Nichole Owen

725 total citations
20 papers, 483 citations indexed

About

Nichole Owen is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Nichole Owen has authored 20 papers receiving a total of 483 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Plant Science. Recurrent topics in Nichole Owen's work include DNA Repair Mechanisms (6 papers), Carcinogens and Genotoxicity Assessment (3 papers) and Prenatal Screening and Diagnostics (3 papers). Nichole Owen is often cited by papers focused on DNA Repair Mechanisms (6 papers), Carcinogens and Genotoxicity Assessment (3 papers) and Prenatal Screening and Diagnostics (3 papers). Nichole Owen collaborates with scholars based in United States, Hong Kong and Australia. Nichole Owen's co-authors include Amanda K. McCullough, Allison J. Schaser, Esteban Luna, Kelvin C. Luk, Vivek K. Unni, Jacob Raber, Teresa L. Stackhouse, Sydney Weber Boutros, Tamily A. Weissman and Randall L. Woltjer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Molecular Cell.

In The Last Decade

Nichole Owen

16 papers receiving 482 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nichole Owen United States 9 323 125 94 76 62 20 483
Fabienne Godin France 10 295 0.9× 93 0.7× 56 0.6× 48 0.6× 33 0.5× 17 483
Steven Pierce United States 14 343 1.1× 168 1.3× 48 0.5× 109 1.4× 75 1.2× 21 750
Katrin A. Mooslehner United Kingdom 10 297 0.9× 80 0.6× 121 1.3× 148 1.9× 17 0.3× 15 522
Lin Luo China 7 180 0.6× 96 0.8× 31 0.3× 65 0.9× 15 0.2× 22 343
Timothy A. Bolger United States 13 782 2.4× 58 0.5× 91 1.0× 121 1.6× 61 1.0× 16 915
David B. Rhee United States 6 560 1.7× 50 0.4× 44 0.5× 43 0.6× 211 3.4× 7 741
Michael J. Hipp United States 9 518 1.6× 200 1.6× 51 0.5× 69 0.9× 107 1.7× 12 775
Baojin Ding United States 16 442 1.4× 78 0.6× 58 0.6× 135 1.8× 13 0.2× 36 604
Per Ludvik Brattås Sweden 11 415 1.3× 30 0.2× 59 0.6× 93 1.2× 32 0.5× 13 534
Jenny Blechingberg Denmark 10 294 0.9× 41 0.3× 67 0.7× 34 0.4× 26 0.4× 18 388

Countries citing papers authored by Nichole Owen

Since Specialization
Citations

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

Fields of papers citing papers by Nichole Owen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nichole Owen

This figure shows the co-authorship network connecting the top 25 collaborators of Nichole Owen. A scholar is included among the top collaborators of Nichole Owen 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 Nichole Owen. Nichole Owen 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.
Chau, Matthew Hoi Kin, Stephanie A. Anderson, Patricia A. Ward, et al.. (2025). Detection of Clinically Relevant Monogenic Copy-Number Variants by a Comprehensive Genome-Wide Microarray with Exonic Coverage. Clinical Chemistry. 71(1). 141–154.
2.
Owen, Nichole, Elizabeth Wilson, Lorraine Potocki, et al.. (2025). De Novo Chromosomes 3q and 5q Chromothripsis Leads to a 5q14.3 Microdeletion Syndrome Presentation: Case Report and Review of the Literature. American Journal of Medical Genetics Part A. 197(6). e63975–e63975.
3.
Chau, Matthew Hoi Kin, Stephanie A. Anderson, Patricia A. Ward, et al.. (2024). P593: Detection of single-gene copy-number variations through high-resolution exon-targeted chromosomal microarray analysis. SHILAP Revista de lepidopterología. 2. 101499–101499.
4.
Saeidian, Amir Hossein, Michael March, Leila Youssefian, et al.. (2024). Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participants. Genetics in Medicine. 26(11). 101225–101225. 7 indexed citations
5.
Vossaert, Liesbeth, et al.. (2024). Novel hemizygous single‐nucleotide duplication in RPGR in a patient with retinal dystrophy and sensorineural hearing loss. Molecular Genetics & Genomic Medicine. 12(2). e2404–e2404. 1 indexed citations
6.
Littlejohn, Rebecca O., et al.. (2023). Precision therapy for a medically actionable ATP1A3 variant from a genomic medicine program in an underserved population. Molecular Genetics & Genomic Medicine. 11(12). e2272–e2272. 1 indexed citations
7.
Murali, Chaya N., Christian M. Parobek, Lorraine Potocki, et al.. (2023). P573: Biallelic missense NEXN variants lead to recessive severe neonatal cardiomyopathy. SHILAP Revista de lepidopterología. 1(1). 100620–100620.
8.
Owen, Nichole, Lisa Forbes Satter, Susan E. Kirk, et al.. (2021). Expansion of the clinical phenotype of GALE deficiency. American Journal of Medical Genetics Part A. 185(10). 3118–3121. 7 indexed citations
9.
Owen, Nichole, et al.. (2021). Enhanced cytarabine-induced killing in OGG1-deficient acute myeloid leukemia cells. Proceedings of the National Academy of Sciences. 118(11). 14 indexed citations
10.
Schaser, Allison J., Valerie R. Osterberg, Teresa L. Stackhouse, et al.. (2019). Alpha-synuclein is a DNA binding protein that modulates DNA repair with implications for Lewy body disorders. Scientific Reports. 9(1). 10919–10919. 189 indexed citations
11.
Chambwe, Nyasha, Weiliang Tang, Nichole Owen, et al.. (2018). An RNAi screen in human cell lines reveals conserved DNA damage repair pathways that mitigate formaldehyde sensitivity. DNA repair. 72. 1–9. 9 indexed citations
12.
Vartanian, Vladimir L., Nichole Owen, Marcus J. Calkins, et al.. (2018). Modulation of UVB-induced Carcinogenesis by Activation of Alternative DNA Repair Pathways. Scientific Reports. 8(1). 705–705. 6 indexed citations
13.
Owen, Nichole, Irina G. Minko, Sabine S. Lange, et al.. (2016). DNA polymerase ζ limits chromosomal damage and promotes cell survival following aflatoxin exposure. Proceedings of the National Academy of Sciences. 113(48). 13774–13779. 21 indexed citations
14.
Calkins, Marcus J., Vladimir L. Vartanian, Nichole Owen, et al.. (2016). Enhanced sensitivity of Neil1−/− mice to chronic UVB exposure. DNA repair. 48. 43–50. 14 indexed citations
15.
Madireddy, Advaitha, Settapong T Kosiyatrakul, Emilia Herrera‐Moyano, et al.. (2016). FANCD2 Facilitates Replication through Common Fragile Sites. Molecular Cell. 64(2). 388–404. 132 indexed citations
16.
Owen, Nichole, Helen J. Lawce, & Susan B. Olson. (2016). A New Rhesus Macaque Karyotype Based on Human-rhesus Synteny.. PubMed. 42(4). 178–179. 1 indexed citations
17.
Kumari, Anuradha, et al.. (2015). BLM protein mitigates formaldehyde-induced genomic instability. DNA repair. 28. 73–82. 13 indexed citations
18.
Owen, Nichole, et al.. (2014). Bloom Syndrome Radials Are Predominantly Non-Homologous and Are Suppressed by Phosphorylated BLM. Cytogenetic and Genome Research. 144(4). 255–263. 7 indexed citations
19.
Murdoch, Brenda M., Nichole Owen, Michelle Stevense, et al.. (2013). Altered Cohesin Gene Dosage Affects Mammalian Meiotic Chromosome Structure and Behavior. PLoS Genetics. 9(2). e1003241–e1003241. 36 indexed citations
20.
Murdoch, Brenda M., et al.. (2010). Multiple loci contribute to genome-wide recombination levels in male mice. Mammalian Genome. 21(11-12). 550–555. 25 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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