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The complex genetics of hypoplastic left heart syndrome.
Liu X, Yagi H, Saeed S, Bais AS, Gabriel GC, Chen Z, Peterson KA, Li Y, Schwartz MC, Reynolds WT, Saydmohammed M, Gibbs B, Wu Y, Devine W, Chatterjee B, Klena NT, Kostka D, de Mesy Bentley KL, Ganapathiraju MK, Dexheimer P, Leatherbury L, Khalifa O, Bhagat A, Zahid M, Pu W, Watkins S, Grossfeld P, Murray SA, Porter GA Jr, Tsang M, Martin LJ, Benson DW, Aronow BJ, Lo CW. Liu X, et al. Among authors: wu y. Nat Genet. 2017 Jul;49(7):1152-1159. doi: 10.1038/ng.3870. Epub 2017 May 22. Nat Genet. 2017. PMID: 28530678 Free PMC article.
Diverse application of MRI for mouse phenotyping.
Wu YL, Lo CW. Wu YL, et al. Birth Defects Res. 2017 Jun 1;109(10):758-770. doi: 10.1002/bdr2.1051. Epub 2017 May 22. Birth Defects Res. 2017. PMID: 28544650 Free PMC article. Review.
The Genetic Landscape of Hypoplastic Left Heart Syndrome.
Yagi H, Liu X, Gabriel GC, Wu Y, Peterson K, Murray SA, Aronow BJ, Martin LJ, Benson DW, Lo CW. Yagi H, et al. Among authors: wu y. Pediatr Cardiol. 2018 Aug;39(6):1069-1081. doi: 10.1007/s00246-018-1861-4. Epub 2018 Mar 22. Pediatr Cardiol. 2018. PMID: 29569026 Free PMC article.
Control of cytokinesis by β-adrenergic receptors indicates an approach for regulating cardiomyocyte endowment.
Liu H, Zhang CH, Ammanamanchi N, Suresh S, Lewarchik C, Rao K, Uys GM, Han L, Abrial M, Yimlamai D, Ganapathy B, Guillermier C, Chen N, Khaladkar M, Spaethling J, Eberwine JH, Kim J, Walsh S, Choudhury S, Little K, Francis K, Sharma M, Viegas M, Bais A, Kostka D, Ding J, Bar-Joseph Z, Wu Y, Yechoor V, Moulik M, Johnson J, Weinberg J, Reyes-Múgica M, Steinhauser ML, Kühn B. Liu H, et al. Among authors: wu y. Sci Transl Med. 2019 Oct 9;11(513):eaaw6419. doi: 10.1126/scitranslmed.aaw6419. Sci Transl Med. 2019. PMID: 31597755 Free PMC article.
Cardiovascular Development and Congenital Heart Disease Modeling in the Pig.
Gabriel GC, Devine W, Redel BK, Whitworth KM, Samuel M, Spate LD, Cecil RF, Prather RS, Wu Y, Wells KD, Lo CW. Gabriel GC, et al. Among authors: wu y. J Am Heart Assoc. 2021 Jul 20;10(14):e021631. doi: 10.1161/JAHA.121.021631. Epub 2021 Jul 3. J Am Heart Assoc. 2021. PMID: 34219463 Free PMC article.
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease.
Teekakirikul P, Zhu W, Gabriel GC, Young CB, Williams K, Martin LJ, Hill JC, Richards T, Billaud M, Phillippi JA, Wang J, Wu Y, Tan T, Devine W, Lin JH, Bais AS, Klonowski J, Moreau de Bellaing A, Saini A, Wang MX, Emerel L, Salamacha N, Wyman SK, Lee C, Sing Li H, Miron A, Zhang J, Xing J, McNamara DM, Fung E, Kirshbom P, Mahle W, Kochilas LK, He Y, Garg V, White P, McBride KL, Benson DW, Gleason TG, Mital S, Lo CW. Teekakirikul P, et al. Among authors: wu y. HGG Adv. 2021 Jul 8;2(3):100037. doi: 10.1016/j.xhgg.2021.100037. Epub 2021 Jul 29. HGG Adv. 2021. PMID: 34888534 Free PMC article.
Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability.
Teekakirikul P, Zhu W, Xu X, Young CB, Tan T, Smith AM, Wang C, Peterson KA, Gabriel GC, Ho S, Sheng Y, Moreau de Bellaing A, Sonnenberg DA, Lin JH, Fotiou E, Tenin G, Wang MX, Wu YL, Feinstein T, Devine W, Gou H, Bais AS, Glennon BJ, Zahid M, Wong TC, Ahmad F, Rynkiewicz MJ, Lehman WJ, Keavney B, Alastalo TP, Freckmann ML, Orwig K, Murray S, Ware SM, Zhao H, Feingold B, Lo CW. Teekakirikul P, et al. Among authors: wu yl. Cell Rep Med. 2022 Feb 15;3(2):100501. doi: 10.1016/j.xcrm.2021.100501. eCollection 2022 Feb 15. Cell Rep Med. 2022. PMID: 35243414 Free PMC article.
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