A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma.
Nature Communications
Seviiri, Mathias M; Law, Matthew H MH; Ong, Jue-Sheng JS; Gharahkhani, Puya P; Fontanillas, Pierre P; , ; Olsen, Catherine M CM; Whiteman, David C DC; MacGregor, Stuart S
Modified eQTL and Somatic DNA Segment Alterations in Esophageal Squamous Cell Carcinoma for Genes Related to Immunity, DNA Repair, and Inflammation.
Cancers
Yang, Howard H HH; Liu, Huaitian H; Hu, Nan N; Su, Hua H; Wang, Chaoyu C; Giffen, Carol C; Goldstein, Alisa M AM; Taylor, Philip R PR; Lee, Maxwell P MP
Hypertension and the roles of the 9p21.3 risk locus: Classic findings and new association data.
International Journal Of Cardiology. Hypertension
Gallo, Juan E JE; Ochoa, Juan E JE; Warren, Helen R HR; Misas, Elizabeth E; Correa, Monica M MM; Gallo-Villegas, Jaime A JA; Bedoya, Gabriel G; Aristizábal, Dagnóvar D; McEwen, Juan G JG; Caulfield, Mark J MJ; Parati, Gianfranco G; Clay, Oliver K OK
Genetic variants of chromosome 9p21.3 region associated with coronary artery disease and premature coronary artery disease in an Asian Indian population.
Indian Heart Journal
Kalpana, Bellary B; Murthy, Dwarkanath K DK; Balakrishna, Nagalla N; Aiyengar, Mohini T MT
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
Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F
Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer.
Nature Genetics
Lesseur, Corina C; Diergaarde, Brenda B; Olshan, Andrew F AF; Wünsch-Filho, Victor V; Ness, Andrew R AR; Liu, Geoffrey G; Lacko, Martin M; Eluf-Neto, José J; Franceschi, Silvia S; Lagiou, Pagona P; Macfarlane, Gary J GJ; Richiardi, Lorenzo L; Boccia, Stefania S; Polesel, Jerry J; Kjaerheim, Kristina K; Zaridze, David D; Johansson, Mattias M; Menezes, Ana M AM; Curado, Maria Paula MP; Robinson, Max M; Ahrens, Wolfgang W; Canova, Cristina C; Znaor, Ariana A; Castellsagué, Xavier X; Conway, David I DI; Holcátová, Ivana I; Mates, Dana D; Vilensky, Marta M; Healy, Claire M CM; Szeszenia-Dąbrowska, Neonila N; Fabiánová, Eleonóra E; Lissowska, Jolanta J; Grandis, Jennifer R JR; Weissler, Mark C MC; Tajara, Eloiza H EH; Nunes, Fabio D FD; de Carvalho, Marcos B MB; Thomas, Steve S; Hung, Rayjean J RJ; Peters, Wilbert H M WH; Herrero, Rolando R; Cadoni, Gabriella G; Bueno-de-Mesquita, H Bas HB; Steffen, Annika A; Agudo, Antonio A; Shangina, Oxana O; Xiao, Xiangjun X; Gaborieau, Valérie V; Chabrier, Amélie A; Anantharaman, Devasena D; Boffetta, Paolo P; Amos, Christopher I CI; McKay, James D JD; Brennan, Paul P
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.
Nature Genetics
Bailey, Jessica N Cooke JN; Loomis, Stephanie J SJ; Kang, Jae H JH; Allingham, R Rand RR; Gharahkhani, Puya P; Khor, Chiea Chuen CC; Burdon, Kathryn P KP; Aschard, Hugues H; Chasman, Daniel I DI; Igo, Robert P RP; Hysi, Pirro G PG; Glastonbury, Craig A CA; Ashley-Koch, Allison A; Brilliant, Murray M; Brown, Andrew A AA; Budenz, Donald L DL; Buil, Alfonso A; Cheng, Ching-Yu CY; Choi, Hyon H; Christen, William G WG; Curhan, Gary G; De Vivo, Immaculata I; Fingert, John H JH; Foster, Paul J PJ; Fuchs, Charles C; Gaasterland, Douglas D; Gaasterland, Terry T; Hewitt, Alex W AW; Hu, Frank F; Hunter, David J DJ; Khawaja, Anthony P AP; Lee, Richard K RK; Li, Zheng Z; Lichter, Paul R PR; Mackey, David A DA; McGuffin, Peter P; Mitchell, Paul P; Moroi, Sayoko E SE; Perera, Shamira A SA; Pepper, Keating W KW; Qi, Qibin Q; Realini, Tony T; Richards, Julia E JE; Ridker, Paul M PM; Rimm, Eric E; Ritch, Robert R; Ritchie, Marylyn M; Schuman, Joel S JS; Scott, William K WK; Singh, Kuldev K; Sit, Arthur J AJ; Song, Yeunjoo E YE; Tamimi, Rulla M RM; Topouzis, Fotis F; Viswanathan, Ananth C AC; Verma, Shefali Setia SS; Vollrath, Douglas D; Wang, Jie Jin JJ; Weisschuh, Nicole N; Wissinger, Bernd B; Wollstein, Gadi G; Wong, Tien Y TY; Yaspan, Brian L BL; Zack, Donald J DJ; Zhang, Kang K; Study, Epic-Norfolk Eye EN; , ; Weinreb, Robert N RN; Pericak-Vance, Margaret A MA; Small, Kerrin K; Hammond, Christopher J CJ; Aung, Tin T; Liu, Yutao Y; Vithana, Eranga N EN; MacGregor, Stuart S; Craig, Jamie E JE; Kraft, Peter P; Howell, Gareth G; Hauser, Michael A MA; Pasquale, Louis R LR; Haines, Jonathan L JL; Wiggs, Janey L JL
A GWAS Meta-analysis and Replication Study Identifies a Novel Locus within CLPTM1L/TERT Associated with Nasopharyngeal Carcinoma in Individuals of Chinese Ancestry.
Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers.
Carcinogenesis
Li, Wen-Qing WQ; Pfeiffer, Ruth M RM; Hyland, Paula L PL; Shi, Jianxin J; Gu, Fangyi F; Wang, Zhaoming Z; Bhattacharjee, Samsiddhi S; Luo, Jun J; Xiong, Xiaoqin X; Yeager, Meredith M; Deng, Xiang X; Hu, Nan N; Taylor, Philip R PR; Albanes, Demetrius D; Caporaso, Neil E NE; Gapstur, Susan M SM; Amundadottir, Laufey L; Chanock, Stephen J SJ; Chatterjee, Nilanjan N; Landi, Maria Teresa MT; Tucker, Margaret A MA; Goldstein, Alisa M AM; Yang, Xiaohong R XR
The relationship between diastolic blood pressure and coronary artery calcification is dependent on single nucleotide polymorphisms on chromosome 9p21.3.
Bmc Medical Genetics
Kim, Daniel S DS; Smith, Jennifer A JA; Bielak, Lawrence F LF; Wu, Chun-Yi CY; Sun, Yan V YV; Sheedy, Patrick F PF; Turner, Stephen T ST; Peyser, Patricia A PA; Kardia, Sharon L R SL
Genetic variants in ARID5B and CEBPE are childhood ALL susceptibility loci in Hispanics.
Cancer Causes & Control : Ccc
Chokkalingam, Anand P AP; Hsu, Ling-I LI; Metayer, Catherine C; Hansen, Helen M HM; Month, Stacy R SR; Barcellos, Lisa F LF; Wiemels, Joseph L JL; Buffler, Patricia A PA
Common genetic variants in the 9p21 region and their associations with multiple tumours.
British Journal Of Cancer
Gu, F F; Pfeiffer, R M RM; Bhattacharjee, S S; Han, S S SS; Taylor, P R PR; Berndt, S S; Yang, H H; Sigurdson, A J AJ; Toro, J J; Mirabello, L L; Greene, M H MH; Freedman, N D ND; Abnet, C C CC; Dawsey, S M SM; Hu, N N; Qiao, Y-L YL; Ding, T T; Brenner, A V AV; Garcia-Closas, M M; Hayes, R R; Brinton, L A LA; Lissowska, J J; Wentzensen, N N; Kratz, C C; Moore, L E LE; Ziegler, R G RG; Chow, W-H WH; Savage, S A SA; Burdette, L L; Yeager, M M; Chanock, S J SJ; Chatterjee, N N; Tucker, M A MA; Goldstein, A M AM; Yang, X R XR
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk.
Nature Genetics
Sherborne, Amy L AL; Hosking, Fay J FJ; Prasad, Rashmi B RB; Kumar, Rajiv R; Koehler, Rolf R; Vijayakrishnan, Jayaram J; Papaemmanuil, Elli E; Bartram, Claus R CR; Stanulla, Martin M; Schrappe, Martin M; Gast, Andreas A; Dobbins, Sara E SE; Ma, Yussanne Y; Sheridan, Eamonn E; Taylor, Malcolm M; Kinsey, Sally E SE; Lightfoot, Tracey T; Roman, Eve E; Irving, Julie A E JA; Allan, James M JM; Moorman, Anthony V AV; Harrison, Christine J CJ; Tomlinson, Ian P IP; Richards, Sue S; Zimmermann, Martin M; Szalai, Csaba C; Semsei, Agnes F AF; Erdelyi, Daniel J DJ; Krajinovic, Maja M; Sinnett, Daniel D; Healy, Jasmine J; Gonzalez Neira, Anna A; Kawamata, Norihiko N; Ogawa, Seishi S; Koeffler, H Phillip HP; Hemminki, Kari K; Greaves, Mel M; Houlston, Richard S RS
Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk.
Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Goode, Ellen L EL; Fridley, Brooke L BL; Vierkant, Robert A RA; Cunningham, Julie M JM; Phelan, Catherine M CM; Anderson, Stephanie S; Rider, David N DN; White, Kristin L KL; Pankratz, V Shane VS; Song, Honglin H; Hogdall, Estrid E; Kjaer, Susanne K SK; Whittemore, Alice S AS; DiCioccio, Richard R; Ramus, Susan J SJ; Gayther, Simon A SA; Schildkraut, Joellen M JM; Pharaoh, Paul P D PP; Sellers, Thomas A TA
Common genetic variation in candidate genes and susceptibility to subtypes of breast cancer.
Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Mavaddat, Nasim N; Dunning, Alison M AM; Ponder, Bruce A J BA; Easton, Douglas F DF; Pharoah, Paul D PD
Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British population.
Carcinogenesis
Driver, Kristy E KE; Song, Honglin H; Lesueur, Fabienne F; Ahmed, Shahana S; Barbosa-Morais, Nuno L NL; Tyrer, Jonathan P JP; Ponder, Bruce A J BA; Easton, Douglas F DF; Pharoah, Paul D P PD; Dunning, Alison M AM; ,