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Results: 1 to 20 of 134

1.

Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease.

Simón-Sánchez J, Kilarski LL, Nalls MA, Martinez M, Schulte C, Holmans P; International Parkinson's Disease Genomics Consortium; Wellcome Trust Case Control Consortium, Gasser T, Hardy J, Singleton AB, Wood NW, Brice A, Heutink P, Williams N, Morris HR.

PLoS One. 2012;7(3):e28787. doi: 10.1371/journal.pone.0028787. Epub 2012 Mar 12.

PMID:
22427796
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Evidence of recessive Alzheimer disease loci in a Caribbean Hispanic data set: genome-wide survey of runs of homozygosity.

Ghani M, Sato C, Lee JH, Reitz C, Moreno D, Mayeux R, St George-Hyslop P, Rogaeva E.

JAMA Neurol. 2013 Oct;70(10):1261-7. doi: 10.1001/jamaneurol.2013.3545.

PMID:
23978990
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

A genome-wide homozygosity association study identifies runs of homozygosity associated with rheumatoid arthritis in the human major histocompatibility complex.

Yang HC, Chang LC, Liang YJ, Lin CH, Wang PL.

PLoS One. 2012;7(4):e34840. doi: 10.1371/journal.pone.0034840. Epub 2012 Apr 20.

PMID:
22536334
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease.

Kilarski LL, Pearson JP, Newsway V, Majounie E, Knipe MD, Misbahuddin A, Chinnery PF, Burn DJ, Clarke CE, Marion MH, Lewthwaite AJ, Nicholl DJ, Wood NW, Morrison KE, Williams-Gray CH, Evans JR, Sawcer SJ, Barker RA, Wickremaratchi MM, Ben-Shlomo Y, Williams NM, Morris HR.

Mov Disord. 2012 Oct;27(12):1522-9. doi: 10.1002/mds.25132. Epub 2012 Sep 6. Review.

PMID:
22956510
[PubMed - indexed for MEDLINE]
5.

PINK1 mutations in sporadic early-onset Parkinson's disease.

Tan EK, Yew K, Chua E, Puvan K, Shen H, Lee E, Puong KY, Zhao Y, Pavanni R, Wong MC, Jamora D, de Silva D, Moe KT, Woon FP, Yuen Y, Tan L.

Mov Disord. 2006 Jun;21(6):789-93.

PMID:
16482571
[PubMed - indexed for MEDLINE]
6.

Regions of homozygosity and their impact on complex diseases and traits.

Ku CS, Naidoo N, Teo SM, Pawitan Y.

Hum Genet. 2011 Jan;129(1):1-15. doi: 10.1007/s00439-010-0920-6. Epub 2010 Nov 23. Review.

PMID:
21104274
[PubMed - indexed for MEDLINE]
7.

Colorectal cancer risk is not associated with increased levels of homozygosity in a population from the United Kingdom.

Spain SL, Cazier JB; CORGI Consortium,, Houlston R, Carvajal-Carmona L, Tomlinson I.

Cancer Res. 2009 Sep 15;69(18):7422-9. doi: 10.1158/0008-5472.CAN-09-0659. Epub 2009 Sep 1.

PMID:
19723657
[PubMed - indexed for MEDLINE]
Free Article
8.

Genomic patterns of homozygosity in worldwide human populations.

Pemberton TJ, Absher D, Feldman MW, Myers RM, Rosenberg NA, Li JZ.

Am J Hum Genet. 2012 Aug 10;91(2):275-92. doi: 10.1016/j.ajhg.2012.06.014.

PMID:
22883143
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Molecular genetic analysis of retinitis pigmentosa in Indonesia using genome-wide homozygosity mapping.

Siemiatkowska AM, Arimadyo K, Moruz LM, Astuti GD, de Castro-Miro M, Zonneveld MN, Strom TM, de Wijs IJ, Hoefsloot LH, Faradz SM, Cremers FP, den Hollander AI, Collin RW.

Mol Vis. 2011;17:3013-24. Epub 2011 Nov 18.

PMID:
22128245
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations.

Camargos ST, Dornas LO, Momeni P, Lees A, Hardy J, Singleton A, Cardoso F.

Mov Disord. 2009 Apr 15;24(5):662-6. doi: 10.1002/mds.22365.

PMID:
19205068
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Analysis of mutations and the association between polymorphisms in the cerebral dopamine neurotrophic factor (CDNF) gene and Parkinson disease.

Choi JM, Hong JH, Chae MJ, Ngyuen PH, Kang HS, Ma HI, Kim YJ.

Neurosci Lett. 2011 Apr 15;493(3):97-101. doi: 10.1016/j.neulet.2011.02.013. Epub 2011 Feb 12.

PMID:
21320571
[PubMed - indexed for MEDLINE]
12.

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.

Laaksovirta H, Peuralinna T, Schymick JC, Scholz SW, Lai SL, Myllykangas L, Sulkava R, Jansson L, Hernandez DG, Gibbs JR, Nalls MA, Heckerman D, Tienari PJ, Traynor BJ.

Lancet Neurol. 2010 Oct;9(10):978-85. doi: 10.1016/S1474-4422(10)70184-8.

PMID:
20801718
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Runs of homozygosity identify a recessive locus 12q21.31 for human adult height.

Yang TL, Guo Y, Zhang LS, Tian Q, Yan H, Papasian CJ, Recker RR, Deng HW.

J Clin Endocrinol Metab. 2010 Aug;95(8):3777-82. doi: 10.1210/jc.2009-1715. Epub 2010 May 13.

PMID:
20466785
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

PINK1 mutations in a Brazilian cohort of early-onset Parkinson's disease patients.

Godeiro-Junior C, de Carvalho-Aguiar PM, Felício AC, Barsottini OG, Silva SM, Borges V, Andrade LA, Ferraz HB.

Mov Disord. 2009 Aug 15;24(11):1693-6. doi: 10.1002/mds.22685.

PMID:
19562775
[PubMed - indexed for MEDLINE]
15.

Parkinson's disease genes do not segregate with breast cancer genes' loci.

Kravitz E, Laitman Y, Hassin-Baer S, Inzelberg R, Friedman E.

Cancer Epidemiol Biomarkers Prev. 2013 Aug;22(8):1464-72. doi: 10.1158/1055-9965.EPI-13-0472. Epub 2013 Jun 13.

PMID:
23765085
[PubMed - indexed for MEDLINE]
16.

GCH1 in early-onset Parkinson's disease.

Cobb SA, Wider C, Ross OA, Mata IF, Adler CH, Rajput A, Rajput AH, Wu RM, Hauser R, Josephs KA, Carr J, Gwinn K, Heckman MG, Aasly JO, Lynch T, Uitti RJ, Wszolek ZK, Kapatos G, Farrer MJ.

Mov Disord. 2009 Oct 30;24(14):2070-5. doi: 10.1002/mds.22729.

PMID:
19735094
[PubMed - indexed for MEDLINE]
17.

P268S in NOD2 associates with susceptibility to Parkinson's disease in Chinese population.

Ma Q, An X, Li Z, Zhang H, Huang W, Cai L, Hu P, Lin Q, Tzeng CM.

Behav Brain Funct. 2013 May 7;9:19. doi: 10.1186/1744-9081-9-19.

PMID:
23651603
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Runs of homozygosity in European populations.

McQuillan R, Leutenegger AL, Abdel-Rahman R, Franklin CS, Pericic M, Barac-Lauc L, Smolej-Narancic N, Janicijevic B, Polasek O, Tenesa A, Macleod AK, Farrington SM, Rudan P, Hayward C, Vitart V, Rudan I, Wild SH, Dunlop MG, Wright AF, Campbell H, Wilson JF.

Am J Hum Genet. 2008 Sep;83(3):359-72. doi: 10.1016/j.ajhg.2008.08.007. Epub 2008 Aug 28. Erratum in: Am J Hum Genet. 2008 Nov;83(5):658.

PMID:
18760389
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk.

Moskvina V, Harold D, Russo G, Vedernikov A, Sharma M, Saad M, Holmans P, Bras JM, Bettella F, Keller MF, Nicolaou N, Simón-Sánchez J, Gibbs JR, Schulte C, Durr A, Guerreiro R, Hernandez D, Brice A, Stefánsson H, Majamaa K, Gasser T, Heutink P, Wood N, Martinez M, Singleton AB, Nalls MA, Hardy J, Owen MJ, O'Donovan MC, Williams J, Morris HR, Williams NM; IPDGC and GERAD Investigators.

JAMA Neurol. 2013 Oct;70(10):1268-76.

PMID:
23921447
[PubMed - indexed for MEDLINE]
20.

Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia.

Lencz T, Lambert C, DeRosse P, Burdick KE, Morgan TV, Kane JM, Kucherlapati R, Malhotra AK.

Proc Natl Acad Sci U S A. 2007 Dec 11;104(50):19942-7. Epub 2007 Dec 5.

PMID:
18077426
[PubMed - indexed for MEDLINE]
Free PMC Article

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