Jaclyn A. Biegel

29.2k total citations · 3 hit papers
244 papers, 13.9k citations indexed

About

Jaclyn A. Biegel is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Neurology. According to data from OpenAlex, Jaclyn A. Biegel has authored 244 papers receiving a total of 13.9k indexed citations (citations by other indexed papers that have themselves been cited), including 157 papers in Molecular Biology, 78 papers in Pathology and Forensic Medicine and 48 papers in Neurology. Recurrent topics in Jaclyn A. Biegel's work include Chromatin Remodeling and Cancer (95 papers), Cancer Mechanisms and Therapy (58 papers) and Glioma Diagnosis and Treatment (38 papers). Jaclyn A. Biegel is often cited by papers focused on Chromatin Remodeling and Cancer (95 papers), Cancer Mechanisms and Therapy (58 papers) and Glioma Diagnosis and Treatment (38 papers). Jaclyn A. Biegel collaborates with scholars based in United States, Canada and United Kingdom. Jaclyn A. Biegel's co-authors include Lucy B. Rorke, Roger J. Packer, Alexander R. Judkins, Luanne Wainwright, Frederic G. Barr, Beverly S. Emanuel, Charles W.M. Roberts, Benjamin Fogelgren, Junying Zhou and Richard J. Davis and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Jaclyn A. Biegel

236 papers receiving 13.7k citations

Hit Papers

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What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors.

1999 629 citations Jaclyn A. Biegel, Lucy B. Rorke et al. PubMed profile →
Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood: definition of an entity

1996 567 citations Lucy B. Rorke, Roger J. Packer et al. profile →
Frequent expression of a mutant epidermal growth factor receptor in multiple human tumors.

1995 507 citations Jaclyn A. Biegel et al. PubMed profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Jaclyn A. Biegel	10.0k	4.8k	2.5k	2.4k	2.4k	244	13.9k
R. S. K. Chaganti	6.7k 0.7×	3.7k 0.8×	853 0.3×	2.5k 1.0×	1.5k 0.6×	199	14.5k
Yasuhiko Kaneko	5.3k 0.5×	1.5k 0.3×	1.2k 0.5×	1.0k 0.4×	1.6k 0.6×	269	10.1k
Alain Aurias	5.8k 0.6×	2.6k 0.5×	1.1k 0.5×	582 0.2×	5.5k 2.3×	179	12.3k
Wolfram Klapper	2.6k 0.3×	7.0k 1.5×	1.7k 0.7×	2.8k 1.2×	1.1k 0.5×	339	11.4k
Anne Hagemeijer	3.4k 0.3×	1.7k 0.4×	623 0.3×	2.4k 1.0×	2.0k 0.8×	151	9.8k
Nils Mandahl	5.7k 0.6×	4.0k 0.8×	1.2k 0.5×	645 0.3×	8.9k 3.7×	389	18.1k
Sverre Heim	4.1k 0.4×	2.6k 0.5×	361 0.1×	940 0.4×	3.4k 1.4×	432	11.9k
Azra H. Ligon	4.5k 0.5×	2.7k 0.6×	1.0k 0.4×	2.2k 0.9×	1.8k 0.7×	89	11.5k
Winand N.M. Dinjens	3.2k 0.3×	1.4k 0.3×	919 0.4×	2.4k 1.0×	2.1k 0.9×	256	9.6k
Gordon W. Dewald	4.4k 0.4×	2.6k 0.5×	321 0.1×	5.2k 2.1×	905 0.4×	212	13.1k

Countries citing papers authored by Jaclyn A. Biegel

Since Specialization

Citations

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

Fields of papers citing papers by Jaclyn A. Biegel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jaclyn A. Biegel. 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 Jaclyn A. Biegel. The network helps show where Jaclyn A. Biegel may publish in the future.

Co-authorship network of co-authors of Jaclyn A. Biegel

This figure shows the co-authorship network connecting the top 25 collaborators of Jaclyn A. Biegel. A scholar is included among the top collaborators of Jaclyn A. Biegel 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 Jaclyn A. Biegel. Jaclyn A. Biegel 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

Crotty, Erin, Sarah Leary, Alexandra Miller, et al.. (2025). Targeted detection of sequence variants in cell-free DNA from cerebrospinal fluid in pediatric central nervous system tumors. Frontiers in Oncology. 14. 1513073–1513073.

Tseng, Alexander M., Rachana Shah, Rima Jubran, et al.. (2025). The use of aqueous humor cfDNA for low-pass whole genome sequencing as a clinical test to identify intraocular retinoblastoma recurrence. PubMed. 2025.

Paulson, Vera, Bonnie Cole, Ashley Margol, et al.. (2025). Low-Pass Whole Genome Sequencing of Cell-Free DNA from Cerebrospinal Fluid: A Focus on Pediatric Central Nervous System Tumors. Clinical Chemistry. 71(1). 87–96.

Lee, Brian, Li Shen, Dennis T. Maglinte, et al.. (2024). Significance Associated with Phenotype Score Aids in Variant Prioritization for Exome Sequencing Analysis. Journal of Molecular Diagnostics. 26(5). 337–348. 2 indexed citations

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

Hiemenz, Matthew, Matthew J. Oberley, Andrew Doan, et al.. (2021). A multimodal genomics approach to diagnostic evaluation of pediatric hematologic malignancies. Cancer Genetics. 254-255. 25–33. 7 indexed citations

Xu, Liya, Ashley Polski, Rishvanth K. Prabakar, et al.. (2021). Establishing the Clinical Utility of ctDNA Analysis for Diagnosis, Prognosis, and Treatment Monitoring of Retinoblastoma: The Aqueous Humor Liquid Biopsy. Cancers. 13(6). 1282–1282. 42 indexed citations

Tříska, Petr, Kristiyana Kaneva, Daria Merkurjev, et al.. (2019). Landscape of Germline and Somatic Mitochondrial DNA Mutations in Pediatric Malignancies. Cancer Research. 79(7). 1318–1330. 29 indexed citations

Tamrazi, Benita, Sriram Venneti, Ashley Margol, et al.. (2019). Pediatric Atypical Teratoid/Rhabdoid Tumors of the Brain: Identification of Metabolic Subgroups Using In Vivo ¹H-MR Spectroscopy. American Journal of Neuroradiology. 40(5). 872–877. 6 indexed citations

10.

Ji, Jianling, David M. Parham, Li Shen, et al.. (2017). Inherited germline ATRX mutation in two brothers with ATR‐X syndrome and osteosarcoma. American Journal of Medical Genetics Part A. 173(5). 1390–1395. 23 indexed citations

11.

Wang, Xiaofeng, Ryan S. Lee, B. Alver, et al.. (2016). SMARCB1-mediated SWI/SNF complex function is essential for enhancer regulation. Nature Genetics. 49(2). 289–295. 239 indexed citations

12.

Fahiminiya, Somayyeh, Leora Witkowski, Javad Nadaf, et al.. (2015). Molecular analyses reveal close similarities between small cell carcinoma of the ovary, hypercalcemic type and atypical teratoid/rhabdoid tumor. Oncotarget. 7(2). 1732–1740. 32 indexed citations

13.

Hertwig, Falk, Katharina Meyer, Sebastian Braun, et al.. (2012). Definition of Genetic Events Directing the Development of Distinct Types of Brain Tumors from Postnatal Neural Stem/Progenitor Cells. Cancer Research. 72(13). 3381–3392. 12 indexed citations

14.

Tatard, Valérie M., Chaomei Xiang, Jaclyn A. Biegel, & Nadia Dahmane. (2010). ZNF238 Is Expressed in Postmitotic Brain Cells and Inhibits Brain Tumor Growth. Cancer Research. 70(3). 1236–1246. 40 indexed citations

15.

Jackson, Eric M., Angela J. Sievert, Xiaowu Gai, et al.. (2009). Genomic Analysis Using High-Density Single Nucleotide Polymorphism-Based Oligonucleotide Arrays and Multiplex Ligation-Dependent Probe Amplification Provides a Comprehensive Analysis of INI1/SMARCB1 in Malignant Rhabdoid Tumors. Clinical Cancer Research. 15(6). 1923–1930. 142 indexed citations

16.

Chi, Susan, Mary Ann Zimmerman, Xiaopan Yao, et al.. (2008). Intensive Multimodality Treatment for Children With Newly Diagnosed CNS Atypical Teratoid Rhabdoid Tumor. Journal of Clinical Oncology. 27(3). 385–389. 297 indexed citations

17.

Lun, Xueqing, Hongyuan Zhou, Limei Wang, et al.. (2008). Oncolytic Efficacy of Recombinant Vesicular Stomatitis Virus and Myxoma Virus in Experimental Models of Rhabdoid Tumors. Clinical Cancer Research. 14(4). 1218–1227. 46 indexed citations

18.

Packer, Roger J., Jaclyn A. Biegel, Susan M. Blaney, et al.. (2002). Atypical Teratoid/Rhabdoid Tumor of the Central Nervous System: Report on Workshop. Journal of Pediatric Hematology/Oncology. 24(5). 337–342. 164 indexed citations

19.

Davis, R. J., et al.. (1996). In Vivo Amplification of the PAX3-FKHR and PAX7-FKHR Fusion Genes in Alveolar Rhabdomyosarcoma. Human Molecular Genetics. 5(1). 15–21. 115 indexed citations

20.

Giovannini, Marco, Jaclyn A. Biegel, Massimo Serra, et al.. (1994). EWS-erg and EWS-Fli1 fusion transcripts in Ewing's sarcoma and primitive neuroectodermal tumors with variant translocations.. Journal of Clinical Investigation. 94(2). 489–496. 116 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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