Sara Sivan

1.2k total citations
18 papers, 842 citations indexed

About

Sara Sivan is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Sara Sivan has authored 18 papers receiving a total of 842 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Cell Biology and 4 papers in Genetics. Recurrent topics in Sara Sivan's work include ATP Synthase and ATPases Research (3 papers), RNA modifications and cancer (3 papers) and Skin and Cellular Biology Research (2 papers). Sara Sivan is often cited by papers focused on ATP Synthase and ATPases Research (3 papers), RNA modifications and cancer (3 papers) and Skin and Cellular Biology Research (2 papers). Sara Sivan collaborates with scholars based in Israel, United States and United Kingdom. Sara Sivan's co-authors include Varda Shoshan‐Barmatz, Salah Abu‐Hamad, Ohad S. Birk, Idan Cohen, Hagit Flusser, Barak Markus, Rivka Ofir, Rotem Kadir, Esther Leshinsky‐Silver and Dorit Lev and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Sara Sivan

18 papers receiving 838 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sara Sivan Israel 13 553 105 82 79 77 18 842
Xiaohua Huang Germany 18 649 1.2× 167 1.6× 43 0.5× 87 1.1× 91 1.2× 33 953
Shelley A. Phelan United States 18 888 1.6× 77 0.7× 123 1.5× 90 1.1× 65 0.8× 34 1.2k
Young-Sun Kang South Korea 12 700 1.3× 90 0.9× 36 0.4× 43 0.5× 60 0.8× 13 987
Joanna Lipecka France 19 548 1.0× 104 1.0× 31 0.4× 64 0.8× 47 0.6× 41 951
Franck Galland France 8 405 0.7× 103 1.0× 79 1.0× 52 0.7× 29 0.4× 8 708
Brent D. Butts United States 12 500 0.9× 67 0.6× 37 0.5× 53 0.7× 58 0.8× 16 761
Motoko Ohnishi Japan 17 899 1.6× 160 1.5× 45 0.5× 60 0.8× 117 1.5× 42 1.2k
Hisao Ueyama Japan 19 503 0.9× 83 0.8× 40 0.5× 61 0.8× 31 0.4× 52 852
Catriona M. H. Anderson United Kingdom 18 514 0.9× 114 1.1× 67 0.8× 78 1.0× 43 0.6× 32 1.2k
Xunsheng Chen United States 17 399 0.7× 186 1.8× 83 1.0× 49 0.6× 39 0.5× 28 767

Countries citing papers authored by Sara Sivan

Since Specialization
Citations

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

Fields of papers citing papers by Sara Sivan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sara Sivan

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

All Works

18 of 18 papers shown
1.
Sivan, Sara, et al.. (2024). Non-coding RNAs mediating the regulation of genes and signaling pathways in aortic valve calcification. Gene. 936. 149117–149117. 1 indexed citations
2.
Kadir, Rotem, Hagit Flusser, Yonatan Perez, et al.. (2017). PAX7mutation in a syndrome of failure to thrive, hypotonia, and global neurodevelopmental delay. Human Mutation. 38(12). 1671–1683. 10 indexed citations
3.
Kadir, Rotem, Tamar Harel, Barak Markus, et al.. (2016). ALFY-Controlled DVL3 Autophagy Regulates Wnt Signaling, Determining Human Brain Size. PLoS Genetics. 12(3). e1005919–e1005919. 62 indexed citations
4.
Flusser, Hagit, Tally Lerman‐Sagie, Bruria Ben‐Zeev, et al.. (2014). VPS53 mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2). Journal of Medical Genetics. 51(5). 303–308. 58 indexed citations
5.
Cohen, Idan, Eldad Silberstein, Yonatan Perez, et al.. (2013). Autosomal recessive Adams–Oliver syndrome caused by homozygous mutation in EOGT, encoding an EGF domain-specific O-GlcNAc transferase. European Journal of Human Genetics. 22(3). 374–378. 45 indexed citations
6.
Cohen, Idan, et al.. (2012). ZNF750 Is Expressed in Differentiated Keratinocytes and Regulates Epidermal Late Differentiation Genes. PLoS ONE. 7(8). e42628–e42628. 38 indexed citations
7.
Cohen, Idan, Daniella Landau, Baruch Yerushalmi, et al.. (2012). Meconium Ileus Caused by Mutations in GUCY2C, Encoding the CFTR-Activating Guanylate Cyclase 2C. The American Journal of Human Genetics. 90(5). 893–899. 73 indexed citations
8.
Flusser, Hagit, Barak Markus, Ilan Shelef, et al.. (2011). The desmosterolosis phenotype: spasticity, microcephaly and micrognathia with agenesis of corpus callosum and loss of white matter. European Journal of Human Genetics. 19(9). 942–946. 37 indexed citations
9.
Markus, Barak, Iris Noyman, Hagit Flusser, et al.. (2011). Response to Biancheri et al. and Boepsflug-Tanguy et al.: AIMP1/p43 Connatal PMLD. The American Journal of Human Genetics. 88(3). 393–395. 1 indexed citations
10.
Zeev, Bruria Ben, Dorit Lev, Dan Su, et al.. (2010). Mutations Disrupting Selenocysteine Formation Cause Progressive Cerebello-Cerebral Atrophy. The American Journal of Human Genetics. 87(4). 538–544. 107 indexed citations
11.
Markus, Barak, Iris Noyman, Hagit Flusser, et al.. (2010). Pelizaeus-Merzbacher-like Disease Caused by AIMP1/p43 Homozygous Mutation. The American Journal of Human Genetics. 87(6). 820–828. 62 indexed citations
12.
Yerushalmi, Baruch, Daniela Vullo, Rivka Ofir, et al.. (2010). Hyperchlorhidrosis Caused by Homozygous Mutation in CA12, Encoding Carbonic Anhydrase XII. The American Journal of Human Genetics. 87(5). 713–720. 31 indexed citations
13.
Abu‐Hamad, Salah, Sara Sivan, & Varda Shoshan‐Barmatz. (2006). The expression level of the voltage-dependent anion channel controls life and death of the cell. Proceedings of the National Academy of Sciences. 103(15). 5787–5792. 208 indexed citations
14.
Yehezkel, Galit, Nurit Hadad, Hilal Zaid, Sara Sivan, & Varda Shoshan‐Barmatz. (2005). Nucleotide-binding Sites in the Voltage-dependent Anion Channel. Journal of Biological Chemistry. 281(9). 5938–5946. 48 indexed citations
15.
Davis, Claytus, et al.. (2003). The P4 promoter of the parvovirus minute virus of mice is developmentally regulated in transgenic P4-LacZ mice. Virology. 306(2). 268–279. 7 indexed citations
16.
Boudreau, Eric, Monique Turmel, Michel Goldschmidt‐Clermont, et al.. (1997). A large open reading frame (orf1995 ) in the chloroplast DNA of Chlamydomonas reinhardtii encodes an essential protein. Molecular and General Genetics MGG. 253(5). 649–653. 37 indexed citations
17.
Sivan, Sara, Arieh Zaritsky, & Varda Kagan‐Zur. (1988). Replication forks of Escherichia coli are not the preferred sites for lysogenic integration of bacteriophage Mu. Journal of Bacteriology. 170(7). 3089–3093. 2 indexed citations
18.
Sivan, Sara, Toshitaka Nabeshima, Dae‐Kwang Lim, Beth Hoskins, & I.K. Ho. (1984). Diisopropylfluorophosphate and GABA Synaptic Function: Effect on Levels, Enzymes, Release and Uptake in the Rat Striatum. The Journal of Urology. 131(4). 837–837. 15 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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