1. IARC, Globocan 2018 [Electronic resource] / World Health Organization. - Paris, 2018. - Mode of access : https://www.uicc.org/news/new-global-cancer-data-globocan-2018. - Date of access : 30.09.2019.
2. Gastric cancer and Helicobacter pylori: a combined analysis of 12 case control studies nested within prospective cohorts // Gut. - 2001. - Vol. 49, N 3. - P. 347-353. https://doi.org/10.1136/gut.49.3.347
3. Cover, T. L. Diet, microbial virulence, and Helicobacter pylori-induced gastric cancer / T. L. Cover, R. M. Peek // Gut Microbes. - 2013. - Vol. 4, N 6. - P. 482-493. https://doi.org/10.4161/gmic.26262
4. Choi, Y. J. Gastric cancer in family history / Y. J. Choi, N. Kim // Korean J. Intern. Med. - 2016. - Vol. 31, N 6. - P. 1042-1053. https://doi.org/10.3904/kjim.2016.147
5. Nagini, S. Carcinoma of the stomach: a review of epidemiology, pathogenesis, molecular genetics and chemoprevention / S. Nagini // World J. Gastroint. Oncol. - 2012. - Vol. 4, N 7. - P. 156-169. https://doi.org/10.4251/wjgo.v4.i7.156
6. Lansdorp-Vogelaar, I. Screening for gastric cancer in Western countries / I. Lansdorp-Vogelaar, E. J. Kuipers // Gut. - 2015. - Vol. 65, N 4. - P. 543-544. https://doi.org/10.1136/gutjnl-2015-310356
7. Management of precancerous conditions and lesions in the stomach (MAPS): guideline from the European Society of Gastrointestinal Endoscopy (ESGE), European Helicobacter Study Group (EHSG), European Society of Pathology (ESP), and the Sociedade Portuguesa de Endoscopia Digestiva (SPED) Endoscopy / M. Dinis-Ribeiro [et al.]. - 2012. - Vol. 44, N 01. - P. 74-94. https://doi.org/10.1055/s-0031-1291491
8. First-degree relatives of patients with early-onset gastric carcinoma show even at young ages a high prevalence of advanced OLGA/OLGIM stages and dysplasia / R. Marcos-Pinto [et al.] // Aliment. Pharmac. Ther. - 2012. - Vol. 35, N 12. - P. 1451-1459. https://doi.org/10.1111/j.1365-2036.2012.05111.x
9. Intrafamilial aggregation of gastric cancer: a comprehensive approach including environmental factors, Helicobacter pylori virulence, and genetic susceptibility / C. M. Shin [et al.] // Eur. J. Gastr. Hepat. - 2011. - Vol. 23, N 5. - P. 411-417. https://doi.org/10.1097/meg.0b013e328343b7f5
10. Precancerous lesions and Helicobacter pylori in relatives of gastric cancer patients / C. R. A. Motta [et al.] // Digestion. - 2008. - Vol. 78, N 1. - P. 3-8. https://doi.org/10.1159/000151297
11. Helicobacter pylori infection and gastric histology in first-degree relatives of gastric cancer patients: a metaanalysis / T. Rokkas [еt al.] // Eur. J. Gastr. Hepat. - 2010. - Vol. 22, N 9. - P. 1128-1133. https://doi.org/10.1097/meg.0b013e3283398d37
12. Prevalence and risk factors of atrophic gastritis and intestinal metaplasia: a nationwide multicenter prospective study in Korea / Y.-E. Joo [et al.] // Gut Liver. - 2013. - Vol. 7, N 3. - P. 303-310. https://doi.org/10.5009/gnl.2013.7.3.303
13. Gastric precancerous lesions in first degree relatives of patients with known gastric cancer: a cross-sectional prospective study in Guilan Province, north of Iran / F. Mansour-Ghanaei [et al.] // Asian. Pac. J. Canc. Prev. - 2012. - Vol. 13, N 5. - P. 1779-1782. https://doi.org/10.7314/apjcp.2012.13.5.1779
14. Classification of gastritis in first-degree relatives of patients with gastric cancer in a high cancer-risk area in Italy / C. Saieva [et al.] // Anticancer Res. - 2012. - Vol. 32, N 5. - P. 1711-1716.
15. Helicobacter pylori infection in 1st degree relatives of Chinese gastric cancer patients / W. K. Leung [et al.] // Scand. J. Gastr. - 2006. - Vol. 41, N 3. - P. 274-279. https://doi.org/10.1080/00365520510024269
16. Role of Helicobacter pylori infection among offspring or siblings of gastric cancer patients / Y. W. Chang [et al.] // Int. J. Canc. - 2002. - Vol. 101, N 5. - P. 469-474. https://doi.org/10.1002/ijc.10637
17. Gómez, Z. М. First-degree relatives of patients with gastric cancer have high frequencies of achlorhydria and premalignant gastric lesions / Z. М. Gómez, D. N. Garzón, R. W. Otero // Rev. Col. Gastr. - 2014. - Vol. 29, N 1. - P. 3-10.
18. Risk factors of atrophic gastritis and intestinal metaplasia in first-degree relatives of gastric cancer patients compared with age-sex matched controls / S. Oh [et al.] // J. Canc. Prev. - 2013. - Vol. 18, N 2. - P. 149-160. https://doi.org/10.15430/jcp.2013.18.2.149
19. Prevalence of H. pylori infection and precancerous gastric lesion in family relative of gastric cancer in South West of Iran / A. R. Masjedizadeh [et al.] // J. Gastr. Hepat. Res. - 2013. - Vol. 2, N 11. - P. 878-882.
20. Classification and grading of gastritis. The updated Sydney system / M. F. Dixon [et al.] // Am. J. Surg. Pathol. - 1996. - Vol. 20, N 10. - P. 1161-1181. https://doi.org/10.1097/00000478-199610000-00001
21. OLGA staging for gastritis: a tutorial / M. Rugge [et al.] // Dig. Liver Dis. - 2008. - Vol. 40, N 8. - P. 650-658. https:// https://doi.org/doi.org/10.1016/j.dld.2008.02.030
22. Особенности верхних отделов пищеварительного тракта при эндоскопии и гастробиопсии у мужчин с синдpомом диспепсии в период призыва на срочную военную службу / А. Н. Януль [и др.] // Мед. журн. - 2015. - № 2. - C. 113-117.
23. Роль полиморфизма гена IL-1RN и IL-1 Β в желудочном канцерогенезе у белорусов / А. В. Воропаева [и др.] // Современные проблемы радиационной медицины: от теории к практике : материалы Междунар. науч.-практ. конф. (г. Гомель, 21-22 апр. 2016 г.) / под общ. ред. А. В. Рожко. - Гомель, 2016. - C. 92-94.
24. Януль, А. Н. Особенности патологии верхнего отдела желудочно-кишечного тракта при диспепсии у военнослужащих срочной военной службы : автореф. дис. … кандидат медицинских наук : 14.01.28 / А. Н. Януль ; Белорус. мед. акад. последиплом. образования. - Минск, 2018. - 24 с.
25. Association between alcohol consumption and the risk of gastric cancer: a meta-analysis of prospective cohort studies / Z. He [et al.] // Oncotarget. - 2017. - Vol. 8, N 48. - P. 84459-84472. https://doi.org/10.18632/oncotarget.20880
26. Analysis of risk factors associated with precancerous lesion of gastric cancer in patients from eastern China: a comparative study / M. Wei [et al.] // J. Can. Res. Ther. - 2013. - Vol. 9, N 2. - P. 205-209. https://doi.org/10.4103/09731482.113351
27. Tobacco smoking and intestinal metaplasia: Systematic review and meta-analysis / S. Morais [et al.] // Dig. Liver Dis. - 2014. - Vol. 46, N 11. - P. 1031-1037. https://doi.org/10.1016/j.dld.2014.08.034
28. Population-based prospective study of the combined influence of cigarette smoking and Helicobacter pylori infection on gastric cancer incidence: the Hisayama study / K. Shikata [et al.] // Am. J. Epidem. - 2008. - Vol. 168, N 12. - P. 1409-1415. https://doi.org/10.1093/aje/kwn276
29. Salt intake and risk of gastric intestinal metaplasia: systematic review and meta-analysis / M. Dias-Neto [et al.] // Nutrit. Canc. - 2010. - Vol. 62, N 2. - P. 133-147. https://doi.org/10.1080/01635580903305391
30. Operative link on gastritis assessment stage is an appropriate predictor of early gastric cancer / Y. Zhou [et al.] // World J. Gastr. - 2016. - Vol. 22, N 13. - P. 3670-3678. https://doi.org/10.3748/wjg.v22.i13.3670
31. Gastritis staging: interobserver agreement by applying OLGA and OLGIM systems / S. Isajevs [et al.] // Virchows Archiv. - 2014. - Vol. 464, N 4. - P. 403-407. https://doi.org/10.1007/s00428-014-1544-3
32. Gastrites chroniques à Hélicobacter pylori: évaluation des systèmes OLGA et OLGIM / S. B. Slama [et al.] // Pan. Afr. Med. J. - 2016. - Vol. 23. - P. 23-28. https://doi.org/10.11604/pamj.2016.23.28.8839