Kathryn E. Pearce

1.4k total citations
31 papers, 512 citations indexed

About

Kathryn E. Pearce is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Kathryn E. Pearce has authored 31 papers receiving a total of 512 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Hematology, 14 papers in Molecular Biology and 8 papers in Genetics. Recurrent topics in Kathryn E. Pearce's work include Acute Myeloid Leukemia Research (9 papers), Multiple Myeloma Research and Treatments (8 papers) and Chronic Myeloid Leukemia Treatments (7 papers). Kathryn E. Pearce is often cited by papers focused on Acute Myeloid Leukemia Research (9 papers), Multiple Myeloma Research and Treatments (8 papers) and Chronic Myeloid Leukemia Treatments (7 papers). Kathryn E. Pearce collaborates with scholars based in United States, Spain and Canada. Kathryn E. Pearce's co-authors include Jennelle C. Hodge, Anne E. Wiktor, William R. Sukov, Patricia T. Greipp, Christine M. Lohse, John C. Cheville, R. Houston Thompson, Linda B. Baughn, Bradley C. Leibovich and Rhett P. Ketterling and has published in prestigious journals such as Blood, Clinical Cancer Research and The FASEB Journal.

In The Last Decade

Kathryn E. Pearce

29 papers receiving 508 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kathryn E. Pearce United States 13 258 187 184 106 88 31 512
Stefan Gröschel Germany 14 319 1.2× 136 0.7× 303 1.6× 86 0.8× 162 1.8× 25 712
Melissa Dainton United Kingdom 9 174 0.7× 139 0.7× 212 1.2× 38 0.4× 112 1.3× 15 382
Yacov Goshen Israel 13 162 0.6× 127 0.7× 56 0.3× 65 0.6× 88 1.0× 18 443
Su Y. Kim United States 9 119 0.5× 99 0.5× 87 0.5× 48 0.5× 88 1.0× 11 391
Sonja Kiuru‐Kuhlefelt Finland 8 259 1.0× 209 1.1× 43 0.2× 135 1.3× 152 1.7× 12 594
Abhinita Mohanty United States 9 97 0.4× 78 0.4× 105 0.6× 102 1.0× 74 0.8× 17 378
Ricardo Alvarez United States 11 92 0.4× 98 0.5× 72 0.4× 58 0.5× 133 1.5× 20 374
Jo-Anne Vergilio United States 7 147 0.6× 36 0.2× 198 1.1× 97 0.9× 64 0.7× 8 457
Markéta Kalinová Czechia 13 300 1.2× 71 0.4× 232 1.3× 48 0.5× 121 1.4× 38 581
Dariusz Woszczyk Poland 12 109 0.4× 46 0.2× 139 0.8× 51 0.5× 119 1.4× 27 397

Countries citing papers authored by Kathryn E. Pearce

Since Specialization
Citations

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

Fields of papers citing papers by Kathryn E. Pearce

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kathryn E. Pearce. 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 Kathryn E. Pearce. The network helps show where Kathryn E. Pearce may publish in the future.

Co-authorship network of co-authors of Kathryn E. Pearce

This figure shows the co-authorship network connecting the top 25 collaborators of Kathryn E. Pearce. A scholar is included among the top collaborators of Kathryn E. Pearce 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 Kathryn E. Pearce. Kathryn E. Pearce 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.
2.
Gomes, Maria Aparecida, Laura Morsberger, Nicole L. Hoppman, et al.. (2024). An Integrated Approach Including CRISPR/Cas9-Mediated Nanopore Sequencing, Mate Pair Sequencing, and Cytogenomic Methods to Characterize Complex Structural Rearrangements in Acute Myeloid Leukemia. Biomedicines. 12(3). 598–598. 1 indexed citations
3.
Baughn, Linda B., Erik Jessen, Neeraj Sharma, et al.. (2023). Mass Cytometry reveals unique phenotypic patterns associated with subclonal diversity and outcomes in multiple myeloma. Blood Cancer Journal. 13(1). 84–84. 4 indexed citations
4.
Sharma, Neeraj, James B. Smadbeck, Nadine Abdallah, et al.. (2021). The Prognostic Role of MYC Structural Variants Identified by NGS and FISH in Multiple Myeloma. Clinical Cancer Research. 27(19). 5430–5439. 22 indexed citations
5.
Hou, Yanli, Krishna M. Roskin, Daniel A. Arber, et al.. (2021). Lymphoid blast transformation in an MPN with BCR-JAK2 treated with ruxolitinib: putative mechanisms of resistance. Blood Advances. 5(17). 3492–3496. 14 indexed citations
6.
Smadbeck, James B., Neeraj Sharma, Reid G. Meyer, et al.. (2021). Increased complexity of t(11;14) rearrangements in plasma cell neoplasms compared with mantle cell lymphoma. Genes Chromosomes and Cancer. 60(10). 678–686. 5 indexed citations
7.
Guenzel, Adam J., James B. Smadbeck, George Vasmatzis, et al.. (2021). Clinical utility of next generation sequencing to detect IGH/IL3 rearrangements [t(5;14)(q31.1;q32.1)] in B-lymphoblastic leukemia/lymphoma. Annals of Diagnostic Pathology. 53. 151761–151761. 8 indexed citations
8.
Pitel, Beth A., Kathryn E. Pearce, James B. Smadbeck, et al.. (2020). Characterizing false-positive fluorescence in situ hybridization results by mate-pair sequencing in a patient with chronic myeloid leukemia and progression to myeloid blast crisis. Cancer Genetics. 243. 48–51. 8 indexed citations
9.
10.
Jia, Yuyan, Linda B. Baughn, Kathryn E. Pearce, et al.. (2020). IGH rearrangement in myeloid neoplasms. Haematologica. 105(6). e315–e317. 2 indexed citations
11.
Xing, Deyin, Gang Zheng, Aparna Pallavajjala, et al.. (2019). Lineage-Specific Alterations in Gynecologic Neoplasms with Choriocarcinomatous Differentiation: Implications for Origin and Therapeutics. Clinical Cancer Research. 25(14). 4516–4529. 22 indexed citations
12.
Smadbeck, James B., Jess F. Peterson, Kathryn E. Pearce, et al.. (2019). Mate pair sequencing outperforms fluorescence in situ hybridization in the genomic characterization of multiple myeloma. Blood Cancer Journal. 9(12). 103–103. 29 indexed citations
13.
Peterson, Jess F., Reid G. Meyer, Stephanie A. Smoley, et al.. (2019). Whole Genome Mate-pair Sequencing of Plasma Cell Neoplasm as a Novel Diagnostic Strategy: A Case of Unrecognized t(2;11) Structural Variation. Clinical Lymphoma Myeloma & Leukemia. 19(9). 598–602. 2 indexed citations
14.
Baughn, Linda B., Kathryn E. Pearce, Dirk R. Larson, et al.. (2018). Differences in genomic abnormalities among African individuals with monoclonal gammopathies using calculated ancestry. Blood Cancer Journal. 8(10). 96–96. 44 indexed citations
15.
16.
González‐Calle, Verónica, Niamh Keane, Kathryn E. Pearce, et al.. (2018). Evaluation of Revised International Staging System (R-ISS) for transplant-eligible multiple myeloma patients. Annals of Hematology. 97(8). 1453–1462. 24 indexed citations
17.
Hodge, Jennelle C., et al.. (2016). Molecular Cytogenetic Analysis of JAZF1, PHF1, and YWHAE in Endometrial Stromal Tumors. Journal of Molecular Diagnostics. 18(4). 516–526. 21 indexed citations
18.
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
19.
Hodge, Jennelle C., Kathryn E. Pearce, Amy C. Clayton, Florin‐Andrei Taran, & Elizabeth A. Stewart. (2014). Uterine cellular leiomyomata with chromosome 1p deletions represent a distinct entity. American Journal of Obstetrics and Gynecology. 210(6). 572.e1–572.e7. 27 indexed citations
20.
Sukov, William R., Jennelle C. Hodge, Christine M. Lohse, et al.. (2012). TFE3 Rearrangements in Adult Renal Cell Carcinoma. The American Journal of Surgical Pathology. 36(5). 663–670. 118 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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