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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2010 3
2013 4
2014 2
2015 2
2016 1
2018 5
2019 4
2020 3
2021 3
2022 4
2023 4
2024 2

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32 results

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Page 1
Hereditary cancer syndromes.
Imyanitov EN, Kuligina ES, Sokolenko AP, Suspitsin EN, Yanus GA, Iyevleva AG, Ivantsov AO, Aleksakhina SN. Imyanitov EN, et al. Among authors: yanus ga. World J Clin Oncol. 2023 Feb 24;14(2):40-68. doi: 10.5306/wjco.v14.i2.40. World J Clin Oncol. 2023. PMID: 36908677 Free PMC article. Review.
Hereditary Renal Cancer Syndromes.
Yanus GA, Kuligina ES, Imyanitov EN. Yanus GA, et al. Med Sci (Basel). 2024 Feb 18;12(1):12. doi: 10.3390/medsci12010012. Med Sci (Basel). 2024. PMID: 38390862 Free PMC article. Review.
KRAS, NRAS, BRAF, HER2 and MSI Status in a Large Consecutive Series of Colorectal Carcinomas.
Martianov AS, Mitiushkina NV, Ershova AN, Martynenko DE, Bubnov MG, Amankwah P, Yanus GA, Aleksakhina SN, Tiurin VI, Venina AR, Anuskina AA, Gorgul YA, Shestakova AD, Maidin MA, Belyaev AM, Baboshkina LS, Iyevleva AG, Imyanitov EN. Martianov AS, et al. Among authors: yanus ga. Int J Mol Sci. 2023 Mar 2;24(5):4868. doi: 10.3390/ijms24054868. Int J Mol Sci. 2023. PMID: 36902296 Free PMC article.
The spectrum of Lynch syndrome-associated germ-line mutations in Russia.
Yanus GA, Akhapkina TA, Iyevleva AG, Kornilov AV, Suspitsin EN, Kuligina ES, Ivantsov AO, Aleksakhina SN, Sokolova TN, Sokolenko AP, Togo AV, Imyanitov EN. Yanus GA, et al. Eur J Med Genet. 2020 Mar;63(3):103753. doi: 10.1016/j.ejmg.2019.103753. Epub 2019 Sep 3. Eur J Med Genet. 2020. PMID: 31491536
Exome-based search for recurrent disease-causing alleles in Russian population.
Yanus GA, Akhapkina TA, Whitehead AJ, Bizin IV, Iyevleva AG, Kuligina ES, Aleksakhina SN, Anisimova MO, Holmatov MM, Romanko AA, Zaitseva OA, Yatsuk OS, Zagorodnev KA, Matsneva MA, Koloskov AV, Togo AV, Suspitsin EN, Imyanitov EN. Yanus GA, et al. Eur J Med Genet. 2019 Jul;62(7):103656. doi: 10.1016/j.ejmg.2019.04.013. Epub 2019 Apr 24. Eur J Med Genet. 2019. PMID: 31028847
32 results