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Record W2099989980 · doi:10.1093/hmg/ddr270

Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration

2011· review· en· W2099989980 on OpenAlex

Why this work is in the frame

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

affAt least one author lists a Canadian institution in the pinned OpenAlex snapshot.

Bibliographic record

VenueHuman Molecular Genetics · 2011
Typereview
Languageen
FieldMedicine
TopicRetinal Diseases and Treatments
Canadian institutionsQueen's University
FundersAlcon Research InstituteNational Eye InstituteNational Institute of Arthritis and Musculoskeletal and Skin DiseasesTufts University School of MedicineMedical Research CouncilNational Institutes of HealthNational Health and Medical Research CouncilNational Institute of Mental HealthNorthwestern UniversityState Government of VictoriaMassachusetts Lions Eye Research FundMacula Vision Research FoundationTufts Medical CenterBrigham and Women's HospitalResearch to Prevent Blindness
KeywordsBiologyGeneticsSingle-nucleotide polymorphismGenome-wide association studyMacular degenerationGenotypeLocus (genetics)Genetic associationAllele1000 Genomes ProjectGeneOphthalmologyMedicine

Abstract

fetched live from OpenAlex

Despite significant progress in the identification of genetic loci for age-related macular degeneration (AMD), not all of the heritability has been explained. To identify variants which contribute to the remaining genetic susceptibility, we performed the largest meta-analysis of genome-wide association studies to date for advanced AMD. We imputed 6 036 699 single-nucleotide polymorphisms with the 1000 Genomes Project reference genotypes on 2594 cases and 4134 controls with follow-up replication of top signals in 5640 cases and 52 174 controls. We identified two new common susceptibility alleles, rs1999930 on 6q21-q22.3 near FRK/COL10A1 [odds ratio (OR) 0.87; P 5 1.1 3 10 28 ] and rs4711751 on 6p12 near VEGFA (OR 1.15; P 5 8.7 3 10 29 ). In addition to the two novel loci, 10 previously reported loci in ARMS2/HTRA1 (rs10490924), CFH (rs1061170, and rs1410996), CFB (rs641153), C3 (rs2230199), C2 (rs9332739), CFI (rs10033900), LIPC (rs10468017), TIMP3 (rs9621532) and CETP (rs3764261) were confirmed with genomewide significant signals in this large study. Loci in the recently reported genes ABCA1 and COL8A1 were also detected with suggestive evidence of association with advanced AMD. The novel variants identified in this study suggest that angiogenesis (VEGFA) and extracellular collagen matrix (FRK/COL10A1) pathways contribute to the development of advanced AMD. c Replication P-values and ORs were derived from meta-analysis results of all replication samples independent of the TMMG sample. d Samples participated in the combined analysis for each SNP were indicated by letters (A/a to K/k). A capital letter indicates the effective allele of the SNP-increased risk of AMD in the specific sample. A lower case letter indicates the effective allele of the SNP-reduced risk of AMD in the specific sample. 'a' represents Tufts/MMAP/MIGen/GAIN (TMMG) samples; 'b', deCODE genetics sample replication (Iceland); 'c', the Columbia University sample replication (COL); 'd', the Johns Hopkins University sample replication (JHU); 'e', Genentech sample replication (Genentech); 'f', Washington University sample replication (WASH-U); 'g', the Centre for Eye Research Australia sample replication (AUS); 'h', the Rotterdam study sample replication (RS); 'i', the independent replication sample of Tufts/MGH (Tufts/MGH replication); 'j', the Hopital Intercommunal de Creteil sample replication (FR-CRET); 'k', the Queen's University of Belfast sample replication (Irish). e The result of this SNP was from imputation data based on HapMap2 Project; all other SNPs were imputed based on 1000 Genomes Project.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Other design · Consensus signal: none
GenreCandidate signal: Review · Consensus signal: Review
Teacher disagreement score0.915
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.036
GPT teacher head0.315
Teacher spread0.279 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it