Arama Sonuçları - Robyn Reynolds
- Gösterilen 1 - 20 sonuçlar arası kayıtlar. 25
- Sonraki Sayfaya Git
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Dietary Omega-3 Fatty Acids, Other Fat Intake, Genetic Susceptibility, and Progression to Incident Geographic Atrophy Yazar: Robyn Reynolds, Bernard Rosner, Johanna M. Seddon
Baskı/Yayın Bilgisi 2013Artigo -
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Serum Lipid Biomarkers and Hepatic Lipase Gene Associations with Age-Related Macular Degeneration Yazar: Robyn Reynolds, Bernard Rosner, Johanna M. Seddon
Baskı/Yayın Bilgisi 2010Artigo -
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Validation of a Prediction Algorithm for Progression to Advanced Macular Degeneration Subtypes Yazar: Johanna M. Seddon, Robyn Reynolds, Yi Yu, Bernard Rosner
Baskı/Yayın Bilgisi 2013Artigo -
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Kidney function, albuminuria and age-related macular degeneration in NHANES III Yazar: Daniel E. Weiner, Hocine Tighiouart, Robyn Reynolds, Johanna M. Seddon
Baskı/Yayın Bilgisi 2011Artigo -
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Prediction Model for Prevalence and Incidence of Advanced Age-Related Macular Degeneration Based on Genetic, Demographic, and Environmental Variables Yazar: Johanna M. Seddon, Robyn Reynolds, Julian Maller, Jesen Fagerness, Mark J. Daly, Bernard Rosner
Baskı/Yayın Bilgisi 2009Artigo -
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Variation near complement factor I is associated with risk of advanced AMD Yazar: Jesen Fagerness, Julian Maller, Benjamin M. Neale, Robyn Reynolds, Mark J. Daly, Johanna M. Seddon
Baskı/Yayın Bilgisi 2008Artigo -
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ARMS2/HTRA1 Locus Can Confer Differential Susceptibility to the Advanced Subtypes of Age-Related Macular Degeneration Yazar: Lucia Sobrin, Robyn Reynolds, Yi Yu, Jesen Fagerness, Nicolas Leveziel, Paul S. Bernstein, Eric H. Souied, Mark J. Daly, Johanna M. Seddon
Baskı/Yayın Bilgisi 2010Artigo -
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Genetic Factors for Choroidal Neovascularization Associated with High Myopia Yazar: Nicolas Leveziel, Yi Yu, Robyn Reynolds, Albert Tai, Weihua Meng, Violaine Caillaux, Patrick Calvas, Bernard Rosner, François Malecaze, Eric H. Souied, Johanna M. Seddon
Baskı/Yayın Bilgisi 2012Artigo -
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Associations of CFHR1–CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent Yazar: Soumya Raychaudhuri, Stephan Ripke, Mingyao Li, Benjamin M. Neale, Jesen Fagerness, Robyn Reynolds, Lucia Sobrin, Anand Swaroop, Gonçalo R. Abecasis, Johanna M. Seddon, Mark J. Daly
Baskı/Yayın Bilgisi 2010Carta -
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rs5888 Variant of SCARB1 Gene Is a Possible Susceptibility Factor for Age-Related Macular Degeneration Yazar: Jennyfer Zerbib, Johanna M. Seddon, Florence Richard, Robyn Reynolds, Nicolas Leveziel, Pascale Benlian, Patrick Borel, Josué Feingold, Arnold Münnich, G. Soubrane, Josseline Kaplan, Jean‐Michel Rozet, Eric H. Souied
Baskı/Yayın Bilgisi 2009Artigo -
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Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration Yazar: Yi Yu, Michael Triebwasser, Edwin Wong, Elizabeth C. Schramm, Brett Thomas, Robyn Reynolds, Elaine R. Mardis, John P. Atkinson, Mark J. Daly, Soumya Raychaudhuri, David Kavanagh, Johanna M. Seddon
Baskı/Yayın Bilgisi 2014Artigo -
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A rare penetrant mutation in CFH confers high risk of age-related macular degeneration Yazar: Soumya Raychaudhuri, Oleg Iartchouk, Kimberly Chin, Perciliz L. Tan, Albert Tai, Stephan Ripke, Sivakumar Gowrisankar, Soumya Vemuri, Kate Montgomery, Yi Yu, Robyn Reynolds, Donald J. Zack, Betsy Campochiaro, Peter A. Campochiaro, Nicholas Katsanis, Mark J. Daly, Johanna M. Seddon
Baskı/Yayın Bilgisi 2011Artigo -
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Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration Yazar: Johanna M. Seddon, Yi Yu, Elizabeth C. Miller, Robyn Reynolds, Perciliz L. Tan, Sivakumar Gowrisankar, Jacqueline I. Goldstein, Michael Triebwasser, Holly E. Anderson, Jennyfer Zerbib, David Kavanagh, Eric H. Souied, Nicholas Katsanis, Mark J. Daly, John P. Atkinson, Soumya Raychaudhuri
Baskı/Yayın Bilgisi 2013Artigo
Arama Araçları:
İlgili Konular
Medicine
Ophthalmology
Biology
Macular degeneration
Genetics
Internal medicine
Gene
Genotype
Single-nucleotide polymorphism
Oncology
Allele
Odds ratio
Confidence interval
Drusen
Proportional hazards model
Complement system
Endocrinology
Factor H
Genetic association
Genome-wide association study
Mutation
SNP
Antibody
Genotyping
Hazard ratio
Locus (genetics)
Biomarker
Cholesterol
Choroidal neovascularization
Complement factor I