Kelle Steenblock

567 total citations
8 papers, 407 citations indexed

About

Kelle Steenblock is a scholar working on Pathology and Forensic Medicine, Oncology and Genetics. According to data from OpenAlex, Kelle Steenblock has authored 8 papers receiving a total of 407 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Pathology and Forensic Medicine, 4 papers in Oncology and 3 papers in Genetics. Recurrent topics in Kelle Steenblock's work include Genetic factors in colorectal cancer (5 papers), Colorectal Cancer Treatments and Studies (4 papers) and Colorectal Cancer Screening and Detection (2 papers). Kelle Steenblock is often cited by papers focused on Genetic factors in colorectal cancer (5 papers), Colorectal Cancer Treatments and Studies (4 papers) and Colorectal Cancer Screening and Detection (2 papers). Kelle Steenblock collaborates with scholars based in United States, Ireland and Canada. Kelle Steenblock's co-authors include Stephen N. Thibodeau, Lawrence J. Burgart, Linnea M. Baudhuin, Amy J. French, Noralane M. Lindor, Hidewaki Nakagawa, Wendy L. Frankel, Albert de la Chapelle, Heather Hampel and Janet Lockman and has published in prestigious journals such as Gastroenterology, Cancer Research and Genetics in Medicine.

In The Last Decade

Kelle Steenblock

8 papers receiving 400 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kelle Steenblock United States 7 347 221 158 99 96 8 407
Isabella Gazzoli Netherlands 8 235 0.7× 162 0.7× 164 1.0× 71 0.7× 247 2.6× 13 444
Deborah Packham Australia 11 288 0.8× 195 0.9× 202 1.3× 89 0.9× 245 2.6× 14 490
Elsa C. Bik Netherlands 5 179 0.5× 91 0.4× 90 0.6× 69 0.7× 83 0.9× 6 270
Anneke Middeldorp Netherlands 9 228 0.7× 146 0.7× 137 0.9× 91 0.9× 126 1.3× 12 348
Raffaella Liccardo Italy 11 227 0.7× 144 0.7× 161 1.0× 43 0.4× 118 1.2× 23 330
Reetta Kariola Finland 13 473 1.4× 235 1.1× 291 1.8× 102 1.0× 156 1.6× 15 520
Tiina Raevaara Finland 7 180 0.5× 86 0.4× 116 0.7× 83 0.8× 117 1.2× 8 274
Constanze Walldorf Germany 7 193 0.6× 117 0.5× 129 0.8× 130 1.3× 120 1.3× 7 350
L Bowles United Kingdom 9 119 0.3× 98 0.4× 90 0.6× 75 0.8× 91 0.9× 12 291
Alexandra E. Gylfe Finland 10 148 0.4× 111 0.5× 104 0.7× 67 0.7× 201 2.1× 14 334

Countries citing papers authored by Kelle Steenblock

Since Specialization
Citations

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

Fields of papers citing papers by Kelle Steenblock

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kelle Steenblock

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

All Works

8 of 8 papers shown
1.
Weissman, Scott M., Cecelia Bellcross, Joy Larsen Haidle, et al.. (2010). Genetic Counseling Considerations in the Evaluation of Families for Lynch Syndrome—A Review. Journal of Genetic Counseling. 20(1). 5–19. 43 indexed citations
2.
Sutphen, Rebecca, et al.. (2010). Abstract P2-10-06: Identification and Referral of Appropriate Patients for Genetic Services in the Community Setting: An innovative Approach. Cancer Research. 70(24_Supplement). P2–10. 1 indexed citations
3.
Redman, Joy B., et al.. (2008). Molecular testing: improving patient care through partnering with laboratory genetic counselors. Genetics in Medicine. 10(5). 337–342. 13 indexed citations
4.
Steenblock, Kelle, et al.. (2008). Premutations in theFMR1Gene Are Uncommon in Men Undergoing Genetic Testing for Spinocerebellar Ataxia. Journal of Neurogenetics. 22(1). 77–92. 14 indexed citations
5.
Baudhuin, Linnea M., Matthew J. Ferber, Jennifer L. Winters, et al.. (2005). Characterization of hMLH1 and hMSH2 Gene Dosage Alterations in Lynch Syndrome Patients. Gastroenterology. 129(3). 846–854. 37 indexed citations
6.
Wang, Liang, Linnea M. Baudhuin, Lisa A. Boardman, et al.. (2004). MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps. Gastroenterology. 127(1). 9–16. 151 indexed citations
7.
Nakagawa, Hidewaki, Janet Lockman, Wendy L. Frankel, et al.. (2004). Mismatch Repair Gene PMS2 . Cancer Research. 64(14). 4721–4727. 127 indexed citations
8.
Hahnloser, Dieter, Gloria M. Petersen, Kari G. Rabe, et al.. (1969). ELECTRON MICROSCOPE INVESTIGATION OF STRUCTURE OF INDIUM OXIDE FILMS.. OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information). 12(10). 1023–8. 21 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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