BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 27007659)

  • 1. Whole Exome Sequencing in Patients with the Cuticular Drusen Subtype of Age-Related Macular Degeneration.
    Duvvari MR; van de Ven JP; Geerlings MJ; Saksens NT; Bakker B; Henkes A; Neveling K; del Rosario M; Westra D; van den Heuvel LP; Schick T; Fauser S; Boon CJ; Hoyng CB; de Jong EK; den Hollander AI
    PLoS One; 2016; 11(3):e0152047. PubMed ID: 27007659
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of rare variants in the CFH gene in patients with the cuticular drusen subtype of age-related macular degeneration.
    Duvvari MR; Saksens NT; van de Ven JP; de Jong-Hesse Y; Schick T; Nillesen WM; Fauser S; Hoefsloot LH; Hoyng CB; de Jong EK; den Hollander AI
    Mol Vis; 2015; 21():285-92. PubMed ID: 25814826
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association analysis of genetic and environmental risk factors in the cuticular drusen subtype of age-related macular degeneration.
    van de Ven JP; Smailhodzic D; Boon CJ; Fauser S; Groenewoud JM; Chong NV; Hoyng CB; Klevering BJ; den Hollander AI
    Mol Vis; 2012; 18():2271-8. PubMed ID: 22933840
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Loss-of-Function Mutations in the CFH Gene Affecting Alternatively Encoded Factor H-like 1 Protein Cause Dominant Early-Onset Macular Drusen.
    Taylor RL; Poulter JA; Downes SM; McKibbin M; Khan KN; Inglehearn CF; Webster AR; Hardcastle AJ; Michaelides M; Bishop PN; Clark SJ; Black GC;
    Ophthalmology; 2019 Oct; 126(10):1410-1421. PubMed ID: 30905644
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rare genetic variants in Tunisian Jewish patients suffering from age-related macular degeneration.
    Pras E; Kristal D; Shoshany N; Volodarsky D; Vulih I; Celniker G; Isakov O; Shomron N; Pras E
    J Med Genet; 2015 Jul; 52(7):484-92. PubMed ID: 25986072
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mapping rare, deleterious mutations in Factor H: Association with early onset, drusen burden, and lower antigenic levels in familial AMD.
    Wagner EK; Raychaudhuri S; Villalonga MB; Java A; Triebwasser MP; Daly MJ; Atkinson JP; Seddon JM
    Sci Rep; 2016 Aug; 6():31531. PubMed ID: 27572114
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rare Genetic Variants in Jewish Patients Suffering from Age-Related Macular Degeneration.
    Shoshany N; Weiner C; Safir M; Einan-Lifshitz A; Pokroy R; Kol A; Modai S; Shomron N; Pras E
    Genes (Basel); 2019 Oct; 10(10):. PubMed ID: 31635417
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Phenotype Characteristics of Patients With Age-Related Macular Degeneration Carrying a Rare Variant in the Complement Factor H Gene.
    Kersten E; Geerlings MJ; den Hollander AI; de Jong EK; Fauser S; Peto T; Hoyng CB
    JAMA Ophthalmol; 2017 Oct; 135(10):1037-1044. PubMed ID: 28859202
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phenotypic Characterization of Complement Factor H R1210C Rare Genetic Variant in Age-Related Macular Degeneration.
    Ferrara D; Seddon JM
    JAMA Ophthalmol; 2015 Jul; 133(7):785-91. PubMed ID: 25880396
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evaluating the Occurrence of Rare Variants in the Complement Factor H Gene in Patients With Early-Onset Drusen Maculopathy.
    de Breuk A; Heesterbeek TJ; Bakker B; Verzijden T; Lechanteur YTE; Klaver CCW; den Hollander AI; Hoyng CB
    JAMA Ophthalmol; 2021 Nov; 139(11):1218-1226. PubMed ID: 34647987
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Basal laminar drusen caused by compound heterozygous variants in the CFH gene.
    Boon CJ; Klevering BJ; Hoyng CB; Zonneveld-Vrieling MN; Nabuurs SB; Blokland E; Cremers FP; den Hollander AI
    Am J Hum Genet; 2008 Feb; 82(2):516-23. PubMed ID: 18252232
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of the Arg345Trp disease-associated allele of the EFEMP1 gene in individuals with early onset drusen or familial age-related macular degeneration.
    Guymer RH; McNeil R; Cain M; Tomlin B; Allen PJ; Dip CL; Baird PN
    Clin Exp Ophthalmol; 2002 Dec; 30(6):419-23. PubMed ID: 12427233
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of variants in the complement factor H, the elongation of very long chain fatty acids-like 4 and the hemicentin 1 genes of age-related macular degeneration in the Finnish population.
    Seitsonen S; Lemmelä S; Holopainen J; Tommila P; Ranta P; Kotamies A; Moilanen J; Palosaari T; Kaarniranta K; Meri S; Immonen I; Järvelä I
    Mol Vis; 2006 Jul; 12():796-801. PubMed ID: 16885922
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration.
    Ratnapriya R; Zhan X; Fariss RN; Branham KE; Zipprer D; Chakarova CF; Sergeev YV; Campos MM; Othman M; Friedman JS; Maminishkis A; Waseem NH; Brooks M; Rajasimha HK; Edwards AO; Lotery A; Klein BE; Truitt BJ; Li B; Schaumberg DA; Morgan DJ; Morrison MA; Souied E; Tsironi EE; Grassmann F; Fishman GA; Silvestri G; Scholl HP; Kim IK; Ramke J; Tuo J; Merriam JE; Merriam JC; Park KH; Olson LM; Farrer LA; Johnson MP; Peachey NS; Lathrop M; Baron RV; Igo RP; Klein R; Hagstrom SA; Kamatani Y; Martin TM; Jiang Y; Conley Y; Sahel JA; Zack DJ; Chan CC; Pericak-Vance MA; Jacobson SG; Gorin MB; Klein ML; Allikmets R; Iyengar SK; Weber BH; Haines JL; Léveillard T; Deangelis MM; Stambolian D; Weeks DE; Bhattacharya SS; Chew EY; Heckenlively JR; Abecasis GR; Swaroop A
    Hum Mol Genet; 2014 Nov; 23(21):5827-37. PubMed ID: 24899048
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analysis of the EFEMP1 gene in individuals and families with early onset drusen.
    Narendran N; Guymer RH; Cain M; Baird PN
    Eye (Lond); 2005 Jan; 19(1):11-5. PubMed ID: 15218514
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rare complement factor H variant associated with age-related macular degeneration in the Amish.
    Hoffman JD; Cooke Bailey JN; D'Aoust L; Cade W; Ayala-Haedo J; Fuzzell D; Laux R; Adams LD; Reinhart-Mercer L; Caywood L; Whitehead-Gay P; Agarwal A; Wang G; Scott WK; Pericak-Vance MA; Haines JL
    Invest Ophthalmol Vis Sci; 2014 Jun; 55(7):4455-60. PubMed ID: 24906858
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Extramacular drusen are highly associated with age-related macular degeneration, but not with CFH and ARMS2 genotypes.
    Ersoy L; Schick T; de Graft D; Felsch M; Hoyng CB; den Hollander AI; Kirchhof B; Fauser S; Liakopoulos S
    Br J Ophthalmol; 2016 Aug; 100(8):1047-51. PubMed ID: 26614632
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Complement factor H polymorphism p.Tyr402His and cuticular Drusen.
    Grassi MA; Folk JC; Scheetz TE; Taylor CM; Sheffield VC; Stone EM
    Arch Ophthalmol; 2007 Jan; 125(1):93-7. PubMed ID: 17210858
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Family-based exome sequencing identifies rare coding variants in age-related macular degeneration.
    Ratnapriya R; Acar İE; Geerlings MJ; Branham K; Kwong A; Saksens NTM; Pauper M; Corominas J; Kwicklis M; Zipprer D; Starostik MR; Othman M; Yashar B; Abecasis GR; Chew EY; Ferrington DA; Hoyng CB; Swaroop A; den Hollander AI
    Hum Mol Genet; 2020 Jul; 29(12):2022-2034. PubMed ID: 32246154
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Early-onset macular degeneration with drusen in a cynomolgus monkey (Macaca fascicularis) pedigree: exclusion of 13 candidate genes and loci.
    Umeda S; Ayyagari R; Allikmets R; Suzuki MT; Karoukis AJ; Ambasudhan R; Zernant J; Okamoto H; Ono F; Terao K; Mizota A; Yoshikawa Y; Tanaka Y; Iwata T
    Invest Ophthalmol Vis Sci; 2005 Feb; 46(2):683-91. PubMed ID: 15671300
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.