Israela Lerer

4.4k total citations
77 papers, 2.5k citations indexed

About

Israela Lerer is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Israela Lerer has authored 77 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 31 papers in Genetics and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Israela Lerer's work include Genetic Syndromes and Imprinting (13 papers), Prenatal Screening and Diagnostics (13 papers) and Genomic variations and chromosomal abnormalities (13 papers). Israela Lerer is often cited by papers focused on Genetic Syndromes and Imprinting (13 papers), Prenatal Screening and Diagnostics (13 papers) and Genomic variations and chromosomal abnormalities (13 papers). Israela Lerer collaborates with scholars based in Israel, United States and France. Israela Lerer's co-authors include Dvorah Abeliovich, Joël Zlotogora, Michal Sagi, Tamar Peretz, Vardiella Meiner, Haya Levi, Ziva Ben‐Neriah, M. Sagi, Luna Kaduri and N. Weinberg and has published in prestigious journals such as Science, Gastroenterology and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Israela Lerer

77 papers receiving 2.5k citations

Peers

Israela Lerer

GENET

PRM

PPCH

Dvorah Abeliovich Israel

Mordechai Shohat Israel

Andreas Winterpacht Germany

Mohnish Suri United Kingdom

Maxime Bouchard Canada

Sue Malcolm United Kingdom

Oliver Bartsch Germany

Shigemi Hayashi United States

H Kääriäinen Finland

Keiko Wakui Japan

Dvorah Abeliovich Israel

Israela Lerer

1.5k ×1.2

1.4k ×1.4

GENET

291 ×0.8

PRM

450 ×1.5

PPCH

186 ×0.7

Citations per year, relative to Israela Lerer Israela Lerer (= 1×) peers Dvorah Abeliovich

Countries citing papers authored by Israela Lerer

Since Specialization

Citations

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

Fields of papers citing papers by Israela Lerer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Israela Lerer

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

All Works

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20 of 20 papers shown

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

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

Arkadir, David, Israela Lerer, Laurent Klapholz, et al.. (2013). Lipoid proteinosis with bilateral amygdalae calcifications, headache, and cognitive impairments. Neurology. 81(3). 303–304. 3 indexed citations

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

Edvardson, Simon, Chaim Jalas, Avraham Shaag, et al.. (2011). A deleterious mutation in the LOXHD1 gene causes autosomal recessive hearing loss in Ashkenazi Jews. American Journal of Medical Genetics Part A. 155(5). 1170–1172. 29 indexed citations

Basel‐Vanagaite, Lina, Liora Kornreich, Adi Har‐Zahav, et al.. (2010). Familial hydrocephalus with normal cognition and distinctive radiological features. American Journal of Medical Genetics Part A. 152A(11). 2743–2748. 3 indexed citations

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

Goldberg, Yael, Rinnat M. Porat, Inbal Kedar, et al.. (2009). An Ashkenazi founder mutation in the MSH6 gene leading to HNPCC. Familial Cancer. 9(2). 141–150. 21 indexed citations

Molho‐Pessach, Vered, Israela Lerer, Dvorah Abeliovich, et al.. (2008). The H Syndrome Is Caused by Mutations in the Nucleoside Transporter hENT3. The American Journal of Human Genetics. 83(4). 529–534. 129 indexed citations

10.

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

11.

Elleuch, Nizar, Naïma Bouslam, Sylvain Hanein, et al.. (2007). Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families. Neurogenetics. 8(4). 307–315. 15 indexed citations

12.

Boneh, Avihu, Stanley H. Korman, Ken‐ichi Sato, et al.. (2005). A single nucleotide substitution that abolishes the initiator methionine codon of the GLDC gene is prevalent among patients with glycine encephalopathy in Jerusalem. Journal of Human Genetics. 50(5). 230–234. 19 indexed citations

13.

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

14.

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

15.

Reish, Orit, Israela Lerer, Aliza Amiel, et al.. (2002). Wiedemann‐Beckwith syndrome: Further prenatal characterization of the condition. American Journal of Medical Genetics. 107(3). 209–213. 45 indexed citations

16.

Lerer, Israela, et al.. (2001). The 28-kb Deletion Spanning D15S63 Is a Polymorphic Variant in the Ashkenazi Jewish Population. The American Journal of Human Genetics. 68(1). 261–263. 4 indexed citations

17.

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

18.

Buiting, Karin, Bärbel Dittrich, Bernd Dworniczak, et al.. (1999). A 28-kb Deletion Spanning D15S63 (PW71) in Five Families: A Rare Neutral Variant?. The American Journal of Human Genetics. 65(6). 1588–1594. 7 indexed citations

19.

Abeliovich, Dvorah, et al.. (1996). t(15;21)(q15;q22.1)pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring. American Journal of Medical Genetics. 66(1). 45–51. 5 indexed citations

20.

Abeliovich, Dvorah, Iris Lavon, Israela Lerer, et al.. (1992). Screening for five mutations detects 97% of cystic fibrosis (CF) chromosomes and predicts a carrier frequency of 1:29 in the Jewish Ashkenazi population.. PubMed. 51(5). 951–6. 114 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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