CammonBArringtonMD

PubMed

• 5 citations
  The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele
  Shannon Hateley, Angelica Lopez-Izquierdo, Chuanchau J. Jou, Scott Cho, Joshua G. Schraiber, Shiya Song, Colin T. Maguire, Natalia S. Torres, Michael Riedel, Neil E. B...> ;Nature Communications. 2021 Nov 8
• 14 citations
  Assessment of large copy number variants in patients with apparently isolated congenital left-sided cardiac lesions reveals clinically relevant genomic events
  Neil A. Hanchard, Luis A. Umaña, Lisa C.A. D'Alessandro, Mahshid S. Azamian, Mojisola Poopola, Shaine A. Morris, Susan D. Fernbach, Seema R. Lalani, Jeffrey A. Towbin,...> ;American Journal of Medical Genetics. Part A. 2017 Jun 27
• 10 citations
  A Functional Assay for Sick Sinus Syndrome Genetic Variants.
  Chuanchau J. Jou, Cammon B. Arrington, Spencer M. Barnett, Jiaxiang Shen, Scott Cho, Xiaoming Sheng, Patrick C McCullagh, Neil E. Bowles, Chase Pribble, Elizabeth V. S...> ;Cellular Physiology and Biochemistry. 2017 Aug 11
• 22 citations
  Kawasaki Disease and Exposure to Fine Particulate Air Pollution
  Andrew Zeft, Jane C. Burns, Rae S. M. Yeung, Brian W. McCrindle, Jane W. Newburger, Samuel R. Dominguez, Marsha S. Anderson, Cammon B. Arrington, Stanford T. Shulman, ...> ;The Journal of Pediatrics. 2016 Oct 1
• 13 citations
  Exome analysis of a family with Wolff-Parkinson-White syndrome identifies a novel disease locus.
  Neil E. Bowles, Chuanchau J. Jou, Cammon B. Arrington, Brett Kennedy, Aubree M. Earl, Norisada Matsunami, Lindsay Meyers, Susan P. Etheridge, Elizabeth V. Saarel, Stev...> ;American Journal of Medical Genetics. Part A. 2015 Dec 1
• 13 citations
  Shared Segment Analysis and Next-Generation Sequencing Implicates the Retinoic Acid Signaling Pathway in Total Anomalous Pulmonary Venous Return (TAPVR).
  Dustin Nash, Cammon B. Arrington, Brett Kennedy, Mark Yandell, Wilfred Wu, Wenying Zhang, Stephanie M. Ware, Lynn B. Jorde, Peter J. Gruber, H. Joseph Yost, Neil E. Bo...> ;Plos One. 2015 Jun 29
• 16 citations
  Novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome.
  Taisuke Ishikawa, Chuanchau J. Jou, Akihiko Nogami, Shinya Kowase, Cammon B. Arrington, Spencer M. Barnett, Daniel Toshio Harrell, Takuro Arimura, Yukiomi Tsuji, Akino...> ;Circulation. Arrhythmia and Electrophysiology. 2015 Apr 1
• 18 citations
  The role of screening and prophylactic surgery for malrotation in heterotaxy patients.
  Craig T. Elder, Ryan R. Metzger, Cammon B. Arrington, Michael D. Rollins, Eric R. Scaife> ;Journal of Pediatric Surgery. 2014 Dec 1
• 40 citations
  Validation of association of the apolipoprotein E ε2 allele with neurodevelopmental dysfunction after cardiac surgery in neonates and infants.
  J. William Gaynor, Daniel Seung Kim, Cammon B. Arrington, Andrew M. Atz, David C. Bellinger, Amber A. Burt, Nancy S. Ghanayem, Jeffery P. Jacobs, Teresa M. Lee, Alan B...> ;The Journal of Thoracic and Cardiovascular Surgery. 2014 Dec 1
• 6 citations
  Neonatal flail tricuspid valve: diagnosis and management.
  Patrick D. Loftus, Cammon B. Arrington, Aditya K. Kaza> ;The Annals of Thoracic Surgery. 2014 Sep 1
• 3 citations
  Kawasaki disease patients homozygous for the rs12252-C variant of interferon-induced transmembrane protein-3 are significantly more likely to develop coronary artery l...
  Neil E. Bowles, Cammon B. Arrington, Keiichi Hirono, Tsuneyuki Nakamura, Long Ngo, Yin Shen Wee, Fukiko Ichida, John H. Weis> ;Molecular Genetics & Genomic Medicine. 2014 Jul 1
• 8 citations
  Heterotaxy Syndrome: Impact of Ventricular Morphology on Resource Utilization
  Venugopal Amula, German L. Ellsworth, Susan L. Bratton, Cammon B. Arrington, Madolin K. Witte> ;Pediatric Cardiology. 2014 Jan 1
• 20 citations
  White matter lesions in children and adolescents with migraine.
  Meghan Candee, Rachel T. McCandless, Kevin R. Moore, Cammon B. Arrington, L. LuAnn Minich, James F. Bale> ;Pediatric Neurology. 2013 Dec 1
• 13 citations
  Sdc2 and Tbx16 regulate Fgf2-dependent epithelial cell morphogenesis in the ciliated organ of asymmetry.
  Cammon B. Arrington, Annita G. Peterson, H. Joseph Yost> ;Development. 2013 Oct 1
• 4 citations
  Family-based studies to identify genetic variants that cause congenital heart defects.
  Cammon B. Arrington, Steven B. Bleyl, Luca Brunelli, Neil E. Bowles> ;Future Cardiology. 2013 Jul 8
• 24 citations
  Rer1p maintains ciliary length and signaling by regulating γ-secretase activity and Foxj1a levels.
  Nathalie Jurisch-Yaksi, Applonia Josephine Rose, Huiqi Lu, Tim Raemaekers, Sebastian Munck, Pieter Baatsen, Veerle Baert, Wendy Vermeire, Suzie J. Scales, Daphne Verle...> ;The Journal of Cell Biology. 2013 Mar 18
• 25 citations
  A family‐based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia
  Cammon B. Arrington, Steven B. Bleyl, Nori Matsunami, Neil E. Bowles, Tami Leppert, Bradley L. Demarest, Karen A. Osborne, Bradley A. Yoder, Janice L. B. Byrne, Joshua...> ;American Journal of Medical Genetics. Part A. 2012 Dec 1
• 47 citations
  Exome analysis of a family with pleiotropic congenital heart disease.
  Cammon B. Arrington, Steven B. Bleyl, Norisada Matsunami, Gabriel D. Bonnell, Brith Otterud, Douglas C. Nielsen, Jeff Stevens, Shawn Levy, Mark Leppert, Neil E. Bowles> ;Circulation. Cardiovascular Genetics. 2012 Apr 1
• 24 citations
  Non-synonymous variants in Pre B-cell leukemia homeobox (PBX) genes are associated with congenital heart defects
  Cammon B. Arrington, Benjamin R. Dowse, Steven B. Bleyl, Neil E. Bowles> ;European Journal of Medical Genetics. 2012 Apr 1
• 39 citations
  Somatic mosaicism contributes to phenotypic variation in Timothy syndrome
  Susan P. Etheridge, Neil E. Bowles, Cammon B. Arrington, Thomas A. Pilcher, Alan F. Rope, Arthur A.M. Wilde, Marielle Alders, Elizabeth V. Saarel, Rene Tavernier, Kath...> ;American Journal of Medical Genetics. Part A. 2011 Oct 1
• 18 citations
  Patent foramen ovale in children with migraine headaches.
  Rachel T. McCandless, Cammon B. Arrington, Douglas C. Nielsen, James F. Bale, L. LuAnn Minich> ;The Journal of Pediatrics. 2011 Aug 1
• 45 citations
  Renin-Angiotensin-Aldosterone Genotype Influences Ventricular Remodeling in Infants With Single Ventricle
  Seema Mital, Wendy K. Chung, Steven D. Colan, Lynn A. Sleeper, Cedric Manlhiot, Cammon B. Arrington, James F. Cnota, Eric M. Graham, Michael E. Mitchell, Elizabeth Gol...> ;Circulation. 2011 May 31
• 22 citations
  Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development.
  Elizabeth J. Bhoj, Purita Ramos, Linda A. Baker, Nicholas G. Cost, Agneta Nordenskjöld, Frederick F.B. Elder, Steven B. Bleyl, Neil E. Bowles, Cammon B. Arrington, Bri...> ;European Journal of Human Genetics. 2011 Feb 2
• 26 citations
  Haploinsufficiency of the LIM domain containing preferred translocation partner in lipoma (LPP) gene in patients with tetralogy of Fallot and VACTERL association.
  Cammon B. Arrington, Ankita Patel, Carlos A. Bacino, Neil E. Bowles> ;American Journal of Medical Genetics. Part A. 2010 Nov 1
• 54 citations
  Extra-embryonic syndecan 2 regulates organ primordia migration and fibrillogenesis throughout the zebrafish embryo
  Cammon B. Arrington, H. Joseph Yost> ;Development. 2009 Sep 15
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