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

Year Number of Results
1955 2
1956 5
1957 3
1958 1
1959 3
1960 9
1961 3
1962 3
1963 8
1964 6
1965 10
1966 5
1967 12
1968 9
1969 6
1970 8
1971 10
1972 6
1973 7
1974 11
1975 14
1976 9
1977 9
1978 9
1979 9
1980 5
1981 11
1982 12
1983 12
1984 20
1985 19
1986 7
1987 15
1988 6
1989 7
1990 7
1991 6
1992 7
1993 7
1994 9
1995 3
1996 10
1997 9
1998 6
1999 4
2000 4
2001 3
2002 5
2003 7
2004 10
2005 13
2006 19
2007 16
2008 14
2009 15
2010 23
2011 14
2012 18
2013 10
2014 30
2015 28
2016 29
2017 25
2018 27
2019 26
2020 33
2021 17
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Article type
Publication date

Search Results

696 results
Results by year
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Page 1
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: cohen asa. Nat Commun. 2018 Nov 5;9(1):4619. doi: 10.1038/s41467-018-06014-6. Nat Commun. 2018. PMID: 30397230 Free PMC article.
NSD1 mutations generate a genome-wide DNA methylation signature.
Choufani S, Cytrynbaum C, Chung BH, Turinsky AL, Grafodatskaya D, Chen YA, Cohen AS, Dupuis L, Butcher DT, Siu MT, Luk HM, Lo IF, Lam ST, Caluseriu O, Stavropoulos DJ, Reardon W, Mendoza-Londono R, Brudno M, Gibson WT, Chitayat D, Weksberg R. Choufani S, et al. Among authors: cohen as. Nat Commun. 2015 Dec 22;6:10207. doi: 10.1038/ncomms10207. Nat Commun. 2015. PMID: 26690673 Free PMC article.
Bone turnover, calcium homeostasis, and vitamin D status in Danish vegans.
Hansen TH, Madsen MTB, Jørgensen NR, Cohen AS, Hansen T, Vestergaard H, Pedersen O, Allin KH. Hansen TH, et al. Among authors: cohen as. Eur J Clin Nutr. 2018 Jul;72(7):1046-1054. doi: 10.1038/s41430-017-0081-y. Epub 2018 Jan 23. Eur J Clin Nutr. 2018. PMID: 29362456
The linker histone H1.0 generates epigenetic and functional intratumor heterogeneity.
Torres CM, Biran A, Burney MJ, Patel H, Henser-Brownhill T, Cohen AS, Li Y, Ben-Hamo R, Nye E, Spencer-Dene B, Chakravarty P, Efroni S, Matthews N, Misteli T, Meshorer E, Scaffidi P. Torres CM, et al. Among authors: cohen as. Science. 2016 Sep 30;353(6307):aaf1644. doi: 10.1126/science.aaf1644. Science. 2016. PMID: 27708074 Free PMC article.
DNA Methylation Signature for EZH2 Functionally Classifies Sequence Variants in Three PRC2 Complex Genes.
Choufani S, Gibson WT, Turinsky AL, Chung BHY, Wang T, Garg K, Vitriolo A, Cohen ASA, Cyrus S, Goodman S, Chater-Diehl E, Brzezinski J, Brudno M, Ming LH, White SM, Lynch SA, Clericuzio C, Temple IK, Flinter F, McConnell V, Cushing T, Bird LM, Splitt M, Kerr B, Scherer SW, Machado J, Imagawa E, Okamoto N, Matsumoto N, Testa G, Iascone M, Tenconi R, Caluseriu O, Mendoza-Londono R, Chitayat D, Cytrynbaum C, Tatton-Brown K, Weksberg R. Choufani S, et al. Among authors: cohen asa. Am J Hum Genet. 2020 May 7;106(5):596-610. doi: 10.1016/j.ajhg.2020.03.008. Epub 2020 Apr 2. Am J Hum Genet. 2020. PMID: 32243864 Free PMC article.
Review: history of the amyloid fibril.
Sipe JD, Cohen AS. Sipe JD, et al. Among authors: cohen as. J Struct Biol. 2000 Jun;130(2-3):88-98. doi: 10.1006/jsbi.2000.4221. J Struct Biol. 2000. PMID: 10940217 Review.
Amyloidosis.
Cohen AS, Jones LA. Cohen AS, et al. Curr Opin Rheumatol. 1991 Feb;3(1):125-38. doi: 10.1097/00002281-199102000-00018. Curr Opin Rheumatol. 1991. PMID: 2043438 Review.
Amyloidosis.
Cohen AS. Cohen AS. Bull Rheum Dis. 1991;40(2):1-12. Bull Rheum Dis. 1991. PMID: 2059761 Review. No abstract available.
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