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Correction: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Patrick Tarpey
Shery Thomas
Irene Gottlob
Amendments and Corrections28 Jun 2011
Nature Genetics

Volume: 43, P: 720
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Patrick Tarpey
Shery Thomas
Irene Gottlob
Research01 Oct 2006
Nature Genetics

Volume: 38, P: 1242-1244
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

Iris Heid, Gonçalo Abecasis, Sudha Iyengar and colleagues report the results of a large genome-wide association meta-analysis of macular degeneration based on over 43,000 subjects. They identify 16 new risk loci, including some very rare coding variants.

Lars G Fritsche
Wilmar Igl
Iris M Heid
Research21 Dec 2015
Nature Genetics

Volume: 48, P: 134-143
Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries

Multi-ancestry genome-wide analyses identify new risk loci for age-related macular degeneration. Ancestry-specific analyses identify distinct effects at major risk loci, including smaller effect sizes for CFH risk alleles in haplotypes of African ancestry.

Bryan R. Gorman
Georgios Voloudakis
Sudha K. Iyengar
Research02 Dec 2024
Nature Genetics

Volume: 56, P: 2659-2671
A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration

Tobias Strunz
Susette Lauwen
Bernhard H. F. Weber
ResearchOpen Access31 Jan 2020
Scientific Reports

Volume: 10, P: 1-16

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Correction: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

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

Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries

A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration

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Correction: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

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

Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries

A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration

Search

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