Amir Peleg

742 total citations
21 papers, 191 citations indexed

About

Amir Peleg is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Amir Peleg has authored 21 papers receiving a total of 191 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 6 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Amir Peleg's work include Prenatal Screening and Diagnostics (8 papers), Genomics and Rare Diseases (4 papers) and Neurological diseases and metabolism (3 papers). Amir Peleg is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomics and Rare Diseases (4 papers) and Neurological diseases and metabolism (3 papers). Amir Peleg collaborates with scholars based in Israel, United States and Italy. Amir Peleg's co-authors include Lena Sagi‐Dain, Lior Löwenstein, Amir Weissman, Israel Thaler, Etan Z. Zimmer, Shlomi Sagi, Idit Maya, Amihood Singer, Shay Ben‐Shachar and Anat Bar‐Shira and has published in prestigious journals such as Diabetes Care, Human Molecular Genetics and Pediatric Research.

In The Last Decade

Amir Peleg

20 papers receiving 188 citations

Peers

Amir Peleg

PPCH

CCM

GENET

Pin Fee Chong Japan

Natàlia Pujol‐Gualdo Estonia

Randall M. Wilson United States

Jamila Ibrahim United Kingdom

Despoina Tramma Greece

Máté Katona Hungary

M. Zhang Canada

A. Hagemann United Kingdom

Kristiina Ruutiainen Finland

Sunthara Rajan Perumal Australia

Pin Fee Chong Japan

Amir Peleg

26 ×0.4

PPCH

55 ×0.9

35 ×1.0

CCM

47 ×1.7

GENET

3 ×0.1

Citations per year, relative to Amir Peleg Amir Peleg (= 1×) peers Pin Fee Chong

Countries citing papers authored by Amir Peleg

Since Specialization

Citations

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

Fields of papers citing papers by Amir Peleg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amir Peleg

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

Peleg, Amir, et al.. (2024). The effect of opting‐in versus opting‐out forming on the rate of reported variants of questionable significance in prenatal microarray. International Journal of Gynecology & Obstetrics. 167(3). 1231–1236. 2 indexed citations

Sagi‐Dain, Lena, Amir Peleg, Shlomi Sagi, & Amihood Singer. (2022). The anxiety caused by abnormal results of Down syndrome screening tests. Journal of Obstetrics and Gynaecology. 42(7). 2893–2898. 1 indexed citations

German, Alina, Amir Peleg, Claudia Gonzaga‐Jauregui, et al.. (2021). A novel truncating variant in the FGD1 gene associated with Aarskog–Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactyly. American Journal of Medical Genetics Part A. 185(10). 3161–3166.

Sagi‐Dain, Lena, Amihood Singer, Tzipora C. Falik‐Zaccai, et al.. (2021). The effect of polyhydramnios degree on chromosomal microarray results: a retrospective cohort analysis of 742 singleton pregnancies. Archives of Gynecology and Obstetrics. 304(3). 649–656. 8 indexed citations

Peleg, Amir, Lena Sagi‐Dain, & Daniel Golan. (2021). Diagnostic yield and recognized barriers of an adult neurogenetics clinic. Journal of Community Genetics. 12(4). 569–576. 3 indexed citations

Peleg, Amir, Alina Kurolap, Lena Sagi‐Dain, et al.. (2020). A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1. Clinical Dysmorphology. 30(2). 71–75. 2 indexed citations

Sagi‐Dain, Lena, Alina Kurolap, Anat Ilivitzki, et al.. (2019). A novel heterozygous loss‐of‐function DCC Netrin 1 receptor variant in prenatal agenesis of corpus callosum and review of the literature. American Journal of Medical Genetics Part A. 182(1). 205–212. 8 indexed citations

Motta, Marialetizia, Lena Sagi‐Dain, Oliver H.F. Krumbach, et al.. (2019). Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy. Human Molecular Genetics. 29(11). 1772–1783. 24 indexed citations

Sagi‐Dain, Lena, Yael Goldberg, Amir Peleg, et al.. (2019). The rare 13q33–q34 microdeletions: eight new patients and review of the literature. Human Genetics. 138(10). 1145–1153. 11 indexed citations

10.

Sagi‐Dain, Lena, Idit Maya, Amir Peleg, et al.. (2018). Microarray analysis in pregnancies with isolated unilateral kidney agenesis. Pediatric Research. 83(4). 825–828. 10 indexed citations

11.

Sagi‐Dain, Lena, et al.. (2018). Whole‐exome sequencing reveals a novel missense mutation in the MARS gene related to a rare Charcot‐Marie‐Tooth neuropathy type 2U. Journal of the Peripheral Nervous System. 23(2). 138–142. 14 indexed citations

12.

Sagi‐Dain, Lena, Amihood Singer, Amir Peleg, et al.. (2018). Microarray analysis has no additional value in fetal aberrant right subclavian artery: description of 268 pregnancies and systematic literature review. Ultrasound in Obstetrics and Gynecology. 53(6). 810–815. 18 indexed citations

13.

Peleg, Amir, et al.. (2017). Whole-Exome Sequencing Identifies a Novel Homozygous Frameshift Mutation in the MTMR2 Gene as a Causative Mutation in a Patient with Charcot-Marie-Tooth Disease Type 4B1. Molecular Neurobiology. 55(4). 3546–3550. 2 indexed citations

14.

Peleg, Amir, et al.. (2017). The yield and complications of amniocentesis performed after 24 weeks of gestation. Archives of Gynecology and Obstetrics. 296(1). 69–75. 10 indexed citations

15.

Cespedes, Frank V. & Amir Peleg. (2017). How the Water Industry Learned to Embrace Data. 1 indexed citations

16.

Sagi‐Dain, Lena, Amir Peleg, & Shlomi Sagi. (2017). First-Trimester Crown-Rump Length and Risk of Chromosomal Aberrations—A Systematic Review and Meta-analysis. Obstetrical & Gynecological Survey. 72(10). 603–609. 8 indexed citations

17.

Sagi‐Dain, Lena, Amir Peleg, & Shlomi Sagi. (2017). Risk for chromosomal aberrations in apparently isolated intrauterine growth restriction: A systematic review. Prenatal Diagnosis. 37(11). 1061–1066. 18 indexed citations

18.

Weissman, Amir, Lior Löwenstein, Amir Peleg, Israel Thaler, & Etan Z. Zimmer. (2006). Power Spectral Analysis of Heart Rate Variability During the 100-g Oral Glucose Tolerance Test in Pregnant Women. Diabetes Care. 29(3). 571–574. 47 indexed citations

19.

Löwenstein, Lior, Ido Solt, Amir Peleg, Benjamin Brenner, & Arie Drugan. (2004). [Is there an association between PUPPP and preeclampsia, abruptio placentae and fetal death?].. PubMed. 143(12). 861–2, 911. 2 indexed citations

20.

Peleg, Amir. (2003). Dream and reality. Modern architecture in Palestine: 1930-1939. RACO (Revistes Catalanes amb Accés Obert) (Consorci de Serveis Universitaris de Catalunya). 47–60. 1 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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