Full text
PDF





Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Apfelstedt-Sylla E., Theischen M., Rüther K., Wedemann H., Gal A., Zrenner E. Extensive intrafamilial and interfamilial phenotypic variation among patients with autosomal dominant retinal dystrophy and mutations in the human RDS/peripherin gene. Br J Ophthalmol. 1995 Jan;79(1):28–34. doi: 10.1136/bjo.79.1.28. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bird A. C. Doyne Lecture. Pathogenesis of retinal pigment epithelial detachment in the elderly; the relevance of Bruch's membrane change. Eye (Lond) 1991;5(Pt 1):1–12. doi: 10.1038/eye.1991.2. [DOI] [PubMed] [Google Scholar]
- Bird A. C. Retinal photoreceptor dystrophies LI. Edward Jackson Memorial Lecture. Am J Ophthalmol. 1995 May;119(5):543–562. doi: 10.1016/s0002-9394(14)70212-0. [DOI] [PubMed] [Google Scholar]
- Bodington M. J., Muzulu S. I., Burden A. C. Spatial clustering in childhood diabetes: evidence of an environmental cause. Diabet Med. 1995 Oct;12(10):865–867. doi: 10.1111/j.1464-5491.1995.tb00387.x. [DOI] [PubMed] [Google Scholar]
- Chew E. Y. Nutritional supplement use and age-related macular degeneration. Curr Opin Ophthalmol. 1995 Jun;6(3):19–24. doi: 10.1097/00055735-199506000-00004. [DOI] [PubMed] [Google Scholar]
- Chowdhury T. A., Kumar S., Barnett A. H., Bain S. C. Nephropathy in type 1 diabetes: the role of genetic factors. Diabet Med. 1995 Dec;12(12):1059–1067. doi: 10.1111/j.1464-5491.1995.tb00422.x. [DOI] [PubMed] [Google Scholar]
- Cordell H. J., Todd J. A., Bennett S. T., Kawaguchi Y., Farrall M. Two-locus maximum lod score analysis of a multifactorial trait: joint consideration of IDDM2 and IDDM4 with IDDM1 in type 1 diabetes. Am J Hum Genet. 1995 Oct;57(4):920–934. [PMC free article] [PubMed] [Google Scholar]
- Cordell H. J., Todd J. A. Multifactorial inheritance in type 1 diabetes. Trends Genet. 1995 Dec;11(12):499–504. doi: 10.1016/s0168-9525(00)89160-x. [DOI] [PubMed] [Google Scholar]
- Cotton R. G. Current methods of mutation detection. Mutat Res. 1993 Jan;285(1):125–144. doi: 10.1016/0027-5107(93)90060-s. [DOI] [PubMed] [Google Scholar]
- Cotton R. G., Rodrigues N. R., Campbell R. D. Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations. Proc Natl Acad Sci U S A. 1988 Jun;85(12):4397–4401. doi: 10.1073/pnas.85.12.4397. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Davies J. L., Kawaguchi Y., Bennett S. T., Copeman J. B., Cordell H. J., Pritchard L. E., Reed P. W., Gough S. C., Jenkins S. C., Palmer S. M. A genome-wide search for human type 1 diabetes susceptibility genes. Nature. 1994 Sep 8;371(6493):130–136. doi: 10.1038/371130a0. [DOI] [PubMed] [Google Scholar]
- Davis A., Cowell J. K. Mutations in the PAX6 gene in patients with hereditary aniridia. Hum Mol Genet. 1993 Dec;2(12):2093–2097. doi: 10.1093/hmg/2.12.2093. [DOI] [PubMed] [Google Scholar]
- Devlin B., Risch N. A comparison of linkage disequilibrium measures for fine-scale mapping. Genomics. 1995 Sep 20;29(2):311–322. doi: 10.1006/geno.1995.9003. [DOI] [PubMed] [Google Scholar]
- Dizier M. H., Babron M. C., Clerget-Darpoux F. Interactive effect of two candidate genes in a disease: extension of the marker-association-segregation chi(2) method. Am J Hum Genet. 1994 Nov;55(5):1042–1049. [PMC free article] [PubMed] [Google Scholar]
- Dosso A. A., Bovet J. Monozygotic twin brothers with age-related macular degeneration. Ophthalmologica. 1992;205(1):24–28. doi: 10.1159/000310307. [DOI] [PubMed] [Google Scholar]
- Drance S. M., Schulzer M., Thomas B., Douglas G. R. Multivariate analysis in glaucoma. Use of discriminant analysis in predicting glaucomatous visual field damage. Arch Ophthalmol. 1981 Jun;99(6):1019–1022. doi: 10.1001/archopht.1981.03930011019007. [DOI] [PubMed] [Google Scholar]
- Evans J., Wormald R. Is the incidence of registrable age-related macular degeneration increasing? Br J Ophthalmol. 1996 Jan;80(1):9–14. doi: 10.1136/bjo.80.1.9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- François J. Genetics and primary open-angle glaucoma. Am J Ophthalmol. 1966 Apr;61(4):652–665. doi: 10.1016/0002-9394(66)91201-3. [DOI] [PubMed] [Google Scholar]
- Gauguier D., Froguel P., Parent V., Bernard C., Bihoreau M. T., Portha B., James M. R., Penicaud L., Lathrop M., Ktorza A. Chromosomal mapping of genetic loci associated with non-insulin dependent diabetes in the GK rat. Nat Genet. 1996 Jan;12(1):38–43. doi: 10.1038/ng0196-38. [DOI] [PubMed] [Google Scholar]
- Genĉk A. Epidemiology and genetics of primary congenital glaucoma in Slovakia. Description of a form of primary congenital glaucoma in gypsies with autosomal-recessive inheritance and complete penetrance. Dev Ophthalmol. 1989;16:76–115. [PubMed] [Google Scholar]
- Gerbitz K. D., Gempel K., Brdiczka D. Mitochondria and diabetes. Genetic, biochemical, and clinical implications of the cellular energy circuit. Diabetes. 1996 Feb;45(2):113–126. doi: 10.2337/diab.45.2.113. [DOI] [PubMed] [Google Scholar]
- Ghosh S. Probability and complex disease genes. Nat Genet. 1995 Mar;9(3):223–224. doi: 10.1038/ng0395-223. [DOI] [PubMed] [Google Scholar]
- Hager J., Hansen L., Vaisse C., Vionnet N., Philippi A., Poller W., Velho G., Carcassi C., Contu L., Julier C. A missense mutation in the glucagon receptor gene is associated with non-insulin-dependent diabetes mellitus. Nat Genet. 1995 Mar;9(3):299–304. doi: 10.1038/ng0395-299. [DOI] [PubMed] [Google Scholar]
- Heiba I. M., Elston R. C., Klein B. E., Klein R. Sibling correlations and segregation analysis of age-related maculopathy: the Beaver Dam Eye Study. Genet Epidemiol. 1994;11(1):51–67. doi: 10.1002/gepi.1370110106. [DOI] [PubMed] [Google Scholar]
- Holmans P. Asymptotic properties of affected-sib-pair linkage analysis. Am J Hum Genet. 1993 Feb;52(2):362–374. [PMC free article] [PubMed] [Google Scholar]
- Holz F. G., Piguet B., Minassian D. C., Bird A. C., Weale R. A. Decreasing stromal iris pigmentation as a risk factor for age-related macular degeneration. Am J Ophthalmol. 1994 Jan 15;117(1):19–23. doi: 10.1016/s0002-9394(14)73010-7. [DOI] [PubMed] [Google Scholar]
- Hyman L. G., Lilienfeld A. M., Ferris F. L., 3rd, Fine S. L. Senile macular degeneration: a case-control study. Am J Epidemiol. 1983 Aug;118(2):213–227. doi: 10.1093/oxfordjournals.aje.a113629. [DOI] [PubMed] [Google Scholar]
- Hästbacka J., de la Chapelle A., Mahtani M. M., Clines G., Reeve-Daly M. P., Daly M., Hamilton B. A., Kusumi K., Trivedi B., Weaver A. The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping. Cell. 1994 Sep 23;78(6):1073–1087. doi: 10.1016/0092-8674(94)90281-x. [DOI] [PubMed] [Google Scholar]
- Héon E., Piguet B., Munier F., Sneed S. R., Morgan C. M., Forni S., Pescia G., Schorderet D., Taylor C. M., Streb L. M. Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21. Arch Ophthalmol. 1996 Feb;114(2):193–198. doi: 10.1001/archopht.1996.01100130187014. [DOI] [PubMed] [Google Scholar]
- Johnson A. T., Drack A. V., Kwitek A. E., Cannon R. L., Stone E. M., Alward W. L. Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucoma. Ophthalmology. 1993 Apr;100(4):524–529. doi: 10.1016/s0161-6420(13)31615-7. [DOI] [PubMed] [Google Scholar]
- Kahn H. A., Leibowitz H. M., Ganley J. P., Kini M. M., Colton T., Nickerson R. S., Dawber T. R. The Framingham Eye Study. II. Association of ophthalmic pathology with single variables previously measured in the Framingham Heart Study. Am J Epidemiol. 1977 Jul;106(1):33–41. doi: 10.1093/oxfordjournals.aje.a112429. [DOI] [PubMed] [Google Scholar]
- Kaprio J., Tuomilehto J., Koskenvuo M., Romanov K., Reunanen A., Eriksson J., Stengård J., Kesäniemi Y. A. Concordance for type 1 (insulin-dependent) and type 2 (non-insulin-dependent) diabetes mellitus in a population-based cohort of twins in Finland. Diabetologia. 1992 Nov;35(11):1060–1067. doi: 10.1007/BF02221682. [DOI] [PubMed] [Google Scholar]
- Keen T. J., Inglehearn C. F., Green E. D., Cunningham A. F., Patel R. J., Peacock R. E., Gerken S., White R., Weissenbach J., Bhattacharya S. S. A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7p. Genomics. 1995 Aug 10;28(3):383–388. doi: 10.1006/geno.1995.1165. [DOI] [PubMed] [Google Scholar]
- Keen T. J., Inglehearn C. F., Kim R., Bird A. C., Bhattacharya S. Retinal pattern dystrophy associated with a 4 bp insertion at codon 140 in the RDS-peripherin gene. Hum Mol Genet. 1994 Feb;3(2):367–368. doi: 10.1093/hmg/3.2.367. [DOI] [PubMed] [Google Scholar]
- Kennedy G. C., German M. S., Rutter W. J. The minisatellite in the diabetes susceptibility locus IDDM2 regulates insulin transcription. Nat Genet. 1995 Mar;9(3):293–298. doi: 10.1038/ng0395-293. [DOI] [PubMed] [Google Scholar]
- Kerem B., Rommens J. M., Buchanan J. A., Markiewicz D., Cox T. K., Chakravarti A., Buchwald M., Tsui L. C. Identification of the cystic fibrosis gene: genetic analysis. Science. 1989 Sep 8;245(4922):1073–1080. doi: 10.1126/science.2570460. [DOI] [PubMed] [Google Scholar]
- Kitsos G., Cote G., Psilas K. Un exemple d'hérédité dominante our la transmission du glaucome primitif à angle ouvert dans une région du nord-ouest de la Grèce. J Fr Ophtalmol. 1988;11(12):859–864. [PubMed] [Google Scholar]
- Klein M. L., Mauldin W. M., Stoumbos V. D. Heredity and age-related macular degeneration. Observations in monozygotic twins. Arch Ophthalmol. 1994 Jul;112(7):932–937. doi: 10.1001/archopht.1994.01090190080025. [DOI] [PubMed] [Google Scholar]
- Klein R., Klein B. E., Linton K. L., DeMets D. L. The Beaver Dam Eye Study: the relation of age-related maculopathy to smoking. Am J Epidemiol. 1993 Jan 15;137(2):190–200. doi: 10.1093/oxfordjournals.aje.a116659. [DOI] [PubMed] [Google Scholar]
- Klein R., Klein B. E., Moss S. E., Davis M. D., DeMets D. L. Glycosylated hemoglobin predicts the incidence and progression of diabetic retinopathy. JAMA. 1988 Nov 18;260(19):2864–2871. [PubMed] [Google Scholar]
- Klein R., Klein B. E., Moss S. E., Davis M. D., DeMets D. L. The Wisconsin epidemiologic study of diabetic retinopathy. II. Prevalence and risk of diabetic retinopathy when age at diagnosis is less than 30 years. Arch Ophthalmol. 1984 Apr;102(4):520–526. doi: 10.1001/archopht.1984.01040030398010. [DOI] [PubMed] [Google Scholar]
- Klein R., Klein B. E., Moss S. E., Davis M. D., DeMets D. L. The Wisconsin epidemiologic study of diabetic retinopathy. III. Prevalence and risk of diabetic retinopathy when age at diagnosis is 30 or more years. Arch Ophthalmol. 1984 Apr;102(4):527–532. doi: 10.1001/archopht.1984.01040030405011. [DOI] [PubMed] [Google Scholar]
- Lander E., Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet. 1995 Nov;11(3):241–247. doi: 10.1038/ng1195-241. [DOI] [PubMed] [Google Scholar]
- Lee D. A., Brubaker R. F., Hruska L. Hereditary glaucoma: a report of two pedigrees. Ann Ophthalmol. 1985 Dec;17(12):739–741. [PubMed] [Google Scholar]
- Leighton D. A. Survey of the first-degree relatives of glaucoma patients. Trans Ophthalmol Soc U K. 1976 Apr;96(1):28–32. [PubMed] [Google Scholar]
- Mares-Perlman J. A., Brady W. E., Klein R., Klein B. E., Bowen P., Stacewicz-Sapuntzakis M., Palta M. Serum antioxidants and age-related macular degeneration in a population-based case-control study. Arch Ophthalmol. 1995 Dec;113(12):1518–1523. doi: 10.1001/archopht.1995.01100120048007. [DOI] [PubMed] [Google Scholar]
- Mashal R. D., Koontz J., Sklar J. Detection of mutations by cleavage of DNA heteroduplexes with bacteriophage resolvases. Nat Genet. 1995 Feb;9(2):177–183. doi: 10.1038/ng0295-177. [DOI] [PubMed] [Google Scholar]
- Meyers S. M. A twin study on age-related macular degeneration. Trans Am Ophthalmol Soc. 1994;92:775–843. [PMC free article] [PubMed] [Google Scholar]
- Mitchell P., Smith W., Attebo K., Wang J. J. Prevalence of age-related maculopathy in Australia. The Blue Mountains Eye Study. Ophthalmology. 1995 Oct;102(10):1450–1460. doi: 10.1016/s0161-6420(95)30846-9. [DOI] [PubMed] [Google Scholar]
- Morissette J., Côté G., Anctil J. L., Plante M., Amyot M., Héon E., Trope G. E., Weissenbach J., Raymond V. A common gene for juvenile and adult-onset primary open-angle glaucomas confined on chromosome 1q. Am J Hum Genet. 1995 Jun;56(6):1431–1442. [PMC free article] [PubMed] [Google Scholar]
- Myers R. M., Larin Z., Maniatis T. Detection of single base substitutions by ribonuclease cleavage at mismatches in RNA:DNA duplexes. Science. 1985 Dec 13;230(4731):1242–1246. doi: 10.1126/science.4071043. [DOI] [PubMed] [Google Scholar]
- Newman B., Selby J. V., King M. C., Slemenda C., Fabsitz R., Friedman G. D. Concordance for type 2 (non-insulin-dependent) diabetes mellitus in male twins. Diabetologia. 1987 Oct;30(10):763–768. doi: 10.1007/BF00275741. [DOI] [PubMed] [Google Scholar]
- Nichols B. E., Sheffield V. C., Vandenburgh K., Drack A. V., Kimura A. E., Stone E. M. Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene. Nat Genet. 1993 Mar;3(3):202–207. doi: 10.1038/ng0393-202. [DOI] [PubMed] [Google Scholar]
- Nickerson D. A., Kaiser R., Lappin S., Stewart J., Hood L., Landegren U. Automated DNA diagnostics using an ELISA-based oligonucleotide ligation assay. Proc Natl Acad Sci U S A. 1990 Nov;87(22):8923–8927. doi: 10.1073/pnas.87.22.8923. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nyström L., Dahlquist G., Rewers M., Wall S. The Swedish childhood diabetes study. An analysis of the temporal variation in diabetes incidence 1978-1987. Int J Epidemiol. 1990 Mar;19(1):141–146. doi: 10.1093/ije/19.1.141. [DOI] [PubMed] [Google Scholar]
- Olmos P., A'Hern R., Heaton D. A., Millward B. A., Risley D., Pyke D. A., Leslie R. D. The significance of the concordance rate for type 1 (insulin-dependent) diabetes in identical twins. Diabetologia. 1988 Oct;31(10):747–750. doi: 10.1007/BF00274777. [DOI] [PubMed] [Google Scholar]
- Orita M., Suzuki Y., Sekiya T., Hayashi K. Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. Genomics. 1989 Nov;5(4):874–879. doi: 10.1016/0888-7543(89)90129-8. [DOI] [PubMed] [Google Scholar]
- Owerbach D., Gabbay K. H. The HOXD8 locus (2q31) is linked to type I diabetes. Interaction with chromosome 6 and 11 disease susceptibility genes. Diabetes. 1995 Jan;44(1):132–136. doi: 10.2337/diab.44.1.132. [DOI] [PubMed] [Google Scholar]
- Pak C. Y., Eun H. M., McArthur R. G., Yoon J. W. Association of cytomegalovirus infection with autoimmune type 1 diabetes. Lancet. 1988 Jul 2;2(8601):1–4. doi: 10.1016/s0140-6736(88)92941-8. [DOI] [PubMed] [Google Scholar]
- Parimoo S., Kolluri R., Weissman S. M. cDNA selection from total yeast DNA containing YACs. Nucleic Acids Res. 1993 Sep 11;21(18):4422–4423. doi: 10.1093/nar/21.18.4422. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Paterson A. H. Molecular dissection of quantitative traits: progress and prospects. Genome Res. 1995 Nov;5(4):321–333. doi: 10.1101/gr.5.4.321. [DOI] [PubMed] [Google Scholar]
- Perkins E. S. Family studies in glaucoma. Br J Ophthalmol. 1974 May;58(5):529–535. doi: 10.1136/bjo.58.5.529. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Permutt M. A., Ghosh S. Rat model contributes new loci for NIDDM susceptibility in man. Nat Genet. 1996 Jan;12(1):4–6. doi: 10.1038/ng0196-4. [DOI] [PubMed] [Google Scholar]
- Pickles A., Bolton P., Macdonald H., Bailey A., Le Couteur A., Sim C. H., Rutter M. Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism. Am J Hum Genet. 1995 Sep;57(3):717–726. [PMC free article] [PubMed] [Google Scholar]
- Pieramici D. J., Bressler N. M., Bressler S. B., Schachat A. P. Choroidal neovascularization in black patients. Arch Ophthalmol. 1994 Aug;112(8):1043–1046. doi: 10.1001/archopht.1994.01090200049020. [DOI] [PubMed] [Google Scholar]
- Piguet B., Wells J. A., Palmvang I. B., Wormald R., Chisholm I. H., Bird A. C. Age-related Bruch's membrane change: a clinical study of the relative role of heredity and environment. Br J Ophthalmol. 1993 Jul;77(7):400–403. doi: 10.1136/bjo.77.7.400. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rand L. I., Krolewski A. S., Aiello L. M., Warram J. H., Baker R. S., Maki T. Multiple factors in the prediction of risk of proliferative diabetic retinopathy. N Engl J Med. 1985 Dec 5;313(23):1433–1438. doi: 10.1056/NEJM198512053132302. [DOI] [PubMed] [Google Scholar]
- Rich S. S. Mapping genes in diabetes. Genetic epidemiological perspective. Diabetes. 1990 Nov;39(11):1315–1319. doi: 10.2337/diab.39.11.1315. [DOI] [PubMed] [Google Scholar]
- Richards J. E., Lichter P. R., Boehnke M., Uro J. L., Torrez D., Wong D., Johnson A. T. Mapping of a gene for autosomal dominant juvenile-onset open-angle glaucoma to chromosome Iq. Am J Hum Genet. 1994 Jan;54(1):62–70. [PMC free article] [PubMed] [Google Scholar]
- Risch N. Linkage strategies for genetically complex traits. I. Multilocus models. Am J Hum Genet. 1990 Feb;46(2):222–228. [PMC free article] [PubMed] [Google Scholar]
- Risch N. Linkage strategies for genetically complex traits. II. The power of affected relative pairs. Am J Hum Genet. 1990 Feb;46(2):229–241. [PMC free article] [PubMed] [Google Scholar]
- Risch N. Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs. Am J Hum Genet. 1990 Feb;46(2):242–253. [PMC free article] [PubMed] [Google Scholar]
- Risch N., Zhang H. Extreme discordant sib pairs for mapping quantitative trait loci in humans. Science. 1995 Jun 16;268(5217):1584–1589. doi: 10.1126/science.7777857. [DOI] [PubMed] [Google Scholar]
- Ritter L. L., Klein R., Klein B. E., Mares-Perlman J. A., Jensen S. C. Alcohol use and age-related maculopathy in the Beaver Dam Eye Study. Am J Ophthalmol. 1995 Aug;120(2):190–196. doi: 10.1016/s0002-9394(14)72607-8. [DOI] [PubMed] [Google Scholar]
- Rommens J. M., Iannuzzi M. C., Kerem B., Drumm M. L., Melmer G., Dean M., Rozmahel R., Cole J. L., Kennedy D., Hidaka N. Identification of the cystic fibrosis gene: chromosome walking and jumping. Science. 1989 Sep 8;245(4922):1059–1065. doi: 10.1126/science.2772657. [DOI] [PubMed] [Google Scholar]
- Sarfarazi M., Akarsu A. N., Hossain A., Turacli M. E., Aktan S. G., Barsoum-Homsy M., Chevrette L., Sayli B. S. Assignment of a locus (GLC3A) for primary congenital glaucoma (Buphthalmos) to 2p21 and evidence for genetic heterogeneity. Genomics. 1995 Nov 20;30(2):171–177. doi: 10.1006/geno.1995.9888. [DOI] [PubMed] [Google Scholar]
- Schork N. J., Boehnke M., Terwilliger J. D., Ott J. Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits. Am J Hum Genet. 1993 Nov;53(5):1127–1136. [PMC free article] [PubMed] [Google Scholar]
- Sham P. Sequential analysis and case-control candidate gene association studies: reply to Sobell et al. Am J Med Genet. 1994 Jun 15;54(2):154–157. doi: 10.1002/ajmg.1320540212. [DOI] [PubMed] [Google Scholar]
- Silvestri G., Johnston P. B., Hughes A. E. Is genetic predisposition an important risk factor in age-related macular degeneration? Eye (Lond) 1994;8(Pt 5):564–568. doi: 10.1038/eye.1994.138. [DOI] [PubMed] [Google Scholar]
- Spielman R. S., McGinnis R. E., Ewens W. J. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet. 1993 Mar;52(3):506–516. [PMC free article] [PubMed] [Google Scholar]
- Stewart W. C. The effect of lifestyle on the relative risk to develop open-angle glaucoma. Curr Opin Ophthalmol. 1995 Apr;6(2):3–9. doi: 10.1097/00055735-199504000-00002. [DOI] [PubMed] [Google Scholar]
- Teikari J. M. Genetic factors in open-angle (simple and capsular) glaucoma. A population-based twin study. Acta Ophthalmol (Copenh) 1987 Dec;65(6):715–720. doi: 10.1111/j.1755-3768.1987.tb07069.x. [DOI] [PubMed] [Google Scholar]
- Todd J. A. A protective role of the environment in the development of type 1 diabetes? Diabet Med. 1991 Dec;8(10):906–910. doi: 10.1111/j.1464-5491.1991.tb01528.x. [DOI] [PubMed] [Google Scholar]
- Todd J. A., Aitman T. J., Cornall R. J., Ghosh S., Hall J. R., Hearne C. M., Knight A. M., Love J. M., McAleer M. A., Prins J. B. Genetic analysis of autoimmune type 1 diabetes mellitus in mice. Nature. 1991 Jun 13;351(6327):542–547. doi: 10.1038/351542a0. [DOI] [PubMed] [Google Scholar]
- Todd J. A. Lawrence Lecture. The Emperor's new genes: 1993 RD Lawrence Lecture. Diabet Med. 1994 Jan-Feb;11(1):6–16. doi: 10.1111/j.1464-5491.1994.tb00222.x. [DOI] [PubMed] [Google Scholar]
- Vialettes B., Paquis-Fluckinger V., Silvestre-Aillaud P., Ben Dahan D., Pelissier J. F., Etchary-Bouyx F., Raccah D., Gin H., Guillausseau P. J., Vanuxen D. Extra-pancreatic manifestations in diabetes secondary to mitochondrial DNA point mutation within the tRNALeu(UUR) gene. Diabetes Care. 1995 Jul;18(7):1023–1028. doi: 10.2337/diacare.18.7.1023. [DOI] [PubMed] [Google Scholar]
- Vingerling J. R., Dielemans I., Bots M. L., Hofman A., Grobbee D. E., de Jong P. T. Age-related macular degeneration is associated with atherosclerosis. The Rotterdam Study. Am J Epidemiol. 1995 Aug 15;142(4):404–409. doi: 10.1093/oxfordjournals.aje.a117648. [DOI] [PubMed] [Google Scholar]
- Vingerling J. R., Dielemans I., Witteman J. C., Hofman A., Grobbee D. E., de Jong P. T. Macular degeneration and early menopause: a case-control study. BMJ. 1995 Jun 17;310(6994):1570–1571. doi: 10.1136/bmj.310.6994.1570. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weber B. H., Vogt G., Pruett R. C., Stöhr H., Felbor U. Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy. Nat Genet. 1994 Dec;8(4):352–356. doi: 10.1038/ng1294-352. [DOI] [PubMed] [Google Scholar]
- Weeks D. E., Lathrop G. M. Polygenic disease: methods for mapping complex disease traits. Trends Genet. 1995 Dec;11(12):513–519. doi: 10.1016/s0168-9525(00)89163-5. [DOI] [PubMed] [Google Scholar]
- West S., Vitale S., Hallfrisch J., Muñoz B., Muller D., Bressler S., Bressler N. M. Are antioxidants or supplements protective for age-related macular degeneration? Arch Ophthalmol. 1994 Feb;112(2):222–227. doi: 10.1001/archopht.1994.01090140098031. [DOI] [PubMed] [Google Scholar]
- Wiggs J. L., Haines J. L., Paglinauan C., Fine A., Sporn C., Lou D. Genetic linkage of autosomal dominant juvenile glaucoma to 1q21-q31 in three affected pedigrees. Genomics. 1994 May 15;21(2):299–303. doi: 10.1006/geno.1994.1269. [DOI] [PubMed] [Google Scholar]
