Academic Content and Language Evaluation of This Article
CrossCheck and Google Search of This Article
Academic Rules and Norms of This Article
Citation of this article
Corresponding Author of This Article
Research Domain of This Article
Article-Type of This Article
Open-Access Policy of This Article
Times Cited Counts in Google of This Article
Number of Hits and Downloads for This Article
- Total Article Views (12323)
All Articles published online
|
Publishing Process of This Article
|
Feb 26, 2016 (publication date) through Dec 24, 2024
Times Cited of This Article
Journal Information of This Article
Publication Name
World Journal of Cardiology
ISSN
1949-8462
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| 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 |
Ahmad Fikri Azfar Ahmad Azahari, Wan Naimah Wan Ab Naim, Nor Ashikin Md Sari, Einly Lim, Mohd Jamil Mohamed Mokhtarudin. Advancement in computational simulation and validation of congenital heart disease: a review. Computer Methods in Biomechanics and Biomedical Engineering 2024; : 1 doi: 10.1080/10255842.2024.2377338
|
| 2 |
Gregory Costain, Candice K Silversides, Anne S Bassett. The importance of copy number variation in congenital heart disease. npj Genomic Medicine 2016; 1(1) doi: 10.1038/npjgenmed.2016.31
|
| 3 |
|
| 4 |
Florencia Petracchi, Silvina Sisterna, Laura Igarzabal, Louise Wilkins‐Haug. Fetal cardiac abnormalities: Genetic etiologies to be considered. Prenatal Diagnosis 2019; 39(9): 758 doi: 10.1002/pd.5480
|
| 5 |
Teodoro Jerves, Andrea Beaton, Paul Kruszka. The genetic workup for structural congenital heart disease. American Journal of Medical Genetics Part C: Seminars in Medical Genetics 2020; 184(1): 178 doi: 10.1002/ajmg.c.31759
|
| 6 |
Frauke Hausburg, Julia Jeannine Jung, Matti Hoch, Markus Wolfien, Arash Yavari, Christian Rimmbach, Robert David. (Re-)programming of subtype specific cardiomyocytes. Advanced Drug Delivery Reviews 2017; 120: 142 doi: 10.1016/j.addr.2017.09.005
|
| 7 |
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 review. Jornal de Pediatria 2020; 96(3): 279 doi: 10.1016/j.jped.2019.07.004
|
| 8 |
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 Disease. Journal of Genetic Counseling 2017; 26(4): 669 doi: 10.1007/s10897-017-0081-z
|
| 9 |
Dorota Szumska, Robert Wilson, Wolfgang Weninger, Tim Mohun. Fetal Therapy. 2019; : 133 doi: 10.1017/9781108564434.015
|
| 10 |
Rabina Shrestha, Jaret Lieberth, Savanna Tillman, Joseph Natalizio, Joshua Bloomekatz. Animal Models of Human Birth Defects. Advances in Experimental Medicine and Biology 2020; 1236: 189 doi: 10.1007/978-981-15-2389-2_8
|
| 11 |
NKX2-5 variants screening in patients with atrial septal defect in Indonesia. BMC Medical Genomics 2022; 15(1) doi: 10.1186/s12920-022-01242-8
|
| 12 |
Bo Wang, Guoling You, Qihua Fu. Human fetal heart specific coexpression network involves congenital heart disease/defect candidate genes. Scientific Reports 2017; 7(1) doi: 10.1038/srep46760
|
| 13 |
Gulrez Chahal, Sonika Tyagi, Mirana Ramialison. Navigating the non-coding genome in heart development and Congenital Heart Disease. Differentiation 2019; 107: 11 doi: 10.1016/j.diff.2019.05.001
|
| 14 |
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 offspring. Medicine 2019; 98(18): e15352 doi: 10.1097/MD.0000000000015352
|
| 15 |
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 Study. Circulation: Genomic and Precision Medicine 2023; 16(2) doi: 10.1161/CIRCGEN.122.003791
|
| 16 |
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 review. Jornal de Pediatria (Versão em Português) 2020; 96(3): 279 doi: 10.1016/j.jpedp.2019.07.002
|
| 17 |
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 disease. European Heart Journal 2022; 43(22): 2103 doi: 10.1093/eurheartj/ehac104
|
| 18 |
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 unit. Journal of Perinatology 2024; 44(8): 1196 doi: 10.1038/s41372-024-01935-1
|
| 19 |
A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship. Genetics in Medicine Open 2024; 2: 101842 doi: 10.1016/j.gimo.2024.101842
|
| 20 |
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 study. Indian Journal of Medical Sciences 2022; 74: 126 doi: 10.25259/IJMS_414_2021
|
| 21 |
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 China. Italian Journal of Pediatrics 2024; 50(1) doi: 10.1186/s13052-024-01630-z
|
| 22 |
Joshua D. Kurtz, Katerina Boucek, Minoo Kavarana, Andrew M. Atz. Two Brothers With Dextro-Transposition of the Great Arteries. World Journal for Pediatric and Congenital Heart Surgery 2020; 11(4): NP155 doi: 10.1177/2150135118768718
|
| 23 |
Jeroen Breckpot. Genetic counselling and testing in congenital heart defects and hereditary thoracic aortic disease: Complex but essential. European Journal of Preventive Cardiology 2019; 26(15): 1670 doi: 10.1177/2047487319860296
|
| 24 |
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 defects. The Kaohsiung Journal of Medical Sciences 2017; 33(9): 442 doi: 10.1016/j.kjms.2017.05.016
|
| 25 |
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 research. Congenital Heart Disease 2018; 13(5): 685 doi: 10.1111/chd.12630
|
| 26 |
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 review. Trends in Cardiovascular Medicine 2022; 32(5): 311 doi: 10.1016/j.tcm.2021.04.011
|
| 27 |
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 China. Scientific Reports 2018; 8(1) doi: 10.1038/s41598-018-26727-4
|
| 28 |
Anne S. Bassett, Miriam S. Reuter, Sarah Malecki, Candice Silversides, Erwin Oechslin. Clinically Relevant Genetic Considerations for Patients With Tetralogy of Fallot. CJC Pediatric and Congenital Heart Disease 2023; 2(6): 426 doi: 10.1016/j.cjcpc.2023.10.002
|
| 29 |
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 death. Experimental and Molecular Pathology 2024; 137: 104907 doi: 10.1016/j.yexmp.2024.104907
|
| 30 |
Kylia Williams, Jason Carson, Cecilia Lo. Genetics of Congenital Heart Disease. Biomolecules 2019; 9(12): 879 doi: 10.3390/biom9120879
|
| 31 |
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 patients. Balkan Journal of Medical Genetics 2021; 24(1): 15 doi: 10.2478/bjmg-2021-0014
|
| 32 |
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 Testing. Genes 2024; 15(4): 505 doi: 10.3390/genes15040505
|
| 33 |
Leong Tung Ong. Editor’s Pick: Genetics and Pathophysiology of Co-occurrence of Congenital Heart Disease and Autism Spectrum Disorder. European Medical Journal 2024; : 73 doi: 10.33590/emj/MKPN4473
|
| 34 |
Anna Tsepokina, Svetlana Shmulevich, Anastasia Ponasenko, Andrey Shabaldin. Genetic predisposition to the development of congenital heart diseases: Role of xenobiotic biotransformation genes. Birth Defects Research 2021; 113(7): 579 doi: 10.1002/bdr2.1841
|
| 35 |
Lisa J. Martin, D. Woodrow Benson. Focused Strategies for Defining the Genetic Architecture of Congenital Heart Defects. Genes 2021; 12(6): 827 doi: 10.3390/genes12060827
|
| 36 |
Liya Popova, Valerie J. Carabetta. High Throughput Gene Screening. Methods in Molecular Biology 2025; 2866: 287 doi: 10.1007/978-1-0716-4192-7_16
|
| 37 |
Kamalvir Gill, Jun Sasaki, Parul Jayakar, Lisa Sosa, Elizabeth Welch. Chromosomal microarray detects genetic risks of neurodevelopmental disorders in newborns with congenital heart disease. Cardiology in the Young 2021; 31(8): 1275 doi: 10.1017/S1047951121000202
|
| 38 |
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 inclusion. European Journal of Epidemiology 2019; 34(1): 79 doi: 10.1007/s10654-018-0448-y
|
| 39 |
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 polymorphisms. Human Gene 2024; 41: 201296 doi: 10.1016/j.humgen.2024.201296
|
| 40 |
Robin D. Clark, Cynthia J. Curry, Robin D. Clark, Cynthia J. Curry. Genetic Consultations in the Newborn. 2019; : 49 doi: 10.1093/med/9780199990993.003.0007
|
| 41 |
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 offspring. Birth Defects Research 2024; 116(3) doi: 10.1002/bdr2.2282
|
| 42 |
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 disease. Journal of International Medical Research 2019; 47(10): 5270 doi: 10.1177/0300060519869079
|
| 43 |
Seham Osman Babiker Omer, Riyadh Mahdi Abu-Sulaiman, Majid Alfadhel. Manual of Pediatric Cardiac Care. 2024; : 485 doi: 10.1007/978-981-19-8357-3_57
|
| 44 |
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 disease. Frontiers in Genetics 2024; 15 doi: 10.3389/fgene.2024.1398887
|
| 45 |
Leitong Wang, Guangrui Lai, Guoming Chu, Xiaoyan Liang, Yanyan Zhao. cMyBP-C was decreased via KLHL3-mediated proteasomal degradation in congenital heart diseases. Experimental Cell Research 2017; 355(1): 18 doi: 10.1016/j.yexcr.2017.03.025
|
| 46 |
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 Dysplasia. Open Access Macedonian Journal of Medical Sciences 2022; 10(B): 1258 doi: 10.3889/oamjms.2022.8253
|
| 47 |
Neeta Sethi, Stephen Miller, Kevin D. Hill. Prenatal Diagnosis, Management, and Treatment of Fetal Cardiac Disease. NeoReviews 2023; 24(5): e285 doi: 10.1542/neo.24-5-e285
|