Stavit Shalev

1.1k total citations
29 papers, 536 citations indexed

About

Stavit Shalev is a scholar working on Molecular Biology, Surgery and Hematology. According to data from OpenAlex, Stavit Shalev has authored 29 papers receiving a total of 536 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Surgery and 7 papers in Hematology. Recurrent topics in Stavit Shalev's work include Blood Coagulation and Thrombosis Mechanisms (4 papers), Hemoglobinopathies and Related Disorders (4 papers) and Pregnancy and preeclampsia studies (3 papers). Stavit Shalev is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (4 papers), Hemoglobinopathies and Related Disorders (4 papers) and Pregnancy and preeclampsia studies (3 papers). Stavit Shalev collaborates with scholars based in Israel, United States and Germany. Stavit Shalev's co-authors include Ariel Koren, Ronen Spiegel, Carina Levin, Eliezer Shalev, Hanna Mandel, Gideon Bach, Marsha Zeigler, Batya Engel‐Yeger, Hillel Pratt and Minerva M. Carrasquillo and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Investigative Dermatology and Cells.

In The Last Decade

Stavit Shalev

29 papers receiving 524 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stavit Shalev Israel 14 172 111 92 86 85 29 536
Mariko Taniguchi‐Ikeda Japan 15 430 2.5× 144 1.3× 40 0.4× 56 0.7× 25 0.3× 60 760
Guilhem Solé France 15 250 1.5× 27 0.2× 48 0.5× 119 1.4× 94 1.1× 62 731
Fraser Fellows Canada 15 203 1.2× 192 1.7× 256 2.8× 18 0.2× 93 1.1× 17 717
Ye Jee Shim South Korea 9 144 0.8× 33 0.3× 115 1.3× 47 0.5× 88 1.0× 49 422
Virginia Fano Argentina 15 206 1.2× 123 1.1× 83 0.9× 32 0.4× 15 0.2× 55 634
Manuela Seia Italy 22 235 1.4× 97 0.9× 230 2.5× 42 0.5× 47 0.6× 70 1.3k
Karsten Nielsen Denmark 12 214 1.2× 49 0.4× 43 0.5× 28 0.3× 43 0.5× 30 573
M. S. Pembrey United Kingdom 4 216 1.3× 97 0.9× 81 0.9× 46 0.5× 14 0.2× 7 664
Frederick V. Schaefer United States 13 231 1.3× 41 0.4× 30 0.3× 27 0.3× 29 0.3× 29 506
Joy B. Redman United States 17 301 1.8× 71 0.6× 31 0.3× 27 0.3× 15 0.2× 27 781

Countries citing papers authored by Stavit Shalev

Since Specialization
Citations

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

Fields of papers citing papers by Stavit Shalev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stavit Shalev

This figure shows the co-authorship network connecting the top 25 collaborators of Stavit Shalev. A scholar is included among the top collaborators of Stavit Shalev 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 Stavit Shalev. Stavit Shalev 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
2.
Key, Jana, Sylvia Torres-Odio, Nina C. Bach, et al.. (2021). Inactivity of Peptidase ClpP Causes Primary Accumulation of Mitochondrial Disaggregase ClpX with Its Interacting Nucleoid Proteins, and of mtDNA. Cells. 10(12). 3354–3354. 9 indexed citations
3.
Shalev, Stavit, Sharon Orbach‐Zinger, Pervez Sultan, et al.. (2020). Obstetric quality of recovery scoring tool: assessment of validity, reliability and feasibility in an Israeli cesarean delivery population. International Journal of Obstetric Anesthesia. 44. 51–51. 16 indexed citations
4.
Cohen‐Barak, Eran, et al.. (2018). Desmoglein 4 Mutation Underlies Autosomal Recessive Keratosis Pilaris Atrophicans. Acta Dermato Venereologica. 98(8). 809–810. 5 indexed citations
5.
Mohamad, Janan, N. Malchin, Stavit Shalev, Ofer Sarig, & Eli Sprecher. (2016). ARCI7 Revisited and Repositioned. Journal of Investigative Dermatology. 137(4). 970–972. 5 indexed citations
6.
Shamaly, Hussein, et al.. (2013). Congenital chloride diarrhea presenting in newborn as a rare cause of meconium ileus. Journal of Perinatology. 33(2). 154–156. 6 indexed citations
7.
Huber, Céline, Eissa Faqeih, Deborah Bartholdi, et al.. (2012). Exome Sequencing Identifies INPPL1 Mutations as a Cause of Opsismodysplasia. The American Journal of Human Genetics. 92(1). 144–149. 41 indexed citations
8.
Shalev, Stavit, et al.. (2011). Novel mutations of MYO7A and USH1G in Israeli Arab families with Usher syndrome type 1.. PubMed Central. 9 indexed citations
9.
Marcus-Braun, Naama, Ohad S. Birk, David Segal, et al.. (2009). Dependence of maternal serum [AFP]/[hCG] median ratios on age of gestation: comparison of trisomy 21 to euploid pregnancies. Prenatal Diagnosis. 29(12). 1130–1134. 4 indexed citations
10.
Koren, Ariel, et al.. (2009). Sickle cell anemia in northern Israel: screening and prevention.. PubMed. 11(4). 229–34. 10 indexed citations
11.
Shalev, Stavit, Eliezer Shalev, Elon Pras, et al.. (2006). Evidence for blood chimerism in dizygotic spontaneous twin pregnancy discordant for Down syndrome. Prenatal Diagnosis. 26(9). 782–784. 26 indexed citations
12.
Stoupel, E, Z. Appelman, Ziva Ben‐Neriah, et al.. (2005). Chromosome aberration and environmental physical activity: Down syndrome and solar and cosmic ray activity, Israel, 1990–2000. International Journal of Biometeorology. 50(1). 1–5. 20 indexed citations
13.
Daniel‐Spiegel, Etty, Arash Ghalamkarpour, Ronen Spiegel, et al.. (2005). Hydrops fetalis: an unusual prenatal presentation of hereditary congenital lymphedema. Prenatal Diagnosis. 25(11). 1015–1018. 37 indexed citations
14.
Spiegel, Ronen, Stavit Shalev, Angela Huebner, & Yoseph Horovitz. (2005). Association of Chronic Symptomatic Neutropenia With the Triple A Syndrome. Journal of Pediatric Hematology/Oncology. 27(1). 53–55. 6 indexed citations
15.
Spiegel, Ronen, et al.. (2004). A mutation in the saposin A coding region of the prosaposin gene in an infant presenting as Krabbe disease: first report of saposin A deficiency in humans. Molecular Genetics and Metabolism. 84(2). 160–166. 87 indexed citations
16.
Shohat, Mordechai, Z. Appelman, Ziva Ben‐Neriah, et al.. (2003). Prenatal diagnosis of Down syndrome: Ten year experience in the Israeli population. American Journal of Medical Genetics Part A. 122A(3). 215–222. 24 indexed citations
17.
Engel‐Yeger, Batya, et al.. (2003). Otoacoustic emissions and brainstem evoked potentials in compound carriers of connexin 26 mutations. Hearing Research. 175(1-2). 140–151. 18 indexed citations
18.
Weiss, Amir, et al.. (2003). Prenatal diagnosis of 5p deletion syndrome following abnormally low maternal serum human chorionic gonadotrophin. Prenatal Diagnosis. 23(7). 572–574. 10 indexed citations
19.
Engel‐Yeger, Batya, et al.. (2002). The effects of a connexin 26 mutation – 35delG – on oto-acoustic emissions and brainstem evoked potentials: homozygotes and carriers. Hearing Research. 163(1-2). 93–100. 35 indexed citations
20.
Ben‐Ami, Moshe, Yuri Perlitz, Stavit Shalev, Ibrahim Shajrawi, & Françoise Müller. (2002). Prenatal diagnosis of extrahepatic biliary duct atresia. Prenatal Diagnosis. 22(7). 583–585. 26 indexed citations

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