What is she best known for?
The fields of study she is best known for:
- Gene
- Internal medicine
- Mutation
Terri L. Young spends much of her time researching Genetics, Genome-wide association study, Locus, Single-nucleotide polymorphism and Ophthalmology.
Her work on Kidney as part of general Genetics research is frequently linked to Eye disorder, thereby connecting diverse disciplines of science.
Her Genome-wide association study research integrates issues from Odds ratio, Refractive error and Genetic association.
Within one scientific family, Terri L. Young focuses on topics pertaining to Optometry under Refractive error, and may sometimes address concerns connected to Retinoscopy.
The concepts of her Locus study are interwoven with issues in Allele frequency, Genetic linkage, Stickler syndrome, Genetic heterogeneity and Marfan syndrome.
Her work on SNP as part of general Single-nucleotide polymorphism study is frequently linked to Metric, Binary segmentation and Rank, therefore connecting diverse disciplines of science.
Her most cited work include:
- Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma (299 citations)
- Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (296 citations)
- Outdoor activity and myopia in Singapore teenage children (285 citations)
What are the main themes of her work throughout her whole career to date?
Terri L. Young mostly deals with Genetics, Genome-wide association study, Ophthalmology, Single-nucleotide polymorphism and Locus.
Her study involves Genetic association, Gene, SNP, Candidate gene and Genetic linkage, a branch of Genetics.
Her biological study deals with issues like Refractive error, which deal with fields such as Optometry, Strabismus and Astigmatism.
Her study on Ophthalmology is mostly dedicated to connecting different topics, such as Surgery.
Her Single-nucleotide polymorphism study integrates concerns from other disciplines, such as Quantitative trait locus, Internal medicine and Genetic marker.
Her Locus study incorporates themes from Allele frequency and Haplotype.
She most often published in these fields:
- Genetics (59.74%)
- Genome-wide association study (28.38%)
- Ophthalmology (23.76%)
What were the highlights of her more recent work (between 2015-2021)?
- Genetics (59.74%)
- Genome-wide association study (28.38%)
- Glaucoma (14.19%)
In recent papers she was focusing on the following fields of study:
Her main research concerns Genetics, Genome-wide association study, Glaucoma, Ophthalmology and Refractive error.
Her work in Gene, Proband, Exome sequencing, Mutation and Exon are all subfields of Genetics research.
Her Genome-wide association study research integrates issues from SNP, Missing data, Meta-analysis, Genetic association and Haplotype.
She combines subjects such as Haploinsufficiency, Intraocular pressure, Angiopoietin receptor and Pathology with her study of Glaucoma.
Her work deals with themes such as Optometry and Pupil, which intersect with Ophthalmology.
Her biological study spans a wide range of topics, including Zebrafish, Single-nucleotide polymorphism and Polymorphism.
Between 2015 and 2021, her most popular works were:
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (273 citations)
- Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity (83 citations)
- Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity (83 citations)
In her most recent research, the most cited papers focused on:
- Gene
- Internal medicine
- Mutation
Her primary scientific interests are in Genome-wide association study, Genetics, Glaucoma, Ophthalmology and Polymorphism.
Her study in Genome-wide association study is interdisciplinary in nature, drawing from both Kidney, Kidney disease and Renal function.
Her Genetics research is multidisciplinary, incorporating perspectives in Nephrology and Internal medicine.
Her Glaucoma research is multidisciplinary, incorporating elements of Optic neuropathy, Loss function and Angiopoietin receptor.
Her work carried out in the field of Polymorphism brings together such families of science as SNP, Evolutionary biology, Heritability, Meta-analysis and Refractive error.
Her Refractive error study integrates concerns from other disciplines, such as Mendelian randomization, Vitamin D and neurology, Endocrinology, Single-nucleotide polymorphism and Genetic variation.
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