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1
Genetics of Congenital Heart Disease: The Glass Half Empty
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Genetics of Congenital Heart Disease: The Glass Half Empty

Circulation research, 2013-02, Vol.112 (4), p.707-720 [Peer Reviewed Journal]

2013 American Heart Association, Inc. ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/CIRCRESAHA.112.300853 ;PMID: 23410880

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2
Lifespan Perspective on Congenital Heart Disease Research: JACC State-of-the-Art Review
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Lifespan Perspective on Congenital Heart Disease Research: JACC State-of-the-Art Review

Journal of the American College of Cardiology, 2021-05, Vol.77 (17), p.2219-2235 [Peer Reviewed Journal]

Copyright © 2021. Published by Elsevier Inc. ;COPYRIGHT 2021 Elsevier B.V. ;ISSN: 0735-1097 ;ISSN: 1558-3597 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2021.03.012 ;PMID: 33926659

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3
Associations and Disease-Disease Interactions of COVID-19 with Congenital and Genetic Disorders: A Comprehensive Review
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Associations and Disease-Disease Interactions of COVID-19 with Congenital and Genetic Disorders: A Comprehensive Review

Viruses, 2022-04, Vol.14 (5), p.910 [Peer Reviewed Journal]

2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2022 by the authors. 2022 ;ISSN: 1999-4915 ;EISSN: 1999-4915 ;DOI: 10.3390/v14050910 ;PMID: 35632654

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4
Breastfeeding in primiparous women with congenital heart disease - a register study
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Breastfeeding in primiparous women with congenital heart disease - a register study

International breastfeeding journal, 2024-03, Vol.19 (1), p.19-19 [Peer Reviewed Journal]

2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;The Author(s) 2024 ;ISSN: 1746-4358 ;EISSN: 1746-4358 ;DOI: 10.1186/s13006-024-00627-y ;PMID: 38509505

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5
Parental occupational exposure and congenital heart diseases in a Hungarian case–control study
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Parental occupational exposure and congenital heart diseases in a Hungarian case–control study

International archives of occupational and environmental health, 2021-04, Vol.94 (3), p.515-527 [Peer Reviewed Journal]

The Author(s) 2020 ;COPYRIGHT 2021 Springer ;The Author(s) 2020. 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: 0340-0131 ;EISSN: 1432-1246 ;DOI: 10.1007/s00420-020-01589-4 ;PMID: 33170344

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6
COVID-19 in Adults With Congenital Heart Disease
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COVID-19 in Adults With Congenital Heart Disease

Journal of the American College of Cardiology, 2021-04, Vol.77 (13), p.1644-1655 [Peer Reviewed Journal]

Copyright © 2021 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;COPYRIGHT 2021 Elsevier B.V. ;2021 by the American College of Cardiology Foundation. Published by Elsevier. 2021 American College of Cardiology Foundation ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2021.02.023 ;PMID: 33795039

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7
Genetic basis of human congenital anomalies of the kidney and urinary tract
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Genetic basis of human congenital anomalies of the kidney and urinary tract

The Journal of clinical investigation, 2018-01, Vol.128 (1), p.4-15 [Peer Reviewed Journal]

COPYRIGHT 2018 American Society for Clinical Investigation ;Copyright American Society for Clinical Investigation Jan 2018 ;Copyright © 2018, American Society for Clinical Investigation 2018 American Society for Clinical Investigation ;ISSN: 0021-9738 ;EISSN: 1558-8238 ;DOI: 10.1172/jci95300 ;PMID: 29293093

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8
Estimating the effect size of the 15Q11.2 BP1–BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice
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Estimating the effect size of the 15Q11.2 BP1–BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice

Journal of medical genetics, 2019-10, Vol.56 (10), p.701-710 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;2019 Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Distributed under a Creative Commons Attribution 4.0 International License ;Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2019 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmedgenet-2018-105879 ;PMID: 31451536

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9
Unplanned hospital readmissions following congenital heart diseases surgery. Prevalence and predictors
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Unplanned hospital readmissions following congenital heart diseases surgery. Prevalence and predictors

Saudi medical journal, 2019-08, Vol.40 (8), p.802-809 [Peer Reviewed Journal]

COPYRIGHT 2019 Saudi Medical Journal ;Copyright: © Saudi Medical Journal 2019 ;ISSN: 0379-5284 ;EISSN: 1658-3175 ;DOI: 10.15537/smj.2019.8.24405 ;PMID: 31423517

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10
Copy-Number Disorders Are a Common Cause of Congenital Kidney Malformations
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Copy-Number Disorders Are a Common Cause of Congenital Kidney Malformations

American journal of human genetics, 2012-12, Vol.91 (6), p.987-997 [Peer Reviewed Journal]

2012 The American Society of Human Genetics ;2014 INIST-CNRS ;Copyright © 2012 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Dec 7, 2012 ;2012 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2012 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2012.10.007 ;PMID: 23159250 ;CODEN: AJHGAG

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11
Infants with Congenital Diseases Identified through Newborn Screening-United States, 2018-2020
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Infants with Congenital Diseases Identified through Newborn Screening-United States, 2018-2020

International journal of neonatal screening, 2023-04, Vol.9 (2), p.23 [Peer Reviewed Journal]

COPYRIGHT 2023 MDPI AG ;2023 by the authors. 2023 ;ISSN: 2409-515X ;EISSN: 2409-515X ;DOI: 10.3390/ijns9020023 ;PMID: 37092517

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12
How I do it: Novel technique to "Unmask" and treat congenital portosystemic venous connections in congenital heart disease
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How I do it: Novel technique to "Unmask" and treat congenital portosystemic venous connections in congenital heart disease

Annals of pediatric cardiology, 2022-07, Vol.15 (4), p.394-398 [Peer Reviewed Journal]

Copyright: © 2023 Annals of Pediatric Cardiology. ;COPYRIGHT 2022 Medknow Publications and Media Pvt. Ltd. ;Copyright: © 2023 Annals of Pediatric Cardiology 2023 ;ISSN: 0974-2069 ;EISSN: 0974-5149 ;DOI: 10.4103/apc.apc_34_22 ;PMID: 36935837

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13
The spectrum of congenital heart diseases in down syndrome. A retrospective study from Northwest Saudi Arabia
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The spectrum of congenital heart diseases in down syndrome. A retrospective study from Northwest Saudi Arabia

Saudi medical journal, 2016-07, Vol.37 (7), p.767-772 [Peer Reviewed Journal]

COPYRIGHT 2016 Saudi Medical Journal ;Copyright: © Saudi Medical Journal 2016 ;ISSN: 0379-5284 ;EISSN: 1658-3175 ;DOI: 10.15537/smj.2016.7.14536 ;PMID: 27381537

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14
Risk factors for prolonged mechanical ventilation after surgical repair of congenital heart disease. Experience from a single cardiac center
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Risk factors for prolonged mechanical ventilation after surgical repair of congenital heart disease. Experience from a single cardiac center

Saudi medical journal, 2019-04, Vol.40 (4), p.367-371 [Peer Reviewed Journal]

COPYRIGHT 2019 Saudi Medical Journal ;Copyright: © Saudi Medical Journal 2019 ;ISSN: 0379-5284 ;EISSN: 1658-3175 ;DOI: 10.15537/smj.2019.4.23682 ;PMID: 30957130

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15
CHARGE syndrome: an update
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CHARGE syndrome: an update

European journal of human genetics : EJHG, 2007-04, Vol.15 (4), p.389-399 [Peer Reviewed Journal]

2007 INIST-CNRS ;Copyright Nature Publishing Group Apr 2007 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/sj.ejhg.5201778 ;PMID: 17299439

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16
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
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Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

Nature genetics, 2017-11, Vol.49 (11), p.1593-1601 [Peer Reviewed Journal]

COPYRIGHT 2017 Nature Publishing Group ;COPYRIGHT 2017 Nature Publishing Group ;Copyright Nature Publishing Group Nov 2017 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.3970 ;PMID: 28991257

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17
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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18
Counseling for Prenatal Congenital Heart Disease-Recommendations Based on Empirical Assessment of Counseling Success
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Counseling for Prenatal Congenital Heart Disease-Recommendations Based on Empirical Assessment of Counseling Success

Frontiers in pediatrics, 2020-02, Vol.8, p.26-26 [Peer Reviewed Journal]

Copyright © 2020 Kovacevic, Simmelbauer, Starystach, Elsässer, Müller, Bär and Gorenflo. ;COPYRIGHT 2020 Frontiers Research Foundation ;Copyright © 2020 Kovacevic, Simmelbauer, Starystach, Elsässer, Müller, Bär and Gorenflo. 2020 Kovacevic, Simmelbauer, Starystach, Elsässer, Müller, Bär and Gorenflo ;ISSN: 2296-2360 ;EISSN: 2296-2360 ;DOI: 10.3389/fped.2020.00026 ;PMID: 32175290

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19
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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20
Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management: A Scientific Statement From the American Heart Association
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Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management: A Scientific Statement From the American Heart Association

Circulation (New York, N.Y.), 2012-08, Vol.126 (9), p.1143-1172 [Peer Reviewed Journal]

2015 INIST-CNRS ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIR.0b013e318265ee8a ;PMID: 22851541 ;CODEN: CIRCAZ

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