Jeaneen L. Andorf

Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease

Edwin M. Stone, Jeaneen L. Andorf, S. Scott Whitmore et al. · Ophthalmology · 2017 · 468 citations · Full text

Medicine, Genetics, Molecular Genetics +16

<i>Bbs2</i> -null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin

Darryl Nishimura, Melissa A. Fath, Robert F. Mullins et al. · Proceedings of the National Academy of Sciences · 2004 · 368 citations

Medicine, Genetics, Molecular Genetics +15

Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease

Terry A. Braun, Robert F. Mullins, Alex H. Wagner et al. · Human Molecular Genetics · 2013 · 182 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Using CRISPR-Cas9 to Generate Gene-Corrected Autologous iPSCs for the Treatment of Inherited Retinal Degeneration

Erin R. Burnight, Manav Gupta, Luke A. Wiley et al. · Molecular Therapy · 2017 · 144 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathy

Michel Michaelides, Lingkan Chen, Milam A. Brantley et al. · British Journal of Ophthalmology · 2007 · 84 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16