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Publications

Filtres: Autor és Mukherjee, B  [Clear All Filters]
2011
Mukherjee B, Rennert G, Ahn J, Dishon S, Lejbkowicz F, Rennert HS, et al. High risk of colorectal and endometrial cancer in Ashkenazi families with the MSH2 A636P founder mutation. Gastroenterology. 2011;140(7):1919-26. Abstract
Boonstra PS, Mukherjee B, Taylor JM, Nilbert M, Moreno V, Gruber SB. Bayesian modeling for genetic anticipation in presence of mutational heterogeneity: a case study in Lynch syndrome. Biometrics. 2011;67(4):1627-37. Abstract
Vilar E, Bartnik CM, Stenzel SL, Raskin L, Ahn J, Moreno V, et al. MRE11 deficiency increases sensitivity to poly(ADP-ribose) polymerase inhibition in microsatellite unstable colorectal cancers. Cancer research. 2011;71(7):2632-42. Abstract
2010
Borràs E, Pineda M, Blanco I, Jewett EM, Wang F, Teulé A, et al. MLH1 founder mutations with moderate penetrance in Spanish Lynch syndrome families. Cancer research. 2010;70(19):7379-91. Abstract
2009
Zhang L, Mukherjee B, Hu B, Moreno V, Cooney KA. Semiparametric Bayesian modeling of random genetic effects in family-based association studies. Statistics in medicine. 2009;28(1):113-39.
2008
Mukherjee B, Ahn J, Gruber SB, Rennert G, Moreno V, Chatterjee N. Tests for gene-environment interaction from case-control data: a novel study of type I error, power and designs. Genetic epidemiology. 2008;32(7):615-26.
Aguado A, Guinó E, Mukherjee B, Sicras A, Serrat J, Acedo M, et al. Variability in prescription drug expenditures explained by adjusted clinical groups (ACG) case-mix: a cross-sectional study of patient electronic records in primary care. BMC health services research. 2008;8:53. Abstract
Zhang L, Mukherjee B, Ghosh M, Gruber S, Moreno V. Accounting for error due to misclassification of exposures in case-control studies of gene-environment interaction. Statistics in medicine. 2008;27(15):2756-83.