Variation at 10p12.2 and 10p14 influences risk of childhood b-cell acute lymphoblastic leukemia and phenotype
In press
Migliorini G, Fiege B, Hosking FJ, et al. Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype. Blood. 2013. In press.
Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia
Yang JJ, Cheng C, Yang W, et al. Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. JAMA. 2009;301(4):393-403.
Patterns of leukemia incidence in the united states by subtype and demographic characteristics, 1997-2002
Yamamoto JF, Goodman MT. Patterns of leukemia incidence in the United States by subtype and demographic characteristics, 1997-2002. Cancer Causes Control. 2008;19(4):379-390.
Racial and ethnic disparities in survival of us children with acute lymphoblastic leukemia: Evidence from the seer database 1988-2008
Goggins WB, Lo FF. Racial and ethnic disparities in survival of US children with acute lymphoblastic leukemia: evidence from the SEER database 1988-2008. Cancer Causes Control. 2012;23(5):737-743.
Novel childhood all susceptibility locus bmi1-pip4k2a is specifically associated with the hyperdiploid subtype
Walsh KM, de Smith AJ, Chokkalingam AP, et al. Novel childhood ALL susceptibility locus BMI1-PIP4K2A is specifically associated with the hyperdiploid subtype. Blood. 2013;121(23):4808-4809.
Associations between genome-wide native american ancestry, known risk alleles and b-cell all risk in hispanic children
published online ahead of print April 25, 2013
Walsh KM, Chokkalingam AP, Hsu LI, et al. Associations between genome-wide Native American ancestry, known risk alleles and B-cell ALL risk in Hispanic children [published online ahead of print April 25, 2013]. Leukemia.