Works matching AU Druley, Todd E.

Results: 21

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

Published in:

Viruses (1999-4915), 2020, v. 12, n. 1, p. 12, doi. 10.3390/v12010012

By:

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.

Publication type:

Article

Commentary.

Published in:

Clinical Chemistry, 2013, v. 59, n. 1, p. 50, doi. 10.1373/clinchem.2012.192310

By:

Druley, Todd E.

Publication type:

Article

Parental Age and Risk of Infant Leukaemia: A Pooled Analysis.

Published in:

2017

By:

Marcotte, Erin L.;
Druley, Todd E.;
Johnson, Kimberly J.;
Richardson, Michaela;
Behren, Julie;
Mueller, Beth A.;
Carozza, Susan;
McLaughlin, Colleen;
Chow, Eric J.;
Reynolds, Peggy;
Spector, Logan G.;
von Behren, Julie

Publication type:

journal article

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

Published in:

BMC Medical Genomics, 2020, v. 13, n. 1, p. 1, doi. 10.1186/s12920-020-0671-8

By:

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

Publication type:

Article

Cardiac signaling genes exhibit unexpected sequence diversity in sporadic cardiomyopathy, revealing HSPB7 polymorphisms associated with disease.

Published in:

2010

By:

Matkovich, Scot J.;
Van Booven, Derek J.;
Hindes, Anna;
Mm Young Kang;
Druley, Todd E.;
Vallania, Francesco L. M.;
Mitra, Robi D.;
Reilly, Muredach P.;
Cappola, Thomas P.;
Dorn II, Gerald W.;
Kang, Min Young;
Dorn, Gerald W 2nd

Publication type:

journal article

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

Published in:

PLoS ONE, 2017, v. 12, n. 7, p. 1, doi. 10.1371/journal.pone.0181246

By:

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

Publication type:

Article

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

Published in:

BMC Genomics, 2012, v. 13, n. 1, p. 683, doi. 10.1186/1471-2164-13-683

By:

Ramos, Enrique;
Levinson, Benjamin T.;
Chasnoff, Sara;
Hughes, Andrew;
Young, Andrew L.;
Thornton, Katherine;
Li, Allie;
Vallania, Francesco L. M.;
Province, Michael;
Druley, Todd E.

Publication type:

Article

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

Published in:

Cancer Medicine, 2023, v. 12, n. 6, p. 7234, doi. 10.1002/cam4.5443

By:

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

Publication type:

Article

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

Published in:

Nature Communications, 2016, v. 7, n. 8, p. 12484, doi. 10.1038/ncomms12484

By:

Young, Andrew L.;
Challen, Grant A.;
Birmann, Brenda M.;
Druley, Todd E.

Publication type:

Article

Integrated analysis of germline and somatic variants in ovarian cancer.

Published in:

Nature Communications, 2014, v. 5, n. 1, p. 3156, doi. 10.1038/ncomms4156

By:

Kanchi, Krishna L.;
Johnson, Kimberly J.;
Lu, Charles;
McLellan, Michael D.;
Leiserson, Mark D. M.;
Wendl, Michael C.;
Zhang, Qunyuan;
Koboldt, Daniel C.;
Xie, Mingchao;
Kandoth, Cyriac;
McMichael, Joshua F.;
Wyczalkowski, Matthew A.;
Larson, David E.;
Schmidt, Heather K.;
Miller, Christopher A.;
Fulton, Robert S.;
Spellman, Paul T.;
Mardis, Elaine R.;
Druley, Todd E.;
Graubert, Timothy A.

Publication type:

Article

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

Published in:

Application of Clinical Genetics, 2020, v. 13, p. 127, doi. 10.2147/TACG.S245093

By:

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

Publication type:

Article

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

Published in:

PLoS ONE, 2018, v. 13, n. 9, p. 1, doi. 10.1371/journal.pone.0203147

By:

Uli, Nishanth;
Michelen-Gomez, Eduardo;
Ramos, Enrique I.;
Druley, Todd E.

Publication type:

Article

Candidate gene resequencing to identify rare, pedigree-specific variants influencing healthy aging phenotypes in the long life family study.

Published in:

2016

By:

Druley, Todd E.;
Lihua Wang;
Lin, Shiow J.;
Lee, Joseph H.;
Qunyuan Zhang;
Warwick Daw, E.;
Abel, Haley J.;
Chasnoff, Sara E.;
Ramos, Enrique I.;
Levinson, Benjamin T.;
Thyagarajan, Bharat;
Newman, Anne B.;
Christensen, Kaare;
Mayeux, Richard;
Province, Michael A.;
Wang, Lihua;
Zhang, Qunyuan;
Daw, E Warwick

Publication type:

journal article

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

Published in:

Nucleic Acids Research, 2014, v. 42, n. 10, p. e82, doi. 10.1093/nar/gku218

By:

Alvarado, David M.;
Yang, Ping;
Druley, Todd E.;
Lovett, Michael;
Gurnett, Christina A.

Publication type:

Article

Congenital neurodevelopmental anomalies in pediatric and young adult cancer.

Published in:

American Journal of Medical Genetics. Part A, 2017, v. 173, n. 10, p. 2670, doi. 10.1002/ajmg.a.38387

By:

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

Publication type:

Article

Quantification of rare allelic variants from pooled genomic DNA.

Published in:

Nature Methods, 2009, v. 6, n. 4, p. 263, doi. 10.1038/nmeth.1307

By:

Druley, Todd E.;
Vallania, Francesco L. M.;
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.

Publication type:

Article

Pooled Sequencing of Candidate Genes Implicates Rare Variants in the Development of Asthma Following Severe RSV Bronchiolitis in Infancy.

Published in:

PLoS ONE, 2015, v. 10, n. 11, p. 1, doi. 10.1371/journal.pone.0142649

By:

Torgerson, Dara G.;
Giri, Tusar;
Druley, Todd E.;
Zheng, Jie;
Huntsman, Scott;
Seibold, Max A.;
Young, Andrew L.;
Schweiger, Toni;
Yin-Declue, Huiqing;
Sajol, Geneline D.;
Schechtman, Kenneth B;
Hernandez, Ryan D.;
Randolph, Adrienne G.;
Bacharier, Leonard B.;
Castro, Mario

Publication type:

Article

Engraftment of rare, pathogenic donor hematopoietic mutations in unrelated hematopoietic stem cell transplantation.

Published in:

Science Translational Medicine, 2020, v. 12, n. 526, p. 1, doi. 10.1126/scitranslmed.aax6249

By:

Wong, Wing Hing;
Bhatt, Sima;
Trinkaus, Kathryn;
Pusic, Iskra;
Elliott, Kevin;
Mahajan, Nitin;
Wan, Fei;
Switzer, Galen E.;
Confer, Dennis L.;
DiPersio, John;
Pulsipher, Michael A.;
Shah, Nirali N.;
Sees, Jennifer;
Bystry, Amelia;
Blundell, Jamie R.;
Shaw, Bronwen E.;
Druley, Todd E.

Publication type:

Article

Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 7, p. 1165, doi. 10.1093/hmg/ddp587

By:

Gurnett, Christina A.;
Desruisseau, David M.;
McCall, Kevin;
Choi, Ryan;
Meyer, Zachary I.;
Talerico, Michael;
Miller, Sara E.;
Ju, Jeong-Sun;
Pestronk, Alan;
Connolly, Anne M.;
Druley, Todd E.;
Weihl, Conrad C.;
Dobbs, Mathew B.

Publication type:

Article

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

Published in:

Epigenetics, 2022, v. 17, n. 2, p. 220, doi. 10.1080/15592294.2021.1954780

By:

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.

Publication type:

Article

Adaptation of the targeted capture Methyl-Seq platform for the mouse genome identifies novel tissue-specific DNA methylation patterns of genes involved in neurodevelopment.

Published in:

Epigenetics, 2015, v. 10, n. 7, p. 581, doi. 10.1080/15592294.2015.1045179

By:

Hing, Benjamin;
Ramos, Enrique;
Braun, Patricia;
McKane, Melissa;
Jancic, Dubravka;
Tamashiro, Kellie L K;
Lee, Richard S;
Michaelson, Jacob J;
Druley, Todd E;
Potash, James B

Publication type:

Article