Katie Beierl

1.1k total citations
24 papers, 683 citations indexed

About

Katie Beierl is a scholar working on Cancer Research, Pediatrics, Perinatology and Child Health and Oncology. According to data from OpenAlex, Katie Beierl has authored 24 papers receiving a total of 683 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cancer Research, 7 papers in Pediatrics, Perinatology and Child Health and 7 papers in Oncology. Recurrent topics in Katie Beierl's work include Cancer Genomics and Diagnostics (10 papers), Prenatal Screening and Diagnostics (7 papers) and Gestational Trophoblastic Disease Studies (6 papers). Katie Beierl is often cited by papers focused on Cancer Genomics and Diagnostics (10 papers), Prenatal Screening and Diagnostics (7 papers) and Gestational Trophoblastic Disease Studies (6 papers). Katie Beierl collaborates with scholars based in United States, Taiwan and Italy. Katie Beierl's co-authors include James R. Eshleman, Ming‐Tseh Lin, Brigitte M. Ronnett, Christopher D. Gocke, Cheryl DeScipio, Russell Vang, Kathleen M. Murphy, Lisa Haley, Stacy Mosier and Marija Debeljak and has published in prestigious journals such as Clinical Cancer Research, The American Journal of Surgical Pathology and Human Pathology.

In The Last Decade

Katie Beierl

24 papers receiving 680 citations

Peers

Katie Beierl

ONCOL

PHEOH

PPCH

Constantine Alifrangis United Kingdom

Natalie Banet United States

Chimene Kesserwan United States

Sarah A. Bannon United States

C. Michel Zwaan Netherlands

Hiroaki Kase Japan

Joan Murphy Canada

Sylvie Ramond France

Iris H.I.M. Hollink Netherlands

Elisabeth M. P. Steeghs Netherlands

Constantine Alifrangis United Kingdom

Katie Beierl

130 ×0.5

ONCOL

163 ×0.7

PHEOH

127 ×0.6

PPCH

96 ×0.5

277 ×1.7

Citations per year, relative to Katie Beierl Katie Beierl (= 1×) peers Constantine Alifrangis

Countries citing papers authored by Katie Beierl

Since Specialization

Citations

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

Fields of papers citing papers by Katie Beierl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katie Beierl

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

All Works

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20 of 20 papers shown

Dbouk, Mohamad, Toshiya Abe, Anne M. Macgregor‐Das, et al.. (2023). Diagnostic Performance of a Tumor Marker Gene Test to Personalize Serum CA19–9 Reference Ranges. Clinical Cancer Research. 29(20). 4178–4185. 16 indexed citations

Xing, Deyin, et al.. (2021). Loss of p57 Expression in Conceptions Other Than Complete Hydatidiform Mole. The American Journal of Surgical Pathology. 46(1). 18–32. 11 indexed citations

Beierl, Katie, Christopher D. Gocke, Daniel J. Zabransky, et al.. (2017). Whole-Exome Sequencing of Metaplastic Breast Carcinoma Indicates Monoclonality with Associated Ductal Carcinoma Component. Clinical Cancer Research. 23(16). 4875–4884. 29 indexed citations

Debeljak, Marija, Evelina Mocci, Aparna Pallavajjalla, et al.. (2017). Haplotype Counting for Sensitive Chimerism Testing. Journal of Molecular Diagnostics. 19(3). 427–436. 9 indexed citations

Illei, Peter B., Deborah Belchis, Li‐Hui Tseng, et al.. (2017). Clinical mutational profiling of 1006 lung cancers by next generation sequencing. Oncotarget. 8(57). 96684–96696. 24 indexed citations

Murphy, Kathleen M., Cheryl DeScipio, Katie Beierl, et al.. (2015). Invasive Complete Hydatidiform Moles. International Journal of Gynecological Pathology. 35(2). 134–141. 15 indexed citations

Rodić, Nemanja, Robert A. Anders, James R. Eshleman, et al.. (2014). PD-L1 Expression in Melanocytic Lesions Does Not Correlate with the BRAF V600E Mutation. Cancer Immunology Research. 3(2). 110–115. 42 indexed citations

McCall, Chad M., Stacy Mosier, Marija Debeljak, et al.. (2014). False Positives in Multiplex PCR-Based Next-Generation Sequencing Have Unique Signatures. Journal of Molecular Diagnostics. 16(5). 541–549. 35 indexed citations

Debeljak, Marija, Donald Freed, Lisa Haley, et al.. (2014). Haplotype Counting by Next-Generation Sequencing for Ultrasensitive Human DNA Detection. Journal of Molecular Diagnostics. 16(5). 495–503. 13 indexed citations

10.

Tseng, Li‐Hui, Jih‐Luh Tang, Lisa Haley, et al.. (2014). Microsatellite Instability Confounds Engraftment Analysis of Hematopoietic Stem-cell Transplantation. Applied immunohistochemistry & molecular morphology. 22(6). 416–420. 12 indexed citations

11.

Beierl, Katie, Li‐Hui Tseng, Lisa Haley, et al.. (2013). Detection of Minor Clones With Internal Tandem Duplication Mutations of FLT3 Gene in Acute Myeloid Leukemia Using Delta-PCR. Diagnostic Molecular Pathology. 22(1). 1–9. 9 indexed citations

12.

Banet, Natalie, Cheryl DeScipio, Kathleen M. Murphy, et al.. (2013). Characteristics of hydatidiform moles: analysis of a prospective series with p57 immunohistochemistry and molecular genotyping. Modern Pathology. 27(2). 238–254. 92 indexed citations

13.

Lin, Ming‐Tseh, Li‐Hui Tseng, Katie Beierl, et al.. (2013). Tandem Duplication PCR. Diagnostic Molecular Pathology. 22(3). 149–155. 9 indexed citations

14.

Robertson, Scott, Omar Hyder, Rebecca M. Dodson, et al.. (2013). The frequency of KRAS and BRAF mutations in intrahepatic cholangiocarcinomas and their correlation with clinical outcome. Human Pathology. 44(12). 2768–2773. 84 indexed citations

15.

DeScipio, Cheryl, Kathleen M. Murphy, Lisa Haley, et al.. (2013). Characterization of Androgenetic/Biparental Mosaic/Chimeric Conceptions, Including Those With a Molar Component. International Journal of Gynecological Pathology. 32(2). 199–214. 54 indexed citations

16.

Chen, Guoli, Matthew T. Olson, Alan M. O’Neill, et al.. (2012). A Virtual Pyrogram Generator to Resolve Complex Pyrosequencing Results. Journal of Molecular Diagnostics. 14(2). 149–159. 16 indexed citations

17.

Murphy, Kathleen M., et al.. (2011). Tetraploid Partial Hydatidiform Mole. International Journal of Gynecological Pathology. 31(1). 73–79. 21 indexed citations

18.

Lin, Ming‐Tseh, Li‐Hui Tseng, Katie Beierl, et al.. (2011). Analysis of Hematopoietic Stem Cell Transplant Engraftment. Diagnostic Molecular Pathology. 20(4). 194–202. 3 indexed citations

19.

DeScipio, Cheryl, et al.. (2011). Diandric Triploid Hydatidiform Mole With Loss of Maternal Chromosome 11. The American Journal of Surgical Pathology. 35(10). 1586–1591. 28 indexed citations

20.

Cesarani, Federico, et al.. (2011). Primary synovial sarcoma of the kidney. A case report with pathologic appraisal investigation and literature review.. PubMed. 103(5). 271–8. 4 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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