Publications by authors named "Jeremy Hoffmann"

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MACULAR ATROPHY AND PHENOTYPIC VARIABILITY IN AUTOSOMAL DOMINANT STARGARDT-LIKE MACULAR DYSTROPHY DUE TO PROM1 MUTATION.
Aaron M Ricca, Ian C Han, Jeremy Hoffmann, Edwin M Stone, Elliott H Sohn

Retina· July 2023

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Long-term functional and structural outcomes in X-linked retinoschisis: implications for clinical trials.
Beau J Fenner, Jonathan F Russell, Arlene V Drack, Alina V Dumitrescu, Elliott H Sohn, Jeremy M Hoffmann

Front Med (Lausanne)· June 2023

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Intrafamilial Variability of Ocular Manifestations of von Hippel-Lindau Disease.
Randy Christopher Bowen, H Culver Boldt, Robert F Mullins, Matthew G Field, Louisa M Affatigato, Jeremy M Hoffmann

Ophthalmol Retina· January 2022

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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, Jeremy M Hoffmann

Sci Rep· October 2020

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Using CRISPR-Cas9 to Generate Gene-Corrected Autologous iPSCs for the Treatment of Inherited Retinal Degeneration.
Erin R Burnight, Manav Gupta, Luke A Wiley, Kristin R Anfinson, Audrey Tran, Jeremy M Hoffmann

Mol Ther· September 2017

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Comparison of drusen and modifying genes in autosomal dominant radial drusen and age-related macular degeneration.
Elliott H Sohn, Kai Wang, Stewart Thompson, Megan J Riker, Jeremy M Hoffmann

Retina· January 2015

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Human photoreceptor outer segments shorten during light adaptation.
Michael D Abràmoff, Robert F Mullins, Kyungmoo Lee, Jeremy M Hoffmann, Milan Sonka

Invest Ophthalmol Vis Sci· May 2013

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Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosa.
Budd A Tucker, Todd E Scheetz, Robert F Mullins, Adam P DeLuca, Jeremy M Hoffmann

Proc Natl Acad Sci U S A· August 2011

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