Janina Suchy

1.9k total citations
42 papers, 807 citations indexed

About

Janina Suchy is a scholar working on Pathology and Forensic Medicine, Oncology and Genetics. According to data from OpenAlex, Janina Suchy has authored 42 papers receiving a total of 807 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Pathology and Forensic Medicine, 21 papers in Oncology and 12 papers in Genetics. Recurrent topics in Janina Suchy's work include Genetic factors in colorectal cancer (29 papers), Colorectal Cancer Screening and Detection (13 papers) and Cancer Genomics and Diagnostics (8 papers). Janina Suchy is often cited by papers focused on Genetic factors in colorectal cancer (29 papers), Colorectal Cancer Screening and Detection (13 papers) and Cancer Genomics and Diagnostics (8 papers). Janina Suchy collaborates with scholars based in Poland, Australia and Latvia. Janina Suchy's co-authors include Grzegorz Kurzawski, Jan Lubiński, Rodney J. Scott, Cliff Meldrum, Bente A. Talseth‐Palmer, Cezary Cybulski, Józef Kładny, Krzysztof Safranow, Mateusz Kurzawski and Dariusz Chlubek and has published in prestigious journals such as SHILAP Revista de lepidopterología, Cancer Research and British Journal of Cancer.

In The Last Decade

Janina Suchy

41 papers receiving 796 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Janina Suchy 324 299 290 189 170 42 807
Min Sun Shin 302 0.9× 639 2.1× 262 0.9× 189 1.0× 93 0.5× 17 1.0k
Shinsuke Funakoshi 271 0.8× 327 1.1× 107 0.4× 100 0.5× 319 1.9× 44 955
Jan Kornafel 411 1.3× 246 0.8× 81 0.3× 144 0.8× 87 0.5× 73 832
Rong‐Miao Zhou 294 0.9× 459 1.5× 113 0.4× 231 1.2× 74 0.4× 61 868
Takahisa Kayahara 394 1.2× 321 1.1× 109 0.4× 86 0.5× 165 1.0× 29 884
Gábor Lakatos 158 0.5× 144 0.5× 158 0.5× 154 0.8× 136 0.8× 21 570
Koeffler Hp 282 0.9× 383 1.3× 151 0.5× 78 0.4× 102 0.6× 25 755
Alexander Gaber 296 0.9× 365 1.2× 156 0.5× 224 1.2× 72 0.4× 29 791
Kimishige Akino 277 0.9× 933 3.1× 149 0.5× 219 1.2× 66 0.4× 24 1.3k

Countries citing papers authored by Janina Suchy

Since Specialization
Citations

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

Fields of papers citing papers by Janina Suchy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Janina Suchy

This figure shows the co-authorship network connecting the top 25 collaborators of Janina Suchy. A scholar is included among the top collaborators of Janina Suchy 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 Janina Suchy. Janina Suchy 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.
Talseth‐Palmer, Bente A., Juul Wijnen, Shantie Jagmohan–Changur, et al.. (2012). Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers. International Journal of Cancer. 132(7). 1556–1564. 20 indexed citations
2.
Rać, Monika, Monika Rać, Janina Suchy, et al.. (2010). Analysis of Human CD36 Gene Sequence Alterations in the Oxidized Low-Density Lipoprotein-Binding Region Using Denaturing High-Performance Liquid Chromatography. Genetic Testing and Molecular Biomarkers. 14(4). 551–557. 8 indexed citations
3.
Trubicka, Joanna, Janina Suchy, Bartłomiej Masojć, et al.. (2010). Variant alleles of the CYP1B1 gene are associated with colorectal cancer susceptibility. BMC Cancer. 10(1). 420–420. 28 indexed citations
4.
Safranow, Krzysztof, Janina Suchy, Katarzyna Jakubowska, et al.. (2010). AMPD1 gene mutations are associated with obesity and diabetes in Polish patients with cardiovascular diseases. Journal of Applied Genetics. 52(1). 67–76. 18 indexed citations
5.
Gronwald, Jacek, Cezary Cybulski, Janina Suchy, et al.. (2009). Cancer risks in first-degree relatives of CHEK2 mutation carriers: effects of mutation type and cancer site in proband. British Journal of Cancer. 100(9). 1508–1512. 25 indexed citations
6.
Dymerska, Dagmara, Pablo Serrano‐Fernández, Janina Suchy, et al.. (2009). Combined iPLEX and TaqMan Assays to Screen for 45 Common Mutations in Lynch Syndrome and FAP Patients. Journal of Molecular Diagnostics. 12(1). 82–90. 6 indexed citations
7.
Shi, Zumin, Daniel M. Johnstone, Bente A. Talseth‐Palmer, et al.. (2009). Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age. International Journal of Cancer. 125(1). 78–83. 28 indexed citations
8.
9.
Suchy, Janina, Cezary Cybulski, Dominika Wokołorczyk, et al.. (2009). CHEK2 mutations and HNPCC‐related colorectal cancer. International Journal of Cancer. 126(12). 3005–3009. 33 indexed citations
10.
Kurzawski, Grzegorz, Janina Suchy, Cezary Cybulski, et al.. (2008). DNA testing for variants conferring low or moderate increase in the risk of cancer. SHILAP Revista de lepidopterología. 3 indexed citations
11.
Raszeja‐Wyszomirska, Joanna, et al.. (2008). Frequency of mutations related to hereditary haemochromatosis in northwestern Poland. Journal of Applied Genetics. 49(1). 105–107. 8 indexed citations
12.
Suchy, Janina & Jan Lubiński. (2008). MSH6 syndrome. Hereditary Cancer in Clinical Practice. 6(2). 103–103. 1 indexed citations
13.
Suchy, Janina, Józef Kładny, Cezary Cybulski, et al.. (2008). Inflammatory response gene polymorphisms and their relationship with colorectal cancer risk. BMC Cancer. 8(1). 112–112. 37 indexed citations
14.
Reeves, Stuart G., Cliff Meldrum, Kim Colyvas, et al.. (2008). IGF1 is a modifier of disease risk in hereditary non‐polyposis colorectal cancer. International Journal of Cancer. 123(6). 1339–1343. 20 indexed citations
15.
Irmejs, Arvīds, Marianna Bitiņa, Grzegorz Kurzawski, et al.. (2007). Nationwide study of clinical and molecular features of hereditary non-polyposis colorectal cancer (HNPCC) in Latvia.. PubMed. 27(1B). 653–8. 3 indexed citations
16.
Talseth‐Palmer, Bente A., Cliff Meldrum, Janina Suchy, et al.. (2007). Lack of association between genetic polymorphisms in cytokine genes and disease expression in patients with hereditary non-polyposis colorectal cancer. Scandinavian Journal of Gastroenterology. 42(5). 628–632. 17 indexed citations
17.
Irmejs, Arvīds, et al.. (2006). Pilot Study on Low Penetrance Breast and Colorectal Cancer Predisposition Markers in Latvia. Hereditary Cancer in Clinical Practice. 4(1). 48–51. 16 indexed citations
18.
Ashton, Katie A., Cliff Meldrum, Mary McPhillips, et al.. (2006). The Association of the COMT V158M Polymorphism with Endometrial/Ovarian Cancer in HNPCC Families Adhering to the Amsterdam Criteria. Hereditary Cancer in Clinical Practice. 4(2). 94–94. 8 indexed citations
19.
Huzarski, Tomasz, Marcin Lener, W Domagała, et al.. (2005). The 3020insC allele of NOD2 predisposes to early-onset breast cancer. Breast Cancer Research and Treatment. 89(1). 91–93. 34 indexed citations
20.
Irmejs, Arvīds, Edvīns Miklaševičs, Marianna Bitiņa, et al.. (2005). Clinical, Molecular and Geographical Features of Hereditary Breast/Ovarian Cancer in Latvia. Hereditary Cancer in Clinical Practice. 3(2). 71–6. 9 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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