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

Year Number of Results
2008 1
2009 2
2010 2
2011 2
2012 4
2013 3
2014 1
2015 3
2016 4
2017 1
2019 1
2022 0
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18 results
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Page 1
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature.
Rice GI, Kasher PR, Forte GM, Mannion NM, Greenwood SM, Szynkiewicz M, Dickerson JE, Bhaskar SS, Zampini M, Briggs TA, Jenkinson EM, Bacino CA, Battini R, Bertini E, Brogan PA, Brueton LA, Carpanelli M, De Laet C, de Lonlay P, del Toro M, Desguerre I, Fazzi E, Garcia-Cazorla A, Heiberg A, Kawaguchi M, Kumar R, Lin JP, Lourenco CM, Male AM, Marques W Jr, Mignot C, Olivieri I, Orcesi S, Prabhakar P, Rasmussen M, Robinson RA, Rozenberg F, Schmidt JL, Steindl K, Tan TY, van der Merwe WG, Vanderver A, Vassallo G, Wakeling EL, Wassmer E, Whittaker E, Livingston JH, Lebon P, Suzuki T, McLaughlin PJ, Keegan LP, O'Connell MA, Lovell SC, Crow YJ. Rice GI, et al. Among authors: dickerson je. Nat Genet. 2012 Nov;44(11):1243-8. doi: 10.1038/ng.2414. Epub 2012 Sep 23. Nat Genet. 2012. PMID: 23001123 Free PMC article.
Cataloguing the HIV type 1 human protein interaction network.
Ptak RG, Fu W, Sanders-Beer BE, Dickerson JE, Pinney JW, Robertson DL, Rozanov MN, Katz KS, Maglott DR, Pruitt KD, Dieffenbach CW. Ptak RG, et al. Among authors: dickerson je. AIDS Res Hum Retroviruses. 2008 Dec;24(12):1497-502. doi: 10.1089/aid.2008.0113. AIDS Res Hum Retroviruses. 2008. PMID: 19025396 Free PMC article. Review.
The genetic basis of DOORS syndrome: an exome-sequencing study.
Campeau PM, Kasperaviciute D, Lu JT, Burrage LC, Kim C, Hori M, Powell BR, Stewart F, Félix TM, van den Ende J, Wisniewska M, Kayserili H, Rump P, Nampoothiri S, Aftimos S, Mey A, Nair LD, Begleiter ML, De Bie I, Meenakshi G, Murray ML, Repetto GM, Golabi M, Blair E, Male A, Giuliano F, Kariminejad A, Newman WG, Bhaskar SS, Dickerson JE, Kerr B, Banka S, Giltay JC, Wieczorek D, Tostevin A, Wiszniewska J, Cheung SW, Hennekam RC, Gibbs RA, Lee BH, Sisodiya SM. Campeau PM, et al. Among authors: dickerson je. Lancet Neurol. 2014 Jan;13(1):44-58. doi: 10.1016/S1474-4422(13)70265-5. Epub 2013 Nov 29. Lancet Neurol. 2014. PMID: 24291220 Free PMC article.
LRIG2 mutations cause urofacial syndrome.
Stuart HM, Roberts NA, Burgu B, Daly SB, Urquhart JE, Bhaskar S, Dickerson JE, Mermerkaya M, Silay MS, Lewis MA, Olondriz MB, Gener B, Beetz C, Varga RE, Gülpınar O, Süer E, Soygür T, Ozçakar ZB, Yalçınkaya F, Kavaz A, Bulum B, Gücük A, Yue WW, Erdogan F, Berry A, Hanley NA, McKenzie EA, Hilton EN, Woolf AS, Newman WG. Stuart HM, et al. Among authors: dickerson je. Am J Hum Genet. 2013 Feb 7;92(2):259-64. doi: 10.1016/j.ajhg.2012.12.002. Epub 2013 Jan 11. Am J Hum Genet. 2013. PMID: 23313374 Free PMC article.
Should medical students be taught ultrasonography?
Dickerson JE, Paul KF, Vila P. Dickerson JE, et al. Med Teach. 2016;38(4):426-7. doi: 10.3109/0142159X.2015.1072269. Epub 2015 Aug 13. Med Teach. 2016. PMID: 26312446 No abstract available.
The role of junior doctors in medical education.
Boufersaoui A, Dickerson JE. Boufersaoui A, et al. Among authors: dickerson je. Med Teach. 2016;38(2):211. doi: 10.3109/0142159X.2015.1083963. Epub 2015 Oct 5. Med Teach. 2016. PMID: 26437252 No abstract available.
Publications and the foundation programme application.
Dickerson JE, Blundell JE. Dickerson JE, et al. Med Teach. 2016 May;38(5):531. doi: 10.3109/0142159X.2015.1078892. Epub 2015 Sep 15. Med Teach. 2016. PMID: 26371888 No abstract available.
On the origins of Mendelian disease genes in man: the impact of gene duplication.
Dickerson JE, Robertson DL. Dickerson JE, et al. Mol Biol Evol. 2012 Jan;29(1):61-9. doi: 10.1093/molbev/msr111. Epub 2011 Jun 24. Mol Biol Evol. 2012. PMID: 21705381 Free PMC article.
These relationships are similar for different disease types and the disease-associated gene's cellular function. This indicates that the emergence of duplication-associated diseases has been ongoing and approximately constant (relative to the retention of duplicate genes) …
These relationships are similar for different disease types and the disease-associated gene's cellular function. This indicates that …
18 results