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For: Chaix MA, Andelfinger G, Khairy P. Genetic testing in congenital heart disease: A clinical approach. World J Cardiol 2016; 8(2): 180-191 [PMID: 26981213 DOI: 10.4330/wjc.v8.i2.180]
URL: https://www.wjgnet.com/1949-8462/full/v8/i2/180.htm
Number Citing Articles
1
Gregory Costain, Candice K Silversides, Anne S Bassett. The importance of copy number variation in congenital heart diseasenpj Genomic Medicine 2016; 1(1) doi: 10.1038/npjgenmed.2016.31
2
Marlon De Ita Ley. Encyclopedia of Life Sciences2022; : 1 doi: 10.1002/9780470015902.a0029332
3
Florencia Petracchi, Silvina Sisterna, Laura Igarzabal, Louise Wilkins‐Haug. Fetal cardiac abnormalities: Genetic etiologies to be consideredPrenatal Diagnosis 2019; 39(9): 758 doi: 10.1002/pd.5480
4
Teodoro Jerves, Andrea Beaton, Paul Kruszka. The genetic workup for structural congenital heart diseaseAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics 2020; 184(1): 178 doi: 10.1002/ajmg.c.31759
5
Frauke Hausburg, Julia Jeannine Jung, Matti Hoch, Markus Wolfien, Arash Yavari, Christian Rimmbach, Robert David. (Re-)programming of subtype specific cardiomyocytesAdvanced Drug Delivery Reviews 2017; 120: 142 doi: 10.1016/j.addr.2017.09.005
6
Aline Saliba, Ana Carolina Vaqueiro Figueiredo, José Eduardo Baroneza, Jorge Yuseff Afiune, Aline Pic-Taylor, Silviene Fabiana de Oliveira, Juliana Forte Mazzeu. Genetic and genomics in congenital heart disease: a clinical reviewJornal de Pediatria 2020; 96(3): 279 doi: 10.1016/j.jped.2019.07.004
7
Ana Morales, Dawn C. Allain, Patricia Arscott, Emily James, Gretchen MacCarrick, Brittney Murray, Crystal Tichnell, Amy R. Shikany, Sara Spencer, Sara M. Fitzgerald‐Butt, Jessica D. Kushner, Christi Munn, Emily Smith, Katherine G. Spoonamore, Harikrishna S. Tandri, W. Aaron Kay. At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart DiseaseJournal of Genetic Counseling 2017; 26(4): 669 doi: 10.1007/s10897-017-0081-z
8
Dorota Szumska, Robert Wilson, Wolfgang Weninger, Tim Mohun. Fetal Therapy2019; : 133 doi: 10.1017/9781108564434.015
9
Rabina Shrestha, Jaret Lieberth, Savanna Tillman, Joseph Natalizio, Joshua Bloomekatz. Animal Models of Human Birth DefectsAdvances in Experimental Medicine and Biology 2020; 1236: 189 doi: 10.1007/978-981-15-2389-2_8
10
NKX2-5 variants screening in patients with atrial septal defect in IndonesiaBMC Medical Genomics 2022; 15(1) doi: 10.1186/s12920-022-01242-8
11
Bo Wang, Guoling You, Qihua Fu. Human fetal heart specific coexpression network involves congenital heart disease/defect candidate genesScientific Reports 2017; 7(1) doi: 10.1038/srep46760
12
Gulrez Chahal, Sonika Tyagi, Mirana Ramialison. Navigating the non-coding genome in heart development and Congenital Heart DiseaseDifferentiation 2019; 107: 11 doi: 10.1016/j.diff.2019.05.001
13
Nannan Zhang, Ming Chen, Jun Li, Ying Deng, Sheng-li Li, Yi-xiong Guo, Nana Li, Yuan Lin, Ping Yu, Zhen Liu, Jun Zhu. Metal nickel exposure increase the risk of congenital heart defects occurrence in offspringMedicine 2019; 98(18): e15352 doi: 10.1097/MD.0000000000015352
14
Emily L. Griffin, Shannon N. Nees, Sarah U. Morton, Julia Wynn, Nihir Patel, Vaidehi Jobanputra, Scott Robinson, Stephanie M. Kochav, Alice Tao, Carli Andrews, Nancy Cross, Judith Geva, Kristen Lanzilotta, Alyssa Ritter, Eileen Taillie, Alexandra Thompson, Chris Meyer, Rachel Akers, Eileen C. King, James F Cnota, Richard W. Kim, George A. Porter, Martina Brueckner, Christine E. Seidman, Yufeng Shen, Bruce D. Gelb, Elizabeth Goldmuntz, Jane W. Newburger, Amy E. Roberts, Wendy K. Chung. Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic StudyCirculation: Genomic and Precision Medicine 2023; 16(2) doi: 10.1161/CIRCGEN.122.003791
15
Aline Saliba, Ana Carolina Vaqueiro Figueiredo, José Eduardo Baroneza, Jorge Yuseff Afiune, Aline Pic‐Taylor, Silviene Fabiana de Oliveira, Juliana Forte Mazzeu. Genetic and genomics in congenital heart disease: a clinical reviewJornal de Pediatria (Versão em Português) 2020; 96(3): 279 doi: 10.1016/j.jpedp.2019.07.002
16
Paul Khairy, Michael J Silka, Jeremy P Moore, James A DiNardo, Jim T Vehmeijer, Mary N Sheppard, Alexander van de Bruaene, Marie-A Chaix, Margarita Brida, Benjamin M Moore, Maully J Shah, Blandine Mondésert, Seshadri Balaji, Michael A Gatzoulis, Magalie Ladouceur. Sudden cardiac death in congenital heart diseaseEuropean Heart Journal 2022; 43(22): 2103 doi: 10.1093/eurheartj/ehac104
17
Erica E. D’Souza, Tina O. Findley, Rachel Hu, Zahra S. H. Khazal, Rachel Signorello, Camille Dash, Alissa M. D’Gama, Henry A. Feldman, Pankaj B. Agrawal, Monica H. Wojcik, Sarah U. Morton. Genomic testing and molecular diagnosis among infants with congenital heart disease in the neonatal intensive care unitJournal of Perinatology 2024;  doi: 10.1038/s41372-024-01935-1
18
A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders FlagshipGenetics in Medicine Open 2024; 2: 101842 doi: 10.1016/j.gimo.2024.101842
19
Ankush Bala, Jyotdeep Kour Raina, Amrit Sudershan, Sanjeev Digra, Manoj K. Dhar, Rakesh K. Panjaliya, Parvinder Kumar. Relationship of MTHFD1 G1958A and CBS 844ins68 polymorphism with congenital heart defects in North Indian population (Jammu and Kashmir): A case-control studyIndian Journal of Medical Sciences 2022; 74: 126 doi: 10.25259/IJMS_414_2021
20
Ye Jin, Miao Zhao, Qiuzhe Guo, Wanyu Zhao, Min Lei, Yifei Zhang, Yunhan zhang, Yan Shen, Keqin Lin, Zhaoqing Yang, Jiayou Chu, Hao Sun, Zhiling Luo. Association study of FLT4 and HYDIN single nucleotide polymorphisms with atrial septal defect susceptibility in the Han Chinese population of Southwest ChinaItalian Journal of Pediatrics 2024; 50(1) doi: 10.1186/s13052-024-01630-z
21
Joshua D. Kurtz, Katerina Boucek, Minoo Kavarana, Andrew M. Atz. Two Brothers With Dextro-Transposition of the Great ArteriesWorld Journal for Pediatric and Congenital Heart Surgery 2020; 11(4): NP155 doi: 10.1177/2150135118768718
22
Jeroen Breckpot. Genetic counselling and testing in congenital heart defects and hereditary thoracic aortic disease: Complex but essentialEuropean Journal of Preventive Cardiology 2019; 26(15): 1670 doi: 10.1177/2047487319860296
23
Mehri Khatami, Farzaneh Morteza Ratki, Saba Tajfar, Fatemeh Akrami. Relationship of the MTHFD1 (rs2236225), eNOS (rs1799983), CBS (rs2850144) and ACE (rs4343) gene polymorphisms in a population of Iranian pediatric patients with congenital heart defectsThe Kaohsiung Journal of Medical Sciences 2017; 33(9): 442 doi: 10.1016/j.kjms.2017.05.016
24
Paul C. Helm, Ulrike M. M. Bauer, Hashim Abdul‐Khaliq, Helmut Baumgartner, Hans‐Heiner Kramer, Christian Schlensak, Thomas Pickardt, Anne‐Karin Kahlert, Marc‐Phillip Hitz. Patients with congenital heart defect and their families support genetic heart researchCongenital Heart Disease 2018; 13(5): 685 doi: 10.1111/chd.12630
25
Ansley M. Morrish, Janine Smith, Annabelle Enriquez, Gary F. Sholler, Jonathan Mervis, Sally L. Dunwoodie, Edwin P. Kirk, David S. Winlaw, Gillian M. Blue. A new era of genetic testing in congenital heart disease: A reviewTrends in Cardiovascular Medicine 2022; 32(5): 311 doi: 10.1016/j.tcm.2021.04.011
26
Yaobin Yin, Jianguang Ji, Yan Borné, Yanqing Wang, Junhui Zhao, Shanlin Chen, Wen Tian. Clinical and epidemiological features of Heart-Hand Syndrome: a hospital-based study in ChinaScientific Reports 2018; 8(1) doi: 10.1038/s41598-018-26727-4
27
Anne S. Bassett, Miriam S. Reuter, Sarah Malecki, Candice Silversides, Erwin Oechslin. Clinically Relevant Genetic Considerations for Patients With Tetralogy of FallotCJC Pediatric and Congenital Heart Disease 2023; 2(6): 426 doi: 10.1016/j.cjcpc.2023.10.002
28
Francesco Sessa, Mario Chisari, Monica Salerno, Massimiliano Esposito, Pietro Zuccarello, Emanuele Capasso, Edmondo Scoto, Giuseppe Cocimano. Congenital heart diseases (CHDs) and forensic investigations: Searching for the cause of deathExperimental and Molecular Pathology 2024; 137: 104907 doi: 10.1016/j.yexmp.2024.104907
29
Kylia Williams, Jason Carson, Cecilia Lo. Genetics of Congenital Heart DiseaseBiomolecules 2019; 9(12): 879 doi: 10.3390/biom9120879
30
L Aidinidou, A Chatzikyriakidou, A Giannopoulos, V Karpa, I Tzimou, E Aidinidou, L Fidani. Association of NFKB1, NKX2-5, GATA4 and RANKL gene polymorphisms with sporadic congenital heart disease in Greek patientsBalkan Journal of Medical Genetics 2021; 24(1): 15 doi: 10.2478/bjmg-2021-0014
31
Benjamin M. Helm, Stephanie M. Ware. Clinical Decision Analysis of Genetic Evaluation and Testing in 1013 Intensive Care Unit Infants with Congenital Heart Defects Supports Universal Genetic TestingGenes 2024; 15(4): 505 doi: 10.3390/genes15040505
32
Leong Tung Ong. Editor’s Pick: Genetics and Pathophysiology of Co-occurrence of Congenital Heart Disease and Autism Spectrum DisorderEuropean Medical Journal 2024; : 73 doi: 10.33590/emj/MKPN4473
33
Anna Tsepokina, Svetlana Shmulevich, Anastasia Ponasenko, Andrey Shabaldin. Genetic predisposition to the development of congenital heart diseases: Role of xenobiotic biotransformation genesBirth Defects Research 2021; 113(7): 579 doi: 10.1002/bdr2.1841
34
Lisa J. Martin, D. Woodrow Benson. Focused Strategies for Defining the Genetic Architecture of Congenital Heart DefectsGenes 2021; 12(6): 827 doi: 10.3390/genes12060827
35
Kamalvir Gill, Jun Sasaki, Parul Jayakar, Lisa Sosa, Elizabeth Welch. Chromosomal microarray detects genetic risks of neurodevelopmental disorders in newborns with congenital heart diseaseCardiology in the Young 2021; 31(8): 1275 doi: 10.1017/S1047951121000202
36
Anne-Sophie Sillesen, Anna Axelsson Raja, Christian Pihl, Ruth Ottilia Birgitta Vøgg, Morten Hedegaard, Pernille Emmersen, Karin Sundberg, Ann Tabor, Cathrine Vedel, Helle Zingenberg, Charlotte Kruse, Charlotte Wilken-Jensen, Tina Holm Nielsen, Finn Stener Jørgensen, Dorthe Lisbeth Jeppesen, Lars Søndergaard, Pia R. Kamstrup, Børge G. Nordestgaard, Ruth Frikke-Schmidt, Niels Vejlstrup, Heather A. Boyd, Henning Bundgaard, Kasper Iversen. Copenhagen Baby Heart Study: a population study of newborns with prenatal inclusionEuropean Journal of Epidemiology 2019; 34(1): 79 doi: 10.1007/s10654-018-0448-y
37
Ankush Bala, Amrit Sudershan, Dharminder Kumar, Sanjeev K. Digra, Rakesh K. Panjaliya, Parvinder Kumar. Genetic links to congenital heart defects: A comprehensive meta-analysis of MTHFD1 and CBS polymorphismsHuman Gene 2024; 41: 201296 doi: 10.1016/j.humgen.2024.201296
38
Jianli Gu, Zhen Jin, Guiqing Wu, Shaonong Dang, Feng Yao, Zihan Zheng, Lingxuan Ren, Jianjun Yang, Danli Chen, Li Zhang, Rong Lin. Correlation between essential and toxic elements in maternal blood during early pregnancy and atrial septal defects/ventricular septal defects/patent ductus arteriosus in offspringBirth Defects Research 2024; 116(3) doi: 10.1002/bdr2.2282
39
Yaobin Zhu, Yaping Zhang, Nan Ding, Yudong Zhao, Zankai Ye, Xing Fan, Yang Liu, Lei Shen, Hanlu Yi, Zhiqiang Li. The role of cardiac surgeons in online prenatal counselling for congenital heart diseaseJournal of International Medical Research 2019; 47(10): 5270 doi: 10.1177/0300060519869079
40
Laura B. Oehlman, Alexander R. Opotowsky, Kathryn N. Weaver, Nicole M. Brown, Cara L. Barnett, Erin M. Miller, Hua He, Amy R. Shikany. Current approach to genetic testing and genetic evaluation referrals for adults with congenital heart diseaseFrontiers in Genetics 2024; 15 doi: 10.3389/fgene.2024.1398887
41
Leitong Wang, Guangrui Lai, Guoming Chu, Xiaoyan Liang, Yanyan Zhao. cMyBP-C was decreased via KLHL3-mediated proteasomal degradation in congenital heart diseasesExperimental Cell Research 2017; 355(1): 18 doi: 10.1016/j.yexcr.2017.03.025
42
Madina Madiyeva, Tamara Rymbaeva . Congenital Heart Disease in Children Living Close to the Former Semipalatinsk Nuclear Test Site: Frequency, Structure, and Links with Connective Tissue DysplasiaOpen Access Macedonian Journal of Medical Sciences 2022; 10(B): 1258 doi: 10.3889/oamjms.2022.8253
43
Neeta Sethi, Stephen Miller, Kevin D. Hill. Prenatal Diagnosis, Management, and Treatment of Fetal Cardiac DiseaseNeoReviews 2023; 24(5): e285 doi: 10.1542/neo.24-5-e285