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

Year Number of Results
1974 1
1982 1
1983 1
1984 2
1985 5
1986 8
1987 2
1988 3
1989 3
1990 5
1991 8
1992 8
1993 5
1994 1
1995 1
1996 5
1997 2
1998 1
1999 3
2000 3
2001 3
2002 1
2003 1
2005 1
2006 1
2007 1
2008 1
2009 4
2011 4
2012 5
2013 6
2014 2
2016 5
2017 5
2018 3
2019 3
2020 2
2021 4
2022 2
2023 0

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114 results

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Page 1
Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.
Page DJ, Miossec MJ, Williams SG, Monaghan RM, Fotiou E, Cordell HJ, Sutcliffe L, Topf A, Bourgey M, Bourque G, Eveleigh R, Dunwoodie SL, Winlaw DS, Bhattacharya S, Breckpot J, Devriendt K, Gewillig M, Brook JD, Setchfield KJ, Bu'Lock FA, O'Sullivan J, Stuart G, Bezzina CR, Mulder BJM, Postma AV, Bentham JR, Baron M, Bhaskar SS, Black GC, Newman WG, Hentges KE, Lathrop GM, Santibanez-Koref M, Keavney BD. Page DJ, et al. Among authors: brook jd. Circ Res. 2019 Feb 15;124(4):553-563. doi: 10.1161/CIRCRESAHA.118.313250. Circ Res. 2019. PMID: 30582441 Free PMC article.
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.
Sifrim A, Hitz MP, Wilsdon A, Breckpot J, Turki SH, Thienpont B, McRae J, Fitzgerald TW, Singh T, Swaminathan GJ, Prigmore E, Rajan D, Abdul-Khaliq H, Banka S, Bauer UM, Bentham J, Berger F, Bhattacharya S, Bu'Lock F, Canham N, Colgiu IG, Cosgrove C, Cox H, Daehnert I, Daly A, Danesh J, Fryer A, Gewillig M, Hobson E, Hoff K, Homfray T; INTERVAL Study; Kahlert AK, Ketley A, Kramer HH, Lachlan K, Lampe AK, Louw JJ, Manickara AK, Manase D, McCarthy KP, Metcalfe K, Moore C, Newbury-Ecob R, Omer SO, Ouwehand WH, Park SM, Parker MJ, Pickardt T, Pollard MO, Robert L, Roberts DJ, Sambrook J, Setchfield K, Stiller B, Thornborough C, Toka O, Watkins H, Williams D, Wright M, Mital S, Daubeney PE, Keavney B, Goodship J; UK10K Consortium; Abu-Sulaiman RM, Klaassen S, Wright CF, Firth HV, Barrett JC, Devriendt K, FitzPatrick DR, Brook JD; Deciphering Developmental Disorders Study; Hurles ME. Sifrim A, et al. Among authors: brook jd. Nat Genet. 2016 Sep;48(9):1060-5. doi: 10.1038/ng.3627. Epub 2016 Aug 1. Nat Genet. 2016. PMID: 27479907 Free PMC article.
Disrupting the Molecular Pathway in Myotonic Dystrophy.
Xing X, Kumari A, Brown J, Brook JD. Xing X, et al. Among authors: brook jd. Int J Mol Sci. 2021 Dec 8;22(24):13225. doi: 10.3390/ijms222413225. Int J Mol Sci. 2021. PMID: 34948025 Free PMC article. Review.
T-Box Genes in Human Development and Disease.
Ghosh TK, Brook JD, Wilsdon A. Ghosh TK, et al. Among authors: brook jd. Curr Top Dev Biol. 2017;122:383-415. doi: 10.1016/bs.ctdb.2016.08.006. Epub 2016 Oct 5. Curr Top Dev Biol. 2017. PMID: 28057271 Review.
Recent advances in congenital heart disease genomics.
Wilsdon A, Sifrim A, Hitz MP, Hurles M, Brook JD. Wilsdon A, et al. Among authors: brook jd. F1000Res. 2017 Jun 12;6:869. doi: 10.12688/f1000research.10113.1. eCollection 2017. F1000Res. 2017. PMID: 28663792 Free PMC article. Review.
The impact of mechanical forces in heart morphogenesis.
Granados-Riveron JT, Brook JD. Granados-Riveron JT, et al. Among authors: brook jd. Circ Cardiovasc Genet. 2012 Feb 1;5(1):132-42. doi: 10.1161/CIRCGENETICS.111.961086. Circ Cardiovasc Genet. 2012. PMID: 22337926 Review. No abstract available.
T-box genes in human disorders.
Packham EA, Brook JD. Packham EA, et al. Among authors: brook jd. Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R37-44. doi: 10.1093/hmg/ddg077. Hum Mol Genet. 2003. PMID: 12668595 Review.
Gene mapping and chromosome 19.
Shaw DJ, Brook JD, Meredith AL, Harley HG, Sarfarazi M, Harper PS. Shaw DJ, et al. Among authors: brook jd. J Med Genet. 1986 Feb;23(1):2-10. doi: 10.1136/jmg.23.1.2. J Med Genet. 1986. PMID: 3081724 Free PMC article. Review.
114 results