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

Year Number of Results
1946 2
1950 1
1951 1
1968 1
1972 1
1973 1
1974 1
1975 1
1980 2
1983 2
1986 2
1989 2
1990 4
1992 3
1993 1
1994 1
1995 1
1996 3
1997 2
1998 1
1999 2
2000 3
2001 2
2002 5
2004 2
2005 2
2007 2
2008 4
2009 2
2010 1
2011 4
2012 2
2013 5
2014 6
2015 4
2016 7
2017 10
2018 9
2019 11
2020 10
2021 3
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Article type
Publication date

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118 results
Results by year
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Page 1
Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease.
Flanagan SE, Haapaniemi E, Russell MA, Caswell R, Allen HL, De Franco E, McDonald TJ, Rajala H, Ramelius A, Barton J, Heiskanen K, Heiskanen-Kosma T, Kajosaari M, Murphy NP, Milenkovic T, Seppänen M, Lernmark Å, Mustjoki S, Otonkoski T, Kere J, Morgan NG, Ellard S, Hattersley AT. Flanagan SE, et al. Among authors: caswell r. Nat Genet. 2014 Aug;46(8):812-814. doi: 10.1038/ng.3040. Epub 2014 Jul 20. Nat Genet. 2014. PMID: 25038750 Free PMC article.
Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability.
Hamilton MJ, Caswell RC, Canham N, Cole T, Firth HV, Foulds N, Heimdal K, Hobson E, Houge G, Joss S, Kumar D, Lampe AK, Maystadt I, McKay V, Metcalfe K, Newbury-Ecob R, Park SM, Robert L, Rustad CF, Wakeling E, Wilkie AOM, Study TDDD, Twigg SRF, Suri M. Hamilton MJ, et al. Among authors: caswell rc. J Med Genet. 2018 Jan;55(1):28-38. doi: 10.1136/jmedgenet-2017-104620. Epub 2017 Oct 11. J Med Genet. 2018. PMID: 29021403 Free PMC article.
Mitochondrial Retinopathy.
Birtel J, von Landenberg C, Gliem M, Gliem C, Reimann J, Kunz WS, Herrmann P, Betz C, Caswell R, Nesbitt V, Kornblum C, Issa PC. Birtel J, et al. Among authors: caswell r. Ophthalmol Retina. 2021 Jul 10:S2468-6530(21)00071-3. doi: 10.1016/j.oret.2021.02.017. Online ahead of print. Ophthalmol Retina. 2021. PMID: 34257060
Preface.
Caswell RS, Deluca PM, Seltzer SM, Wambersie A. Caswell RS, et al. J ICRU. 2004 Dec;4(2):9. doi: 10.1093/jicru/ndh021. J ICRU. 2004. PMID: 24170824 No abstract available.
Copy number variation of LINGO1 in familial dystonic tremor.
Alakbarzade V, Iype T, Chioza BA, Singh R, Harlalka GV, Hardy H, Sreekantan-Nair A, Proukakis C, Peall K, Clark LN, Caswell R, Lango Allen H, Wakeling M, Chilton JK, Baple EL, Louis ED, Warner TT, Crosby AH. Alakbarzade V, et al. Among authors: caswell r. Neurol Genet. 2019 Feb 4;5(1):e307. doi: 10.1212/NXG.0000000000000307. eCollection 2019 Feb. Neurol Genet. 2019. PMID: 30842974 Free PMC article.
118 results
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