Ramakrishna P. Alur

Expression profiling during ocular development identifies 2 <i>Nlz</i> genes with a critical role in optic fissure closure

Jacob D. Brown, Sunit Dutta, Kapil Bharti et al. · Proceedings of the National Academy of Sciences · 2009 · 69 citations · Full text

Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRL

Lorenzo Nichols, Ramakrishna P. Alur, Elangovan Boobalan et al. · Human Mutation · 2010 · 64 citations · Full text

Nitisinone improves eye and skin pigmentation defects in a mouse model of oculocutaneous albinism

Ighovie F. Onojafe, David R. Adams, Dimitre R. Simeonov et al. · Journal of Clinical Investigation · 2011 · 57 citations · Full text

Ocular Disease, Genetics, Plasma Tyrosine Concentrations +16

A secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant coloboma

Chunqiao Liu, Sonya A. Widen, Kathleen A. Williamson et al. · Human Molecular Genetics · 2016 · 45 citations · Full text

One-year pilot study on the effects of nitisinone on melanin in patients with OCA-1B

David R. Adams, Supriya Menezes, Ramon Jauregui et al. · JCI Insight · 2019 · 34 citations · Full text