Genome-wide association studies in the hunt for genes causing primary open-angle glaucoma: a review

Long Noncoding RNA, Polycomb, and the Ghosts Haunting INK4b-ARF-INK4a Expression

(2011) F. Aguilo et al.   CANCER RESEARCH

Primary open-angle glaucoma genes

(2011) J H Fingert   EYE

Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area

(2011) Chiea Chuen Khor et al.   HUMAN MOLECULAR GENETICS

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA

(2011) Janey L. Wiggs et al.   HUMAN MOLECULAR GENETICS

Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations

(2011) Belinda K. Cornes et al.   HUMAN MOLECULAR GENETICS

Common genetic variants associated with open-angle glaucoma

(2011) Wishal D. Ramdas et al.   HUMAN MOLECULAR GENETICS

Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1

(2011) Kathryn P Burdon et al.   NATURE GENETICS

Lack of Association BetweenLOXL1Gene Polymorphisms and Primary Open Angle Glaucoma in the Saudi Arabian Population

(2011) Khaled K. Abu-Amero et al.   OPHTHALMIC GENETICS

Collagen-related genes influence the glaucoma risk factor, central corneal thickness

(2010) Eranga N. Vithana et al.   HUMAN MOLECULAR GENETICS

New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8

(2010) Veronique Vitart et al.   HUMAN MOLECULAR GENETICS

Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

(2010) Stuart Macgregor et al.   HUMAN MOLECULAR GENETICS

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

(2010) Gudmar Thorleifsson et al.   NATURE GENETICS

Genome-wide Association Study of Normal Tension Glaucoma: Common Variants in SRBD1 and ELOVL5 Contribute to Disease Susceptibility

(2010)   OPHTHALMOLOGY

A Genome-Wide Association Study of Optic Disc Parameters

(2010) Wishal D. Ramdas et al.   PLoS Genetics

Homozygous frameshift mutation in TMCO1 causes a syndrome with craniofacial dysmorphism, skeletal anomalies, and mental retardation

(2009) B. Xin et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Three susceptible loci associated with primary open-angle glaucoma identified by genome-wide association study in a Japanese population

(2009) M. Nakano et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Estimation of significance thresholds for genomewide association scans

(2008) Frank Dudbridge et al.   GENETIC EPIDEMIOLOGY