liat;
Assaf, Sari;
Malki, Liron;
Malovitski, Kiril;
Meijers, Odile;
Adir, Noam;
Granot, Ester;
Pavlovsky, Mor;
Sarig, Ofer;
Sprecher, Eli

Publication type:

Article

Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expression.

Published in:

Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-09951-x

By:

Assaf, Sari;
Vodo, Dan;
Malovitski, Kiril;
Mohamad, Janan;
Bergson, Shir;
Feller, Yarden;
Malki, Liron;
Sarig, Ofer;
Sprecher, Eli

Publication type:

Article