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Results by year

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

Year Number of Results
1945 1
1946 2
1947 2
1949 1
1950 3
1951 4
1952 3
1954 1
1955 3
1956 1
1958 3
1959 3
1960 2
1963 2
1964 1
1965 6
1966 1
1967 4
1968 4
1969 5
1970 5
1971 5
1972 3
1973 3
1974 4
1975 1
1976 7
1977 4
1978 3
1979 5
1980 3
1981 2
1982 2
1983 3
1984 3
1985 5
1986 4
1987 6
1988 6
1989 12
1990 11
1991 6
1992 8
1993 10
1994 7
1995 7
1996 8
1997 11
1998 10
1999 10
2000 7
2001 6
2002 3
2003 8
2004 4
2005 9
2006 9
2007 6
2008 5
2009 10
2010 8
2011 9
2012 9
2013 17
2014 11
2015 14
2016 16
2017 17
2018 11
2019 13
2020 16
2021 41
2022 26
2023 40
2024 17

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519 results

Results by year

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Page 1
A novel paradigm for observational learning in rats.
Rautio IV, Holmberg EH, Kurup D, Dunn BA, Whitlock JR. Rautio IV, et al. Among authors: whitlock jr. Cogn Neurodyn. 2024 Apr;18(2):757-767. doi: 10.1007/s11571-023-10022-8. Epub 2023 Nov 16. Cogn Neurodyn. 2024. PMID: 38699625 Free PMC article.
Access to innovative therapies in pediatric oncology: Report of the nationwide experience in Canada.
Judd S, Revon-Riviere G, Grover SA, Deyell RJ, Vanan MI, Lewis VA, Pecheux L, Zorzi AP, Goudie C, Santiago R, Tran TH, Abbott LS, Brossard J, Moorehead P, Alvi S, Portwine C, Denburg A, Whitlock JA, Cohen-Gogo S, Morgenstern DA. Judd S, et al. Among authors: whitlock ja. Cancer Med. 2024 Feb;13(3):e7033. doi: 10.1002/cam4.7033. Cancer Med. 2024. PMID: 38400668 Free PMC article.
De novo variants in DENND5B cause a neurodevelopmental disorder.
Scala M, Tomati V, Ferla M, Lena M, Cohen JS, Fatemi A, Brokamp E, Bican A, Phillips JA 3rd, Koziura ME, Nicouleau M, Rio M, Siquier K, Boddaert N, Musante I, Tamburro S, Baldassari S, Iacomino M, Scudieri P; Undiagnosed Diseases Network; Rosenfeld JA, Bellus G, Reed S, Al Saif H, Russo RS, Walsh MB, Cantagrel V, Crunk A, Gustincich S, Ruggiero SM, Fitzgerald MP, Helbig I, Striano P, Severino M, Salpietro V, Pedemonte N, Zara F. Scala M, et al. Am J Hum Genet. 2024 Mar 7;111(3):529-543. doi: 10.1016/j.ajhg.2024.02.001. Epub 2024 Feb 21. Am J Hum Genet. 2024. PMID: 38387458 Free PMC article.
RANKL inhibition reduces lesional cellularity and Gαs variant expression and enables osteogenic maturation in fibrous dysplasia.
de Castro LF, Whitlock JM, Michel Z, Pan K, Taylor J, Szymczuk V, Boyce B, Martin D, Kram V, Galisteo R, Melikov K, Chernomordik LV, Collins MT, Boyce AM. de Castro LF, et al. Among authors: whitlock jm. Bone Res. 2024 Feb 20;12(1):10. doi: 10.1038/s41413-023-00311-7. Bone Res. 2024. PMID: 38378678 Free PMC article. Clinical Trial.
Recurring homozygous ACTN2 variant (p.Arg506Gly) causes a recessive myopathy.
Donkervoort S, Mohassel P, O'Leary M, Bonner DE, Hartley T, Acquaye N, Brull A, Mozaffar T, Saporta MA, Dyment DA, Sampson JB, Pajusalu S, Austin-Tse C, Hurth K, Cohen JS, McWalter K, Warman-Chardon J, Crunk A, Foley AR; Undiagnosed Diseases Network; Mammen AL, Wheeler MT, O'Donnell-Luria A, Bönnemann CG. Donkervoort S, et al. Ann Clin Transl Neurol. 2024 Mar;11(3):629-640. doi: 10.1002/acn3.51983. Epub 2024 Feb 4. Ann Clin Transl Neurol. 2024. PMID: 38311799 Free PMC article.
519 results