Author details

Full Name

Terri L Young

Affiliation

ORCID

Career Start Year

1989

Papers

183

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37386247	Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci.	Nat Genet	2023
37757997	Disparities in Promotion and Retention Rates Among Underrepresented in Medicine Faculty in U.S. Ophthalmology Departments.		2023
37615948	Using Adjustable-Focus Spectacles in Young Children to Meet Increasing Eyecare Needs.		2023
35131981	Glaucoma Cascade Screening in a High Risk Afro-Caribbean Haitian Population: A Pilot Study.	J Glaucoma	2022
36217948	Specifications of the ACMG/AMP variant curation guidelines for myocilin: Recommendations from the clingen glaucoma expert panel.	Hum Mutat	2022
35749127	Sonic Hedgehog Intron Variant Associated With an Unusual Pediatric Cortical Cataract.	Invest Ophthalmol Vis Sci	2022
34612139	Ophthalmic manifestations in Costello syndrome caused by Ras pathway dysregulation during development.	Ophthalmic Genetics	2022
34698770	Genetic Variants Associated With Human Eye Size Are Distinct From Those Conferring Susceptibility to Myopia.	Invest Ophthalmol Vis Sci	2021
33627673	Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.	Nat Commun	2021
34663817	Cellular crosstalk regulates the aqueous humor outflow pathway and provides new targets for glaucoma therapies.	Nature Communications	2021
33027505	SVEP1 as a Genetic Modifier of TEK-Related Primary Congenital Glaucoma.	Invest Ophthalmol Vis Sci	2020
31323684	Determining Possible Shared Genetic Architecture Between Myopia and Primary Open-Angle Glaucoma.	Invest Ophthalmol Vis Sci	2019
31600355	Correction: Genetic variants linked to myopic macular degeneration in persons with high myopia: CREAM Consortium.	PLoS One	2019
32672544	Comparative Intraoperative Anterior Segment OCT Findings in Pediatric Patients with and without Glaucoma.	Ophthalmology. Glaucoma	2019
31415580	Genetic variants linked to myopic macular degeneration in persons with high myopia: CREAM Consortium.	PLoS One	2019
31100065	In-utero epigenetic factors are associated with early-onset myopia in young children.	PLoS ONE	2019
29808027	Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error.	Nat Genet	2018
29865051	Accuracy of Inferred APOE Genotypes for a Range of Genotyping Arrays and Imputation Reference Panels.	J Alzheimers Dis	2018
28095098	Reduced penetrance in a large Caucasian pedigree with Stickler syndrome.	Ophthalmic Genet	2017
28384719	Exome Sequence Analysis of 14 Families With High Myopia.	Investigative Ophthalmology and Visual Science	2017
28380103	Hypotrichosis with juvenile macular dystrophy: a case report with molecular study.	Arquivos Brasileiros de Oftalmologia	2017
28758139	Assaying the Effects of Splice Site Variants by Exon Trapping in a Mammalian Cell Line.	Bio-protocol	2017
28586461	Genetically low vitamin D concentrations and myopic refractive error: a Mendelian randomization study.	Int J Epidemiol	2017
28373534	Trio-based exome sequencing arrests de novo mutations in early-onset high myopia.	Proceedings of the National Academy of Sciences of the United States of America	2017
29106382	Angiopoietin-1 is required for Schlemm's canal development in mice and humans.	J Clin Invest	2017
28073927	New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics.	Hum Mol Genet	2017
27622715	Large-Scale microRNA Expression Profiling Identifies Putative Retinal miRNA-mRNA Signaling Pathways Underlying Form-Deprivation Myopia in Mice.	PLoS ONE	2016
27020472	Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error.	Nat Commun	2016
27409473	Posterior Eye Shape Measurement With Retinal OCT Compared to MRI.	Invest Ophthalmol Vis Sci	2016
27174397	Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium.	Sci Rep	2016
27270174	Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity.	J Clin Invest	2016
27167468	Response: Cycloplegia in refraction: age and cycloplegics.	Acta Ophthalmol	2016
25187374	Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians.		2015
25631615	Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology.	Genet Epidemiol	2015
25367360	Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.	Hum Genet	2015
25429064	Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci.	Hum Mol Genet	2015
26390057	Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.	Nat Genet	2015
24641244	What is the appropriate age cut-off for cycloplegia in refraction?	Acta Ophthalmol	2014
24264139	Common mechanisms underlying refractive error identified in functional analysis of gene lists from genome-wide association study results in 2 European British cohorts.	JAMA Ophthalmol	2014
24105470	A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2.	Hum Mol Genet	2014
23802135	Sequencing analysis of the ATOH7 gene in individuals with optic nerve hypoplasia.	Ophthalmic Genet	2014
24861553	Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index.	Hum Mol Genet	2014
25173106	Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma.	Nat Genet	2014
24518671	A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125B in the TwinsUK cohort.	Hum Mol Genet	2014
25118269	Genetic variants associated with severe retinopathy of prematurity in extremely low birth weight infants.	Invest Ophthalmol Vis Sci	2014
24512587	Refraction issues in childhood: when to prescribe glasses.	Journal of Pediatric Ophthalmology and Strabismus	2014
25072831	Myopia in young adults is inversely related to an objective marker of ocular sun exposure: the Western Australian Raine cohort study.	Am J Ophthalmol	2014
24647736	Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians.	Diabetes	2014
25241763	Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process.	Nat Commun	2014
24954895	Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.	Am J Hum Genet	2014