Kollu N. Rao

The Transcription Factor Gene<i>FOXC1</i>Exhibits a Limited Role in Primary Congenital Glaucoma

Subhabrata Chakrabarti, Kiranpreet Kaur, Kollu N. Rao et al. · Investigative Ophthalmology & Visual Science · 2009 · 65 citations

Medicine, Genetics, Molecular Genetics +17

Variations in<i>NTF4, VAV2</i>, and<i>VAV3</i>Genes Are Not Involved with Primary Open-Angle and Primary Angle-Closure Glaucomas in an Indian Population

Kollu N. Rao, Inderjeet Kaur, Rajul Parikh et al. · Investigative Ophthalmology & Visual Science · 2010 · 41 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Ciliopathy-associated protein CEP290 modifies the severity of retinal degeneration due to loss of RPGR

Kollu N. Rao, Wei Zhang, Linjing Li et al. · Human Molecular Genetics · 2016 · 38 citations · Full text

Medicine, Genetics, Ophthalmology +16

Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma.

Kollu N. Rao, Robert Ritch, Syril K. Dorairaj et al. · PubMed · 2008 · 35 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

The carboxyl terminal mutational hotspot of the ciliary disease protein RPGRORF15 (retinitis pigmentosa GTPase regulator) is glutamylated <i>in vivo</i>

Kollu N. Rao, Manisha Anand, Hemant Khanna · Biology Open · 2016 · 35 citations · Full text

Medicine, Genetics, Molecular Biology +10