Odelia Nahum

2.7k total citations
13 papers, 352 citations indexed

About

Odelia Nahum is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Oncology. According to data from OpenAlex, Odelia Nahum has authored 13 papers receiving a total of 352 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Pediatrics, Perinatology and Child Health, 5 papers in Genetics and 4 papers in Oncology. Recurrent topics in Odelia Nahum's work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Cancer-related Molecular Pathways (2 papers). Odelia Nahum is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Cancer-related Molecular Pathways (2 papers). Odelia Nahum collaborates with scholars based in United States, Switzerland and Denmark. Odelia Nahum's co-authors include Brynn Levy, Konstantinos Evangelou, Thanos D. Halazonetis, Jiří Bártek, Vassilis Zoumpourlis, Zoi Lygerou, Christos Kittas, Vassilis G. Gorgoulis, Athanassios Kotsinas and Dimitris Kletsas and has published in prestigious journals such as Cancer Research, Fertility and Sterility and Journal of General Virology.

In The Last Decade

Odelia Nahum

13 papers receiving 338 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Odelia Nahum United States 9 193 88 62 58 46 13 352
Rosalind Codrington United Kingdom 7 185 1.0× 86 1.0× 33 0.5× 26 0.4× 31 0.7× 8 339
Michele Cook Australia 7 337 1.7× 132 1.5× 24 0.4× 43 0.7× 18 0.4× 10 498
Michael Rusch United States 10 301 1.6× 43 0.5× 37 0.6× 30 0.5× 17 0.4× 14 376
Amita Limaye India 8 352 1.8× 64 0.7× 62 1.0× 23 0.4× 13 0.3× 8 515
Jean-François Spinella Canada 13 273 1.4× 83 0.9× 77 1.2× 26 0.4× 26 0.6× 23 489
Regina Lichti Binz United States 10 193 1.0× 66 0.8× 58 0.9× 24 0.4× 31 0.7× 21 310
Sheryl Gere United States 5 466 2.4× 78 0.9× 206 3.3× 35 0.6× 24 0.5× 5 605
Ashley N. Kamimae-Lanning United States 7 317 1.6× 53 0.6× 34 0.5× 17 0.3× 13 0.3× 8 415
Wenbing Xie China 13 636 3.3× 94 1.1× 70 1.1× 32 0.6× 39 0.8× 19 739
Ivor Hickey United Kingdom 9 231 1.2× 86 1.0× 54 0.9× 63 1.1× 19 0.4× 16 382

Countries citing papers authored by Odelia Nahum

Since Specialization
Citations

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

Fields of papers citing papers by Odelia Nahum

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Odelia Nahum

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

All Works

13 of 13 papers shown
1.
Buchovecky, Christie M., Odelia Nahum, & Brynn Levy. (2018). Assessment of Maternal Cell Contamination in Prenatal Samples by Quantitative Fluorescent PCR (QF-PCR). Methods in molecular biology. 1885. 117–127. 5 indexed citations
2.
Ganapathi, Mythily, Odelia Nahum, & Brynn Levy. (2018). Prenatal Diagnosis Using Chromosomal SNP Microarrays. Methods in molecular biology. 1885. 187–205. 16 indexed citations
3.
Borczuk, Alain, Jianming Pei, Robert N. Taub, et al.. (2016). Genome-wide analysis of abdominal and pleural malignant mesothelioma with DNA arrays reveals both common and distinct regions of copy number alteration. Cancer Biology & Therapy. 17(3). 328–335. 38 indexed citations
4.
Ganapathi, Karthik A., Vaidehi Jobanputra, Fábio M. Iwamoto, et al.. (2016). The genetic landscape of dural marginal zone lymphomas. Oncotarget. 7(28). 43052–43061. 22 indexed citations
5.
Margolskee, Elizabeth, Vaidehi Jobanputra, Preti Jain, et al.. (2016). Genetic landscape of T- and NK-cell post-transplant lymphoproliferative disorders. Oncotarget. 7(25). 37636–37648. 41 indexed citations
6.
Levy, Brynn, David Tegay, Peter Papenhausen, et al.. (2012). Tetrasomy 15q26: a distinct syndrome or Shprintzen-Goldberg syndrome phenocopy?. Genetics in Medicine. 14(9). 811–818. 4 indexed citations
7.
Shanske, Alan, Kwame Anyane‐Yeboa, Odelia Nahum, et al.. (2011). The proximal chromosome 14q microdeletion syndrome: Delineation of the phenotype using high resolution SNP oligonucleotide microarray analysis (SOMA) and review of the literature. American Journal of Medical Genetics Part A. 155(8). 1884–1896. 9 indexed citations
8.
Levy, Brynn, Dong Wang, Kristin Engelstad, et al.. (2010). Uncovering microdeletions in patients with severe Glut-1 deficiency syndrome using SNP oligonucleotide microarray analysis. Molecular Genetics and Metabolism. 100(2). 129–135. 19 indexed citations
9.
Shanske, Alan, et al.. (2010). Delineation of the breakpoints of pure duplication 3q due to a de novo duplication event using SOMA. American Journal of Medical Genetics Part A. 152A(12). 3185–3188. 19 indexed citations
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Liontos, Michalis, Maria Sideridou, Konstantinos Evangelou, et al.. (2007). Deregulated Overexpression of hCdt1 and hCdc6 Promotes Malignant Behavior. Cancer Research. 67(22). 10899–10909. 160 indexed citations
13.
Faktor, Ouriel, et al.. (1997). The p10 gene of Spodoptera littoralis nucleopolyhedrovirus: nucleotide sequence, transcriptional analysis and unique gene organization in the p10 locus.. Journal of General Virology. 78(8). 2119–2128. 15 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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