BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Pierpont ME, Brueckner M, Chung WK, Garg V, Lacro RV, McGuire AL, Mital S, Priest JR, Pu WT, Roberts A, Ware SM, Gelb BD, Russell MW; American Heart Association Council on Cardiovascular Disease in the Young; Council on Cardiovascular and Stroke Nursing; and Council on Genomic and Precision Medicine. Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association. Circulation 2018;138:e653-711. [PMID: 30571578 DOI: 10.1161/CIR.0000000000000606] [Cited by in Crossref: 125] [Cited by in F6Publishing: 60] [Article Influence: 41.7] [Reference Citation Analysis]
Number Citing Articles
1 Sharma M, Choueiter N. 50 Years Ago in TheJournalofPediatrics: Congenital Heart Disease and Genetic Counseling: Shifting Paradigm. J Pediatr 2022;244:e6. [PMID: 35534172 DOI: 10.1016/j.jpeds.2022.01.021] [Reference Citation Analysis]
2 Ware SM. Pediatric cardiomyopathy and the PCM Genes study: A summary with insights on genetic testing, variant interpretation, race and ethnicity. Progress in Pediatric Cardiology 2021;63:101468. [DOI: 10.1016/j.ppedcard.2021.101468] [Reference Citation Analysis]
3 Yu B, Yao S, Liu L, Li H, Zhu J, Li M, Han S, Yu Z. The role of polypeptide PDTLN1 in suppression of PI3K/AKT signaling causes cardiogenetic disorders in vitro and in vivo. Life Sci 2022;289:120244. [PMID: 34922940 DOI: 10.1016/j.lfs.2021.120244] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Akerberg BN, Pu WT. Genetic and Epigenetic Control of Heart Development. Cold Spring Harb Perspect Biol 2020;12:a036756. [PMID: 31818853 DOI: 10.1101/cshperspect.a036756] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
5 Kodo K, Uchida K, Yamagishi H. Genetic and Cellular Interaction During Cardiovascular Development Implicated in Congenital Heart Diseases. Front Cardiovasc Med 2021;8:653244. [PMID: 33796576 DOI: 10.3389/fcvm.2021.653244] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Zhan X, Chen L, Jiang M, Fu B. Get insight into the cause of death distribution and epidemiology of penile squamous cell carcinoma: A population-based study. Cancer Med 2022. [PMID: 35238488 DOI: 10.1002/cam4.4614] [Reference Citation Analysis]
7 Assimopoulos S, Hammill C, Fernandes DJ, Spencer Noakes TL, Zhou YQ, Nutter LMJ, Ellegood J, Anagnostou E, Sled JG, Lerch JP. Genetic mouse models of autism spectrum disorder present subtle heterogenous cardiac abnormalities. Autism Res 2022. [PMID: 35445787 DOI: 10.1002/aur.2728] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Geddes GC, Syverson E, Earing MG. Three year experience of a clinical cardiovascular genetics program for infants with congenital heart disease. Congenit Heart Dis 2019;14:832-7. [PMID: 31222963 DOI: 10.1111/chd.12817] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
9 Afifi HH, Gaber KR, Thomas MM, Taher MB, Tosson AMS. Genetic Implications in High-Risk Pregnancy and Its Outcome: A 2-year Study. Am J Perinatol 2021. [PMID: 33636738 DOI: 10.1055/s-0041-1724002] [Reference Citation Analysis]
10 Benjamin RH, Scheuerle AE, Scott DA, Navarro Sanchez ML, Langlois PH, Canfield MA, Northrup H, Schaaf CP, Ray JW, McLean SD, Chen H, Swartz MD, Lupo PJ, Agopian AJ. Birth defect co-occurrence patterns in the Texas Birth Defects Registry. Pediatr Res 2021. [PMID: 34193968 DOI: 10.1038/s41390-021-01629-w] [Reference Citation Analysis]
11 Ni P, Chen X, Zhang Y, Zhang M, Xu Z, Luo W. High-Energy Enteral Nutrition in Infants After Complex Congenital Heart Surgery. Front Pediatr 2022;10:869415. [DOI: 10.3389/fped.2022.869415] [Reference Citation Analysis]
12 Udholm LF, Gaml‐sørensen A, Arendt LH, Brix N, Lunddorf LLH, Ernst A, Knudsen UB, Hjortdal VE, Ramlau‐hansen CH. Timing of Pubertal Development in Boys and Girls With Congenital Heart Defects: A Nationwide Cohort Study. JAHA. [DOI: 10.1161/jaha.121.023135] [Reference Citation Analysis]
13 Wang H, Xiao F, Qian Y, Wu B, Dong X, Lu Y, Cheng G, Wang L, Yan K, Yang L, Chen L, Kang W, Li L, Pan X, Wei Q, Zhuang D, Chen D, Yin Z, Yang L, Ni Q, Liu R, Li G, Zhang P, Li X, Peng X, Wang Y, Chen H, Ma X, Liu F, Cao Y, Huang G, Zhou W. Genetic architecture in neonatal intensive care unit patients with congenital heart defects: a retrospective study from the China Neonatal Genomes Project. J Med Genet 2022:jmedgenet-2021-108354. [PMID: 35595280 DOI: 10.1136/jmedgenet-2021-108354] [Reference Citation Analysis]
14 Jiang WF, Xu YJ, Zhao CM, Wang XH, Qiu XB, Liu X, Wu SH, Yang YQ. A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve. Genet Mol Biol 2020;43:e20200142. [PMID: 33306779 DOI: 10.1590/1678-4685-GMB-2020-0142] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
15 Matos-Nieves A, Manivannan S, Majumdar U, McBride KL, White P, Garg V. A Multi-Omics Approach Using a Mouse Model of Cardiac Malformations for Prioritization of Human Congenital Heart Disease Contributing Genes. Front Cardiovasc Med 2021;8:683074. [PMID: 34504875 DOI: 10.3389/fcvm.2021.683074] [Reference Citation Analysis]
16 Waldmann V, Guichard J, Marijon E, Khairy P. Tachyarrhythmias in Congenital Heart Diseases: From Ion Channels to Catheter Ablation. JCDD 2022;9:39. [DOI: 10.3390/jcdd9020039] [Reference Citation Analysis]
17 Choudhury TZ, Garg V. Molecular genetic mechanisms of congenital heart disease. Curr Opin Genet Dev 2022;75:101949. [PMID: 35816939 DOI: 10.1016/j.gde.2022.101949] [Reference Citation Analysis]
18 Seidl-mlczoch E, Kasprian G, Kitzmueller E, Zimpfer D, Steiner I, Jowett V, Stuempflen M, Wielandner A, Ulm B, Michel-behnke I. Discordant Post-natal Patterns in Fetuses With Heterotaxy Syndrome: A Retrospective Single-Centre Series on Outcome After Fetal Diagnosis. Front Pediatr 2022;10:908505. [DOI: 10.3389/fped.2022.908505] [Reference Citation Analysis]
19 Findley TO, Northrup H. The current state of prenatal detection of genetic conditions in congenital heart defects. Transl Pediatr 2021;10:2157-70. [PMID: 34584888 DOI: 10.21037/tp-20-315] [Reference Citation Analysis]
20 Morales-Demori R, Montañes E, Erkonen G, Chance M, Anders M, Denfield S. Epidemiology of Pediatric Heart Failure in the USA-a 15-Year Multi-Institutional Study. Pediatr Cardiol 2021;42:1297-307. [PMID: 33871685 DOI: 10.1007/s00246-021-02611-3] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Woodward AA, Taylor DM, Goldmuntz E, Mitchell LE, Agopian A, Moore JH, Urbanowicz RJ. Gene-Interaction-Sensitive enrichment analysis in congenital heart disease. BioData Mining 2022;15. [DOI: 10.1186/s13040-022-00287-w] [Reference Citation Analysis]
22 Alam S, Claxton JS, Mortillo M, Sassis L, Kefala-Karli P, Silberbach M, Kochilas L, Wechsler SB. Thirty-Year Survival after Cardiac Surgery for Patients with Turner Syndrome. J Pediatr 2021;239:187-192.e1. [PMID: 34450123 DOI: 10.1016/j.jpeds.2021.08.034] [Reference Citation Analysis]
23 Helm BM, Landis BJ, Ware SM. Genetic Evaluation of Inpatient Neonatal and Infantile Congenital Heart Defects: New Findings and Review of the Literature. Genes (Basel) 2021;12:1244. [PMID: 34440418 DOI: 10.3390/genes12081244] [Reference Citation Analysis]
24 Hendrix JA, Amon A, Abbeduto L, Agiovlasitis S, Alsaied T, Anderson HA, Bain LJ, Baumer N, Bhattacharyya A, Bogunovic D, Botteron KN, Capone G, Chandan P, Chase I, Chicoine B, Cieuta-Walti C, DeRuisseau LR, Durand S, Esbensen A, Fortea J, Giménez S, Granholm AC, Hahn LJ, Head E, Hillerstrom H, Jacola LM, Janicki MP, Jasien JM, Kamer AR, Kent RD, Khor B, Lawrence JB, Lemonnier C, Lewanda AF, Mobley W, Moore PE, Nelson LP, Oreskovic NM, Osorio RS, Patterson D, Rasmussen SA, Reeves RH, Roizen N, Santoro S, Sherman SL, Talib N, Tapia IE, Walsh KM, Warren SF, White AN, Wong GW, Yi JS. Opportunities, barriers, and recommendations in down syndrome research. Transl Sci Rare Dis 2021;5:99-129. [PMID: 34268067 DOI: 10.3233/trd-200090] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
25 Dong J, Peng T, Li M, Xie F, Wu J, Perez-lopez FR. Association between Maternal Thyroxine and Risk of Fetal Congenital Heart Defects: A Hospital-Based Cohort Study. International Journal of Endocrinology 2022;2022:1-8. [DOI: 10.1155/2022/3859388] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
26 Findley TO, Crain AK, Mahajan S, Deniwar A, Davis J, Solis Zavala AS, Corno AF, Rodriguez-Buritica D. Congenital heart defects and copy number variants associated with neurodevelopmental impairment. Am J Med Genet A 2022;188:13-23. [PMID: 34472185 DOI: 10.1002/ajmg.a.62484] [Reference Citation Analysis]
27 Martin LJ, Benson DW. Focused Strategies for Defining the Genetic Architecture of Congenital Heart Defects. Genes (Basel) 2021;12:827. [PMID: 34071175 DOI: 10.3390/genes12060827] [Reference Citation Analysis]
28 Zhang H, Cao X, Wang J, Li Q, Zhao Y, Jin X. LZTR1: A promising adaptor of the CUL3 family. Oncol Lett 2021;22:564. [PMID: 34113392 DOI: 10.3892/ol.2021.12825] [Reference Citation Analysis]
29 Atli EI, Atli E, Yalcintepe S, Demir S, Kalkan R, Akurut C, Ozen Y, Gurkan H. Investigation of Genetic Alterations in Congenital Heart Diseases in Prenatal Period. Glob Med Genet 2022;09:029-33. [DOI: 10.1055/s-0041-1736566] [Reference Citation Analysis]
30 Zhao Y, Kang X, Gao F, Guzman A, Lau RP, Biniwale R, Wadehra M, Reemtsen B, Garg M, Halnon N, Quintero-Rivera F, Van Arsdell G, Coppola G, Nelson SF, Touma M; UCLA Congenital Heart Defects BioCore Faculty. Gene-environment regulatory circuits of right ventricular pathology in tetralogy of fallot. J Mol Med (Berl) 2019;97:1711-22. [PMID: 31834445 DOI: 10.1007/s00109-019-01857-y] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
31 Gug C, Gorduza EV, Lăcătuşu A, Vaida MA, Bîrsăşteanu F, Puiu M, Stoicănescu D. CHARGE syndrome associated with de novo (I1460Rfs*15) frameshift mutation of CHD7 gene in a patient with arteria lusoria and horseshoe kidney. Exp Ther Med 2020;20:479-85. [PMID: 32509017 DOI: 10.3892/etm.2020.8683] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
32 Peyvandi S, Baer RJ, Chambers CD, Norton ME, Rajagopal S, Ryckman KK, Moon-Grady A, Jelliffe-Pawlowski LL, Steurer MA. Environmental and Socioeconomic Factors Influence the Live-Born Incidence of Congenital Heart Disease: A Population-Based Study in California. J Am Heart Assoc 2020;9:e015255. [PMID: 32306820 DOI: 10.1161/JAHA.119.015255] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 3.5] [Reference Citation Analysis]
33 Nees SN, Chung WK. Genetic Basis of Human Congenital Heart Disease. Cold Spring Harb Perspect Biol 2020;12:a036749. [PMID: 31818857 DOI: 10.1101/cshperspect.a036749] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
34 Lin H, McBride KL, Garg V, Zhao MT. Decoding Genetics of Congenital Heart Disease Using Patient-Derived Induced Pluripotent Stem Cells (iPSCs). Front Cell Dev Biol 2021;9:630069. [PMID: 33585486 DOI: 10.3389/fcell.2021.630069] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
35 Cirillo A, Lioncino M, Maratea A, Passariello A, Fusco A, Fratta F, Monda E, Caiazza M, Signore G, Esposito A, Baban A, Versacci P, Putotto C, Marino B, Pignata C, Cirillo E, Giardino G, Sarubbi B, Limongelli G, Russo MG. Clinical Manifestations of 22q11.2 Deletion Syndrome. Heart Fail Clin 2022;18:155-64. [PMID: 34776076 DOI: 10.1016/j.hfc.2021.07.009] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
36 Ji H, Liang H, Yu Y, Wang Z, Yuan W, Qian X, Mikkelsen EM, Laursen ASD, Fang G, Huang G, Miao M, Li J. Association of Maternal History of Spontaneous Abortion and Stillbirth With Risk of Congenital Heart Disease in Offspring of Women With vs Without Type 2 Diabetes. JAMA Netw Open 2021;4:e2133805. [PMID: 34757411 DOI: 10.1001/jamanetworkopen.2021.33805] [Reference Citation Analysis]
37 Lim TB, Foo SYR, Chen CK. The Role of Epigenetics in Congenital Heart Disease. Genes (Basel) 2021;12:390. [PMID: 33803261 DOI: 10.3390/genes12030390] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
38 Ji W, Ferdman D, Copel J, Scheinost D, Shabanova V, Brueckner M, Khokha MK, Ment LR. De novo damaging variants associated with congenital heart diseases contribute to the connectome. Sci Rep 2020;10:7046. [PMID: 32341405 DOI: 10.1038/s41598-020-63928-2] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
39 Fa J, Zhang X, Zhang X, Qi M, Zhang X, Fu Q, Xu Z, Gao Y, Wang B. Long Noncoding RNA lnc-TSSK2-8 Activates Canonical Wnt/β-Catenin Signaling Through Small Heat Shock Proteins HSPA6 and CRYAB. Front Cell Dev Biol 2021;9:660576. [PMID: 34041241 DOI: 10.3389/fcell.2021.660576] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
40 Ramlakhan KP, Tobler D, Greutmann M, Schwerzmann M, Baris L, Yetman AT, Nihoyannopoulos P, Manga P, Boersma E, Maggioni AP, Johnson MR, Hall R, Roos-Hesselink JW; ROPAC investigators group. Pregnancy outcomes in women with aortic coarctation. Heart 2020:heartjnl-2020-317513. [PMID: 33122301 DOI: 10.1136/heartjnl-2020-317513] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
41 Yi K, Ma YH, Wang W, Zhang X, Gao J, He SE, Xu XM, Ji M, Guo WF, You T. The Roles of Reduced Folate Carrier-1 (RFC1) A80G (rs1051266) Polymorphism in Congenital Heart Disease: A Meta-Analysis. Med Sci Monit 2021;27:e929911. [PMID: 33935279 DOI: 10.12659/MSM.929911] [Reference Citation Analysis]
42 Keller BB, Kowalski WJ, Tinney JP, Tobita K, Hu N. Validating the Paradigm That Biomechanical Forces Regulate Embryonic Cardiovascular Morphogenesis and Are Fundamental in the Etiology of Congenital Heart Disease. J Cardiovasc Dev Dis 2020;7:E23. [PMID: 32545681 DOI: 10.3390/jcdd7020023] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
43 Diab NS, Barish S, Dong W, Zhao S, Allington G, Yu X, Kahle KT, Brueckner M, Jin SC. Molecular Genetics and Complex Inheritance of Congenital Heart Disease. Genes (Basel) 2021;12:1020. [PMID: 34209044 DOI: 10.3390/genes12071020] [Reference Citation Analysis]
44 Rashkin SR, Cleves M, Shaw GM, Nembhard WN, Nestoridi E, Jenkins MM, Romitti PA, Lou XY, Browne ML, Mitchell LE, Olshan AF, Lomangino K, Bhattacharyya S, Witte JS, Hobbs CA; National Birth Defects Prevention Study. A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study. Am J Med Genet A 2022. [PMID: 35451555 DOI: 10.1002/ajmg.a.62759] [Reference Citation Analysis]
45 Theis JL, Vogler G, Missinato MA, Li X, Nielsen T, Zeng XI, Martinez-Fernandez A, Walls SM, Kervadec A, Kezos JN, Birker K, Evans JM, O'Byrne MM, Fogarty ZC, Terzic A, Grossfeld P, Ocorr K, Nelson TJ, Olson TM, Colas AR, Bodmer R. Patient-specific genomics and cross-species functional analysis implicate LRP2 in hypoplastic left heart syndrome. Elife 2020;9:e59554. [PMID: 33006316 DOI: 10.7554/eLife.59554] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
46 Smith KA, Uribe V. Getting to the Heart of Left-Right Asymmetry: Contributions from the Zebrafish Model. J Cardiovasc Dev Dis 2021;8:64. [PMID: 34199828 DOI: 10.3390/jcdd8060064] [Reference Citation Analysis]
47 Henry S, Szabó V, Sutus E, Pirity MK. RYBP is important for cardiac progenitor cell development and sarcomere formation. PLoS One 2020;15:e0235922. [PMID: 32673370 DOI: 10.1371/journal.pone.0235922] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
48 Myers SM, Challman TD, Bernier R, Bourgeron T, Chung WK, Constantino JN, Eichler EE, Jacquemont S, Miller DT, Mitchell KJ, Zoghbi HY, Martin CL, Ledbetter DH. Insufficient Evidence for "Autism-Specific" Genes. Am J Hum Genet 2020;106:587-95. [PMID: 32359473 DOI: 10.1016/j.ajhg.2020.04.004] [Cited by in Crossref: 66] [Cited by in F6Publishing: 45] [Article Influence: 33.0] [Reference Citation Analysis]
49 Diz OM, Toro R, Cesar S, Gomez O, Sarquella-Brugada G, Campuzano O. Personalized Genetic Diagnosis of Congenital Heart Defects in Newborns. J Pers Med 2021;11:562. [PMID: 34208491 DOI: 10.3390/jpm11060562] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
50 Garcia AM, Beatty JT, Nakano SJ. Heart failure in single right ventricle congenital heart disease: physiological and molecular considerations. Am J Physiol Heart Circ Physiol 2020;318:H947-65. [PMID: 32108525 DOI: 10.1152/ajpheart.00518.2019] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
51 Liu J, Wu Y, Sun H, Liu X, Gu X, Zhao Y, Zhang Y, Han J, He Y. Placental DNA Methylation Abnormalities in Prenatal Conotruncal Heart Defects. Front Genet 2022;13:878063. [DOI: 10.3389/fgene.2022.878063] [Reference Citation Analysis]
52 Hedermann G, Hedley PL, Thagaard IN, Krebs L, Ekelund CK, Sørensen TIA, Christiansen M. Maternal obesity and metabolic disorders associate with congenital heart defects in the offspring: A systematic review. PLoS One 2021;16:e0252343. [PMID: 34043700 DOI: 10.1371/journal.pone.0252343] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
53 Hall B, Alonzo M, Texter K, Garg V, Zhao MT. Probing single ventricle heart defects with patient-derived induced pluripotent stem cells and emerging technologies. Birth Defects Res 2022. [PMID: 35199491 DOI: 10.1002/bdr2.1989] [Reference Citation Analysis]
54 Gonzalez-Teran B, Pittman M, Felix F, Thomas R, Richmond-Buccola D, Hüttenhain R, Choudhary K, Moroni E, Costa MW, Huang Y, Padmanabhan A, Alexanian M, Lee CY, Maven BEJ, Samse-Knapp K, Morton SU, McGregor M, Gifford CA, Seidman JG, Seidman CE, Gelb BD, Colombo G, Conklin BR, Black BL, Bruneau BG, Krogan NJ, Pollard KS, Srivastava D. Transcription factor protein interactomes reveal genetic determinants in heart disease. Cell 2022;185:794-814.e30. [PMID: 35182466 DOI: 10.1016/j.cell.2022.01.021] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
55 Deniz E, Jonas S, Khokha MK, Choma MA. Quantitative Phenotyping of Xenopus Embryonic Heart Pathophysiology Using Hemoglobin Contrast Subtraction Angiography to Screen Human Cardiomyopathies. Front Physiol 2019;10:1197. [PMID: 31620018 DOI: 10.3389/fphys.2019.01197] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
56 Katz OL, Wild KT, McEldrew D, Kaur M, Raible S, Skraban CM, Zackai EH, Medne L, Izumi K, Fortunato S, Weatherly J, Hartman T, Deppen P, Blair J, Devkota B, Schindler E, Hedrick HL, Peranteau W, Krantz ID. Molecular Mechanisms Contributing to the Etiology of Congenital Diaphragmatic Hernia: A Review and Novel Cases. J Pediatr 2022;246:251-265.e2. [PMID: 35314152 DOI: 10.1016/j.jpeds.2022.03.023] [Reference Citation Analysis]
57 Zu B, Zheng Z, Fu Q. Molecular diagnostics for congenital heart disease: a narrative review of the current technologies and applications. Journal of Bio-X Research 2020;3:92-6. [DOI: 10.1097/jbr.0000000000000068] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
58 Chen X, Jiang Y, Chen R, Qi Q, Zhang X, Zhao S, Liu C, Wang W, Li Y, Sun G, Song J, Huang H, Cheng C, Zhang J, Cheng L, Liu J. Clinical efficiency of simultaneous CNV-seq and whole-exome sequencing for testing fetal structural anomalies. J Transl Med 2022;20:10. [PMID: 34980134 DOI: 10.1186/s12967-021-03202-9] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
59 Alser M, Shurbaji S, Yalcin HC. Mechanosensitive Pathways in Heart Development: Findings from Chick Embryo Studies. J Cardiovasc Dev Dis 2021;8:32. [PMID: 33810288 DOI: 10.3390/jcdd8040032] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
60 Jin JY, Wu LP, Dong Y, Pi HC, Wu HF, Xiang R. Identification of a novel GATA binding protein 5 variant (c.830C>T/p.P277L) damaging the nuclear translocation and causing tetralogy of Fallot. QJM 2021:hcab317. [PMID: 34904678 DOI: 10.1093/qjmed/hcab317] [Reference Citation Analysis]
61 Evans WN, Acherman RJ, Restrepo H. Prenatal and Neonatal Detection of Isomeric Situs and the Association with Maternal Comorbidities. J Fetal Med 2021;8:273-7. [DOI: 10.1007/s40556-021-00325-3] [Reference Citation Analysis]
62 Jill Glidewell M, Farr SL, Book WM, Botto L, Li JS, Soim AS, Downing KF, Riehle-Colarusso T, D'Ottavio AA, Feldkamp ML, Khanna AD, Raskind-Hood CL, Sommerhalter KM, Crume TL. Individuals aged 1-64 years with documented congenital heart defects at healthcare encounters, five U.S. surveillance sites, 2011-2013. Am Heart J 2021;238:100-8. [PMID: 33951414 DOI: 10.1016/j.ahj.2021.04.007] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
63 Loss KL, Shaddy RE, Kantor PF. Recent and Upcoming Drug Therapies for Pediatric Heart Failure. Front Pediatr 2021;9:681224. [PMID: 34858897 DOI: 10.3389/fped.2021.681224] [Reference Citation Analysis]
64 Wang T, Li Q, Chen L, Ni B, Sheng X, Huang P, Zhang S, Qin J. Maternal Viral Infection in Early Pregnancy and Risk of Congenital Heart Disease in Offspring: A Prospective Cohort Study in Central China. CLEP 2022;Volume 14:71-82. [DOI: 10.2147/clep.s338870] [Reference Citation Analysis]
65 Robson A, Makova SZ, Barish S, Zaidi S, Mehta S, Drozd J, Jin SC, Gelb BD, Seidman CE, Chung WK, Lifton RP, Khokha MK, Brueckner M. Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility. Proc Natl Acad Sci U S A 2019;116:14049-54. [PMID: 31235600 DOI: 10.1073/pnas.1808341116] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 5.3] [Reference Citation Analysis]
66 Geddes GC, Przybylowski LF 3rd, Ware SM. Variants of significance: medical genetics and surgical outcomes in congenital heart disease. Curr Opin Pediatr 2020;32:730-8. [PMID: 33009125 DOI: 10.1097/MOP.0000000000000949] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
67 Mohamed AM, Kamel AK, Eid MM, Eid OM, Mekkawy M, Hussein SH, Zaki MS, Esmail S, Afifi HH, El-Kamah GY, Otaify GA, El-Awady HA, Elaidy A, Essa MY, El-Ruby M, Ashaat EA, Hammad SA, Mazen I, Abdel-Salam GMH, Aglan M, Temtamy S. Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly. Mol Genet Genomic Med 2021;9:e1829. [PMID: 34609792 DOI: 10.1002/mgg3.1829] [Reference Citation Analysis]
68 Knutson AK, Williams AL, Boisvert WA, Shohet RV. HIF in the heart: development, metabolism, ischemia, and atherosclerosis. J Clin Invest 2021;131:e137557. [PMID: 34623330 DOI: 10.1172/JCI137557] [Reference Citation Analysis]
69 Yao Y, Marra AN, Yelon D. Pathways Regulating Establishment and Maintenance of Cardiac Chamber Identity in Zebrafish. J Cardiovasc Dev Dis 2021;8:13. [PMID: 33572830 DOI: 10.3390/jcdd8020013] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
70 Morton SU, Quiat D, Seidman JG, Seidman CE. Genomic frontiers in congenital heart disease. Nat Rev Cardiol 2021. [PMID: 34272501 DOI: 10.1038/s41569-021-00587-4] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
71 Sevim Bayrak C, Zhang P, Tristani-Firouzi M, Gelb BD, Itan Y. De novo variants in exomes of congenital heart disease patients identify risk genes and pathways. Genome Med 2020;12:9. [PMID: 31941532 DOI: 10.1186/s13073-019-0709-8] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 6.5] [Reference Citation Analysis]
72 Uveges MK, Holm IA. Current Trends in Genetics and Neonatal Care. Adv Neonatal Care 2021;21:473-81. [PMID: 33538495 DOI: 10.1097/ANC.0000000000000834] [Reference Citation Analysis]
73 Delea M, Massara L, Espeche L, Bidondo M, Barbero P, Oliveri J, Brun P, Fabro M, Galain M, Fernández C, Taboas M, Bruque C, Kolomenski J, Izquierdo A, Berenstein A, Cosentino V, Martinoli C, Vilas M, Rittler M, Mendez R, Furforo L, Liascovich R, Groisman B, Rozental S, Dain L; on behalf of the PID ACM-CC Group. Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease. Genes 2022;13:1172. [DOI: 10.3390/genes13071172] [Reference Citation Analysis]
74 Mullen M, Zhang A, Lui GK, Romfh AW, Rhee JW, Wu JC. Race and Genetics in Congenital Heart Disease: Application of iPSCs, Omics, and Machine Learning Technologies. Front Cardiovasc Med 2021;8:635280. [PMID: 33681306 DOI: 10.3389/fcvm.2021.635280] [Reference Citation Analysis]
75 Zhang X, Wang B, You G, Xiang Y, Fu Q, Yu Y, Zhang X. Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle. BMC Med Genomics 2021;14:243. [PMID: 34627233 DOI: 10.1186/s12920-021-01090-y] [Reference Citation Analysis]
76 Freud LR, Seed M. Prenatal Diagnosis and Management of Single Ventricle Heart Disease. Canadian Journal of Cardiology 2022. [DOI: 10.1016/j.cjca.2022.04.003] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
77 Xie Y, Li M, Dong W, Jiang W, Zhao H. M-DATA: A statistical approach to jointly analyzing de novo mutations for multiple traits. PLoS Genet 2021;17:e1009849. [PMID: 34735430 DOI: 10.1371/journal.pgen.1009849] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
78 Edwards JJ, Rouillard AD, Fernandez NF, Wang Z, Lachmann A, Shankaran SS, Bisgrove BW, Demarest B, Turan N, Srivastava D, Bernstein D, Deanfield J, Giardini A, Porter G, Kim R, Roberts AE, Newburger JW, Goldmuntz E, Brueckner M, Lifton RP, Seidman CE, Chung WK, Tristani-Firouzi M, Yost HJ, Ma'ayan A, Gelb BD. Systems Analysis Implicates WAVE2 Complex in the Pathogenesis of Developmental Left-Sided Obstructive Heart Defects. JACC Basic Transl Sci 2020;5:376-86. [PMID: 32368696 DOI: 10.1016/j.jacbts.2020.01.012] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
79 Fan D, Pang S, Chen J, Shan J, Cheng Q, Yan B. Identification and functional study of GATA4 gene regulatory variants in atrial septal defects. BMC Cardiovasc Disord 2021;21:321. [PMID: 34193080 DOI: 10.1186/s12872-021-02136-w] [Reference Citation Analysis]
80 Ramlakhan KP, Johnson MR, Lelonek M, Saad A, Gasimov Z, Sharashkina NV, Thornton P, Arstall M, Hall R, Roos-hesselink JW, Hall R, Roos-hesselink J, Stein J, Parsonage WA, Budts W, De Backer J, Grewal J, Marelli A, Kaemmerer H, Jondeau G, Johnson M, Maggioni AP, Tavazzi L, Thilen U, Elkayam U, Otto C, Sliwa K, Aquieri A, Saad A, Vega HR, Hojman J, Caparros J, Blanco MV, Arstall M, Chung C, Mahadavan G, Aldridge E, Wittwer M, Chow Y, Parsonage W, Lust K, Collins N, Warner G, Hatton R, Gordon A, Nyman E, Stein J, Donhauser E, Gabriel H, Bahshaliyev A, Guliyev F, Hasanova I, Jahangirov T, Gasimov Z, Salim A, Ahmed C, Begum F, Hoque M, Mahmood M, Islam M, Haque P, Banerjee S, Parveen T, Morissens M, De Backer J, Demulier L, de Hosson M, Budts W, Beckx M, Kozic M, Lovric M, Kovacevic-preradovic T, Chilingirova N, Kratunkov P, Wahab N, Mclean S, Gordon E, Walter L, Marelli A, Montesclaros A, Monsalve G, Rodriguez C, Balthazar F, Quintero V, Palacio W, Cadavid LM, Ortiz EM, Hoyos FF, Guerrero EA, Ricardo JG, Penagos JV, Vavera Z, Prague, Popelova J, Vejlstrup N, Grønbeck L, Johansen M, Ersboll A, Elrakshy Y, Eltamawy K, Abd-el Aziz MG, El Nagar A, Ebaid H, Elenin HA, Saed M, Farag S, Makled W, Sorour K, Ashour Z, El-sayed G, Meguid Mahdy MA, Taha N, Dardeer A, Shabaan M, Saad A, Ali M, Moceri P, Duthoit G, Gouton M, Nizard J, Baris L, Cohen S, Ladouceur M, Khimoud D, Iung B, Berger F, Olsson A, Gembruch U, Merz W, Reinert E, Clade S, Kliesch Y, Wald C, Sinning C, Kozlik-feldmann R, Blankenberg S, Zengin-sahm E, Mueller G, Hillebrand M, Hauck P, von Kodolitsch Y, Zarniko N, Baumgartner MH, Schmidt R, Hellige A, Tutarel O, Kaemmerer H, Kuschel B, Nagdyman N, Motz R, Maisuradze D, Frogoudaki A, Iliodromitis E, Anastasiou-nana M, Marousi, Triantafyllis D, Bekiaris G, Karvounis H, Giannakoulas G, Ntiloudi D, Mouratoglou S, Temesvari A, Balint H, Kohalmi D, Merkely B, Liptai C, Nemes A, Forster T, Kalapos A, Berek K, Havasi K, Ambrus N, Shelke A, Kawade R, Patil S, Martanto E, Aprami T, Purnomowati A, Cool C, Hasan M, Akbar R, Hidayat S, Dewi T, Permadi W, Soedarsono D, Ansari-ramandi M, Samiei N, Tabib A, Kashfi F, Ansari-ramandi S, Rezaei S, Farhan HA, Al-hussein A, Al-saedi G, Mahmood G, Yaseen I, Al-yousuf L, Albayati M, Mahmood S, Raheem S, Alhaidari T, Dakhil Z, Thornton P, Donnelly J, Bowen M, Blatt A, Elbaz-greener G, Shotan A, Yalonetsky S, Goland S, Biener M, Assenza GE, Bonvicini M, Donti A, Bulgarelli A, Prandstraller D, Romeo C, Crepaz R, Sciatti E, Metra M, Orabona R, Ali LA, Festa P, Fesslova V, Bonanomi C, Calcagnino M, Lombardi F, Colli A, Ossola M, Gobbi C, Gherbesi E, Tondi L, Schiavone M, Squillace M, Carmina M, Maina A, Macchi C, Gollo E, Comoglio F, Montali N, Re P, Bordese R, Todros T, Donvito V, Marra WG, Sinagra G, D'agata Mottolese B, Bobbo M, Gesuete V, Rakar S, Ramani F, Niwa K, Mekebekova D, Mussagaliyeva A, Lee T, Mirrakhimov E, Abilova S, Bektasheva E, Neronova K, Lunegova O, Žaliūnas R, Jonkaitienė R, Petrauskaitė J, Laucevicius A, Jancauskaite D, Lauciuviene L, Gumbiene L, Lankutiene L, Glaveckaite S, Laukyte M, Solovjova S, Rudiene V, Chee K, Yim C, Ang H, Kuppusamy R, Watson T, Caruana M, Estensen M, Kayani MM, Munir R, Tomaszuk-kazberuk A, Sobkowicz B, Przepiesc J, Lesniak-sobelga A, Tomkiewicz-pajak L, Komar M, Olszowska M, Podolec P, Wisniowska-smialek S, Lelonek M, Faflik U, Cichocka-radwan A, Plaskota K, Trojnarska O, Guerra N, de Sousa L, Cruz C, Ribeiro V, Jovanova S, Petrescu V, Jurcut R, Ginghina C, Coman IM, Musteata M, Osipova O, Golivets T, Khamnagadaev I, Golovchenko O, Nagibina A, Ropatko I, Gaisin I, Shilina LV, Sharashkina N, Shlyakhto E, Irtyuga O, Moiseeva O, Karelkina E, Zazerskaya I, Kozlenok A, Sukhova I, Jovovic L, Prokšelj K, Koželj M, Askar A, Abdilaahi A, Mohamed M, Dirir A, Sliwa K, Manga P, Pijuan-domenech A, Galian-gay L, Tornos P, Subirana M, T M, Subirana, Oliver J, Garcia-aranda Dominguez B, Gonzalez IH, Jimenez JD, Subias PE, Murga N, Elbushi A, Suliman A, Jazzar K, Murtada M, Ahamed N, Dellborg M, Furenas E, Jinesjo M, Skoglund K, Eriksson P, Gilljam T, Thilen U, Tobler D, Wustmann K, Schwitz F, Schwerzmann M, Rutz T, Bouchardy J, Greutmann M, Lopes BS, Meier L, Arrigo M, de Boer K, Konings T, Wajon E, Wagenaar L, Polak P, Pieper E, Roos-hesselink J, Baris L, van Hagen I, Duvekot H, Cornette J, De Groot C, van Oppen C, Sarac L, Esen OB, Enar SC, Mondo C, Ingabire P, Nalwanga B, Semu T, Salih B, Almahmeed W, Wani S, Farook FM, Ain A, Gerges F, Komaranchath A, Al bakshi F, Al Mulla A, Yusufali A, Al Hatou E, Bazargani N, Hussain F, Hudsmith L, Thompson P, Thorne S, Bowater S, Money-kyrle A, Clifford P, Ramrakha P, Firoozan S, Chaplin J, Bowers N, Adamson D, Schroeder F, Wendler R, Hammond S, Nihoyannopoulos P, Norfolk N, Hall R, Freeman L, Veldtman G, Kerr J, Tellett L, Scott N, Bhatt A, Defaria Yeh D, Youniss M, Wood M, Sarma A, Tsiaras S, Stefanescu A, Duran J, Stone L, Majdalany D, Chapa J, Chintala K, Gupta P, Botti J, Ting J, Davidson W, Wells G, Sparks D, Paruchuri V, Marzo K, Patel D, Wagner W, Ahanya S, Colicchia L, Jentink T, Han K, Loichinger M, Parker M, Wagner W, Longtin C, Yetman A, Erickson K, Cramer J, Tsai S, Fletcher B, Warta S, Cohen C, Lindblade C, Puntel R, Nagaran K, Croft N, Gurvitz M, Otto C, Talluto C, Murphy D, Perlroth M. Congenital heart disease in the ESC EORP Registry of Pregnancy and Cardiac disease (ROPAC). International Journal of Cardiology Congenital Heart Disease 2021;3:100107. [DOI: 10.1016/j.ijcchd.2021.100107] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
81 Ahmad A, Fitzgerald-Butt SM, Ware SM, Ison HE, Elmore LR, Helm BM. Assessing genetic counselors' graduate school education and training in congenital heart defects. J Genet Couns 2021. [PMID: 34877755 DOI: 10.1002/jgc4.1540] [Reference Citation Analysis]
82 Blue GM, Smith J, Sholler GF, Semsarian C, Winlaw DS; Australian Genomics Cardiovascular Genetic Disorders Flagship. Current Practice of Genetic Testing and Counselling in Congenital Heart Disease: An Australian Perspective. Heart Lung Circ 2020;29:1733-6. [PMID: 32868177 DOI: 10.1016/j.hlc.2020.07.013] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
83 Qu Y, Lin S, Bloom MS, Wang X, Nie Z, Ou Y, Mai J, Gao X, Wu Y, Chen J, Justino J, Tan H, Zhuang J, Liu X. First-Trimester Maternal Folic Acid Supplementation Modifies the Effects of Risk Factors Exposures on Congenital Heart Disease in Offspring. Life (Basel) 2021;11:724. [PMID: 34440469 DOI: 10.3390/life11080724] [Reference Citation Analysis]
84 Rufaihah AJ, Chen CK, Yap CH, Mattar CNZ. Mending a broken heart: In vitro, in vivo and in silico models of congenital heart disease. Dis Model Mech 2021;14:dmm047522. [PMID: 33787508 DOI: 10.1242/dmm.047522] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
85 Landstrom AP, Kim JJ, Gelb BD, Helm BM, Kannankeril PJ, Semsarian C, Sturm AC, Tristani-Firouzi M, Ware SM; American Heart Association Council on Genomic and Precision Medicine; Council on Lifelong Congenital Heart Disease and Heart Health in the Young; Council on Arteriosclerosis, Thrombosis and Vascular Biology; and Council on Lifestyle and Cardiometabolic Health. Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association. Circ Genom Precis Med 2021;14:e000086. [PMID: 34412507 DOI: 10.1161/HCG.0000000000000086] [Reference Citation Analysis]
86 Wichert-schmitt B, D‘souza R, Silversides CK. Reproductive Issues in Patients with the Fontan Operation. Canadian Journal of Cardiology 2022. [DOI: 10.1016/j.cjca.2022.04.020] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
87 Ison HE, Griffin EL, Parrott A, Shikany AR, Meyers L, Thomas MJ, Syverson E, Demo EM, Fitzgerald KK, Fitzgerald-Butt S, Ziegler KL, Schartman AF, Stone KM, Helm BM. Genetic counseling for congenital heart disease - Practice resource of the national society of genetic counselors. J Genet Couns 2021. [PMID: 34510635 DOI: 10.1002/jgc4.1498] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
88 Chicoine B, Rivelli A, Fitzpatrick V, Chicoine L, Jia G, Rzhetsky A. Prevalence of Common Disease Conditions in a Large Cohort of Individuals With Down Syndrome in the United States. J Patient Cent Res Rev 2021;8:86-97. [PMID: 33898640 DOI: 10.17294/2330-0698.1824] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
89 Chen X, Zhang M, Song Y, Luo Y, Wang L, Xu Z, Bao N. Early high-energy feeding in infants following cardiac surgery: a randomized controlled trial. Transl Pediatr 2021;10:2439-48. [PMID: 34765467 DOI: 10.21037/tp-21-360] [Reference Citation Analysis]
90 Iacobazzi D, Alvino VV, Caputo M, Madeddu P. Accelerated Cardiac Aging in Patients With Congenital Heart Disease. Front Cardiovasc Med 2022;9:892861. [DOI: 10.3389/fcvm.2022.892861] [Reference Citation Analysis]
91 Izarzugaza JMG, Ellesøe SG, Doganli C, Ehlers NS, Dalgaard MD, Audain E, Dombrowsky G, Banasik K, Sifrim A, Wilsdon A, Thienpont B, Breckpot J, Gewillig M, Brook JD, Hitz MP, Larsen LA, Brunak S; Competence Network for Congenital Heart Defects, Germany. Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease. Genome Med 2020;12:76. [PMID: 32859249 DOI: 10.1186/s13073-020-00772-z] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
92 Matos-Nieves A, Yasuhara J, Garg V. Another Notch in the Genetic Puzzle of Tetralogy of Fallot. Circ Res 2019;124:462-4. [PMID: 30763217 DOI: 10.1161/CIRCRESAHA.118.314520] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
93 Jia L, Limeng D, Xiaoyin T, Junwen W, Xintong Z, Gang X, Yun B, Hong G. A Novel Splicing Mutation c.335-1 G > A in the Cardiac Transcription Factor NKX2-5 Leads to Familial Atrial Septal Defect Through miR-19 and PYK2. Stem Cell Rev Rep 2022. [PMID: 35778654 DOI: 10.1007/s12015-022-10400-5] [Reference Citation Analysis]
94 Nees SN, Chung WK. The genetics of isolated congenital heart disease. Am J Med Genet C Semin Med Genet 2020;184:97-106. [PMID: 31876989 DOI: 10.1002/ajmg.c.31763] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
95 Williams K, Carson J, Lo C. Genetics of Congenital Heart Disease. Biomolecules 2019;9:E879. [PMID: 31888141 DOI: 10.3390/biom9120879] [Cited by in Crossref: 18] [Cited by in F6Publishing: 17] [Article Influence: 6.0] [Reference Citation Analysis]
96 Sousa A, Moldovan O, Lebreiro A, Bourbon M, António N, Rato Q, Rodrigues P, Toste A, Gonçalves Rocha M, Oliveira R, Granja S, Cruz C, Almeida J, Martins E. Recommendations for genetic testing in cardiology: Review of major international guidelines. Rev Port Cardiol (Engl Ed) 2020;39:597-610. [PMID: 33036867 DOI: 10.1016/j.repc.2020.03.016] [Reference Citation Analysis]
97 Gal DB, Deuitch N, Lee SSJ, Simon RT, Char DS. Parental Attitudes Toward Clinical Genomic Sequencing in Children With Critical Cardiac Disease. Pediatr Crit Care Med 2021;22:e419-26. [PMID: 33591072 DOI: 10.1097/PCC.0000000000002669] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
98 Hao L, Ma J, Wu F, Ma X, Qian M, Sheng W, Yan T, Tang N, Jiang X, Zhang B, Xiao D, Qian Y, Zhang J, Jiang N, Zhou W, Chen W, Ma D, Huang G. WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation. Clin Transl Med 2022;12:e941. [PMID: 35808830 DOI: 10.1002/ctm2.941] [Reference Citation Analysis]
99 Mansfield C, Zhao MT, Basu M. Translational potential of hiPSCs in predictive modeling of heart development and disease. Birth Defects Res 2022. [PMID: 35261209 DOI: 10.1002/bdr2.1999] [Reference Citation Analysis]
100 Majumdar U, Yasuhara J, Garg V. In Vivo and In Vitro Genetic Models of Congenital Heart Disease. Cold Spring Harb Perspect Biol 2021;13:a036764. [PMID: 31818859 DOI: 10.1101/cshperspect.a036764] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
101 Parker LE, Landstrom AP. Genetic Etiology of Left-Sided Obstructive Heart Lesions: A Story in Development. J Am Heart Assoc 2021;10:e019006. [PMID: 33432820 DOI: 10.1161/JAHA.120.019006] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
102 Maran S, Faten SA, Lim SE, Lai KS, Ibrahim WPW, Ankathil R, Gan SH, Tan HL. Screening of 22q11.2DS Using Multiplex Ligation-Dependent Probe Amplification as an Alternative Diagnostic Method. Biomed Res Int 2020;2020:6945730. [PMID: 33062692 DOI: 10.1155/2020/6945730] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
103 Helle E, Pihkala J, Turunen R, Ruotsalainen H, Tuupanen S, Koskenvuo J, Ojala T. Rare Variants in Genes Associated With Cardiomyopathy Are Not Common in Hypoplastic Left Heart Syndrome Patients With Myocardial Dysfunction. Front Pediatr 2020;8:596840. [PMID: 33194928 DOI: 10.3389/fped.2020.596840] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
104 Shen H, He Q, Shao X, Li S, Zhou Z. Deep Phenotypic Analysis for Transposition of the Great Arteries and Prognosis Implication. J Am Heart Assoc 2022;11:e023181. [PMID: 35001652 DOI: 10.1161/JAHA.121.023181] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
105 Miller DB, Piccolo SR. A Survey of Compound Heterozygous Variants in Pediatric Cancers and Structural Birth Defects. Front Genet 2021;12:640242. [PMID: 33828584 DOI: 10.3389/fgene.2021.640242] [Reference Citation Analysis]
106 Musfee FI, Agopian AJ, Goldmuntz E, Hakonarson H, Morrow BE, Taylor DM, Tristani-Firouzi M, Watkins WS, Yandell M, Mitchell LE. Common Variation in Cytoskeletal Genes is Associated with Conotruncal Heart Defects. Genes (Basel) 2021;12:655. [PMID: 33925651 DOI: 10.3390/genes12050655] [Reference Citation Analysis]
107 Ni P, Zhang M, Wu Y, Luo W, Xu Z. What is the postoperative nutrition intake in children with congenital heart disease? A single-center analysis in China. BMC Pediatr 2022;22:470. [PMID: 35922774 DOI: 10.1186/s12887-022-03530-9] [Reference Citation Analysis]
108 Yasuhara J, Garg V. Genetics of congenital heart disease: a narrative review of recent advances and clinical implications. Transl Pediatr 2021;10:2366-86. [PMID: 34733677 DOI: 10.21037/tp-21-297] [Reference Citation Analysis]
109 Chelu A, Williams SG, Keavney BD, Talavera D. Joint analysis of functionally related genes yields further candidates associated with Tetralogy of Fallot. J Hum Genet 2022. [PMID: 35718831 DOI: 10.1038/s10038-022-01051-y] [Reference Citation Analysis]
110 Sidhwani P, Leerberg DM, Boezio GLM, Capasso TL, Yang H, Chi NC, Roman BL, Stainier DYR, Yelon D. Cardiac function modulates endocardial cell dynamics to shape the cardiac outflow tract. Development 2020;147:dev185900. [PMID: 32439760 DOI: 10.1242/dev.185900] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
111 Tang H, Zhang Y, Dai C, Ru T, Li J, Chen J, Zhang B, Zhou K, Lv P, Liu R, Zhou Q, Zheng M. Postmortem 9.4-T MRI for Fetuses With Congenital Heart Defects Diagnosed in the First Trimester. Front Cardiovasc Med 2022;8:764587. [DOI: 10.3389/fcvm.2021.764587] [Reference Citation Analysis]
112 Balistreri CR, Ammoscato CL, Scola L, Fragapane T, Giarratana RM, Lio D, Piccione M. Susceptibility to Heart Defects in Down Syndrome Is Associated with Single Nucleotide Polymorphisms in HAS 21 Interferon Receptor Cluster and VEGFA Genes. Genes (Basel) 2020;11:E1428. [PMID: 33260695 DOI: 10.3390/genes11121428] [Reference Citation Analysis]
113 Scher MS. Gene-Environment Interactions During the First Thousand Days Influence Childhood Neurological Diagnosis. Seminars in Pediatric Neurology 2022. [DOI: 10.1016/j.spen.2022.100970] [Reference Citation Analysis]
114 Gerardin JF, Cohen S. Counseling for Perinatal Outcomes in Women with Congenital Heart Disease. Clinics in Perinatology 2022. [DOI: 10.1016/j.clp.2021.11.004] [Reference Citation Analysis]
115 Yuan Y, Zhang Y, Wang J, Fang P, Ramirez G. Classification of Electrocardiogram of Congenital Heart Disease Patients by Neural Network Algorithms. Scientific Programming 2021;2021:1-8. [DOI: 10.1155/2021/3801675] [Reference Citation Analysis]
116 Pierick AR, Pierick TA, Scholz TD, Zimmerman MB, Reinking BE. Increased interstage morbidity and mortality following stage 1 palliation in patients with genetic abnormalities. Cardiol Young 2022;:1-6. [PMID: 35137681 DOI: 10.1017/S1047951122000166] [Reference Citation Analysis]
117 Okashah S, Vasudeva D, El Jerbi A, Khodjet-el-khil H, Al-shafai M, Syed N, Kambouris M, Udassi S, Saraiva LR, Al-saloos H, Udassi J, Al-shafai KN. Investigation of Genetic Causes in Patients with Congenital Heart Disease in Qatar: Findings from the Sidra Cardiac Registry. Genes 2022;13:1369. [DOI: 10.3390/genes13081369] [Reference Citation Analysis]
118 Richter F, Morton SU, Kim SW, Kitaygorodsky A, Wasson LK, Chen KM, Zhou J, Qi H, Patel N, DePalma SR, Parfenov M, Homsy J, Gorham JM, Manheimer KB, Velinder M, Farrell A, Marth G, Schadt EE, Kaltman JR, Newburger JW, Giardini A, Goldmuntz E, Brueckner M, Kim R, Porter GA Jr, Bernstein D, Chung WK, Srivastava D, Tristani-Firouzi M, Troyanskaya OG, Dickel DE, Shen Y, Seidman JG, Seidman CE, Gelb BD. Genomic analyses implicate noncoding de novo variants in congenital heart disease. Nat Genet 2020;52:769-77. [PMID: 32601476 DOI: 10.1038/s41588-020-0652-z] [Cited by in Crossref: 29] [Cited by in F6Publishing: 21] [Article Influence: 14.5] [Reference Citation Analysis]