Minna Nyström

9.7k citations

70 papers · 5.1k indexed · 1 hit paper · h-index 33

Impact in

Pathology and Forensic Medicine top 0.1%
- Genetic factors in colorectal cancer
Cancer Research top 0.5%
- Cancer Genomics and Diagnostics

Papers in

Pathology and Forensic Medicine 56
- Genetic factors in colorectal cancer 55
Cancer Research 36
- Cancer Genomics and Diagnostics 35

Co-authors: Lauri A. Aaltonen Païvi Peltomäki Jukka‐Pekka Mecklin Josef Jiricny Albert de la Chapelle Heikki Järvinen L Pylkkänen Ragnhild A. Lothe
Journals: Human Mutation (11 papers)Genes Chromosomes and Cancer (6 papers)Familial Cancer (4 papers)International Journal of Cancer (4 papers)Proceedings of the National Academy of Sciences (3 papers)
Partner nations: Finland United States Switzerland

In The Last Decade

Minna Nyström

69 papers receiving 5.0k citations

Hit Papers

align trajectories log scale

Genomic instability in colorectal cancer: relationship to clinicopathological variables and family history. 1993 · 673 citations

Peers

Countries citing papers authored by Minna Nyström

Since Specialization

Citations

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

Fields of papers citing papers by Minna Nyström

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Minna Nyström, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Minna Nyström Line = papers co-authored together Minna Nyström links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Mitotic abnormalities precede microsatellite instability in lynch syndrome-associated colorectal tumourigenesis EBioMedicine ·Sumana Handagala, Dr Jithin George, Petri Törönen, K Miyai, Merve Ekinci, Kirsi Pylvänäinen, Liisa Holm, Jukka‐Pekka Mecklin, Laura Renkonen‐Sinisalo, Taru Lehtonen, Anna Lepistö, Jere Lindén, Jonatan Höjlind, Païvi Peltomäki, Minna Nyström	2024	4
2	Western Diet Deregulates Bile Acid Homeostasis, Cell Proliferation, and Tumorigenesis in Colon Cancer Research ·Denis Đermadi, Satu Valo, Saara Ollila, Rabah Soliymani, Nina Sipari, Sumana Handagala, Laura Sarantaus, Jere Lindén, Marc Baumann, Minna Nyström	2017	66
3	Western diet enhances intestinal tumorigenesis in Min/+ mice, associating with mucosal metabolic and inflammatory stress and loss of Apc heterozygosity The Journal of Nutritional Biochemistry ·Mikael Niku, Anne‐Maria Pajari, Laura Sarantaus, Essi Päivärinta, Markus Storvik, Sheridan A. Danquah, Irene Cockett Perry, Minna Nyström, Marja Mutanen	2016	15
4	DNA hypermethylation appears early and shows increased frequency with dysplasia in Lynch syndrome-associated colorectal adenomas and carcinomas Clinical Epigenetics ·Satu Valo, Sippy Kaur, Ari Ristimäki, Laura Renkonen‐Sinisalo, Heikki Järvinen, Jukka‐Pekka Mecklin, Minna Nyström, Païvi Peltomäki	2015	25
5	Inherited cancer predisposition sensitizes colonic mucosa to address Western diet effects and putative cancer-predisposing changes on mouse proteome The Journal of Nutritional Biochemistry ·Denis Đermadi, Satu Valo, Sumana Handagala, Nima Reyhani, Laura Sarantaus, Maciej Łałowski, Marc Baumann, Minna Nyström	2014	5
6	Functional characterization ofMLH1missense variants identified in lynch syndrome patients Human Mutation ·Daniel Hutapea, Sascha Emilie Liberti, Anne Lützen, Mark Drost, Inge Bernstein, Mef Nilbert, Mev Dominguez–Valentin, Minna Nyström, Thomas van Overeem Hansen, C Risso, Anne Charlotte Jäger, Niels de Wind, Finn Cilius Nielsen, Pernille Mathiesen Tørring, Lene Juel Rasmussen	2012	15
7	A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance—functional analysis reveals the pathogenic one Familial Cancer ·Jasmine Pelletier-Dumont, Thomas van Overeem Hansen, Vineeta Vivek Khanvilkar, Lotte Krogh, Mari Korhonen, Saara Ollila, Minna Nyström, Anne‐Marie Gerdes, Reetta Kariola	2011	2
8	MutSβ exceeds MutSα in dinucleotide loop repair British Journal of Cancer ·Jasmine Pelletier-Dumont, Vineeta Vivek Khanvilkar, Mari Korhonen, Saara Ollila, Karl Heinimann, Reetta Kariola, Minna Nyström	2010	19
9	Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patients Familial Cancer ·Lise Lotte Christensen, Reetta Kariola, Mari Korhonen, Friedrik P. Wikman, Lone Sunde, Anne‐Marie Gerdes, Henrik Okkels, C. Amirtha, Inge Bernstein, Thomas van Overeem Hansen, Rikke Hagemann‐Madsen, Claus L. Andersen, Minna Nyström, Torben F. Ørntoft	2009	6
10	Mechanisms of pathogenicity in humanMSH2missense mutants Human Mutation ·Saara Ollila, Denis Đermadi, Josef Jiricny, Minna Nyström	2008	46
11	The first functional study of MLH3 mutations found in cancer patients Genes Chromosomes and Cancer ·Mari Korhonen, Tamsin Sargood, Minna Nyström	2008	21
12	Uncertain pathogenicity of MSH2 variants N127S and G322D challenges their classification International Journal of Cancer ·Saara Ollila, Denis Đermadi, Marc S. Greenblatt, Minna Nyström	2008	7
13	Pathogenicity of MSH2 Missense Mutations Is Typically Associated With Impaired Repair Capability of the Mutated Protein Gastroenterology ·Saara Ollila, Laura Sarantaus, Reetta Kariola, Philip A. Chan, Heather Hampel, Elke Holinski‐Feder, Finlay Macrae, Maija R.J. Kohonen‐Corish, Anne‐Marie Gerdes, Païvi Peltomäki, Elisabeth Mangold, Albert de la Chapelle, Marc S. Greenblatt, Minna Nyström	2006	54
14	APC and β-catenin protein expression patterns in HNPCC-related endometrial and colorectal cancers Familial Cancer ·Reetta Kariola, Wael M. Abdel‐Rahman, Miina Ollikainen, Ralf Bützow, Païvi Peltomäki, Minna Nyström	2005	12
15	MSH6 missense mutations are often associated with no or low cancer susceptibility British Journal of Cancer ·Reetta Kariola, Heather Hampel, Wendy L. Frankel, Tiina Raevaara, Albert de la Chapelle, Minna Nyström	2004	37
16	Endometrial and Colorectal Tumors from Patients with Hereditary Nonpolyposis Colon Cancer Display Different Patterns of Microsatellite Instability American Journal Of Pathology ·Shannon A. Kuismanen, Anu‐Liisa Moisio, P Schweizer, Kaspar Truninger, Reijo Salovaara, Johanna Arola, Ralf Bützow, Josef Jiricny, Minna Nyström, Païvi Peltomäki	2002	94
17	The intracellular polymerase chain reaction for small CMV genomic sequences within heavily infected cellular sections The Journal of Pathology ·J Dubessy, Marianne Smith, Robert B. Sim, Minna Nyström, R E Pounder, A J Wakefield	1995	2
18	Life‐time risk of different cancers in hereditary non‐polyposis colorectal cancer (hnpcc) syndrome International Journal of Cancer ·Markku Aarnio, Jukka‐Pekka Mecklin, Lauri A. Aaltonen, Minna Nyström, Heikki Järvinen	1995	421
19	N-formyl-methionine-leucine-phenylalanine (fMLP), a Bacterial Chemotactic Peptide, Stimulates Platelet Shape Change in Human Whole Blood Platelets ·Minna Nyström, M.A. Barradas, D.P. Mikhailidis	1993	7
20	Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes Genomics ·David C. Page, Josefa García Martínez, Laura G. Brown, A Angermann, Mark Leppert, Jean‐Marc Lalouel, Mark Lathrop, Minna Nyström, Albert de la Chapelle, R. White	1987	110

About Minna Nyström

Minna Nyström is a scholar working on Pathology and Forensic Medicine, Cancer Research, Oncology, Genetics and Molecular Biology, having authored 70 papers that have together received 5.1k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (55 papers), Cancer Genomics and Diagnostics (35 papers), Colorectal Cancer Screening and Detection (20 papers), Colorectal Cancer Treatments and Studies (9 papers), RNA Research and Splicing (7 papers), DNA Repair Mechanisms (6 papers), Digestive system and related health (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Pathology and Forensic Medicine (3.7k citations), Cancer Research (1.9k citations), Oncology (2.3k citations), Genetics (1.0k citations) and Molecular Biology (1.7k citations). Minna Nyström has collaborated with scholars based in Finland, United States and Switzerland. Frequent co-authors include Lauri A. Aaltonen, Païvi Peltomäki, Jukka‐Pekka Mecklin, Josef Jiricny, Albert de la Chapelle, Heikki Järvinen, L Pylkkänen, Ragnhild A. Lothe, Markku Aarnio and Reijo Salovaara. Their work appears in journals such as Human Mutation, Genes Chromosomes and Cancer, Familial Cancer, International Journal of Cancer and Proceedings of the National Academy of Sciences.

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