Related references
Note: Only part of the references are listed.Age-related macular degeneration: genetic and clinical findings
Haris Kokotas et al.
CLINICAL CHEMISTRY AND LABORATORY MEDICINE (2011)
Collagen-related genes influence the glaucoma risk factor, central corneal thickness
Eranga N. Vithana et al.
HUMAN MOLECULAR GENETICS (2011)
GWAF: an R package for genome-wide association analyses with family data
Ming-Huei Chen et al.
BIOINFORMATICS (2010)
LocusZoom: regional visualization of genome-wide association scan results
Randall J. Pruim et al.
BIOINFORMATICS (2010)
New RAB3GAP1 mutations in patients with Warburg Micro Syndrome from different ethnic backgrounds and a possible founder effect in the Danish
Deborah J. Morris-Rosendahl et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2010)
New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8
Veronique Vitart et al.
HUMAN MOLECULAR GENETICS (2010)
Glaucoma: genes, phenotypes, and new directions for therapy
Bao Jian Fan et al.
JOURNAL OF CLINICAL INVESTIGATION (2010)
Common Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal Thickness
Yi Lu et al.
PLOS GENETICS (2010)
Four Novel Loci (19q13, 6q24, 12q24, and 5q14) Influence the Microcirculation In Vivo
M. Kamran Ikram et al.
PLOS GENETICS (2010)
Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Design of Prospective Meta-Analyses of Genome-Wide Association Studies From 5 Cohorts
Bruce M. Psaty et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2009)
Linkage Analysis in Keratoconus: Replication of Locus 5q21.2 and Identification of Other Suggestive Loci
Luigi Bisceglia et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2009)
Three VSX1 gene mutations, L159M, R166W, and H244R, are not associated with keratoconus
Yongming G. Tang et al.
CORNEA (2008)
A second generation human haplotype map of over 3.1 million SNPs
Kelly A. Frazer et al.
NATURE (2007)
PLINK: A tool set for whole-genome association and population-based linkage analyses
Shaun Purcell et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Complex trait genetics of refractive error
Terri L. Young et al.
ARCHIVES OF OPHTHALMOLOGY (2007)
Principal components analysis corrects for stratification in genome-wide association studies
Alkes L. Price et al.
NATURE GENETICS (2006)
Whole-genome genotyping of haplotype tag single nucleotide polymorphisms
KL Gunderson et al.
PHARMACOGENOMICS (2006)
Mutation in rab3 GTPase-activating protein (RAB3GAP) noncatalytic subunit in a kindred with Martsolf syndrome
IA Aligianis et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Two-stage genome-wide linkage scan in keratoconus sib pair families
Xiaohui Li et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2006)
Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1
YMG Tang et al.
GENETICS IN MEDICINE (2005)
A genome-wide scalable SNP genotyping assay using microarray technology
KL Gunderson et al.
NATURE GENETICS (2005)
Complement factor H polymorphism in age-related macular degeneration
RJ Klein et al.
SCIENCE (2005)
Gene expression profile studies of human keratoconus cornea for NEIBank: A novel cornea-expressed gene and the absence of transcripts for aquaporin 5
YS Rabinowitz et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2005)
Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndrome
IA Aligianis et al.
NATURE GENETICS (2005)
VSX1 mutational analysis in a series of Italian patients affected by keratoconus: Detection of a novel mutation
L Bisceglia et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2005)
Haploview: analysis and visualization of LD and haplotype maps
JC Barrett et al.
BIOINFORMATICS (2005)
Identification of a new locus for isolated familial keratoconus at 2p24
H Hutchings et al.
JOURNAL OF MEDICAL GENETICS (2005)
A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13
F Brancati et al.
JOURNAL OF MEDICAL GENETICS (2004)
Localization versus function of Rab3 proteins -: Evidence for a common regulatory role in controlling fusion
OM Schlüter et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
VSX1:: A gene for posterior polymorphous dystrophy and keratoconus
E Héon et al.
HUMAN MOLECULAR GENETICS (2002)
Identity-by-descent approach to gene localisation in eight individuals affected by keratoconus from north-west Tasmania, Australia
J Fullerton et al.
HUMAN GENETICS (2002)
Multiple aspects of Rab protein action in the secretory pathway: Focus on Rab3 and Rab6
F Darchen et al.
BIOCHIMIE (2000)