Patricia B S Celestino-Soper

Patricia B S Celestino-Soper

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Patricia B S Celestino-Soper

Patricia B S Celestino-Soper

Publications by authors named "Patricia B S Celestino-Soper"

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Genetic analyses in a bonobo (Pan paniscus) with arrhythmogenic right ventricular cardiomyopathy.

Sci Rep 2018 03 12;8(1):4350. Epub 2018 Mar 12.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.

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http://dx.doi.org/10.1038/s41598-018-22334-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5847517PMC
March 2018

Validation and Utilization of a Clinical Next-Generation Sequencing Panel for Selected Cardiovascular Disorders.

Front Cardiovasc Med 2017 15;4:11. Epub 2017 Mar 15.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA; Division of Cardiology, Department of Medicine, Krannert Institute of Cardiology, Indiana University School of Medicine, Indianapolis, IN, USA.

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http://dx.doi.org/10.3389/fcvm.2017.00011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350117PMC
March 2017

Intragenic CFTR Duplication and 5T/12TG Variant in a Patient with Non-Classic Cystic Fibrosis.

Sci Rep 2016 12 20;6:38776. Epub 2016 Dec 20.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.

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http://dx.doi.org/10.1038/srep38776DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5172161PMC
December 2016

Taking a peek at the border of the sarcomere in heart failure and cardiac resynchronization therapy.

J Mol Cell Cardiol 2014 Sep 2;74:1-3. Epub 2014 May 2.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indianapolis, IN, USA; Krannert Institute of Cardiology and the Division of Cardiology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indianapolis, IN, USA. Electronic address:

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http://dx.doi.org/10.1016/j.yjmcc.2014.04.015DOI Listing
September 2014

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.

Neuron 2011 Jun;70(5):863-85

Program on Neurogenetics, Yale University School of Medicine, 230 South Frontage Road, New Haven, CT 06520, USA.

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http://dx.doi.org/10.1016/j.neuron.2011.05.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3939065PMC
June 2011