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

Year Number of Results
2002 3
2003 3
2004 3
2005 3
2006 5
2007 4
2008 4
2009 3
2010 5
2011 6
2012 5
2013 4
2014 12
2015 7
2016 2
2017 3
2018 3
2019 2
2020 2
2021 1
2022 5
2023 3
2024 0

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81 results

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Page 1
Nanoparticle-coated microcrystals.
Murugesan M, Cunningham D, Martinez-Albertos JL, Vrcelj RM, Moore BD. Murugesan M, et al. Among authors: moore bd. Chem Commun (Camb). 2005 Jun 7;(21):2677-9. doi: 10.1039/b501046b. Epub 2005 Apr 20. Chem Commun (Camb). 2005. PMID: 15917917 Free article.
Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning.
Peterson B, Hernandez EJ, Hobbs C, Malone Jenkins S, Moore B, Rosales E, Zoucha S, Sanford E, Bainbridge MN, Frise E, Oriol A, Brunelli L, Kingsmore SF, Yandell M. Peterson B, et al. Among authors: moore b. Genome Med. 2023 Mar 16;15(1):18. doi: 10.1186/s13073-023-01166-7. Genome Med. 2023. PMID: 36927505 Free PMC article.
Predictors of Survival after Vaccination in a Pneumonic Plague Model.
Moore BD, Macleod C, Henning L, Krile R, Chou YL, Laws TR, Butcher WA, Moore KM, Walker NJ, Williamson ED, Galloway DR. Moore BD, et al. Vaccines (Basel). 2022 Jan 19;10(2):145. doi: 10.3390/vaccines10020145. Vaccines (Basel). 2022. PMID: 35214604 Free PMC article.
SOBA: sequence ontology bioinformatics analysis.
Moore B, Fan G, Eilbeck K. Moore B, et al. Nucleic Acids Res. 2010 Jul;38(Web Server issue):W161-4. doi: 10.1093/nar/gkq426. Epub 2010 May 21. Nucleic Acids Res. 2010. PMID: 20494974 Free PMC article.
A dominant negative ADIPOQ mutation in a diabetic family with renal disease, hypoadiponectinemia, and hyperceramidemia.
Simeone CA, Wilkerson JL, Poss AM, Banks JA, Varre JV, Guevara JL, Hernandez EJ, Gorsi B, Atkinson DL, Turapov T, Frodsham SG, Morales JCF, O'Neil K, Moore B, Yandell M, Summers SA, Krolewski AS, Holland WL, Pezzolesi MG. Simeone CA, et al. Among authors: moore b. NPJ Genom Med. 2022 Jul 22;7(1):43. doi: 10.1038/s41525-022-00314-z. NPJ Genom Med. 2022. PMID: 35869090 Free PMC article.
Comprehensive variant calling from whole-genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic hernia.
Nicholas TJ, Al-Sweel N, Farrell A, Mao R, Bayrak-Toydemir P, Miller CE, Bentley D, Palmquist R, Moore B, Hernandez EJ, Cormier MJ, Fredrickson E, Noble K, Rynearson S, Holt C, Karren MA, Bonkowsky JL, Tristani-Firouzi M, Yandell M, Marth G, Quinlan AR, Brunelli L, Toydemir RM, Shayota BJ, Carey JC, Boyden SE, Malone Jenkins S. Nicholas TJ, et al. Among authors: moore b. Mol Genet Genomic Med. 2022 Apr;10(4):e1888. doi: 10.1002/mgg3.1888. Epub 2022 Feb 4. Mol Genet Genomic Med. 2022. PMID: 35119225 Free PMC article.
Genome Annotation and Curation Using MAKER and MAKER-P.
Campbell MS, Holt C, Moore B, Yandell M. Campbell MS, et al. Among authors: moore b. Curr Protoc Bioinformatics. 2014 Dec 12;48:4.11.1-4.11.39. doi: 10.1002/0471250953.bi0411s48. Curr Protoc Bioinformatics. 2014. PMID: 25501943 Free PMC article.
81 results