検索結果 - Robyn Reynolds
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Associations of CFHR1–CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent 著者: 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
出版事項 2010Carta -
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rs5888 Variant of SCARB1 Gene Is a Possible Susceptibility Factor for Age-Related Macular Degeneration 著者: 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
出版事項 2009Artigo -
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Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration 著者: 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
出版事項 2014Artigo -
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A rare penetrant mutation in CFH confers high risk of age-related macular degeneration 著者: 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
出版事項 2011Artigo -
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Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration 著者: 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
出版事項 2013Artigo
関連主題
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