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

Year Number of Results
1964 2
1965 2
1966 25
1967 37
1968 31
1969 37
1970 40
1971 45
1972 54
1973 94
1974 138
1975 87
1976 84
1977 97
1978 112
1979 152
1980 151
1981 195
1982 206
1983 238
1984 270
1985 251
1986 251
1987 283
1988 270
1989 356
1990 724
1991 1285
1992 1715
1993 1037
1994 1230
1995 1199
1996 1312
1997 1503
1998 2518
1999 2376
2000 3544
2001 3478
2002 3006
2003 3143
2004 4596
2005 4440
2006 4263
2007 4536
2008 4823
2009 4756
2010 5395
2011 5891
2012 5615
2013 5884
2014 5855
2015 5702
2016 5630
2017 5202
2018 5238
2019 2748
2020 109
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102,484 results
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Page 1
Reliability of Whole-Exome Sequencing for Assessing Intratumor Genetic Heterogeneity.
Shi W, Ng CKY, Lim RS, Jiang T, Kumar S, Li X, Wali VB, Piscuoglio S, Gerstein MB, Chagpar AB, Weigelt B, Pusztai L, Reis-Filho JS, Hatzis C. Shi W, et al. Cell Rep. 2018 Nov 6;25(6):1446-1457. doi: 10.1016/j.celrep.2018.10.046. Cell Rep. 2018. PMID: 30404001 Free PMC article.
SvABA: genome-wide detection of structural variants and indels by local assembly.
Wala JA, Bandopadhayay P, Greenwald NF, O'Rourke R, Sharpe T, Stewart C, Schumacher S, Li Y, Weischenfeldt J, Yao X, Nusbaum C, Campbell P, Getz G, Meyerson M, Zhang CZ, Imielinski M, Beroukhim R. Wala JA, et al. Genome Res. 2018 Apr;28(4):581-591. doi: 10.1101/gr.221028.117. Epub 2018 Mar 13. Genome Res. 2018. PMID: 29535149 Free PMC article.
Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles.
Coban-Akdemir Z, White JJ, Song X, Jhangiani SN, Fatih JM, Gambin T, Bayram Y, Chinn IK, Karaca E, Punetha J, Poli C; Baylor-Hopkins Center for Mendelian Genomics, Boerwinkle E, Shaw CA, Orange JS, Gibbs RA, Lappalainen T, Lupski JR, Carvalho CMB. Coban-Akdemir Z, et al. Am J Hum Genet. 2018 Aug 2;103(2):171-187. doi: 10.1016/j.ajhg.2018.06.009. Epub 2018 Jul 19. Am J Hum Genet. 2018. PMID: 30032986 Free PMC article.
Authors' Reply.
Li MM, Datto M, Duncavage EJ, Kulkarni S, Lindeman NI, Roy S, Tsimberidou AM, Vnencak-Jones CL, Wolff DJ, Younes A, Nikiforova MN. Li MM, et al. J Mol Diagn. 2018 Jan;20(1):125-126. doi: 10.1016/j.jmoldx.2017.11.002. J Mol Diagn. 2018. PMID: 29249244 Free PMC article.
Technical laboratory standards for interpretation and reporting of acquired copy-number abnormalities and copy-neutral loss of heterozygosity in neoplastic disorders: a joint consensus recommendation from the American College of Medical Genetics and Genomics (ACMG) and the Cancer Genomics Consortium (CGC).
Mikhail FM, Biegel JA, Cooley LD, Dubuc AM, Hirsch B, Horner VL, Newman S, Shao L, Wolff DJ, Raca G. Mikhail FM, et al. Genet Med. 2019 Sep;21(9):1903-1916. doi: 10.1038/s41436-019-0545-7. Epub 2019 May 29. Genet Med. 2019. PMID: 31138931
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