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Items: 1 to 20 of 61

1.

Common variants in the COL4A4 gene confer susceptibility to lattice degeneration of the retina.

Meguro A, Ideta H, Ota M, Ito N, Ideta R, Yonemoto J, Takeuchi M, Uemoto R, Nishide T, Iijima Y, Kawagoe T, Okada E, Shiota T, Hagihara Y, Oka A, Inoko H, Mizuki N.

PLoS One. 2012;7(6):e39300. doi: 10.1371/journal.pone.0039300. Epub 2012 Jun 19.

2.

Genetic linkage of snowflake vitreoretinal degeneration to chromosome 2q36.

Jiao X, Ritter R 3rd, Hejtmancik JF, Edwards AO.

Invest Ophthalmol Vis Sci. 2004 Dec;45(12):4498-503.

PMID:
15557460
3.

Evaluation of possible relationship between COL4A4 gene polymorphisms and risk of keratoconus.

Saravani R, Hasanian-Langroudi F, Validad MH, Yari D, Bahari G, Faramarzi M, Khateri M, Bahadoram S.

Cornea. 2015 Mar;34(3):318-22. doi: 10.1097/ICO.0000000000000356.

PMID:
25651396
4.

Analysis of six genetic risk factors highly associated with AMD in the region surrounding ARMS2 and HTRA1 on chromosome 10, region q26.

Hadley D, Orlin A, Brown G, Brucker AJ, Ho AC, Regillo CD, Donoso LA, Tian L, Kaderli B, Stambolian D.

Invest Ophthalmol Vis Sci. 2010 Apr;51(4):2191-6. doi: 10.1167/iovs.09-3798. Epub 2009 Nov 20.

PMID:
19933195
5.

Genetic association study of synphilin-1 in idiopathic Parkinson's disease.

Myhre R, Klungland H, Farrer MJ, Aasly JO.

BMC Med Genet. 2008 Mar 21;9:19. doi: 10.1186/1471-2350-9-19.

6.

Tumor necrosis factor-associated susceptibility to type 1 diabetes is caused by linkage disequilibrium with HLA-DR3 haplotypes.

Kumar N, Kaur G, Tandon N, Mehra N.

Hum Immunol. 2012 May;73(5):566-73. doi: 10.1016/j.humimm.2012.01.012. Epub 2012 Feb 9.

PMID:
22366579
7.

Genetics of Behçet disease inside and outside the MHC.

Meguro A, Inoko H, Ota M, Katsuyama Y, Oka A, Okada E, Yamakawa R, Yuasa T, Fujioka T, Ohno S, Bahram S, Mizuki N.

Ann Rheum Dis. 2010 Apr;69(4):747-54. doi: 10.1136/ard.2009.108571. Epub 2009 Aug 13.

PMID:
19684014
8.

Polymorphisms in COL4A3 and COL4A4 genes associated with keratoconus.

Stabuc-Silih M, Ravnik-Glavac M, Glavac D, Hawlina M, Strazisar M.

Mol Vis. 2009 Dec 20;15:2848-60.

9.

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
10.

A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma.

Osman W, Low SK, Takahashi A, Kubo M, Nakamura Y.

Hum Mol Genet. 2012 Jun 15;21(12):2836-42. doi: 10.1093/hmg/dds103. Epub 2012 Mar 13.

PMID:
22419738
11.

Characterization of the 10q26-orthologue in rhesus monkeys corroborates a functional connection between ARMS2 and HTRA1.

Pahl L, Spangenberg A, Schubert S, Schönmann U, Schmidtke J, Stuhrmann M.

Exp Eye Res. 2012 May;98:75-8. doi: 10.1016/j.exer.2012.03.007. Epub 2012 Mar 21.

PMID:
22465519
12.

Lattice degeneration of the retina and retinal detachment.

Semes LP.

Optom Clin. 1992;2(3):71-91. Review.

PMID:
1463916
13.

A meta-analysis of genome-wide association studies of follicular lymphoma.

Skibola CF, Conde L, Foo JN, Riby J, Humphreys K, Sillé FC, Darabi H, Sanchez S, Hjalgrim H, Liu J, Bracci PM, Smedby KE.

BMC Genomics. 2012 Oct 1;13:516. doi: 10.1186/1471-2164-13-516.

14.

Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibility.

Spencer KL, Olson LM, Schnetz-Boutaud N, Gallins P, Wang G, Scott WK, Agarwal A, Jakobsdottir J, Conley Y, Weeks DE, Gorin MB, Pericak-Vance MA, Haines JL.

Invest Ophthalmol Vis Sci. 2011 Mar 28;52(3):1748-54. doi: 10.1167/iovs.09-5112. Print 2011 Mar.

15.

Support for NRG1 as a susceptibility factor for schizophrenia in a northern Swedish isolated population.

Alaerts M, Ceulemans S, Forero D, Moens LN, De Zutter S, Heyrman L, Lenaerts AS, Norrback KF, De Rijk P, Nilsson LG, Goossens D, Adolfsson R, Del-Favero J.

Arch Gen Psychiatry. 2009 Aug;66(8):828-37. doi: 10.1001/archgenpsychiatry.2009.82.

PMID:
19652122
16.

Analyses of single nucleotide polymorphisms and haplotype linkage of LOC387715 and the HTRA1 gene in exudative age-related macular degeneration in a Chinese cohort.

Jiang H, Qu Y, Dang G, Zhang X, Yin N, Zhang Y, Bi H, Pan X, Xu X, Zhou F, Dai H.

Retina. 2009 Jul-Aug;29(7):974-9. doi: 10.1097/IAE.0b013e3181a3b90e.

PMID:
19491722
17.

Power of genome-wide linkage disequilibrium testing by using microsatellite markers.

Ohashi J, Tokunaga K.

J Hum Genet. 2003;48(9):487-91. Epub 2003 Aug 22.

PMID:
12938017
18.

Variants in the 17q21 asthma susceptibility locus are associated with allergic rhinitis in the Japanese population.

Tomita K, Sakashita M, Hirota T, Tanaka S, Masuyama K, Yamada T, Fujieda S, Miyatake A, Hizawa N, Kubo M, Nakamura Y, Tamari M.

Allergy. 2013 Jan;68(1):92-100. doi: 10.1111/all.12066. Epub 2012 Nov 12.

19.

PLEKHA1-LOC387715-HTRA1 polymorphisms and exudative age-related macular degeneration in the French population.

Leveziel N, Souied EH, Richard F, Barbu V, Zourdani A, Morineau G, Zerbib J, Coscas G, Soubrane G, Benlian P.

Mol Vis. 2007 Nov 26;13:2153-9.

PMID:
18079691
20.

Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.

Nakabayashi K, Tajima A, Yamamoto K, Takahashi A, Hata K, Takashima Y, Koyanagi M, Nakaoka H, Akamizu T, Ishikawa N, Kubota S, Maeda S, Tsunoda T, Kubo M, Kamatani N, Nakamura Y, Sasazuki T, Shirasawa S.

J Hum Genet. 2011 Nov;56(11):772-8. doi: 10.1038/jhg.2011.99. Epub 2011 Sep 8.

PMID:
21900946

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