Todd E Druley

Todd E Druley

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Todd E Druley

Todd E Druley

Publications by authors named "Todd E Druley"

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28Publications

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

PLoS One 2018 26;13(9):e0203147. Epub 2018 Sep 26.

Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, Missouri, United States of America.

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September 2018

Rare Event Detection Using Error-corrected DNA and RNA Sequencing.

J Vis Exp 2018 08 3(138). Epub 2018 Aug 3.

Department of Pediatrics, Division of Hematology and Oncology, Washington University School of Medicine; Center for Genome Sciences and Systems Biology, Washington University School of Medicine;

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August 2018

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

Paediatr Perinat Epidemiol 2017 11 22;31(6):563-572. Epub 2017 Sep 22.

Division of Epidemiology & Clinical Research, Department of Pediatrics, University of Minnesota, Minneapolis, MN.

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November 2017

Congenital neurodevelopmental anomalies in pediatric and young adult cancer.

Am J Med Genet A 2017 Oct 29;173(10):2670-2679. Epub 2017 Aug 29.

Division of Hematology and Oncology, Department of Pediatrics, Washington University School of Medicine, Saint Louis, Missouri.

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October 2017

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

PLoS One 2017 27;12(7):e0181246. Epub 2017 Jul 27.

Department of Pediatrics, Washington University School of Medicine, Washington University in St. Louis, St. Louis, Missouri, United States of America.

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September 2017

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

Nat Commun 2016 08 22;7:12484. Epub 2016 Aug 22.

Department of Pediatrics, Division of Hematology and Oncology, Washington University School of Medicine, Saint Louis, Missouri 63108, USA.

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August 2016

Integrated analysis of germline and somatic variants in ovarian cancer.

Nat Commun 2014 ;5:3156

1] The Genome Institute, Washington University, St. Louis, Missouri 63108, USA [2] Department of Genetics, Washington University, St. Louis, Missouri 63108, USA [3] Siteman Cancer Center, Washington University, St. Louis, Missouri 63108, USA [4] Department of Medicine, Washington University, St. Louis, Missouri 63108, USA.

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March 2016

Late toxicity of a novel allogeneic stem cell transplant using single fraction total body irradiation for hematologic malignancies in children.

J Pediatr Hematol Oncol 2015 Mar;37(2):e94-e101

Division of Pediatric Hematology-Oncology, Washington University School of Medicine, St Louis, MO.

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March 2015

The cyclic AMP pathway is a sex-specific modifier of glioma risk in type I neurofibromatosis patients.

Cancer Res 2015 Jan 7;75(1):16-21. Epub 2014 Nov 7.

Division of Pediatric Hematology/Oncology, Department of Pediatrics, Washington University School of Medicine, St Louis, Missouri. Department of Anatomy and Neurobiology, Washington University School of Medicine, St Louis, Missouri.

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January 2015

Synonymous ABCA3 variants do not increase risk for neonatal respiratory distress syndrome.

J Pediatr 2014 Jun 20;164(6):1316-21.e3. Epub 2014 Mar 20.

Edward Mallinckrodt Department of Pediatrics, Washington University School of Medicine, St. Louis, MO.

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June 2014

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

Nucleic Acids Res 2014 Jun 20;42(10):e82. Epub 2014 Mar 20.

Department of Orthopaedic Surgery, Washington University School of Medicine, 660 S Euclid Ave., St Louis, MO 63110, USA Department of Pediatrics, Washington University School of Medicine, 660 S Euclid Ave., St Louis, MO 63110, USA Department of Neurology, Washington University School of Medicine, 660 S Euclid Ave., St Louis, MO 63110, USA

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June 2014

Commentary.

Authors:
Todd E Druley

Clin Chem 2013 Jan;59(1):50-1

Department of Pediatrics, Division of Hematology and Oncology, Washington University School of Medicine, St. Louis, MO 63110, USA.

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January 2013

Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome.

Pediatrics 2012 Dec 19;130(6):e1575-82. Epub 2012 Nov 19.

Division of Newborn Medicine, The Edward Mallinckrodt Department of Pediatrics, Washington University School of Medicine, St Louis, MO 63110.

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December 2012

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

BMC Genomics 2012 Dec 6;13:683. Epub 2012 Dec 6.

Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St, Louis, MO 63108, USA.

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December 2012

Detection of rare genomic variants from pooled sequencing using SPLINTER.

J Vis Exp 2012 Jun 23(64). Epub 2012 Jun 23.

Center for Genome Sciences and Systems Biology, Department of Genetics, Washington University School of Medicine.

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June 2012

High-throughput discovery of rare insertions and deletions in large cohorts.

Genome Res 2010 Dec 1;20(12):1711-8. Epub 2010 Nov 1.

Center for Genome Sciences and Systems Biology, Department of Genetics, Washington University in St. Louis School of Medicine, St. Louis, Missouri 63108, USA.

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December 2010

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

J Clin Invest 2010 Jan 14;120(1):280-9. Epub 2009 Dec 14.

Center for Pharmacogenomics, Department of Medicine, Washington University School of Medicine, 660 S. Eucliud Avenue, St. Louis, Missouri 63110, USA.

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January 2010

Severe ceftriaxone-induced hemolysis complicated by diffuse cerebral ischemia in a child with sickle cell disease.

J Pediatr Hematol Oncol 2009 Nov;31(11):870-2

Division of Hematology and Oncology, Department of Pediatrics, Washington University School of Medicine, St Louis, MO 63110, USA.

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November 2009

Quantification of rare allelic variants from pooled genomic DNA.

Nat Methods 2009 Apr 1;6(4):263-5. Epub 2009 Mar 1.

Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.

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April 2009