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Items: 1 to 20 of 98

1.

Genomewide association, Parkinson disease, and PARK10.

Farrer MJ, Haugarvoll K, Ross OA, Stone JT, Milkovic NM, Cobb SA, Whittle AJ, Lincoln SJ, Hulihan MM, Heckman MG, White LR, Aasly JO, Gibson JM, Gosal D, Lynch T, Wszolek ZK, Uitti RJ, Toft M.

Am J Hum Genet. 2006 Jun;78(6):1084-8; author reply 1092-4. No abstract available.

2.

PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease.

Beecham GW, Dickson DW, Scott WK, Martin ER, Schellenberg G, Nuytemans K, Larson EB, Buxbaum JD, Trojanowski JQ, Van Deerlin VM, Hurtig HI, Mash DC, Beach TG, Troncoso JC, Pletnikova O, Frosch MP, Ghetti B, Foroud TM, Honig LS, Marder K, Vonsattel JP, Goldman SM, Vinters HV, Ross OA, Wszolek ZK, Wang L, Dykxhoorn DM, Pericak-Vance MA, Montine TJ, Leverenz JB, Dawson TM, Vance JM.

Neurology. 2015 Mar 10;84(10):972-80. doi: 10.1212/WNL.0000000000001332. Epub 2015 Feb 6.

3.

A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.

Li Y, Rowland C, Schrodi S, Laird W, Tacey K, Ross D, Leong D, Catanese J, Sninsky J, Grupe A.

Am J Hum Genet. 2006 Jun;78(6):1090-2; author reply 1092-4. No abstract available.

4.

Fine-mapping and candidate gene investigation within the PARK10 locus.

Haugarvoll K, Toft M, Skipper L, Heckman MG, Crook JE, Soto A, Ross OA, Hulihan MM, Kachergus JM, Sando SB, White LR, Lynch T, Gibson JM, Uitti RJ, Wszolek ZK, Aasly JO, Farrer MJ.

Eur J Hum Genet. 2009 Mar;17(3):336-43. doi: 10.1038/ejhg.2008.187. Epub 2008 Oct 15.

5.

Genetics. Can SNPs deliver on susceptibility genes?

Gura T.

Science. 2001 Jul 27;293(5530):593-5. No abstract available.

PMID:
11474081
6.

Tumor necrosis factor-alpha promoter polymorphism is associated with the risk of Parkinson's disease.

Wu YR, Feng IH, Lyu RK, Chang KH, Lin YY, Chan H, Hu FJ, Lee-Chen GJ, Chen CM.

Am J Med Genet B Neuropsychiatr Genet. 2007 Apr 5;144B(3):300-4.

PMID:
17192953
7.

Genome studies: genetics by numbers.

Baker M.

Nature. 2008 Jan 31;451(7178):516-8. doi: 10.1038/451516a. No abstract available.

PMID:
18235474
8.

Positive association of the PDE4B (phosphodiesterase 4B) gene with schizophrenia in the Japanese population.

Numata S, Ueno S, Iga J, Song H, Nakataki M, Tayoshi S, Sumitani S, Tomotake M, Itakura M, Sano A, Ohmori T.

J Psychiatr Res. 2008 Nov;43(1):7-12. doi: 10.1016/j.jpsychires.2008.01.013. Epub 2008 Mar 10.

PMID:
18329668
9.

A quantitative trait locus for body fat on chromosome 1q43 in French Canadians: linkage and association studies.

Aissani B, Perusse L, Lapointe G, Chagnon YC, Bouchard L, Walts B, Bouchard C.

Obesity (Silver Spring). 2006 Sep;14(9):1605-15.

10.

High-resolution whole-genome association study of Parkinson disease.

Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, Pant PV, Frazer KA, Cox DR, Ballinger DG.

Am J Hum Genet. 2005 Nov;77(5):685-93. Epub 2005 Sep 9.

11.

Mapping a role for SNPs in drug development.

Rothberg BE.

Nat Biotechnol. 2001 Mar;19(3):209-11. No abstract available.

PMID:
11231544
12.

alpha-Synuclein and Parkinson disease susceptibility.

Winkler S, Hagenah J, Lincoln S, Heckman M, Haugarvoll K, Lohmann-Hedrich K, Kostic V, Farrer M, Klein C.

Neurology. 2007 Oct 30;69(18):1745-50. Epub 2007 Sep 13.

PMID:
17872362
13.

Genomewide linkage scan for nicotine dependence: identification of a chromosome 5 risk locus.

Gelernter J, Panhuysen C, Weiss R, Brady K, Poling J, Krauthammer M, Farrer L, Kranzler HR.

Biol Psychiatry. 2007 Jan 1;61(1):119-26. Epub 2006 Nov 1.

PMID:
17081504
14.

Evidence for gene x smoking exposure interactions in a genome-wide linkage screen of asthma and bronchial hyper-responsiveness in EGEA families.

Dizier MH, Bouzigon E, Guilloud-Bataille M, Siroux V, Lemainque A, Boland A, Lathrop M, Demenais F.

Eur J Hum Genet. 2007 Jul;15(7):810-5. Epub 2007 Apr 11.

15.

Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11q14-q22 and Xq23.

Everett KV, Chioza BA, Georgoula C, Reece A, Capon F, Parker KA, Cord-Udy C, McKeigue P, Mitton S, Pierro A, Puri P, Mitchison HM, Chung EM, Gardiner RM.

Am J Hum Genet. 2008 Mar;82(3):756-62. doi: 10.1016/j.ajhg.2007.12.023. Epub 2008 Feb 28.

16.

Genetics of pigment changes and geographic atrophy.

Thompson CL, Jun G, Klein BE, Klein R, Capriotti J, Lee KE, Iyengar SK.

Invest Ophthalmol Vis Sci. 2007 Jul;48(7):3005-13.

PMID:
17591865
17.

Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.

Holliday EG, McLean DE, Nyholt DR, Mowry BJ.

Arch Gen Psychiatry. 2009 Oct;66(10):1058-67. doi: 10.1001/archgenpsychiatry.2009.136.

PMID:
19805696
18.

Genetic linkage and association analysis of COPD-related traits on chromosome 8p.

Hersh CP, DeMeo DL, Raby BA, Litonjua AA, Sylvia JS, Sparrow D, Reilly JJ, Silverman EK.

COPD. 2006 Dec;3(4):189-94.

PMID:
17361499
19.

[Association of single nucleotide polymorphism rs599839 on chromosome 1p13.3 with premature coronary heart disease in a Chinese Han population].

Huang H, Pan L, Zhang L, Chen Y, Zeng Z.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Dec;25(6):686-9. Chinese.

PMID:
19065533
20.

Identification and replication of a novel obesity locus on chromosome 1q24 in isolated populations of Cilento.

Ciullo M, Nutile T, Dalmasso C, Sorice R, Bellenguez C, Colonna V, Persico MG, Bourgain C.

Diabetes. 2008 Mar;57(3):783-90. Epub 2007 Dec 27.

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