Sali Usher

730 total citations
20 papers, 480 citations indexed

About

Sali Usher is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Sali Usher has authored 20 papers receiving a total of 480 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Hematology and 4 papers in Genetics. Recurrent topics in Sali Usher's work include Coagulation, Bradykinin, Polyphosphates, and Angioedema (4 papers), Platelet Disorders and Treatments (3 papers) and Metabolism and Genetic Disorders (3 papers). Sali Usher is often cited by papers focused on Coagulation, Bradykinin, Polyphosphates, and Angioedema (4 papers), Platelet Disorders and Treatments (3 papers) and Metabolism and Genetic Disorders (3 papers). Sali Usher collaborates with scholars based in Israel, Germany and United Kingdom. Sali Usher's co-authors include Hava Peretz, Raphael N. Pollack, Michael Krämer, Uri Seligsohn, Shlomo Berliner, Itzhak Shapira, David B. Goldstein, Neil Bradman, David Reich and Shani Shenhar‐Tsarfaty and has published in prestigious journals such as Blood, The American Journal of Human Genetics and Clinical Chemistry.

In The Last Decade

Sali Usher

20 papers receiving 465 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sali Usher Israel 11 141 133 118 88 70 20 480
Akiyo Sekimoto Japan 16 50 0.4× 161 1.2× 179 1.5× 21 0.2× 160 2.3× 33 618
Florin Tripon Romania 12 81 0.6× 50 0.4× 37 0.3× 39 0.4× 140 2.0× 42 381
Arianna Maiorana Italy 17 28 0.2× 253 1.9× 131 1.1× 26 0.3× 226 3.2× 52 839
Robert G. Cheron United States 7 184 1.3× 76 0.6× 28 0.2× 176 2.0× 57 0.8× 9 497
Ilana Koren Israel 11 165 1.2× 53 0.4× 8 0.1× 86 1.0× 119 1.7× 26 632
Sally Chappell United Kingdom 12 29 0.2× 115 0.9× 135 1.1× 12 0.1× 138 2.0× 24 623
F. Bourgeois United States 12 22 0.2× 104 0.8× 110 0.9× 22 0.3× 89 1.3× 28 368
Vicência Sales Brazil 11 14 0.1× 149 1.1× 68 0.6× 72 0.8× 243 3.5× 15 598
Soichiro Okubo Japan 10 24 0.2× 202 1.5× 90 0.8× 53 0.6× 476 6.8× 18 1.1k
Jong Yun Hwang South Korea 14 17 0.1× 128 1.0× 213 1.8× 13 0.1× 178 2.5× 44 603

Countries citing papers authored by Sali Usher

Since Specialization
Citations

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

Fields of papers citing papers by Sali Usher

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sali Usher

This figure shows the co-authorship network connecting the top 25 collaborators of Sali Usher. A scholar is included among the top collaborators of Sali Usher 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 Sali Usher. Sali Usher 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.
Peretz, Hava, Ayala Lagziel, Florian Bittner, et al.. (2021). Classical Xanthinuria in Nine Israeli Families and Two Isolated Cases from Germany: Molecular, Biochemical and Population Genetics Aspects. Biomedicines. 9(7). 788–788. 4 indexed citations
2.
Peretz, Hava, Michael Korostishevsky, David M. Steinberg, et al.. (2019). An ancestral variant causing type I xanthinuria in Turkmen and Arab families is predicted to prevail in the Afro‐Asian stone‐forming belt. JIMD Reports. 51(1). 45–52. 4 indexed citations
3.
Tene, Oren, Hen Hallevi, Amos D. Korczyn, et al.. (2018). The Price of Stress: High Bedtime Salivary Cortisol Levels Are Associated with Brain Atrophy and Cognitive Decline in Stroke Survivors. Results from the TABASCO Prospective Cohort Study. Journal of Alzheimer s Disease. 65(4). 1365–1375. 20 indexed citations
4.
Peretz, Hava, Ophira Salomon, Ronit Mor-Cohen, et al.. (2013). Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews. Journal of Thrombosis and Haemostasis. 11(4). 724–730. 6 indexed citations
5.
Shenhar‐Tsarfaty, Shani, Nir Waiskopf, Keren Ofek, et al.. (2013). Atherosclerosis and arteriosclerosis parameters in stroke patients associate with paraoxonase polymorphism and esterase activities. European Journal of Neurology. 20(6). 891–898. 29 indexed citations
6.
Peretz, Hava, David G. Watson, Gavin Blackburn, et al.. (2011). Urine metabolomics reveals novel physiologic functions of human aldehyde oxidase and provides biomarkers for typing xanthinuria. Metabolomics. 8(5). 951–959. 21 indexed citations
7.
Assayag, Einor Ben, Shani Shenhar‐Tsarfaty, Irena Bova, et al.. (2009). Association of the -757T>C polymorphism in the CRP gene with circulating C-reactive protein levels and carotid atherosclerosis. Thrombosis Research. 124(4). 458–462. 15 indexed citations
8.
Shenhar‐Tsarfaty, Shani, Irena Bova, Shlomo Berliner, et al.. (2007). Triggered C‐reactive protein (CRP) concentrations and the CRP gene −717A>G polymorphism in acute stroke or transient ischemic attack. European Journal of Neurology. 14(3). 315–320. 21 indexed citations
9.
Assayag, Einor Ben, Irena Bova, Shlomo Berliner, et al.. (2006). Gender differences in the expression of erythrocyte aggregation in relation to Bβ-fibrinogen gene polymorphisms in apparently healthy individuals. Thrombosis and Haemostasis. 95(3). 428–433. 12 indexed citations
10.
Goldstein, David B., David Reich, Neil Bradman, et al.. (1999). Age Estimates of Two Common Mutations Causing Factor XI Deficiency: Recent Genetic Drift Is Not Necessary for Elevated Disease Incidence among Ashkenazi Jews. The American Journal of Human Genetics. 64(4). 1071–1075. 50 indexed citations
11.
Thornton, Michael A., Mortimer Poncz, M. Korostishevsky, et al.. (1999). The Human Platelet IIb Gene Is Not Closely Linked to Its Integrin Partner β3. Blood. 94(6). 2039–2047. 27 indexed citations
12.
Yakobson, Emanuel, et al.. (1998). Screening for Tumour Suppressor p16(CDKN2A) Germline Mutations in Israeli Melanoma Families. Clinical Chemistry and Laboratory Medicine (CCLM). 36(8). 645–648. 7 indexed citations
13.
Krämer, Michael, et al.. (1997). Etiologic determinants of abruptio placentae. Obstetrics and Gynecology. 89(2). 221–226. 144 indexed citations
14.
15.
16.
Dardik, Rima, Hava Peretz, Sali Usher, Uri Seligsohn, & U. Martinowitz. (1996). Current strategy for genetic analysis of haemophilia A families. Haemophilia. 2(1). 11–17. 9 indexed citations
17.
Peretz, Hava, Nurit Rosenberg, Sali Usher, et al.. (1995). Glanzmann's thrombasthenia associated with deletion-insertion and alternative splicing in the glycoprotein IIb gene. Blood. 85(2). 414–420. 4 indexed citations
18.
Peretz, Hava, Nurit Rosenberg, Sali Usher, et al.. (1995). Glanzmann's thrombasthenia associated with deletion-insertion and alternative splicing in the glycoprotein IIb gene. Blood. 85(2). 414–420. 28 indexed citations
19.
Peretz, Hava, et al.. (1994). Factor VIII gene rearrangement in hemophilia A carrier detection: a word of caution [letter]. Blood. 84(4). 1351–1352. 5 indexed citations
20.
Peretz, Hava, et al.. (1988). Enzyme analysis of amniotic fluid for prenatal diagnosis of cystic fibrosis in high-risk pregnancies.. Clinical Chemistry. 34(12). 2401–2405. 2 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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