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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2002 | 1 |
2003 | 1 |
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2012 | 2 |
2013 | 1 |
2016 | 1 |
2018 | 1 |
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7 results
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Page 1
Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease.
Sci Transl Med. 2018 Jan 10;10(423):eaai7795. doi: 10.1126/scitranslmed.aai7795.
Sci Transl Med. 2018.
PMID: 29321258
Free PMC article.
Identification of TMEM230 mutations in familial Parkinson's disease.
Deng HX, Shi Y, Yang Y, Ahmeti KB, Miller N, Huang C, Cheng L, Zhai H, Deng S, Nuytemans K, Corbett NJ, Kim MJ, Deng H, Tang B, Yang Z, Xu Y, Chan P, Huang B, Gao XP, Song Z, Liu Z, Fecto F, Siddique N, Foroud T, Jankovic J, Ghetti B, Nicholson DA, Krainc D, Melen O, Vance JM, Pericak-Vance MA, Ma YC, Rajput AH, Siddique T.
Deng HX, et al.
Nat Genet. 2016 Jul;48(7):733-9. doi: 10.1038/ng.3589. Epub 2016 Jun 6.
Nat Genet. 2016.
PMID: 27270108
Free PMC article.
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A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies.
Nalls MA, Duran R, Lopez G, Kurzawa-Akanbi M, McKeith IG, Chinnery PF, Morris CM, Theuns J, Crosiers D, Cras P, Engelborghs S, De Deyn PP, Van Broeckhoven C, Mann DM, Snowden J, Pickering-Brown S, Halliwell N, Davidson Y, Gibbons L, Harris J, Sheerin UM, Bras J, Hardy J, Clark L, Marder K, Honig LS, Berg D, Maetzler W, Brockmann K, Gasser T, Novellino F, Quattrone A, Annesi G, De Marco EV, Rogaeva E, Masellis M, Black SE, Bilbao JM, Foroud T, Ghetti B, Nichols WC, Pankratz N, Halliday G, Lesage S, Klebe S, Durr A, Duyckaerts C, Brice A, Giasson BI, Trojanowski JQ, Hurtig HI, Tayebi N, Landazabal C, Knight MA, Keller M, Singleton AB, Wolfsberg TG, Sidransky E.
Nalls MA, et al.
JAMA Neurol. 2013 Jun;70(6):727-35. doi: 10.1001/jamaneurol.2013.1925.
JAMA Neurol. 2013.
PMID: 23588557
Free PMC article.
Clinical Trial.
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Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation.
Dumitriu A, Latourelle JC, Hadzi TC, Pankratz N, Garza D, Miller JP, Vance JM, Foroud T, Beach TG, Myers RH.
Dumitriu A, et al.
PLoS Genet. 2012 Jun;8(6):e1002794. doi: 10.1371/journal.pgen.1002794. Epub 2012 Jun 28.
PLoS Genet. 2012.
PMID: 22761592
Free PMC article.
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Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
Pankratz N, Beecham GW, DeStefano AL, Dawson TM, Doheny KF, Factor SA, Hamza TH, Hung AY, Hyman BT, Ivinson AJ, Krainc D, Latourelle JC, Clark LN, Marder K, Martin ER, Mayeux R, Ross OA, Scherzer CR, Simon DK, Tanner C, Vance JM, Wszolek ZK, Zabetian CP, Myers RH, Payami H, Scott WK, Foroud T; PD GWAS Consortium.
Pankratz N, et al.
Ann Neurol. 2012 Mar;71(3):370-84. doi: 10.1002/ana.22687.
Ann Neurol. 2012.
PMID: 22451204
Free PMC article.
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A recommended scale for cognitive screening in clinical trials of Parkinson's disease.
Chou KL, Amick MM, Brandt J, Camicioli R, Frei K, Gitelman D, Goldman J, Growdon J, Hurtig HI, Levin B, Litvan I, Marsh L, Simuni T, Tröster AI, Uc EY; Parkinson Study Group Cognitive/Psychiatric Working Group.
Chou KL, et al.
Mov Disord. 2010 Nov 15;25(15):2501-7. doi: 10.1002/mds.23362.
Mov Disord. 2010.
PMID: 20878991
Free PMC article.
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Natural selection shaped regional mtDNA variation in humans.
Mishmar D, Ruiz-Pesini E, Golik P, Macaulay V, Clark AG, Hosseini S, Brandon M, Easley K, Chen E, Brown MD, Sukernik RI, Olckers A, Wallace DC.
Mishmar D, et al.
Proc Natl Acad Sci U S A. 2003 Jan 7;100(1):171-6. doi: 10.1073/pnas.0136972100. Epub 2002 Dec 30.
Proc Natl Acad Sci U S A. 2003.
PMID: 12509511
Free PMC article.
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