Reetta Kariola

689 total citations
15 papers, 520 citations indexed

About

Reetta Kariola is a scholar working on Pathology and Forensic Medicine, Cancer Research and Oncology. According to data from OpenAlex, Reetta Kariola has authored 15 papers receiving a total of 520 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Pathology and Forensic Medicine, 12 papers in Cancer Research and 7 papers in Oncology. Recurrent topics in Reetta Kariola's work include Genetic factors in colorectal cancer (15 papers), Cancer Genomics and Diagnostics (12 papers) and Colorectal Cancer Screening and Detection (5 papers). Reetta Kariola is often cited by papers focused on Genetic factors in colorectal cancer (15 papers), Cancer Genomics and Diagnostics (12 papers) and Colorectal Cancer Screening and Detection (5 papers). Reetta Kariola collaborates with scholars based in Finland, Denmark and United States. Reetta Kariola's co-authors include Minna Nyström, Païvi Peltomäki, Wael M. Abdel‐Rahman, Miina Ollikainen, Tiina Raevaara, Ralf Bützow, Heather Hampel, Anne‐Marie Gerdes, Anu‐Liisa Moisio and Irma Järvelä and has published in prestigious journals such as Journal of Clinical Oncology, Gastroenterology and Oncogene.

In The Last Decade

Reetta Kariola

15 papers receiving 510 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Reetta Kariola Finland	13	473	291	235	156	102	15	520
Renée C. Niessen Netherlands	14	594 1.3×	327 1.1×	385 1.6×	163 1.0×	123 1.2×	17	694
Shannon A. Kuismanen United States	6	563 1.2×	282 1.0×	390 1.7×	189 1.2×	82 0.8×	6	627
Raffaella Liccardo Italy	11	227 0.5×	161 0.6×	144 0.6×	118 0.8×	43 0.4×	23	330
Deborah Packham Australia	11	288 0.6×	202 0.7×	195 0.8×	245 1.6×	89 0.9×	14	490
Jeff Bacher United States	7	206 0.4×	129 0.4×	127 0.5×	77 0.5×	41 0.4×	8	312
Theofanis Zagoras Sweden	8	173 0.4×	100 0.3×	87 0.4×	72 0.5×	67 0.7×	10	269
Fernando Bellido Spain	6	176 0.4×	119 0.4×	118 0.5×	109 0.7×	43 0.4×	8	280
Ester Borràs United States	13	279 0.6×	186 0.6×	256 1.1×	139 0.9×	56 0.5×	21	465
Alexandra E. Gylfe Finland	10	148 0.3×	104 0.4×	111 0.5×	201 1.3×	67 0.7×	14	334
Mark Drost Netherlands	11	214 0.5×	165 0.6×	57 0.2×	132 0.8×	76 0.7×	16	302

Countries citing papers authored by Reetta Kariola

Since Specialization

Citations

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

Fields of papers citing papers by Reetta Kariola

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Reetta Kariola

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

All Works

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15 of 15 papers shown

Hampel, Heather, et al.. (2012). Mismatch repair analysis of inherited MSH2 and/or MSH6 variation pairs found in cancer patients. Human Mutation. 33(8). 1294–1301. 12 indexed citations

Hansen, Thomas van Overeem, Lotte Krogh, Mari Korhonen, et al.. (2011). A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance—functional analysis reveals the pathogenic one. Familial Cancer. 10(3). 515–520. 2 indexed citations

Korhonen, Mari, et al.. (2010). MutSβ exceeds MutSα in dinucleotide loop repair. British Journal of Cancer. 102(6). 1068–1073. 19 indexed citations

Kariola, Reetta, et al.. (2010). Verification of the three-step model in assessing the pathogenicity of mismatch repair gene variants. Human Mutation. 32(1). 107–115. 29 indexed citations

Christensen, Lise Lotte, Reetta Kariola, Mari Korhonen, et al.. (2009). Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patients. Familial Cancer. 8(4). 489–500. 6 indexed citations

Ollila, Saara, Laura Sarantaus, Reetta Kariola, et al.. (2006). Pathogenicity of MSH2 Missense Mutations Is Typically Associated With Impaired Repair Capability of the Mutated Protein. Gastroenterology. 131(5). 1408–1417. 54 indexed citations

Ollila, Saara, Laura Sarantaus, Reetta Kariola, et al.. (2006). The importance of functional testing in the genetic assessment of Muir-Torre syndrome, a clinical subphenotype of HNPCC. International Journal of Oncology. 16 indexed citations

Kariola, Reetta, Wael M. Abdel‐Rahman, Miina Ollikainen, et al.. (2005). APC and β-catenin protein expression patterns in HNPCC-related endometrial and colorectal cancers. Familial Cancer. 4(2). 187–190. 12 indexed citations

Abdel‐Rahman, Wael M., Miina Ollikainen, Reetta Kariola, et al.. (2005). Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutations. Oncogene. 24(9). 1542–1551. 71 indexed citations

10.

Ollikainen, Miina, Wael M. Abdel‐Rahman, Anu‐Liisa Moisio, et al.. (2005). Molecular Analysis of Familial Endometrial Carcinoma: A Manifestation of Hereditary Nonpolyposis Colorectal Cancer or a Separate Syndrome?. Journal of Clinical Oncology. 23(21). 4609–4616. 98 indexed citations

11.

Kariola, Reetta, Heather Hampel, Wendy L. Frankel, et al.. (2004). MSH6 missense mutations are often associated with no or low cancer susceptibility. British Journal of Cancer. 91(7). 1287–1292. 37 indexed citations

12.

Raevaara, Tiina, Anne‐Marie Gerdes, Anne Tybjærg‐Hansen, et al.. (2004). HNPCC mutation MLH1 P648S makes the functional protein unstable, and homozygosity predisposes to mild neurofibromatosis type 1. Genes Chromosomes and Cancer. 40(3). 261–265. 43 indexed citations

13.

Kariola, Reetta, Robyn Otway, Tiina Raevaara, et al.. (2003). Two mismatch repair gene mutations found in a colon cancer patient – which one is pathogenic?. Human Genetics. 112(2). 105–109. 28 indexed citations

14.

Raevaara, Tiina, Carlos Vaccaro, Wael M. Abdel‐Rahman, et al.. (2003). Pathogenicity of the hereditary colorectal cancer mutation hMLH1 del616 linked to shortage of the functional protein. Gastroenterology. 125(2). 501–509. 32 indexed citations

15.

Kariola, Reetta. (2002). Functional analysis of MSH6 mutations linked to kindreds with putative hereditary non-polyposis colorectal cancer syndrome. Human Molecular Genetics. 11(11). 1303–1310. 61 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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