These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
264 related articles for article (PubMed ID: 30826882)
1. Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33. Musolf AM; Simpson CL; Alexander TA; Portas L; Murgia F; Ciner EB; Stambolian D; Bailey-Wilson JE Hum Genet; 2019 Apr; 138(4):339-354. PubMed ID: 30826882 [TBL] [Abstract][Full Text] [Related]
2. Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families. Simpson CL; Musolf AM; Li Q; Portas L; Murgia F; Cordero RY; Cordero JB; Moiz BA; Holzinger ER; Middlebrooks CD; Lewis DD; Bailey-Wilson JE; Stambolian D BMC Med Genet; 2019 Jan; 20(1):27. PubMed ID: 30704416 [TBL] [Abstract][Full Text] [Related]
3. Candidate high myopia loci on chromosomes 18p and 12q do not play a major role in susceptibility to common myopia. Ibay G; Doan B; Reider L; Dana D; Schlifka M; Hu H; Holmes T; O'Neill J; Owens R; Ciner E; Bailey-Wilson JE; Stambolian D BMC Med Genet; 2004 Aug; 5():20. PubMed ID: 15291966 [TBL] [Abstract][Full Text] [Related]
4. Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p. Musolf AM; Simpson CL; Moiz BA; Long KA; Portas L; Murgia F; Ciner EB; Stambolian D; Bailey-Wilson JE Invest Ophthalmol Vis Sci; 2017 Jul; 58(9):3547-3554. PubMed ID: 28715588 [TBL] [Abstract][Full Text] [Related]
5. Genome-wide scan for myopia in the Old Order Amish. Stambolian D; Ciner EB; Reider LC; Moy C; Dana D; Owens R; Schlifka M; Holmes T; Ibay G; Bailey-Wilson JE Am J Ophthalmol; 2005 Sep; 140(3):469-76. PubMed ID: 16084785 [TBL] [Abstract][Full Text] [Related]
6. Myopia in Chinese families shows linkage to 10q26.13. Musolf AM; Simpson CL; Long KA; Moiz BA; Lewis DD; Middlebrooks CD; Portas L; Murgia F; Ciner EB; Bailey-Wilson JE; Stambolian D Mol Vis; 2018; 24():29-42. PubMed ID: 29383007 [TBL] [Abstract][Full Text] [Related]
7. Rare variants and loci for age-related macular degeneration in the Ohio and Indiana Amish. Waksmunski AR; Igo RP; Song YE; Cooke Bailey JN; Laux R; Fuzzell D; Fuzzell S; Adams LD; Caywood L; Prough M; Stambolian D; Scott WK; Pericak-Vance MA; Haines JL Hum Genet; 2019 Oct; 138(10):1171-1182. PubMed ID: 31367973 [TBL] [Abstract][Full Text] [Related]
8. Myopia in African Americans Is Significantly Linked to Chromosome 7p15.2-14.2. Simpson CL; Musolf AM; Cordero RY; Cordero JB; Portas L; Murgia F; Lewis DD; Middlebrooks CD; Ciner EB; Bailey-Wilson JE; Stambolian D Invest Ophthalmol Vis Sci; 2021 Jul; 62(9):16. PubMed ID: 34241624 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. An international collaborative family-based whole genome quantitative trait linkage scan for myopic refractive error. Abbott D; Li YJ; Guggenheim JA; Metlapally R; Malecaze F; Calvas P; Rosenberg T; Paget S; Zayats T; Mackey DA; Feng S; Young TL Mol Vis; 2012; 18():720-9. PubMed ID: 22509102 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Identification of novel suggestive loci for high-grade myopia in Polish families. Rydzanicz M; Nath SK; Sun C; Podfigurna-Musielak M; Frajdenberg A; Mrugacz M; Winters D; Ratnamala U; Radhakrishna U; Bejjani BA; Gajecka M Mol Vis; 2011; 17():2028-39. PubMed ID: 21850178 [TBL] [Abstract][Full Text] [Related]
13. Linkage analysis of high myopia susceptibility locus in 26 families. Paget S; Julia S; Vitezica ZG; Soler V; Malecaze F; Calvas P Mol Vis; 2008; 14():2566-74. PubMed ID: 19122830 [TBL] [Abstract][Full Text] [Related]
14. Parkinson disease loci in the mid-western Amish. Davis MF; Cummings AC; D'Aoust LN; Jiang L; Velez Edwards DR; Laux R; Reinhart-Mercer L; Fuzzell D; Scott WK; Pericak-Vance MA; Lee SL; Haines JL Hum Genet; 2013 Nov; 132(11):1213-21. PubMed ID: 23793441 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Genome-wide linkage and haplotype sharing analysis implicates the MCDR3 locus as a candidate region for a developmental macular disorder in association with digit abnormalities. Cipriani V; Kalhoro A; Arno G; Silva RS; Pontikos N; Puech V; McClements ME; Hunt DM; van Heyningen V; Michaelides M; Webster AR; Moore AT; Puech B Ophthalmic Genet; 2017 Dec; 38(6):511-519. PubMed ID: 28635424 [TBL] [Abstract][Full Text] [Related]
18. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14. Ma DQ; Cuccaro ML; Jaworski JM; Haynes CS; Stephan DA; Parod J; Abramson RK; Wright HH; Gilbert JR; Haines JL; Pericak-Vance MA Mol Psychiatry; 2007 Apr; 12(4):376-84. PubMed ID: 17179998 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene. Cummings AC; Jiang L; Velez Edwards DR; McCauley JL; Laux R; McFarland LL; Fuzzell D; Knebusch C; Caywood L; Reinhart-Mercer L; Nations L; Gilbert JR; Konidari I; Tramontana M; Cuccaro ML; Scott WK; Pericak-Vance MA; Haines JL Ann Hum Genet; 2012 Sep; 76(5):342-51. PubMed ID: 22881374 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]