Dejerianne Ostrow

1.2k total citations
31 papers, 431 citations indexed

About

Dejerianne Ostrow is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Dejerianne Ostrow has authored 31 papers receiving a total of 431 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Genetics and 9 papers in Cancer Research. Recurrent topics in Dejerianne Ostrow's work include Cancer Genomics and Diagnostics (8 papers), Evolution and Genetic Dynamics (7 papers) and Genetics, Aging, and Longevity in Model Organisms (5 papers). Dejerianne Ostrow is often cited by papers focused on Cancer Genomics and Diagnostics (8 papers), Evolution and Genetic Dynamics (7 papers) and Genetics, Aging, and Longevity in Model Organisms (5 papers). Dejerianne Ostrow collaborates with scholars based in United States, Czechia and Canada. Dejerianne Ostrow's co-authors include Charles F. Baer, Matthew P. Salomon, Naomi Phillips, Laura Levy, Thomas E. Keller, Chikako Matsuba, Jill G. Joseph, Camille B. Wortman, Ronald C. Kessler and John Phair and has published in prestigious journals such as Journal of Clinical Oncology, American Journal of Psychiatry and Cancer Research.

In The Last Decade

Dejerianne Ostrow

29 papers receiving 425 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dejerianne Ostrow United States 12 168 122 91 66 65 31 431
William Beggs United States 11 462 2.8× 296 2.4× 44 0.5× 83 1.3× 26 0.4× 18 823
Xue Liang China 10 115 0.7× 120 1.0× 9 0.1× 12 0.2× 73 1.1× 27 430
Wendy K. Kiso United States 11 150 0.9× 179 1.5× 42 0.5× 84 1.3× 7 0.1× 21 523
Jorge Azofeifa Costa Rica 11 200 1.2× 172 1.4× 10 0.1× 13 0.2× 21 0.3× 29 409
George Nicholson United Kingdom 12 164 1.0× 341 2.8× 3 0.0× 46 0.7× 43 0.7× 23 715
Joshua Zhang United States 10 44 0.3× 138 1.1× 28 0.3× 13 0.2× 14 0.2× 15 278
Yohann Nédélec Canada 10 261 1.6× 348 2.9× 7 0.1× 101 1.5× 144 2.2× 11 842
Chih-Ting Yang Taiwan 4 283 1.7× 436 3.6× 5 0.1× 8 0.1× 53 0.8× 7 699
Anand Vasudevan United States 8 62 0.4× 173 1.4× 3 0.0× 92 1.4× 220 3.4× 9 643
Amy M. Boddy United States 4 149 0.9× 163 1.3× 25 0.3× 97 1.5× 5 0.1× 10 406

Countries citing papers authored by Dejerianne Ostrow

Since Specialization
Citations

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

Fields of papers citing papers by Dejerianne Ostrow

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dejerianne Ostrow

This figure shows the co-authorship network connecting the top 25 collaborators of Dejerianne Ostrow. A scholar is included among the top collaborators of Dejerianne Ostrow 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 Dejerianne Ostrow. Dejerianne Ostrow 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.
Maggo, Simran, et al.. (2025). Clinical impact of pharmacogenomics in pediatric care: insights extracted from clinical exome sequencing. Frontiers in Genetics. 16. 1574325–1574325.
2.
Buckley, Jonathan D., Scott A. Mitchell, Dejerianne Ostrow, et al.. (2025). Combined genomic profiling of cell-free DNA (cfDNA) and circulating tumor cell DNA (ctcDNA) in S1802, a prospective phase 3 trial for metastatic prostate cancer (mHSPC).. Journal of Clinical Oncology. 43(16_suppl). 1 indexed citations
3.
Momcilovic, Milica, Dejerianne Ostrow, Simran Maggo, et al.. (2024). Trafficking of mitochondrial double-stranded RNA from mitochondria to the cytosol. Life Science Alliance. 7(9). e202302396–e202302396. 5 indexed citations
4.
Maggo, Simran, Dejerianne Ostrow, Jennifer Cotter, et al.. (2024). A method for measuring mitochondrial DNA copy number in pediatric populations. Frontiers in Pediatrics. 12. 1401737–1401737. 3 indexed citations
5.
Bootwalla, Moiz, Dejerianne Ostrow, Jennifer Cotter, et al.. (2024). Pediatric Chordoma: A Tale of Two Genomes. Molecular Cancer Research. 22(8). 721–729. 1 indexed citations
6.
Buckley, Jonathan D., Ryan J. Schmidt, Dejerianne Ostrow, et al.. (2023). An Exome Capture-Based RNA-Sequencing Assay for Genome-Wide Identification and Prioritization of Clinically Important Fusions in Pediatric Tumors. Journal of Molecular Diagnostics. 26(2). 127–139. 3 indexed citations
7.
Hu, Zunsong, Alexandra E. Kovach, Venkata D. Yellapantula, et al.. (2023). Transcriptome Sequencing Allows Comprehensive Genomic Characterization of Pediatric B-Acute Lymphoblastic Leukemia in an Academic Clinical Laboratory. Journal of Molecular Diagnostics. 26(1). 49–60. 7 indexed citations
8.
Yellapantula, Venkata, Jianling Ji, Jesse L. Berry, et al.. (2023). Abstract 3322: Diagnosis and monitoring of pediatric cancer patients using low-pass whole genome and targeted sequencing of cell-free DNA. Cancer Research. 83(7_Supplement). 3322–3322.
9.
Zhou, Shengmei, Stephen F. Sarabia, Dejerianne Ostrow, et al.. (2023). Comparative Clinicopathologic and Genomic Analysis of Hepatocellular Neoplasm, Not Otherwise Specified, and Hepatoblastoma. Modern Pathology. 37(2). 100385–100385. 3 indexed citations
10.
Yellapantula, Venkata, Liya Xu, Jesse L. Berry, et al.. (2023). Combined low-pass whole genome and targeted sequencing in liquid biopsies for pediatric solid tumors. npj Precision Oncology. 7(1). 21–21. 33 indexed citations
11.
Buckley, Jonathan D., Dejerianne Ostrow, Bino Varghese, et al.. (2022). Non-Invasive Profiling of Advanced Prostate Cancer via Multi-Parametric Liquid Biopsy and Radiomic Analysis. International Journal of Molecular Sciences. 23(5). 2571–2571. 12 indexed citations
12.
Zhou, Shengmei, Meng Li, Dejerianne Ostrow, et al.. (2022). Potential methylation-regulated genes and pathways in hepatocellular neoplasm, not otherwise specified. Frontiers in Oncology. 12. 952325–952325. 2 indexed citations
13.
Ryutov, Alex, Xiaowu Gai, Dejerianne Ostrow, et al.. (2021). Utility of viral whole-genome sequencing for institutional infection surveillance during the coronavirus disease 2019 (COVID-19) pandemic. Infection Control and Hospital Epidemiology. 43(8). 1086–1088. 4 indexed citations
14.
Kaneva, Kristiyana, Daria Merkurjev, Dejerianne Ostrow, et al.. (2020). Detection of mitochondrial DNA variants at low level heteroplasmy in pediatric CNS and extra-CNS solid tumors with three different enrichment methods. Mitochondrion. 51. 97–103. 6 indexed citations
15.
Pandey, Utsav, Rebecca Yee, Li Shen, et al.. (2020). High Prevalence of SARS-CoV-2 Genetic Variation and D614G Mutation in Pediatric Patients With COVID-19. Open Forum Infectious Diseases. 8(6). ofaa551–ofaa551. 12 indexed citations
16.
Oberley, Matthew J., Christopher Denton, Jianling Ji, et al.. (2017). A neoplasm with FIP1L1-PDGFRA fusion presenting as pediatric T-cell lymphoblastic leukemia/lymphoma without eosinophilia. Cancer Genetics. 216-217. 91–99. 3 indexed citations
17.
Buckley, Jonathan D., Pedro A. Sanchez‐Lara, Dennis T. Maglinte, et al.. (2016). A Rapid and Sensitive Next-Generation Sequencing Method to Detect RB1 Mutations Improves Care for Retinoblastoma Patients and Their Families. Journal of Molecular Diagnostics. 18(4). 480–493. 25 indexed citations
18.
Baer, Charles F., et al.. (2010). RAPID DECLINE IN FITNESS OF MUTATION ACCUMULATION LINES OF GONOCHORISTIC (OUTCROSSING) CAENORHABDITIS NEMATODES. Evolution. 64(11). 3242–3253. 13 indexed citations
19.
Salomon, Matthew P., Dejerianne Ostrow, Naomi Phillips, et al.. (2009). Comparing Mutational and Standing Genetic Variability for Fitness and Size inCaenorhabditis briggsaeandC. elegans. Genetics. 183(2). 685–692. 18 indexed citations
20.
Phillips, Naomi, Matthew P. Salomon, Andrew W. Custer, Dejerianne Ostrow, & Charles F. Baer. (2008). Spontaneous Mutational and Standing Genetic (Co)variation at Dinucleotide Microsatellites in Caenorhabditis briggsae and Caenorhabditis elegans. Molecular Biology and Evolution. 26(3). 659–669. 29 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by William Beggs Breakdown of academic impact, for papers by Xue Liang Breakdown of academic impact, for papers by Wendy K. Kiso Breakdown of academic impact, for papers by Jorge Azofeifa Breakdown of academic impact, for papers by George Nicholson Breakdown of academic impact, for papers by Joshua Zhang Breakdown of academic impact, for papers by Yohann Nédélec Breakdown of academic impact, for papers by Chih-Ting Yang Breakdown of academic impact, for papers by Anand Vasudevan Breakdown of academic impact, for papers by Amy M. Boddy
Rankless by CCL
2026