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

Year Number of Results
1920 1
1947 3
1949 1
1952 1
1954 1
1955 1
1956 1
1961 2
1964 2
1965 4
1966 1
1967 1
1968 4
1969 3
1970 5
1971 2
1972 2
1973 6
1974 4
1975 3
1976 6
1977 9
1978 3
1979 5
1980 5
1981 4
1982 8
1984 5
1985 5
1986 7
1987 10
1988 10
1989 11
1990 8
1991 16
1992 18
1993 18
1994 18
1995 26
1996 13
1997 14
1998 12
1999 19
2000 27
2001 25
2002 24
2003 26
2004 35
2005 44
2006 65
2007 51
2008 49
2009 56
2010 61
2011 68
2012 64
2013 71
2014 78
2015 87
2016 87
2017 79
2018 86
2019 90
2020 98
2021 56
Text availability
Article attribute
Article type
Publication date

Search Results

1,480 results
Results by year
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Page 1
Non-alcoholic fatty liver disease and diabetes.
Hazlehurst JM, Woods C, Marjot T, Cobbold JF, Tomlinson JW. Hazlehurst JM, et al. Among authors: woods c. Metabolism. 2016 Aug;65(8):1096-108. doi: 10.1016/j.metabol.2016.01.001. Epub 2016 Jan 11. Metabolism. 2016. PMID: 26856933 Free PMC article. Review.
Congenital Insensitivity to Pain Overview.
Schon KR, Parker APJ, Woods CG. Schon KR, et al. Among authors: woods cg. 2018 Feb 8 [updated 2020 Jun 11]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. 2018 Feb 8 [updated 2020 Jun 11]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. PMID: 29419974 Free Books & Documents. Review.
Valganciclovir for symptomatic congenital cytomegalovirus disease.
Kimberlin DW, Jester PM, Sánchez PJ, Ahmed A, Arav-Boger R, Michaels MG, Ashouri N, Englund JA, Estrada B, Jacobs RF, Romero JR, Sood SK, Whitworth MS, Abzug MJ, Caserta MT, Fowler S, Lujan-Zilbermann J, Storch GA, DeBiasi RL, Han JY, Palmer A, Weiner LB, Bocchini JA, Dennehy PH, Finn A, Griffiths PD, Luck S, Gutierrez K, Halasa N, Homans J, Shane AL, Sharland M, Simonsen K, Vanchiere JA, Woods CR, Sabo DL, Aban I, Kuo H, James SH, Prichard MN, Griffin J, Giles D, Acosta EP, Whitley RJ; National Institute of Allergy and Infectious Diseases Collaborative Antiviral Study Group. Kimberlin DW, et al. Among authors: woods cr. N Engl J Med. 2015 Mar 5;372(10):933-43. doi: 10.1056/NEJMoa1404599. N Engl J Med. 2015. PMID: 25738669 Free PMC article. Clinical Trial.
Glucocorticoids and non-alcoholic fatty liver disease.
Woods CP, Hazlehurst JM, Tomlinson JW. Woods CP, et al. J Steroid Biochem Mol Biol. 2015 Nov;154:94-103. doi: 10.1016/j.jsbmb.2015.07.020. Epub 2015 Aug 1. J Steroid Biochem Mol Biol. 2015. PMID: 26241028 Review.
A Pediatric Infectious Diseases Perspective of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and Novel Coronavirus Disease 2019 (COVID-19) in Children.
Shane AL, Sato AI, Kao C, Adler-Shohet FC, Vora SB, Auletta JJ, Nachman S, Raabe VN, Inagaki K, Akinboyo IC, Woods C, Alsulami AO, Kainth MK, Santos RP, Espinosa CM, Burns JE, Cunningham CK, Dominguez SR, Martinez BL, Zhu F, Crews J, Kitano T, Saiman L, Kotloff K. Shane AL, et al. Among authors: woods c. J Pediatric Infect Dis Soc. 2020 Nov 10;9(5):596-608. doi: 10.1093/jpids/piaa099. J Pediatric Infect Dis Soc. 2020. PMID: 32840614 Free PMC article. Review.
ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm.
Gould RA, Aziz H, Woods CE, Seman-Senderos MA, Sparks E, Preuss C, Wünnemann F, Bedja D, Moats CR, McClymont SA, Rose R, Sobreira N, Ling H, MacCarrick G, Kumar AA, Luyckx I, Cannaerts E, Verstraeten A, Björk HM, Lehsau AC, Jaskula-Ranga V, Lauridsen H, Shah AA, Bennett CL, Ellinor PT, Lin H, Isselbacher EM, Lino Cardenas CL, Butcher JT, Hughes GC, Lindsay ME; Baylor-Hopkins Center for Mendelian Genomics; MIBAVA Leducq Consortium, Mertens L, Franco-Cereceda A, Verhagen JMA, Wessels M, Mohamed SA, Eriksson P, Mital S, Van Laer L, Loeys BL, Andelfinger G, McCallion AS, Dietz HC. Gould RA, et al. Among authors: woods ce. Nat Genet. 2019 Jan;51(1):42-50. doi: 10.1038/s41588-018-0265-y. Epub 2018 Nov 19. Nat Genet. 2019. PMID: 30455415 Free PMC article.
Autosomal recessive primary microcephaly due to ASPM mutations: An update.
Létard P, Drunat S, Vial Y, Duerinckx S, Ernault A, Amram D, Arpin S, Bertoli M, Busa T, Ceulemans B, Desir J, Doco-Fenzy M, Elalaoui SC, Devriendt K, Faivre L, Francannet C, Geneviève D, Gérard M, Gitiaux C, Julia S, Lebon S, Lubala T, Mathieu-Dramard M, Maurey H, Metreau J, Nasserereddine S, Nizon M, Pierquin G, Pouvreau N, Rivier-Ringenbach C, Rossi M, Schaefer E, Sefiani A, Sigaudy S, Sznajer Y, Tunca Y, Guilmin Crepon S, Alberti C, Elmaleh-Bergès M, Benzacken B, Wollnick B, Woods CG, Rauch A, Abramowicz M, El Ghouzzi V, Gressens P, Verloes A, Passemard S. Létard P, et al. Among authors: woods cg. Hum Mutat. 2018 Mar;39(3):319-332. doi: 10.1002/humu.23381. Epub 2018 Jan 16. Hum Mutat. 2018. PMID: 29243349
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