Umut Aypar

1.0k total citations
33 papers, 557 citations indexed

About

Umut Aypar is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Umut Aypar has authored 33 papers receiving a total of 557 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Genetics. Recurrent topics in Umut Aypar's work include Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Lymphoma Diagnosis and Treatment (6 papers). Umut Aypar is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Lymphoma Diagnosis and Treatment (6 papers). Umut Aypar collaborates with scholars based in United States, Netherlands and Germany. Umut Aypar's co-authors include Janet E. Baulch, William F. Morgan, Nicole L. Hoppman, Robert B. Jenkins, Beth A. Pitel, James B. Smadbeck, Sarah H. Johnson, Stephanie A. Smoley, Hutton M. Kearney and Roman M. Zenka and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Umut Aypar

30 papers receiving 546 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Umut Aypar United States 12 273 127 118 111 88 33 557
Pamela Brock United States 15 277 1.0× 286 2.3× 103 0.9× 59 0.5× 68 0.8× 39 712
Olaug K. Rødningen Norway 20 410 1.5× 310 2.4× 181 1.5× 110 1.0× 112 1.3× 50 949
Hinke F. van Thuijl Netherlands 7 200 0.7× 96 0.8× 216 1.8× 193 1.7× 95 1.1× 11 693
George A. Tanteles Cyprus 14 336 1.2× 233 1.8× 79 0.7× 79 0.7× 61 0.7× 72 646
Catherine Dehainault France 14 343 1.3× 119 0.9× 71 0.6× 51 0.5× 295 3.4× 21 637
Jonathan P. Park United States 19 462 1.7× 267 2.1× 83 0.7× 49 0.4× 177 2.0× 36 898
Takaya Ichimura Japan 13 706 2.6× 179 1.4× 55 0.5× 52 0.5× 152 1.7× 34 943
Ken C. Lo United States 14 291 1.1× 92 0.7× 123 1.0× 38 0.3× 64 0.7× 21 473
Cecilia Surace Italy 12 328 1.2× 201 1.6× 128 1.1× 58 0.5× 68 0.8× 33 595
Shlomit Rienstein Israel 14 277 1.0× 161 1.3× 94 0.8× 49 0.4× 60 0.7× 28 559

Countries citing papers authored by Umut Aypar

Since Specialization
Citations

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

Fields of papers citing papers by Umut Aypar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Umut Aypar

This figure shows the co-authorship network connecting the top 25 collaborators of Umut Aypar. A scholar is included among the top collaborators of Umut Aypar 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 Umut Aypar. Umut Aypar 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.
Agaram, Narasimhan P., Konstantinos Linos, Carol D. Morris, et al.. (2025). 31 SNP Array Analysis of Synovial Chondromatosis with Atypical Features. Laboratory Investigation. 105(3). 102254–102254.
2.
3.
Hurwitz, Stephanie N., Brian Lockhart, Özlem Önder, et al.. (2023). Proteogenomic Profiling of High-Grade B-Cell Lymphoma With 11q Aberrations and Burkitt Lymphoma Reveals Lymphoid Enhancer Binding Factor 1 as a Novel Biomarker. Modern Pathology. 36(7). 100170–100170. 3 indexed citations
4.
Gao, Qi, Ying Liu, Umut Aypar, et al.. (2023). Highly sensitive single tube B‐lymphoblastic leukemia/lymphoma minimal/measurable residual disease test robust to surface antigen directed therapy. Cytometry Part B Clinical Cytometry. 104(4). 279–293. 8 indexed citations
5.
Argyropoulos, Kimon V., Umut Aypar, Mark D. Ewalt, et al.. (2023). Chronic lymphocytic leukemia transdifferentiated to blastic neoplasm with T/plasmacytoid dendritic cell immunophenotype. Leukemia & lymphoma. 64(3). 734–737.
6.
Aypar, Umut & Mark D. Ewalt. (2022). A very Burkitt-like case of Burkitt-like lymphoma with 11q aberration. Blood. 139(11). 1771–1771. 1 indexed citations
7.
Aypar, Umut, et al.. (2022). A novel case of cutaneous myxoid spindle cell neoplasm with FMR1‐ALK gene fusion and CD34/S100 co‐expression. Journal of Cutaneous Pathology. 50(6). 505–510. 5 indexed citations
8.
Uraoka, Naohiro, et al.. (2021). Automated 3D scoring of fluorescence in situ hybridization (FISH) using a confocal whole slide imaging scanner. Han-guk hyeonmigyeong hakoeji/Applied microscopy. 51(1). 4–4. 10 indexed citations
9.
Yang, Soo‐Ryum, Umut Aypar, Ezra Y. Rosen, et al.. (2020). A Performance Comparison of Commonly Used Assays to Detect RET Fusions. Clinical Cancer Research. 27(5). 1316–1328. 50 indexed citations
10.
Gliem, Troy J. & Umut Aypar. (2017). Development of a Chromosomal Microarray Test for the Detection of Abnormalities in Formalin-Fixed, Paraffin-Embedded Products of Conception Specimens. Journal of Molecular Diagnostics. 19(6). 843–847. 14 indexed citations
11.
Johnson, Sarah H., James B. Smadbeck, Stephanie A. Smoley, et al.. (2017). SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq). Cancer Genetics. 221. 1–18. 61 indexed citations
12.
Allyse, Megan, Umut Aypar, Natasha Bonhomme, et al.. (2017). Offering Prenatal Screening in the Age of Genomic Medicine: A Practical Guide. Journal of Women s Health. 26(7). 755–761. 9 indexed citations
13.
Faqeih, Eissa, et al.. (2017). A novel deletion of SNURF/SNRPN exon 1 in a patient with Prader-Willi-like phenotype. European Journal of Medical Genetics. 60(8). 416–420. 14 indexed citations
14.
Aypar, Umut, Nicole L. Hoppman, Erik C. Thorland, & D. Brian Dawson. (2016). Patients with mosaic methylation patterns of the Prader-Willi/Angelman Syndrome critical region exhibit AS-like phenotypes with some PWS features. Molecular Cytogenetics. 9(1). 26–26. 6 indexed citations
15.
Cocanougher, Ben, Umut Aypar, Linda Hasadsri, et al.. (2015). Biochemical and computational analyses of two phenotypically related GALT mutations (S222N and S135L) that lead to atypical galactosemia. Data in Brief. 3. 34–39. 2 indexed citations
16.
Cocanougher, Ben, Umut Aypar, Linda Hasadsri, et al.. (2015). Compound heterozygosity with a novel S222N GALT mutation leads to atypical galactosemia with loss of GALT activity in erythrocytes but little evidence of clinical disease. SHILAP Revista de lepidopterología. 2. 61–64. 2 indexed citations
17.
Aypar, Umut, Ryan A. Knudson, Kathryn E. Pearce, Anne E. Wiktor, & Rhett P. Ketterling. (2014). Development of an NPM1/MLF1 D-FISH Probe Set for the Detection of t(3;5)(q25;q35) Identified in Patients with Acute Myeloid Leukemia. Journal of Molecular Diagnostics. 16(5). 527–532. 7 indexed citations
18.
Baulch, Janet E., Umut Aypar, Katrina M. Waters, Austin J. Yang, & William F. Morgan. (2014). Genetic and Epigenetic Changes in Chromosomally Stable and Unstable Progeny of Irradiated Cells. PLoS ONE. 9(9). e107722–e107722. 16 indexed citations
19.
Aypar, Umut, William F. Morgan, & Janet E. Baulch. (2010). Radiation-induced genomic instability: Are epigenetic mechanisms the missing link?. International Journal of Radiation Biology. 87(2). 179–191. 68 indexed citations
20.
Aypar, Umut, William F. Morgan, & Janet E. Baulch. (2010). Radiation-induced epigenetic alterations after low and high LET irradiations. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 707(1-2). 24–33. 97 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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