Kristen Hanson

655 total citations
9 papers, 371 citations indexed

About

Kristen Hanson is a scholar working on Pathology and Forensic Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Kristen Hanson has authored 9 papers receiving a total of 371 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Pathology and Forensic Medicine, 5 papers in Genetics and 2 papers in Molecular Biology. Recurrent topics in Kristen Hanson's work include Genetic factors in colorectal cancer (5 papers), Genomics and Rare Diseases (3 papers) and BRCA gene mutations in cancer (2 papers). Kristen Hanson is often cited by papers focused on Genetic factors in colorectal cancer (5 papers), Genomics and Rare Diseases (3 papers) and BRCA gene mutations in cancer (2 papers). Kristen Hanson collaborates with scholars based in United States, Belgium and France. Kristen Hanson's co-authors include Elena M. Stoffel, Stephen B. Gruber, Laura S. Rozek, Erika Koeppe, Peter Ulintz, Linford Williams, Mark J. Kiel, Jessica N. Everett, Kristen J. Vogel and Anna Johnson and has published in prestigious journals such as Journal of Clinical Oncology, Gastroenterology and Cancer.

In The Last Decade

Kristen Hanson

9 papers receiving 366 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kristen Hanson United States	6	216	187	121	91	90	9	371
Amal Yussuf United States	11	90 0.4×	95 0.5×	178 1.5×	125 1.4×	92 1.0×	29	322
Chantal Perret Canada	10	76 0.4×	122 0.7×	189 1.6×	82 0.9×	92 1.0×	11	329
Fernando Bellido Spain	6	176 0.8×	118 0.6×	43 0.4×	119 1.3×	109 1.2×	8	280
Neal Clark Norway	9	126 0.6×	104 0.6×	232 1.9×	120 1.3×	83 0.9×	12	352
Rohini Rau‐Murthy United States	8	58 0.3×	137 0.7×	76 0.6×	119 1.3×	98 1.1×	14	256
María Carolina Sanabria‐Salas Colombia	11	55 0.3×	131 0.7×	91 0.8×	110 1.2×	66 0.7×	34	289
Jeffrey S. Skilling United States	11	69 0.3×	187 1.0×	146 1.2×	110 1.2×	150 1.7×	12	436
Vida Stegel Slovenia	11	56 0.3×	75 0.4×	135 1.1×	87 1.0×	143 1.6×	36	334
Belinda Nagler Australia	6	185 0.9×	200 1.1×	42 0.3×	100 1.1×	121 1.3×	7	353
William M. Grady United States	7	154 0.7×	145 0.8×	44 0.4×	44 0.5×	77 0.9×	9	250

Countries citing papers authored by Kristen Hanson

Since Specialization

Citations

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

Fields of papers citing papers by Kristen Hanson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kristen Hanson

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

All Works

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9 of 9 papers shown

Yin, Rui, Maxime Wack, Cartik R. Kothari, et al.. (2024). Phenome-wide profiling identifies genotype-phenotype associations in Phelan-McDermid syndrome using family-sourced data from an international registry. Molecular Autism. 15(1). 40–40. 3 indexed citations

Hanson, Kristen, Michael P. Mullane, Dean C. Pavlick, et al.. (2021). Identification of potential germline (GL) variants by routine clinical comprehensive genomic profiling (CGP) and confirmatory GL testing in 24 tumor types.. Journal of Clinical Oncology. 39(15_suppl). 10596–10596. 2 indexed citations

Stoffel, Elena M., Erika Koeppe, Jessica N. Everett, et al.. (2017). Germline Genetic Features of Young Individuals With Colorectal Cancer. Gastroenterology. 154(4). 897–905.e1. 227 indexed citations

Pilié, Patrick G., Anna Johnson, Kristen Hanson, et al.. (2017). Germline genetic variants in men with prostate cancer and one or more additional cancers. Cancer. 123(20). 3925–3932. 42 indexed citations

Stoffel, Elena M., Erika Koeppe, Kristen Hanson, et al.. (2016). Sa1765 Incidental Finding of Germline CDH1 Mutations: Implications for Clinical Management. Gastroenterology. 150(4). S360–S360. 1 indexed citations

Gunaratnam, Naresh T., Mehmet Akce, Angela N. Bartley, et al.. (2016). Screening for Cancer Genetic Syndromes With a Simple Risk-Assessment Tool in a Community-Based Open-Access Colonoscopy Practice. The American Journal of Gastroenterology. 111(5). 589–593. 7 indexed citations

Hanson, Kristen, et al.. (2014). Soil Solarization in High Tunnels in the Semiarid Southwestern United States. HortScience. 49(9). 1165–1170. 6 indexed citations

Vogel, Kristen J., et al.. (2014). The Evolution of Cancer Risk Assessment in the Era of Next Generation Sequencing. Journal of Genetic Counseling. 23(4). 633–639. 54 indexed citations

Thiel, Christian, Georg F. Hoffmann, Kristen Hanson, et al.. (2011). Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip. Human Mutation. 33(3). 485–487. 29 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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