Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1962 1
1963 1
1964 1
1965 1
1969 2
1970 1
1971 2
1972 2
1973 1
1975 1
1979 1
1980 1
1982 1
1983 2
1987 2
1989 3
1990 1
1991 1
1993 2
1994 3
1995 1
1997 3
1998 5
1999 2
2001 4
2002 5
2003 5
2004 4
2005 1
2007 1
2008 2
2009 1
2010 2
2011 1
2012 1
2013 5
2014 6
2015 4
2016 1
2017 2
2018 2
2019 6
2020 4
2021 0
Text availability
Article attribute
Article type
Publication date

Search Results

97 results
Results by year
Filters applied: . Clear all
Page 1
Somatic mutations in neurodegeneration: An update.
Proukakis C. Proukakis C. Neurobiol Dis. 2020 Oct;144:105021. doi: 10.1016/j.nbd.2020.105021. Epub 2020 Jul 24. Neurobiol Dis. 2020. PMID: 32712267 Free article. Review.
Genetic and phenotypic characterization of complex hereditary spastic paraplegia.
Kara E, Tucci A, Manzoni C, Lynch DS, Elpidorou M, Bettencourt C, Chelban V, Manole A, Hamed SA, Haridy NA, Federoff M, Preza E, Hughes D, Pittman A, Jaunmuktane Z, Brandner S, Xiromerisiou G, Wiethoff S, Schottlaender L, Proukakis C, Morris H, Warner T, Bhatia KP, Korlipara LV, Singleton AB, Hardy J, Wood NW, Lewis PA, Houlden H. Kara E, et al. Among authors: proukakis c. Brain. 2016 Jul;139(Pt 7):1904-18. doi: 10.1093/brain/aww111. Epub 2016 May 23. Brain. 2016. PMID: 27217339 Free PMC article.
Selective vulnerability in α-synucleinopathies.
Alegre-Abarrategui J, Brimblecombe KR, Roberts RF, Velentza-Almpani E, Tilley BS, Bengoa-Vergniory N, Proukakis C. Alegre-Abarrategui J, et al. Among authors: proukakis c. Acta Neuropathol. 2019 Nov;138(5):681-704. doi: 10.1007/s00401-019-02010-2. Epub 2019 Apr 20. Acta Neuropathol. 2019. PMID: 31006067 Free PMC article. Review.
Review: Somatic mutations in neurodegeneration.
Leija-Salazar M, Piette C, Proukakis C. Leija-Salazar M, et al. Among authors: proukakis c. Neuropathol Appl Neurobiol. 2018 Apr;44(3):267-285. doi: 10.1111/nan.12465. Epub 2018 Feb 28. Neuropathol Appl Neurobiol. 2018. PMID: 29369391 Review.
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: proukakis c. Neurol Genet. 2019 Feb 4;5(1):e307. doi: 10.1212/NXG.0000000000000307. eCollection 2019 Feb. Neurol Genet. 2019. PMID: 30842974 Free PMC article.
Complex mosaic structural variations in human fetal brains.
Sekar S, Tomasini L, Proukakis C, Bae T, Manlove L, Jang Y, Scuderi S, Zhou B, Kalyva M, Amiri A, Mariani J, Sedlazeck FJ, Urban AE, Vaccarino FM, Abyzov A. Sekar S, et al. Among authors: proukakis c. Genome Res. 2020 Dec;30(12):1695-1704. doi: 10.1101/gr.262667.120. Epub 2020 Oct 29. Genome Res. 2020. PMID: 33122304 Free PMC article.
Evolution and clustering of prodromal parkinsonian features in GBA1 carriers.
Mullin S, Beavan M, Bestwick J, McNeill A, Proukakis C, Cox T, Hughes D, Mehta A, Zetterberg H, Schapira AHV. Mullin S, et al. Among authors: proukakis c. Mov Disord. 2019 Sep;34(9):1365-1373. doi: 10.1002/mds.27775. Epub 2019 Jun 28. Mov Disord. 2019. PMID: 31251436 Free PMC article.
A crowdsourced set of curated structural variants for the human genome.
Chapman LM, Spies N, Pai P, Lim CS, Carroll A, Narzisi G, Watson CM, Proukakis C, Clarke WE, Nariai N, Dawson E, Jones G, Blankenberg D, Brueffer C, Xiao C, Kolora SRR, Alexander N, Wolujewicz P, Ahmed AE, Smith G, Shehreen S, Wenger AM, Salit M, Zook JM. Chapman LM, et al. Among authors: proukakis c. PLoS Comput Biol. 2020 Jun 19;16(6):e1007933. doi: 10.1371/journal.pcbi.1007933. eCollection 2020 Jun. PLoS Comput Biol. 2020. PMID: 32559231 Free PMC article.
97 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page