Suzanne M Lewis

Suzanne M E Lewis

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Suzanne M Lewis

Suzanne M E Lewis

Publications by authors named "Suzanne M E Lewis"

10Publications

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1PubMed Central Citations

Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplication.

Eur J Med Genet 2019 Feb 13;62(2):103-108. Epub 2018 Jun 13.

Department of Pathology and Laboratory Medicine, UBC, Vancouver, BC, Canada; BC Children's Hospital Research Institute, Vancouver, BC, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2018.06.010DOI Listing
February 2019

Whole exome sequencing of families with 1q21.1 microdeletion or microduplication.

Am J Med Genet A 2017 Jul 5;173(7):1782-1791. Epub 2017 May 5.

Department of Pathology, University of British Columbia (UBC), Vancouver, British Columbia, Canada.

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http://dx.doi.org/10.1002/ajmg.a.38247DOI Listing
July 2017

miRNA and miRNA target genes in copy number variations occurring in individuals with intellectual disability.

BMC Genomics 2013 Aug 10;14:544. Epub 2013 Aug 10.

Department of Pathology and Lab Medicine, BC Child and Family Research Institute, University of British Columbia, Vancouver, BC V5Z 4H4, Canada.

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http://bmcgenomics.biomedcentral.com/articles/10.1186/1471-2
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http://dx.doi.org/10.1186/1471-2164-14-544DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750877PMC
August 2013

The DLX1and DLX2 genes and susceptibility to autism spectrum disorders.

Eur J Hum Genet 2009 Feb 27;17(2):228-35. Epub 2008 Aug 27.

Department of Psychiatry, Queen's University, Kingston, Ontario, Canada.

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http://dx.doi.org/10.1038/ejhg.2008.148DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2986060PMC
February 2009

Complete rescue of lipoprotein lipase-deficient mice by somatic gene transfer of the naturally occurring LPLS447X beneficial mutation.

Arterioscler Thromb Vasc Biol 2005 Oct 7;25(10):2143-50. Epub 2005 Jul 7.

Department of Medical Genetics, University of British Columbia, Centre for Molecular Medicine and Therapeutics, Vancouver, Canada.

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http://dx.doi.org/10.1161/01.ATV.0000176971.27302.b0DOI Listing
October 2005

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy.

Nat Genet 2002 Apr 11;30(4):441-5. Epub 2002 Mar 11.

Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital, North Adelaide, South Australia 5006, Australia.

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http://dx.doi.org/10.1038/ng862DOI Listing
April 2002