Lily Bazak

2.0k total citations
33 papers, 1.1k citations indexed

About

Lily Bazak is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Lily Bazak has authored 33 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 15 papers in Genetics and 3 papers in Surgery. Recurrent topics in Lily Bazak's work include Genomics and Rare Diseases (11 papers), RNA regulation and disease (8 papers) and RNA modifications and cancer (7 papers). Lily Bazak is often cited by papers focused on Genomics and Rare Diseases (11 papers), RNA regulation and disease (8 papers) and RNA modifications and cancer (7 papers). Lily Bazak collaborates with scholars based in Israel, United States and Greece. Lily Bazak's co-authors include Erez Y. Levanon, Eli Eisenberg, Gideon Rechavi, Michal Barák, Rui Zhang, Patricia Deng, Jasmine Jacob‐Hirsch, Farren J. Isaacs, Jin Billy Li and Ilana Buchumenski and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and SHILAP Revista de lepidopterología.

In The Last Decade

Lily Bazak

31 papers receiving 1.1k citations

Peers

Lily Bazak

GENET

IMMUN

CCM

Noélia Custódio Portugal

Thomas J. Nicholls United Kingdom

Bruno Passet France

David F. Read United States

Heidi Cook‐Andersen United States

Aleksandr V. Makeyev United States

Shruti Bhide United States

Eugene J. Gardner United Kingdom

Daniel Ardeljan United States

Noélia Custódio Portugal

Lily Bazak

749 ×0.8

127 ×0.8

GENET

65 ×0.5

50 ×0.5

IMMUN

27 ×0.4

CCM

Citations per year, relative to Lily Bazak Lily Bazak (= 1×) peers Noélia Custódio

Countries citing papers authored by Lily Bazak

Since Specialization

Citations

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

Fields of papers citing papers by Lily Bazak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lily Bazak

This figure shows the co-authorship network connecting the top 25 collaborators of Lily Bazak. A scholar is included among the top collaborators of Lily Bazak 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 Lily Bazak. Lily Bazak 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

Bazak, Lily, et al.. (2024). Potentially Missed Diagnoses in Prenatal Versus Postnatal Exome Sequencing in the Lack of Informative Phenotype: Lessons Learned From a Postnatal Cohort. Prenatal Diagnosis. 44(12). 1423–1434.

Levy, Michal, Lily Bazak, Uri Hamiel, et al.. (2024). Exome sequencing in every pregnancy? Results of trio exome sequencing in structurally normal fetuses. Prenatal Diagnosis. 45(3). 276–286. 12 indexed citations

Kedar, Inbal, Lily Bazak, Lina Basel‐Salmon, et al.. (2024). A POT1 Founder Variant Associated with Early Onset Recurrent Melanoma and Various Solid Malignancies. Genes. 15(3). 355–355.

Orenstein, Naama, Lily Bazak, Gabriel Lidzbarsky, et al.. (2024). High frequency of MEFV disease-causing variants in children with very-early-onset inflammatory bowel disease. Pediatric Research. 97(1). 268–272. 2 indexed citations

Basel‐Salmon, Lina, Noa Ruhrman‐Shahar, Naama Orenstein, et al.. (2023). Clinically actionable incidental and secondary parental genomic findings after proband exome sequencing: Yield and dilemmas. SHILAP Revista de lepidopterología. 1(1). 100813–100813. 1 indexed citations

Orenstein, Naama, Lina Basel‐Salmon, Irina Lagovsky, et al.. (2023). Severe early-onset Wilson disease caused by a common pathogenic variant in the Bukharan Jewish population in Israel. Gene. 887. 147728–147728. 1 indexed citations

Einhorn, Moshe, Alina Kurolap, Adi Mory, et al.. (2023). Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panels. Human Genomics. 17(1). 30–30. 2 indexed citations

Eliyahu, Aviva, Ortal Barel, Lior Greenbaum, et al.. (2022). Refining the Phenotypic Spectrum of KMT5B-Associated Developmental Delay. Frontiers in Pediatrics. 10. 844845–844845. 10 indexed citations

Ruhrman‐Shahar, Noa, Nurit Assia Batzir, Gabriel Lidzbarsky, et al.. (2021). A nonsense variant in the second exon of the canonical transcript of NSD1 does not cause Sotos syndrome. American Journal of Medical Genetics Part A. 188(1). 369–372. 1 indexed citations

10.

Fellner, Avi, Noa Ruhrman‐Shahar, Naama Orenstein, et al.. (2021). The role of phenotype-based search approaches using public online databases in diagnostics of Mendelian disorders. Genetics in Medicine. 23(6). 1095–1100. 4 indexed citations

11.

Basel‐Salmon, Lina, Noa Ruhrman‐Shahar, Ortal Barel, et al.. (2021). Biallelic variants in ETV2 in a family with congenital heart defects, vertebral abnormalities and preaxial polydactyly. European Journal of Medical Genetics. 64(2). 104124–104124. 7 indexed citations

12.

Basel‐Vanagaite, Lina, Noa Ruhrman‐Shahar, Naama Orenstein, et al.. (2020). When phenotype does not match genotype: importance of “real-time” refining of phenotypic information for exome data interpretation. Genetics in Medicine. 23(1). 215–221. 14 indexed citations

13.

Reches, Adi, Karin Weiss, Lily Bazak, Hagit Baris Feldman, & Idit Maya. (2019). From phenotyping to genotyping - bioinformatics for the busy clinician. European Journal of Medical Genetics. 62(8). 103689–103689. 2 indexed citations

14.

Cohen, Lior, et al.. (2018). Variant in SCYL1 gene causes aberrant splicing in a family with cerebellar ataxia, recurrent episodes of liver failure, and growth retardation. European Journal of Human Genetics. 27(2). 263–268. 19 indexed citations

15.

Basel‐Vanagaite, Lina, Naama Orenstein, Noa Ruhrman‐Shahar, et al.. (2018). Improved diagnostics by exome sequencing following raw data reevaluation by clinical geneticists involved in the medical care of the individuals tested. Genetics in Medicine. 21(6). 1443–1451. 55 indexed citations

16.

Mei‐Zahav, Meir, Patrick Stafler, Hanoch Senderowitz, et al.. (2018). The Q359K/T360K mutation causes cystic fibrosis in Georgian Jews. Journal of Cystic Fibrosis. 17(5). e41–e45. 4 indexed citations

17.

Orenstein, Naama, Hadassa Goldberg‐Stern, Rachel Straussberg, et al.. (2017). A de novo GABRA2 missense mutation in severe early-onset epileptic encephalopathy with a choreiform movement disorder. European Journal of Paediatric Neurology. 22(3). 516–524. 23 indexed citations

18.

Paz-Yaacov, Nurit, Lily Bazak, Ilana Buchumenski, et al.. (2015). Elevated RNA Editing Activity Is a Major Contributor to Transcriptomic Diversity in Tumors. Cell Reports. 13(2). 267–276. 247 indexed citations

19.

Bazak, Lily, Erez Y. Levanon, & Eli Eisenberg. (2014). Genome-wide analysis of Alu editability. Nucleic Acids Research. 42(11). 6876–6884. 90 indexed citations

20.

Bazak, Lily, Michal Barák, Jasmine Jacob‐Hirsch, et al.. (2013). A-to-I RNA editing occurs at over a hundred million genomic sites, located in a majority of human genes. Genome Research. 24(3). 365–376. 444 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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