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1
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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2
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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3
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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4
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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5
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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6
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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7
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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8
Increased prevalence of inattention-related symptoms in a large cohort of patients with congenital heart disease
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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9
Prevalence of Mental Illness in Adolescents and Adults With Congenital Heart Disease from the Colorado Congenital Heart Defect Surveillance System
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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10
Association of congenital heart disease and neurodevelopmental disorders: an observational and Mendelian randomization study
Association of congenital heart disease and neurodevelopmental disorders: an observational and Mendelian randomization study
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Association of congenital heart disease and neurodevelopmental disorders: an observational and Mendelian randomization study

Italian journal of pediatrics, 2024-04, Vol.50 (1), p.63-63 [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. ;The Author(s) 2024 ;ISSN: 1720-8424 ;EISSN: 1824-7288 ;DOI: 10.1186/s13052-024-01610-3 ;PMID: 38589916

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11
Utility of next generation sequencing in genetic diagnosis of early onset neuromuscular disorders
Utility of next generation sequencing in genetic diagnosis of early onset neuromuscular disorders
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Utility of next generation sequencing in genetic diagnosis of early onset neuromuscular disorders

Journal of medical genetics, 2015-03, Vol.52 (3), p.208-216 [Peer Reviewed Journal]

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. ;Copyright: 2015 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmedgenet-2014-102819 ;PMID: 25635128 ;CODEN: JMDGAE

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12
Value of Galectin-3 assay in children with heart failure secondary to congenital heart diseases: a prospective study
Value of Galectin-3 assay in children with heart failure secondary to congenital heart diseases: a prospective study
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Value of Galectin-3 assay in children with heart failure secondary to congenital heart diseases: a prospective study

BMC pediatrics, 2020-11, Vol.20 (1), p.537-537, Article 537 [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/s12887-020-02427-9 ;PMID: 33248453

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13
Invasive cardiovascular magnetic resonance (iCMR) for diagnostic right and left heart catheterization using an MR-conditional guidewire and passive visualization in congenital heart disease
Invasive cardiovascular magnetic resonance (iCMR) for diagnostic right and left heart catheterization using an MR-conditional guidewire and passive visualization in congenital heart disease
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Invasive cardiovascular magnetic resonance (iCMR) for diagnostic right and left heart catheterization using an MR-conditional guidewire and passive visualization in congenital heart disease

Journal of cardiovascular magnetic resonance, 2020-03, Vol.22 (1), p.20-11, Article 20 [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/s12968-020-0605-9 ;PMID: 32213193

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14
Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease
Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease
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Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease

Human genetics, 2021-02, Vol.140 (2), p.333-348 [Peer Reviewed Journal]

Springer-Verlag GmbH Germany, part of Springer Nature 2020 ;COPYRIGHT 2020 Springer ;Springer-Verlag GmbH Germany, part of Springer Nature 2020. ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/s00439-020-02200-z ;PMID: 32696347

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15
Telemedicine in Adult Congenital Heart Disease: Usefulness of Digital Health Technology in the Assistance of Critical Patients
Telemedicine in Adult Congenital Heart Disease: Usefulness of Digital Health Technology in the Assistance of Critical Patients
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Telemedicine in Adult Congenital Heart Disease: Usefulness of Digital Health Technology in the Assistance of Critical Patients

International journal of environmental research and public health, 2023-05, Vol.20 (10), p.5775 [Peer Reviewed Journal]

COPYRIGHT 2023 MDPI AG ;2023 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. ;2023 by the authors. 2023 ;ISSN: 1660-4601 ;ISSN: 1661-7827 ;EISSN: 1660-4601 ;DOI: 10.3390/ijerph20105775 ;PMID: 37239504

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16
Physical activity for children with chronic disease; a narrative review and practical applications
Physical activity for children with chronic disease; a narrative review and practical applications
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Physical activity for children with chronic disease; a narrative review and practical applications

BMC pediatrics, 2019-01, Vol.19 (1), p.12-12, Article 12 [Peer Reviewed Journal]

COPYRIGHT 2019 BioMed Central Ltd. ;Copyright © 2019. 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). 2019 ;ISSN: 1471-2431 ;EISSN: 1471-2431 ;DOI: 10.1186/s12887-018-1377-3 ;PMID: 30621667

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17
Characteristic face: a key indicator for direct diagnosis of 22q11.2 deletions in Chinese velocardiofacial syndrome patients
Characteristic face: a key indicator for direct diagnosis of 22q11.2 deletions in Chinese velocardiofacial syndrome patients
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Characteristic face: a key indicator for direct diagnosis of 22q11.2 deletions in Chinese velocardiofacial syndrome patients

PloS one, 2013-01, Vol.8 (1), p.e54404 [Peer Reviewed Journal]

COPYRIGHT 2013 Public Library of Science ;COPYRIGHT 2013 Public Library of Science ;2013 Wu et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://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. ;2013 Wu et al 2013 Wu et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0054404 ;PMID: 23342150

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18
Children with a rare congenital genetic disorder: a systematic review of parent experiences
Children with a rare congenital genetic disorder: a systematic review of parent experiences
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Children with a rare congenital genetic disorder: a systematic review of parent experiences

Orphanet journal of rare diseases, 2022-10, Vol.17 (1), p.1-375, Article 375 [Peer Reviewed Journal]

COPYRIGHT 2022 BioMed Central Ltd. ;2022. 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) 2022 ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-022-02525-0

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19
A case report of children of the same family presenting with congenital cataract- as part of a rare genetic disorder-Sengers Syndrome
A case report of children of the same family presenting with congenital cataract- as part of a rare genetic disorder-Sengers Syndrome
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A case report of children of the same family presenting with congenital cataract- as part of a rare genetic disorder-Sengers Syndrome

Indian journal of ophthalmology, 2020-11, Vol.68 (11), p.2567-2569 [Peer Reviewed Journal]

COPYRIGHT 2020 Medknow Publications and Media Pvt. Ltd. ;2020. This article is published under (http://creativecommons.org/licenses/by-nc-sa/3.0/) (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright: © 2020 Indian Journal of Ophthalmology 2020 ;ISSN: 0301-4738 ;EISSN: 1998-3689 ;DOI: 10.4103/ijo.IJO_760_20 ;PMID: 33120694

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20
Variations of CITED2 are associated with congenital heart disease (CHD) in Chinese population
Variations of CITED2 are associated with congenital heart disease (CHD) in Chinese population
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Variations of CITED2 are associated with congenital heart disease (CHD) in Chinese population

PloS one, 2014-05, Vol.9 (5), p.e98157 [Peer Reviewed Journal]

COPYRIGHT 2014 Public Library of Science ;2014 Liu 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 Liu et al 2014 Liu et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0098157 ;PMID: 24848765

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