AuthorArranger automates formatting title pages and author affiliations for manuscript submissions

por Machiela, Mitchell J., Tobias, Geoffrey
Publicado 2022

GWAS is going to the dogs

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

LDexpress: an online tool for integrating population-specific linkage disequilibrium patterns with tissue-specific expression data

por Lin, Shu-Hong, Thakur, Rohit, Machiela, Mitchell J.
Publicado 2021

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

por Myers, Timothy A., Chanock, Stephen J., Machiela, Mitchell J.
Publicado 2020

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 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 2015

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 2021

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 2021

Genetic analyses identify evidence for a causal relationship between Ewing sarcoma and hernias

por Yang, Tianzhong, Mills, Lauren J., Hubbard, Aubrey K., Cao, Rui, Raduski, Andrew, Machiela, Mitchell J., Spector, Logan G.
Publicado 2023

Predictors of mosaic chromosome Y loss and associations with mortality in the UK Biobank

por Loftfield, Erikka, Zhou, Weiyin, Graubard, Barry I., Yeager, Meredith, Chanock, Stephen J., Freedman, Neal D., Machiela, Mitchell J.
Publicado 2018

Genetically predicted telomere length is associated with clonal somatic copy number alterations in peripheral leukocytes

por Brown, Derek W., Lin, Shu-Hong, Loh, Po-Ru, Chanock, Stephen J., Savage, Sharon A., Machiela, Mitchell J.
Publicado 2020

An investigation of the association of genetic susceptibility risk with somatic mutation burden in breast cancer

por Zhu, Bin, Mukherjee, Anwesha, Machiela, Mitchell J, Song, Lei, Hua, Xing, Shi, Jianxin, Garcia-Closas, Montserrat, Chanock, Stephen J, Chatterjee, Nilanjan
Publicado 2016

Mosaic chromosome Y loss is associated with alterations in blood cell counts in UK Biobank men

por Lin, Shu-Hong, Loftfield, Erikka, Sampson, Josh N., Zhou, Weiyin, Yeager, Meredith, Freedman, Neal D., Chanock, Stephen J., Machiela, Mitchell J.
Publicado 2020

Mosaic 13q14 deletions in peripheral leukocytes of non-hematologic cancer cases and healthy controls

por Machiela, Mitchell J., Zhou, Weiyin, Caporaso, Neil, Dean, Michael, Gapstur, Susan M., Goldin, Lynn, Stevens, Victoria L., Yeager, Meredith, Chanock, Stephen J.
Publicado 2016

Increase in power by obtaining 10 or more controls per case when type-1 error is small in large-scale association studies

por Katki, Hormuzd A., Berndt, Sonja I., Machiela, Mitchell J., Stewart, Douglas R., Garcia-Closas, Montserrat, Kim, Jung, Shi, Jianxin, Yu, Kai, Rothman, Nathaniel
Publicado 2023

Mosaic chromosome Y loss and testicular germ cell tumor risk

por Machiela, Mitchell J., Dagnall, Casey L., Pathak, Anand, Loud, Jennifer T., Chanock, Stephen J., Greene, Mark H., McGlynn, Katherine A., Stewart, Douglas R.
Publicado 2017

Integrating Clinical and Multiple Omics Data for Prognostic Assessment across Human Cancers

por Zhu, Bin, Song, Nan, Shen, Ronglai, Arora, Arshi, Machiela, Mitchell J., Song, Lei, Landi, Maria Teresa, Ghosh, Debashis, Chatterjee, Nilanjan, Baladandayuthapani, Veera, Zhao, Hongyu
Publicado 2017

Functional characterization of the 12p12.1 renal cancer-susceptibility locus implicates BHLHE41

por Bigot, Pierre, Colli, Leandro M., Machiela, Mitchell J., Jessop, Lea, Myers, Timothy A., Carrouget, Julie, Wagner, Sarah, Roberson, David, Eymerit, Caroline, Henrion, Daniel, Chanock, Stephen J.
Publicado 2016

Incident disease associations with mosaic chromosomal alterations on autosomes, X and Y chromosomes: insights from a phenome-wide association study in the UK Biobank

por Lin, Shu-Hong, Brown, Derek W., Rose, Brandon, Day, Felix, Lee, Olivia W., Khan, Sairah M., Hislop, Jada, Chanock, Stephen J., Perry, John R. B., Machiela, Mitchell J.
Publicado 2021

Different Pigmentation Risk Loci for High-Risk Monosomy 3 and Low-Risk Disomy 3 Uveal Melanomas

por Mobuchon, Lenha, Derrien, Anne-Céline, Houy, Alexandre, Verrier, Thibault, Pierron, Gaëlle, Cassoux, Nathalie, Milder, Maud, Deleuze, Jean-François, Boland, Anne, Scelo, Ghislaine, Cancel-Tassin, Géraldine, Cussenot, Olivier, Rodrigues, Manuel, Noirel, Josselin, Machiela, Mitchell J, Stern, Marc-Henri
Publicado 2021