Publications

The following are recent publications from the members of this lab. Click on the title of a publication to read its abstract, or follow the Pubmed ID link to view the Pubmed entry.

Therapeutic antisense oligonucleotide mitigates retinal dysfunction in a pig model of CLN3 Batten disease

Matthew Stratton, Jessica Centa, Vicki Swier, Wanda Pfeifer, Clarissa Booth, Karlee Albert, John Hunyara, Mitchell Rechtzigel, Fox Duelli, Hannah Leppert, Frank Rigo, Trisha Smit, Paymaan Jafar-Nejad, Jill Weimer, Arlene V Drack, Michelle L Hastings

Nucleic acids research Nov 11 2025
Pubmed ID: 40501755
PEDIATRIC ELECTRORETINOGRAPHY

Wanda L Pfeifer, Arlene V Drack

Genetic Diseases of the Eye Sep 12 2025
Pubmed ID:
Immune landscape in children with X-linked retinoschisis

Ying Hsu, Giulia Del Valle, Sarah Stanley, Brianna Lobeck, Sergei I Syrbu, Christine Sinkey, Christopher R Fortenbach, Alina Dumitrescu, Arlene V Drack

BMC immunology Aug 8 2025
Pubmed ID: 40781274
My child can’t see”—workup and management of children with low vision: a joint workshop of the AAPOS Low Vision Rehabilitation and Genetic Eye Diseases Committees

Lauren Ditta, Virginia Miraldi Utz, Arvind Chandna, Arlene Drack, Margaret Reynolds, Matthew Weed, Alina Dumitrescu, Melinda Y Chang

Journal of American Association for Pediatric Ophthalmology and Strabismus May 27 2025
Pubmed ID: 40441479
Splice-Switching Antisense Oligonucleotide Drug Discovery for CLN3 Batten Disease

Jessica Centa, Matthew Stratton, Vicki Swier, Wanda Pfeifer, Clarissa Booth, Karlee Albert, Mitchell Rechtzigel, Fox Duelli, Hannah Leppert, Trisha Smit, Jill Weimer, Arlene Drack, Michelle Hastings

MOLECULAR THERAPY Apr 28 2025
Pubmed ID:
Prevention of Vision Loss using Subretinal Gene Therapy in a Mouse Model of Bardet-Biedl Syndrome Type 10

Ying Hsu, Brianna Lobeck, Tyler Rankin, Sarah Stanley, Emma VandeLune, Ethan Brandauer, Joseph Laird, Salma Hassan, Neda Mokhberian, Emily Kalmanek, Izabela Klaska, Sophia Kleine Holthaus, Tassos Georgiadis, Arlene Drack

MOLECULAR THERAPY Apr 28 2025
Pubmed ID:
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders

Julie A Jurgens, Brenda J Barry, Wai-Man Chan, Sarah MacKinnon, Mary C Whitman, Paola M Matos Ruiz, Brandon M Pratt, Eleina M England, Lynn Pais, Gabrielle Lemire, Emily Groopman, Carmen Glaze, Kathryn A Russell, Moriel Singer-Berk, Silvio Alessandro Di G

Genetics in medicine Apr 1 2025
Pubmed ID: 39033378
N-Acetylcysteine Ameliorates Loss of the Electroretinogram b-wave in a Bardet-Biedl Syndrome Type 10 Mouse Model

Tyler J Rankin, Sara Mayer, Joseph G Laird, Brianna Lobeck, Emily Kalmanek, Arlene V Drack

Journal of Experimental Neurology Mar 13 2025
Pubmed ID: 41001250
Electroretinography as a Tool in Distinguishing Bardet-Biedl and Alström Syndromes in Early Childhood

Amy V Whittington, Scott R Lambert, William B Dasher, Arlene V Drack

Update on Strabismus and Pediatric Ophthalmology Proceedings of the June, 1994 Joint ISA and AAPO&S Meeting, Vancouver, Canada Dec 20 2024
Pubmed ID:
Children often present to the pediatric ophthalmologist because of a family history of eye disease. A common cause for such referrals is an autosomal dominant retinal dystrophy diagnosed in older family members. Clinical evaluation of the children in the

Arlene V Drack, Brian E Nichols, Val C Sheffield, Edwin M Stone

Update on Strabismus and Pediatric Ophthalmology Proceedings of the June, 1994 Joint ISA and AAPO&S Meeting, Vancouver, Canada Dec 20 2024
Pubmed ID:

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