Ofer Sarig

4.5k citations

87 papers · 2.1k indexed · 1 hit paper · h-index 23

Impact in

Dermatology top 1%
- Dermatology and Skin Diseases
Cell Biology top 2%
- Skin and Cellular Biology Research

Papers in ⓘ

Cell Biology 47
- Skin and Cellular Biology Research 43
Dermatology 17

Co-authors: Eli Sprecher (81 shared papers)Jan Ihmels (1 shared paper)Yaniv Ziv (1 shared paper)Sven Bergmann (1 shared paper)Naama Barkai (1 shared paper)Gilgi Friedlander (1 shared paper)Dana Fuchs‐Telem (15 shared papers)Janna Nousbeck (12 shared papers)
Journals: Clinical and Experimental Dermatology (16 papers)Journal of Investigative Dermatology (15 papers)British Journal of Dermatology (13 papers)Pediatric Dermatology (6 papers)The American Journal of Human Genetics (6 papers)
Partner nations: Israel United States Germany

In The Last Decade

Ofer Sarig

79 papers receiving 2.0k citations

Hit Papers

align trajectories log scale

Revealing modular organization in the yeast transcriptional network 2002 · 520 citations

Peers

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-authors

The 25 scholars most cited alongside Ofer Sarig, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ofer Sarig Line = papers co-authored together Ofer Sarig links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 87 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Revealing modular organization in the yeast transcriptional network Nature Genetics ·Jan Ihmels, Gilgi Friedlander, Sven Bergmann, Ofer Sarig, Yaniv Ziv, Naama Barkai Hit paper breakdown →	2002	520
2	Familial Pityriasis Rubra Pilaris Is Caused by Mutations in CARD14 The American Journal of Human Genetics ·Dana Fuchs‐Telem, Ofer Sarig, Maurice A. M. Van Steensel, Ofer Isakov, Shirli Israeli, Janna Nousbeck, Katharina Richard, Véronique Winnepenninckx, Marigje Vernooij, Noam Shomron, Jouni Uitto, Philip Fleckman, Gabriele Richard, Eli Sprecher	2012	161
3	Desmoglein-1/Erbin interaction suppresses ERK activation to support epidermal differentiation Journal of Clinical Investigation ·Robert M. Harmon, Cory L. Simpson, Jodi Johnson, Jennifer L. Koetsier, Adi D. Dubash, Nicole A. Najor, Ofer Sarig, Eli Sprecher, Kathleen J. Green	2013	103
4	Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakin Journal of Allergy and Clinical Immunology ·Maeve A. McAleer, Elizabeth Pöhler, Frances J.D. Smith, Neil Wilson, Christian Cole, Stuart A. MacGowan, Jennifer L. Koetsier, Lisa M. Godsel, Robert M. Harmon, Robert Gruber, Debra Crumrine, Peter M. Elias, Michael McDermott, Karina Butler, Annemarie Broderick, Ofer Sarig, Eli Sprecher, Kathleen J. Green, W.H. Irwin McLean, Alan D. Irvine	2015	82
5	CEDNIK syndrome results from loss-of-function mutations in SNAP29 British Journal of Dermatology ·Dana Fuchs‐Telem, Helen Stewart, David Rapaport, Janna Nousbeck, Andrea Gat, M. Gini, Yarine Lugassy, Steffen Emmert, Katja‐Martina Eckl, H.-C. Hennies, Ofer Sarig, Dorith Goldsher, Benjamin Meilik, Akemi Ishida‐Yamamoto, Mia Horowitz, Eli Sprecher	2010	64
6	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Syndrome Is Caused by a POC1A Mutation The American Journal of Human Genetics ·Ofer Sarig, Sagi Nahum, Debora Rapaport, Akemi Ishida‐Yamamoto, Dana Fuchs‐Telem, Qiaoli Li, Ksenya Cohen‐Katsenelson, Ronen Spiegel, Janna Nousbeck, Shirli Israeli, Z Borochowitz, Gilly Padalon‐Brauch, Jouni Uitto, Mia Horowitz, Stavit A. Shalev, Eli Sprecher	2012	53
7	A Mutation in LIPN, Encoding Epidermal Lipase N, Causes a Late-Onset Form of Autosomal-Recessive Congenital Ichthyosis The American Journal of Human Genetics ·Shirli Israeli, Ziad Khamaysi, Dana Fuchs‐Telem, Janna Nousbeck, Richard N. Bergman, Ofer Sarig, Eli Sprecher	2011	53
8	Functional Characterization of SAMD9, a Protein Deficient in Normophosphatemic Familial Tumoral Calcinosis Journal of Investigative Dermatology ·Dov Hershkovitz, Yonit Gross, Sagi Nahum, Shiran Yehezkel, Ofer Sarig, Jouni Uitto, Eli Sprecher	2010	53
9	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 ·A. Peled, Ofer Sarig, Guangping Sun, Liat Samuelov, Chi A., Yuan Zhang, Tom DiMaggio, Celeste Nelson, Kelly D. Stone, Alexandra F. Freeman, Liron Malki, Lucia Seminario‐Vidal, Latha M. Chamarthy, Valeria Briskin, Janan Mohamad, Mor Pavlovsky, Jolán E. Walter, Joshua D. Milner, Eli Sprecher	2018	52
10	The Genetics of Pemphigus Vulgaris Frontiers in Medicine ·Dan Vodo, Ofer Sarig, Eli Sprecher	2018	51
11	Autosomal dominant inheritance of central centrifugal cicatricial alopecia in black South Africans Journal of the American Academy of Dermatology ·Ncoza C. Dlova, Francois H. Jordaan, Ofer Sarig, Eli Sprecher	2014	44
12	Pyoderma gangrenosum, acne and ulcerative colitis in a patient with a novel mutation in thePSTPIP1gene Clinical and Experimental Dermatology ·Tal Zeeli, Gilly Padalon‐Brauch, Eran Ellenbogen, Andrea Gat, Ofer Sarig, Eli Sprecher	2015	43
13	A phenotype combining hidradenitis suppurativa with Dowling-Degos disease caused by a founder mutation in PSENEN British Journal of Dermatology ·Mor Pavlovsky, Ofer Sarig, Marina Eskin‐Schwartz, N. Malchin, Ron Bochner, Janan Mohamad, Andrea Gat, A. Peled, A. Häfner, Eli Sprecher	2017	37
14	Cole Disease Results from Mutations in ENPP1 The American Journal of Human Genetics ·Ori Eytan, Fanny Morice‐Picard, Ofer Sarig, Khaled Ezzedine, Ofer Isakov, Qiaoli Li, Akemi Ishida‐Yamamoto, Noam Shomron, Tomer Goldsmith, Dana Fuchs‐Telem, Noam Adir, Jouni Uitto, Seth J. Orlow, Alain Taı̈eb, Eli Sprecher	2013	36
15	Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene PLoS Genetics ·Dan Vodo, Ofer Sarig, Shamir Geller, Edna Ben‐Asher, Tsviya Olender, Ron Bochner, Ilan Goldberg, Judith Nosgorodsky, Anna Alkelai, Pavel Tatarskyy, A. Peled, Sharon Baum, Aviv Barzilai, Saleh Ibrahim, Detlef Zillikens, Doron Lancet, Eli Sprecher	2016	35
16	Insulin-Like Growth Factor-Binding Protein 7 Regulates Keratinocyte Proliferation, Differentiation and Apoptosis Journal of Investigative Dermatology ·Janna Nousbeck, Ofer Sarig, Nili Avidan, Margarita Indelman, Richard N. Bergman, Michal Ramon, Claes D. Enk, Eli Sprecher	2009	34
17	Epstein–Barr virus antibodies mark systemic lupus erythematosus and scleroderma patients negative for anti‐DNA Immunology ·Ittai Fattal, Noam Shental, Yair Molad, Armando Gabrielli, Elisheva Pokroy‐Shapira, Shirly Oren, Avi Livneh, Pnina Langevitz, Rachel Pauzner, Ofer Sarig, Uzi Gafter, Eytan Domany, Irun R. Cohen	2013	33
18	A Mutation in a Skin-Specific Isoform of SMARCAD1 Causes Autosomal-Dominant Adermatoglyphia The American Journal of Human Genetics ·Janna Nousbeck, Bettina Burger, Dana Fuchs‐Telem, Mor Pavlovsky, Shlomit Fenig, Ofer Sarig, Peter Itin, Eli Sprecher	2011	32
19	Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3‐Methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and leigh‐Like Syndrome) caused by novel mutations in SERAC1 American Journal of Medical Genetics Part A ·Ofer Sarig, Dorit Goldsher, Janna Nousbeck, Dana Fuchs‐Telem, Ksenya Cohen‐Katsenelson, Theodore C. Iancu, Irena Manov, Ann Saada, Eli Sprecher, Hanna Mandel	2013	32
20	Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A Journal of Investigative Dermatology ·Janan Mohamad, Ofer Sarig, Lisa M. Godsel, A. Peled, N. Malchin, Ron Bochner, Dan Vodo, Tom Rabinowitz, Mor Pavlovsky, Shahar Taiber, Maya Fried, Marina Eskin‐Schwartz, Siwar Assi, Noam Shomron, Jouni Uitto, Jennifer L. Koetsier, Richard N. Bergman, Kathleen J. Green, Eli Sprecher	2018	30

About Ofer Sarig

Ofer Sarig is a scholar working on Cell Biology, Dermatology, Urology, Immunology and Allergy and Pathology and Forensic Medicine, having authored 87 papers that have together received 2.1k indexed citations. Recurring topics across this work include Skin and Cellular Biology Research (43 papers), Wnt/β-catenin signaling in development and cancer (21 papers), Autoimmune Bullous Skin Diseases (12 papers), Genetic and rare skin diseases. (11 papers), Dermatological and Skeletal Disorders (10 papers), Hair Growth and Disorders (10 papers), Plant Reproductive Biology (8 papers) and Cell Adhesion Molecules Research (7 papers). The work is most often cited by research in Dermatology (359 citations), Cell Biology (521 citations), Immunology and Allergy (102 citations), Molecular Biology (1.1k citations) and Urology (96 citations). Ofer Sarig has collaborated with scholars based in Israel, United States and Germany. Frequent co-authors include Eli Sprecher, Jan Ihmels, Yaniv Ziv, Sven Bergmann, Naama Barkai, Gilgi Friedlander, Dana Fuchs‐Telem, Janna Nousbeck, Shirli Israeli and Dan Vodo. Their work appears in journals such as Clinical and Experimental Dermatology, Journal of Investigative Dermatology, British Journal of Dermatology, Pediatric Dermatology and The American Journal of Human Genetics.

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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