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Page 1
Profiling development of abdominal organs in the pig.
Gabriel GC, Devine WA, Redel BK, Whitworth KM, Samuel M, Spate LD, Cecil RF, Prather RS, Wu YL, Wells KD, Lo CW. Gabriel GC, et al. Sci Rep. 2022 Sep 28;12(1):16245. doi: 10.1038/s41598-022-19960-5. Sci Rep. 2022. PMID: 36171243 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. 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.
Clinical factors associated with microstructural connectome related brain dysmaturation in term neonates with congenital heart disease.
Votava-Smith JK, Gaesser J, Harbison AL, Lee V, Tran N, Rajagopalan V, Del Castillo S, Kumar SR, Herrup E, Baust T, Johnson JA, Gabriel GC, Reynolds WT 3rd, Wallace J, Meyers B, Ceschin R, Lo CW, Schmithorst VJ, Panigrahy A. Votava-Smith JK, et al. Front Neurosci. 2022 Nov 18;16:952355. doi: 10.3389/fnins.2022.952355. eCollection 2022. Front Neurosci. 2022. PMID: 36466162 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. 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.
Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract.
Münch J, Engesser M, Schönauer R, Hamm JA, Hartig C, Hantmann E, Akay G, Pehlivan D, Mitani T, Coban Akdemir Z, Tüysüz B, Shirakawa T, Dateki S, Claus LR, van Eerde AM; Genomics England Research Consortium; Smol T, Devisme L, Franquet H, Attié-Bitach T, Wagner T, Bergmann C, Höhn AK, Shril S, Pollack A, Wenger T, Scott AA, Paolucci S, Buchan J, Gabriel GC, Posey JE, Lupski JR, Petit F, McCarthy AA, Pazour GJ, Lo CW, Popp B, Halbritter J. Münch J, et al. Kidney Int. 2022 May;101(5):1039-1053. doi: 10.1016/j.kint.2022.01.028. Epub 2022 Feb 26. Kidney Int. 2022. PMID: 35227688 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. 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.