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Showing 1–11 of 11 results

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Synchronous extreme spectral variability of BE Ursae Majoris

Bruce Margon
Ronald A. Downes
Jonathan I. Katz
Research17 Sept 1981
Nature

Volume: 293, P: 200-202
Essential requirement for major histocompatibility complex recognition in T-cell tolerance induction

Jonathan R. Lamb
Marc Feldmann
Research01 Mar 1984
Nature

Volume: 308, P: 72-74
Structural and functional restoration by collateral sprouting of hippocampal 5-HT axons

EFRAIN C. AZMITIA
ALASTAIR M. BUCHAN
JONATHAN H. WILLIAMS
Research27 Jul 1978
Nature

Volume: 274, P: 374-376
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression

Multitrait genome-wide analysis of glaucoma and related phenotypes identifies new risk loci and enables development of a polygenic risk score to predict disease susceptibility and key clinical outcomes.

Jamie E. Craig
Xikun Han
Stuart MacGregor
Research20 Jan 2020
Nature Genetics

Volume: 52, P: 160-166
Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma

A combined analysis of participants from the UK Biobank and the International Glaucoma Genetic Consortium identifies 85 new loci for intraocular pressure (IOP). Pathway analysis uncovers new pathways associated with both IOP and glaucoma.

Stuart MacGregor
Jue-Sheng Ong
Alex W. Hewitt
Research27 Jul 2018
Nature Genetics

Volume: 50, P: 1067-1071
Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma

Jamie Craig, Puya Gharahkhani and colleagues report results of a genome-wide association study of primary open-angle glaucoma. They identify common variants near ABCA1, AFAP1 and GMDS that are associated with risk of this disease.

Puya Gharahkhani
Kathryn P Burdon
Jamie E Craig
Research31 Aug 2014
Nature Genetics

Volume: 46, P: 1120-1125
Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma

Puya Gharahkhani
Kathryn P. Burdon
Donald J. Zack
ResearchOpen Access15 Feb 2018
Scientific Reports

Volume: 8, P: 1-12
Patient experiences and perceived value of genetic testing in inherited retinal diseases: a cross-sectional survey

Alexis Ceecee Britten-Jones
Joshua Schultz
Lauren N. Ayton
ResearchOpen Access05 Mar 2024
Scientific Reports

Volume: 14, P: 1-9
Erratum: Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants

Emmanuelle Souzeau
Owen M Siggs
Jamie E Craig
Amendments and Corrections12 Oct 2017
European Journal of Human Genetics

Volume: 25, P: 1290
Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants

Emmanuelle Souzeau
Owen M Siggs
Jamie E Craig
ResearchOpen Access17 May 2017
European Journal of Human Genetics

Volume: 25, P: 839-847
Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium

Qiao Fan
Xiaobo Guo
Zoran Vatavuk
ResearchOpen Access13 May 2016
Scientific Reports

Volume: 6, P: 1-14

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Synchronous extreme spectral variability of BE Ursae Majoris

Essential requirement for major histocompatibility complex recognition in T-cell tolerance induction

Structural and functional restoration by collateral sprouting of hippocampal 5-HT axons

Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression

Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma

Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma

Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma

Patient experiences and perceived value of genetic testing in inherited retinal diseases: a cross-sectional survey

Erratum: Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants

Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants

Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium

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