About: Jamie E Craig

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About: Jamie E Craig Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

ophthalmologist-scientist

Attributes	Values
rdf:type	Item
field of work	wds:Q82048083-219c56be-446f-92db-aa9b-0e273a7bab93 wds:Q82048083-41929b92-4070-150e-699b-4455e6710f2c
field of work	glaucoma diabetic retinopathy
description	investigador (es) araştırmacı (tr) wetenschapper (nl) дослідник (uk) ophthalmologist-scientist (en)
rdfs:label	Jamie E Craig (en) Jamie E Craig (nl) Jamie E. Craig (it)
skos:prefLabel	Jamie E Craig (en) Jamie E Craig (nl) Jamie E. Craig (it)
name	Jamie E Craig (en) Jamie E Craig (nl) Jamie E. Craig (it)
Scopus author ID	wds:Q82048083-037EDFAD-46DC-4270-8978-E926ED053660
Scopus author ID	35510868100
given name	wds:Q82048083-717DE1F5-7A2F-45AF-96BC-25B19E4BC85F
given name	Jamie
instance of	wds:Q82048083-3FF0FD4E-1A50-436C-ACFE-68E493C01E96
described at URL	wds:Q82048083-dca8e12b-4ed6-8634-7b6d-3b28c5cb86b5
instance of	Homo sapiens
described at URL	https://www.flinders.edu.au/people/jamie.craig
award received	wds:Q82048083-9C1FCF23-9F0C-4586-B1E5-D6D31BCB847F
award received	Fellow of the Australian Academy of Health and Medical Sciences
skos:altLabel	Jamie Craig (en) Jamie E. Craig (en)
occupation	wds:Q82048083-6DCFED2C-6F45-4783-BF66-75686C80FB11
employer	wds:Q82048083-D5DD4592-DD80-4F2E-9212-908FF1A74F64
NLA Trove people ID	wds:Q82048083-be92a5b7-4d9d-6e09-3ecf-1460dc26bbb9 wds:Q82048083-cad9fdae-4b64-3740-c799-f63c7c085314
VIAF ID	wds:Q82048083-c00306f5-78f5-4aae-86c4-ff3ed5b14420
Libraries Australia ID	wds:Q82048083-1b55d021-41bc-c2c8-b624-6c0e00c580be
educated at	wds:Q82048083-34add74d-48ab-c5b3-3b68-86d3e5a5aaa9 wds:Q82048083-7f8a9016-4763-fa8a-6883-7d976cd65a3c
family name	wds:Q82048083-4BE20D2A-84D9-4E3D-B187-EAA2A4C5114F
official website	wds:Q82048083-6C43C992-0A2B-4D6A-BA20-195833B3542E
VIAF ID	http://viaf.org/viaf/4873148390838310830007
occupation	ophthalmologist
employer	Flinders University
NLA Trove people ID	1509542 1867632
VIAF ID	4873148390838310830007
Libraries Australia ID	58815778
educated at	University of Oxford University of Adelaide
family name	Craig
official website	https://researchnow.flinders.edu.au/en/persons/67336231-d6d2-473a-876f-60f89789759a
ORCID iD	wds:Q82048083-4AE03762-A26A-44B7-9D6F-74E69207A9AC
Dimensions author ID	wds:Q82048083-EB0514F7-926E-4150-9512-8C5C83088713
ORCID iD	https://orcid.org/0000-0001-9955-9696
ORCID iD	0000-0001-9955-9696
Dimensions author ID	010011541707.44
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q82048083
is author of	Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q. Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process Intravitreal triamcinolone-induced elevated intraocular pressure is associated with the development of posterior subcapsular cataract Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus The genetics of central corneal thickness Analysis of myocilin mutations in 1703 glaucoma patients from five different populations Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis The PITX3 gene in posterior polar congenital cataract in Australia The optic nerve head in myocilin glaucoma Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy The apolipoprotein epsilon4 gene is associated with elevated risk of normal tension glaucoma. Association of genetic variants in the TMCO1 gene with clinical parameters related to glaucoma and characterization of the protein in the eye. The reliability of single-field fundus photography in screening for diabetic retinopathy: the Central Australian Ocular Health Study. Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 gene Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucoma A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance Mutation spectrum in Australian pedigrees with hereditary hyperferritinaemia-cataract syndrome reveals novel and de novo mutations Null mutations in LTBP2 cause primary congenital glaucoma A systematic meta-analysis of genetic association studies for diabetic retinopathy Association between erythropoietin gene polymorphisms and diabetic retinopathy Common sequence variation in the VEGFA gene predicts risk of diabetic retinopathy. Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1 Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy Sequence variation in DDAH1 and DDAH2 genes is strongly and additively associated with serum ADMA concentrations in individuals with type 2 diabetes The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ratio, and central corneal thickness Central corneal thickness is highly heritable: the twin eye studies. Heritability of Central Corneal Thickness in Nuclear Families Retinopathy of prematurity: recent advances in our understanding. Complex genetics of complex traits: the case of primary open-angle glaucoma Investigation of crystallin genes in familial cataract, and report of two disease associated mutations. Prevalence and associations of cataract in indigenous Australians within central Australia: the Central Australian Ocular Health Study Genetic analysis of the clusterin gene in pseudoexfoliation syndrome Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people Functional and structural implications of the complement factor H Y402H polymorphism associated with age-related macular degeneration

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