KathrynCollierChatfieldMD

Pediatric Cardiology • Aurora, CO

Pediatric Cardiac Genetics, Pediatric Heart Failure and Heart Transplantation

Associate Professor of Pediatrics, Section of Pediatric Cardiology

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Office
13123 E 16th Ave
Aurora, CO 80045
Phone(720) 777-6820
Fax(720) 777-7290
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Education & Training

University of ColoradoFellowship, Pediatric Cardiology, 2010 - 2013
Children's Hospital of PhiladelphiaResidency, Pediatrics/Medical Genetics, 2006 - 2010
Geisel School of Medicine at DartmouthClass of 2006

Certifications & Licensure

CO State Medical License 2010 - 2021
PA State Medical License 2006 - 2010
American Board of Medical Genetics and Genomics Clinical Genetics
American Board of Pediatrics Pediatrics
American Board of Pediatrics Pediatric Cardiology

Clinical Trials

Micro RNAs as a Marker of Aortic Aneurysm in Hereditary Aortopathy Syndromes Start of enrollment: 2014 Aug 01Taylor, A.L.,Chatfield, K.C.,Chatfield, K.

Publications & Presentations

PubMed

Tafazzin deficiency impairs CoA-dependent oxidative metabolism in cardiac mitochondria.
Catherine H. Le, Lindsay G. Benage, Kalyn S. Specht, Lance C. Li Puma, Christopher M. Mulligan, Adam L. Heuberger, Jessica E. Prenni, Steven M. Claypool, Kathryn C. Ch...> ;Journal of Biological Chemistry. 2020 Jul 14
1 citations
Automated syndrome diagnosis by three-dimensional facial imaging.
Benedikt Hallgrímsson, J. David Aponte, David C. Katz, Jordan J. Bannister, Sheri L. Riccardi, Nick Mahasuwan, Brenda McInnes, Tracey M. Ferrara, Danika M. Lipman, Ama...> ;Genetics in Medicine. 2020 Jun 1
Alteration of cardiolipin biosynthesis and remodeling in single right ventricle congenital heart disease.
Garcia, A. M., McPhaul, J. C., Sparagna, G. C., Jeffrey, D. A., Jonscher, R., Patel, S. S., Sucharov, C. C., Stauffer, B. L., Miyamoto, S. D., Chatfield, K. C.> ;American journal of physiology. Heart and circulatory physiology. 2020 Feb 15
Cardiac transplantation in children with Noonan syndrome.
McCallen, L. M., Ameduri, R. K., Denfield, S. W., Dodd, D. A., Everitt, M. D., Johnson, J. N., Lee, T. M., Lin, A. E., Lohr, J. L., May, L. J., Pierpont, M. E., Steven...> ;Pediatric transplantation. 2019 Jul 2
8 citations
Costello syndrome: Clinical phenotype, genotype, and management guidelines.
Gripp, K. W., Morse, L. A., Axelrad, M., Chatfield, K. C., Chidekel, A., Dobyns, W., Doyle, D., Kerr, B., Lin, A. E., Schwartz, D. D., Sibbles, B. J., Siegel, D., Shan...> ;American journal of medical genetics. Part A. 2019 Jun 22
17 citations
Elamipretide Improves Mitochondrial Function in the Failing Human Heart.
Kathryn C. Chatfield, Genevieve C. Sparagna, Sarah Chau, Elisabeth K Phillips, Amrut V. Ambardekar, Muhammad Aftab, Max B. Mitchell, Carmen C. Sucharov, Shelley D. Miy...> ;JACC: Basic to Translational Science. 2019 Apr 1
Aortic stiffness in adolescent Turner and Marfan syndrome patients.
Michal Schäfer, Lorna P. Browne, Uyen Truong, James Jaggers, Max B. Mitchell, Ladonna Malone, Gareth J. Morgan, Kathryn C. Chatfield, Daniel McLennan, Harma K. Turbend...> ;European Journal of Cardio-Thoracic Surgery. 2018 Nov 1
Biallelic B3GALT6 mutations cause spondylodysplastic Ehlers-Danlos syndrome.
Tim Van Damme, Xiaomeng Pang, Brecht Guillemyn, Sandrine Gulberti, Delfien Syx, Riet De Rycke, Olivier Kaye, Christine E. M. de Die-Smulders, Rolph Pfundt, Ariana Kari...> ;Human Molecular Genetics. 2018 Oct 15
7 citations
Pathogenic variants in glutamyl-tRNA(Gln) amidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorder
Marisa W. Friederich, Sharita Timal, Christopher A. Powell, Cristina Dallabona, Alina Kurolap, Sara Palacios-Zambrano, Drago Bratkovic, Terry G. J. Derks, David Bick, ...> ;Nature Communications. 2018 Oct 3
In-utero idiopathic ductal constriction: a prenatal manifestation of Alagille and Williams syndrome arteriopathy.
Shardha Srinivasan, Lisa Howley, Bettina F. Cuneo, Kathryn C. Chatfield> ;Journal of Perinatology. 2018 Sep 10
Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients.
Mark D. Levin, Sulagna C. Saitta, Karen W. Gripp, Tara L. Wenger, Jaya Ganesh, Jennifer M. Kalish, Michael R. Epstein, Rosemarie Smith, Richard J. Czosek, Stephanie M....> ;American Journal of Medical Genetics Part A. 2018 Aug 1
Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations.
Ellen S. Regalado, Lauren Mellor-Crummey, Julie De Backer, Alan C. Braverman, Lesley C. Adès, Susan L. Benedict, Timothy J. Bradley, M. Elizabeth Brickner, Kathryn C. ...> ;Genetics in Medicine. 2018 Jan 4
5 citations
Mutations in the accessory subunit NDUFB10 result in isolated complex I deficiency and illustrate the critical role of intermembrane space import for complex I holoenz...
Marisa W. Friederich, Alican J. Erdogan, Curtis R. Coughlin, Mihret T. Elos, Hua Jiang, Courtney P. O’Rourke, Mark A. Lovell, Eric P. Wartchow, Katherine Gowan, Kathry...> ;Human Molecular Genetics. 2016 Dec 30
2 citations
Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital ...
Yu, H., Coughlin, C. R., Geiger, E. A., Salvador, B. J., Elias, E. R., Cavanaugh, J. L., Chatfield, K. C., Miyamoto, S. D., Shaikh, T. H.> ;Cold Spring Harbor molecular case studies. 2016 May 6
19 citations
Mitochondrial energy failure in HSD10 disease is due to defective mtDNA transcript processing.
Kathryn C. Chatfield, Curtis R. Coughlin, Marisa W. Friederich, Renata C. Gallagher, Jay R. Hesselberth, Mark A. Lovell, Rob Ofman, Michael A. Swanson, Janet A. Thomas...> ;Mitochondrion. 2015 Mar 1
4 citations
Genome-wide expression analysis in fibroblast cell lines from probands with Pallister Killian syndrome.
Kaur, M., Izumi, K., Wilkens, A. B., Chatfield, K. C., Spinner, N. B., Conlin, L. K., Zhang, Z., Krantz, I. D.> ;PloS one. 2014 Oct 21
Dysregulation of cardiolipin biosynthesis in pediatric heart failure.
Kathryn C. Chatfield, Genevieve C. Sparagna, Carmen C. Sucharov, Shelley D. Miyamoto, Jonathan E. Grudis, Rebecca D. Sobus, Jamie G. Hijmans, Brian L. Stauffer> ;Journal of Molecular and Cellular Cardiology. 2014 Sep 1
17 citations
Congenital Heart Disease in Cornelia de Lange Syndrome: Phenotype and Genotype Analysis
Kathryn C. Chatfield, Samantha A. Schrier, Jennifer R. Li, Dinah Clark, Maninder Kaur, Antonie D. Kline, Matthew A. Deardorff, Laird S. Jackson, Elizabeth Goldmuntz, I...> ;American Journal of Medical Genetics Part A. 2012 Oct 1
Inhibitors of protein phosphatases 1 and 2A differentially prevent intrinsic and extrinsic apoptosis pathways.
Kathryn Chatfield, Alan Eastman> ;Biochemical and Biophysical Research Communications. 2004 Oct 29
Effect of Caffeine on Acetaminophen Hepatotoxicity in Cultured Hepatocytes Treated with Ethanol and Isopentanol
Keith DiPetrillo, Sheryl G. Wood, Vsevolod E. Kostrubsky, Kathryn Chatfield, Jenna L. Bement, Steven A. Wrighton, Elizabeth H. Jeffery, Peter R. Sinclair, Jacqueline F...> ;Toxicology and Applied Pharmacology. 2002 Dec 1
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