Christina Chakarova
University College London(GB)
Publications by Year
Research Areas
Retinal Development and Disorders, Retinal Diseases and Treatments, Cellular transport and secretion, Connexins and lens biology, RNA regulation and disease
Most-Cited Works
- → Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait(2010)632 cited
- → A Human Homolog of Yeast Pre-mRNA Splicing Gene, PRP31, Underlies Autosomal Dominant Retinitis Pigmentosa on Chromosome 19q13.4 (RP11)(2001)330 cited
- → A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies(2009)267 cited
- → Mutations in HPRP3, a third member ofpre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa(2002)237 cited
- → EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa(2008)213 cited
- → NMNAT1 mutations cause Leber congenital amaurosis(2012)199 cited
- → Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa(2016)130 cited
- → Premature Truncation of a Novel Protein, RD3, Exhibiting Subnuclear Localization Is Associated with Retinal Degeneration(2006)120 cited
- → Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa(2009)100 cited
- → Mutant carbonic anhydrase 4 impairs pH regulation and causes retinal photoreceptor degeneration(2004)89 cited