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1
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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2
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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3
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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4
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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5
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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6
Increased prevalence of inattention-related symptoms in a large cohort of patients with congenital heart disease
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Increased prevalence of inattention-related symptoms in a large cohort of patients with congenital heart disease

European child & adolescent psychiatry, 2021-04, Vol.30 (4), p.647-655 [Peer Reviewed Journal]

Springer-Verlag GmbH Germany, part of Springer Nature 2020 ;COPYRIGHT 2021 Springer ;Springer-Verlag GmbH Germany, part of Springer Nature 2020. ;ISSN: 1018-8827 ;EISSN: 1435-165X ;DOI: 10.1007/s00787-020-01547-y ;PMID: 32394091

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7
A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
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A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)

PloS one, 2016-05, Vol.11 (5), p.e0154412-e0154412 [Peer Reviewed Journal]

COPYRIGHT 2016 Public Library of Science ;COPYRIGHT 2016 Public Library of Science ;This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication: https://creativecommons.org/publicdomain/zero/1.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0154412 ;PMID: 27149523

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8
Deletions of chromosomal regulatory boundaries are associated with congenital disease
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Deletions of chromosomal regulatory boundaries are associated with congenital disease

Genome biology, 2014-09, Vol.15 (9), p.423-423, Article 423 [Peer Reviewed Journal]

Ibn-Salem et al.; licensee BioMed Central Ltd. 2014 ;ISSN: 1474-760X ;ISSN: 1465-6906 ;EISSN: 1474-760X ;EISSN: 1465-6914 ;DOI: 10.1186/s13059-014-0423-1 ;PMID: 25315429

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9
Risk factors for congenital heart disease: The Baby Hearts Study, a population-based case-control study
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Risk factors for congenital heart disease: The Baby Hearts Study, a population-based case-control study

PloS one, 2020-02, Vol.15 (2), p.e0227908 [Peer Reviewed Journal]

COPYRIGHT 2020 Public Library of Science ;COPYRIGHT 2020 Public Library of Science ;2020 Dolk 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. ;2020 Dolk et al 2020 Dolk et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0227908 ;PMID: 32092068

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10
Maternal cardiovascular health in early pregnancy and the risk of congenital heart defects in offspring
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Maternal cardiovascular health in early pregnancy and the risk of congenital heart defects in offspring

BMC pregnancy and childbirth, 2024-04, Vol.24 (1), p.325-325 [Peer Reviewed Journal]

2024. The Author(s). ;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. ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-024-06529-5 ;PMID: 38671408

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11
Autoimmune-associated Congenital Heart Block: A New Insight in Fetal Life
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Autoimmune-associated Congenital Heart Block: A New Insight in Fetal Life

Chinese medical journal, 2017-12, Vol.130 (23), p.2863-2871 [Peer Reviewed Journal]

COPYRIGHT 2017 Medknow Publications and Media Pvt. Ltd. ;COPYRIGHT 2017 Medknow Publications and Media Pvt. Ltd. ;Copyright Medknow Publications & Media Pvt. Ltd. Dec 2017 ;Copyright © Wanfang Data Co. Ltd. All Rights Reserved. ;Copyright: © 2017 Chinese Medical Journal 2017 ;ISSN: 0366-6999 ;EISSN: 2542-5641 ;DOI: 10.4103/0366-6999.219160 ;PMID: 29176145

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12
De novo variants in exomes of congenital heart disease patients identify risk genes and pathways
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De novo variants in exomes of congenital heart disease patients identify risk genes and pathways

Genome medicine, 2020-01, Vol.12 (1), p.9-9, Article 9 [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: 1756-994X ;EISSN: 1756-994X ;DOI: 10.1186/s13073-019-0709-8 ;PMID: 31941532

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13
Maternal obesity and metabolic disorders associate with congenital heart defects in the offspring: A systematic review
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Maternal obesity and metabolic disorders associate with congenital heart defects in the offspring: A systematic review

PloS one, 2021-05, Vol.16 (5), p.e0252343-e0252343 [Peer Reviewed Journal]

COPYRIGHT 2021 Public Library of Science ;2021 Hedermann 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. ;2021 Hedermann et al 2021 Hedermann et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0252343 ;PMID: 34043700

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14
Hypoxic/ischemic hits predispose to necrotizing enterocolitis in (near) term infants with congenital heart disease: a case control study
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Hypoxic/ischemic hits predispose to necrotizing enterocolitis in (near) term infants with congenital heart disease: a case control study

BMC pediatrics, 2020-12, Vol.20 (1), p.553-553, Article 553 [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: 1471-2431 ;EISSN: 1471-2431 ;DOI: 10.1186/s12887-020-02446-6 ;PMID: 33287760

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15
Prenatal echocardiographic diagnosis of congenital heart disease in high-risk antenatal mothers in a tertiary care center and their postnatal outcome: An experience from third world
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Prenatal echocardiographic diagnosis of congenital heart disease in high-risk antenatal mothers in a tertiary care center and their postnatal outcome: An experience from third world

Heart India, 2020-04, Vol.8 (2), p.103-110 [Peer Reviewed Journal]

ISSN: 2321-449X ;DOI: 10.4103/heartindia.heartindia_9_19

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16
Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformations
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Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformations

Nature genetics, 2017-04, Vol.49 (4), p.613-617 [Peer Reviewed Journal]

COPYRIGHT 2017 Nature Publishing Group ;COPYRIGHT 2017 Nature Publishing Group ;Copyright Nature Publishing Group Apr 2017 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.3815 ;PMID: 28288113

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17
Unraveling the genomic basis of congenital heart disease
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Article
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Unraveling the genomic basis of congenital heart disease

The Journal of clinical investigation, 2021-01, Vol.131 (2), p.1-2 [Peer Reviewed Journal]

COPYRIGHT 2021 American Society for Clinical Investigation ;COPYRIGHT 2021 American Society for Clinical Investigation ;Copyright American Society for Clinical Investigation Jan 2021 ;2021 American Society for Clinical Investigation 2021 American Society for Clinical Investigation ;ISSN: 0021-9738 ;EISSN: 1558-8238 ;DOI: 10.1172/JCI145377 ;PMID: 33463545

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18
Genetic variant in MTRR, but not MTR, is associated with risk of congenital heart disease: an integrated meta-analysis
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Genetic variant in MTRR, but not MTR, is associated with risk of congenital heart disease: an integrated meta-analysis

PloS one, 2014-03, Vol.9 (3), p.e89609 [Peer Reviewed Journal]

COPYRIGHT 2014 Public Library of Science ;COPYRIGHT 2014 Public Library of Science ;2014 Cai 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. ;2014 Cai et al 2014 Cai et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0089609 ;PMID: 24595101

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19
Bone fragility in patients affected by congenital diseases non skeletal in origin
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Bone fragility in patients affected by congenital diseases non skeletal in origin

Orphanet journal of rare diseases, 2021-01, Vol.16 (1), p.11-11, Article 11 [Peer Reviewed Journal]

COPYRIGHT 2021 BioMed Central Ltd. ;2021. 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) 2021 ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-020-01611-5 ;PMID: 33407701

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20
The risk of cancer in patients with congenital heart disease: a nationwide population-based cohort study in Taiwan
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The risk of cancer in patients with congenital heart disease: a nationwide population-based cohort study in Taiwan

PloS one, 2015-02, Vol.10 (2), p.e0116844-e0116844 [Peer Reviewed Journal]

COPYRIGHT 2015 Public Library of Science ;COPYRIGHT 2015 Public Library of Science ;2015 Lee 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 Lee et al 2015 Lee et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0116844 ;PMID: 25706872

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