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Items: 1 to 20 of 1201

1.

Identification of novel candidate loci for anorexia nervosa at 1q41 and 11q22 in Japanese by a genome-wide association analysis with microsatellite markers.

Nakabayashi K, Komaki G, Tajima A, Ando T, Ishikawa M, Nomoto J, Hata K, Oka A, Inoko H, Sasazuki T; Japanese Genetic Research Group for Eating Disorders (JGRED)., Shirasawa S.

J Hum Genet. 2009 Sep;54(9):531-7. doi: 10.1038/jhg.2009.74.

PMID:
19680270
2.

Candidate genes for anorexia nervosa in the 1p33-36 linkage region: serotonin 1D and delta opioid receptor loci exhibit significant association to anorexia nervosa.

Bergen AW, van den Bree MB, Yeager M, Welch R, Ganjei JK, Haque K, Bacanu S, Berrettini WH, Grice DE, Goldman D, Bulik CM, Klump K, Fichter M, Halmi K, Kaplan A, Strober M, Treasure J, Woodside B, Kaye WH.

Mol Psychiatry. 2003 Apr;8(4):397-406.

PMID:
12740597
3.

Linkage and association of schizophrenia with genetic variations in the locus of neuregulin 1 in Korean population.

Kim JW, Lee YS, Cho EY, Jang YL, Park DY, Choi KS, Jeun HO, Cho SH, Jang SY, Hong KS.

Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):281-6.

PMID:
16526041
4.

A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population.

Nakashima M, Chung S, Takahashi A, Kamatani N, Kawaguchi T, Tsunoda T, Hosono N, Kubo M, Nakamura Y, Zembutsu H.

Nat Genet. 2010 Sep;42(9):768-71. doi: 10.1038/ng.645.

PMID:
20711176
5.

A genome-wide association scan for asthma in a general Australian population.

Hui J, Oka A, James A, Palmer LJ, Musk AW, Beilby J, Inoko H.

Hum Genet. 2008 Apr;123(3):297-306. doi: 10.1007/s00439-008-0477-9.

PMID:
18253752
6.

Genomewide linkage and linkage disequilibrium analyses identify COL6A1, on chromosome 21, as the locus for ossification of the posterior longitudinal ligament of the spine.

Tanaka T, Ikari K, Furushima K, Okada A, Tanaka H, Furukawa K, Yoshida K, Ikeda T, Ikegawa S, Hunt SC, Takeda J, Toh S, Harata S, Nakajima T, Inoue I.

Am J Hum Genet. 2003 Oct;73(4):812-22.

7.

Role of STAT4 polymorphisms in systemic lupus erythematosus in a Japanese population: a case-control association study of the STAT1-STAT4 region.

Kawasaki A, Ito I, Hikami K, Ohashi J, Hayashi T, Goto D, Matsumoto I, Ito S, Tsutsumi A, Koga M, Arinami T, Graham RR, Hom G, Takasaki Y, Hashimoto H, Behrens TW, Sumida T, Tsuchiya N.

Arthritis Res Ther. 2008;10(5):R113. doi: 10.1186/ar2516.

8.

Fine mapping by genetic association implicates the chromosome 1q23.3 gene UHMK1, encoding a serine/threonine protein kinase, as a novel schizophrenia susceptibility gene.

Puri V, McQuillin A, Choudhury K, Datta S, Pimm J, Thirumalai S, Krasucki R, Lawrence J, Quested D, Bass N, Moorey H, Morgan J, Punukollu B, Kandasami G, Curtis D, Gurling H.

Biol Psychiatry. 2007 Apr 1;61(7):873-9.

PMID:
16978587
9.

A genome-wide scan maps a novel high myopia locus to 5p15.

Lam CY, Tam PO, Fan DS, Fan BJ, Wang DY, Lee CW, Pang CP, Lam DS.

Invest Ophthalmol Vis Sci. 2008 Sep;49(9):3768-78. doi: 10.1167/iovs.07-1126.

PMID:
18421076
10.

An autosome-wide scan for linkage disequilibrium-based association in sporadic breast cancer cases in eastern Finland: three candidate regions found.

Hartikainen JM, Tuhkanen H, Kataja V, Dunning AM, Antoniou A, Smith P, Arffman A, Pirskanen M, Easton DF, Eskelinen M, Uusitupa M, Kosma VM, Mannermaa A.

Cancer Epidemiol Biomarkers Prev. 2005 Jan;14(1):75-80.

11.

Association of CNR1 and FAAH endocannabinoid gene polymorphisms with anorexia nervosa and bulimia nervosa: evidence for synergistic effects.

Monteleone P, Bifulco M, Di Filippo C, Gazzerro P, Canestrelli B, Monteleone F, Proto MC, Di Genio M, Grimaldi C, Maj M.

Genes Brain Behav. 2009 Oct;8(7):728-32. doi: 10.1111/j.1601-183X.2009.00518.x.

12.

A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1.

Hmani-Aifa M, Ben Salem S, Benzina Z, Bouassida W, Messaoud R, Turki K, Khairallah M, Rebaï A, Fakhfekh F, Söderkvist P, Ayadi H.

Hum Genet. 2009 Oct;126(4):575-87. doi: 10.1007/s00439-009-0688-8.

PMID:
19526372
13.

Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

Tamiya G, Shinya M, Imanishi T, Ikuta T, Makino S, Okamoto K, Furugaki K, Matsumoto T, Mano S, Ando S, Nozaki Y, Yukawa W, Nakashige R, Yamaguchi D, Ishibashi H, Yonekura M, Nakami Y, Takayama S, Endo T, Saruwatari T, Yagura M, Yoshikawa Y, Fujimoto K, Oka A, Chiku S, Linsen SE, Giphart MJ, Kulski JK, Fukazawa T, Hashimoto H, Kimura M, Hoshina Y, Suzuki Y, Hotta T, Mochida J, Minezaki T, Komai K, Shiozawa S, Taniguchi A, Yamanaka H, Kamatani N, Gojobori T, Bahram S, Inoko H.

Hum Mol Genet. 2005 Aug 15;14(16):2305-21.

14.

Fine mapping and single nucleotide polymorphism association results of candidate genes for asthma and related phenotypes.

Immervoll T, Loesgen S, Dütsch G, Gohlke H, Herbon N, Klugbauer S, Dempfle A, Bickeböller H, Becker-Follmann J, Rüschendorf F, Saar K, Reis A, Wichmann HE, Wjst M.

Hum Mutat. 2001 Oct;18(4):327-36.

PMID:
11668616
16.

A genome-wide association screen identifies regions on chromosomes 1q25 and 7p21 as risk loci for sporadic prostate cancer.

Nam RK, Zhang WW, Loblaw DA, Klotz LH, Trachtenberg J, Jewett MA, Stanimirovic A, Davies TO, Toi A, Venkateswaran V, Sugar L, Siminovitch KA, Narod SA.

Prostate Cancer Prostatic Dis. 2008;11(3):241-6.

PMID:
17876339
17.

Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data.

Bahlo M, Stankovich J, Speed TP, Rubio JP, Burfoot RK, Foote SJ.

Hum Genet. 2006 Mar;119(1-2):38-50.

PMID:
16362347
18.

Population-based association study and contrasting linkage disequilibrium pattern reveal genetic association of SLC6A4 with autism in the Indian population from West Bengal.

Guhathakurta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Gangopadhyay PK, Usha R.

Brain Res. 2008 Nov 13;1240:12-21. doi: 10.1016/j.brainres.2008.08.063.

PMID:
18804097
19.

Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellites.

John S, Shephard N, Liu G, Zeggini E, Cao M, Chen W, Vasavda N, Mills T, Barton A, Hinks A, Eyre S, Jones KW, Ollier W, Silman A, Gibson N, Worthington J, Kennedy GC.

Am J Hum Genet. 2004 Jul;75(1):54-64.

20.

A genome-wide DNA microsatellite association screen to identify chromosomal regions harboring candidate genes in diabetic nephropathy.

McKnight AJ, Maxwell AP, Sawcer S, Compston A, Setakis E, Patterson CC, Brady HR, Savage DA.

J Am Soc Nephrol. 2006 Mar;17(3):831-6.

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