205 related articles for article (PubMed ID: 29383007)
21. Haplotype analysis of the ARMS2/HTRA1 region in Japanese patients with typical neovascular age-related macular degeneration or polypoidal choroidal vasculopathy.
Gotoh N; Yamashiro K; Nakanishi H; Saito M; Iida T; Yoshimura N
Jpn J Ophthalmol; 2010 Nov; 54(6):609-14. PubMed ID: 21191724
[TBL] [Abstract][Full Text] [Related]
22. Linkage analysis of quantitative refraction and refractive errors in the Beaver Dam Eye Study.
Klein AP; Duggal P; Lee KE; Cheng CY; Klein R; Bailey-Wilson JE; Klein BE
Invest Ophthalmol Vis Sci; 2011 Jul; 52(8):5220-5. PubMed ID: 21571680
[TBL] [Abstract][Full Text] [Related]
23. Risk- and non-risk-associated variants at the 10q26 AMD locus influence ARMS2 mRNA expression but exclude pathogenic effects due to protein deficiency.
Friedrich U; Myers CA; Fritsche LG; Milenkovich A; Wolf A; Corbo JC; Weber BH
Hum Mol Genet; 2011 Apr; 20(7):1387-99. PubMed ID: 21252205
[TBL] [Abstract][Full Text] [Related]
24. Linkage analysis of the genetic loci for high myopia on 18p, 12q, and 17q in 51 U.K. families.
Farbrother JE; Kirov G; Owen MJ; Pong-Wong R; Haley CS; Guggenheim JA
Invest Ophthalmol Vis Sci; 2004 Sep; 45(9):2879-85. PubMed ID: 15326098
[TBL] [Abstract][Full Text] [Related]
25. Linkage Analysis of the Chromosome 5q31-33 Region Identifies JAKMIP2 as a Risk Factor for Graves' Disease in the Chinese Han Population.
Li J; Teng W; Yu Y; Hou X; Shan Z
Med Sci Monit; 2019 Feb; 25():1439-1451. PubMed ID: 30796769
[TBL] [Abstract][Full Text] [Related]
26. Age-related maculopathy: a genomewide scan with continued evidence of susceptibility loci within the 1q31, 10q26, and 17q25 regions.
Weeks DE; Conley YP; Tsai HJ; Mah TS; Schmidt S; Postel EA; Agarwal A; Haines JL; Pericak-Vance MA; Rosenfeld PJ; Paul TO; Eller AW; Morse LS; Dailey JP; Ferrell RE; Gorin MB
Am J Hum Genet; 2004 Aug; 75(2):174-89. PubMed ID: 15168325
[TBL] [Abstract][Full Text] [Related]
27. Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12.
Stambolian D; Ibay G; Reider L; Dana D; Moy C; Schlifka M; Holmes T; Ciner E; Bailey-Wilson JE
Am J Hum Genet; 2004 Sep; 75(3):448-59. PubMed ID: 15273935
[TBL] [Abstract][Full Text] [Related]
28. Dissecting the genetic heterogeneity of myopia susceptibility in an Ashkenazi Jewish population using ordered subset analysis.
Simpson CL; Wojciechowski R; Ibay G; Stambolian D; Bailey-Wilson JE
Mol Vis; 2011; 17():1641-51. PubMed ID: 21738393
[TBL] [Abstract][Full Text] [Related]
29. The 10q26 Risk Haplotype of Age-Related Macular Degeneration Aggravates Subretinal Inflammation by Impairing Monocyte Elimination.
Beguier F; Housset M; Roubeix C; Augustin S; Zagar Y; Nous C; Mathis T; Eandi C; Benchaboune M; Drame-Maigné A; Carpentier W; Chardonnet S; Touhami S; Blot G; Conart JB; Charles-Messance H; Potey A; Girmens JF; Paques M; Blond F; Leveillard T; Koertvely E; Roger JE; Sahel JA; Sapieha P; Delarasse C; Guillonneau X; Sennlaub F
Immunity; 2020 Aug; 53(2):429-441.e8. PubMed ID: 32814029
[TBL] [Abstract][Full Text] [Related]
30. TGIF1 is a potential candidate gene for high myopia in ethnic Kashmiri population.
Ahmed I; Rasool S; Jan T; Qureshi T; Naykoo NA; Andrabi KI
Curr Eye Res; 2014 Mar; 39(3):282-90. PubMed ID: 24215395
[TBL] [Abstract][Full Text] [Related]
31. Genomewide scan of ocular refraction in African-American families shows significant linkage to chromosome 7p15.
Ciner E; Wojciechowski R; Ibay G; Bailey-Wilson JE; Stambolian D
Genet Epidemiol; 2008 Jul; 32(5):454-63. PubMed ID: 18293391
[TBL] [Abstract][Full Text] [Related]
32. Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing.
Ratnamala U; Lyle R; Rawal R; Singh R; Vishnupriya S; Himabindu P; Rao V; Aggarwal S; Paluru P; Bartoloni L; Young TL; Paoloni-Giacobino A; Morris MA; Nath SK; Antonarakis SE; Radhakrishna U
Invest Ophthalmol Vis Sci; 2011 Aug; 52(9):6814-9. PubMed ID: 21357393
[TBL] [Abstract][Full Text] [Related]
33. Variants in the 10q26 gene cluster (LOC387715 and HTRA1) exhibit enhanced risk of age-related macular degeneration along with CFH in Indian patients.
Kaur I; Katta S; Hussain A; Hussain N; Mathai A; Narayanan R; Hussain A; Reddy RK; Majji AB; Das T; Chakrabarti S
Invest Ophthalmol Vis Sci; 2008 May; 49(5):1771-6. PubMed ID: 18436811
[TBL] [Abstract][Full Text] [Related]
34. [A genome-wide screening for pathological myopia suggests a novel locus on chromosome 15q12 - 13].
Yu ZQ; Li YB; Huang CX; Chu RY; Hu DN; Shen ZH; Huang W
Zhonghua Yan Ke Za Zhi; 2007 Mar; 43(3):233-8. PubMed ID: 17605906
[TBL] [Abstract][Full Text] [Related]
35. Genomewide linkage scans for ocular refraction and meta-analysis of four populations in the Myopia Family Study.
Wojciechowski R; Stambolian D; Ciner E; Ibay G; Holmes TN; Bailey-Wilson JE
Invest Ophthalmol Vis Sci; 2009 May; 50(5):2024-32. PubMed ID: 19151385
[TBL] [Abstract][Full Text] [Related]
36. An international collaborative family-based whole-genome linkage scan for high-grade myopia.
Li YJ; Guggenheim JA; Bulusu A; Metlapally R; Abbott D; Malecaze F; Calvas P; Rosenberg T; Paget S; Creer RC; Kirov G; Owen MJ; Zhao B; White T; Mackey DA; Young TL
Invest Ophthalmol Vis Sci; 2009 Jul; 50(7):3116-27. PubMed ID: 19324860
[TBL] [Abstract][Full Text] [Related]
37. Familial high myopia linkage to chromosome 18p.
Lam DS; Tam PO; Fan DS; Baum L; Leung YF; Pang CP
Ophthalmologica; 2003; 217(2):115-8. PubMed ID: 12592049
[TBL] [Abstract][Full Text] [Related]
38. A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612.
Zhang Q; Guo X; Xiao X; Jia X; Li S; Hejtmancik JF
Mol Vis; 2005 Jul; 11():554-60. PubMed ID: 16052171
[TBL] [Abstract][Full Text] [Related]
39. Replication study of significant single nucleotide polymorphisms associated with myopia from two genome-wide association studies.
Wang Q; Gao Y; Wang P; Li S; Jia X; Xiao X; Guo X; Zhang Q
Mol Vis; 2011; 17():3290-9. PubMed ID: 22194655
[TBL] [Abstract][Full Text] [Related]
40. Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family.
Zhang Q; Guo X; Xiao X; Yi J; Jia X; Hejtmancik JF
Mol Vis; 2004 Nov; 10():890-900. PubMed ID: 15570218
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
