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341 results

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Patient genotypes impact survival after surgery for isolated congenital heart disease.
Kim DS, Kim JH, Burt AA, Crosslin DR, Burnham N, McDonald-McGinn DM, Zackai EH, Nicolson SC, Spray TL, Stanaway IB, Nickerson DA, Russell MW, Hakonarson H, Gaynor JW, Jarvik GP. Kim DS, et al. Among authors: russell mw. Ann Thorac Surg. 2014 Jul;98(1):104-10; discussion 110-1. doi: 10.1016/j.athoracsur.2014.03.017. Epub 2014 May 6. Ann Thorac Surg. 2014. PMID: 24811984 Free PMC article.
Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development.
Thorsson T, Russell WW, El-Kashlan N, Soemedi R, Levine J, Geisler SB, Ackley T, Tomita-Mitchell A, Rosenfeld JA, Töpf A, Tayeh M, Goodship J, Innis JW, Keavney B, Russell MW. Thorsson T, et al. Among authors: russell mw, russell ww. Congenit Heart Dis. 2015 May-Jun;10(3):193-208. doi: 10.1111/chd.12179. Epub 2014 Apr 11. Congenit Heart Dis. 2015. PMID: 24720490 Free article.
Damaging Variants in Proangiogenic Genes Impair Growth in Fetuses with Cardiac Defects.
Russell MW, Moldenhauer JS, Rychik J, Burnham NB, Zullo E, Parry SI, Simmons RA, Elovitz MA, Nicolson SC, Linn RL, Johnson MP, Yu S, Sampson MG, Hakonarson H, Gaynor JW. Russell MW, et al. J Pediatr. 2019 Oct;213:103-109. doi: 10.1016/j.jpeds.2019.05.013. Epub 2019 Jun 18. J Pediatr. 2019. PMID: 31227283 Free PMC article.
Failure to validate association of mannose-binding lectin deficiency with adverse neurodevelopmental outcomes after cardiac surgery in infants.
Kim DS, Newburger JW, Bellinger DC, Russell MW, Goldberg CS, Jarvik GP, Gaynor JW. Kim DS, et al. Among authors: russell mw. J Thorac Cardiovasc Surg. 2019 Jun;157(6):e397-e398. doi: 10.1016/j.jtcvs.2018.10.099. Epub 2019 May 16. J Thorac Cardiovasc Surg. 2019. PMID: 31307150 Free article. No abstract available.
Effect of parental origin of damaging variants in pro-angiogenic genes on fetal growth in patients with congenital heart defects: Data and analyses.
Russell MW, Moldenhauer JS, Rychik J, Burnham NB, Zullo E, Parry SI, Simmons RA, Elovitz MA, Nicolson SC, Linn RL, Johnson MP, Yu S, Sampson MG, Hakonarson H, Gaynor JW. Russell MW, et al. Data Brief. 2019 Jul 26;25:104311. doi: 10.1016/j.dib.2019.104311. eCollection 2019 Aug. Data Brief. 2019. PMID: 31453292 Free PMC article.
Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls.
Mamasoula C, Prentice RR, Pierscionek T, Pangilinan F, Mills JL, Druschel C, Pass K, Russell MW, Hall D, Töpf A, Brown DL, Zelenika D, Bentham J, Cosgrove C, Bhattacharya S, Riveron JG, Setchfield K, Brook JD, Bu'Lock FA, Thornborough C, Rahman TJ, Doza JP, Tan HL, O'Sullivan J, Stuart AG, Blue G, Winlaw D, Postma AV, Mulder BJ, Zwinderman AH, van Engelen K, Moorman AF, Rauch A, Gewillig M, Breckpot J, Devriendt K, Lathrop GM, Farrall M, Goodship JA, Cordell HJ, Brody LC, Keavney BD. Mamasoula C, et al. Among authors: russell mw. Circ Cardiovasc Genet. 2013 Aug;6(4):347-53. doi: 10.1161/CIRCGENETICS.113.000191. Epub 2013 Jul 22. Circ Cardiovasc Genet. 2013. PMID: 23876493 Free PMC article.
341 results