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

Year Number of Results
1973 1
1975 1
1976 2
1977 1
1981 2
1983 1
1985 2
1987 5
1988 4
1989 4
1990 6
1991 6
1992 5
1993 5
1994 8
1995 8
1996 3
1997 4
1998 11
1999 6
2000 6
2001 11
2002 10
2003 7
2004 8
2005 19
2006 13
2007 21
2008 32
2009 38
2010 45
2011 36
2012 35
2013 29
2014 24
2015 21
2016 18
2017 18
2018 19
2019 22
2020 26
2021 16
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493 results
Results by year
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Page 1
Smell and taste symptom-based predictive model for COVID-19 diagnosis.
Roland LT, Gurrola JG 2nd, Loftus PA, Cheung SW, Chang JL. Roland LT, et al. Among authors: cheung sw. Int Forum Allergy Rhinol. 2020 Jul;10(7):832-838. doi: 10.1002/alr.22602. Epub 2020 Jun 7. Int Forum Allergy Rhinol. 2020. PMID: 32363809 Free PMC article.
Phenotypic manifestations of copy number variation in chromosome 16p13.11.
Nagamani SC, Erez A, Bader P, Lalani SR, Scott DA, Scaglia F, Plon SE, Tsai CH, Reimschisel T, Roeder E, Malphrus AD, Eng PA, Hixson PM, Kang SH, Stankiewicz P, Patel A, Cheung SW. Nagamani SC, et al. Among authors: cheung sw. Eur J Hum Genet. 2011 Mar;19(3):280-6. doi: 10.1038/ejhg.2010.184. Epub 2010 Dec 8. Eur J Hum Genet. 2011. PMID: 21150890 Free PMC article.
A Dynamic Protein Interaction Landscape of the Human Centrosome-Cilium Interface.
Gupta GD, Coyaud É, Gonçalves J, Mojarad BA, Liu Y, Wu Q, Gheiratmand L, Comartin D, Tkach JM, Cheung SW, Bashkurov M, Hasegan M, Knight JD, Lin ZY, Schueler M, Hildebrandt F, Moffat J, Gingras AC, Raught B, Pelletier L. Gupta GD, et al. Among authors: cheung sw. Cell. 2015 Dec 3;163(6):1484-99. doi: 10.1016/j.cell.2015.10.065. Cell. 2015. PMID: 26638075 Free PMC article.
Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage.
Dong Z, Yan J, Xu F, Yuan J, Jiang H, Wang H, Chen H, Zhang L, Ye L, Xu J, Shi Y, Yang Z, Cao Y, Chen L, Li Q, Zhao X, Li J, Chen A, Zhang W, Wong HG, Qin Y, Zhao H, Chen Y, Li P, Ma T, Wang WJ, Kwok YK, Jiang Y, Pursley AN, Chung JPW, Hong Y, Kristiansen K, Yang H, Piña-Aguilar RE, Leung TY, Cheung SW, Morton CC, Choy KW, Chen ZJ. Dong Z, et al. Among authors: cheung sw. Am J Hum Genet. 2019 Dec 5;105(6):1102-1111. doi: 10.1016/j.ajhg.2019.10.003. Epub 2019 Oct 31. Am J Hum Genet. 2019. PMID: 31679651 Free PMC article.
Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies.
Yuan B, Neira J, Pehlivan D, Santiago-Sim T, Song X, Rosenfeld J, Posey JE, Patel V, Jin W, Adam MP, Baple EL, Dean J, Fong CT, Hickey SE, Hudgins L, Leon E, Madan-Khetarpal S, Rawlins L, Rustad CF, Stray-Pedersen A, Tveten K, Wenger O, Diaz J, Jenkins L, Martin L, McGuire M, Pietryga M, Ramsdell L, Slattery L; DDD Study, Abid F, Bertuch AA, Grange D, Immken L, Schaaf CP, Van Esch H, Bi W, Cheung SW, Breman AM, Smith JL, Shaw C, Crosby AH, Eng C, Yang Y, Lupski JR, Xiao R, Liu P. Yuan B, et al. Among authors: cheung sw. Genet Med. 2019 Mar;21(3):663-675. doi: 10.1038/s41436-018-0085-6. Epub 2018 Aug 30. Genet Med. 2019. PMID: 30158690 Free PMC article.
Hep G2 is a hepatoblastoma-derived cell line.
López-Terrada D, Cheung SW, Finegold MJ, Knowles BB. López-Terrada D, et al. Among authors: cheung sw. Hum Pathol. 2009 Oct;40(10):1512-5. doi: 10.1016/j.humpath.2009.07.003. Hum Pathol. 2009. PMID: 19751877 No abstract available.
493 results
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