GordonCGowansMD

PubMed

• 4 citations
  Characterization of an APC Promoter 1B deletion in a Patient Diagnosed with Familial Adenomatous Polyposis via Whole Genome Shotgun Sequencing
  Ted Kalbfleisch, Pamela L. Brock, Angela K. Snow, Deborah W. Neklason, Gordon C. Gowans, Jon B. Klein> ;F1000research. 2015 Jun 26
• 14 citations
  Molecular characterization of distal 4q duplication in two patients using oligonucleotide array-based comparative genomic hybridization (oaCGH) analysis
  Monika Thapa, Alexander Asamoah, Gordon C. Gowans, Kathryn C. Platky, J Margaret, Patricia Mouchrani, Cecilia Rajakaruna, Joseph H. Hersh> ;American Journal of Medical Genetics. Part A. 2014 Apr 1
• 396 citations
  Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants
  Santhosh Girirajan, Jill A. Rosenfeld, Bradley P. Coe, Sumit Parikh, Neil R. Friedman, Amy Goldstein, Robyn A. Filipink, Juliann Mcconnell, Brad Angle, Wendy S. Meschi...> ;The New England Journal of Medicine. 2012 Oct 3
• 14 citations
  Neurotransmitter abnormalities and response to supplementation in SPG11
  Adeline Vanderver, Davide Tonduti, Sarah Auerbach, Johanna L. Schmidt, Sumit Parikh, Gordon C. Gowans, Kelly E. Jackson, Pamela L. Brock, Marc C. Patterson, Michelle N...> ;Molecular Genetics and Metabolism. 2012 Sep 1
• 16 citations
  NF1 microduplications: identification of seven nonrelated individuals provides further characterization of the phenotype
  Kimberly J. Moles, Gordon C. Gowans, Satyanarayana Gedela, David Q. Beversdorf, Arthur Yu, Laurie H. Seaver, Roger A. Schultz, Jill A. Rosenfeld, Beth S. Torchia, Lisa...> ;Genetics in Medicine. 2012 Jan 12
• 49 citations
  Case series: 2q33.1 microdeletion syndrome—further delineation of the phenotype
  Meena Balasubramanian, Kath Smith, Lina Basel-Vanagaite, M F Feingold, Pamela L. Brock, Gordon C. Gowans, Pradeep C. Vasudevan, Lara Cresswell, E J Taylor, Catharine J...> ;Journal of Medical Genetics. 2011 May 1
• 1 citations
  A two-month-old infant with respiratory distress and left ventricular hypertrophy.
  Ilana L. Kayrouz, Bibhuti B. Das, Gordon C. Gowans, Christopher L. Johnsrude> ;The Journal of Pediatrics. 2011 Jan 1
• 12 citations
  Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome.
  Ariel M. Pani, Holly H. Hobart, Colleen A. Morris, Carolyn B. Mervis, Patricia Bray-Ward, Kendra W. Kimberley, Cecilia M. Rios, Robin C. Clark, Maricela D. Gulbronson,...> ;Plos One. 2010 Aug 31
• 218 citations
  Haploinsufficiency of HDAC4 Causes Brachydactyly Mental Retardation Syndrome, with Brachydactyly Type E, Developmental Delays, and Behavioral Problems
  Stephen R. Williams, Micheala A. Aldred, Vazken M. Der Kaloustian, Fahed Halal, Gordon C. Gowans, D. Ross McLeod, Sara Zondag, Helga V. Toriello, R. Ellen Magenis, Sar...> ;American Journal of Human Genetics. 2010 Aug 13
• 72 citations
  Identification of a Recurrent Microdeletion at 17q23.1q23.2 Flanked by Segmental Duplications Associated with Heart Defects and Limb Abnormalities
  Blake C. Ballif, Aaron Theisen, Jill A. Rosenfeld, Ryan N. Traylor, Julie M. Gastier-Foster, Devon Lamb Thrush, Caroline Astbury, Dennis Bartholomew, Kim L. McBride, R...> ;American Journal of Human Genetics. 2010 Mar 12
• 5 citations
  Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global...
  Roland Haj, Kelly E. Jackson, Beth A. Torchia, Lisa G. Shaffer, Bassem A. Bejjani, Gordon C. Gowans, Michael E Ruff> ;Molecular Cytogenetics. 2009 Jan 7
• 180 citations
  Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication.
  Blake C. Ballif, Aaron Theisen, Justine Coppinger, Gordon C. Gowans, Joseph H. Hersh, Suneeta Madan-Khetarpal, Karen R Schmidt, Raymond Tervo, Luis F. Escobar, Christo...> ;Molecular Cytogenetics. 2008 Apr 28
• 155 citations
  Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2.
  Blake C. Ballif, Sara A Hornor, Elizabeth Jenkins, Suneeta Madan-Khetarpal, Urvashi Surti, Kelly E. Jackson, Alexander Asamoah, Pamela L. Brock, Gordon C. Gowans, Robe...> ;Nature Genetics. 2007 Sep 1
• 10 citations
  Patient with terminal duplication 3q and terminal deletion 5q: comparison with the 3q duplication syndrome and distal 5q deletion syndrome
  Brad Angle, Frank Yen, Joseph H. Hersh, Gordon C. Gowans> ;American Journal of Medical Genetics. Part A. 2003 Feb 1
• 6 citations
  Partial duplication 4q and deletion 1p36 in monozygotic twins with discordant phenotypes.
  Brad Angle, Frank Yen, Joseph H. Hersh, Gordon C. Gowans, Margaret> ;American Journal of Medical Genetics. 2002 Aug 15
• 13 citations
  Developmental field defects: Coming together of associations and sequences during blastogenesis
  Joseph H. Hersh, Brad Angle, Terry L. Fox, Rolf F. Barth, Robert W. Bendon, Gordon C. Gowans> ;American Journal of Medical Genetics. 2002 Jul 15
• 39 citations
  Effects of cocaine and d-amphetamine on sustained and selective attention in rats.
  David M. Grilly, Gordon C. Gowans, Don S. McCann, Timothy W. Grogan> ;Pharmacology, Biochemistry, and Behavior. 1989 Aug 1
• 18 citations
  Effects of naltrexone, and d -amphetamine, and their interaction on the stimulus control of choice behavior of rats
  David M. Grilly, Gordon C. Gowans> ;Psychopharmacology. 1988 Jan 1
• 5 citations
  Comparison of the effects of morphine and immobilization stress on discrimination performance of rats.
  David M. Grilly, Gordon C. Gowans> ;Behavioral Neuroscience. 1986 Aug 1
• 12 citations
  Acute morphine dependence: effects observed in shock and light discrimination tasks.
  David M. Grilly, Gordon C. Gowans> ;Psychopharmacology. 1986 Jan 1
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