Daphna Marom

2.8k total citations
26 papers, 510 citations indexed

About

Daphna Marom is a scholar working on Molecular Biology, Epidemiology and Genetics. According to data from OpenAlex, Daphna Marom has authored 26 papers receiving a total of 510 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Epidemiology and 6 papers in Genetics. Recurrent topics in Daphna Marom's work include Infective Endocarditis Diagnosis and Management (4 papers), Metabolism and Genetic Disorders (3 papers) and Streptococcal Infections and Treatments (3 papers). Daphna Marom is often cited by papers focused on Infective Endocarditis Diagnosis and Management (4 papers), Metabolism and Genetic Disorders (3 papers) and Streptococcal Infections and Treatments (3 papers). Daphna Marom collaborates with scholars based in Israel, United States and Canada. Daphna Marom's co-authors include Shai Ashkenazi, Avraham Zeharia, Orit Pappo, Anne-Marie Mager-Heckel, Reeval Segel, Ivan Tarassov, Agnès Rötig, Ann Saada, Marine Beinat and Hanna Mandel and has published in prestigious journals such as PEDIATRICS, The American Journal of Human Genetics and American Journal of Obstetrics and Gynecology.

In The Last Decade

Daphna Marom

24 papers receiving 494 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daphna Marom Israel 11 227 113 86 77 65 26 510
Stefania Gaspari Italy 15 218 1.0× 50 0.4× 17 0.2× 107 1.4× 35 0.5× 46 659
Mila Barak Israel 9 414 1.8× 50 0.4× 306 3.6× 14 0.2× 42 0.6× 18 560
Tai‐Ju Hwang South Korea 11 179 0.8× 60 0.5× 24 0.3× 32 0.4× 21 0.3× 25 489
Indira Sahdev United States 12 64 0.3× 119 1.1× 23 0.3× 65 0.8× 104 1.6× 25 547
Shiming Lü China 12 133 0.6× 62 0.5× 5 0.1× 43 0.6× 37 0.6× 25 462
Kaushik Sen India 12 75 0.3× 58 0.5× 18 0.2× 33 0.4× 51 0.8× 32 452
Toshinori Hori Japan 11 87 0.4× 158 1.4× 25 0.3× 108 1.4× 22 0.3× 26 467
Kei Takasawa Japan 13 247 1.1× 15 0.1× 33 0.4× 31 0.4× 187 2.9× 64 456
Eunhee Han South Korea 11 119 0.5× 65 0.6× 23 0.3× 37 0.5× 70 1.1× 44 387
J Masopust Czechia 10 78 0.3× 54 0.5× 25 0.3× 31 0.4× 22 0.3× 21 351

Countries citing papers authored by Daphna Marom

Since Specialization
Citations

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

Fields of papers citing papers by Daphna Marom

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daphna Marom

This figure shows the co-authorship network connecting the top 25 collaborators of Daphna Marom. A scholar is included among the top collaborators of Daphna Marom 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 Daphna Marom. Daphna Marom 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.
Hamiel, Uri, Alina Kurolap, Adi Mory, et al.. (2025). Deletion of RAI1 noncoding exons 1–2 causes Smith–Magenis syndrome. Journal of Genetics. 104(1).
2.
Rothschild, Ehud, Guy Baruch, Daphna Marom, et al.. (2024). Cardiac screening in pediatric patients with neurofibromatosis type 1: similarities with Noonan syndrome?. The International Journal of Cardiovascular Imaging. 40(7). 1475–1482.
3.
Hamiel, Uri, et al.. (2023). Telemedicine Versus Traditional In-Person Consultations: Comparison of Patient Satisfaction Rates. Telemedicine Journal and e-Health. 30(4). 1013–1019. 4 indexed citations
4.
Zerem, Ayelet, Liat Ben‐Sira, Moran Hausman‐Kedem, et al.. (2023). Utility of genetic testing in children with leukodystrophy. European Journal of Paediatric Neurology. 45. 29–35. 2 indexed citations
5.
Yaron, Yuval, Adi Mory, Alina Kurolap, et al.. (2022). Exome sequencing as first‐tier test for fetuses with severe central nervous system structural anomalies. Ultrasound in Obstetrics and Gynecology. 60(1). 59–67. 48 indexed citations
6.
Hausman‐Kedem, Moran, Liat Ben‐Sira, Debora Kidron, et al.. (2021). Deletion in COL4A2 is associated with a three-generation variable phenotype: from fetal to adult manifestations. European Journal of Human Genetics. 29(11). 1654–1662. 5 indexed citations
7.
Cohen‐Barak, Eran, Hagit Toledano‐Alhadef, Ido Livneh, et al.. (2021). Concomitant variants in NF1, LZTR1 and GNAZ genes probably contribute to the aggressiveness of plexiform neurofibroma and warrant treatment with MEK inhibitor. Experimental Dermatology. 31(5). 775–780. 2 indexed citations
8.
Marom, Daphna. (2020). Genetics of tuberous sclerosis complex: an update. Child s Nervous System. 36(10). 2489–2496. 5 indexed citations
9.
Mozer‐Glassberg, Yael, et al.. (2018). [TRMU MUTATIONS - REVERSIBLE INFANTILE LIVER FAILURE OR MULTISYSTEM DISORDER?]. PubMed. 157(1). 52–57. 5 indexed citations
10.
Gilad, Oded, et al.. (2015). Nonbullous Erythema Multiforme in Hospitalized Children: A 10‐Year Survey. Pediatric Dermatology. 32(5). 701–703. 4 indexed citations
11.
Straussberg, Rachel, Daphna Marom, Gadi Horev, et al.. (2014). A Possible Genotype-Phenotype Correlation in Ashkenazi-Jewish Individuals With Aicardi-Goutières Syndrome Associated With SAMHD1 Mutation. Journal of Child Neurology. 30(4). 490–495. 1 indexed citations
12.
Marom, Daphna, Shai Ashkenazi, Zmira Samra, & Einat Birk. (2013). Infective Endocarditis in Previously Healthy Children With Structurally Normal Hearts. Pediatric Cardiology. 34(6). 1415–1421. 19 indexed citations
13.
Basel‐Vanagaite, Lina, Noam Zevit, Liang Guo, et al.. (2012). Transient Infantile Hypertriglyceridemia, Fatty Liver, and Hepatic Fibrosis Caused by Mutated GPD1, Encoding Glycerol-3-Phosphate Dehydrogenase 1. The American Journal of Human Genetics. 90(1). 49–60. 73 indexed citations
14.
Marom, Daphna, Charles E. Schwartz, Adi Har‐Zahav, et al.. (2011). X‐linked mental retardation with alacrima and achalasia—Triple A syndrome or a new syndrome?. American Journal of Medical Genetics Part A. 155(8). 1959–1963. 4 indexed citations
15.
Marom, Daphna, Itzhak Levy, Odit Gutwein, Einat Birk, & Shai Ashkenazi. (2011). Healthcare-associated Versus Community-associated Infective Endocarditis in Children. The Pediatric Infectious Disease Journal. 30(7). 585–588. 22 indexed citations
16.
Zeharia, Avraham, Avraham Shaag, Orit Pappo, et al.. (2010). Acute Infantile Liver Failure Due to Mutations in the TRMU Gene. The American Journal of Human Genetics. 86(2). 295–295. 4 indexed citations
17.
Zeharia, Avraham, Avraham Shaag, Orit Pappo, et al.. (2009). Acute Infantile Liver Failure Due to Mutations in the TRMU Gene. The American Journal of Human Genetics. 85(3). 401–407. 161 indexed citations
18.
19.
Weintrob, Naomi, Jacques Drouin, Sophie Vallette-Kasic, et al.. (2006). Low Estriol Levels in the Maternal Triple-Marker Screen as a Predictor of Isolated Adrenocorticotropic Hormone Deficiency Caused by a New Mutation in the TPIT Gene. PEDIATRICS. 117(2). e322–e327. 26 indexed citations
20.
Marom, Daphna, et al.. (1998). Intravenous leiomyomatosis with cardiac involvement in a pregnant woman. American Journal of Obstetrics and Gynecology. 178(3). 620–621. 10 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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