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Genetic determinants of childhood and adult height associated with osteosarcoma risk

CITE Title : Genetic determinants of childhood and adult height associated with osteosarcoma risk Personal Author(s) : Zhang, Chenan;Morimoto, Libby M.;de Smith, Adam J.;Hansen, Helen M.;Gonzalez-Maya, Julio;Endicott, Alyson A.;Smirnov, Ivan V.;Metayer, Catherine;Wei, Qingyi;Eward, William C.;Wiemels, Joseph L.;Walsh, Kyle M.; Published Date : October 12 2018 Source : Cancer. 124(18):3742-3752 URL : https://stacks.cdc.gov/view/cdc/60318 Zhang, Chenan et al. (2018). Genetic determinants of childhood and adult height associated with osteosarcoma risk. 124(18). Zhang, Chenan et al. "Genetic determinants of childhood and adult height associated with osteosarcoma risk" 124, no. 18 (2018) Zhang, Chenan et al. "Genetic determinants of childhood and adult height associated with osteosarcoma risk" vol. 124, no. 18, 2018 Export RIS Citation Information.

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Zhang, Chenan ;

Morimoto, Libby M.

October 12 2018 | Cancer. 124(18):3742-3752

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Background:Although increased height has been associated with osteosarcoma risk in previous epidemiologic studies, the relative contribution of statur...
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...
Germline polymorphisms in myeloid-associated genes are not associated with survival in glioma patients

CITE Title : Germline polymorphisms in myeloid-associated genes are not associated with survival in glioma patients Personal Author(s) : Jacobs, Daniel I.;Liu, Yanhong;Gabrusiewicz, Konrad;Tsavachidis, Spiridon;Armstrong, Georgina N.;Zhou, Renke;Wei, Jun;Ivan, Cristina;Calin, George;Molinaro, Annette M.;Rice, Terri;Bracci, Paige M.;Hansen, Helen M.;Wiencke, John K.;Wrensch, Margaret R.;Heimberger, Amy B.;Bondy, Melissa L.; Published Date : Sep 30 2017 Source : J Neurooncol. 136(1):33-39 URL : https://stacks.cdc.gov/view/cdc/61782 Jacobs, Daniel I. et al. (2017). Germline polymorphisms in myeloid-associated genes are not associated with survival in glioma patients. 136(1). Jacobs, Daniel I. et al. "Germline polymorphisms in myeloid-associated genes are not associated with survival in glioma patients" 136, no. 1 (2017) Jacobs, Daniel I. et al. "Germline polymorphisms in myeloid-associated genes are not associated with survival in glioma patients" vol. 136, no. 1, 2017 Export RIS Citation Information.

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Jacobs, Daniel I. ;

Liu, Yanhong

Sep 30 2017 | J Neurooncol. 136(1):33-39

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Immune cells of myeloid origin, including microglia, macrophages, and myeloid-derived suppressor cells adopt immunosuppressive phenotypes that support...
Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome

CITE Title : Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome Personal Author(s) : de Smith, Adam J.;Walsh, Kyle M.;Morimoto, Libby M.;Francis, Stephen S.;Hansen, Helen M.;Jeon, Soyoung;Gonseth, Semira;Chen, Minhui;Sun, Hanxiao;Luna-Fineman, Sandra;Antillón, Federico;Girón, Verónica;Kang, Alice Y.;Smirnov, Ivan;Shao, Xiaorong;Whitehead, Todd P.;Barcellos, Lisa F.;Jolly, Kent W.;Healy, Jasmine;Laverdière, Caroline;Sinnett, Daniel;Taub, Jeffrey W.;Birch, Jillian M.;Thompson, Pamela D.;Pombo-de-Oliveira, Maria S.;Spector, Logan G.;DeWan, Andrew T.;Mueller, Beth A.;Chiang, Charleston;Metayer, Catherine;Ma, Xiaomei;Wiemels, Joseph L.; Published Date : July 11 2019 Source : Leukemia. 33(11):2746-2751 URL : https://stacks.cdc.gov/view/cdc/83099 de Smith, Adam J. et al. (2019). Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome. 33(11). de Smith, Adam J. et al. "Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome" 33, no. 11 (2019) de Smith, Adam J. et al. "Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome" vol. 33, no. 11, 2019 Export RIS Citation Information.

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de Smith, Adam J. ;

Walsh, Kyle M.

July 11 2019 | Leukemia. 33(11):2746-2751

No Description
Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk

CITE Title : Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk Personal Author(s) : Walsh, Kyle M.;Codd, Veryan;Smirnov, Ivan V.;Rice, Terri;Decker, Paul A.;Hansen, Helen M.;Kollmeyer, Thomas;Kosel, Matthew L.;Molinaro, Annette M.;McCoy, Lucie S.;Bracci, Paige M.;Cabriga, Belinda S.;Pekmezci, Melike;Zheng, Shichun;Wiemels, Joseph L.;Pico, Alexander R.;Tihan, Tarik;Berger, Mitchell S.;Chang, Susan M.;Prados, Michael D.;Lachance, Daniel H.;O’Neill, Brian P.;Sicotte, Hugues;Eckel-Passow, Jeanette E.;van der Harst, Pim;Wiencke, John K.;Samani, Nilesh J.;Jenkins, Robert B.;Wrensch, Margaret R.; Corporate Authors(s) : ENGAGE Consortium Telomere Group Published Date : 7 2014;7-2014; Source : Nat Genet. 46(7):731-735 URL : https://stacks.cdc.gov/view/cdc/27881 Walsh, Kyle M. et al. (2014). Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk. 46(7). Walsh, Kyle M. et al. "Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk" 46, no. 7 (2014) Walsh, Kyle M. et al. "Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk" vol. 46, no. 7, 2014 Export RIS Citation Information.

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Walsh, Kyle M. ;

Codd, Veryan

7 2014 | Nat Genet. 46(7):731-735

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Glioma, the most common central nervous system cancer in adults, has poor prognosis. Here we identify a new SNP associated with glioma risk, rs1920116...
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...
SSBP2 variants are associated with survival in glioblastoma patients

CITE Title : SSBP2 variants are associated with survival in glioblastoma patients Personal Author(s) : Xiao, Yuanyuan;Decker, Paul A.;Rice, Terri;McCoy, Lucie S.;Smirnov, Ivan;Patoka, Joseph S.;Hansen, Helen M.;Wiemels, Joe L.;Tihan, Tarik;Prados, Michael D.;Chang, Susan M.;Berger, Mitchel S.;Kosel, Matthew L.;Fridley, Brooke L.;Lachance, Daniel H.;O’Neill, Brian Patrick;Buckner, Jan C.;Thompson, Reid C.;Nabors, L. B.;Olson, Jeffrey J.;Brem, Steve;Madden, Melissa H.;Browning, James E.;Wiencke, John K.;Egan, Kathleen M.;Jenkins, Robert B.;Wrensch, Margaret R.; Published Date : 6 1 2012;6-1-; Source : Clin Cancer Res. 18(11):3154-3162 URL : https://stacks.cdc.gov/view/cdc/33534 Xiao, Yuanyuan et al. (2012). SSBP2 variants are associated with survival in glioblastoma patients. 18(11). Xiao, Yuanyuan et al. "SSBP2 variants are associated with survival in glioblastoma patients" 18, no. 11 (2012) Xiao, Yuanyuan et al. "SSBP2 variants are associated with survival in glioblastoma patients" vol. 18, no. 11, 2012 Export RIS Citation Information.

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Xiao, Yuanyuan ;

Decker, Paul A.

6 1 2012 | Clin Cancer Res. 18(11):3154-3162

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PurposeGlioblastoma is a devastating, incurable disease with few known prognostic factors. Here we present the first genome-wide survival and validati...
Age-specific genome-wide association study in glioblastoma identifies increased proportion of ‘lower grade glioma’-like features associated with younger age

CITE Title : Age-specific genome-wide association study in glioblastoma identifies increased proportion of ‘lower grade glioma’-like features associated with younger age Personal Author(s) : Ostrom, Quinn T.;Kinnersley, Ben;Armstrong, Georgina;Rice, Terri;Chen, Yanwen;Wiencke, John K.;McCoy, Lucie S.;Hansen, Helen M.;Amos, Christopher I.;Bernstein, Jonine L.;Claus, Elizabeth B.;Eckel-Passow, Jeanette E.;Il’yasova, Dora;Johansen, Christoffer;Lachance, Daniel H.;Lai, Rose K.;Merrell, Ryan T.;Olson, Sara H.;Sadetzki, Siegal;Schildkraut, Joellen M.;Shete, Sanjay;Rubin, Joshua B.;Andersson, Ulrika;Rajaraman, Preetha;Chanock, Stephen J.;Linet, Martha S.;Wang, Zhaoming;Yeager, Meredith;Houlston, Richard S.;Jenkins, Robert B.;Wrensch, Margaret R.;Melin, Beatrice;Bondy, Melissa L.;Barnholtz-Sloan, Jill. S.; Published Date : 11 15 2018;11-15-; Source : Int J Cancer. 143(10):2359-2366 URL : https://stacks.cdc.gov/view/cdc/60142 Ostrom, Quinn T. et al. (2018). Age-specific genome-wide association study in glioblastoma identifies increased proportion of ‘lower grade glioma’-like features associated with younger age. 143(10). Ostrom, Quinn T. et al. "Age-specific genome-wide association study in glioblastoma identifies increased proportion of ‘lower grade glioma’-like features associated with younger age" 143, no. 10 (2018) Ostrom, Quinn T. et al. "Age-specific genome-wide association study in glioblastoma identifies increased proportion of ‘lower grade glioma’-like features associated with younger age" vol. 143, no. 10, 2018 Export RIS Citation Information.

:

Ostrom, Quinn T. ;

Kinnersley, Ben

11 15 2018 | Int J Cancer. 143(10):2359-2366

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Glioblastoma (GBM) is the most common malignant brain tumor in the United States. Incidence of GBM increases with age, and younger age-at-diagnosis is...
BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemia

CITE Title : BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemia Personal Author(s) : de Smith, Adam J.;Walsh, Kyle M.;Francis, Stephen S.;Zhang, Chenan;Hansen, Helen M.;Smirnov, Ivan;Morimoto, Libby;Whitehead, Todd P.;Kang, Alice;Shao, Xiaorong;Barcellos, Lisa F.;McKean-Cowdin, Roberta;Zhang, Luoping;Fu, Cecilia;Wang, Rong;Yu, Herbert;Hoh, Josephine;Dewan, Andrew T.;Metayer, Catherine;Ma, Xiaomei;Wiemels, Joseph L.; Published Date : 12 01 2018;12-01-; Source : Int J Cancer. 143(11):2647-2658 URL : https://stacks.cdc.gov/view/cdc/60718 de Smith, Adam J. et al. (2018). BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemia. 143(11). de Smith, Adam J. et al. "BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemia" 143, no. 11 (2018) de Smith, Adam J. et al. "BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemia" vol. 143, no. 11, 2018 Export RIS Citation Information.

:

de Smith, Adam J. ;

Walsh, Kyle M.

12 01 2018 | Int J Cancer. 143(11):2647-2658

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Genome-wide association studies of childhood acute lymphoblastic leukemia (ALL) have identified regions of association at PIP4K2A and upstream of BMI1...
Common genetic variation and risk of osteosarcoma in a multi-ethnic pediatric and adolescent population

CITE Title : Common genetic variation and risk of osteosarcoma in a multi-ethnic pediatric and adolescent population Personal Author(s) : Zhang, Chenan;Hansen, Helen M.;Semmes, Eleanor C.;Gonzalez-Maya, Julio;Morimoto, Libby;Wei, Qingyi;Eward, William C.;DeWitt, Suzanne B.;Hurst, Jillian H.;Metayer, Catherine;de Smith, Adam J.;Wiemels, Joseph L.;Walsh, Kyle M.; Published Date : 1 2020;1-2020; Source : Bone. 130:115070 URL : https://stacks.cdc.gov/view/cdc/149754 Zhang, Chenan et al. (2020). Common genetic variation and risk of osteosarcoma in a multi-ethnic pediatric and adolescent population. 130 Zhang, Chenan et al. "Common genetic variation and risk of osteosarcoma in a multi-ethnic pediatric and adolescent population" 130 (2020) Zhang, Chenan et al. "Common genetic variation and risk of osteosarcoma in a multi-ethnic pediatric and adolescent population" vol. 130, 2020 Export RIS Citation Information.

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Zhang, Chenan ;

Hansen, Helen M.

1 2020 | Bone. 130:115070

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Osteosarcoma, a malignant primary bone tumor most commonly diagnosed in children and adolescents, has a poorly understood genetic etiology. Genome-wid...