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Section of Genetics

Genetic Cancer Susceptibility Group

Previous Publications

All Publications 2020-2015

1. Bosse, Y., Li, Z., Xia, J., Manem, V., Carreras-Torres, R., Gabriel, A., . . . McKay, J. D. (2020). Transcriptome-wide association study reveals candidate causal genes for lung cancer. Int J Cancer. 146(7): 1862-1878. PMID: 31696517 doi: 10.1002/ijc.32771

2. Gupta, P., Shahzad, N., Harold, A., Shuda, M., Venuti, A., Romero-Medina, M. C., . . . Tommasino, M. (2020). Merkel Cell Polyomavirus Downregulates N-myc Downstream-Regulated Gene 1, Leading to Cellular Proliferation and Migration. J Virol. 94(3). PMID: 31694959 doi: 10.1128/jvi.00899-19

3. Hosen, M. I., Sheikh, M., Zvereva, M., Scelo, G., Forey, N., Durand, G., . . . Calvez-Kelm, F. L. (2020). Urinary TERT promoter mutations are detectable up to 10 years prior to clinical diagnosis of bladder cancer: Evidence from the Golestan Cohort Study. EBioMedicine. 53: 102643. PMID: 32081602 doi: 10.1016/j.ebiom.2020.102643

4. Kleinstern, G., Yan, H., Hildebrandt, M. A. T., Vijai, J., Berndt, S. I., Ghesquieres, H., . . . Cerhan, J. R. (2020). Inherited variants at 3q13.33 and 3p24.1 are associated with risk of diffuse large B-cell lymphoma and implicate immune pathways. Hum Mol Genet. 29(1): 70-79. PMID: 31600786 doi: 10.1093/hmg/ddz228

5. Nicholson, A. G., Sauter, J. L., Nowak, A. K., Kindler, H. L., Gill, R. R., Remy-Jardin, M., . . . Galateau-Salle, F. (2020). EURACAN/IASLC Proposals for Updating the Histologic Classification of Pleural Mesothelioma: Towards a More Multidisciplinary Approach. J Thorac Oncol. 15(1): 29-49. PMID: 31546041 doi: 10.1016/j.jtho.2019.08.2506

6. Saraiya, V., Bradshaw, P., Meyer, K., Gammon, M., Slade, G., Brennan, P., . . . Olshan, A. (2020). The association between diet quality and cancer incidence of the head and neck. Cancer Causes Control. 31(2): 193-202. PMID: 31894494 doi: 10.1007/s10552-019-01261-4

7. Alcala, N., Leblay, N., Gabriel, A. A. G., Mangiante, L., Hervas, D., Giffon, T., . . . Fernandez-Cuesta, L. (2019). Integrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids. Nat Commun. 10(1): 3407. PMID: 31431620 doi: 10.1038/s41467-019-11276-9

8. Alcala, N., Mangiante, L., Le-Stang, N., Gustafson, C. E., Boyault, S., Damiola, F., . . . Fernandez-Cuesta, L. (2019). Redefining malignant pleural mesothelioma types as a continuum uncovers immune-vascular interactions. EBioMedicine. 48: 191-202. PMID: 31648983 doi: 10.1016/j.ebiom.2019.09.003

9. Alcala, N., & Rosenberg, N. A. (2019). G(ST)’, Jost’s D, and F-ST are similarly constrained by allele frequencies: A mathematical, simulation, and empirical study. Mol Ecol. 28(7): 1624-1636. doi: 10.1111/mec.15000

10. Avogbe, P. H., Manel, A., Vian, E., Durand, G., Forey, N., Voegele, C., . . . Le Calvez-Kelm, F. (2019). Urinary TERT promoter mutations as non-invasive biomarkers for the comprehensive detection of urothelial cancer. EBioMedicine. 44: 431-438. PMID: 31122840 doi: 10.1016/j.ebiom.2019.05.004

11. Barrett, R. D. H., Laurent, S., Mallarino, R., Pfeifer, S. P., Xu, C. C. Y., Foll, M., . . . Hoekstra, H. E. (2019). Linking a mutation to survival in wild mice. Science. 363(6426): 499-504. PMID: 30705186 doi: 10.1126/science.aav3824

12. Dai, J., Li, Z., Amos, C. I., Hung, R. J., Tardon, A., Andrew, A. S., . . . Shen, H. (2019). Systematic analyses of regulatory variants in DNase I hypersensitive sites identified two novel lung cancer susceptibility loci. Carcinogenesis. 40(3): 432-440. PMID: 30590402 doi: 10.1093/carcin/bgy187

13. Din, L., Sheikh, M., Kosaraju, N., Smedby, K. E., Bernatsky, S., Berndt, S. I., . . . Khankhanian, P. (2019). Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. Genet Epidemiol. 43(7): 844-863. PMID: 31407831 doi: 10.1002/gepi.22242

14. Du, E., Mazul, A. L., Farquhar, D., Brennan, P., Anantharaman, D., Abedi-Ardekani, B., . . . Zevallos, J. P. (2019). Long-term Survival in Head and Neck Cancer: Impact of Site, Stage, Smoking, and Human Papillomavirus Status. Laryngoscope. 129(11): 2506-2513. PMID: 30637762 doi: 10.1002/lary.27807

15. Fernandez-Cuesta, L., & Foll, M. (2019). Molecular studies of lung neuroendocrine neoplasms uncover new concepts and entities. Translational Lung Cancer Research. 8: S430-S434. PMID: 32038931 doi: 10.21037/tlcr.2019.11.08

16. Jiang, X., Finucane, H. K., Schumacher, F. R., Schmit, S. L., Tyrer, J. P., Han, Y., . . . Lindstrom, S. (2019). Shared heritability and functional enrichment across six solid cancers. Nat Commun. 10(1): 431. PMID: 30683880 doi: 10.1038/s41467-018-08054-4

17. Johansson, M., Carreras-Torres, R., Scelo, G., Purdue, M. P., Mariosa, D., Muller, D. C., . . . Brennan, P. (2019). The influence of obesity-related factors in the etiology of renal cell carcinoma-A mendelian randomization study. PLoS Med. 16(1): e1002724. PMID: 30605491 doi: 10.1371/journal.pmed.1002724

18. Kachuri, L., Saarela, O., Bojesen, S. E., Davey Smith, G., Liu, G., Landi, M. T., . . . Hung, R. J. (2019). Mendelian Randomization and mediation analysis of leukocyte telomere length and risk of lung and head and neck cancers. Int J Epidemiol. 48(3): 751-766. PMID: 30059977 doi: 10.1093/ije/dyy140

19. Mendy, M., Caboux, E., & Wild, C. P. (2019). Centralization of the IARC Biobank: Combining Multiple Sample Collections into a Common Platform. Biopreserv Biobank. 17(5): 433-443. PMID: 31091138 doi: 10.1089/bio.2018.0036

20. Menya, D., Maina, S. K., Kibosia, C., Kigen, N., Oduor, M., Some, F., . . . McCormack, V. A. (2019). Dental fluorosis and oral health in the African Esophageal Cancer Corridor: Findings from the Kenya ESCCAPE case-control study and a pan-African perspective. Int J Cancer. 145(1): 99-109. PMID: 30582155 doi: 10.1002/ijc.32086

21. Olivier, M., Bouaoun, L., Villar, S., Robitaille, A., Cahais, V., Heguy, A., . . . Rinaldi, S. (2019). Molecular features of premenopausal breast cancers in Latin American women: Pilot results from the PRECAMA study. PLoS ONE. 14(1): e0210372. PMID: 30653559 doi: 10.1371/journal.pone.0210372

22. Pertesi, M., Vallee, M., Wei, X., Revuelta, M. V., Galia, P., Demangel, D., . . . Dumontet, C. (2019). Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma. Leukemia. 33(9): 2324-2330. PMID: 30967618 doi: 10.1038/s41375-019-0452-6

23. Sheikh, M., Poustchi, H., Pourshams, A., Etemadi, A., Islami, F., Khoshnia, M., . . . Malekzadeh, R. (2019). Individual and Combined Effects of Environmental Risk Factors for Esophageal Cancer Based on Results From the Golestan Cohort Study. Gastroenterology. 156(5): 1416-1427. PMID: 30611753 doi: 10.1053/j.gastro.2018.12.024

24. Stahl, E. A., Breen, G., Forstner, A. J., McQuillin, A., Ripke, S., Trubetskoy, V., . . . Sklar, P. (2019). Genome-wide association study identifies 30 loci associated with bipolar disorder. Nat Genet. 51(5): 793-803. PMID: 31043756 doi: 10.1038/s41588-019-0397-8

25. Vargas-Ayala, R. C., Jay, A., Manara, F., Maroui, M. A., Hernandez-Vargas, H., Diederichs, A., . . . Accardi, R. (2019). Interplay between the Epigenetic Enzyme Lysine (K)-Specific Demethylase 2B and Epstein-Barr Virus Infection. J Virol. 93(13). PMID: 30996097 doi: 10.1128/JVI.00273-19

26. Vrieling, A., Bueno-De-Mesquita, H. B., Ros, M. M., Kampman, E., Aben, K. K., Buchner, F. L., . . . Kiemeney, L. A. (2019). One-carbon metabolism biomarkers and risk of urothelial cell carcinoma in the European prospective investigation into cancer and nutrition. Int J Cancer. 145(9): 2349-2359. PMID: 30694528 doi: 10.1002/ijc.32165

27. Zhivagui, M., Ng, A. W. T., Ardin, M., Churchwell, M. I., Pandey, M., Renard, C., . . . Zavadil, J. (2019). Experimental and pan-cancer genome analyses reveal widespread contribution of acrylamide exposure to carcinogenesis in humans. Genome Res. 29(4): 521-531. PMID: 30846532 doi: 10.1101/gr.242453.118

28. Zhu, Y., Wei, Y., Zhang, R., Dong, X., Shen, S., Zhao, Y., . . . Christiani, D. C. (2019). Elevated Platelet Count Appears to Be Causally Associated with Increased Risk of Lung Cancer: A Mendelian Randomization Analysis. Cancer Epidemiol Biomarkers Prev. 28(5): 935-942. PMID: 30700444 doi: 10.1158/1055-9965.Epi-18-0356

29. Abelson, S., Collord, G., Ng, S. W. K., Weissbrod, O., Mendelson Cohen, N., Niemeyer, E., . . . Shlush, L. I. (2018). Prediction of acute myeloid leukaemia risk in healthy individuals. Nature. 559(7714): 400-404. PMID: 29988082 doi: 10.1038/s41586-018-0317-6

30. Anantharaman, D., Billot, A., Waterboer, T., Gheit, T., Abedi-Ardekani, B., Lagiou, P., . . . Brennan, P. (2018). Predictors of oropharyngeal cancer survival in Europe. Oral Oncol. 81: 89-94. PMID: 29884419 doi: 10.1016/j.oraloncology.2018.04.016

31. Byun, J., Schwartz, A. G., Lusk, C., Wenzlaff, A. S., de Andrade, M., Mandal, D., . . . Amos, C. I. (2018). Genome-wide association study of familial lung cancer. Carcinogenesis. 39(9): 1135-1140. PMID: 29924316 doi: 10.1093/carcin/bgy080

32. Churg, A., Nabeshima, K., Ali, G., Bruno, R., Fernandez-Cuesta, L., & Galateau-Salle, F. (2018). Highlights of the 14th international mesothelioma interest group meeting: Pathologic separation of benign from malignant mesothelial proliferations and histologic/molecular analysis of malignant mesothelioma subtypes. Lung Cancer. 124: 95-101. PMID: 30268487 doi: 10.1016/j.lungcan.2018.07.041

33. Derks, J. L., Leblay, N., Lantuejoul, S., Dingemans, A. C., Speel, E. M., & Fernandez-Cuesta, L. (2018). New Insights into the Molecular Characteristics of Pulmonary Carcinoids and Large Cell Neuroendocrine Carcinomas, and the Impact on Their Clinical Management. J Thorac Oncol. 13(6): 752-766. PMID: 29454048 doi: 10.1016/j.jtho.2018.02.002

34. Derks, J. L., Leblay, N., Thunnissen, E., van Suylen, R. J., den Bakker, M., Groen, H. J. M., . . . Dingemans, A. C. (2018). Molecular Subtypes of Pulmonary Large-cell Neuroendocrine Carcinoma Predict Chemotherapy Treatment Outcome. Clin Cancer Res. 24(1): 33-42. PMID: 29066508 doi: 10.1158/1078-0432.Ccr-17-1921

35. Ferreiro-Iglesias, A., Lesseur, C., McKay, J., Hung, R. J., Han, Y., Zong, X., . . . Brennan, P. (2018). Fine mapping of MHC region in lung cancer highlights independent susceptibility loci by ethnicity. Nat Commun. 9(1): 3927. PMID: 30254314 doi: 10.1038/s41467-018-05890-2

36. George, J., Walter, V., Peifer, M., Alexandrov, L. B., Seidel, D., Leenders, F., . . . Thomas, R. K. (2018). Integrative genomic profiling of large-cell neuroendocrine carcinomas reveals distinct subtypes of high-grade neuroendocrine lung tumors. Nat Commun. 9(1): 1048. PMID: 29535388 doi: 10.1038/s41467-018-03099-x

37. Ghesquieres, H., Larrabee, B. R., Casasnovas, O., Maurer, M. J., McKay, J. D., Ansell, S. M., . . . Salles, G. (2018). A susceptibility locus for classical Hodgkin lymphoma at 8q24 near MYC/PVT1 predicts patient outcome in two independent cohorts. Br J Haematol. 180(2): 286-290. PMID: 27716907 doi: 10.1111/bjh.14306

38. Hancock, D. B., Guo, Y., Reginsson, G. W., Gaddis, N. C., Lutz, S. M., Sherva, R., . . . Johnson, E. O. (2018). Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence. Mol Psychiatry. 23(9): 1911-1919. PMID: 28972577 doi: 10.1038/mp.2017.193

39. Ji, X., Bosse, Y., Landi, M. T., Gui, J., Xiao, X., Qian, D., . . . Amos, C. I. (2018). Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk. Nat Commun. 9(1): 3221. PMID: 30104567 doi: 10.1038/s41467-018-05074-y

40. Kleinstern, G., Camp, N. J., Goldin, L. R., Vachon, C. M., Vajdic, C. M., de Sanjose, S., . . . Slager, S. L. (2018). Association of polygenic risk score with the risk of chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis. Blood. 131(23): 2541-2551. PMID: 29674426 doi: 10.1182/blood-2017-11-814608

41. Li, Y., Xiao, X., Han, Y., Gorlova, O., Qian, D., Leighl, N., . . . Amos, C. I. (2018). Genome-wide interaction study of smoking behavior and non-small cell lung cancer risk in Caucasian population. Carcinogenesis. 39(3): 336-346. PMID: 29059373 doi: 10.1093/carcin/bgx113

42. Liu, Y., Lusk, C. M., Cho, M. H., Silverman, E. K., Qiao, D., Zhang, R., . . . Spitz, M. R. (2018). Rare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer. J Thorac Oncol. 13(10): 1483-1495. PMID: 29981437 doi: 10.1016/j.jtho.2018.06.016

43. Machiela, M. J., Hofmann, J. N., Carreras-Torres, R., Brown, K. M., Johansson, M., Wang, Z., . . . Purdue, M. P. (2018). Corrigendum re “Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma” [Eur Urol 2017;72:747-54]. Eur Urol. 74(3): e85-e86. PMID: 29853305 doi: 10.1016/j.eururo.2018.05.017

44. McMaster, M. L., Berndt, S. I., Zhang, J., Slager, S. L., Li, S. A., Vajdic, C. M., . . . Caporaso, N. E. (2018). Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenstrom macroglobulinemia. Nat Commun. 9(1): 4182. PMID: 30305637 doi: 10.1038/s41467-018-06541-2

45. Muhleisen, T. W., Reinbold, C. S., Forstner, A. J., Abramova, L. I., Alda, M., Babadjanova, G., . . . Cichon, S. (2018). Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder. J Affect Disord. 228: 20-25. PMID: 29197740 doi: 10.1016/j.jad.2017.11.068

46. Pastorino, R., Iuliano, L., Vecchioni, A., Arzani, D., Milic, M., Annunziata, F., . . . Boccia, S. (2018). Effect of alcohol dehydrogenase-1B and -7 polymorphisms on blood ethanol and acetaldehyde concentrations in healthy subjects with a history of moderate alcohol consumption. Drug Test Anal. 10(3): 488-495. PMID: 28731573 doi: 10.1002/dta.2251

47. Perdomo, S., Anantharaman, D., Foll, M., Abedi-Ardekani, B., Durand, G., Reis Rosa, L. A., . . . Brennan, P. (2018). Genomic analysis of head and neck cancer cases from two high incidence regions. PLoS ONE. 13(1): e0191701. PMID: 29377909 doi: 10.1371/journal.pone.0191701

48. Rindi, G., Klimstra, D. S., Abedi-Ardekani, B., Asa, S. L., Bosman, F. T., Brambilla, E., . . . Cree, I. A. (2018). A common classification framework for neuroendocrine neoplasms: an International Agency for Research on Cancer (IARC) and World Health Organization (WHO) expert consensus proposal. Mod Pathol. 31(12): 1770-1786. PMID: 30140036 doi: 10.1038/s41379-018-0110-y

49. Ronellenfitsch, M. W., Oh, J. E., Satomi, K., Sumi, K., Harter, P. N., Steinbach, J. P., . . . Ohgaki, H. (2018). CASP9 germline mutation in a family with multiple brain tumors. Brain Pathol. 28(1): 94-102. PMID: 27935156 doi: 10.1111/bpa.12471

50. Stanford-Moore, G., Bradshaw, P. T., Weissler, M. C., Zevallos, J. P., Brennan, P., Anantharaman, D., . . . Olshan, A. F. (2018). Interaction between known risk factors for head and neck cancer and socioeconomic status: the Carolina Head and Neck Cancer Study. Cancer Causes Control. 29(9): 863-873. PMID: 30069657 doi: 10.1007/s10552-018-1062-8

51. Viarisio, D., Muller-Decker, K., Accardi, R., Robitaille, A., Durst, M., Beer, K., . . . Tommasino, M. (2018). Beta HPV38 oncoproteins act with a hit-and-run mechanism in ultraviolet radiation-induced skin carcinogenesis in mice. PLoS Pathog. 14(1): e1006783. PMID: 29324843 doi: 10.1371/journal.ppat.1006783

52. Waller, R. G., Darlington, T. M., Wei, X., Madsen, M. J., Thomas, A., Curtin, K., . . . Camp, N. J. (2018). Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk. PLoS Genet. 14(2): e1007111. PMID: 29389935 doi: 10.1371/journal.pgen.1007111

53. Wang, S. S., Carrington, M., Berndt, S. I., Slager, S. L., Bracci, P. M., Voutsinas, J., . . . Skibola, C. F. (2018). HLA Class I and II Diversity Contributes to the Etiologic Heterogeneity of Non-Hodgkin Lymphoma Subtypes. Cancer Res. 78(14): 4086-4096. PMID: 29735552 doi: 10.1158/0008-5472.Can-17-2900

54. Wang, Z., Wei, Y., Zhang, R., Su, L., Gogarten, S. M., Liu, G., . . . Christiani, D. C. (2018). Multi-Omics Analysis Reveals a HIF Network and Hub Gene EPAS1 Associated with Lung Adenocarcinoma. EBioMedicine. 32: 93-101. PMID: 29859855 doi: 10.1016/j.ebiom.2018.05.024

55. Wei, X., Calvo-Vidal, M. N., Chen, S., Wu, G., Revuelta, M. V., Sun, J., . . . Lipkin, S. M. (2018). Germline Lysine-Specific Demethylase 1 (LSD1/KDM1A) Mutations Confer Susceptibility to Multiple Myeloma. Cancer Res. 78(10): 2747-2759. PMID: 29559475 doi: 10.1158/0008-5472.Can-17-1900

56. Zuo, H., Ueland, P. M., Midttun, O., Vollset, S. E., Tell, G. S., Theofylaktopoulou, D., . . . Ulvik, A. (2018). Results from the European Prospective Investigation into Cancer and Nutrition Link Vitamin B6 Catabolism and Lung Cancer Risk. Cancer Res. 78(1): 302-308. PMID: 29070616 doi: 10.1158/0008-5472.Can-17-1923

57. Ambatipudi, S., Horvath, S., Perrier, F., Cuenin, C., Hernandez-Vargas, H., Le Calvez-Kelm, F., . . . Herceg, Z. (2017). DNA methylome analysis identifies accelerated epigenetic ageing associated with postmenopausal breast cancer susceptibility. Eur J Cancer. 75: 299-307. PMID: 28259012 doi: 10.1016/j.ejca.2017.01.014

58. Amorim, C. E., Hofer, T., Ray, N., Foll, M., Ruiz-Linares, A., & Excoffier, L. (2017). Long-distance dispersal suppresses introgression of local alleles during range expansions. Heredity (Edinb). 118(2): 135-142. PMID: 27577693 doi: 10.1038/hdy.2016.68

59. Amos, C. I., Dennis, J., Wang, Z., Byun, J., Schumacher, F. R., Gayther, S. A., . . . Easton, D. F. (2017). The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers. Cancer Epidemiol Biomarkers Prev. 26(1): 126-135. PMID: 27697780 doi: 10.1158/1055-9965.epi-16-0106

60. Anantharaman, D., Abedi-Ardekani, B., Beachler, D. C., Gheit, T., Olshan, A. F., Wisniewski, K., . . . D’Souza, G. (2017). Geographic heterogeneity in the prevalence of human papillomavirus in head and neck cancer. Int J Cancer. 140(9): 1968-1975. PMID: 28108990 doi: 10.1002/ijc.30608

61. Bernatsky, S., Velasquez Garcia, H. A., Spinelli, J. J., Gaffney, P., Smedby, K. E., Ramsey-Goldman, R., . . . Clarke, A. E. (2017). Lupus-related single nucleotide polymorphisms and risk of diffuse large B-cell lymphoma. Lupus Sci Med. 4(1): e000187. PMID: 29214033 doi: 10.1136/lupus-2016-000187

62. Botteri, E., Ferrari, P., Roswall, N., Tjonneland, A., Hjartaker, A., Huerta, J. M., . . . Weiderpass, E. (2017). Alcohol consumption and risk of urothelial cell bladder cancer in the European prospective investigation into cancer and nutrition cohort. Int J Cancer. 141(10): 1963-1970. PMID: 28722206 doi: 10.1002/ijc.30894

63. Carreras-Torres, R., Johansson, M., Haycock, P. C., Wade, K. H., Relton, C. L., Martin, R. M., . . . Brennan, P. (2017). Obesity, metabolic factors and risk of different histological types of lung cancer: A Mendelian randomization study. PLoS ONE. 12(6): e0177875. PMID: 28594918 doi: 10.1371/journal.pone.0177875

64. Forstner, A. J., Hecker, J., Hofmann, A., Maaser, A., Reinbold, C. S., Muhleisen, T. W., . . . Nothen, M. M. (2017). Identification of shared risk loci and pathways for bipolar disorder and schizophrenia. PLoS ONE. 12(2): e0171595. PMID: 28166306 doi: 10.1371/journal.pone.0171595

65. Gheit, T., Dutta, S., Oliver, J., Robitaille, A., Hampras, S., Combes, J. D., . . . Tommasino, M. (2017). Isolation and characterization of a novel putative human polyomavirus. Virology. 506: 45-54. PMID: 28342387 doi: 10.1016/j.virol.2017.03.007

66. Gonzalez-Vela, M. D., Curiel-Olmo, S., Derdak, S., Beltran, S., Santibanez, M., Martinez, N., . . . Vaque, J. P. (2017). Shared Oncogenic Pathways Implicated in Both Virus-Positive and UV-Induced Merkel Cell Carcinomas. J Invest Dermatol. 137(1): 197-206. PMID: 27592799 doi: 10.1016/j.jid.2016.08.015

67. Gu, F., Zhang, H., Hyland, P. L., Berndt, S., Gapstur, S. M., Wheeler, W., . . . Caporaso, N. E. (2017). Inherited variation in circadian rhythm genes and risks of prostate cancer and three other cancer sites in combined cancer consortia. Int J Cancer. 141(9): 1794-1802. PMID: 28699174 doi: 10.1002/ijc.30883

68. Haycock, P. C., Burgess, S., Nounu, A., Zheng, J., Okoli, G. N., Bowden, J., . . . Davey Smith, G. (2017). Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study. JAMA Oncol. 3(5): 636-651. PMID: 28241208 doi: 10.1001/jamaoncol.2016.5945

69. Hernandez-Vargas, H., Gruffat, H., Cros, M. P., Diederichs, A., Sirand, C., Vargas-Ayala, R. C., . . . Accardi, R. (2017). Viral driven epigenetic events alter the expression of cancer-related genes in Epstein-Barr-virus naturally infected Burkitt lymphoma cell lines. Sci Rep. 7(1): 5852. PMID: 28724958 doi: 10.1038/s41598-017-05713-2

70. Holmila, R., Sklias, A., Muller, D. C., Degli Esposti, D., Guilloreau, P., McKay, J., . . . Nogueira da Costa, A. (2017). Targeted deep sequencing of plasma circulating cell-free DNA reveals Vimentin and Fibulin 1 as potential epigenetic biomarkers for hepatocellular carcinoma. PLoS ONE. 12(3): e0174265. PMID: 28333958 doi: 10.1371/journal.pone.0174265

71. Huang, M. N., Yu, W., Teoh, W. W., Ardin, M., Jusakul, A., Ng, A. W. T., . . . Rozen, S. G. (2017). Genome-scale mutational signatures of aflatoxin in cells, mice, and human tumors. Genome Res. 27(9): 1475-1486. PMID: 28739859 doi: 10.1101/gr.220038.116

72. Kettunen, E., Hernandez-Vargas, H., Cros, M. P., Durand, G., Le Calvez-Kelm, F., Stuopelyte, K., . . . Husgafvel-Pursiainen, K. (2017). Asbestos-associated genome-wide DNA methylation changes in lung cancer. Int J Cancer. 141(10): 2014-2029. PMID: 28722770 doi: 10.1002/ijc.30897

73. Law, P. J., Berndt, S. I., Speedy, H. E., Camp, N. J., Sava, G. P., Skibola, C. F., . . . Slager, S. (2017). Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia. Nat Commun. 8: 14175. PMID: 28165464 doi: 10.1038/ncomms14175

74. Leblay, N., Lepretre, F., Le Stang, N., Gautier-Stein, A., Villeneuve, L., Isaac, S., . . . Brevet, M. (2017). BAP1 Is Altered by Copy Number Loss, Mutation, and/or Loss of Protein Expression in More Than 70% of Malignant Peritoneal Mesotheliomas. J Thorac Oncol. 12(4): 724-733. PMID: 28034829 doi: 10.1016/j.jtho.2016.12.019

75. Lonjou, C., Damiola, F., Moissonnier, M., Durand, G., Malakhova, I., Masyakin, V., . . . Lesueur, F. (2017). Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation. BMC cancer. 17(1): 328. PMID: 28499365 doi: 10.1186/s12885-017-3314-5

76. Machiela, M. J., Hofmann, J. N., Carreras-Torres, R., Brown, K. M., Johansson, M., Wang, Z., . . . Purdue, M. P. (2017). Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma. Eur Urol. 72(5): 747-754. PMID: 28797570 doi: 10.1016/j.eururo.2017.07.015

77. Mazul, A. L., Taylor, J. M., Divaris, K., Weissler, M. C., Brennan, P., Anantharaman, D., . . . Zevallos, J. P. (2017). Oral health and human papillomavirus-associated head and neck squamous cell carcinoma. Cancer. 123(1): 71-80. PMID: 27571516 doi: 10.1002/cncr.30312

78. McKay, J., Tenet, V., Franceschi, S., Chabrier, A., Gheit, T., Gaborieau, V., . . . Vaccarella, S. (2017). Immuno-related polymorphisms and cervical cancer risk: The IARC multicentric case-control study. PLoS ONE. 12(5): e0177775. PMID: 28505207 doi: 10.1371/journal.pone.0177775

79. McKay, J. D., Hung, R. J., Han, Y., Zong, X., Carreras-Torres, R., Christiani, D. C., . . . Amos, C. I. (2017). Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. Nat Genet. 49(7): 1126-1132. PMID: 28604730 doi: 10.1038/ng.3892

80. Michailidou, K., Lindstrom, S., Dennis, J., Beesley, J., Hui, S., Kar, S., . . . Easton, D. F. (2017). Association analysis identifies 65 new breast cancer risk loci. Nature. 551(7678): 92-94. PMID: 29059683 doi: 10.1038/nature24284

81. Murphy, G., McCormack, V., Abedi-Ardekani, B., Arnold, M., Camargo, M. C., Dar, N. A., . . . Brennan, P. (2017). International cancer seminars: a focus on esophageal squamous cell carcinoma. Ann Oncol. 28(9): 2086-2093. PMID: 28911061 doi: 10.1093/annonc/mdx279

82. Perdomo, S., Avogbe, P. H., Foll, M., Abedi-Ardekani, B., Facciolla, V. L., Anantharaman, D., . . . Brennan, P. (2017). Circulating tumor DNA detection in head and neck cancer: evaluation of two different detection approaches. Oncotarget. 8(42): 72621-72632. PMID: 29069814 doi: 10.18632/oncotarget.20004

83. Scelo, G., Purdue, M. P., Brown, K. M., Johansson, M., Wang, Z., Eckel-Passow, J. E., . . . Chanock, S. J. (2017). Genome-wide association study identifies multiple risk loci for renal cell carcinoma. Nat Commun. 8: 15724. PMID: 28598434 doi: 10.1038/ncomms15724

84. Wang, T., Moon, J. Y., Wu, Y., Amos, C. I., Hung, R. J., Tardon, A., . . . Ho, G. Y. F. (2017). Pleiotropy of genetic variants on obesity and smoking phenotypes: Results from the Oncoarray Project of The International Lung Cancer Consortium. PLoS ONE. 12(9): e0185660. PMID: 28957450 doi: 10.1371/journal.pone.0185660

85. Witt, S. H., Streit, F., Jungkunz, M., Frank, J., Awasthi, S., Reinbold, C. S., . . . Rietschel, M. (2017). Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia. Transl Psychiatry. 7(6): e1155. PMID: 28632202 doi: 10.1038/tp.2017.115

86. Yong, S. K., Ha, T. C., Yeo, M. C., Gaborieau, V., McKay, J. D., & Wee, J. (2017). Associations of lifestyle and diet with the risk of nasopharyngeal carcinoma in Singapore: a case-control study. Chin J Cancer. 36(1): 3. PMID: 28063457 doi: 10.1186/s40880-016-0174-3

87. Ambatipudi, S., Cuenin, C., Hernandez-Vargas, H., Ghantous, A., Le Calvez-Kelm, F., Kaaks, R., . . . Herceg, Z. (2016). Tobacco smoking-associated genome-wide DNA methylation changes in the EPIC study. Epigenomics. 8(5): 599-618. PMID: 26864933 doi: 10.2217/epi-2016-0001

88. Amos, C. I., Hung, R., Bosse, Y., Christiani, D. C., Field, J. K., Landi, M. T., . . . McKay, J. P. (2016). P1.04: Defining the Genetic Architecture of Lung Cancer Etiology: Track: Prevention, Early Detection, Epidemiology and Tobacco Control. J Thorac Oncol. 11(10s): S182. PMID: 27676490 doi: 10.1016/j.jtho.2016.08.026

89. Bank, C., Renzette, N., Liu, P., Matuszewski, S., Shim, H., Foll, M., . . . Jensen, J. D. (2016). An experimental evaluation of drug-induced mutational meltdown as an antiviral treatment strategy. Evolution. 70(11): 2470-2484. PMID: 27566611 doi: 10.1111/evo.13041

90. Bei, J. X., Su, W. H., Ng, C. C., Yu, K., Chin, Y. M., Lou, P. J., . . . Hildesheim, A. (2016). A GWAS Meta-analysis and Replication Study Identifies a Novel Locus within CLPTM1L/TERT Associated with Nasopharyngeal Carcinoma in Individuals of Chinese Ancestry. Cancer Epidemiol Biomarkers Prev. 25(1): 188-192. PMID: 26545403 doi: 10.1158/1055-9965.epi-15-0144

91. Berndt, S. I., Camp, N. J., Skibola, C. F., Vijai, J., Wang, Z., Gu, J., . . . Slager, S. L. (2016). Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia. Nat Commun. 7: 10933. PMID: 26956414 doi: 10.1038/ncomms10933

92. Carreras-Torres, R., Haycock, P. C., Relton, C. L., Martin, R. M., Smith, G. D., Kraft, P., . . . Brennan, P. (2016). The causal relevance of body mass index in different histological types of lung cancer: A Mendelian randomization study. Sci Rep. 6: 31121. PMID: 27487993 doi: 10.1038/srep31121

93. Darabi, H., Beesley, J., Droit, A., Kar, S., Nord, S., Moradi Marjaneh, M., . . . Dunning, A. M. (2016). Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs). Sci Rep. 6: 32512. PMID: 27600471 doi: 10.1038/srep32512

94. D’Souza, G., Anantharaman, D., Gheit, T., Abedi-Ardekani, B., Beachler, D. C., Conway, D. I., . . . Cadoni, G. (2016). Effect of HPV on head and neck cancer patient survival, by region and tumor site: A comparison of 1362 cases across three continents. Oral Oncol. 62: 20-27. PMID: 27865368 doi: 10.1016/j.oraloncology.2016.09.005

95. Easton, D. F., Lesueur, F., Decker, B., Michailidou, K., Li, J., Allen, J., . . . Chenevix-Trench, G. (2016). No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing. J Med Genet. 53(5): 298-309. PMID: 26921362 doi: 10.1136/jmedgenet-2015-103529

96. Esposti, D. D., Hernandez-Vargas, H., Voegele, C., Fernandez-Jimenez, N., Forey, N., Bancel, B., . . . Herceg, Z. (2016). Identification of novel long non-coding RNAs deregulated in hepatocellular carcinoma using RNA-sequencing. Oncotarget. 7(22): 31862-31877. PMID: 26887054 doi: 10.18632/oncotarget.7364

97. Fernandez-Cuesta, L., & McKay, J. D. (2016). Genomic architecture of lung cancers. Curr Opin Oncol. 28(1): 52-57. PMID: 26569422 doi: 10.1097/cco.0000000000000251

98. Fernandez-Cuesta, L., Perdomo, S., Avogbe, P. H., Leblay, N., Delhomme, T. M., Gaborieau, V., . . . Brennan, P. (2016). Identification of Circulating Tumor DNA for the Early Detection of Small-cell Lung Cancer. EBioMedicine. 10: 117-123. PMID: 27377626 doi: 10.1016/j.ebiom.2016.06.032

99. Golozar, A., Etemadi, A., Kamangar, F., Fazeltabar Malekshah, A., Islami, F., Nasrollahzadeh, D., . . . Malekzadeh, R. (2016). Food preparation methods, drinking water source, and esophageal squamous cell carcinoma in the high-risk area of Golestan, Northeast Iran. Eur J Cancer Prev. 25(2): 123-129. PMID: 25851181 doi: 10.1097/cej.0000000000000156

100. Jensen, J. D., Foll, M., & Bernatchez, L. (2016). The past, present and future of genomic scans for selection INTRODUCTION. Mol Ecol. 25(1): 1-4. PMID: 26745554 doi: 10.1111/mec.13493

101. Kachuri, L., Amos, C. I., McKay, J. D., Johansson, M., Vineis, P., Bueno-de-Mesquita, H. B., . . . Hung, R. J. (2016). Fine mapping of chromosome 5p15.33 based on a targeted deep sequencing and high density genotyping identifies novel lung cancer susceptibility loci. Carcinogenesis. 37(1): 96-105. PMID: 26590902 doi: 10.1093/carcin/bgv165

102. Karami, S., Han, Y., Pande, M., Cheng, I., Rudd, J., Pierce, B. L., . . . Doherty, J. A. (2016). Telomere structure and maintenance gene variants and risk of five cancer types. Int J Cancer. 139(12): 2655-2670. PMID: 27459707 doi: 10.1002/ijc.30288

103. Khankhanian, P., Cozen, W., Himmelstein, D. S., Madireddy, L., Din, L., van den Berg, A., . . . Hjalgrim, H. (2016). Meta-analysis of genome-wide association studies reveals genetic overlap between Hodgkin lymphoma and multiple sclerosis. Int J Epidemiol. 45(3): 728-740. PMID: 26971321 doi: 10.1093/ije/dyv364

104. Kousathanas, A., Leuenberger, C., Helfer, J., Quinodoz, M., Foll, M., & Wegmann, D. (2016). Likelihood-Free Inference in High-Dimensional Models. Genetics. 203(2): 893-904. PMID: 27052569 doi: 10.1534/genetics.116.187567

105. Le Calvez-Kelm, F., Foll, M., Wozniak, M. B., Delhomme, T. M., Durand, G., Chopard, P., . . . Scelo, G. (2016). KRAS mutations in blood circulating cell-free DNA: a pancreatic cancer case-control. Oncotarget. 7(48): 78827-78840. PMID: 27705932 doi: 10.18632/oncotarget.12386

106. Lesseur, C., Diergaarde, B., Olshan, A. F., Wunsch-Filho, V., Ness, A. R., Liu, G., . . . Brennan, P. (2016). Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Nat Genet. 48(12): 1544-1550. PMID: 27749845 doi: 10.1038/ng.3685

107. Lorenz, S., Baroy, T., Sun, J., Nome, T., Vodak, D., Bryne, J. C., . . . Meza-Zepeda, L. A. (2016). Unscrambling the genomic chaos of osteosarcoma reveals extensive transcript fusion, recurrent rearrangements and frequent novel TP53 aberrations. Oncotarget. 7(5): 5273-5288. PMID: 26672768 doi: 10.18632/oncotarget.6567

108. Machiela, M. J., Lan, Q., Slager, S. L., Vermeulen, R. C., Teras, L. R., Camp, N. J., . . . Rothman, N. (2016). Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes. Hum Mol Genet. 25(8): 1663-1676. PMID: 27008888 doi: 10.1093/hmg/ddw027

109. Mazul, A. L., Rodriguez-Ormaza, N., Taylor, J. M., Desai, D. D., Brennan, P., Anantharaman, D., . . . Zevallos, J. P. (2016). Prognostic significance of non-HPV16 genotypes in oropharyngeal squamous cell carcinoma. Oral Oncol. 61: 98-103. PMID: 27688111 doi: 10.1016/j.oraloncology.2016.08.019

110. McKenzie, F., Zietsman, A., Galukande, M., Anele, A., Adisa, C., Cubasch, H., . . . McCormack, V. (2016). African Breast Cancer-Disparities in Outcomes (ABC-DO): protocol of a multicountry mobile health prospective study of breast cancer survival in sub-Saharan Africa. BMJ Open. 6(8): e011390. PMID: 27554102 doi: 10.1136/bmjopen-2016-011390

111. Ormond, L., Foll, M., Ewing, G. B., Pfeifer, S. P., & Jensen, J. D. (2016). Inferring the age of a fixed beneficial allele. Mol Ecol. 25(1): 157-169. PMID: 26576754 doi: 10.1111/mec.13478

112. Ortiz-Cuaran, S., Scheffler, M., Plenker, D., Dahmen, L., Scheel, A. H., Fernandez-Cuesta, L., . . . Sos, M. L. (2016). Heterogeneous Mechanisms of Primary and Acquired Resistance to Third-Generation EGFR Inhibitors. Clin Cancer Res. 22(19): 4837-4847. PMID: 27252416 doi: 10.1158/1078-0432.ccr-15-1915

113. Palmero, E. I., Alemar, B., Schuler-Faccini, L., Hainaut, P., Moreira-Filho, C. A., Ewald, I. P., . . . Ashton-Prolla, P. (2016). Screening for germline BRCA1, BRCA2, TP53 and CHEK2 mutations in families at-risk for hereditary breast cancer identified in a population-based study from Southern Brazil. Genet Mol Biol. 39(2): 210-222. PMID: 27223485 doi: 10.1590/1678-4685-gmb-2014-0363

114. Parroche, P., Roblot, G., Le Calvez-Kelm, F., Tout, I., Marotel, M., Malfroy, M., . . . Hasan, U. A. (2016). TLR9 re-expression in cancer cells extends the S-phase and stabilizes p16(INK4a) protein expression. Oncogenesis. 5(7): e244. PMID: 27454079 doi: 10.1038/oncsis.2016.49

115. Patel, Y. M., Park, S. L., Han, Y., Wilkens, L. R., Bickeboller, H., Rosenberger, A., . . . Le Marchand, L. (2016). Novel Association of Genetic Markers Affecting CYP2A6 Activity and Lung Cancer Risk. Cancer Res. 76(19): 5768-5776. PMID: 27488534 doi: 10.1158/0008-5472.can-16-0446

116. Price, A. J., Travis, R. C., Appleby, P. N., Albanes, D., Barricarte Gurrea, A., Bjorge, T., . . . Allen, N. E. (2016). Circulating Folate and Vitamin B12 and Risk of Prostate Cancer: A Collaborative Analysis of Individual Participant Data from Six Cohorts Including 6875 Cases and 8104 Controls. Eur Urol. 70(6): 941-951. PMID: 27061263 doi: 10.1016/j.eururo.2016.03.029

117. Renault, A. L., Lesueur, F., Coulombe, Y., Gobeil, S., Soucy, P., Hamdi, Y., . . . Simard, J. (2016). ABRAXAS (FAM175A) and Breast Cancer Susceptibility: No Evidence of Association in the Breast Cancer Family Registry. PLoS ONE. 11(6): e0156820. PMID: 27270457 doi: 10.1371/journal.pone.0156820

118. Shim, H., Laurent, S., Matuszewski, S., Foll, M., & Jensen, J. D. (2016). Detecting and Quantifying Changing Selection Intensities from Time-Sampled Polymorphism Data. G3 (Bethesda). 6(4): 893-904. PMID: 26869618 doi: 10.1534/g3.115.023200

119. Vinayanuwattikun, C., Le Calvez-Kelm, F., Abedi-Ardekani, B., Zaridze, D., Mukeria, A., Voegele, C., . . . Scelo, G. (2016). Elucidating Genomic Characteristics of Lung Cancer Progression from In Situ to Invasive Adenocarcinoma. Sci Rep. 6: 31628. PMID: 27545006 doi: 10.1038/srep31628

120. Wyszynski, A., Hong, C. C., Lam, K., Michailidou, K., Lytle, C., Yao, S., . . . Cole, M. D. (2016). An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression. Hum Mol Genet. 25(17): 3863-3876. PMID: 27402876 doi: 10.1093/hmg/ddw223

121. Young, E. L., Feng, B. J., Stark, A. W., Damiola, F., Durand, G., Forey, N., . . . Tavtigian, S. V. (2016). Multigene testing of moderate-risk genes: be mindful of the missense. J Med Genet. 53(6): 366-376. PMID: 26787654 doi: 10.1136/jmedgenet-2015-103398

122. Zevallos, J. P., Mazul, A. L., Rodriguez, N., Weissler, M. C., Brennan, P., Anantharaman, D., . . . Olshan, A. F. (2016). Previous tonsillectomy modifies odds of tonsil and base of tongue cancer. Br J Cancer. 114(7): 832-838. PMID: 26977858 doi: 10.1038/bjc.2016.63

123. Zuber, V., Marconett, C. N., Shi, J., Hua, X., Wheeler, W., Yang, C., . . . Landi, M. T. (2016). Pleiotropic Analysis of Lung Cancer and Blood Triglycerides. J Natl Cancer Inst. 108(12). PMID: 27565901 doi: 10.1093/jnci/djw167

124. Accardi, R., Gruffat, H., Sirand, C., Fusil, F., Gheit, T., Hernandez-Vargas, H., . . . Tommasino, M. (2015). The mycotoxin aflatoxin B1 stimulates Epstein-Barr virus-induced B-cell transformation in in vitro and in vivo experimental models. Carcinogenesis. 36(11): 1440-1451. PMID: 26424750 doi: 10.1093/carcin/bgv142

125. Amorim, C. E., Daub, J. T., Salzano, F. M., Foll, M., & Excoffier, L. (2015). Detection of convergent genome-wide signals of adaptation to tropical forests in humans. PLoS. One. 10(4): e0121557. PMID: 25849546 doi: 10.1371/journal.pone.0121557

126. Ancey, P. B., Testoni, B., Gruffaz, M., Cros, M. P., Durand, G., Le Calvez-Kelm, F., . . . Hernandez-Vargas, H. (2015). Genomic responses to hepatitis B virus (HBV) infection in primary human hepatocytes. Oncotarget. PMID: 26565721 doi: 10.18632/oncotarget.6270

127. Brenner, D. R., Amos, C. I., Brhane, Y., Timofeeva, M. N., Caporaso, N., Wang, Y., . . . Hung, R. J. (2015). Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia. Carcinogenesis. 36(11): 1314-1326. PMID: 26363033 doi: 10.1093/carcin/bgv128

128. Castells, X., Karanovic, S., Ardin, M., Tomic, K., Xylinas, E., Durand, G., . . . Zavadil, J. (2015). Low-Coverage Exome Sequencing Screen in Formalin-Fixed Paraffin-Embedded Tumors Reveals Evidence of Exposure to Carcinogenic Aristolochic Acid. Cancer Epidemiol Biomarkers Prev. 24(12): 1873-1881. PMID: 26383547 doi: 10.1158/1055-9965.epi-15-0553

129. Chen, D., Gaborieau, V., Zhao, Y., Chabrier, A., Wang, H., Waterboer, T., . . . McKay, J. D. (2015). A systematic investigation of the contribution of genetic variation within the MHC region to HPV seropositivity. Hum. Mol. Genet. 24(9): 2681-2688. PMID: 25616963 doi: 10.1093/hmg/ddv015

130. Cheng, T. H., Gorman, M., Martin, L., Barclay, E., Casey, G., Saunders, B., . . . Tomlinson, I. (2015). Common colorectal cancer risk alleles contribute to the multiple colorectal adenoma phenotype, but do not influence colonic polyposis in FAP. Eur. J Hum. Genet. 23(2): 260-263. PMID: 24801760 doi: 10.1038/ejhg.2014.74

131. Darabi, H., McCue, K., Beesley, J., Michailidou, K., Nord, S., Kar, S., . . . Chenevix-Trench, G. (2015). Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression. Am. J Hum. Genet. 97(1): 22-34. PMID: 26073781 doi: 10.1016/j.ajhg.2015.05.002

132. Delahaye-Sourdeix, M., Anantharaman, D., Timofeeva, M. N., Gaborieau, V., Chabrier, A., Vallee, M. P., . . . McKay, J. D. (2015). A Rare Truncating BRCA2 Variant and Genetic Susceptibility to Upper Aerodigestive Tract Cancer. J Natl. Cancer Inst. 107(5): pii: djv037. PMID: 25838448 doi: 10.1093/jnci/djv037

133. Delahaye-Sourdeix, M., Oliver, J., Timofeeva, M. N., Gaborieau, V., Johansson, M., Chabrier, A., . . . McKay, J. D. (2015). The 12p13.33/RAD52 Locus and Genetic Susceptibility to Squamous Cell Cancers of Upper Aerodigestive Tract. PLoS. One. 10(3): e0117639. PMID: 25793373 doi: 10.1371/journal.pone.0117639

134. Delahaye-Sourdeix, M., Urayama, K. Y., Gaborieau, V., Veenstra, R., Foll, M., Chabrier, A., . . . McKay, J. D. (2015). A Novel Risk Locus at 6p21.3 for Epstein-Barr Virus-Positive Hodgkin Lymphoma. Cancer Epidemiol Biomarkers Prev. 24(12): 1838-1843. PMID: 26404960 doi: 10.1158/1055-9965.EPI-15-0534

135. Fernandez-Cuesta, L., Sun, R., Menon, R., George, J., Lorenz, S., Meza-Zepeda, L. A., . . . Thomas, R. K. (2015). Identification of novel fusion genes in lung cancer using breakpoint assembly of transcriptome sequencing data. Genome Biol. 16: 7. PMID: 25650807 doi: 10.1186/s13059-014-0558-0

136. Fernandez-Cuesta, L., & Thomas, R. K. (2015). Molecular Pathways: Targeting NRG1 Fusions in Lung Cancer. Clin. Cancer Res. 21(9): 1989-1994. PMID: 25501131 doi: 10.1158/1078-0432.CCR-14-0854

137. Forstner, A. J., Hofmann, A., Maaser, A., Sumer, S., Khudayberdiev, S., Muhleisen, T. W., . . . Nothen, M. M. (2015). Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder. Transl Psychiatry. 5: e678. PMID: 26556287 doi: 10.1038/tp.2015.159

138. Glubb, D. M., Maranian, M. J., Michailidou, K., Pooley, K. A., Meyer, K. B., Kar, S., . . . French, J. D. (2015). Fine-Scale Mapping of the 5q11.2 Breast Cancer Locus Reveals at Least Three Independent Risk Variants Regulating MAP3K1. Am J Hum Genet. 96(1): 5-20. PMID: 25529635 doi: 10.1016/j.ajhg.2014.11.009

139. Guidoum, M., Kherfi-Kadi, H., Benharkat-Boughaba, O., Djemaa-Bendjazia, A., Keghouche, S., Abedi-Ardekani, B., . . . Bouslama, Z. (2015). Patterns of Benign and Malignant Lesions of the Thyroid in Two Wilayahs of Northeastern Algeria. J Cancer Epidemiol. 2015: 849416. PMID: 26681943 doi: 10.1155/2015/849416

140. Henrion, M. Y., Purdue, M. P., Scelo, G., Broderick, P., Frampton, M., Ritchie, A., . . . Houlston, R. S. (2015). Common Variation at 1q24.1 (ALDH9A1) Is a Potential Risk Factor for Renal Cancer. PLoS. One. 10(3): e0122589. PMID: 25826619 doi: 10.1371/journal.pone.0122589

141. Jhuraney, A., Velkova, A., Johnson, R. C., Kessing, B., Carvalho, R. S., Whiley, P., . . . Monteiro, A. N. (2015). BRCA1 Circos: a visualisation resource for functional analysis of missense variants. J Med. Genet. 52(4): 224-230. PMID: 25643705 doi: 10.1136/jmedgenet-2014-102766

142. Ji, X., Gui, J., Han, Y., Brennan, P., Li, Y., McKay, J., . . . Amos, C. I. (2015). The role of haplotype in 15q25.1 locus in lung cancer risk: results of scanning chromosome 15. Carcinogenesis. 36(11): 1275-1283. PMID: 26282330 doi: 10.1093/carcin/bgv118

143. Lin, W. Y., Camp, N. J., Ghoussaini, M., Beesley, J., Michailidou, K., Hopper, J. L., . . . Cox, A. (2015). Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk. Hum Mol Genet. 24(1): 285-298. PMID: 25168388 doi: 10.1093/hmg/ddu431

144. Maillard, S., Damiola, F., Clero, E., Pertesi, M., Robinot, N., Rachedi, F., . . . de, V. F. (2015). Common variants at 9q22.33, 14q13.3, and ATM loci, and risk of differentiated thyroid cancer in the French Polynesian population. PLoS. One. 10(4): e0123700. PMID: 25849217 doi: 10.1371/journal.pone.0123700

145. Michailidou, K., Beesley, J., Lindstrom, S., Canisius, S., Dennis, J., Lush, M. J., . . . Easton, D. F. (2015). Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer. Nat. Genet. 47(4): 373-380. PMID: 25751625 doi: 10.1038/ng.3242

146. Oh, J. E., Ohta, T., Satomi, K., Foll, M., Durand, G., McKay, J., . . . Ohgaki, H. (2015). Alterations in the NF2/LATS1/LATS2/YAP Pathway in Schwannomas. J Neuropathol. Exp. Neurol. 74(10): 952-959. PMID: 26360373 doi: 10.1097/NEN.0000000000000238

147. Orr, N., Dudbridge, F., Dryden, N., Maguire, S., Novo, D., Perrakis, E., . . . Peto, J. (2015). Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2. Hum. Mol. Genet. 24(10): 2966-2984. PMID: 25652398 doi: 10.1093/hmg/ddv035

148. Pereda, C. M., Lesueur, F., Pertesi, M., Robinot, N., Lence-Anta, J. J., Turcios, S., . . . de, V. F. (2015). Common variants at the 9q22.33, 14q13.3 and ATM loci, and risk of differentiated thyroid cancer in the Cuban population. BMC Genet. 16: 22. PMID: 25879635 doi: 10.1186/s12863-015-0180-5

149. Pertesi, M., Galia, P., Nazaret, N., Vallee, M., Garderet, L., Leleu, X., . . . Dumontet, C. (2015). Rare Circulating Cells in Familial Waldenstrom Macroglobulinemia Displaying the MYD88 L265P Mutation Are Enriched by Epstein-Barr Virus Immortalization. PLoS. One. 10(9): e0136505. PMID: 26352266 doi: 10.1371/journal.pone.0136505

150. Poirier, J. G., Brennan, P., McKay, J. D., Spitz, M. R., Bickeboller, H., Risch, A., . . . Hung, R. J. (2015). Informed genome-wide association analysis with family history as a secondary phenotype identifies novel loci of lung cancer. Genet Epidemiol. 39(3): 197-206. PMID: 25644374 doi: 10.1002/gepi.21882

151. Sampson, J. N., Wheeler, W. A., Yeager, M., Panagiotou, O., Wang, Z., Berndt, S. I., . . . Chatterjee, N. (2015). Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types. J Natl Cancer Inst. 107(12). PMID: 26464424 doi: 10.1093/jnci/djv279

152. Vaca-Paniagua, F., Alvarez-Gomez, R. M., Maldonado-Martinez, H. A., Perez-Plasencia, C., Fragoso-Ontiveros, V., Lasa-Gonsebatt, F., . . . Olivier, M. (2015). Revealing the Molecular Portrait of Triple Negative Breast Tumors in an Understudied Population through Omics Analysis of Formalin-Fixed and Paraffin-Embedded Tissues. PLoS. One. 10(5): e0126762. PMID: 25961742 doi: 10.1371/journal.pone.0126762

153. Vaca-Paniagua, F., Oliver, J., Nogueira da, C. A., Merle, P., McKay, J., Herceg, Z., & Holmila, R. (2015). Targeted deep DNA methylation analysis of circulating cell-free DNA in plasma using massively parallel semiconductor sequencing. Epigenomics. 7(3): 353-362. PMID: 26077425 doi: 10.2217/epi.14.94

154. Vijai, J., Wang, Z., Berndt, S. I., Skibola, C. F., Slager, S. L., de, S. S., . . . Nieters, A. (2015). A genome-wide association study of marginal zone lymphoma shows association to the HLA region. Nat Commun. 6: 5751. PMID: 25569183 doi: 10.1038/ncomms6751

155. Wang, Y., Wei, Y., Gaborieau, V., Shi, J., Han, Y., Timofeeva, M. N., . . . Houlston, R. S. (2015). Deciphering associations for lung cancer risk through imputation and analysis of 12 316 cases and 16 831 controls. Eur J Hum Genet. 23(12): 1723-1728. PMID: 25804397 doi: 10.1038/ejhg.2015.48

156. Zhang, C., Doherty, J. A., Burgess, S., Hung, R. J., Lindstrom, S., Kraft, P., . . . Pierce, B. L. (2015). Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study. Hum. Mol. Genet. 24(18): 5356-5366. PMID: 26138067 doi: 10.1093/hmg/ddv25

 

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