Ofer Sarig

4.5k total citations · 1 hit paper
87 papers, 2.1k citations indexed

About

Ofer Sarig is a scholar working on Cell Biology, Molecular Biology and Genetics. According to data from OpenAlex, Ofer Sarig has authored 87 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Cell Biology, 45 papers in Molecular Biology and 20 papers in Genetics. Recurrent topics in Ofer Sarig's work include Skin and Cellular Biology Research (43 papers), Wnt/β-catenin signaling in development and cancer (21 papers) and Autoimmune Bullous Skin Diseases (12 papers). Ofer Sarig is often cited by papers focused on Skin and Cellular Biology Research (43 papers), Wnt/β-catenin signaling in development and cancer (21 papers) and Autoimmune Bullous Skin Diseases (12 papers). Ofer Sarig collaborates with scholars based in Israel, United States and Germany. Ofer Sarig's co-authors include Eli Sprecher, Gilgi Friedlander, Yaniv Ziv, Sven Bergmann, Jan Ihmels, Naama Barkai, Dana Fuchs‐Telem, Janna Nousbeck, Shirli Israeli and Dan Vodo and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and Scientific Reports.

In The Last Decade

Ofer Sarig

79 papers receiving 2.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Revealing modular organization in the yeast transcriptional network

2002 520 citations Ofer Sarig et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Ofer Sarig Israel	23	1.1k	521	359	343	306	87	2.1k
Meg R. Gerstenblith United States	17	1.2k 1.1×	258 0.5×	328 0.9×	213 0.6×	254 0.8×	35	2.1k
Jesús Pérez‐Losada Spain	27	1.6k 1.4×	348 0.7×	248 0.7×	239 0.7×	254 0.8×	71	2.7k
Satrajit Sinha United States	39	3.5k 3.1×	415 0.8×	203 0.6×	619 1.8×	533 1.7×	112	5.3k
A. Hunter Shain United States	23	2.8k 2.4×	438 0.8×	242 0.7×	426 1.2×	544 1.8×	36	4.6k
Juliane Lüscher‐Firzlaff Germany	21	1.3k 1.2×	132 0.3×	380 1.1×	128 0.4×	436 1.4×	31	2.3k
Philippe Bahadoran France	33	1.4k 1.2×	1.2k 2.3×	814 2.3×	125 0.4×	619 2.0×	89	3.3k
Elsa R. Flores United States	35	3.9k 3.4×	347 0.7×	111 0.3×	416 1.2×	582 1.9×	86	5.5k
Vladimir Bezrookove United States	28	2.1k 1.8×	405 0.8×	65 0.2×	333 1.0×	464 1.5×	48	3.3k
Naohito Hatta Japan	23	900 0.8×	235 0.5×	741 2.1×	163 0.5×	198 0.6×	59	1.8k
Andreas Gast Germany	19	2.1k 1.9×	225 0.4×	66 0.2×	607 1.8×	462 1.5×	28	3.3k

Countries citing papers authored by Ofer Sarig

Since Specialization

Citations

This map shows the geographic impact of Ofer Sarig's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ofer Sarig with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ofer Sarig more than expected).

Fields of papers citing papers by Ofer Sarig

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ofer Sarig. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ofer Sarig. The network helps show where Ofer Sarig may publish in the future.

Co-authorship network of co-authors of Ofer Sarig

This figure shows the co-authorship network connecting the top 25 collaborators of Ofer Sarig. A scholar is included among the top collaborators of Ofer Sarig based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ofer Sarig. Ofer Sarig is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Haxho, Fiona, Richard M. Haber, Janan Mohamad, et al.. (2025). 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. Pediatric Dermatology. 42(6). 1239–1247.

Brunet‐Llobet, Lluís, Marta Ivars, Dèlia Yubero, et al.. (2023). Woolly hair in tricho‐dento‐osseous syndrome. Pediatric Dermatology. 40(6). 1094–1096.

Mohamad, Janan, Ofer Sarig, Paula Beattie, et al.. (2022). A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes. British Journal of Dermatology. 187(5). 773–777. 5 indexed citations

Mohamad, Janan, Ofer Sarig, Liron Malki, et al.. (2021). 162 Loss-of-function variants in SERPINA12 underlie autosomal recessive palmoplantar keratoderma. Journal of Investigative Dermatology. 141(10). S176–S176.

Mohamad, Janan, et al.. (2021). Epidermolytic epidermal nevus caused by a somatic mutation in KRT2. Pediatric Dermatology. 38(2). 538–540. 1 indexed citations

Peled, A., Liat Samuelov, Ofer Sarig, et al.. (2021). 078 Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicin. Journal of Investigative Dermatology. 141(10). S161–S161. 1 indexed citations

Mohamad, Janan, Arti Nanda, Mor Pavlovsky, et al.. (2020). Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis. Experimental Dermatology. 29(8). 742–748. 2 indexed citations

Cohen‐Barak, Eran, Lisa M. Godsel, Jennifer L. Koetsier, et al.. (2019). The Role of Desmoglein 1 in Gap Junction Turnover Revealed through the Study of SAM Syndrome. Journal of Investigative Dermatology. 140(3). 556–567.e9. 16 indexed citations

Hsu, Chao‐Kai, Magdalene Michael, Cédric Duval, et al.. (2019). Coagulation Factor XIII-A Subunit Missense Mutation in the Pathobiology of Autosomal Dominant Multiple Dermatofibromas. Journal of Investigative Dermatology. 140(3). 624–635.e7. 10 indexed citations

10.

Radeva, Mariya Y., Elias Walter, Amir S. Yazdi, et al.. (2019). ST18 Enhances PV-IgG-Induced Loss of Keratinocyte Cohesion in Parallel to Increased ERK Activation. Frontiers in Immunology. 10. 770–770. 20 indexed citations

11.

Peled, A., Ofer Sarig, Guangping Sun, et al.. (2018). Loss-of-function mutations in caspase recruitment domain-containing protein 14 (CARD14) are associated with a severe variant of atopic dermatitis. Journal of Allergy and Clinical Immunology. 143(1). 173–181.e10. 52 indexed citations

12.

Vodo, Dan, Ofer Sarig, & Eli Sprecher. (2018). The Genetics of Pemphigus Vulgaris. Frontiers in Medicine. 5. 226–226. 51 indexed citations

13.

Vodo, Dan, Edel A. O’Toole, N. Malchin, et al.. (2018). 773 Striate palmoplantar keratoderma resulting from a missense mutation in DSG1. Journal of Investigative Dermatology. 138(5). S131–S131. 2 indexed citations

14.

Sarig, Ofer & Eli Sprecher. (2017). The Molecular Revolution in Cutaneous Biology: Era of Next-Generation Sequencing. Journal of Investigative Dermatology. 137(5). e79–e82. 13 indexed citations

15.

Eskin‐Schwartz, Marina, Y. Metzger, A. Peled, et al.. (2016). 378 Somatic mosaicism for the “lethal” GJB2 mutation results in a patterned form of spiny hyperkeratosis without eccrine involvement. Journal of Investigative Dermatology. 136(5). S67–S67. 2 indexed citations

16.

Mohamad, Janan, N. Malchin, Stavit Shalev, Ofer Sarig, & Eli Sprecher. (2016). ARCI7 Revisited and Repositioned. Journal of Investigative Dermatology. 137(4). 970–972. 5 indexed citations

17.

Pigors, Manuela, Ofer Sarig, Vincent Plagnol, et al.. (2016). Loss-of-Function Mutations in SERPINB8 Linked to Exfoliative Ichthyosis with Impaired Mechanical Stability of Intercellular Adhesions. The American Journal of Human Genetics. 99(2). 430–436. 22 indexed citations

18.

Sarig, Ofer, Debora Rapaport, Akemi Ishida‐Yamamoto, et al.. (2012). Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Syndrome Is Caused by a POC1A Mutation. The American Journal of Human Genetics. 91(2). 337–342. 53 indexed citations

19.

Nousbeck, Janna, Bettina Burger, Dana Fuchs‐Telem, et al.. (2011). A Mutation in a Skin-Specific Isoform of SMARCAD1 Causes Autosomal-Dominant Adermatoglyphia. The American Journal of Human Genetics. 89(2). 302–307. 32 indexed citations

20.

Nousbeck, Janna, Ofer Sarig, Nili Avidan, et al.. (2009). Insulin-Like Growth Factor-Binding Protein 7 Regulates Keratinocyte Proliferation, Differentiation and Apoptosis. Journal of Investigative Dermatology. 130(2). 378–387. 34 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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