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Alexander J. Brucker

Researcher at University of Pennsylvania

Publications -  157
Citations -  10628

Alexander J. Brucker is an academic researcher from University of Pennsylvania. The author has contributed to research in topics: Diabetic retinopathy & Retinopathy. The author has an hindex of 45, co-authored 148 publications receiving 9255 citations. Previous affiliations of Alexander J. Brucker include Children's Hospital of Philadelphia & Johns Hopkins University School of Medicine.

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A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

Lars G. Fritsche, +185 more
- 01 Feb 2016 - 
TL;DR: The results support the hypothesis that rare coding variants can pinpoint causal genes within known genetic loci and illustrate that applying the approach systematically to detect new loci requires extremely large sample sizes.
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Seven new loci associated with age-related macular degeneration

Lars G. Fritsche, +185 more
- 01 Apr 2013 - 
TL;DR: A collaborative genome-wide association study, including >17,100 advanced AMD cases and >60,000 controls of European and Asian ancestry, identifies 19 loci associated at P < 5 × 10−8, which show enrichment for genes involved in the regulation of complement activity, lipid metabolism, extracellular matrix remodeling and angiogenesis.
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Aflibercept, Bevacizumab, or Ranibizumab for Diabetic Macular Edema: Two-Year Results from a Comparative Effectiveness Randomized Clinical Trial.

TL;DR: All 3 anti-VEGF groups showed VA improvement from baseline to 2 years with a decreased number of injections in year 2, and among eyes with worse baseline VA, a flibercept had superior 2-year VA outcomes compared with bevacizumab, but superiority of aflibercept over ranibizumAB, noted at 1 year, was no longer identified.
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Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration

Wei Chen, +69 more
TL;DR: A genome-wide association scan for age-related macular degeneration (AMD) showed that 329 of 331 individuals with the highest-risk genotypes were cases, and 85% of these had advanced AMD, consistent with the hypothesis that HDL metabolism is associated with AMD pathogenesis.