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Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects.
Agopian AJ, Goldmuntz E, Hakonarson H, Sewda A, Taylor D, Mitchell LE; Pediatric Cardiac Genomics Consortium*. Agopian AJ, et al. Among authors: sewda a. Circ Cardiovasc Genet. 2017 Jun;10(3):e001449. doi: 10.1161/CIRCGENETICS.116.001449. Circ Cardiovasc Genet. 2017. PMID: 28468790 Free PMC article.
Exon sequencing of PAX3 and T (brachyury) in cases with spina bifida.
Agopian AJ, Bhalla AD, Boerwinkle E, Finnell RH, Grove ML, Hixson JE, Shimmin LC, Sewda A, Stuart C, Zhong Y, Zhu H, Mitchell LE. Agopian AJ, et al. Among authors: sewda a. Birth Defects Res A Clin Mol Teratol. 2013 Sep;97(9):597-601. doi: 10.1002/bdra.23163. Epub 2013 Aug 2. Birth Defects Res A Clin Mol Teratol. 2013. PMID: 23913553 Free PMC article.
Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study.
Hoang TT, Manso PH, Edman S, Mercer-Rosa L, Mitchell LE, Sewda A, Swartz MD, Fogel MA, Agopian AJ, Goldmuntz E. Hoang TT, et al. Among authors: sewda a. J Cardiovasc Magn Reson. 2019 Aug 19;21(1):51. doi: 10.1186/s12968-019-0555-2. J Cardiovasc Magn Reson. 2019. PMID: 31422771 Free PMC article.
Nonsyndromic craniosynostosis: novel coding variants.
Sewda A, White SR, Erazo M, Hao K, García-Fructuoso G, Fernández-Rodriguez I, Heuzé Y, Richtsmeier JT, Romitti PA, Reva B, Jabs EW, Peter I. Sewda A, et al. Pediatr Res. 2019 Mar;85(4):463-468. doi: 10.1038/s41390-019-0274-2. Epub 2019 Jan 14. Pediatr Res. 2019. PMID: 30651579 Free PMC article.
Genetic architecture of cardiometabolic risks in people living with HIV.
Cheng H, Sewda A, Marquez-Luna C, White SR, Whitney BM, Williams-Nguyen J, Nance RM, Lee WJ, Kitahata MM, Saag MS, Willig A, Eron JJ, Mathews WC, Hunt PW, Moore RD, Webel A, Mayer KH, Delaney JA, Crane PK, Crane HM, Hao K, Peter I. Cheng H, et al. Among authors: sewda a. BMC Med. 2020 Oct 28;18(1):288. doi: 10.1186/s12916-020-01762-z. BMC Med. 2020. PMID: 33109212 Free PMC article.
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays.
Ganapathi M, Matsuoka LS, March M, Li D, Brokamp E, Benito-Sanz S, White SM, Lachlan K, Ahimaz P, Sewda A, Bastarache L, Thomas-Wilson A, Stoler JM, Bramswig NC, Baptista J, Stals K, Demurger F, Cogne B, Isidor B, Bedeschi MF, Peron A, Amiel J, Zackai E, Schacht JP, Iglesias AD, Morton J, Schmetz A; Undiagnosed Diseases Network; Seidel V, Lucia S, Baskin SM, Thiffault I, Cogan JD, Gordon CT, Chung WK, Bowdin S, Bhoj E. Ganapathi M, et al. Among authors: sewda a. Eur J Hum Genet. 2023 Oct;31(10):1117-1124. doi: 10.1038/s41431-023-01434-5. Epub 2023 Jul 27. Eur J Hum Genet. 2023. PMID: 37500725
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