Shoshi Shpitzen

974 total citations
15 papers, 400 citations indexed

About

Shoshi Shpitzen is a scholar working on Surgery, Genetics and Molecular Biology. According to data from OpenAlex, Shoshi Shpitzen has authored 15 papers receiving a total of 400 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Surgery, 8 papers in Genetics and 3 papers in Molecular Biology. Recurrent topics in Shoshi Shpitzen's work include Lipoproteins and Cardiovascular Health (7 papers), Cholesterol and Lipid Metabolism (4 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). Shoshi Shpitzen is often cited by papers focused on Lipoproteins and Cardiovascular Health (7 papers), Cholesterol and Lipid Metabolism (4 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). Shoshi Shpitzen collaborates with scholars based in Israel, United States and Canada. Shoshi Shpitzen's co-authors include Eran Leitersdorf, Vardiella Meiner, Yechiel Friedlander, Ronen Durst, Alexander Lossos, V. Barash, Dov Soffer, Zohar Argov, Oded Abramsky and Zeev Meiner and has published in prestigious journals such as Journal of the American College of Cardiology, Neurology and Annals of Neurology.

In The Last Decade

Shoshi Shpitzen

14 papers receiving 393 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shoshi Shpitzen Israel 11 151 118 110 108 98 15 400
John Fernandes Netherlands 11 95 0.6× 164 1.4× 179 1.6× 268 2.5× 148 1.5× 16 631
Roberta Taurisano Italy 14 70 0.5× 257 2.2× 174 1.6× 107 1.0× 63 0.6× 28 501
Ewa Popowska Poland 15 80 0.5× 68 0.6× 346 3.1× 40 0.4× 125 1.3× 36 565
Roberto Della Casa Italy 16 38 0.3× 139 1.2× 138 1.3× 311 2.9× 166 1.7× 34 536
Mary Anne Preece United Kingdom 11 56 0.4× 75 0.6× 162 1.5× 66 0.6× 46 0.5× 20 377
Beatriz Lecumberri Spain 13 145 1.0× 117 1.0× 214 1.9× 24 0.2× 201 2.1× 32 600
Udo Wendel Germany 12 54 0.4× 68 0.6× 245 2.2× 233 2.2× 48 0.5× 18 525
Ubaldo Caruso Italy 15 31 0.2× 136 1.2× 349 3.2× 150 1.4× 48 0.5× 21 662
Eirini I. Bimpaki United States 9 136 0.9× 33 0.3× 283 2.6× 14 0.1× 37 0.4× 12 524
Takahiro Kanatsuna Japan 15 293 1.9× 77 0.7× 116 1.1× 33 0.3× 252 2.6× 30 593

Countries citing papers authored by Shoshi Shpitzen

Since Specialization
Citations

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

Fields of papers citing papers by Shoshi Shpitzen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shoshi Shpitzen

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

All Works

15 of 15 papers shown
1.
Shpitzen, Shoshi, Haim Rosen, Ayal Ben‐Zvi, et al.. (2024). Characterization of LTBP2 mutation causing mitral valve prolapse. European Heart Journal Open. 5(1). oeae106–oeae106.
2.
Winther, Michael D., Shoshi Shpitzen, Daniel Schurr, et al.. (2019). In search of a genetic explanation for LDLc variability in an FH family: common SNPs and a rare mutation in MTTP explain only part of LDL variability in an FH family. Journal of Lipid Research. 60(10). 1733–1740. 2 indexed citations
3.
Durst, Ronen, Shoshi Shpitzen, Daniel Schurr, et al.. (2016). Molecular genetics of familial hypercholesterolemia in Israel–revisited. Atherosclerosis. 257. 55–63. 17 indexed citations
4.
Kakhlon, Or, Jorida Çoku, Lorenzo Peverelli, et al.. (2015). An exon trap with proper poly-A site in the GBE1 is the common missing cause in Adult Polyglucosan Body Disease (S42.006). Neurology. 84(14_supplement). 1 indexed citations
5.
Akman, Hasan O., Or Kakhlon, Jorida Çoku, et al.. (2015). Deep IntronicGBE1Mutation in Manifesting Heterozygous Patients With Adult Polyglucosan Body Disease. JAMA Neurology. 72(4). 441–441. 30 indexed citations
6.
Qi, Qibin, Ronen Durst, Dan Schwarzfuchs, et al.. (2014). CETP genotype and changes in lipid levels in response to weight-loss diet intervention in the POUNDS LOST and DIRECT randomized trials. Journal of Lipid Research. 56(3). 713–721. 34 indexed citations
7.
Durst, Ronen, Shoshi Shpitzen, Dan Schwarzfuchs, et al.. (2012). INSULIN RECEPTOR SUBSTRATE 1 GENE VARIATION MODIFIES INSULIN RESISTANCE RESPONSE TO VARIOUS TYPES OF DIETARY STRATEGIES: RESULTS FROM THE DIRECT INTERVENTION TRIAL. Journal of the American College of Cardiology. 59(13). E1664–E1664. 1 indexed citations
8.
Båvner, Ann, Marjan Shafaati, Magnus Hansson, et al.. (2010). On the mechanism of accumulation of cholestanol in the brain of mice with a disruption of sterol 27-hydroxylase. Journal of Lipid Research. 51(9). 2722–2730. 46 indexed citations
9.
Meiner, Vardiella, Yechiel Friedlander, Shoshi Shpitzen, et al.. (2008). Cholesteryl Ester Transfer Protein (CETP) Genetic Variation and Early Onset of Non‐Fatal Myocardial Infarction. Annals of Human Genetics. 72(6). 732–741. 21 indexed citations
10.
Durst, Ronen, Angelique C.M. Jansen, Gilli Erez, et al.. (2006). The discrete and combined effect of SREBP-2 and SCAP isoforms in the control of plasma lipids among familial hypercholesterolaemia patients. Atherosclerosis. 189(2). 443–450. 22 indexed citations
11.
Durst, Ronen, et al.. (2004). Aplipoprotein E genotyping: accurate, simple, high throughput method using ABI Prism® SNaPshot™ Multiplex System. Journal of Alzheimer s Disease. 6(5). 497–501. 20 indexed citations
12.
Meiner, Vardiella, Shoshi Shpitzen, Hanna Mandel, et al.. (2001). Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type C. Genetics in Medicine. 3(5). 343–348. 28 indexed citations
13.
Durst, Ronen, Roberto Colombo, Shoshi Shpitzen, et al.. (2001). Recent Origin and Spread of a Common Lithuanian Mutation, G197del LDLR, Causing Familial Hypercholesterolemia: Positive Selection Is Not Always Necessary to Account for Disease Incidence among Ashkenazi Jews. The American Journal of Human Genetics. 68(5). 1172–1188. 40 indexed citations
14.
Kark, J.D., Ronit Sinnreich, Eran Leitersdorf, et al.. (2000). Taq1B CETP polymorphism, plasma CETP, lipoproteins, apolipoproteins and sex differences in a Jewish population sample characterized by low HDL-cholesterol. Atherosclerosis. 151(2). 509–518. 51 indexed citations
15.
Lossos, Alexander, Zeev Meiner, V. Barash, et al.. (1998). Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329 Ser mutation in the glycogen‐branching enzyme gene. Annals of Neurology. 44(6). 867–872. 87 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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