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For: LaHaye S, Corsmeier D, Basu M, Bowman JL, Fitzgerald-Butt S, Zender G, Bosse K, McBride KL, White P, Garg V. Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease. Circ Cardiovasc Genet 2016;9:320-9. [PMID: 27418595 DOI: 10.1161/CIRCGENETICS.115.001324] [Cited by in Crossref: 35] [Cited by in F6Publishing: 20] [Article Influence: 5.8] [Reference Citation Analysis]
Number Citing Articles
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4 Wilde AAM, Semsarian C, Márquez MF, Sepehri Shamloo A, Ackerman MJ, Ashley EA, Sternick EB, Barajas-Martinez H, Behr ER, Bezzina CR, Breckpot J, Charron P, Chockalingam P, Crotti L, Gollob MH, Lubitz S, Makita N, Ohno S, Ortiz-Genga M, Sacilotto L, Schulze-Bahr E, Shimizu W, Sotoodehnia N, Tadros R, Ware JS, Winlaw DS, Kaufman ES; ESC Scientific Document Group . European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases. Europace 2022:euac030. [PMID: 35373836 DOI: 10.1093/europace/euac030] [Reference Citation Analysis]
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10 Touma M. Fetal Mouse Cardiovascular Imaging Using a High-frequency Ultrasound (30/45MHZ) System. J Vis Exp 2018. [PMID: 29781990 DOI: 10.3791/57210] [Reference Citation Analysis]
11 Zhou Y, Bai K, Wang Y, Meng Z, Zhou S, Jiang S, Wang H, Wang J, Yang M, Wang Q, Sun K, Chen S. Identification of Rare Variants in Right Ventricular Outflow Tract Obstruction Congenital Heart Disease by Whole-Exome Sequencing. Front Cardiovasc Med 2022;8:811156. [DOI: 10.3389/fcvm.2021.811156] [Reference Citation Analysis]
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13 Qiao F, Wang Y, Zhang C, Zhou R, Wu Y, Wang C, Meng L, Mao P, Cheng Q, Luo C, Hu P, Xu Z. Comprehensive evaluation of genetic variants using chromosomal microarray analysis and exome sequencing in fetuses with congenital heart defect. Ultrasound Obstet Gynecol 2021;58:377-87. [PMID: 33142350 DOI: 10.1002/uog.23532] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
14 Wilde AAM, Semsarian C, Márquez MF, Shamloo AS, Ackerman MJ, Ashley EA, Sternick EB, Barajas-Martinez H, Behr ER, Bezzina CR, Breckpot J, Charron P, Chockalingam P, Crotti L, Gollob MH, Lubitz S, Makita N, Ohno S, Ortiz-Genga M, Sacilotto L, Schulze-Bahr E, Shimizu W, Sotoodehnia N, Tadros R, Ware JS, Winlaw DS, Kaufman ES; Document Reviewers. European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases. Heart Rhythm 2022:S1547-5271(22)01697-6. [PMID: 35390533 DOI: 10.1016/j.hrthm.2022.03.1225] [Reference Citation Analysis]
15 Wang F, Li Z, Song T, Jia Y, Qi L, Ren L, Chen S. Proteomics study on the effect of silybin on cardiomyopathy in obese mice. Sci Rep 2021;11:7136. [PMID: 33785854 DOI: 10.1038/s41598-021-86717-x] [Reference Citation Analysis]
16 El Bouchikhi I, Bouguenouch L, Moufid FZ, Belhassan K, Samri I, Chaouti A, Houssaïni MI, Atmani S, Ouldim K. Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects. Eurasian J Med 2020;52:283-7. [PMID: 33209082 DOI: 10.5152/eurasianjmed.2020.19237] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
17 Li Y, Deshpande P, Hertzman RJ, Palubinsky AM, Gibson A, Phillips EJ. Genomic Risk Factors Driving Immune-Mediated Delayed Drug Hypersensitivity Reactions. Front Genet 2021;12:641905. [PMID: 33936169 DOI: 10.3389/fgene.2021.641905] [Reference Citation Analysis]
18 Pawlak M, Niescierowicz K, Winata CL. Decoding the Heart through Next Generation Sequencing Approaches. Genes (Basel) 2018;9:E289. [PMID: 29880785 DOI: 10.3390/genes9060289] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
19 Alanzi T, Alhashem A, Dagriri K, Alzahrani F, Alkuraya FS. A de novo splicing variant supports the candidacy of TLL1 in ASD pathogenesis. Eur J Hum Genet 2020;28:525-8. [PMID: 31570783 DOI: 10.1038/s41431-019-0524-0] [Reference Citation Analysis]
20 Huang RT, Wang J, Xue S, Qiu XB, Shi HY, Li RG, Qu XK, Yang XX, Liu H, Li N, Li YJ, Xu YJ, Yang YQ. TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus. Int J Med Sci 2017;14:323-32. [PMID: 28553164 DOI: 10.7150/ijms.17834] [Cited by in Crossref: 23] [Cited by in F6Publishing: 21] [Article Influence: 4.6] [Reference Citation Analysis]
21 Chesneau B, Plancke A, Rolland G, Marcheix B, Dulac Y, Edouard T, Plaisancié J, Aubert-Mucca M, Julia S, Langeois M, Lavabre-Bertrand T, Khau Van Kien P. A +3 variant at a donor splice site leads to a skipping of the MYH11 exon 32, a recurrent RNA defect causing Heritable Thoracic Aortic Aneurysm and Dissection and/or Patent Ductus Arteriosus. Mol Genet Genomic Med 2021;9:e1814. [PMID: 34672437 DOI: 10.1002/mgg3.1814] [Reference Citation Analysis]
22 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]
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24 Møller Nielsen AK, Nyboe C, Lund Ovesen AS, Udholm S, Larsen MM, Hjortdal VE, Larsen LA. Mutation burden in patients with small unrepaired atrial septal defects. International Journal of Cardiology Congenital Heart Disease 2021;4:100164. [DOI: 10.1016/j.ijcchd.2021.100164] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
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29 Suwinski P, Ong C, Ling MHT, Poh YM, Khan AM, Ong HS. Advancing Personalized Medicine Through the Application of Whole Exome Sequencing and Big Data Analytics. Front Genet 2019;10:49. [PMID: 30809243 DOI: 10.3389/fgene.2019.00049] [Cited by in Crossref: 57] [Cited by in F6Publishing: 44] [Article Influence: 19.0] [Reference Citation Analysis]
30 Paige SL, Saha P, Priest JR. Beyond Gene Panels: Whole Exome Sequencing for Diagnosis of Congenital Heart Disease. Circ Genom Precis Med 2018;11:e002097. [PMID: 29555674 DOI: 10.1161/CIRCGEN.118.002097] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]