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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1999 2
2000 1
2001 3
2003 3
2004 5
2005 2
2006 4
2007 3
2008 3
2009 3
2010 3
2011 6
2012 5
2013 6
2014 1
2015 5
2016 2
2017 2
2018 11
2019 4
2020 6
2021 8
2022 3
2023 1
2024 3
2025 5

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94 results

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Page 1
Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1).
Laing NG, Dye DE, Wallgren-Pettersson C, Richard G, Monnier N, Lillis S, Winder TL, Lochmüller H, Graziano C, Mitrani-Rosenbaum S, Twomey D, Sparrow JC, Beggs AH, Nowak KJ. Laing NG, et al. Among authors: nowak kj. Hum Mutat. 2009 Sep;30(9):1267-77. doi: 10.1002/humu.21059. Hum Mutat. 2009. PMID: 19562689 Free PMC article.
Early Intratracheal Budesonide to Reduce Bronchopulmonary Dysplasia in Extremely Preterm Infants: The Budesonide in Babies (BiB) Randomized Clinical Trial.
Ambalavanan N, Carlo WA, Nowak KJ, Wiener LE, Cosby SS, Bhatt AJ, Watterberg KL, Poindexter BB, Keszler M, D'Angio CT, Brion LP, Narendran V, Rau CA, Cotten CM, Laughon MM, Das A, Rysavy MA, Hibbs AM, Fuller J, Puopolo KM, Katheria A, Patel RM, Bermick JR, Laptook AR, Prelipcean I, Wyckoff MH, Moore R, Merhar SL, Ohls RK, Yoder BA, Perez M, Ghavam S, Meyer LR, Chock VY, DeMauro SB, Jackson WM, Handa D, Walsh MC; National Institute of Child Health and Human Development Neonatal Research Network. Ambalavanan N, et al. Among authors: nowak kj. JAMA. 2025 Oct 28;334(16):1452-1462. doi: 10.1001/jama.2025.16450. JAMA. 2025. PMID: 41026481 Clinical Trial.
Incidental inequity.
Nowak KJ, Bauskis A, Dawkins HJ, Baynam G. Nowak KJ, et al. Eur J Hum Genet. 2018 May;26(5):616-617. doi: 10.1038/s41431-018-0101-y. Epub 2018 Feb 15. Eur J Hum Genet. 2018. PMID: 29449719 Free PMC article. No abstract available.
Recent advances in understanding congenital myopathies.
Ravenscroft G, Bryson-Richardson RJ, Nowak KJ, Laing NG. Ravenscroft G, et al. Among authors: nowak kj. F1000Res. 2018 Dec 11;7:F1000 Faculty Rev-1921. doi: 10.12688/f1000research.16422.1. eCollection 2018. F1000Res. 2018. PMID: 30631434 Free PMC article. Review.
Optimizing Precision Medicine for Public Health.
Bilkey GA, Burns BL, Coles EP, Mahede T, Baynam G, Nowak KJ. Bilkey GA, et al. Among authors: nowak kj. Front Public Health. 2019 Mar 7;7:42. doi: 10.3389/fpubh.2019.00042. eCollection 2019. Front Public Health. 2019. PMID: 30899755 Free PMC article. Review.
Nemaline myopathies.
Wallgren-Pettersson C, Sewry CA, Nowak KJ, Laing NG. Wallgren-Pettersson C, et al. Among authors: nowak kj. Semin Pediatr Neurol. 2011 Dec;18(4):230-8. doi: 10.1016/j.spen.2011.10.004. Semin Pediatr Neurol. 2011. PMID: 22172418 Review.
Clinical utility gene card for McArdle disease.
Taylor RL, Davis M, Turner E, Brull A, Pinos T, Cabrera M, Nowak KJ. Taylor RL, et al. Among authors: nowak kj. Eur J Hum Genet. 2018 May;26(5):758-764. doi: 10.1038/s41431-017-0070-6. Epub 2018 Jan 25. Eur J Hum Genet. 2018. PMID: 29371640 Free PMC article.
Clinical Utility Gene Card for: Becker muscular dystrophy.
Coote D, Davis MR, Cabrera M, Needham M, Laing NG, Nowak KJ. Coote D, et al. Among authors: nowak kj. Eur J Hum Genet. 2018 Jul;26(7):1065-1071. doi: 10.1038/s41431-017-0064-4. Epub 2018 Feb 21. Eur J Hum Genet. 2018. PMID: 29467387 Free PMC article. No abstract available.
Clinical utility gene card for: Nemaline myopathy - update 2015.
Nowak KJ, Davis MR, Wallgren-Pettersson C, Lamont PJ, Laing NG. Nowak KJ, et al. Eur J Hum Genet. 2015 Nov;23(11). doi: 10.1038/ejhg.2015.12. Epub 2015 Feb 25. Eur J Hum Genet. 2015. PMID: 25712079 Free PMC article. No abstract available.
94 results