Tamar Paperna

1.8k total citations
48 papers, 1.2k citations indexed

About

Tamar Paperna is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Tamar Paperna has authored 48 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 12 papers in Pathology and Forensic Medicine and 12 papers in Genetics. Recurrent topics in Tamar Paperna's work include Multiple Sclerosis Research Studies (6 papers), BRCA gene mutations in cancer (5 papers) and Genomics and Rare Diseases (4 papers). Tamar Paperna is often cited by papers focused on Multiple Sclerosis Research Studies (6 papers), BRCA gene mutations in cancer (5 papers) and Genomics and Rare Diseases (4 papers). Tamar Paperna collaborates with scholars based in Israel, United States and Hungary. Tamar Paperna's co-authors include Ariel Miller, Uta Francke, Lea Glass‐Marmor, Rafael Malach, Ruth Gershoni‐Baruch, Risa Peoples, Izabella Lejbkowicz, Efrat Dagan, L Kasinetz and Nili Avidan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Tamar Paperna

43 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tamar Paperna Israel 21 524 242 212 143 134 48 1.2k
Jami Dwyer United States 14 597 1.1× 194 0.8× 117 0.6× 379 2.7× 102 0.8× 15 1.3k
Jimmy Huynh United States 16 872 1.7× 207 0.9× 177 0.8× 117 0.8× 223 1.7× 25 1.3k
Francesca Galbiati Italy 21 474 0.9× 145 0.6× 104 0.5× 433 3.0× 148 1.1× 52 1.4k
Martin Begemann Germany 23 1.2k 2.2× 339 1.4× 213 1.0× 163 1.1× 66 0.5× 54 2.3k
Martin Graf Switzerland 23 786 1.5× 139 0.6× 78 0.4× 64 0.4× 56 0.4× 54 1.6k
Yu‐Chia Chen Taiwan 23 470 0.9× 61 0.3× 90 0.4× 137 1.0× 104 0.8× 74 1.4k
Lara Kular Sweden 19 608 1.2× 101 0.4× 178 0.8× 255 1.8× 78 0.6× 35 1.1k
Willie Mark United States 18 1.0k 1.9× 197 0.8× 109 0.5× 230 1.6× 278 2.1× 27 1.9k
Yuko Tanabe Japan 25 671 1.3× 227 0.9× 85 0.4× 105 0.7× 46 0.3× 107 1.8k
Tomoko Okamoto Japan 18 636 1.2× 86 0.4× 655 3.1× 338 2.4× 38 0.3× 85 1.9k

Countries citing papers authored by Tamar Paperna

Since Specialization
Citations

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

Fields of papers citing papers by Tamar Paperna

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tamar Paperna

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

All Works

20 of 20 papers shown
1.
Paperna, Tamar, et al.. (2025). A family with an atypical presentation of TBX3-related disorder. European Journal of Medical Genetics. 73. 104994–104994.
2.
Blich, Miry, Yaniv Zohar, Victoria Cohen‐Kaplan, et al.. (2024). Ser194Leu DSG2 mutation, associated with arrhythmogenic left ventricular cardiomyopathy and ventricular tachycardia. Pacing and Clinical Electrophysiology. 47(4). 503–510.
3.
Paperna, Tamar, et al.. (2024). Rapid exome sequencing for children with severe acute encephalopathy – A case series. European Journal of Medical Genetics. 68. 104918–104918. 1 indexed citations
4.
Paperna, Tamar, Mario García‐Domínguez, Eric S. Shinwell, et al.. (2023). Exome sequencing links the SUMO protease SENP7 with fatal arthrogryposis multiplex congenita, early respiratory failure and neutropenia. Journal of Medical Genetics. 60(11). 1133–1141. 6 indexed citations
5.
Goldberg, Yael, Hanna Segev, Itay Maza, et al.. (2023). High prevalence of MUTYH associated polyposis among minority populations in Israel, due to rare founder pathogenic variants. Digestive and Liver Disease. 55(7). 880–887.
6.
German, Alina, Amir Peleg, Claudia Gonzaga‐Jauregui, et al.. (2021). A novel truncating variant in the FGD1 gene associated with Aarskog–Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactyly. American Journal of Medical Genetics Part A. 185(10). 3161–3166.
7.
Ekhilevitch, Nina, et al.. (2021). A recurrent pathogenic BRCA2 exon 5–11 duplication in the Christian Arab population in Israel. Familial Cancer. 21(3). 289–294. 1 indexed citations
8.
Hershkovitz, Tova, Alina Kurolap, Claudia Gonzaga‐Jauregui, et al.. (2019). A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4. Journal of Human Genetics. 64(6). 589–595. 21 indexed citations
9.
Sagi‐Dain, Lena, Alina Kurolap, Anat Ilivitzki, et al.. (2019). A novel heterozygous loss‐of‐function DCC Netrin 1 receptor variant in prenatal agenesis of corpus callosum and review of the literature. American Journal of Medical Genetics Part A. 182(1). 205–212. 8 indexed citations
10.
Kurolap, Alina, Tova Hershkovitz, Adi Mory, et al.. (2016). Loss of Glycine Transporter 1 Causes a Subtype of Glycine Encephalopathy with Arthrogryposis and Mildly Elevated Cerebrospinal Fluid Glycine. The American Journal of Human Genetics. 99(5). 1172–1180. 25 indexed citations
11.
Benedek, Gil, Tamar Paperna, Nili Avidan, et al.. (2010). Opposing effects of the HLA-DRB1*0301-DQB1*0201 haplotype on the risk for multiple sclerosis in diverse Arab populations in Israel. Genes and Immunity. 11(5). 423–431. 19 indexed citations
12.
Paperna, Tamar, et al.. (2010). Cathepsins and their endogenous inhibitors cystatins: expression and modulation in multiple sclerosis. Journal of Cellular and Molecular Medicine. 15(11). 2421–2429. 52 indexed citations
13.
Miller, Ariel, Nili Avidan, Lea Glass‐Marmor, et al.. (2008). Translation towards personalized medicine in Multiple Sclerosis. Journal of the Neurological Sciences. 274(1-2). 68–75. 22 indexed citations
14.
Grossman, I., Nili Avidan, Tamar Paperna, et al.. (2004). Genomic profiling of interpopulation diversity guides prioritization of candidate-genes for autoimmunity. Genes and Immunity. 5(6). 493–504. 10 indexed citations
15.
Nakano, Aoi, Gilles G. Lestringant, Tamar Paperna, et al.. (2002). Junctional epidermolysis bullosa in the Middle East: Clinical and genetic studies in a series of consanguineous families. Journal of the American Academy of Dermatology. 46(4). 510–516. 37 indexed citations
16.
Makhoul, Imad R., Ayala Aviram‐Goldring, Tamar Paperna, et al.. (2001). Caudal dysplasia sequence with penile enlargement: Case report and a potential pathogenic hypothesis. American Journal of Medical Genetics. 99(1). 54–58. 5 indexed citations
17.
Peoples, Risa, et al.. (2000). A Physical Map, Including a BAC/PAC Clone Contig, of the Williams-Beuren Syndrome–Deletion Region at 7q11.23. The American Journal of Human Genetics. 66(1). 47–68. 121 indexed citations
18.
19.
Lupu‐Meiri, Monica, et al.. (1998). How Does the Mongoose Cope with α‐Bungarotoxin?: Analysis of the Mongoose Muscle AChR α‐Subunit. Annals of the New York Academy of Sciences. 841(1). 97–100. 2 indexed citations
20.
Paperna, Tamar & Rafael Malach. (1991). Patterns of sensory intermodality relationships in the cerebral cortex of the rat. The Journal of Comparative Neurology. 308(3). 432–456. 74 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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