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Reference EntriesFull Text
Druley, Todd E
Journal title:American Men & Women of Science : A Biographical Directory of Today’s Leaders in Physical, Biological and Related Sciences: COO-DUQ, 2022, p.2999-2999
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Druley, Todd E
Journal title:American Men & Women of Science : A Biographical Directory of Today’s Leaders in Physical, Biological and Related Sciences: COO-DUQ, 2021, p.2983-2984
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ArticlesPeer ReviewedFull Text
Clonal haematopoiesis harbouring AML-associated mutations is ubiquitous in healthy adults
Author / Creator:Young, Andrew L. ; Challen, Grant A. ; Birmann, Brenda M. ; Druley, Todd E.
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2016-08, Vol.7 (1), p.12484-12484, Article 12484
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ArticlesPeer ReviewedFull Text
Integrated analysis of germline and somatic variants in ovarian cancer
Author / Creator: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. ; Goodfellow, Paul J. ; Raphael, Benjamin J. ; Wilson, Richard K. ; Ding, Li
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2014-01, Vol.5 (1), p.3156-3156, Article 3156
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Pediatric cancer risk in association with birth defects: A systematic review
Author / Creator:Johnson, Kimberly J. ; Lee, Jong Min ; Ahsan, Kazi ; Padda, Hannah ; Feng, Qianxi ; Partap, Sonia ; Fowler, Susan A. ; Druley, Todd E.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2017-07, Vol.12 (7), p.e0181246-e0181246
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ArticlesPeer ReviewedFull Text
Age-specific changes in genome-wide methylation enrich for Foxa2 and estrogen receptor alpha binding sites
Author / Creator:Uli, Nishanth ; Michelen-Gomez, Eduardo ; Ramos, Enrique I. ; Druley, Todd E.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2018-09, Vol.13 (9), p.e0203147-e0203147
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ArticlesPeer ReviewedFull Text
Error-corrected sequencing strategies enable comprehensive detection of leukemic mutations relevant for diagnosis and minimal residual disease monitoring
Author / Creator:Crowgey, Erin L. ; Mahajan, Nitin ; Wong, Wing Hing ; Gopalakrishnapillai, Anilkumar ; Barwe, Sonali P. ; Kolb, E. Anders ; Druley, Todd E.
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genomics, 2020-03, Vol.13 (1), p.32-32, Article 32
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ArticlesPeer ReviewedFull Text
Quantification of rare allelic variants from pooled genomic DNA
Author / Creator: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
Publisher:New York: Nature Publishing Group US
Journal title:Nature methods, 2009-04, Vol.6 (4), p.263-265
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ArticlesPeer ReviewedFull Text
KMT2A‐D pathogenicity, prevalence, and variation according to a population database
Author / Creator:Larson, Jenna K. ; Hunter‐Schlichting, DeVon N. ; Crowgey, Erin L. ; Mills, Lauren J. ; Druley, Todd E. ; Marcotte, Erin L.
Publisher:United States: John Wiley & Sons, Inc
Journal title:Cancer medicine (Malden, MA), 2023-03, Vol.12 (6), p.7234-7245
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ArticlesPeer ReviewedFull Text
Pooled Sequencing of Candidate Genes Implicates Rare Variants in the Development of Asthma Following Severe RSV Bronchiolitis in Infancy
Author / Creator: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
Publisher:United States: Public Library of Science
Journal title:PloS one, 2015-11, Vol.10 (11), p.e0142649-e0142649
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ArticlesPeer ReviewedFull Text
Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing
Author / Creator:Ramos, Enrique ; Levinson, Benjamin T ; Chasnoff, Sara ; Hughes, Andrew ; Young, Andrew L ; Thornton, Katherine ; Li, Allie ; Vallania, Francesco LM ; Province, Michael ; Druley, Todd E
Publisher:England: BioMed Central Ltd
Journal title:BMC genomics, 2012-12, Vol.13 (1), p.683-683, Article 683
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Role of TP53 mutations in the origin and evolution of therapy-related acute myeloid leukaemia
Author / Creator:Wong, Terrence N. ; Ramsingh, Giridharan ; Young, Andrew L. ; Miller, Christopher A. ; Touma, Waseem ; Welch, John S. ; Lamprecht, Tamara L. ; Shen, Dong ; Hundal, Jasreet ; Fulton, Robert S. ; Heath, Sharon ; Baty, Jack D. ; Klco, Jeffery M. ; Ding, Li ; Mardis, Elaine R. ; Westervelt, Peter ; DiPersio, John F. ; Walter, Matthew J. ; Graubert, Timothy A. ; Ley, Timothy J. ; Druley, Todd E. ; Link, Daniel C. ; Wilson, Richard K.
Publisher:London: Nature Publishing Group UK
Journal title:Nature (London), 2015-02, Vol.518 (7540), p.552-555
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ArticlesPeer ReviewedFull Text
Distal chromosome 16p11.2 duplications containing SH2B1 in patients with scoliosis
Author / Creator:Sadler, Brooke ; Haller, Gabe ; Antunes, Lilian ; Bledsoe, Xavier ; Morcuende, Jose ; Giampietro, Philip ; Raggio, Cathleen ; Miller, Nancy ; Kidane, Yared ; Wise, Carol A ; Amarillo, Ina ; Walton, Nephi ; Seeley, Mark ; Johnson, Darren ; Jenkins, Conner ; Jenkins, Troy ; Oetjens, Matthew ; Tong, R Spencer ; Druley, Todd E ; Dobbs, Matthew B ; Gurnett, Christina A
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2019-07, Vol.56 (7), p.427-433
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ArticlesPeer ReviewedFull Text
The Zebrafish Xenograft Platform—A Novel Tool for Modeling KSHV-Associated Diseases
Author / Creator: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.
Publisher:Switzerland: MDPI AG
Journal title:Viruses, 2019-12, Vol.12 (1), p.12
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ArticlesPeer ReviewedFull Text
Cardiac signaling genes exhibit unexpected sequence diversity in sporadic cardiomyopathy, revealing HSPB7 polymorphisms associated with disease
Author / Creator:Matkovich, Scot J. ; Van Booven, Derek J. ; Hindes, Anna ; Kang, Min Young ; Druley, Todd E. ; Vallania, Francesco L.M. ; Mitra, Robi D. ; Reilly, Muredach P. ; Cappola, Thomas P. ; Dorn, Gerald W.
Publisher:United States: American Society for Clinical Investigation
Journal title:The Journal of clinical investigation, 2010-01, Vol.120 (1), p.280-289
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Candidate gene resequencing to identify rare, pedigree-specific variants influencing healthy aging phenotypes in the long life family study
Author / Creator:Druley, Todd E. ; Wang, Lihua ; Lin, Shiow J. ; Lee, Joseph H. ; Zhang, Qunyuan ; Daw, E. Warwick ; Abel, Haley J. ; Chasnoff, Sara E. ; Ramos, Enrique I. ; Levinson, Benjamin T. ; Thyagarajan, Bharat ; Newman, Anne B. ; Christensen, Kaare ; Mayeux, Richard ; Province, Michael A.
Publisher:England: BioMed Central Ltd
Journal title:BMC geriatrics, 2016-04, Vol.16 (1), p.80-80, Article 80
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Germline Sequencing Identifies Rare Variants in Finnish Subjects with Familial Germ Cell Tumors
Author / Creator:Crowgey, Erin L ; Soini, Tea ; Shah, Nidhi ; Pauniaho, Satu-Liisa ; Lahdenne, Pekka ; Wilson, David B ; Heikinheimo, Markku ; Druley, Todd E
Publisher:New Zealand: Taylor & Francis Ltd
Journal title:Application of clinical genetics, 2020-01, Vol.13, p.127-137
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Commentary
Author / Creator:Druley, Todd E
Publisher:Washington: Oxford University Press
Journal title:Clinical chemistry (Baltimore, Md.), 2013-01, Vol.59 (1), p.50
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Commentary
Author / Creator:Druley, Todd E
Journal title:Clinical chemistry (Baltimore, Md.), 2013-01, Vol.59 (1), p.50-51
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KDM6A knockout in human iPSCs alters the genome-wide histone methylation profile at active and poised enhancers, activating expression of ectoderm gene expression pathways
Author / Creator:Maurya, Shailendra S ; Yang, Wei ; Zhang, Qiang ; Erdmann-Gilmore, Petra ; Bystry, Amelia ; Townsend, Reid ; Druley, Todd E
Publisher:Cold Spring Harbor: Cold Spring Harbor Laboratory Press
Journal title:bioRxiv, 2021-03
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Druley, Todd E

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Druley, Todd E

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

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Integrated analysis of germline and somatic variants in ovarian cancer

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

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

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

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Quantification of rare allelic variants from pooled genomic DNA

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

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

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

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Role of TP53 mutations in the origin and evolution of therapy-related acute myeloid leukaemia

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Distal chromosome 16p11.2 duplications containing SH2B1 in patients with scoliosis

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

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

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

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

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Commentary

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Commentary

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KDM6A knockout in human iPSCs alters the genome-wide histone methylation profile at active and poised enhancers, activating expression of ectoderm gene expression pathways

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