Concepedia

Author

Deepa Taranath

Flinders Medical CentreORCID

Also Known As

D. Taranath, Deepa A Taranath, Deepa A. Taranath, Deepa Ajay Taranath, Deepa Taranath

46

Publications

988

Citations

15

H-Index

21

Concepts

All Affiliations

Flinders Medical CentreFlinders UniversityUniversity of TasmaniaRoyal Children's HospitalLions Eye Institute
DT

About

Deepa Taranath is an author at Flinders Medical Centre specializing in ophthalmology, medicine, and glaucoma.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

5

5

176

2

Engineering

1

1

10

3

Genetic Medicine

1

1

44

4

Newborn Medicine

1

1

16

5

Pathology

1

1

44

Deepa Taranath

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18

Publications

888

Citations

15

H-Index

YearCitations

Anterior segment biometry with the Pentacam: Comprehensive assessment of repeatability of automated measurements

Hema Shankar, Deepa Taranath, Chandramalar T. Santhirathelagan,

Journal of Cataract & Refractive Surgery

2008

282

Repeatability of corneal first-surface wavefront aberrations measured with Pentacam corneal topography

Hema Shankar, Deepa Taranath, Chandramalar T. Santhirathelagan,

Journal of Cataract & Refractive Surgery

2008

76

Port-wine vascular malformations and glaucoma risk in Sturge-Weber syndrome

Sapna Sharan, Brighu Swamy, Deepa Taranath,

Journal of American Association for Pediatric Ophthalmology and Strabismus

2009

75

Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma

Owen M. Siggs, Emmanuelle Souzeau, Deepa Taranath,

Ophthalmology

2020

68

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

Emmanuelle Souzeau, Owen M. Siggs, Tiger Zhou,

European Journal of Human Genetics

2017

67

Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry

Lachlan S.W. Knight, Jonathan B. Ruddle, Deepa Taranath,

Ophthalmology

2021

45

Mutations in the EPHA2 Gene Are a Major Contributor to Inherited Cataracts in South-Eastern Australia

Alpana Dave, Kate J. Laurie, Sandra E. Staffieri,

PLoS ONE

2013

44

Prevalence of<i>FOXC1</i>Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma

Owen M. Siggs, Emmanuelle Souzeau, Francesca Pasutto,

JAMA Ophthalmology

2019

43

A comparison between the amblyopic eye and normal fellow eye ocular architecture in children with hyperopic anisometropic amblyopia

Bob Z. Wang, Deepa Taranath

Journal of American Association for Pediatric Ophthalmology and Strabismus

2012

33

High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia

Shari Javadiyan, Jamie E. Craig, Emmanuelle Souzeau,

G3 Genes Genomes Genetics

2017

29

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