Publications by authors named "Adam P Deluca"

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Early-Onset Stargardt Disease Caused by Homozygosity of a Complex Allele from Eastern Africa: Two Case Reports.
Sigrid Aslaksen, Eirik Bratland, Mari Hamre Bu, Ingvild Aukrust, Cecilie Bredrup, Adam P DeLuca

Case Rep Ophthalmol· October 2025

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Demonstration of the pathogenicity of a common non-exomic mutation in ABCA4 using iPSC-derived retinal organoids and retrospective clinical data.
Erin R Burnight, Beau J Fenner, Ian C Han, Adam P DeLuca, S Scott Whitmore

Hum Mol Genet· August 2024

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A Retrospective Longitudinal Study of 460 Patients with ABCA4-Associated Retinal Disease.
Beau J Fenner, S Scott Whitmore, Adam P DeLuca, Jean L Andorf, Heather T Daggett

Ophthalmology· August 2024

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Using Goldmann Visual Field Volume to Track Disease Progression in Choroideremia.
Adam P DeLuca, S Scott Whitmore, Nicole J Tatro, Jeaneen L Andorf, Ben P Faga

Ophthalmol Sci· December 2023

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Propensity of Patient-Derived iPSCs for Retinal Differentiation: Implications for Autologous Cell Replacement.
Jessica A Cooke, Andrew P Voigt, Michael A Collingwood, Nicholas E Stone, S Scott Whitmore, Adam P DeLuca

Stem Cells Transl Med· June 2023

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Modeling rod and cone photoreceptor cell survival in vivo using optical coherence tomography.
S Scott Whitmore, Adam P DeLuca, Jeaneen L Andorf, Justine L Cheng, Mahsaw Mansoor

Sci Rep· April 2023

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AUTOIMMUNE RETINOPATHY MIMICKING HERITABLE RETINAL DEGENERATION IN A PATIENT WITH COMMON VARIABLE IMMUNE DEFICIENCY.
Luke A Wiley, Elaine M Binkley, Adam P DeLuca, Grefachew Workalemahu, Nicole J Tatro

Retin Cases Brief Rep· January 2022

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Label-free microfluidic enrichment of cancer cells from non-cancer cells in ascites.
Nicholas E Stone, Abhishek Raj, Katherine M Young, Adam P DeLuca, Fatima Ezahra Chrit

Sci Rep· September 2021

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Human photoreceptor cells from different macular subregions have distinct transcriptional profiles.
Andrew P Voigt, Nathaniel K Mullin, S Scott Whitmore, Adam P DeLuca, Erin R Burnight

Hum Mol Genet· July 2021

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Exome-based investigation of the genetic basis of human pigmentary glaucoma.
Carly van der Heide, Wes Goar, Kacie J Meyer, Wallace L M Alward, Erin A Boese, Adam P DeLuca

BMC Genomics· June 2021

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Spectacle: An interactive resource for ocular single-cell RNA sequencing data analysis.
Andrew P Voigt, S Scott Whitmore, Nicholas D Lessing, Adam P DeLuca, Budd A Tucker

Exp Eye Res· November 2020

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Analysis of retinal sublayer thicknesses and rates of change in ABCA4-associated Stargardt disease.
S Scott Whitmore, Christopher R Fortenbach, Justine L Cheng, Adam P DeLuca, D Brice Critser

Sci Rep· October 2020

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Single-Cell RNA Sequencing in Human Retinal Degeneration Reveals Distinct Glial Cell Populations.
Andrew P Voigt, Elaine Binkley, Miles J Flamme-Wiese, Shemin Zeng, Adam P DeLuca

Cells· February 2020

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Wide-Field Swept-Source OCT and Angiography in X-Linked Retinoschisis.
Ian C Han, S Scott Whitmore, D Brice Critser, Sun Young Lee, Adam P DeLuca

Ophthalmol Retina· February 2019

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Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients.
Adam P DeLuca, Wallace L M Alward, Jeffrey Liebmann, Robert Ritch, Kazuhide Kawase

J Glaucoma· December 2017

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Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease.
Edwin M Stone, Jeaneen L Andorf, S Scott Whitmore, Adam P DeLuca, Joseph C Giacalone

Ophthalmology· September 2017

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Keeping an Eye on Bardet-Biedl Syndrome: A Comprehensive Review of the Role of Bardet-Biedl Syndrome Genes in the Eye.
Katie Weihbrecht, Wesley A Goar, Thomas Pak, Janelle E Garrison, Adam P DeLuca

Med Res Arch· September 2017

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Primary congenital and developmental glaucomas.
Carly J Lewis, Adam Hedberg-Buenz, Adam P DeLuca, Edwin M Stone, Wallace L M Alward

Hum Mol Genet· August 2017

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SQSTM1 Mutations and Glaucoma.
Todd E Scheetz, Ben R Roos, Frances Solivan-Timpe, Kathy Miller, Adam P DeLuca

PLoS One· July 2017

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cGMP production of patient-specific iPSCs and photoreceptor precursor cells to treat retinal degenerative blindness.
Luke A Wiley, Erin R Burnight, Adam P DeLuca, Kristin R Anfinson, Cathryn M Cranston

Sci Rep· July 2016

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Audioprofile Surfaces: The 21st Century Audiogram.
Kyle R Taylor, Kevin T Booth, Hela Azaiez, Christina M Sloan, Diana L Kolbe, Adam P DeLuca

Ann Otol Rhinol Laryngol· May 2016

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Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis.
Adam P DeLuca, S Scott Whitmore, Jenna Barnes, Tasneem P Sharma, Trudi A Westfall

Hum Mol Genet· January 2016

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North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13.
Kent W Small, Adam P DeLuca, S Scott Whitmore, Thomas Rosenberg, Rosemary Silva-Garcia

Ophthalmology· January 2016

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