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Results by year

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

Year Number of Results
1822 1
1828 1
1839 3
1862 1
1864 1
1896 1
1899 1
1906 1
1930 1
1936 1
1940 1
1945 1
1946 1
1947 6
1948 4
1949 8
1950 6
1951 2
1952 4
1953 2
1954 2
1955 10
1956 10
1957 5
1958 4
1959 4
1960 5
1961 6
1962 8
1963 9
1964 15
1965 11
1966 16
1967 9
1968 14
1969 13
1970 18
1971 13
1972 15
1973 11
1974 14
1975 15
1976 18
1977 12
1978 19
1979 13
1980 16
1981 16
1982 14
1983 24
1984 9
1985 19
1986 15
1987 12
1988 16
1989 14
1990 15
1991 31
1992 11
1993 19
1994 16
1995 26
1996 27
1997 24
1998 15
1999 16
2000 20
2001 13
2002 14
2003 15
2004 19
2005 19
2006 19
2007 24
2008 33
2009 32
2010 21
2011 25
2012 18
2013 18
2014 29
2015 38
2016 41
2017 44
2018 39
2019 31
2020 26
2021 22
2022 25
2023 33
2024 12

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Article type

Publication date

Search Results

1,235 results

Results by year

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Page 1
Meniere's Disease.
Gibson WPR. Gibson WPR. Adv Otorhinolaryngol. 2019;82:77-86. doi: 10.1159/000490274. Epub 2019 Jan 15. Adv Otorhinolaryngol. 2019. PMID: 30947172 Review.
International consensus (ICON) on treatment of Ménière's disease.
Nevoux J, Barbara M, Dornhoffer J, Gibson W, Kitahara T, Darrouzet V. Nevoux J, et al. Among authors: gibson w. Eur Ann Otorhinolaryngol Head Neck Dis. 2018 Feb;135(1S):S29-S32. doi: 10.1016/j.anorl.2017.12.006. Epub 2018 Jan 12. Eur Ann Otorhinolaryngol Head Neck Dis. 2018. PMID: 29338942 Free article. Review.
Pediatric heart transplant.
Barnes A, Gibson W. Barnes A, et al. Among authors: gibson w. Semin Pediatr Surg. 2021 Apr;30(2):151039. doi: 10.1016/j.sempedsurg.2021.151039. Epub 2021 Mar 21. Semin Pediatr Surg. 2021. PMID: 33992306 Review.
Slow Delivery Immunization Enhances HIV Neutralizing Antibody and Germinal Center Responses via Modulation of Immunodominance.
Cirelli KM, Carnathan DG, Nogal B, Martin JT, Rodriguez OL, Upadhyay AA, Enemuo CA, Gebru EH, Choe Y, Viviano F, Nakao C, Pauthner MG, Reiss S, Cottrell CA, Smith ML, Bastidas R, Gibson W, Wolabaugh AN, Melo MB, Cossette B, Kumar V, Patel NB, Tokatlian T, Menis S, Kulp DW, Burton DR, Murrell B, Schief WR, Bosinger SE, Ward AB, Watson CT, Silvestri G, Irvine DJ, Crotty S. Cirelli KM, et al. Among authors: gibson w. Cell. 2019 May 16;177(5):1153-1171.e28. doi: 10.1016/j.cell.2019.04.012. Epub 2019 May 9. Cell. 2019. PMID: 31080066 Free PMC article.
Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study.
Elliott AM, Adam S, du Souich C, Lehman A, Nelson TN, van Karnebeek C, Alderman E, Armstrong L, Aubertin G, Blood K, Boelman C, Boerkoel C, Bretherick K, Brown L, Chijiwa C, Clarke L, Couse M, Creighton S, Watts-Dickens A, Gibson WT, Gill H, Tarailo-Graovac M, Hamilton S, Heran H, Horvath G, Huang L, Hulait GK, Koehn D, Lee HK, Lewis S, Lopez E, Louie K, Niederhoffer K, Matthews A, Meagher K, Peng JJ, Patel MS, Race S, Richmond P, Rupps R, Salvarinova R, Seath K, Selby K, Steinraths M, Stockler S, Tang K, Tyson C, van Allen M, Wasserman W, Mwenifumbo J, Friedman JM. Elliott AM, et al. Among authors: gibson wt. HGG Adv. 2022 Apr 18;3(3):100108. doi: 10.1016/j.xhgg.2022.100108. eCollection 2022 Jul 14. HGG Adv. 2022. PMID: 35599849 Free PMC article.
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Snijders Blok L, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, Nowak CB, Douglas J, Swoboda KJ, Steeves MA, Sahai I, Stumpel CTRM, Stegmann APA, Wheeler P, Willing M, Fiala E, Kochhar A, Gibson WT, Cohen ASA, Agbahovbe R, Innes AM, Au PYB, Rankin J, Anderson IJ, Skinner SA, Louie RJ, Warren HE, Afenjar A, Keren B, Nava C, Buratti J, Isapof A, Rodriguez D, Lewandowski R, Propst J, van Essen T, Choi M, Lee S, Chae JH, Price S, Schnur RE, Douglas G, Wentzensen IM, Zweier C, Reis A, Bialer MG, Moore C, Koopmans M, Brilstra EH, Monroe GR, van Gassen KLI, van Binsbergen E, Newbury-Ecob R, Bownass L, Bader I, Mayr JA, Wortmann SB, Jakielski KJ, Strand EA, Kloth K, Bierhals T; DDD study; Roberts JD, Petrovich RM, Machida S, Kurumizaka H, Lelieveld S, Pfundt R, Jansen S, Deriziotis P, Faivre L, Thevenon J, Assoum M, Shriberg L, Kleefstra T, Brunner HG, Wade PA, Fisher SE, Campeau PM. Snijders Blok L, et al. Among authors: gibson wt. Nat Commun. 2018 Nov 5;9(1):4619. doi: 10.1038/s41467-018-06014-6. Nat Commun. 2018. PMID: 30397230 Free PMC article.
SETD1B-associated neurodevelopmental disorder.
Roston A, Evans D, Gill H, McKinnon M, Isidor B, Cogné B, Mwenifumbo J, van Karnebeek C, An J, Jones SJM, Farrer M, Demos M, Connolly M, Gibson WT; CAUSES Study; EPGEN Study. Roston A, et al. Among authors: gibson wt. J Med Genet. 2021 Mar;58(3):196-204. doi: 10.1136/jmedgenet-2019-106756. Epub 2020 Jun 16. J Med Genet. 2021. PMID: 32546566
1,235 results