Janan Mohamad - Search Results

Year	Number of Results
2016	2
2017	1
2018	3
2019	2
2020	4
2021	2
2022	5
2023	3
2024	0

1

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

Bergson S, Daniely D, Bomze D, Mohamad J, Malovitski K, Meijers O, Briskin V, Bihari O, Malchin N, Israeli S, Mashiah J, Falik-Zaccai T, Avitan-Hersh E, Eskin-Schwartz M, Allon-Shalev S, Sarig O, Sprecher E, Samuelov L. Bergson S, et al. Among authors: mohamad j. Pediatr Dermatol. 2023 Nov-Dec;40(6):1021-1027. doi: 10.1111/pde.15440. Epub 2023 Oct 12. Pediatr Dermatol. 2023. PMID: 37827535

2

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

Peled A, Sarig O, Mohamad J, Eskin-Schwartz M, Vodo D, Bochner R, Malchin N, Isakov O, Shomron N, Fainberg G, Bertolini M, Paus R, Sprecher E. Peled A, et al. Among authors: mohamad j. Am J Med Genet A. 2023 Dec;191(12):2806-2812. doi: 10.1002/ajmg.a.63408. Epub 2023 Sep 19. Am J Med Genet A. 2023. PMID: 37724761

3

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

Malovitski K, Sarig O, Feller Y, Bergson S, Assaf S, Mohamad J, Pavlovsky M, Giladi M, Sprecher E. Malovitski K, et al. Among authors: mohamad j. Br J Dermatol. 2023 Aug 24;189(3):302-311. doi: 10.1093/bjd/ljad167. Br J Dermatol. 2023. PMID: 37210216

4

Cutaneous and Developmental Effects of CARD14 Overexpression in Zebrafish.

Baniel A, Ziv L, Ben-Moshe Z, Sarig O, Mohamad J, Peled A, Rechavi G, Gothilf Y, Sprecher E. Baniel A, et al. Among authors: mohamad j. Biomedicines. 2022 Dec 8;10(12):3192. doi: 10.3390/biomedicines10123192. Biomedicines. 2022. PMID: 36551948 Free PMC article.

5

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

Mohamad J, Samuelov L, Assaf S, Malki L, Malovitski K, Meijers O, Adir N, Granot E, Pavlovsky M, Sarig O, Sprecher E. Mohamad J, et al. Am J Med Genet A. 2022 Oct;188(10):2879-2887. doi: 10.1002/ajmg.a.62924. Epub 2022 Aug 3. Am J Med Genet A. 2022. PMID: 35920354

6

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

Mohamad J, Sarig O, Beattie P, Malovitski K, Assaf S, O'Toole E, Schwartz J, Evans H, Samuelov L, Sprecher E. Mohamad J, et al. Br J Dermatol. 2022 Nov;187(5):773-777. doi: 10.1111/bjd.21766. Epub 2022 Aug 8. Br J Dermatol. 2022. PMID: 35822506

7

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

Assaf S, Vodo D, Malovitski K, Mohamad J, Bergson S, Feller Y, Malki L, Sarig O, Sprecher E. Assaf S, et al. Among authors: mohamad j. Sci Rep. 2022 Apr 8;12(1):5958. doi: 10.1038/s41598-022-09951-x. Sci Rep. 2022. PMID: 35396567 Free PMC article.

8

Loss-of-function variants in KLF4 underlie autosomal dominant palmoplantar keratoderma.

Malovitski K, Sarig O, Assaf S, Mohamad J, Malki L, Bergson S, Peled A, Eskin-Schwartz M, Gat A, Pavlovsky M, Sprecher E. Malovitski K, et al. Among authors: mohamad j. Genet Med. 2022 May;24(5):1085-1095. doi: 10.1016/j.gim.2022.01.009. Epub 2022 Feb 12. Genet Med. 2022. PMID: 35168889 Free article.

9

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

Mohamad J, Samuelov L, Malchin N, Rabinowitz T, Assaf S, Malki L, Malovitski K, Israeli S, Grafi-Cohen M, Bitterman-Deutsch O, Molho-Pessach V, Cohen-Barak E, Bach G, Garty BZ, Bergman R, Harel A, Nanda A, Lestringant GG, McGrath J, Shalev S, Shomron N, Mashiah J, Eskin-Schwartz M, Sprecher E, Sarig O. Mohamad J, et al. Exp Dermatol. 2021 Sep;30(9):1290-1297. doi: 10.1111/exd.14345. Epub 2021 Apr 15. Exp Dermatol. 2021. PMID: 33786896

10

Epidermolytic epidermal nevus caused by a somatic mutation in KRT2.

Mohamad J, Samuelov L, Assaf S, Vodo D, Sarig O, Sprecher E. Mohamad J, et al. Pediatr Dermatol. 2021 Mar;38(2):538-540. doi: 10.1111/pde.14529. Epub 2021 Feb 8. Pediatr Dermatol. 2021. PMID: 33555633

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