Research Groups

Recent Publications - 12 most recent publications

1. Timofeeva M.N., Hung R.J., Rafnar T., Christiani D.C., Field J.K., Bickeboller H., Risch A., McKay J.D., Wang Y., Dai J., Gaborieau V., McLaughlin J., Brenner D., Narod S.A., Caporaso N.E., Albanes D., Thun M., Eisen T., Wichmann H.E., Rosenberger A., Han Y., Chen W., Zhu D., Spitz M., Wu X., Pande M., Zhao Y., Zaridze D., Szeszenia-Dabrowska N., Lissowska J., Rudnai P., Fabianova E., Mates D., Bencko V., Foretova L., Janout V., Krokan H.E., Gabrielsen M.E., Skorpen F., Vatten L., Njolstad I., Chen C., Goodman G., Lathrop M., Benhamou S., Vooder T., Valk K., Nelis M., Metspalu A., Raji O., Chen Y., Gosney J., Liloglou T., Muley T., Dienemann H., Thorleifsson G., Shen H., Stefansson K., Brennan P., Amos C.I., Houlston R., Landi M.T. (2012) Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls Human Molecular Genetics; 21(22):4980-4995. PMID: 22899653

2. Martino A., Campa D., Jamroziak K., Reis R.M., Sainz J., Buda G., Garcia-Sanz R., Lesueur F., Marques H., Moreno V., Jurado M., Rios R., Szemraj-Rogucka Z., Szemraj J., Tjonneland A., Overvad K., Vangsted A.J., Vogel U., Mikala G., Kadar K., Szombath G., Varkonyi J., Orciuolo E., Dumontet C., Gemignani F., Rossi A.M., Landi S., Petrini M., Houlston R.S., Hemminki K., Canzian F. (2012) Impact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myeloma British journal of haematology; 158(6):805-809. PMID: 22823248

3. Campa D., Martino A., Sainz J., Buda G., Jamroziak K., Weinhold N., Vieira Reis R.M., Garcia-Sanz R., Jurado M., Rios R., Szemraj-Rogucka Z., Marques H., Lesueur F., Bugert P., Moreno V., Szemraj J., Orciuolo E., Gemignani F., Rossi A.M., Dumontet C., Petrini M., Goldschmidt H., Landi S., Canzian F. (2012) Comprehensive investigation of genetic variation in the 8q24 region and multiple myeloma risk in the IMMEnSE consortium British journal of haematology; 157(3):331-338. PMID: 22590720

4. Ito H., McKay J.D., Hosono S., Hida T., Yatabe Y., Mitsudomi T., Brennan P., Tanaka H., Matsuo K. (2012) Association between a Genome-Wide Association Study-Identified Locus and the Risk of Lung Cancer in Japanese Population J Thorac Oncol; 7(5):790-798. PMID: 22430809

5. Park D.J., Lesueur F., Nguyen-Dumont T., Pertesi M., Odefrey F., Hammet F., Neuhausen S.L., John E.M., Andrulis I.L., Terry M.B., Daly M., Buys S., Le Calvez-Kelm F., Lonie A., Pope B.J., Tsimiklis H., Voegele C., Hilbers F.M., Hoogerbrugge N., Barroso A., Osorio A., Giles G.G., Devilee P., Benitez J., Hopper J.L., Tavtigian S.V., Goldgar D.E., Southey M.C. (2012) Rare Mutations in XRCC2 Increase the Risk of Breast Cancer American journal of human genetics; 90(4):734-739. PMID: 22464251

6. Tischkowitz M., Capanu M., Sabbaghian N., Li L., Liang X., Vallee M.P., Tavtigian S.V., Concannon P., Foulkes W.D., Bernstein L., Bernstein J.L., Begg C.B. (2012) Rare germline mutations in PALB2 and breast cancer risk: a population-based study Human Mutation; 33(4):674-680. PMID: 22241545

7. Martino A., Sainz J., Buda G., Jamroziak K., Reis R.M., Garcia-Sanz R., Jurado M., Rios R., Szemraj-Rogucka Z., Marques H., Lesueur F., Moreno V., Orciuolo E., Gemignani F., Landi S., Rossi A.M., Dumontet C., Petrini M., Campa D., Canzian F. (2012) Genetics and molecular epidemiology of multiple myeloma: The rationale for the IMMEnSE consortium (Review) International journal of oncology; 40(3):625-638. PMID: 22159523

8. Urayama K.Y., Jarrett R.F., Hjalgrim H., Diepstra A., Kamatani Y., Chabrier A., Gaborieau V., Boland A., Nieters A., Becker N., Foretova L., Benavente Y., Maynadie M., Staines A., Shield L., Lake A., Montgomery D., Taylor M., Smedby K.E., Amini R.M., Adami H.O., Glimelius B., Feenstra B., Nolte I.M., Visser L., van Imhoff G.W., Lightfoot T., Cocco P., Kiemeney L., Vermeulen S.H., Holcatova I., Vatten L., MacFarlane G.J., Thomson P., Conway D.I., Benhamou S., Agudo A., Healy C.M., Overvad K., Tjonneland A., Melin B., Canzian F., Khaw K.T., Travis R.C., Peeters P.H., Gonzalez C.A., Quiros J.R., Sanchez M.J., Huerta J.M., Ardanaz E., Dorronsoro M., Clavel-Chapelon F., Bueno-de-Mesquita H.B., Riboli E., Roman E., Boffetta P., de Sanjose S., Zelenika D., Melbye M., van den Berg A., Lathrop M., Brennan P., McKay J.D. (2012) Genome-wide association study of classical hodgkin lymphoma and epstein-barr virus status-defined subgroups Journal of the National Cancer Institute; 104(3):240-253. PMID: 22286212

9. Lindor N.M., Guidugli L., Wang X., Vallee M.P., Monteiro A.N., Tavtigian S., Goldgar D.E., Couch F.J. (2012) A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS) Human Mutation; 33(1):8-21. PMID: 21990134

10. Vallee M.P., Francy T.C., Judkins M.K., Babikyan D., Lesueur F., Gammon A., Goldgar D.E., Couch F.J., Tavtigian S.V. (2012) Classification of missense substitutions in the BRCA genes: A database dedicated to Ex-UVs Human Mutation; 33(1):22-28. PMID: 21990165

11. Wu X., Scelo G., Purdue M.P., Rothman N., Johansson M., Ye Y., Wang Z., Zelenika D., Moore L.E., Wood C.G., Prokhortchouk E., Gaborieau V., Jacobs K.B., Chow W.H., Toro J.R., Zaridze D., Lin J., Lubinski J., Trubicka J., Szeszenia-Dabrowska N., Lissowska J., Rudnai P., Fabianova E., Mates D., Jinga V., Bencko V., Slamova A., Holcatova I., Navratilova M., Janout V., Boffetta P., Colt J.S., Davis F.G., Schwartz K.L., Banks R.E., Selby P.J., Harnden P., Berg C.D., Hsing A.W., Grubb R.L. III, Boeing H., Vineis P., Clavel-Chapelon F., Palli D., Tumino R., Krogh V., Panico S., Duell E.J., Quiros J.R., Sanchez M.J., Navarro C., Ardanaz E., Dorronsoro M., Khaw K.T., Allen N.E., Bueno-de-Mesquita H.B., Peeters P.H., Trichopoulos D., Linseisen J., Ljungberg B., Overvad K., Tjonneland A., Romieu I., Riboli E., Stevens V.L., Thun M.J., Diver W.R., Gapstur S.M., Pharoah P.D., Easton D.F., Albanes D., Virtamo J., Vatten L., Hveem K., Fletcher T., Koppova K., Cussenot O., Cancel-Tassin G., Benhamou S., Hildebrandt M.A., Pu X., Foglio M., Lechner D., Hutchinson A., Yeager M., Fraumeni J.F. Jr., Lathrop M., Skryabin K.G., McKay J.D., Gu J., Brennan P., Chanock S.J. (2012) A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23 Human Molecular Genetics; 21(2):456-462. PMID: 22010048

12. Heck J.E., Moore L.E., Lee Y.C., McKay J.D., Hung R.J., Karami S., Gaborieau V., Szeszenia-Dabrowska N., Zaridze D.G., Mukeriya A., Mates D., Foretova L., Janout V., Kollarova H., Bencko V., Rothman N., Brennan P., Chow W.H., Boffetta P. (2012) Xenobiotic metabolizing gene variants and renal cell cancer: a multicenter study Frontiers in oncology; 16. PMID: 22645715