Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68(6):394–424.
Article
PubMed
Google Scholar
Islami F, Goding Sauer A, Miller KD, Siegel RL, Fedewa SA, Jacobs EJ, et al. Proportion and number of cancer cases and deaths attributable to potentially modifiable risk factors in the United States. CA Cancer J Clin. 2018;68(1):31–54.
Article
PubMed
Google Scholar
Parkin DM. 2. Tobacco-attributable cancer burden in the UK in 2010. Br J Cancer. 2011;105(Suppl 2):S6–S13.
Article
PubMed
PubMed Central
Google Scholar
Islami F, Chen W, Yu XQ, Lortet-Tieulent J, Zheng R, Flanders WD, et al. Cancer deaths and cases attributable to lifestyle factors and infections in China, 2013. Ann Oncol. 2017;28(10):2567–74.
CAS
PubMed
Google Scholar
Matakidou A, Eisen T, Houlston RS. Systematic review of the relationship between family history and lung cancer risk. Br J Cancer. 2005;93(7):825–33.
Article
CAS
PubMed
PubMed Central
Google Scholar
Gu J, Hua F, Zhong D, Chen J, Liu H, Zhou Q. Systematic review of the relationship between family history of lung cancer and lung cancer risk. Zhongguo Fei Ai Za Zhi. 2010;13(3):224–9.
PubMed
Google Scholar
Lissowska J, Foretova L, Dabek J, Zaridze D, Szeszenia-Dabrowska N, Rudnai P, et al. Family history and lung cancer risk: international multicentre case-control study in eastern and Central Europe and meta-analyses. Cancer Causes Control. 2010;21(7):1091–104.
Article
PubMed
Google Scholar
Cote ML, Liu M, Bonassi S, Neri M, Schwartz AG, Christiani DC, et al. Increased risk of lung cancer in individuals with a family history of the disease: a pooled analysis from the international lung Cancer consortium. Eur J Cancer. 2012;48(13):1957–68.
Article
PubMed
PubMed Central
Google Scholar
Lin H, Huang YS, Yan HH, Yang XN, Zhong WZ, Ye HW, et al. A family history of cancer and lung cancer risk in never-smokers: a clinic-based case-control study. Lung Cancer. 2015;89(2):94–8.
Article
PubMed
Google Scholar
Yu H, Frank C, Hemminki A, Sundquist K, Hemminki K. Other cancers in lung cancer families are overwhelmingly smoking-related cancers. ERJ Open Res. 2017;3(2):00006–2017.
Article
PubMed
PubMed Central
Google Scholar
Li Y, Xiao X, Han Y, Gorlova O, Qian D, Leighl N, et al. Genome-wide interaction study of smoking behavior and non-small cell lung cancer risk in Caucasian population. Carcinogenesis. 2018;39(3):336–46.
Article
CAS
PubMed
Google Scholar
Yu YW, Wang CP, Han YF, Niu JJ, Zhang YZ, Fang Y. Meta-analysis on related risk factors regarding lung cancer in non-smoking Chinese women. Zhonghua Liu Xing Bing Xue Za Zhi. 2016;37(2):268–72.
CAS
PubMed
Google Scholar
Galvan A, Falvella FS, Frullanti E, Spinola M, Incarbone M, Nosotti M, et al. Genome-wide association study in discordant sibships identifies multiple inherited susceptibility alleles linked to lung cancer. Carcinogenesis. 2010;31(3):462–5.
Article
CAS
PubMed
Google Scholar
Li Y, Sheu C-C, Ye Y, de Andrade M, Wang L, Chang S-C, et al. Genetic variants and risk of lung cancer in never smokers: a genome-wide association study. Lancet Oncol. 2010;11(4):321–30.
Article
CAS
PubMed
PubMed Central
Google Scholar
Machiela MJ, Hsiung CA, Shu XO, Seow WJ, Wang Z, Matsuo K, et al. Genetic variants associated with longer telomere length are associated with increased lung cancer risk among never-smoking women in Asia: a report from the female lung cancer consortium in Asia. Int J Cancer. 2015;137(2):311–9.
Article
CAS
PubMed
Google Scholar
Rahman N. Realizing the promise of cancer predisposition genes. Nature. 2014;505(7483):302–8.
Article
CAS
PubMed
PubMed Central
Google Scholar
Park S, Supek F, Lehner B. Systematic discovery of germline cancer predisposition genes through the identification of somatic second hits. Nat Commun. 2018;9(1):2601.
Article
PubMed
PubMed Central
CAS
Google Scholar
Castellanos E, Feld E, Horn L. Driven by mutations: the predictive value of mutation subtype in EGFR-mutated non-small cell lung Cancer. J Thorac Oncol. 2017;12(4):612–23.
Article
PubMed
Google Scholar
Dearden S, Stevens J, Wu YL, Blowers D. Mutation incidence and coincidence in non small-cell lung cancer: meta-analyses by ethnicity and histology (mutMap). Ann Oncol. 2013;24(9):2371–6.
Article
CAS
PubMed
PubMed Central
Google Scholar
Gou LY, Niu FY, Wu YL, Zhong WZ. Differences in driver genes between smoking-related and non-smoking-related lung cancer in the Chinese population. Cancer. 2015;121(Suppl 17):3069–79.
Article
CAS
PubMed
Google Scholar
El-Telbany A, Ma PC. Cancer genes in lung cancer: racial disparities: are there any? Genes Cancer. 2012;3(7–8):467–80.
Article
PubMed
PubMed Central
CAS
Google Scholar
Shigematsu H, Lin L, Takahashi T, Nomura M, Suzuki M, Wistuba II, et al. Clinical and biological features associated with epidermal growth factor receptor gene mutations in lung cancers. J Natl Cancer Inst. 2005;97(5):339–46.
Article
CAS
PubMed
Google Scholar
Stroup DF, Berlin JA, Morton SC, Olkin I, Williamson GD, Rennie D, et al. Meta-analysis of observational studies in epidemiology: a proposal for reporting. Meta-analysis of observational studies in epidemiology (MOOSE) group. JAMA. 2000;283(15):2008–12.
Article
CAS
PubMed
Google Scholar
Higgins J.P.T, Green S (editors). Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0 [updated March 2011]. The Cochrane Collaboration, 2011. https://www.handbook.cochrane.org Accessed on date 25 Jul 2019.
Cheng PC, Cheng YC. Correlation between familial cancer history and epidermal growth factor receptor mutations in Taiwanese never smokers with non-small cell lung cancer: a case-control study. J Thorac Dis. 2015;7(3):281–7.
PubMed
PubMed Central
Google Scholar
Gaughan EM, Cryer SK, Yeap BY, Jackman DM, Costa DB. Family history of lung cancer in never smokers with non-small-cell lung cancer and its association with tumors harboring EGFR mutations. Lung Cancer. 2013;79(3):193–7.
Article
PubMed
Google Scholar
He YY, Li S, Ren SX, Cai WJ, Li XF, Zhao C, et al. Impact of family history of cancer on the incidence of mutation in epidermal growth factor receptor gene in non-small cell lung cancer patients. Lung Cancer. 2013;81(2):162–6.
Article
PubMed
Google Scholar
Hsu KH, Tseng JS, Wang CL, Yang TY, Tseng CH, Chen HY, et al. Higher frequency but random distribution of EGFR mutation subtypes in familial lung cancer patients. Oncotarget. 2016;7(33):53299–308.
Article
PubMed
PubMed Central
Google Scholar
Isla D, Felip E, Vinolas N, Provencio M, Majem M, Artal A, et al. Lung Cancer in women with a family history of Cancer: the Spanish female-specific database WORLD07. Anticancer Res. 2016;36(12):6647–53.
Article
PubMed
Google Scholar
Kawaguchi T, Ando M, Kubo A, Takada M, Atagi S, Okishio K, et al. Long exposure of environmental tobacco smoke associated with activating EGFR mutations in never-smokers with non-small cell lung Cancer. Clin Cancer Res. 2011;17(1):39–45.
Article
CAS
PubMed
Google Scholar
Kim JS, Cho MS, Nam JH, Kim HJ, Choi KW, Ryu JS. Prognostic impact of EGFR mutation in non-small-cell lung cancer patients with family history of lung cancer. PLoS One. 2017;12(5):e0177015.
Article
PubMed
PubMed Central
CAS
Google Scholar
Kim SY, Kim HR, Kim CH, Koh JS, Baek HJ, Choi CM, et al. Association between thyroid cancer and epidermal growth factor receptor mutation in female with nonsmall cell lung cancer. Ann Thorac Med. 2017;12(1):36–41.
Article
CAS
PubMed
PubMed Central
Google Scholar
Okudela K, Woo T, Yazawa T, Ogawa N, Tajiri M, Masuda M, et al. Significant association between EGFR-mutated lung adenocarcinoma and past illness from gastric cancer or uterine myoma: its implication in carcinogenesis. Lung Cancer. 2009;66(3):287–91.
Article
PubMed
Google Scholar
Wang CD, Wang XR, Wang CY, Tang YJ, Hao MW. Relevance of EGFR gene mutation with pathological features and prognosis in patients with non-small-cell lung carcinoma. Asian Pac J Trop Med. 2015;8(3):249–52.
Article
CAS
PubMed
Google Scholar
Zhu J, Cai L, Yang H, Wen Y, Wang J, Rong T, et al. Echinoderm microtubule-associated protein-like 4-anaplastic lymphoma kinase rearrangement and epidermal growth factor receptor mutation coexisting in Chinese patients with lung adenocarcinoma. Thorac Cancer. 2014;5(5):411–6.
Article
CAS
PubMed
PubMed Central
Google Scholar
Bell DW, Gore I, Okimoto RA, Godin-Heymann N, Sordella R, Mulloy R, et al. Inherited susceptibility to lung cancer may be associated with the T790M drug resistance mutation in EGFR. Nat Genet. 2005;37(12):1315–6.
Article
CAS
PubMed
Google Scholar
Prudkin L, Tang X, Wistuba II. Germ-line and somatic presentations of the EGFR T790M mutation in lung cancer. J Thorac Oncol. 2009;4(1):139–41.
Article
PubMed
PubMed Central
Google Scholar
Tibaldi C, Giovannetti E, Vasile E, Boldrini L, Gallegos-Ruiz MI, Bernardini I, et al. Inherited germline T790M mutation and somatic epidermal growth factor receptor mutations in non-small cell lung cancer patients. J Thorac Oncol. 2011;6(2):395–6.
Article
PubMed
Google Scholar
Thomas A, Xi L, Carter CA, Rajan A, Khozin S, Szabo E, et al. Concurrent molecular alterations in tumors with germ line epidermal growth factor receptor T790M mutations. Clin Lung Cancer. 2013;14(4):452–6.
Article
CAS
PubMed
PubMed Central
Google Scholar
Gazdar A, Robinson L, Oliver D, Xing C, Travis WD, Soh J, et al. Hereditary lung cancer syndrome targets never smokers with germline EGFR gene T790M mutations. J Thorac Oncol. 2014;9(4):456–63.
Article
CAS
PubMed
PubMed Central
Google Scholar
Yu HA, Arcila ME, Harlan Fleischut M, Stadler Z, Ladanyi M, Berger MF, et al. Germline EGFR T790M mutation found in multiple members of a familial cohort. J Thorac Oncol. 2014;9(4):554–8.
Article
PubMed
PubMed Central
CAS
Google Scholar
Lou Y, Pecot CV, Tran HT, DeVito VJ, Tang XM, Heymach JV, et al. Germline mutation of T790M and dual/multiple EGFR mutations in patients with lung adenocarcinoma. Clin Lung Cancer. 2016;17(2):e5–11.
Article
CAS
PubMed
Google Scholar
van Noesel J, van der Ven WH, van Os TA, Kunst PW, Weegenaar J, Reinten RJ, et al. Activating germline R776H mutation in the epidermal growth factor receptor associated with lung cancer with squamous differentiation. J Clin Oncol. 2013;31(10):e161–4.
Article
PubMed
CAS
Google Scholar
Hellmann MD, Hayashi T, Reva B, Yu HA, Riely GJ, Adusumilli PS, et al. Identification and functional characterization of EGFR V769M, a novel Germline variant associated with multiple lung adenocarcinomas. JCO Precision Oncology. 2017;1:1–10.
Article
Google Scholar
Ikeda K, Nomori H, Mori T, Sasaki J, Kobayashi T. Novel germline mutation: EGFR V843I in patient with multiple lung adenocarcinomas and family members with lung cancer. Ann Thorac Surg. 2008;85(4):1430–2.
Article
PubMed
Google Scholar
Ohtsuka K, Ohnishi H, Kurai D, Matsushima S, Morishita Y, Shinonaga M, et al. Familial lung adenocarcinoma caused by the EGFR V843I germ-line mutation. J Clin Oncol. 2011;29(8):e191–2.
Article
PubMed
Google Scholar
van der Leest C, Wagner A, Pedrosa RM, Aerts JG, Dinjens WNM, Dubbink HJ. Novel EGFR V834L Germline mutation associated with familial lung adenocarcinoma. JCO Precision Oncology. 2018;2:1–5.
Article
Google Scholar
Yamamoto H, Higasa K, Sakaguchi M, Shien K, Soh J, Ichimura K, et al. Novel germline mutation in the transmembrane domain of HER2 in familial lung adenocarcinomas. J Natl Cancer Inst. 2014;106(1):djt338.
Article
PubMed
CAS
Google Scholar
Tode N, Kikuchi T, Sakakibara T, Hirano T, Inoue A, Ohkouchi S, et al. Exome sequencing deciphers a germline MET mutation in familial epidermal growth factor receptor-mutant lung cancer. Cancer Sci. 2017;108(6):1263–70.
Article
CAS
PubMed
PubMed Central
Google Scholar
Kukita Y, Okami J, Yoneda-Kato N, Nakamae I, Kawabata T, Higashiyama M, et al. Homozygous inactivation of CHEK2 is linked to a familial case of multiple primary lung cancer with accompanying cancers in other organs. Cold Spring Harb Mol Case Stud. 2016;2(6):a001032.
Article
PubMed
PubMed Central
CAS
Google Scholar
Marks JL, Golas B, Kirchoff T, Miller VA, Riely GJ, Offit K, et al. EGFR mutant lung adenocarcinomas in patients with germline BRCA mutations. J Thorac Oncol. 2008;3(7):805.
Article
PubMed
Google Scholar
Bemis LT, Robinson WA, McFarlane R, Buyers E, Kelly K, Varella-Garcia M, et al. EGFR-mutant lung adenocarcinoma in a patient with Li-Fraumeni syndrome. Lancet Oncol. 2007;8(6):559–60.
Article
PubMed
Google Scholar
Jia Y, Ali SM, Saad S, Chan CA, Miller VA, Halmos B. Successful treatment of a patient with Li-Fraumeni syndrome and metastatic lung adenocarcinoma harboring synchronous EGFR L858R and ERBB2 extracellular domain S310F mutations with the pan-HER inhibitor afatinib. Cancer Biol Ther. 2014;15(8):970–4.
Article
CAS
PubMed
PubMed Central
Google Scholar
Michalarea V, Calcasola M, Cane P, Tobal K, Izatt L, Spicer J. EGFR-mutated lung cancer in Li-Fraumeni syndrome. Lung Cancer. 2014;85(3):458–87.
Article
Google Scholar
Ricordel C, Labalette-Tiercin M, Lespagnol A, Kerjouan M, Dugast C, Mosser J, et al. EFGR-mutant lung adenocarcinoma and Li-Fraumeni syndrome: report of two cases and review of the literature. Lung Cancer. 2015;87(1):80–4.
Article
PubMed
Google Scholar
Pathak S, Singh SRK, Katiyar V, McDunn S. Epidermal growth factor receptor-mutated lung Cancer as the initial manifestation of Germline TP53 mutation associated Cancer. Cureus. 2018;10(3):e2395.
PubMed
PubMed Central
Google Scholar
Cardona AF, Zatarain-Barron ZL, Rubio C, Martinez S, Ruiz-Patino A, Ricaurte L, et al. Probable hereditary familial overlap syndrome with multiple synchronous lung tumors. Lung Cancer. 2018;124:279–82.
Article
PubMed
Google Scholar
Serra V, Vivancos A, Puente XS, Felip E, Silberschmidt D, Caratu G, et al. Clinical response to a lapatinib-based therapy for a Li-Fraumeni syndrome patient with a novel HER2V659E mutation. Cancer Discov. 2013;3(11):1238–44.
Article
CAS
PubMed
Google Scholar
Wang Z, Sun Y, Gao B, Lu Y, Fang R, Gao Y, et al. Two co-existing germline mutations P53 V157D and PMS2 R20Q promote tumorigenesis in a familial cancer syndrome. Cancer Lett. 2014;342(1):36–42.
Article
CAS
PubMed
Google Scholar
Shinmura K, Suzuki M, Yamada H, Tao H, Goto M, Kamo T, et al. Characterization of adenocarcinoma of the lung in a familial adenomatous polyposis patient. Pathol Int. 2008;58(11):706–12.
Article
CAS
PubMed
Google Scholar
Lovly C, Horn L, Oxnard G, Pao W. EGFR c.2369C>T (T790M) Mutation in Non-Small Cell Lung Cancer. My Cancer Genome 2016 [https://www.mycancergenome.org/content/disease/lung-cancer/egfr/4/] (Updated November 11).
Seow WJ, Matsuo K, Hsiung CA, Shiraishi K, Song M, Kim HN, et al. Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations. Hum Mol Genet. 2017;26(2):454–65.
CAS
PubMed
Google Scholar
Wei R, Cao L, Pu H, Wang H, Zheng Y, Niu X, et al. TERT polymorphism rs2736100-C is associated with EGFR mutation-positive non-small cell lung Cancer. Clin Cancer Res. 2015;21(22):5173–80.
Article
CAS
PubMed
PubMed Central
Google Scholar
Shiraishi K, Okada Y, Takahashi A, Kamatani Y, Momozawa Y, Ashikawa K, et al. Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma. Nat Commun. 2016;7:12451.
Article
CAS
PubMed
PubMed Central
Google Scholar
Parry EM, Gable DL, Stanley SE, Khalil SE, Antonescu V, Florea L, et al. Germline mutations in DNA repair genes in lung adenocarcinoma. J Thorac Oncol. 2017;12(11):1673–8.
Article
PubMed
PubMed Central
Google Scholar
Lu S, Yu Y, Li Z, Yu R, Wu X, Bao H, et al. Brief report: EGFR and ERBB2 Germline mutations in Chinese lung Cancer patients and their roles in genetic susceptibility to Cancer. J Thorac Oncol. 2019;14(4):732–6.
Article
PubMed
Google Scholar
Centeno I, Blay P, Santamaria I, Astudillo A, Pitiot AS, Osorio FG, et al. Germ-line mutations in epidermal growth factor receptor (EGFR) are rare but may contribute to oncogenesis: a novel germ-line mutation in EGFR detected in a patient with lung adenocarcinoma. BMC Cancer. 2011;11:172.
Article
CAS
PubMed
PubMed Central
Google Scholar
Vikis H, Sato M, James M, Wang D, Wang Y, Wang M, et al. EGFR-T790M is a rare lung cancer susceptibility allele with enhanced kinase activity. Cancer Res. 2007;67(10):4665–70.
Article
CAS
PubMed
PubMed Central
Google Scholar
Oxnard GR, Arcila ME, Chmielecki J, Ladanyi M, Miller VA, Pao W. New strategies in overcoming acquired resistance to epidermal growth factor receptor tyrosine kinase inhibitors in lung cancer. Clin Cancer Res. 2011;17(17):5530–7.
Article
CAS
PubMed
PubMed Central
Google Scholar
Yokoyama T, Kondo M, Goto Y, Fukui T, Yoshioka H, Yokoi K, et al. EGFR point mutation in non-small cell lung cancer is occasionally accompanied by a second mutation or amplification. Cancer Sci. 2006;97(8):753–9.
Article
CAS
PubMed
Google Scholar
Hidaka N, Iwama E, Kubo N, Harada T, Miyawaki K, Tanaka K, et al. Most T790M mutations are present on the same EGFR allele as activating mutations in patients with non-small cell lung cancer. Lung Cancer. 2017;108:75–82.
Article
PubMed
Google Scholar
Godin-Heymann N, Bryant I, Rivera MN, Ulkus L, Bell DW, Riese DJ 2nd, et al. Oncogenic activity of epidermal growth factor receptor kinase mutant alleles is enhanced by the T790M drug resistance mutation. Cancer Res. 2007;67(15):7319–26.
Article
CAS
PubMed
PubMed Central
Google Scholar
Regales L, Balak MN, Gong Y, Politi K, Sawai A, Le C, et al. Development of new mouse lung tumor models expressing EGFR T790M mutants associated with clinical resistance to kinase inhibitors. PLoS One. 2007;2(8):e810.
Article
PubMed
PubMed Central
CAS
Google Scholar
Oxnard GR, Miller VA, Robson ME, Azzoli CG, Pao W, Ladanyi M, et al. Screening for germline EGFR T790M mutations through lung cancer genotyping. J Thorac Oncol. 2012;7(6):1049–52.
Article
CAS
PubMed
PubMed Central
Google Scholar
Catalogue Of Somatic Mutations In Cancer [https://cancer.sanger.ac.uk/cosmic] Accessed on date 25 Jul 2019.
Swift M, Morrell D, Massey RB, Chase CL. Incidence of cancer in 161 families affected by ataxia-telangiectasia. N Engl J Med. 1991;325(26):1831–6.
Article
CAS
PubMed
Google Scholar
Hwang SJ, Cheng LS, Lozano G, Amos CI, Gu X, Strong LC. Lung cancer risk in germline p53 mutation carriers: association between an inherited cancer predisposition, cigarette smoking, and cancer risk. Hum Genet. 2003;113(3):238–43.
Article
CAS
PubMed
Google Scholar
Digennaro M, Sambiasi D, Tommasi S, Pilato B, Diotaiuti S, Kardhashi A, et al. Hereditary and non-hereditary branches of family eligible for BRCA test: cancers in other sites. Hered Cancer Clin Pract. 2017;15:7.
Article
CAS
PubMed
PubMed Central
Google Scholar
Jamal-Hanjani M, Wilson GA, McGranahan N, Birkbak NJ, Watkins TBK, Veeriah S, et al. Tracking the evolution of non-small-cell lung Cancer. N Engl J Med. 2017;376(22):2109–21.
Article
CAS
PubMed
Google Scholar
Soo RA, Kubo A, Ando M, Kawaguchi T, Ahn MJ, Ou SI. Association between environmental tobacco smoke exposure and the occurrence of EGFR mutations and ALK rearrangements in never-smokers with non-small-cell lung Cancer: analyses from a prospective multinational ETS registry. Clin Lung Cancer. 2017;18(5):535–42.
Article
CAS
PubMed
Google Scholar
Lee MN, Tseng RC, Hsu HS, Chen JY, Tzao C, Ho WL, et al. Epigenetic inactivation of the chromosomal stability control genes BRCA1, BRCA2, and XRCC5 in non-small cell lung cancer. Clin Cancer Res. 2007;13(3):832–8.
Article
CAS
PubMed
Google Scholar
Lin EP, Lin CH, Yang CY, Lu TP, Chang SN, Hsiao TH, et al. Population-based cohort study reveals distinct associations between female lung Cancer and breast Cancer in Taiwan. JCO Clin Cancer Inform. 2018;2:1–14.
CAS
PubMed
Google Scholar
Lovly C, Horn L, Gautschi O, Pao W. HER2 (ERBB2) Exon 20 Insertion in Non-Small Cell Lung Cancer. My Cancer Genome 2015 [https://www.mycancergenome.org/content/disease/lung-cancer/erbb2/65/] (Updated June 18).
Yamamoto H, Toyooka S, Ninomiya T, Matsumoto S, Kanai M, Tomida S, et al. Therapeutic potential of Afatinib for cancers with ERBB2 (HER2) Transmembrane domain mutations G660D and V659E. Oncologist. 2018;23(2):150–4.
Article
CAS
PubMed
Google Scholar
Roengvoraphoj M, Tsongalis GJ, Dragnev KH, Rigas JR. Epidermal growth factor receptor tyrosine kinase inhibitors as initial therapy for non-small cell lung cancer: focus on epidermal growth factor receptor mutation testing and mutation-positive patients. Cancer Treat Rev. 2013;39(8):839–50.
Article
CAS
PubMed
Google Scholar
Fiederling J, Shams AZ, Haug U. Validity of self-reported family history of cancer: a systematic literature review on selected cancers. Int J Cancer. 2016;139(7):1449–60.
Article
CAS
PubMed
Google Scholar