Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Julio Gonzalez-Maya"'
Autor:
Ivo S. Muskens, Elad Ziv, Vijay Ramaswamy, Jill S. Barnholtz-Sloan, Joseph L. Wiemels, Cassie Kline, Adam J. de Smith, Francis Ali-Osman, Libby M. Morimoto, Quinn T. Ostrom, Kyle M. Walsh, Melissa L. Bondy, Donglei Hu, Chenan Zhang, Sharon J. Diskin, Catherine Metayer, Zalman Vaksman, Helen M. Hansen, Hakon Hakonarson, Kruchko C, Julio Gonzalez-Maya, Michael D. Taylor
Publikováno v:
Neuro Oncol
Neuro-oncology, vol 22, iss 11
Neuro-oncology, vol 22, iss 11
BackgroundEpendymoma is a histologically defined central nervous system tumor most commonly occurring in childhood. Population-level incidence differences by race/ethnicity are observed, with individuals of European ancestry at highest risk. We aimed
Autor:
Alyson A. Endicott, Adam J. de Smith, John S. Witte, Joseph L. Wiemels, Ivan Smirnov, Kyle M. Walsh, Chenan Zhang, Julio Gonzalez-Maya, Catherine Metayer, Libby M. Morimoto, Helen M. Hansen
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention. 27:1151-1158
Background: The genetic etiology of osteosarcoma remains poorly understood despite the publication of a genome-wide association study. Association between HLA genetic variants and risk of several cancers has been observed, but HLA variation is not we
Autor:
Joseph L. Wiemels, Helen M. Hansen, Alyson A. Endicott, Kyle M. Walsh, Julio Gonzalez-Maya, Qingyi Wei, Chenan Zhang, Catherine Metayer, William C. Eward, Libby M. Morimoto, Ivan Smirnov, Adam J. de Smith
Publikováno v:
Cancer. 124:3742-3752
Background Although increased height has been associated with osteosarcoma risk in previous epidemiologic studies, to the authors' knowledge the relative contribution of stature during different developmental timepoints remains unclear. Furthermore,
Autor:
Qingyi Wei, Helen M. Hansen, Joseph L. Wiemels, Eleanor C. Semmes, Catherine Metayer, Jillian H. Hurst, Kyle M. Walsh, Chenan Zhang, Libby M. Morimoto, William C. Eward, Julio Gonzalez-Maya, Adam J. de Smith, Suzanne Bartholf DeWitt
Publikováno v:
Bone
Osteosarcoma, a malignant primary bone tumor most commonly diagnosed in children and adolescents, has a poorly understood genetic etiology. Genome-wide association studies (GWAS) and candidate-gene analyses have identified putative risk variants in s
Autor:
Kyle M. Walsh, Julio Gonzalez-Maya, Chenan Zhang, Joseph L. Wiemels, Ivan Smirnov, Helen M. Hansen
Publikováno v:
Neuro-Oncology. 20:vi80-vi80
SNPs identified by previous GWAS can serve as instrumental variables for exposures of interest using a process known as Mendelian randomization. We sought to identify risk factors for childhood ependymoma using a Mendelian randomization approach. We