Jenina Capasso - Concepedia

Author

Jenina Capasso

Thomas Jefferson University ORCID

Also Known As

Alex V. Levin, J. E. Capasso, Jenina Capasso, Jenina E Capasso, Jenina E. Capasso, Nanette Zale Refice

Publications

566

Citations

H-Index

Concepts

All Affiliations

Thomas Jefferson University Wills Eye Hospital Aravind Eye Hospital Golisano Children's Hospital University of Rochester

About

Jenina Capasso is an author at Thomas Jefferson University specializing in medicine, ophthalmology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	110
2	Pathology	3	3	54
3	Biology	1	1	13
4	Cell Biology	1	1	56
5	Molecular Genetics	1	1	13

Jenina Capasso

Publications

397

Citations

H-Index

Page 1

	Year	Citations
Axenfeld-Rieger syndrome: more than meets the eye Linda M. Reis, Mohit Maheshwari, Jenina Capasso, Journal of Medical Genetics	2022	67
Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach Simon M. Petersen‐Jones, Laurence M. Occelli, Paige A. Winkler, Journal of Clinical Investigation Ocular DiseaseRetinal TherapiesSynaptic SignalingCngb1 MutationsRetina	2017	56
Spectrum of PEX1 and PEX6 variants in Heimler syndrome Claire E. L. Smith, James A. Poulter, Alex V. Levin, European Journal of Human Genetics	2016	53
Ocular Manifestations of 22q11.2 Microduplication Jose A. Cordovez, Jenina Capasso, Michelle D. Lingao, Ophthalmology Ocular DiseaseOphthalmologySurgical PathologyPathogenesisHistopathology	2013	29
Anirdia‐like phenotype caused by 6p25 dosage aberrations Karthikeyan Arcot Sadagopan, Grace T. Liu, Jenina Capasso, American Journal of Medical Genetics Part A	2015	23
Macular cystoid spaces in patients with retinal dystrophy Michelle D. Lingao, Anuradha Ganesh, Arcot Sadagopan Karthikeyan, Ophthalmic Genetics	2016	23
Retinal Dystrophy with Intraretinal Cystoid Spaces Associated with Mutations in the Crumbs Homologue (<i>CRB1</i>) Gene Jose A. Cordovez, Elias I. Traboulsi, Jenina Capasso, Ophthalmic Genetics	2014	20
Comprehensive phenotypic and functional analysis of dominant and recessive<i>FOXE3</i>alleles in ocular developmental disorders Linda M. Reis, Ľubica Ďuďáková, Jana Moravíková, Human Molecular Genetics	2021	20
Early onset ectopia lentis due to a <i>FBN1</i> mutation with non‐penetrance Li Zhang, Yu‐Hung Lai, Jenina Capasso, American Journal of Medical Genetics Part A	2015	16
Ophthalmic manifestations of Heimler syndrome due to <i>PEX6</i> mutations Nutsuchar Wangtiraumnuay, Waleed Abed Alnabi, Mai Tsukikawa, Ophthalmic Genetics	2018	15

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