Amara Fatima

Prioritized sequencing of the second exon of MYO15A reveals a new mutation segregating in a Pakistani family with moderate to severe hearing loss

Rasheeda Bashir, Amara Fatima, Sadaf Naz · European Journal of Medical Genetics · 2011 · 42 citations · Full text

Second Exon, Mendelian Disorder, Genetic Disorder +10

A p.C343S missense mutation in PJVK causes progressive hearing loss

Ghulam Mujtaba, Ihtisham Bukhari, Amara Fatima et al. · Gene · 2012 · 32 citations · Full text

Pathogenesis, Audiology, P.c343s Missense Mutation +5

A Novel OPA3 Mutation Revealed by Exome Sequencing

Beenish Arif, Kishore R. Kumar, Philip Seibler et al. · JAMA Neurology · 2013 · 28 citations

Mutations in CLDN14 are associated with different hearing thresholds

Rasheeda Bashir, Amara Fatima, Sadaf Naz · Journal of Human Genetics · 2010 · 15 citations · Full text

Auditory Processing, Health Sciences, Genetics +10

Amplification of GC-rich DNA for High-Throughput Family-Based Genetic Studies

Sadaf Naz, Amara Fatima · Molecular Biotechnology · 2012 · 15 citations · Full text

Gc-rich Dna, Dna Sequencing, Natural Sciences +6