Michal Sagi

2.5k total citations
57 papers, 1.7k citations indexed

About

Michal Sagi is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Michal Sagi has authored 57 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 20 papers in Molecular Biology and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Michal Sagi's work include BRCA gene mutations in cancer (18 papers), Prenatal Screening and Diagnostics (11 papers) and Cancer Genomics and Diagnostics (6 papers). Michal Sagi is often cited by papers focused on BRCA gene mutations in cancer (18 papers), Prenatal Screening and Diagnostics (11 papers) and Cancer Genomics and Diagnostics (6 papers). Michal Sagi collaborates with scholars based in Israel, United States and Germany. Michal Sagi's co-authors include Israela Lerer, Dvorah Abeliovich, Shoshana Shiloh, Haya Levi, Joël Zlotogora, Tamar Peretz, Tirza Cohen, Ziva Ben‐Neriah, Vardiella Meiner and Karen Hurley and has published in prestigious journals such as JAMA, Journal of Clinical Oncology and PEDIATRICS.

In The Last Decade

Michal Sagi

57 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michal Sagi Israel 27 621 598 350 303 184 57 1.7k
Uppala Radhakrishna United States 25 758 1.2× 1.0k 1.7× 174 0.5× 80 0.3× 113 0.6× 81 2.1k
Mordechai Shohat Israel 25 699 1.1× 1.6k 2.7× 270 0.8× 225 0.7× 51 0.3× 106 2.9k
Domenico Coviello Italy 32 795 1.3× 1.2k 1.9× 418 1.2× 71 0.2× 360 2.0× 175 3.4k
Michael B. Petersen Greece 34 1.9k 3.0× 1.7k 2.8× 1.1k 3.2× 296 1.0× 96 0.5× 172 4.1k
Joël Zlotogora Israel 35 2.0k 3.2× 1.9k 3.2× 690 2.0× 254 0.8× 115 0.6× 170 5.0k
Ziva Ben‐Neriah Israel 20 404 0.7× 774 1.3× 195 0.6× 206 0.7× 47 0.3× 40 1.4k
Meredith Wilson Australia 31 1.1k 1.8× 1.6k 2.7× 342 1.0× 149 0.5× 96 0.5× 92 3.3k
Faustina Lalatta Italy 24 948 1.5× 714 1.2× 716 2.0× 57 0.2× 55 0.3× 105 1.9k
Lisa A. Schimmenti United States 27 736 1.2× 1.6k 2.7× 337 1.0× 230 0.8× 84 0.5× 106 2.7k
Barbara F. Crandall United States 25 719 1.2× 704 1.2× 740 2.1× 69 0.2× 86 0.5× 88 2.0k

Countries citing papers authored by Michal Sagi

Since Specialization
Citations

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

Fields of papers citing papers by Michal Sagi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michal Sagi

This figure shows the co-authorship network connecting the top 25 collaborators of Michal Sagi. A scholar is included among the top collaborators of Michal Sagi 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 Michal Sagi. Michal Sagi 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.
Frenkel, Shahar, et al.. (2016). Genotype-phenotype correlation in the presentation of retinoblastoma among 149 patients. Experimental Eye Research. 146. 313–317. 13 indexed citations
2.
Rubin, Lisa R., et al.. (2014). ‘TheBRCAClock is Ticking!’: Negotiating medical concerns and reproductive goals in preimplantation genetic diagnosis. Human Fertility. 17(3). 159–164. 22 indexed citations
3.
Kadouri, Luna, Michal Sagi, Yael Goldberg, et al.. (2013). Genetic predisposition to radiation induced sarcoma: possible role for BRCA and p53 mutations. Breast Cancer Research and Treatment. 140(1). 207–211. 37 indexed citations
4.
Goldberg, Yael, Inbal Kedar, Naama Halpern, et al.. (2013). Lynch Syndrome in high risk Ashkenazi Jews in Israel. Familial Cancer. 13(1). 65–73. 16 indexed citations
5.
6.
Francey, Lauren J., Laura K. Conlin, Dinah Clark, et al.. (2011). Genome‐wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment. American Journal of Medical Genetics Part A. 158A(2). 298–308. 70 indexed citations
7.
Sagi, Michal, Yael Goldberg, Dani Bercovich, et al.. (2010). Two BRCA1/2 founder mutations in Jews of Sephardic origin. Familial Cancer. 10(1). 59–63. 18 indexed citations
8.
Goldberg, Yael, Rinnat M. Porat, Inbal Kedar, et al.. (2008). Mutation spectrum in HNPCC in the Israeli population. Familial Cancer. 7(4). 309–317. 15 indexed citations
9.
Kadouri, Luna, Dani Bercovich, Israela Lerer, et al.. (2007). A novel BRCA-1 mutation in Arab kindred from east Jerusalem with breast and ovarian cancer. BMC Cancer. 7(1). 14–14. 30 indexed citations
10.
Lahad, Amnon, Amir Shmueli, Ari Zimran, et al.. (2007). Carrier Screening for Gaucher Disease. JAMA. 298(11). 1281–1281. 59 indexed citations
11.
Lerer, Israela, Michal Sagi, Vardiella Meiner, et al.. (2005). Deletion of the ANKRD15 gene at 9p24.3 causes parent-of-origin-dependent inheritance of familial cerebral palsy. Human Molecular Genetics. 14(24). 3911–3920. 106 indexed citations
12.
Lerer, Israela, et al.. (2005). Mutation spectrum in Jewish cystic fibrosis patients in Israel: Implication to carrier screening. American Journal of Medical Genetics Part A. 136A(3). 246–248. 35 indexed citations
13.
Segel, Reeval, Israela Lerer, Esther Kahana, et al.. (2003). Prevalence of myotonic dystrophy in Israeli Jewish communities: Inter‐community variation and founder premutations. American Journal of Medical Genetics Part A. 119A(3). 273–278. 15 indexed citations
14.
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
15.
Sagi, Michal, et al.. (2001). A deletion/insertion mutation in the BRCA2 gene in a breast cancer family: A possible role of the Alu‐polyA tail in the evolution of the deletion. Genes Chromosomes and Cancer. 31(1). 91–95. 36 indexed citations
16.
Lerer, Israela, et al.. (2000). Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT. American Journal of Medical Genetics. 95(1). 53–56. 68 indexed citations
17.
Sagi, Michal, Luna Kaduri, Joël Zlotogora, & Tamar Peretz. (1998). The Effect of Genetic Counseling on Knowledge and Perceptions Regarding Risks for Breast Cancer. Journal of Genetic Counseling. 7(5). 417–434. 24 indexed citations
18.
Lerer, Israela, Joël Zlotogora, Michal Sagi, et al.. (1994). Neurofibromatosis type I (NFI) in Israeli families: Linkage analysis as a diagnostic tool. American Journal of Medical Genetics. 53(4). 325–334. 6 indexed citations
19.
Shiloh, Shoshana & Michal Sagi. (1989). Effect of framing on the perception of genetic recurrence risks. American Journal of Medical Genetics. 33(1). 130–135. 61 indexed citations
20.
Cohen, Maimon M. & Michal Sagi. (1979). The effect of nitrofurans on mitosis, chromosome breakage and sister-chromatid exchanges in human peripheral lymphocytes. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 59(1). 139–142. 7 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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