Age-specific changes in genome-wide methylation enrich for Foxa2 and estrogen receptor alpha binding sites

por Uli, Nishanth, Michelen-Gomez, Eduardo, Ramos, Enrique I., Druley, Todd E.
Publicado 2018

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER

por Vallania, Francesco, Ramos, Enrique, Cresci, Sharon, Mitra, Robi D., Druley, Todd E.
Publicado 2012

Clonal haematopoiesis harbouring AML-associated mutations is ubiquitous in healthy adults

por Young, Andrew L., Challen, Grant A., Birmann, Brenda M., Druley, Todd E.
Publicado 2016

Rare Event Detection Using Error-corrected DNA and RNA Sequencing

por Wong, Wing H., Tong, R. Spencer, Young, Andrew L., Druley, Todd E.
Publicado 2018

Clonal hematopoiesis and risk of acute myeloid leukemia

por Young, Andrew L., Tong, R. Spencer, Birmann, Brenda M., Druley, Todd E.
Publicado 2019

Multiplexed direct genomic selection (MDiGS): a pooled BAC capture approach for highly accurate CNV and SNP/INDEL detection

por Alvarado, David M., Yang, Ping, Druley, Todd E., Lovett, Michael, Gurnett, Christina A.
Publicado 2014

Late Toxicity of a Novel Allogeneic Stem Cell Transplant Using Single Fraction Total Body Irradiation for Hematologic Malignancies in Children

por Madden, Lisa M., Ngwube, Alexander I., Shenoy, Shalini, Druley, Todd E., Hayashi, Robert J.
Publicado 2015

Strong concordance between RNA structural and single nucleotide variants identified via next generation sequencing techniques in primary pediatric leukemia and patient-derived xeno...

por Barwe, Sonali P., Gopalakrisnapillai, Anilkumar, Mahajan, Nitin, Druley, Todd E., Kolb, E. Anders, Crowgey, Erin L.
Publicado 2020

Quantifying ultra-rare pre-leukemic clones via targeted error-corrected sequencing

por Young, A L, Wong, T N, Hughes, A E O, Heath, S E, Ley, T J, Link, D C, Druley, T E
Publicado 2015

Congenital neurodevelopmental anomalies in pediatric and young adult cancer

por Wong‐Siegel, Jeannette R., Johnson, Kimberly J., Gettinger, Katie, Cousins, Nicole, McAmis, Nicole, Zamarione, Ashley, Druley, Todd E.
Publicado 2017

Error-corrected sequencing strategies enable comprehensive detection of leukemic mutations relevant for diagnosis and minimal residual disease monitoring

por Crowgey, Erin L., Mahajan, Nitin, Wong, Wing Hing, Gopalakrishnapillai, Anilkumar, Barwe, Sonali P., Kolb, E. Anders, Druley, Todd E.
Publicado 2020

KMT2A‐D pathogenicity, prevalence, and variation according to a population database

por Larson, Jenna K., Hunter‐Schlichting, DeVon N., Crowgey, Erin L., Mills, Lauren J., Druley, Todd E., Marcotte, Erin L.
Publicado 2022

Pediatric cancer risk in association with birth defects: A systematic review

por Johnson, Kimberly J., Lee, Jong Min, Ahsan, Kazi, Padda, Hannah, Feng, Qianxi, Partap, Sonia, Fowler, Susan A., Druley, Todd E.
Publicado 2017

Germline Sequencing Identifies Rare Variants in Finnish Subjects with Familial Germ Cell Tumors

por Crowgey, Erin L, Soini, Tea, Shah, Nidhi, Pauniaho, Satu-Liisa, Lahdenne, Pekka, Wilson, David B, Heikinheimo, Markku, Druley, Todd E
Publicado 2020

Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing

por Ramos, Enrique, Levinson, Benjamin T, Chasnoff, Sara, Hughes, Andrew, Young, Andrew L, Thornton, Katherine, Li, Allie, Vallania, Francesco LM, Province, Michael, Druley, Todd E
Publicado 2012

Loss of KMT2C reprograms the epigenomic landscape in hPSCs resulting in NODAL overexpression and a failure of hemogenic endothelium specification

por Maurya, Shailendra, Yang, Wei, Tamai, Minori, Zhang, Qiang, Erdmann-Gilmore, Petra, Bystry, Amelia, Martins Rodrigues, Fernanda, Valentine, Mark C., Wong, Wing H, Townsend, Reid, Druley, Todd E.
Publicado 2021

Excess congenital non-synonymous variation in leukemia-associated genes in MLL− infant leukemia: a Children's Oncology Group report

por Valentine, M C, Linabery, A M, Chasnoff, S, Hughes, A E O, Mallaney, C, Sanchez, N, Giacalone, J, Heerema, N A, Hilden, J M, Spector, L G, Ross, J A, Druley, T E
Publicado 2014

The Zebrafish Xenograft Platform—A Novel Tool for Modeling KSHV-Associated Diseases

por Pringle, Eric S., Wertman, Jaime, Melong, Nicole, Coombs, Andrew J., Young, Andrew L., O’Leary, David, Veinotte, Chansey, Robinson, Carolyn-Ann, Ha, Michael N., Dellaire, Graham, Druley, Todd E., McCormick, Craig, Berman, Jason N.
Publicado 2019

Quantification of rare allelic variants from pooled genomic DNA

por Druley, Todd E, Vallania, Francesco LM, Wegner, Daniel J, Varley, Katherine E, Knowles, Olivia L, Bonds, Jacqueline A, Robison, Sarah W, Doniger, Scott W, Hamvas, Aaron, Cole, F. Sessions, Fay, Justin C, Mitra, Robi D
Publicado 2009

Dnmt3a Regulates T-cell Development and Suppresses T-ALL Transformation

por Kramer, Ashley C., Kothari, Alok, Wilson, W. Casey, Celik, Hamza, Nikitas, John, Mallaney, Cates, Ostrander, Elizabeth L., Eultgen, Elizabeth, Martens, Andrew, Valentine, Mark C., Young, Andrew L., Druley, Todd E., Figueroa, Maria E., Zhang, Bo, Challen, Grant A.
Publicado 2017