Uppala Ratnamala

Localization of a Gene for Keratoconus to a 5.6-Mb Interval on 13q32

Marzena Gajęcka, Uppala Radhakrishna, Daniel Winters et al. · Investigative Ophthalmology & Visual Science · 2009 · 114 citations · Full text

Genomewide Scan for Nonsyndromic Cleft Lip and Palate in Multigenerational Indian Families Reveals Significant Evidence of Linkage at 13q33.1-34

Uppala Radhakrishna, Uppala Ratnamala, Mathew Gaines et al. · The American Journal of Human Genetics · 2006 · 37 citations · Full text

Developmental Biology, Nonsyndromic Cleft Lip, Genetic Disorder +10

Novel homozygous, heterozygous and hemizygous FRMD7 gene mutations segregated in the same consanguineous family with congenital X-linked nystagmus

Uppala Radhakrishna, Uppala Ratnamala, Samuel Deutsch et al. · European Journal of Human Genetics · 2012 · 36 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +9

Genomewide Linkage Scan for Split–Hand/Foot Malformation with Long-Bone Deficiency in a Large Arab Family Identifies Two Novel Susceptibility Loci on Chromosomes 1q42.2-q43 and 6q14.1

Mohammed Naveed, Swapan K. Nath, Mathew Gaines et al. · The American Journal of Human Genetics · 2006 · 35 citations · Full text

Genomewide Linkage Scan, Genetic Disorder, Genetics +8

Epigenetically dysregulated genes and pathways implicated in the pathogenesis of non-syndromic high myopia

Sangeetha Vishweswaraiah, Joanna Swierkowska, Uppala Ratnamala et al. · Scientific Reports · 2019 · 35 citations · Full text