Kristin Zelley

1.7k total citations
43 papers, 1.0k citations indexed

About

Kristin Zelley is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Kristin Zelley has authored 43 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 19 papers in Oncology and 16 papers in Genetics. Recurrent topics in Kristin Zelley's work include Cancer-related Molecular Pathways (12 papers), Neuroendocrine Tumor Research Advances (6 papers) and Childhood Cancer Survivors' Quality of Life (6 papers). Kristin Zelley is often cited by papers focused on Cancer-related Molecular Pathways (12 papers), Neuroendocrine Tumor Research Advances (6 papers) and Childhood Cancer Survivors' Quality of Life (6 papers). Kristin Zelley collaborates with scholars based in United States, Canada and Germany. Kristin Zelley's co-authors include Kim E. Nichols, Jennifer M. Kalish, Susan J. Wiener, Wendy Kohlmann, David T. Teachey, Huaqing Zhao, Deepak Chellapandian, Rupali Das, Katherine L. Nathanson and Sarah Scollon and has published in prestigious journals such as Journal of Clinical Oncology, Blood and Gastroenterology.

In The Last Decade

Kristin Zelley

38 papers receiving 995 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kristin Zelley United States 15 354 334 284 199 181 43 1.0k
Patrick Boutard France 19 245 0.7× 172 0.5× 267 0.9× 208 1.0× 260 1.4× 52 1.0k
Christiane Vermylen Belgium 20 237 0.7× 190 0.6× 330 1.2× 224 1.1× 568 3.1× 64 1.4k
Mouhab Ayas Saudi Arabia 21 316 0.9× 151 0.5× 200 0.7× 261 1.3× 756 4.2× 92 1.3k
J.-L. Stéphan France 17 180 0.5× 154 0.5× 135 0.5× 89 0.4× 426 2.4× 38 983
Dolors Costa Spain 21 299 0.8× 122 0.4× 262 0.9× 190 1.0× 400 2.2× 73 1.2k
Francine R. Dembitzer United States 12 308 0.9× 186 0.6× 110 0.4× 94 0.5× 82 0.5× 21 831
Hisato Kigasawa Japan 21 301 0.9× 144 0.4× 160 0.6× 392 2.0× 988 5.5× 60 1.5k
Osborn B. Eden United Kingdom 15 554 1.6× 175 0.5× 418 1.5× 374 1.9× 416 2.3× 26 1.6k
Kazuko Hamamoto Japan 17 435 1.2× 135 0.4× 113 0.4× 138 0.7× 788 4.4× 47 1.2k
Ram Kumar Marwaha India 17 180 0.5× 92 0.3× 188 0.7× 138 0.7× 342 1.9× 73 904

Countries citing papers authored by Kristin Zelley

Since Specialization
Citations

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

Fields of papers citing papers by Kristin Zelley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kristin Zelley

This figure shows the co-authorship network connecting the top 25 collaborators of Kristin Zelley. A scholar is included among the top collaborators of Kristin Zelley 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 Kristin Zelley. Kristin Zelley 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.
Rednam, Surya P., Junne Kamihara, Garrett M. Brodeur, et al.. (2025). Update on Tumor Surveillance for Children with Hereditary Pheochromocytoma/Paraganglioma Syndromes. Clinical Cancer Research. 31(16). 3368–3376. 1 indexed citations
2.
Le, Anh N., Kristin Zelley, Luke Maese, et al.. (2025). Pancreatic Cancer Risk and Screening Outcomes in Li-Fraumeni Syndrome. Pancreas. 54(7). e618–e623. 1 indexed citations
3.
Rednam, Surya P., Anita Villani, Garrett M. Brodeur, et al.. (2025). Update on Surveillance in Von Hippel–Lindau Disease. Clinical Cancer Research. 31(12). 2271–2277. 1 indexed citations
4.
Berko, Esther R., Arlene Naranjo, Samantha N. McNulty, et al.. (2025). Frequency and Clinical Significance of Clonal and Subclonal Driver Mutations in High-Risk Neuroblastoma at Diagnosis: A Children's Oncology Group Study. Journal of Clinical Oncology. 43(14). 1673–1684. 1 indexed citations
5.
Brzezinski, Jack, Gaëlle Bougeard, Garrett M. Brodeur, et al.. (2024). Update on Surveillance Guidelines in Emerging Wilms Tumor Predisposition Syndromes. Clinical Cancer Research. 31(1). 18–24. 2 indexed citations
6.
Kalish, Jennifer M., Gaëlle Bougeard, Garrett M. Brodeur, et al.. (2024). Update on Surveillance for Wilms Tumor and Hepatoblastoma in Beckwith–Wiedemann Syndrome and Other Predisposition Syndromes. Clinical Cancer Research. 30(23). 5260–5269. 9 indexed citations
7.
Luo, Minjie, Derek Wong, Kristin Zelley, et al.. (2024). Identification of TP53 germline variants in pediatric patients undergoing tumor testing: strategy and prevalence. JNCI Journal of the National Cancer Institute. 116(8). 1356–1365. 2 indexed citations
8.
Kratz, Christian P., Philip J. Lupo, Kristin Zelley, et al.. (2024). Adult-Onset Cancer Predisposition Syndromes in Children and Adolescents—To Test or not to Test?. Clinical Cancer Research. 30(9). 1733–1738. 9 indexed citations
9.
MacFarland, Suzanne P., Kami Wolfe Schneider, Roland P. Kuiper, et al.. (2024). Pediatric Cancer Screening in Hereditary Gastrointestinal Cancer Risk Syndromes: An Update from the AACR Childhood Cancer Predisposition Working Group. Clinical Cancer Research. 30(20). 4566–4571. 6 indexed citations
10.
Zelley, Kristin, Jaclyn Schienda, Bailey Gallinger, et al.. (2024). Update on Genetic Counselor Practice and Recommendations for Pediatric Cancer Predisposition Evaluation and Surveillance. Clinical Cancer Research. 30(18). 3983–3989. 5 indexed citations
11.
Zelley, Kristin, et al.. (2024). Atypical presentations of RECQL4‐related syndromes. Pediatric Blood & Cancer. 71(12). e31315–e31315. 1 indexed citations
12.
Le, Anh N., Jacquelyn Powers, Kristin Zelley, et al.. (2023). Rates of Intervention and Cancer Detection on Initial versus Subsequent Whole-body MRI Screening in Li-Fraumeni Syndrome. Cancer Prevention Research. 16(9). 507–512. 3 indexed citations
13.
Isaza, Amber, Garrett M. Brodeur, Suzanne P. MacFarland, et al.. (2020). The Clinical Spectrum of PTEN Hamartoma Tumor Syndrome: Exploring the Value of Thyroid Surveillance. Hormone Research in Paediatrics. 93(11-12). 634–642. 10 indexed citations
14.
Gao, Fan, Xuedong Pan, Jasmina Bojadzieva, et al.. (2020). A pedigree-based prediction model identifies carriers of deleterious de novo mutations in families with Li-Fraumeni syndrome. Genome Research. 30(8). 1170–1180. 3 indexed citations
15.
Katona, Bryson W., Jacquelyn Powers, Danielle McKenna, et al.. (2020). Upper Gastrointestinal Cancer Risk and Surveillance Outcomes in Li-Fraumeni Syndrome. The American Journal of Gastroenterology. 115(12). 2095–2097. 12 indexed citations
16.
Zhong, Yiming, Jeffrey Schubert, Jinhua Wu, et al.. (2020). A germline PALB2 pathogenic variant identified in a pediatric high-grade glioma. Molecular Case Studies. 6(4). a005397–a005397. 2 indexed citations
17.
Isaza, Amber, Garrett M. Brodeur, Suzanne P. MacFarland, et al.. (2020). OR22-02 PTEN Hamartoma Tumor Syndrome in Pediatrics: Triggers for Evaluation and the Value of Surveillance. Journal of the Endocrine Society. 4(Supplement_1).
18.
Zelley, Kristin, et al.. (2015). Diagnosis of 9q22.3 microdeletion syndrome in utero following identification of craniosynostosis, overgrowth, and skeletal anomalies. American Journal of Medical Genetics Part A. 167(4). 862–865. 7 indexed citations
19.
Alderfer, Melissa A., Kristin Zelley, Robert B. Lindell, et al.. (2014). Parent decision‐making around the genetic testing of children for germline TP53 mutations. Cancer. 121(2). 286–293. 39 indexed citations
20.
Kalish, Jennifer M., Laura K. Conlin, Sogol Mostoufi‐Moab, et al.. (2013). Bilateral Pheochromocytomas, Hemihyperplasia, and Subtle Somatic Mosaicism: The Importance of Detecting Low‐Level Uniparental Disomy. American Journal of Medical Genetics Part A. 161(5). 993–1001. 15 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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