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1
Genetics of Congenital Heart Disease: The Glass Half Empty
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
Breastfeeding in primiparous women with congenital heart disease - a register study
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. ;2024. 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) 2024 ;ISSN: 1746-4358 ;EISSN: 1746-4358 ;DOI: 10.1186/s13006-024-00627-y ;PMID: 38509505

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3
The developmental genetics of congenital heart disease
The developmental genetics of congenital heart disease
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The developmental genetics of congenital heart disease

Nature, 2008-02, Vol.451 (7181), p.943-948 [Peer Reviewed Journal]

COPYRIGHT 2008 Nature Publishing Group ;Copyright Nature Publishing Group Feb 21, 2008 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;EISSN: 1476-4679 ;DOI: 10.1038/nature06801 ;PMID: 18288184 ;CODEN: NATUAS

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4
COVID-19 in Adults With Congenital Heart Disease
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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5
Estimating the effect size of the 15Q11.2 BP1–BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice
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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6
Genetic basis of human congenital anomalies of the kidney and urinary tract
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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7
Unplanned hospital readmissions following congenital heart diseases surgery. Prevalence and predictors
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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8
Copy-Number Disorders Are a Common Cause of Congenital Kidney Malformations
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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9
The spectrum of congenital heart diseases in down syndrome. A retrospective study from Northwest Saudi Arabia
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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10
CHARGE syndrome: an update
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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11
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
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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12
Investigation of infant deaths associated with critical congenital heart diseases; 2018-2021, Türkiye
Investigation of infant deaths associated with critical congenital heart diseases; 2018-2021, Türkiye
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Investigation of infant deaths associated with critical congenital heart diseases; 2018-2021, Türkiye

BMC public health, 2024-02, Vol.24 (1), p.441-441 [Peer Reviewed Journal]

2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;2024. 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) 2024 ;ISSN: 1471-2458 ;EISSN: 1471-2458 ;DOI: 10.1186/s12889-024-17966-4 ;PMID: 38347475

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13
Prognostic value of the model for end-stage liver disease excluding INR score (MELD-XI) in patients with adult congenital heart disease
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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14
Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management: A Scientific Statement From the American Heart Association
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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15
Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors
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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16
The impact of congenital heart diseases on the quality of life of patients and their families in Saudi Arabia. Biological, psychological, and social dimensions
The impact of congenital heart diseases on the quality of life of patients and their families in Saudi Arabia. Biological, psychological, and social dimensions
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The impact of congenital heart diseases on the quality of life of patients and their families in Saudi Arabia. Biological, psychological, and social dimensions

Saudi medical journal, 2016-04, Vol.37 (4), p.392-402 [Peer Reviewed Journal]

COPYRIGHT 2016 Saudi Medical Journal ;Copyright: © Saudi Medical Journal 2016 ;ISSN: 0379-5284 ;EISSN: 1658-3175 ;DOI: 10.15537/smj.2016.4.13626 ;PMID: 27052282

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17
Fully‑automated deep‑learning segmentation of pediatric cardiovascular magnetic resonance of patients with complex congenital heart diseases
Fully‑automated deep‑learning segmentation of pediatric cardiovascular magnetic resonance of patients with complex congenital heart diseases
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Fully‑automated deep‑learning segmentation of pediatric cardiovascular magnetic resonance of patients with complex congenital heart diseases

Journal of cardiovascular magnetic resonance, 2020-11, Vol.22 (1), p.80-80, Article 80 [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/s12968-020-00678-0 ;PMID: 33256762

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18
Three‐dimensional printing in congenital heart disease: A systematic review
Three‐dimensional printing in congenital heart disease: A systematic review
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Three‐dimensional printing in congenital heart disease: A systematic review

Journal of medical radiation sciences, 2018-09, Vol.65 (3), p.226-236 [Peer Reviewed Journal]

2018 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Australian Society of Medical Imaging and Radiation Therapy and New Zealand Institute of Medical Radiation Technology. ;2018 The Authors. Journal of Medical Radiation Sciences published by John Wiley & Sons Australia, Ltd on behalf of Australian Society of Medical Imaging and Radiation Therapy and New Zealand Institute of Medical Radiation Technology. ;2018 Journal of Medical Radiation Sciences published by John Wiley & Sons Australia, Ltd on behalf of Australian Society of Medical Imaging and Radiation Therapy and New Zealand Institute of Medical Radiation Technology ;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. ;ISSN: 2051-3895 ;EISSN: 2051-3909 ;DOI: 10.1002/jmrs.268 ;PMID: 29453808

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19
X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood
X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood
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X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood

European journal of endocrinology, 2019-06, Vol.180 (6), p.397-406 [Peer Reviewed Journal]

2019 European Society of Endocrinology ;Copyright BioScientifica Ltd. Jun 2019 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0804-4643 ;EISSN: 1479-683X ;DOI: 10.1530/EJE-18-0878 ;PMID: 30991358

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20
Contribution of congenital heart disease to neuropsychiatric outcome in school-age children with 22q11.2 deletion syndrome
Contribution of congenital heart disease to neuropsychiatric outcome in school-age children with 22q11.2 deletion syndrome
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Contribution of congenital heart disease to neuropsychiatric outcome in school-age children with 22q11.2 deletion syndrome

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2014-03, Vol.165B (2), p.137-147 [Peer Reviewed Journal]

2013 Wiley Periodicals, Inc. ;2013 Wiley Periodicals, Inc. 2013 ;ISSN: 1552-4841 ;EISSN: 1552-485X ;DOI: 10.1002/ajmg.b.32215 ;PMID: 24265253

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