Detectable Clonal Mosaicism in the Human Genome

por Machiela, Mitchell J., Chanock, Stephen J.
Publicado em 2013

GWAS is going to the dogs

por Machiela, Mitchell J, Chanock, Stephen J
Publicado em 2014

Scanning for Clues to Better Use Selective Estrogen Receptor Modulators

por Machiela, Mitchell J, Chanock, Stephen J
Publicado no Cancer Discov (2013)

LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants

por Machiela, Mitchell J., Chanock, Stephen J.
Publicado no Bioinformatics (2015)

The Ageing Genome, Clonal Mosaicism and Chronic Disease

por Machiela, Mitchell J., Chanock, Stephen J.
Publicado no Curr Opin Genet Dev (2017)

LDassoc: an online tool for interactively exploring genome-wide association study results and prioritizing variants for functional investigation

por Machiela, Mitchell J, Chanock, Stephen J
Publicado no Bioinformatics (2018)

Why Y? Downregulation of Chromosome Y Genes Potentially Contributes to Elevated Cancer Risk

por Brown, Derek W, Machiela, Mitchell J
Publicado no J Natl Cancer Inst (2020)

LDlinkR: An R Package for Rapidly Calculating Linkage Disequilibrium Statistics in Diverse Populations

por Myers, Timothy A., Chanock, Stephen J., Machiela, Mitchell J.
Publicado no Front Genet (2020)

LDtrait: an online tool for identifying published phenotype associations in linkage disequilibrium

por Lin, Shu-Hong, Brown, Derek W., Machiela, Mitchell J.
Publicado no Cancer Res (2020)

Characterization of breakpoint regions of large structural autosomal mosaic events

por Machiela, Mitchell J, Jessop, Lea, Zhou, Weiyin, Yeager, Meredith, Chanock, Stephen J
Publicado no Hum Mol Genet (2017)

Genomic characterization of viral integration sites in HPV-related cancers

por Bodelon, Clara, Untereiner, Michael E., Machiela, Mitchell J., Vinokurova, Svetlana, Wentzensen, Nicolas
Publicado no Int J Cancer (2016)

Re-Ranking Sequencing Variants in the Post-GWAS Era for Accurate Causal Variant Identification

por Faye, Laura L., Machiela, Mitchell J., Kraft, Peter, Bull, Shelley B., Sun, Lei
Publicado em 2013

Limited evidence that cancer susceptibility regions are preferential targets for somatic mutation

por Machiela, Mitchell J., Ho, Brian M., Fisher, Victoria A., Hua, Xing, Chanock, Stephen J.
Publicado no Genome Biol (2015)

Burden of non-synonymous mutations among TCGA cancers and candidate immune checkpoint inhibitor responses

por Colli, Leandro M., Machiela, Mitchell J., Myers, Timothy, Jessop, Lea, Yu, Kai, Chanock, Stephen J.
Publicado no Cancer Res (2016)

Mosaic Y loss is moderately associated with solid tumor risk

por Loftfield, Erikka, Zhou, Weiyin, Yeager, Meredith, Chanock, Stephen J., Freedman, Neal D., Machiela, Mitchell J.
Publicado no Cancer Res (2018)

sparrpowR: a flexible R package to estimate statistical power to identify spatial clustering of two groups and its application

por Buller, Ian D., Brown, Derek W., Myers, Timothy A., Jones, Rena R., Machiela, Mitchell J.
Publicado no Int J Health Geogr (2021)

Evaluation of polygenic risk scores for predicting breast and prostate cancer risk

por Machiela, Mitchell J., Chen, Chia-Yen, Chen, Constance, Chanock, Stephen J., Hunter, David J., Kraft, Peter
Publicado em 2011

Detectable chromosome X mosaicism in males is rarely tolerated in peripheral leukocytes

por Zhou, Weiyin, Lin, Shu-Hong, Khan, Sairah M., Yeager, Meredith, Chanock, Stephen J., Machiela, Mitchell J.
Publicado no Sci Rep (2021)

Comparative international incidence of Ewing Sarcoma 1988-2012

por Spector, Logan G., Hubbard, Aubrey K., Diessner, Brandon J., Machiela, Mitchell J., Webber, Beau, Schiffman, Joshua D.
Publicado no Int J Cancer (2021)

Chromosome 17q12 variants contribute to risk of early-onset prostate cancer

por Levin, Albert M., Machiela, Mitchell J., Zuhlke, Kimberly A., Ray, Anna M., Cooney, Kathleen A., Douglas, Julie A.
Publicado em 2008