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1
Genomic analyses implicate noncoding de novo variants in congenital heart disease
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Genomic analyses implicate noncoding de novo variants in congenital heart disease

Nature genetics, 2020-08, Vol.52 (8), p.769-777 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;Copyright Nature Publishing Group Aug 2020 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-020-0652-z ;PMID: 32601476

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2
Prognostic value of the model for end-stage liver disease excluding INR score (MELD-XI) in patients with adult congenital heart disease
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Prognostic value of the model for end-stage liver disease excluding INR score (MELD-XI) in patients with adult congenital heart disease

PloS one, 2019-11, Vol.14 (11), p.e0225403-e0225403 [Peer Reviewed Journal]

COPYRIGHT 2019 Public Library of Science ;COPYRIGHT 2019 Public Library of Science ;2019 Konno et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2019 Konno et al 2019 Konno et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0225403 ;PMID: 31743362

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3
Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors
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Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors

Nature genetics, 2009-11, Vol.41 (11), p.1247-1252 [Peer Reviewed Journal]

2009 INIST-CNRS ;COPYRIGHT 2009 Nature Publishing Group ;Copyright Nature Publishing Group Nov 2009 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.470 ;PMID: 19855393 ;CODEN: NGENEC

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4
Prevalence of Mental Illness in Adolescents and Adults With Congenital Heart Disease from the Colorado Congenital Heart Defect Surveillance System
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Prevalence of Mental Illness in Adolescents and Adults With Congenital Heart Disease from the Colorado Congenital Heart Defect Surveillance System

The American journal of cardiology, 2019-08, Vol.124 (4), p.618-626 [Peer Reviewed Journal]

2019 Elsevier Inc. ;Copyright © 2019 Elsevier Inc. All rights reserved. ;2019. Elsevier Inc. ;ISSN: 0002-9149 ;EISSN: 1879-1913 ;DOI: 10.1016/j.amjcard.2019.05.023 ;PMID: 31303246

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5
Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease
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Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease

Clinical genetics, 2010-12, Vol.78 (6), p.533-540 [Peer Reviewed Journal]

2010 John Wiley & Sons A/S ;2015 INIST-CNRS ;2010 John Wiley & Sons A/S. ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.2010.01422.x ;PMID: 20456451 ;CODEN: CLGNAY

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6
Ex vivo cardiovascular magnetic resonance diffusion weighted imaging in congenital heart disease, an insight into the microstructures of tetralogy of Fallot, biventricular and univentricular systemic right ventricle
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Ex vivo cardiovascular magnetic resonance diffusion weighted imaging in congenital heart disease, an insight into the microstructures of tetralogy of Fallot, biventricular and univentricular systemic right ventricle

Journal of cardiovascular magnetic resonance, 2020-09, Vol.22 (1), p.69-69, Article 69 [Peer Reviewed Journal]

COPYRIGHT 2020 BioMed Central Ltd. ;COPYRIGHT 2020 BioMed Central Ltd. ;2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 1532-429X ;ISSN: 1097-6647 ;EISSN: 1532-429X ;DOI: 10.1186/s12968-020-00662-8 ;PMID: 32951605

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7
4D flow cardiovascular magnetic resonance for monitoring of aortic valve repair in bicuspid aortic valve disease
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4D flow cardiovascular magnetic resonance for monitoring of aortic valve repair in bicuspid aortic valve disease

Journal of cardiovascular magnetic resonance, 2020-04, Vol.22 (1), p.29-29, Article 29 [Peer Reviewed Journal]

COPYRIGHT 2020 BioMed Central Ltd. ;COPYRIGHT 2020 BioMed Central Ltd. ;2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 1532-429X ;ISSN: 1097-6647 ;EISSN: 1532-429X ;DOI: 10.1186/s12968-020-00608-0 ;PMID: 32354361

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8
NGS-based expanded carrier screening for genetic disorders in North Indian population reveals unexpected results - a pilot study
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NGS-based expanded carrier screening for genetic disorders in North Indian population reveals unexpected results - a pilot study

BMC medical genetics, 2020-11, Vol.21 (1), p.216-216, Article 216 [Peer Reviewed Journal]

COPYRIGHT 2020 BioMed Central Ltd. ;COPYRIGHT 2020 BioMed Central Ltd. ;2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 1471-2350 ;EISSN: 1471-2350 ;DOI: 10.1186/s12881-020-01153-4 ;PMID: 33138774

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9
Prevalence of congenital amusia
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Prevalence of congenital amusia

European journal of human genetics : EJHG, 2017-05, Vol.25 (5), p.625-630 [Peer Reviewed Journal]

Copyright Nature Publishing Group May 2017 ;Copyright © 2017 Macmillan Publishers Limited, part of Springer Nature. 2017 Macmillan Publishers Limited, part of Springer Nature. ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2017.15 ;PMID: 28224991

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10
Orthotopic Heart Transplantation for Congenital Heart Disease with Dextrocardia: A Single-Center Clinic Experience
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Orthotopic Heart Transplantation for Congenital Heart Disease with Dextrocardia: A Single-Center Clinic Experience

BioMed research international, 2020, Vol.2020, p.3487635-9 [Peer Reviewed Journal]

Copyright © 2020 Guohua Wang et al. ;COPYRIGHT 2020 Hindawi Limited ;Copyright © 2020 Guohua Wang et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0 ;Copyright © 2020 Guohua Wang et al. 2020 ;ISSN: 2314-6133 ;EISSN: 2314-6141 ;DOI: 10.1155/2020/3487635 ;PMID: 32596301

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11
Identification of rare de novo epigenetic variations in congenital disorders
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Identification of rare de novo epigenetic variations in congenital disorders

Nature communications, 2018-05, Vol.9 (1), p.2064-11, Article 2064 [Peer Reviewed Journal]

2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2018 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-04540-x ;PMID: 29802345

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12
Imaging of the pulmonary vasculature in congenital heart disease without gadolinium contrast: Intraindividual comparison of a novel Compressed SENSE accelerated 3D modified REACT with 4D contrast-enhanced magnetic resonance angiography
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Imaging of the pulmonary vasculature in congenital heart disease without gadolinium contrast: Intraindividual comparison of a novel Compressed SENSE accelerated 3D modified REACT with 4D contrast-enhanced magnetic resonance angiography

Journal of cardiovascular magnetic resonance, 2020-01, Vol.22 (1), p.8-8, Article 8 [Peer Reviewed Journal]

COPYRIGHT 2020 BioMed Central Ltd. ;COPYRIGHT 2020 BioMed Central Ltd. ;2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s). 2020 ;ISSN: 1532-429X ;ISSN: 1097-6647 ;EISSN: 1532-429X ;DOI: 10.1186/s12968-019-0591-y ;PMID: 31969137

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13
Modified-Release Hydrocortisone in Congenital Adrenal Hyperplasia
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Article
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Modified-Release Hydrocortisone in Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2021-05, Vol.106 (5), p.e2063-e2077 [Peer Reviewed Journal]

The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. 2021 ;The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. ;COPYRIGHT 2021 Oxford University Press ;ISSN: 0021-972X ;ISSN: 1945-7197 ;EISSN: 1945-7197 ;DOI: 10.1210/clinem/dgab051 ;PMID: 33527139

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14
Expanding the phenotype of CACNA1C mutation disorders
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Expanding the phenotype of CACNA1C mutation disorders

Molecular genetics & genomic medicine, 2021-06, Vol.9 (6), p.e1673-n/a [Peer Reviewed Journal]

2021 The Authors. published by Wiley Periodicals LLC ;2021 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1673 ;PMID: 33797204

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15
Stroke in Adults With Congenital Heart Disease: Incidence, Cumulative Risk, and Predictors
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Stroke in Adults With Congenital Heart Disease: Incidence, Cumulative Risk, and Predictors

Circulation (New York, N.Y.), 2015-12, Vol.132 (25), p.2385-2394 [Peer Reviewed Journal]

2015 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;2015 American Heart Association, Inc. ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.115.011241 ;PMID: 26597113

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16
Paternal age and offspring congenital heart defects: a national cohort study
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Paternal age and offspring congenital heart defects: a national cohort study

PloS one, 2015-03, Vol.10 (3), p.e0121030-e0121030 [Peer Reviewed Journal]

COPYRIGHT 2015 Public Library of Science ;COPYRIGHT 2015 Public Library of Science ;2015 Su et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2015 Su et al 2015 Su et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0121030 ;PMID: 25806788

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17
Modified 16-Dot plication technique for correction of penile curvature: prevention of knot-related complications
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Modified 16-Dot plication technique for correction of penile curvature: prevention of knot-related complications

International journal of impotence research, 2018-06, Vol.30 (3), p.117-121 [Peer Reviewed Journal]

COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Jun 2018 ;ISSN: 0955-9930 ;EISSN: 1476-5489 ;DOI: 10.1038/s41443-018-0018-6 ;PMID: 29736012

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18
Anomalous aortic origin of right coronary artery from left coronary cusp: a management conundrum: a case report
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Anomalous aortic origin of right coronary artery from left coronary cusp: a management conundrum: a case report

Journal of medical case reports, 2023-05, Vol.17 (1), p.191-191, Article 191 [Peer Reviewed Journal]

2023. The Author(s). ;COPYRIGHT 2023 BioMed Central Ltd. ;2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2023 ;ISSN: 1752-1947 ;EISSN: 1752-1947 ;DOI: 10.1186/s13256-023-03921-1 ;PMID: 37161579

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19
High Prevalence of Respiratory Ciliary Dysfunction in Congenital Heart Disease Patients With Heterotaxy
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High Prevalence of Respiratory Ciliary Dysfunction in Congenital Heart Disease Patients With Heterotaxy

Circulation (New York, N.Y.), 2012-05, Vol.125 (18), p.2232-2242 [Peer Reviewed Journal]

2015 INIST-CNRS ;2012 American Heart Association, Inc. 2012 ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.111.079780 ;PMID: 22499950 ;CODEN: CIRCAZ

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20
Specialized Adult Congenital Heart Disease Care: The Impact of Policy on Mortality
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Specialized Adult Congenital Heart Disease Care: The Impact of Policy on Mortality

Circulation (New York, N.Y.), 2014-05, Vol.129 (18), p.1804-1812 [Peer Reviewed Journal]

2014 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;2015 INIST-CNRS ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.113.005817 ;PMID: 24589851 ;CODEN: CIRCAZ

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