Sara Fitzgerald-Butt

Sara Fitzgerald-Butt

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Sara Fitzgerald-Butt

Sara Fitzgerald-Butt

Publications by authors named "Sara Fitzgerald-Butt"

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21Publications

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Reclassification of Variants of Uncertain Significance in Children with Inherited Arrhythmia Syndromes is Predicted by Clinical Factors.

Pediatr Cardiol 2019 Sep 18. Epub 2019 Sep 18.

Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH, USA.

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http://dx.doi.org/10.1007/s00246-019-02203-2DOI Listing
September 2019

The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results.

Am J Hum Genet 2019 Apr;104(4):578-595

Social Issues Committee, American Society of Human Genetics, Rockville, MD 20852, USA; Division of General Internal Medicine, Department of Medicine, Johns Hopkins University, Baltimore, MD 21205, USA; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, Baltimore, MD 21205, USA.

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http://dx.doi.org/10.1016/j.ajhg.2019.02.025DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451731PMC
April 2019

Abnormal Longitudinal Growth of the Aorta in Children with Familial Bicuspid Aortic Valve.

Pediatr Cardiol 2017 Dec 25;38(8):1709-1715. Epub 2017 Sep 25.

Center for Cardiovascular Research, Research Institute at Nationwide Children's Hospital, Columbus, OH, 43205, USA.

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http://dx.doi.org/10.1007/s00246-017-1740-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5798863PMC
December 2017

Clinical exome sequencing reports: current informatics practice and future opportunities.

J Am Med Inform Assoc 2017 Nov;24(6):1184-1191

Research Information Solutions and Innovation, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.

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http://dx.doi.org/10.1093/jamia/ocx048DOI Listing
November 2017

A cohort study of multiple families with FBN1 p.R650C variant, ectopia lentis, and low but not absent risk for aortopathy.

Am J Med Genet A 2017 Nov 21;173(11):2995-3002. Epub 2017 Sep 21.

The Heart Center, Nationwide Children's Hospital, Columbus, Ohio.

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http://doi.wiley.com/10.1002/ajmg.a.38489
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http://dx.doi.org/10.1002/ajmg.a.38489DOI Listing
November 2017

Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.

Circ Cardiovasc Genet 2016 Aug 14;9(4):320-9. Epub 2016 Jul 14.

From the Center for Cardiovascular Research, The Research Institute (S.L., M.B., S.F.-B., G.Z., K.B., K.L.M., V.G.), The Heart Center (S.L., M.B., J.L.B., S.F.-B., K.L.M., V.G.), and Biomedical Genomics Core and the Center for Microbial Pathogenesis, The Research Institute (D.C., P.W.), Nationwide Children's Hospital, Columbus, OH; and Department of Molecular Genetics (S.L., V.G.) and Department of Pediatrics (J.L.B., S.F.-B., K.L.M., P.W., V.G.), The Ohio State University, Columbus.

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http://dx.doi.org/10.1161/CIRCGENETICS.115.001324DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412122PMC
August 2016

Lifetime prevalence of sexual intercourse and contraception use at last sex among adolescents and young adults with congenital heart disease.

J Adolesc Health 2015 Apr;56(4):396-401

Center for Cardiovascular and Pulmonary Research, The Research Institute, Nationwide Children's Hospital, Columbus, Ohio; Department of Pediatrics, College of Medicine, The Ohio State University, Columbus, Ohio. Electronic address:

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http://dx.doi.org/10.1016/j.jadohealth.2014.12.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821850PMC
April 2015

Genetic knowledge and attitudes of parents of children with congenital heart defects.

Am J Med Genet A 2014 Dec 24;164A(12):3069-75. Epub 2014 Sep 24.

Center for Cardiovascular and Pulmonary Research, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio; Department of Pediatrics, College of Medicine, The Ohio State University, Columbus, Ohio.

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http://dx.doi.org/10.1002/ajmg.a.36763DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236279PMC
December 2014

Rare GATA5 sequence variants identified in individuals with bicuspid aortic valve.

Pediatr Res 2014 Aug 5;76(2):211-6. Epub 2014 May 5.

1] Department of Pediatrics, The Ohio State University, Columbus, Ohio [2] Center for Cardiovascular and Pulmonary Research, Nationwide Children's Hospital, Columbus, Ohio [3] The Heart Center, Nationwide Children's Hospital, Columbus, Ohio [4] Department of Molecular Genetics, The Ohio State University, Columbus, Ohio.

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http://dx.doi.org/10.1038/pr.2014.67DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717758PMC
August 2014

An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.

Authors:
Catherine A Brownstein Alan H Beggs Nils Homer Barry Merriman Timothy W Yu Katherine C Flannery Elizabeth T DeChene Meghan C Towne Sarah K Savage Emily N Price Ingrid A Holm Lovelace J Luquette Elaine Lyon Joseph Majzoub Peter Neupert David McCallie Peter Szolovits Huntington F Willard Nancy J Mendelsohn Renee Temme Richard S Finkel Sabrina W Yum Livija Medne Shamil R Sunyaev Ivan Adzhubey Christopher A Cassa Paul I W de Bakker Hatice Duzkale Piotr Dworzyński William Fairbrother Laurent Francioli Birgit H Funke Monica A Giovanni Robert E Handsaker Kasper Lage Matthew S Lebo Monkol Lek Ignaty Leshchiner Daniel G MacArthur Heather M McLaughlin Michael F Murray Tune H Pers Paz P Polak Soumya Raychaudhuri Heidi L Rehm Rachel Soemedi Nathan O Stitziel Sara Vestecka Jochen Supper Claudia Gugenmus Bernward Klocke Alexander Hahn Max Schubach Mortiz Menzel Saskia Biskup Peter Freisinger Mario Deng Martin Braun Sven Perner Richard J H Smith Janeen L Andorf Jian Huang Kelli Ryckman Val C Sheffield Edwin M Stone Thomas Bair E Ann Black-Ziegelbein Terry A Braun Benjamin Darbro Adam P DeLuca Diana L Kolbe Todd E Scheetz Aiden E Shearer Rama Sompallae Kai Wang Alexander G Bassuk Erik Edens Katherine Mathews Steven A Moore Oleg A Shchelochkov Pamela Trapane Aaron Bossler Colleen A Campbell Jonathan W Heusel Anne Kwitek Tara Maga Karin Panzer Thomas Wassink Douglas Van Daele Hela Azaiez Kevin Booth Nic Meyer Michael M Segal Marc S Williams Gerard Tromp Peter White Donald Corsmeier Sara Fitzgerald-Butt Gail Herman Devon Lamb-Thrush Kim L McBride David Newsom Christopher R Pierson Alexander T Rakowsky Aleš Maver Luca Lovrečić Anja Palandačić Borut Peterlin Ali Torkamani Anna Wedell Mikael Huss Andrey Alexeyenko Jessica M Lindvall Måns Magnusson Daniel Nilsson Henrik Stranneheim Fulya Taylan Christian Gilissen Alexander Hoischen Bregje van Bon Helger Yntema Marcel Nelen Weidong Zhang Jason Sager Lu Zhang Kathryn Blair Deniz Kural Michael Cariaso Greg G Lennon Asif Javed Saloni Agrawal Pauline C Ng Komal S Sandhu Shuba Krishna Vamsi Veeramachaneni Ofer Isakov Eran Halperin Eitan Friedman Noam Shomron Gustavo Glusman Jared C Roach Juan Caballero Hannah C Cox Denise Mauldin Seth A Ament Lee Rowen Daniel R Richards F Anthony San Lucas Manuel L Gonzalez-Garay C Thomas Caskey Yu Bai Ying Huang Fang Fang Yan Zhang Zhengyuan Wang Jorge Barrera Juan M Garcia-Lobo Domingo González-Lamuño Javier Llorca Maria C Rodriguez Ignacio Varela Martin G Reese Francisco M De La Vega Edward Kiruluta Michele Cargill Reece K Hart Jon M Sorenson Gholson J Lyon David A Stevenson Bruce E Bray Barry M Moore Karen Eilbeck Mark Yandell Hongyu Zhao Lin Hou Xiaowei Chen Xiting Yan Mengjie Chen Cong Li Can Yang Murat Gunel Peining Li Yong Kong Austin C Alexander Zayed I Albertyn Kym M Boycott Dennis E Bulman Paul M K Gordon A Micheil Innes Bartha M Knoppers Jacek Majewski Christian R Marshall Jillian S Parboosingh Sarah L Sawyer Mark E Samuels Jeremy Schwartzentruber Isaac S Kohane David M Margulies

Genome Biol 2014 Mar 25;15(3):R53. Epub 2014 Mar 25.

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http://dx.doi.org/10.1186/gb-2014-15-3-r53DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4073084PMC
March 2014

Understanding of informed consent by parents of children enrolled in a genetic biobank.

Genet Med 2014 Feb 27;16(2):141-8. Epub 2013 Jun 27.

1] Center for Cardiovascular and Pulmonary Research, Nationwide Children's Hospital, Columbus, Ohio, USA [2] Department of Pediatrics, College of Medicine, The Ohio State University, Columbus, Ohio, USA.

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http://www.nature.com/articles/gim201386
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http://dx.doi.org/10.1038/gim.2013.86DOI Listing
February 2014

Association of common variants in ERBB4 with congenital left ventricular outflow tract obstruction defects.

Birth Defects Res A Clin Mol Teratol 2011 Mar 2;91(3):162-8. Epub 2011 Feb 2.

Center for Molecular and Human Genetics, Nationwide Children's Hospital, Department of Pediatrics, Ohio State University, Columbus, Ohio 43205, USA.

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http://dx.doi.org/10.1002/bdra.20764DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3736588PMC
March 2011

Parental knowledge and attitudes toward hypertrophic cardiomyopathy genetic testing.

Pediatr Cardiol 2010 Feb 1;31(2):195-202. Epub 2009 Dec 1.

Center for Molecular and Human Genetics, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.

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http://link.springer.com/10.1007/s00246-009-9583-2
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http://dx.doi.org/10.1007/s00246-009-9583-2DOI Listing
February 2010

NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling.

Hum Mol Genet 2008 Sep 30;17(18):2886-93. Epub 2008 Jun 30.

Center for Molecular and Human Genetics, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.

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http://dx.doi.org/10.1093/hmg/ddn187DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2722892PMC
September 2008