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

Year Number of Results
1954 1
1958 1
1960 2
1961 1
1962 2
1964 1
1965 7
1966 1
1967 1
1970 1
1971 2
1972 2
1973 2
1974 2
1975 3
1976 1
1977 8
1978 3
1979 3
1980 5
1981 6
1982 10
1983 13
1984 10
1985 21
1986 21
1987 10
1988 8
1989 15
1990 14
1991 15
1992 18
1993 17
1994 15
1995 15
1996 19
1997 18
1998 18
1999 19
2000 19
2001 21
2002 22
2003 15
2004 15
2005 18
2006 28
2007 24
2008 21
2009 19
2010 15
2011 23
2012 27
2013 35
2014 29
2015 29
2016 35
2017 35
2018 34
2019 32
2020 35
2021 38
2022 26
2023 23
2024 34
2025 3

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907 results

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Page 1
A metabolic switch orchestrated by IL-18 and the cyclic dinucleotide cGAMP programs intestinal tolerance.
Mertens RT, Misra A, Xiao P, Baek S, Rone JM, Mangani D, Sivanathan KN, Arojojoye AS, Awuah SG, Lee I, Shi GP, Petrova B, Brook JR, Anderson AC, Flavell RA, Kanarek N, Hemberg M, Nowarski R. Mertens RT, et al. Among authors: brook jr. Immunity. 2024 Sep 10;57(9):2077-2094.e12. doi: 10.1016/j.immuni.2024.06.001. Epub 2024 Jun 20. Immunity. 2024. PMID: 38906145
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.
The Alcubierre key.
Brook J. Brook J. Nature. 2024 Jan 17. doi: 10.1038/d41586-024-00095-8. Online ahead of print. Nature. 2024. PMID: 38233547 No abstract available.
Platelet lipoprotein interactions.
Brook JG, Aviram M. Brook JG, et al. Semin Thromb Hemost. 1988 Jul;14(3):258-65. doi: 10.1055/s-2007-1002787. Semin Thromb Hemost. 1988. PMID: 3051391 Review. No abstract available.
From Fetus to Eight: the CHILD Cohort Study.
Miliku K, Reyna ME, Medeleanu M, Dai R, Dubeau A, Lefebvre DL, Wright K, Dawod B, Beck M, Brooks E, Kobor M, Duan Q, Brook JR, Lou W, Brinkman FSL, Winsor GL, Cook J, Becker AB, Simons E, Mandhane PJ, Moraes TJ, Azad MB, Sears MR, Turvey SE, Subbarao P; CHILD Study Investigators. Miliku K, et al. Among authors: brook jr. Am J Epidemiol. 2024 Oct 11:kwae397. doi: 10.1093/aje/kwae397. Online ahead of print. Am J Epidemiol. 2024. PMID: 39393830
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.
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.
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.
Myotonic dystrophy, knockouts, warts and all.
Hamshere MG, Brook JD. Hamshere MG, et al. Among authors: brook jd. Trends Genet. 1996 Sep;12(9):332-4. doi: 10.1016/s0168-9525(96)80002-3. Trends Genet. 1996. PMID: 8855655 Review. No abstract available.
907 results