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O. Sarig · SciRah

Researcher profile · Semantic Scholar

O. Sarig

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O. Sarig — researcher profile on SciRah

h-index: 34
Works: 172
Citations: 4,420

Most-cited papers

Variant PADI3 in Central Centrifugal Cicatricial Alopecia
L. Malki, O. Sarig, M. Romano, M. Méchin +17 more
2019New England Journal of Medicine111 citations Open access
Semantic Scholar
The Genetics of Pemphigus Vulgaris
D. Vodo, O. Sarig, E. Sprecher
2018Frontiers in Medicine81 citations Open access
Semantic Scholar
Loss‐of‐function mutations in caspase recruitment domain‐containing protein 14 (CARD14) are associated with a severe variant of atopic dermatitis
A. Peled, O. Sarig, Guang-Ping Sun, L. Samuelov +15 more
2019Journal of Allergy and Clinical Immunology69 citations Open access
Semantic Scholar
Treatment of epidermolysis bullosa pruriginosa‐associated pruritus with dupilumab
W. Shehadeh, O. Sarig, J. Bär, E. Sprecher +1 more
2020British Journal of Dermatology61 citations
Semantic Scholar
A phenotype combining hidradenitis suppurativa with Dowling–Degos disease caused by a founder mutation in PSENEN
M. Pavlovsky, O. Sarig, M. Eskin-Schwartz, N. Malchin +6 more
2018British Journal of Dermatology56 citations
Semantic Scholar
Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A
J. Mohamad, O. Sarig, L. Godsel, A. Peled +15 more
2018Journal of Investigative Dermatology43 citations Open access
Semantic Scholar
SAM syndrome is characterized by extensive phenotypic heterogeneity
S. Taiber, L. Samuelov, J. Mohamad, E. Barak +4 more
2018Experimental Dermatology30 citations
Semantic Scholar
Loss-of-function variants in SERPINA12 underlie autosomal recessive palmoplantar keratoderma.
J. Mohamad, O. Sarig, L. Malki, T. Rabinowitz +11 more
2020Journal of Investigative Dermatology29 citations Open access
Semantic Scholar
ST18 Enhances PV-IgG-Induced Loss of Keratinocyte Cohesion in Parallel to Increased ERK Activation
M. Radeva, E. Walter, R. Stach, A. Yazdi +4 more
2019Frontiers in Immunology26 citations Open access
Semantic Scholar
Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population
J. Mohamad, L. Samuelov, N. Malchin, T. Rabinowitz +21 more
2021Experimental Dermatology24 citations
Semantic Scholar
Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicin
A. Peled, L. Samuelov, O. Sarig, R. Bochner +5 more
2019British Journal of Dermatology24 citations
Semantic Scholar
The role of Desmoglein 1 in gap junction turnover revealed through the study of SAM syndrome
Eran Cohen Barak, L. Godsel, J. Koetsier, Marihan Hegazy +15 more
2019Journal of Investigative Dermatology22 citations Open access
Semantic Scholar
Vorinostat, a histone deacetylase inhibitor, as a potential novel treatment for psoriasis
L. Samuelov, R. Bochner, L. Magal, K. Malovitski +7 more
2021Experimental Dermatology21 citations
Semantic Scholar
ST18 affects cell–cell adhesion in pemphigus vulgaris in a tumour necrosis factor‐α‐dependent fashion *
S. Assaf, L. Malki, T. Mayer, J. Mohamad +6 more
2020British Journal of Dermatology20 citations
Semantic Scholar
Evidence for cutaneous dysbiosis in dystrophic epidermolysis bullosa
J. Bär, O. Sarig, M. Lotan-Pompan, B. Dassa +5 more
2021Clincal and Experimental Dermatology17 citations
Semantic Scholar
Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis
L. Malki, O. Sarig, N. Cesarato, J. Mohamad +15 more
2020Genetics in Medicine17 citations Open access
Semantic Scholar
Coagulation Factor XIII-A Subunit Missense Mutation in the Pathobiology of Autosomal Dominant Multiple Dermatofibromas.
Chavalit Supsrisunjai, Chao-Kai Hsu, Magdalene Michael, C. Duval +15 more
2020Journal of Investigative Dermatology17 citations Open access
Semantic Scholar
Coexistence of pachyonychia congenita and hidradenitis suppurativa: more than a coincidence
M. Pavlovsky, A. Peled, O. Sarig, N. Astman +8 more
2022British Journal of Dermatology13 citations Open access
Semantic Scholar
Recessive epidermolytic ichthyosis results from loss of keratin 10 expression, regardless of the mutation location
D. Vodo, O. Sarig, A. Peled, L. Samuelov +3 more
2018Clincal and Experimental Dermatology13 citations
Semantic Scholar
Epidermolysis bullosa simplex due to bi‐allelic DST mutations: Case series and review of the literature
Dalit Ganani, K. Malovitski, O. Sarig, A. Gat +2 more
2021Pediatric dermatology12 citations
Semantic Scholar
Identification of a recurrent mutation in ATP2C1 demonstrates that papular acantholytic dyskeratosis and Hailey–Hailey disease are allelic disorders
D. Vodo, N. Malchin, M. Furman, O. Sarig +1 more
2018British Journal of Dermatology12 citations
Semantic Scholar
Striate palmoplantar keratoderma resulting from a missense mutation in DSG1
D. Vodo, E. O'Toole, N. Malchin, A. Lahav +5 more
2018British Journal of Dermatology10 citations Open access
Semantic Scholar
PLACK syndrome shows remarkable phenotypic homogeneity
J. Mohamad, L. Samuelov, D. Ben-Amitai, N. Malchin +2 more
2019Clincal and Experimental Dermatology9 citations
Semantic Scholar
Immune‐regulatory genes as possible modifiers of familial pityriasis rubra pilaris – lessons from a family with PRP and psoriasis
I. Spoerri, S. Herms, O. Eytan, O. Sarig +4 more
2018Journal of the European Academy of Dermatology and Venereology9 citations
Semantic Scholar
Identification of clinically useful predictive genetic variants in pachyonychia congenita
L. Samuelov, O. Sarig, N. Adir, M. Pavlovsky +4 more
2021Clincal and Experimental Dermatology8 citations
Semantic Scholar
Defective cathepsin Z affects EGFR expression and causes autosomal dominant palmoplantar keratoderma.
K. Malovitski, O. Sarig, Yarden Feller, S. Bergson +5 more
2023British Journal of Dermatology7 citations
Semantic Scholar
Neonatal inflammatory skin and bowel disease type 1 caused by a complex genetic defect and responsive to combined anti‐tumour necrosis factor‐α and interleukin‐12/23 blockade
L. Samuelov, O. Sarig, K. Malovitski, S. Bergson +3 more
2022British Journal of Dermatology7 citations
Semantic Scholar
Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expression
S. Assaf, D. Vodo, K. Malovitski, J. Mohamad +5 more
2022Scientific Reports7 citations Open access
Semantic Scholar
miR-200b-mediated reversion of a spectrum of epithelial to mesenchymal transition states in recessive dystrophic epidermolysis bullosa squamous cell carcinomas.
J. Illmer, R. Zauner, Josefina Piñón Hofbauer, M. Wimmer +16 more
2023British Journal of Dermatology6 citations Open access
Semantic Scholar
Ustekinumab therapy for Netherton syndrome
L. Samuelov, Waseem Shehadeh, O. Sarig, A. Gat +2 more
2022Journal of dermatology (Print)6 citations
Semantic Scholar
A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes
J. Mohamad, O. Sarig, P. Beattie, K. Malovitski +6 more
2022British Journal of Dermatology6 citations
Semantic Scholar
HMCN1 variants aggravate epidermolysis bullosa simplex phenotype
S. Bergson, O. Sarig, M. Giladi, J. Mohamad +23 more
2025Journal of Experimental Medicine5 citations Open access
Semantic Scholar
Heterozygous variants in the integrin subunit beta 4 gene (ITGB4) cause autosomal dominant nail dystrophy
K. Malovitski, O. Meijers, E. Cohen-Barak, J. Bergman +8 more
2022British Journal of Dermatology5 citations
Semantic Scholar
Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1
J. Mohamad, L. Samuelov, S. Assaf, L. Malki +7 more
2022American Journal of Medical Genetics. Part A5 citations
Semantic Scholar
Loss-of-function variants in KLF4 underlie autosomal dominant palmoplantar keratoderma.
K. Malovitski, O. Sarig, S. Assaf, J. Mohamad +7 more
2022Genetics in Medicine5 citations Open access
Semantic Scholar
Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia.
Noy Keller-Rosenthal, O. Sarig, M. Giladi, K. Malovitski +7 more
2025Journal of Investigative Dermatology4 citations Open access
Semantic Scholar
Molecular epidemiology of pachyonychia congenita in the Israeli population
M. Pavlovsky, A. Peled, L. Samuelov, L. Malki +7 more
2020Clincal and Experimental Dermatology4 citations
Semantic Scholar
Glutathione S‐transferase polymorphisms in patients with photosensitive and non‐photosensitive drug eruptions
Tal Ben-Ami, O. Sarig, E. Sprecher, I. Goldberg
2019Photodermatology, Photoimmunology & Photomedicine4 citations
Semantic Scholar
Novel POFUT1 mutation associated with hidradenitis suppurativa–Dowling–Degos disease firm up a role for Notch signalling in the pathogenesis of this disorder: reply from the authors
M. Pavlovsky, O. Sarig, M. Eskin-Schwartz, A. Hafner +1 more
2018British Journal of Dermatology4 citations
Semantic Scholar
Woolly hair in tricho‐dento‐osseous syndrome
H. Perandones‐González, Lluis Rusiñol-Batlle, David Bosquez, L. Brunet-Llobet +7 more
2023Pediatric dermatology3 citations
Semantic Scholar
Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4
A. Peled, O. Sarig, J. Mohamad, M. Eskin-Schwartz +9 more
2023American Journal of Medical Genetics. Part A3 citations
Semantic Scholar
Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis
J. Mohamad, A. Nanda, M. Pavlovsky, A. Peled +8 more
2020Experimental Dermatology3 citations
Semantic Scholar
Palmoplantar keratoderma caused by a missense variant in CTSB encoding cathepsin B
J. Mohamad, L. Samuelov, L. Malki, A. Peled +10 more
2020Clincal and Experimental Dermatology3 citations
Semantic Scholar
Identification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome
D. Ralser, S. Kumar, O. Borisov, O. Sarig +6 more
2020British Journal of Dermatology3 citations Open access
Semantic Scholar
Punctate palmoplantar keratoderma: an unusual mutation causing an unusual phenotype
D. Vodo, O. Sarig, D. Jeddah, N. Malchin +8 more
2018British Journal of Dermatology3 citations
Semantic Scholar
Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads (PLACK) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two Patients.
Fiona Haxho, R. Haber, J. Mohamad, O. Sarig +4 more
2025Pediatric dermatology2 citations Open access
Semantic Scholar
Atypical presentation of laryngo‐onycho‐cutaneous syndrome resulting from novel mutations in LAMA3A
D. Vodo, N. Malchin, A. Derowe, E. Sprecher +1 more
2021Clincal and Experimental Dermatology2 citations
Semantic Scholar
Epidermolytic epidermal nevus caused by a somatic mutation in KRT2
J. Mohamad, L. Samuelov, S. Assaf, D. Vodo +2 more
2021Pediatric dermatology2 citations Open access
Semantic Scholar
Acute Respiratory Distress Syndrome in a Carrier of an Interleukin-36 Receptor Antagonist Mutation With Generalized Pustular Psoriasis
A. Baniel, Efract Bar-Ilan, Y. Hilerowicz, Ilan Merdler +4 more
2021Journal of Psoriasis and Psoriatic Arthritis2 citations
Semantic Scholar
[LINEAR MYCOSIS FUNGOIDES IN A BLASCHKOID DISTRIBUTION].
Y. Kaplan, O. Sarig, T. Rabinowitz, J. Mohamad +3 more
2020Harefuah2 citations
Semantic Scholar

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J. Mohamad×24
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M. Pavlovsky — researcher profile on SciRah

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L. Malki — researcher profile on SciRah

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