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Analysis of 60 Reported Glioma Risk SNPs Replicates Published GWAS Findings but Fails to Replicate Associations From Published Candidate-Gene Studies

CITE Title : Analysis of 60 Reported Glioma Risk SNPs Replicates Published GWAS Findings but Fails to Replicate Associations From Published Candidate-Gene Studies Personal Author(s) : Walsh, Kyle M.;Anderson, Erik;Hansen, Helen M.;Decker, Paul A.;Kosel, Matt L.;Kollmeyer, Thomas;Rice, Terri;Zheng, Shichun;Xiao, Yuanyuan;Chang, Jeffrey S.;McCoy, Lucie S.;Bracci, Paige M.;Wiemels, Joe L.;Pico, Alexander R.;Smirnov, Ivan;Lachance, Daniel H.;Sicotte, Hugues;Eckel-Passow, Jeanette E.;Wiencke, John K.;Jenkins, Robert B.;Wrensch, Margaret R.; Published Date : December 31 2012 Source : Genet Epidemiol. 2012; 37(2):222-228 URL : https://stacks.cdc.gov/view/cdc/33575 Walsh, Kyle M. et al. (2012). Analysis of 60 Reported Glioma Risk SNPs Replicates Published GWAS Findings but Fails to Replicate Associations From Published Candidate-Gene Studies. 37(2). Walsh, Kyle M. et al. "Analysis of 60 Reported Glioma Risk SNPs Replicates Published GWAS Findings but Fails to Replicate Associations From Published Candidate-Gene Studies" 37, no. 2 (2012) Walsh, Kyle M. et al. "Analysis of 60 Reported Glioma Risk SNPs Replicates Published GWAS Findings but Fails to Replicate Associations From Published Candidate-Gene Studies" vol. 37, no. 2, 2012 Export RIS Citation Information.

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Walsh, Kyle M. ;

Anderson, Erik

December 31 2012 | Genet Epidemiol. 2012; 37(2):222-228

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Genomewide association studies (GWAS) and candidate-gene studies have implicated single-nucleotide polymorphisms (SNPs) in at least 45 different genes...
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors

CITE Title : Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors Personal Author(s) : Melin, Beatrice S;Barnholtz-Sloan, Jill S;Wrensch, Margaret R;Johansen, Christoffer;Il’yasova, Dora;Kinnersley, Ben;Ostrom, Quinn T;Labreche, Karim;Chen, Yanwen;Armstrong, Georgina;Liu, Yanhong;Eckel-Passow, Jeanette E;Decker, Paul A;Labussière, Marianne;Idbaih, Ahmed;Hoang-Xuan, Khe;Di Stefano, Anna-Luisa;Mokhtari, Karima;Delattre, Jean-Yves;Broderick, Peter;Galan, Pilar;Gousias, Konstantinos;Schramm, Johannes;Schoemaker, Minouk J;Fleming, Sarah J;Herms, Stefan;Heilmann, Stefanie;Nöthen, Markus M;Wichmann, Heinz-Erich;Schreiber, Stefan;Swerdlow, Anthony;Lathrop, Mark;Simon, Matthias;Sanson, Marc;Andersson, Ulrika;Rajaraman, Preetha;Chanock, Stephen;Linet, Martha;Wang, Zhaoming;Yeager, Meredith;Wiencke, John K;Hansen, Helen;McCoy, Lucie;Rice, Terri;Kosel, Matthew L;Sicotte, Hugues;Amos, Christopher I;Bernstein, Jonine L;Davis, Faith;Lachance, Dan;Lau, Ching;Merrell, Ryan T;Shildkraut, Joellen;Ali-Osman, Francis;Sadetzki, Siegal;Scheurer, Michael;Shete, Sanjay;Lai, Rose K;Claus, Elizabeth B;Olson, Sara H;Jenkins, Robert B;Houlston, Richard S;Bondy, Melissa L; Corporate Authors(s) : GliomaScan Consortium Published Date : March 27 2017 Source : Nat Genet. 49(5):789-794 URL : https://stacks.cdc.gov/view/cdc/47599 Melin, Beatrice S et al. (2017). Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. 49(5). Melin, Beatrice S et al. "Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors" 49, no. 5 (2017) Melin, Beatrice S et al. "Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors" vol. 49, no. 5, 2017 Export RIS Citation Information.

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Melin, Beatrice S ;

Barnholtz-Sloan, Jill S

March 27 2017 | Nat Genet. 49(5):789-794

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Genome-wide association studies (GWAS) have transformed our understanding of glioma susceptibility, but individual studies have had limited power to i...
A heritable missense polymorphism in CDKN2A confers strong risk of childhood acute lymphoblastic leukemia and is preferentially selected during clonal evolution

CITE Title : A heritable missense polymorphism in CDKN2A confers strong risk of childhood acute lymphoblastic leukemia and is preferentially selected during clonal evolution Personal Author(s) : Walsh, Kyle M.;de Smith, Adam J.;Hansen, Helen M.;Smirnov, Ivan V.;Gonseth, Semira;Endicott, Alyson A.;Xiao, Jianqiao;Rice, Terri;Fu, Cecilia H.;McCoy, Lucie S.;Lachance, Daniel H.;Eckel-Passow, Jeanette E.;Wiencke, John K.;Jenkins, Robert B.;Wrensch, Margaret R.;Ma, Xiaomei;Metayer, Catherine;Wiemels, Joseph L.; Published Date : Nov 2 2015 Source : Cancer Res. 75(22):4884-4894. URL : https://stacks.cdc.gov/view/cdc/36507 Walsh, Kyle M. et al. (2015). A heritable missense polymorphism in CDKN2A confers strong risk of childhood acute lymphoblastic leukemia and is preferentially selected during clonal evolution. 75(22). Walsh, Kyle M. et al. "A heritable missense polymorphism in CDKN2A confers strong risk of childhood acute lymphoblastic leukemia and is preferentially selected during clonal evolution" 75, no. 22 (2015) Walsh, Kyle M. et al. "A heritable missense polymorphism in CDKN2A confers strong risk of childhood acute lymphoblastic leukemia and is preferentially selected during clonal evolution" vol. 75, no. 22, 2015 Export RIS Citation Information.

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Walsh, Kyle M. ;

de Smith, Adam J.

Nov 2 2015 | Cancer Res. 75(22):4884-4894.

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Genome-wide association studies (GWAS) have identified SNPs in six genes that are associated with childhood acute lymphoblastic leukemia (ALL). A lead...
Adult Infiltrating Gliomas with WHO 2016 Integrated Diagnosis: Additional Prognostic Roles of ATRX and TERT

CITE Title : Adult Infiltrating Gliomas with WHO 2016 Integrated Diagnosis: Additional Prognostic Roles of ATRX and TERT Personal Author(s) : Pekmezci, Melike;Rice, Terri;Molinaro, Annette M.;Walsh, Kyle M.;Decker, Paul A.;Hansen, Helen;Sicotte, Hugues;Kollmeyer, Thomas M.;McCoy, Lucie S.;Sarkar, Gobinda;Perry, Arie;Giannini, Caterina;Tihan, Tarik;Berger, Mitchel S.;Wiemels, Joseph L.;Bracci, Paige M.;Eckel-Passow, Jeanette E.;Lachance, Daniel H.;Clarke, Jennifer;Taylor, Jennie W.;Luks, Tracy;Wiencke, John K.;Jenkins RB, Robert B.;Wrensch, Margaret R; Published Date : Mar 02 2017 Source : Acta Neuropathol. 133(6):1001-1016. URL : https://stacks.cdc.gov/view/cdc/45797 Pekmezci, Melike et al. (2017). Adult Infiltrating Gliomas with WHO 2016 Integrated Diagnosis: Additional Prognostic Roles of ATRX and TERT. 133(6). Pekmezci, Melike et al. "Adult Infiltrating Gliomas with WHO 2016 Integrated Diagnosis: Additional Prognostic Roles of ATRX and TERT" 133, no. 6 (2017) Pekmezci, Melike et al. "Adult Infiltrating Gliomas with WHO 2016 Integrated Diagnosis: Additional Prognostic Roles of ATRX and TERT" vol. 133, no. 6, 2017 Export RIS Citation Information.

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Pekmezci, Melike ;

Rice, Terri

Mar 02 2017 | Acta Neuropathol. 133(6):1001-1016.

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The "integrated diagnosis" for infiltrating gliomas in the 2016 revised World Health Organization (WHO) classification of tumors of the central nervou...