Ian B Stanaway

Ian B Stanaway

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Ian B Stanaway

Ian B Stanaway

Publications by authors named "Ian B Stanaway"

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21Publications

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Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical Setting.

Am J Hum Genet 2019 Sep 15;105(3):526-533. Epub 2019 Aug 15.

Department of Medicine (Medical Genetics), University of Washington School of Medicine, Seattle, WA 98195, USA; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2019.07.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731361PMC
September 2019

An Atlas of Genetic Variation Linking Pathogen-Induced Cellular Traits to Human Disease.

Cell Host Microbe 2018 08;24(2):308-323.e6

Department of Molecular Genetics and Microbiology, School of Medicine, Duke University, Durham, NC 27710, USA; Division of Infectious Diseases, Department of Medicine, School of Medicine, Duke University, Durham, NC 27710, USA. Electronic address:

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http://dx.doi.org/10.1016/j.chom.2018.07.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093297PMC
August 2018

Patient genotypes impact survival after surgery for isolated congenital heart disease.

Ann Thorac Surg 2014 Jul 6;98(1):104-10; discussion 110-1. Epub 2014 May 6.

Department of Medicine, Division of Medical Genetics, University of Washington School of Medicine, Seattle, Washington; Department of Genome Sciences, University of Washington School of Medicine, Seattle, Washington. Electronic address:

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http://dx.doi.org/10.1016/j.athoracsur.2014.03.017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4083015PMC
July 2014

IGF1R variants associated with isolated single suture craniosynostosis.

Am J Med Genet A 2011 Jan;155A(1):91-7

Seattle Children's Hospital Craniofacial Center, University of Washington, 98195, USA.

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http://dx.doi.org/10.1002/ajmg.a.33781DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3059230PMC
January 2011

Single nucleotide polymorphism discovery in TBX1 in individuals with and without 22q11.2 deletion syndrome.

Birth Defects Res A Clin Mol Teratol 2010 Jan;88(1):54-63

Department of Pediatrics, Division of Craniofacial Medicine, University of Washington and Seattle Children's Hospital, Seattle, Washington 98105-5371, USA.

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http://dx.doi.org/10.1002/bdra.20604DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535433PMC
January 2010

The environmental genome project: reference polymorphisms for drug metabolism genes and genome-wide association studies.

Drug Metab Rev 2008 ;40(2):241-61

Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA.

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http://dx.doi.org/10.1080/03602530801952880 DOI Listing
June 2008

Direct detection of null alleles in SNP genotyping data.

Hum Mol Genet 2006 Jun 27;15(12):1931-7. Epub 2006 Apr 27.

Department of Genome Sciences, University of Washington, Seattle, WA 98195-7730, USA.

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http://dx.doi.org/10.1093/hmg/ddl115DOI Listing
June 2006