Hagit Daum

721 total citations
39 papers, 420 citations indexed

About

Hagit Daum is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Surgery. According to data from OpenAlex, Hagit Daum has authored 39 papers receiving a total of 420 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Pediatrics, Perinatology and Child Health, 16 papers in Genetics and 12 papers in Surgery. Recurrent topics in Hagit Daum's work include Prenatal Screening and Diagnostics (18 papers), Genomic variations and chromosomal abnormalities (8 papers) and Congenital Anomalies and Fetal Surgery (7 papers). Hagit Daum is often cited by papers focused on Prenatal Screening and Diagnostics (18 papers), Genomic variations and chromosomal abnormalities (8 papers) and Congenital Anomalies and Fetal Surgery (7 papers). Hagit Daum collaborates with scholars based in Israel, United States and Argentina. Hagit Daum's co-authors include Tamar Peretz, Simcha Yagel, Vardiella Meiner, Neri Laufer, D. V. Valsky, Tamar Harel, Orly Elpeleg, Ayala Frumkin, Michal Lipschuetz and N. Yanai and has published in prestigious journals such as Fertility and Sterility, Obstetrics and Gynecology and Journal of Medical Genetics.

In The Last Decade

Hagit Daum

37 papers receiving 413 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hagit Daum Israel 12 172 141 87 83 70 39 420
Atsushi Yoshida Japan 14 187 1.1× 137 1.0× 171 2.0× 104 1.3× 133 1.9× 41 608
Koji Yamazawa Japan 16 215 1.3× 88 0.6× 113 1.3× 107 1.3× 265 3.8× 42 751
Anjeung Kang Switzerland 9 284 1.7× 100 0.7× 138 1.6× 23 0.3× 20 0.3× 11 463
Cécile Rittore France 12 233 1.4× 130 0.9× 185 2.1× 32 0.4× 230 3.3× 21 450
R. Patrick Weitzel United States 10 128 0.7× 60 0.4× 153 1.8× 16 0.2× 44 0.6× 19 495
L. W. Evans United Kingdom 16 123 0.7× 59 0.4× 404 4.6× 57 0.7× 138 2.0× 21 683
Fenxia Li China 13 77 0.4× 91 0.6× 229 2.6× 36 0.4× 45 0.6× 30 438
Lorenza Romitti Italy 13 205 1.2× 136 1.0× 137 1.6× 56 0.7× 67 1.0× 31 531
Ivana Kuzmiç Prusac Croatia 12 130 0.8× 21 0.1× 98 1.1× 45 0.5× 38 0.5× 40 382
Satoshi Hamanoue Japan 12 45 0.3× 127 0.9× 162 1.9× 54 0.7× 37 0.5× 32 364

Countries citing papers authored by Hagit Daum

Since Specialization
Citations

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

Fields of papers citing papers by Hagit Daum

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hagit Daum

This figure shows the co-authorship network connecting the top 25 collaborators of Hagit Daum. A scholar is included among the top collaborators of Hagit Daum 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 Hagit Daum. Hagit Daum 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.
Slovik, Maya, Shamir Zenvirt, Ilana Livyatan, et al.. (2025). High Concordance of Copy Number Variants Detected by Chromosomal Microarray and Exome Sequencing in Clinical Diagnostics. Clinical Genetics. 109(3). 529–538.
2.
Michaelson‐Cohen, Rachel, Yuval Yaron, Adi Reches, et al.. (2024). Exploring the factors affecting classification and reporting of uncertain prenatal microarray findings, using a “virtual fetus” model‐a pilot study. Prenatal Diagnosis. 44(4). 511–518. 1 indexed citations
3.
Daum, Hagit, et al.. (2023). A Case Report of Familial Mayer-Rokitansky-Küster-Hauser Syndrome as Part of the Phenotypic Spectrum of the 2q37 Deletion. Journal of Pediatric and Adolescent Gynecology. 37(1). 95–97. 1 indexed citations
4.
Daum, Hagit, Tamar Harel, Chaggai Rosenbluh, et al.. (2022). Exome sequencing for structurally normal fetuses—yields and ethical issues. European Journal of Human Genetics. 31(2). 164–168. 12 indexed citations
5.
Daum, Hagit & Joël Zlotogora. (2021). Fanconi Anemia Gene Variants in Patients with Gonadal Dysfunction. Reproductive Sciences. 29(5). 1408–1413. 10 indexed citations
6.
Meiner, Vardiella, Simcha Yagel, Shamir Zenvirt, et al.. (2020). Universal chromosomal microarray analysis reveals high proportion of copy‐number variants in low‐risk pregnancies. Ultrasound in Obstetrics and Gynecology. 57(5). 813–820. 29 indexed citations
7.
Singer, Amihood, Idit Maya, Lena Sagi‐Dain, et al.. (2020). Chromosomal microarray should be performed for cases of fetal short long bones detected prenatally. Archives of Gynecology and Obstetrics. 303(1). 85–92. 5 indexed citations
8.
Hochner, Hagit, et al.. (2019). Information Women Choose to Receive About Prenatal Chromosomal Microarray Analysis. Obstetrics and Gynecology. 135(1). 149–157. 11 indexed citations
9.
Daum, Hagit, Ayala Frumkin, Vardiella Meiner, et al.. (2019). Non‐confined long‐standing blood chimerism in a spontaneous monochorionic dizygotic twin pregnancy. International Journal of Gynecology & Obstetrics. 148(3). 399–400. 3 indexed citations
10.
Daum, Hagit, Israela Lerer, Ayala Frumkin, et al.. (2018). Ultrasound findings provide clues to investigate founder mutations expressed as runs of homozygosity in chromosomal microarray studies. Prenatal Diagnosis. 38(2). 135–139. 8 indexed citations
11.
Tirosh, Amit, Phaedon D. Zavras, Elena Belyavskaya, et al.. (2017). Failure to Thrive in the Context of Carney Complex. Hormone Research in Paediatrics. 89(1). 38–46. 4 indexed citations
12.
Breuer, Oded, Hagit Daum, Malena Cohen‐Cymberknoh, et al.. (2017). Autosomal dominant gain of function STAT1 mutation and severe bronchiectasis. Respiratory Medicine. 126. 39–45. 20 indexed citations
13.
Daum, Hagit, et al.. (2017). Congenital myopathy due to myosin heavy chain 2 mutation presenting as chronic aspiration pneumonia in infancy. Neuromuscular Disorders. 27(10). 947–950. 7 indexed citations
14.
Valsky, D. V., S. M. Cohen, Michal Lipschuetz, et al.. (2016). Third‐ or Fourth‐Degree Intrapartum Anal Sphincter Tears Are Associated With Levator Ani Avulsion in Primiparas. Journal of Ultrasound in Medicine. 35(4). 709–715. 27 indexed citations
15.
Lev‐Sagie, Ahinoam, D. Hochner‐Celnikier, Daphna Stroumsa, et al.. (2016). Group A streptococcus: is there a genital carrier state in women following infection?. European Journal of Clinical Microbiology & Infectious Diseases. 36(1). 91–93. 2 indexed citations
16.
Sagi, Michal, Shai Carmi, Hagit Daum, et al.. (2015). An Ashkenazi founder mutation in the PKHD1 gene. European Journal of Medical Genetics. 59(2). 86–90. 5 indexed citations
17.
Yagel, Simcha, S. M. Cohen, Shay Porat, et al.. (2014). Detailed Transabdominal Fetal Anatomic Scanning in the Late First Trimester Versus the Early Second Trimester of Pregnancy. Journal of Ultrasound in Medicine. 34(1). 143–149. 13 indexed citations
18.
19.
Haimov‐Kochman, Ronit, Hagit Daum, Einat Aizenman, et al.. (2009). Monozygotic multiple gestation after intracytoplasmic sperm injection and preimplantation genetic diagnosis. Fertility and Sterility. 92(6). 2037.e11–2037.e17. 9 indexed citations
20.
Valsky, D. V., Hagit Daum, & Simcha Yagel. (2007). Rectus Sheath Hematoma as a Rare Complication of Genetic Amniocentesis. Journal of Ultrasound in Medicine. 26(3). 371–372. 6 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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