Publications by authors named "Peggy D Robertson"

12Publications

Actionable exomic incidental findings in 6503 participants: challenges of variant classification.

Genome Res 2015 Mar 30;25(3):305-15. Epub 2015 Jan 30.

Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA;

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http://dx.doi.org/10.1101/gr.183483.114DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352885PMC
March 2015

Actionable, pathogenic incidental findings in 1,000 participants' exomes.

Am J Hum Genet 2013 Oct 19;93(4):631-40. Epub 2013 Sep 19.

Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA 98195, USA; Department of Laboratory Medicine, University of Washington, Seattle, WA 98195, USA.

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http://dx.doi.org/10.1016/j.ajhg.2013.08.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3791261PMC
October 2013

Exome sequencing reveals novel rare variants in the ryanodine receptor and calcium channel genes in malignant hyperthermia families.

Anesthesiology 2013 Nov;119(5):1054-65

* Assistant Professor, Department of Anesthesiology and Pain Medicine, † Professor, ‡ Associate Professor, § Biostatistician, Department of Medicine, Division of Medical Genetics, ‖ Graduate Student, # Research Professor, ** Research Scientist, †† Professor, Department of Genome Sciences, University of Washington, Seattle, Washington. ‡‡ Research Scientist, §§ Professor, Leeds Institute of Molecular Medicine, Leeds, United Kingdom.

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http://dx.doi.org/10.1097/ALN.0b013e3182a8a998DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4115638PMC
November 2013

Novel common and rare genetic determinants of paraoxonase activity: FTO, SERPINA12, and ITGAL.

J Lipid Res 2013 Feb 15;54(2):552-60. Epub 2012 Nov 15.

Department of Medicine, University of Washington School of Medicine, Seattle, WA, USA.

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http://dx.doi.org/10.1194/jlr.P033266DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588879PMC
February 2013

Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.

Circ Cardiovasc Genet 2012 Apr 15;5(2):167-74. Epub 2012 Feb 15.

Cardiovascular Division, Department of Medicine and the Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL 33136, USA.

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http://dx.doi.org/10.1161/CIRCGENETICS.111.961805DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3332064PMC
April 2012

IFRD1 is a candidate gene for SMNA on chromosome 7q22-q23.

Am J Hum Genet 2009 May 30;84(5):692-7. Epub 2009 Apr 30.

Department of Psychiatry and Behavioral Sciences, University of Washington School of Medicine, Seattle, WA 98104, USA.

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http://dx.doi.org/10.1016/j.ajhg.2009.04.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680994PMC
May 2009