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Results by year

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

Year Number of Results
1949 1
1955 1
1960 1
1962 1
1964 2
1965 1
1966 1
1969 3
1970 3
1971 2
1973 2
1974 5
1975 3
1976 2
1977 2
1978 3
1979 2
1980 2
1981 2
1982 4
1983 3
1984 7
1985 5
1986 5
1987 3
1988 5
1989 11
1990 8
1991 9
1992 9
1993 7
1994 11
1995 13
1996 23
1997 3
1998 9
1999 9
2000 9
2001 7
2002 5
2003 8
2004 12
2005 24
2006 20
2007 16
2008 20
2009 22
2010 23
2011 19
2012 27
2013 38
2014 41
2015 35
2016 48
2017 39
2018 38
2019 57
2020 59
2021 70
2022 67
2023 60
2024 24

Text availability

Article attribute

Article type

Publication date

Search Results

852 results

Results by year

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Page 1
Costello syndrome: Clinical phenotype, genotype, and management guidelines.
Gripp KW, Morse LA, Axelrad M, Chatfield KC, Chidekel A, Dobyns W, Doyle D, Kerr B, Lin AE, Schwartz DD, Sibbles BJ, Siegel D, Shankar SP, Stevenson DA, Thacker MM, Weaver KN, White SM, Rauen KA. Gripp KW, et al. Among authors: weaver kn. Am J Med Genet A. 2019 Sep;179(9):1725-1744. doi: 10.1002/ajmg.a.61270. Epub 2019 Jun 20. Am J Med Genet A. 2019. PMID: 31222966 Free PMC article.
Enterococcal Genetics.
Weaver KE. Weaver KE. Microbiol Spectr. 2019 Mar;7(2). doi: 10.1128/microbiolspec.GPP3-0055-2018. Microbiol Spectr. 2019. PMID: 30848235 Free article. Review.
Petroclival meningiomas.
Hunter JB, Weaver KD, Thompson RC, Wanna GB. Hunter JB, et al. Among authors: weaver kd. Otolaryngol Clin North Am. 2015 Jun;48(3):477-90. doi: 10.1016/j.otc.2015.02.007. Epub 2015 Apr 9. Otolaryngol Clin North Am. 2015. PMID: 25863570 Review.
ARF1-related disorder: phenotypic and molecular spectrum.
de Sainte Agathe JM, Pode-Shakked B, Naudion S, Michaud V, Arveiler B, Fergelot P, Delmas J, Keren B, Poirsier C, Alkuraya FS, Tabarki B, Bend E, Davis K, Bebin M, Thompson ML, Bryant EM, Wagner M, Hannibal I, Lenberg J, Krenn M, Wigby KM, Friedman JR, Iascone M, Cereda A, Miao T, LeGuern E, Argilli E, Sherr E, Caluseriu O, Tidwell T, Bayrak-Toydemir P, Hagedorn C, Brugger M, Vill K, Morneau-Jacob FD, Chung W, Weaver KN, Owens JW, Husami A, Chaudhari BP, Stone BS, Burns K, Li R, de Lange IM, Biehler M, Ginglinger E, Gérard B, Stottmann RW, Trimouille A. de Sainte Agathe JM, et al. Among authors: weaver kn. J Med Genet. 2023 Oct;60(10):999-1005. doi: 10.1136/jmg-2022-108803. Epub 2023 Apr 25. J Med Genet. 2023. PMID: 37185208 Free PMC article.
POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies.
Smallwood K, Watt KEN, Ide S, Baltrunaite K, Brunswick C, Inskeep K, Capannari C, Adam MP, Begtrup A, Bertola DR, Demmer L, Demo E, Devinsky O, Gallagher ER, Guillen Sacoto MJ, Jech R, Keren B, Kussmann J, Ladda R, Lansdon LA, Lunke S, Mardy A, McWalters K, Person R, Raiti L, Saitoh N, Saunders CJ, Schnur R, Skorvanek M, Sell SL, Slavotinek A, Sullivan BR, Stark Z, Symonds JD, Wenger T, Weber S, Whalen S, White SM, Winkelmann J, Zech M, Zeidler S, Maeshima K, Stottmann RW, Trainor PA, Weaver KN. Smallwood K, et al. Among authors: weaver kn. Am J Hum Genet. 2023 May 4;110(5):809-825. doi: 10.1016/j.ajhg.2023.03.014. Epub 2023 Apr 18. Am J Hum Genet. 2023. PMID: 37075751 Free PMC article.
Irritable Bowel Syndrome.
Weaver KR, Melkus GD, Henderson WA. Weaver KR, et al. Am J Nurs. 2017 Jun;117(6):48-55. doi: 10.1097/01.NAJ.0000520253.57459.01. Am J Nurs. 2017. PMID: 28541989 Free PMC article.
852 results