Dan Vodo

590 total citations
17 papers, 212 citations indexed

About

Dan Vodo is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Dan Vodo has authored 17 papers receiving a total of 212 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Cell Biology and 7 papers in Genetics. Recurrent topics in Dan Vodo's work include Skin and Cellular Biology Research (9 papers), Genetic and rare skin diseases. (5 papers) and Autoimmune Bullous Skin Diseases (5 papers). Dan Vodo is often cited by papers focused on Skin and Cellular Biology Research (9 papers), Genetic and rare skin diseases. (5 papers) and Autoimmune Bullous Skin Diseases (5 papers). Dan Vodo collaborates with scholars based in Israel, United States and Germany. Dan Vodo's co-authors include Eli Sprecher, Ofer Sarig, A. Peled, Liat Samuelov, Janan Mohamad, N. Malchin, Noam Shomron, Ron Bochner, Mor Pavlovsky and Tom Rabinowitz and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and PLoS Genetics.

In The Last Decade

Dan Vodo

16 papers receiving 205 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dan Vodo Israel	9	103	67	65	61	59	17	212
H.N. Liu Taiwan	7	183 1.8×	146 2.2×	132 2.0×	45 0.7×	86 1.5×	8	363
Janan Mohamad Israel	9	26 0.3×	17 0.3×	20 0.3×	79 1.3×	84 1.4×	25	236
Yasuko Takizawa Japan	9	97 0.9×	13 0.2×	26 0.4×	128 2.1×	187 3.2×	14	261
Ana Kljuic United States	9	27 0.3×	20 0.3×	15 0.2×	119 2.0×	89 1.5×	10	222
Shefali Rajpopat United Kingdom	5	23 0.2×	8 0.1×	10 0.2×	53 0.9×	74 1.3×	7	175
Kimberly Nicholson United States	8	50 0.5×	9 0.1×	14 0.2×	63 1.0×	26 0.4×	10	308
Glenda M. Beaman United Kingdom	9	13 0.1×	34 0.5×	18 0.3×	129 2.1×	18 0.3×	20	278
Pei Lin United States	6	36 0.3×	9 0.1×	39 0.6×	93 1.5×	17 0.3×	12	190
Ursula Giussani Italy	9	13 0.1×	14 0.2×	27 0.4×	124 2.0×	32 0.5×	16	226
P.M. Steijlen Netherlands	10	21 0.2×	10 0.1×	6 0.1×	127 2.1×	68 1.2×	18	304

Countries citing papers authored by Dan Vodo

Since Specialization

Citations

This map shows the geographic impact of Dan Vodo'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 Dan Vodo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dan Vodo more than expected).

Fields of papers citing papers by Dan Vodo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dan Vodo. 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 Dan Vodo. The network helps show where Dan Vodo may publish in the future.

Co-authorship network of co-authors of Dan Vodo

This figure shows the co-authorship network connecting the top 25 collaborators of Dan Vodo. A scholar is included among the top collaborators of Dan Vodo 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 Dan Vodo. Dan Vodo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

Vodo, Dan & Eli Sprecher. (2023). The genetic basis of pemphigus vulgaris. SHILAP Revista de lepidopterología. 2(2). 203–212.

Vodo, Dan, et al.. (2022). Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expression. Scientific Reports. 12(1). 5958–5958. 4 indexed citations

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

Vodo, Dan, N. Malchin, Ari DeRowe, Eli Sprecher, & Ofer Sarig. (2021). Atypical presentation of laryngo‐onycho‐cutaneous syndrome resulting from novel mutations in LAMA3A. Clinical and Experimental Dermatology. 46(5). 990–992. 1 indexed citations

Mohamad, Janan, Ofer Sarig, Liron Malki, et al.. (2020). Loss-of-Function Variants in SERPINA12 Underlie Autosomal Recessive Palmoplantar Keratoderma. Journal of Investigative Dermatology. 140(11). 2178–2187. 16 indexed citations

Malki, Liron, Ofer Sarig, Janan Mohamad, et al.. (2020). Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis. Genetics in Medicine. 22(7). 1227–1234. 9 indexed citations

Malki, Liron, Janan Mohamad, A. Peled, et al.. (2020). ST18 affects cell–cell adhesion in pemphigus vulgaris in a tumour necrosis factor‐α‐dependent fashion*. British Journal of Dermatology. 184(6). 1153–1160. 12 indexed citations

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

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

10.

Mohamad, Janan, Ofer Sarig, Lisa M. Godsel, et al.. (2018). 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. 138(8). 1736–1743. 30 indexed citations

11.

Eskin‐Schwartz, Marina, Ofer Sarig, Andrea Gat, et al.. (2017). Epidermolytic Ichthyosis Sine Epidermolysis. American Journal of Dermatopathology. 39(6). 440–444. 12 indexed citations

12.

Vodo, Dan, Ofer Sarig, A. Peled, et al.. (2017). Recessive epidermolytic ichthyosis results from loss of keratin 10 expression, regardless of the mutation location. Clinical and Experimental Dermatology. 43(2). 187–190. 9 indexed citations

13.

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

14.

Vodo, Dan, Ofer Sarig, Shamir Geller, et al.. (2016). Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene. PLoS Genetics. 12(5). e1006008–e1006008. 35 indexed citations

15.

Eskin‐Schwartz, Marina, Ofer Sarig, Ofer Isakov, et al.. (2016). 381 Epidermolytic ichthyosis sine epidermolysis. Journal of Investigative Dermatology. 136(5). S67–S67. 6 indexed citations

16.

Eskin‐Schwartz, Marina, Y. Metzger, A. Peled, et al.. (2016). Somatic Mosaicism for a “Lethal” GJB2 Mutation Results in a Patterned Form of Spiny Hyperkeratosis without Eccrine Involvement. Pediatric Dermatology. 33(3). 322–326. 6 indexed citations

17.

Samuelov, Liat, Ofer Sarig, Dan Vodo, et al.. (2015). RBM28, a protein deficient in ANE syndrome, regulates hair follicle growth via miR‐203 and p63. Experimental Dermatology. 24(8). 618–622. 16 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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