M. Shohat

958 total citations
19 papers, 226 citations indexed

About

M. Shohat is a scholar working on Molecular Biology, Immunology and Dermatology. According to data from OpenAlex, M. Shohat has authored 19 papers receiving a total of 226 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Immunology and 4 papers in Dermatology. Recurrent topics in M. Shohat's work include T-cell and Retrovirus Studies (2 papers), Neonatal Health and Biochemistry (2 papers) and Dermatology and Skin Diseases (2 papers). M. Shohat is often cited by papers focused on T-cell and Retrovirus Studies (2 papers), Neonatal Health and Biochemistry (2 papers) and Dermatology and Skin Diseases (2 papers). M. Shohat collaborates with scholars based in Israel, United States and Germany. M. Shohat's co-authors include Daniella Ben‐Meir, Sara Lavi, B. Shohat, Daniel Mimouni, Alon Harmelin, Michael David, Raanan Berger, Dan Ben‐Amitai, Gideon Rechavi and Raphael Pfeffer and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and American Journal Of Pathology.

In The Last Decade

M. Shohat

19 papers receiving 223 citations

Peers

M. Shohat

DERMA

IMMUN

UROLO

EPIDE

Claudia Stoeger Germany

R S Kelleher United States

Mary A. Crawford United States

Jennifer Doig United Kingdom

Lilia Aikawa da Silveira United States

Faye Haldane United Kingdom

Gert Lykkesfeldt Denmark

Jean Secchi France

Sandra Reichrath Germany

Jinghui Liang China

Claudia Stoeger Germany

M. Shohat

163 ×1.4

13 ×0.3

DERMA

34 ×1.0

IMMUN

16 ×0.6

UROLO

15 ×0.6

EPIDE

Citations per year, relative to M. Shohat M. Shohat (= 1×) peers Claudia Stoeger

Countries citing papers authored by M. Shohat

Since Specialization

Citations

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

Fields of papers citing papers by M. Shohat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Shohat

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

All Works

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19 of 19 papers shown

Alroy, Iris, et al.. (2018). Translational read-through of CTNS nonsense mutations and attenuation of CTNS nonsense-mediated mRNA decay by ELX-02 treatment. Molecular Genetics and Metabolism. 123(2). S18–S18. 3 indexed citations

Shohat, M., Jeong-Ki Kim, Koki Nakanishi, et al.. (2017). A pathogenic S250F missense mutation results in a mouse model of mild aromatic l-amino acid decarboxylase (AADC) deficiency. Human Molecular Genetics. 26(22). 4406–4415. 10 indexed citations

Shalom, Hadas Sar, M. Shohat, Daniella Ben‐Meir, et al.. (2014). Protein Phosphatase Magnesium Dependent 1A Governs the Wound Healing–Inflammation–Angiogenesis Cross Talk on Injury. American Journal Of Pathology. 184(11). 2936–2950. 23 indexed citations

Shohat, M., Daniella Ben‐Meir, & Sara Lavi. (2012). Protein Phosphatase Magnesium Dependent 1A (PPM1A) Plays a Role in the Differentiation and Survival Processes of Nerve Cells. PLoS ONE. 7(2). e32438–e32438. 24 indexed citations

Shohat, M., et al.. (2009). A new method for isolation of human antisperm antibodies. Andrologia. 28(5). 275–279. 1 indexed citations

Baris, Hagit, et al.. (2008). A novelGJB6missense mutation in hidrotic ectodermal dysplasia 2 (Clouston syndrome) broadens its genotypic basis. British Journal of Dermatology. 159(6). 1373–1376. 16 indexed citations

Shohat, M., B. Shohat, Daniel Mimouni, et al.. (2006). Human T-cell lymphotropic virus type 1 provirus and phylogenetic analysis in patients with mycosis fungoides and their family relatives. British Journal of Dermatology. 155(2). 372–378. 8 indexed citations

Shohat, M., Daniel Mimouni, Dan Ben‐Amitai, et al.. (2005). In vitro cytokine profile in childhood alopecia areata and the immunomodulatory effects of AS-101. Clinical and Experimental Dermatology. 30(4). 432–434. 26 indexed citations

Margalit, Ofer, Lea Eisenbach, Ninette Amariglio, et al.. (2003). Overexpression of a set of genes, including WISP-1, common to pulmonary metastases of both mouse D122 Lewis lung carcinoma and B16-F10.9 melanoma cell lines. British Journal of Cancer. 89(2). 314–319. 35 indexed citations

10.

Chkhotua, Archil, M. Shohat, Ana Tobar, et al.. (2002). Replicative senescence in organ transplantation—mechanisms and significance. Transplant Immunology. 9(2-4). 165–171. 20 indexed citations

11.

Shohat, M., et al.. (2001). Cytokine Profile of Patients with Mycosis Fungoides and the Immunomodulatory Effect of AS101. Acta Dermato Venereologica. 81(4). 255–257. 9 indexed citations

12.

Sobe, Tama, Sarah Vreugde, Hashem Shahin, et al.. (2000). The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population. Human Genetics. 106(1). 50–57. 22 indexed citations

13.

Shohat, M., Dan Ben Amitai, B. Shohat, et al.. (1999). Atopic Dermatitis and HTLV-1-Associated Myelopathy: Associated or Coincidental Disorders?. Dermatology. 199(4). 356–360. 4 indexed citations

14.

Achiron, Asaf, et al.. (1994). Myotonic dystrophy gene analysis in affected Israeli families.. PubMed. 30(8). 622–5. 3 indexed citations

15.

Levy, Itzhak, et al.. (1989). Recurrent ascites in an infant with perinatally acquired cytomegalovirus infection. European Journal of Pediatrics. 148(6). 531–532. 3 indexed citations

16.

Shohat, M., et al.. (1989). Nutritional complications in an infant fed exclusively on homemade sesame seed emulsion.. Journal of the American College of Nutrition. 8(2). 167–169. 4 indexed citations

17.

Shohat, M., et al.. (1988). Cerebrospinal fluid findings in infants with nonpolio enteroviral meningitis.. PubMed. 24(4-5). 233–6. 3 indexed citations

18.

Shohat, M., Marc Mimouni, & I. Varsano. (1987). Efficacy of topical application of glucocorticosteroids compared with eosin in infants with seborrheic dermatitis.. PubMed. 40(1). 67–8. 9 indexed citations

19.

Alpert, Gershon, M. Shohat, S H Reisner, & Yehuda L. Danon. (1984). Osmotic Fragility of Erythrocytes in Newborn Infants Treated by Phototherapy. Acta Paediatrica. 73(2). 254–257. 3 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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