Ayesha Imtiaz
Lahore, PB, Pakistan
Last Updated: 09/26/2026
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Found 16 publications
A truncated CDC14A retains catalytic structure and phosphatase activity preserving male fertility but causes nonsyndromic deafness.
Journal: The Journal of biological chemistry
Published: October 17, 2025
Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from Pakistan.
Journal: Scientific reports
Published: July 15, 2025
Taperin bundles F-actin at stereocilia pivot points enabling optimal lifelong mechanosensitivity.
Journal: The Journal of cell biology
Published: August 05, 2024
ARNSHL gene identification: past, present and future.
Journal: Molecular genetics and genomics : MGG
Published: October 26, 2021
Variants of human CLDN9 cause mild to profound hearing loss.
Journal: Human mutation
Published: August 31, 2020
TRIOBP-5 sculpts stereocilia rootlets and stiffens supporting cells enabling hearing.
Journal: JCI insight
Published: March 04, 2019
Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss.
Journal: Human mutation
Published: July 06, 2018
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
Journal: Human molecular genetics
Published: October 06, 2017
Genetic causes of moderate to severe hearing loss point to modifiers.
Journal: Clinical genetics
Published: June 30, 2016
Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness.
Journal: Human mutation
Published: March 29, 2016
Recessive mutations of TMC1 associated with moderate to severe hearing loss.
Journal: Neurogenetics
Published: January 18, 2016
A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss.
Journal: Journal of medical genetics
Published: January 16, 2015
Last Updated: 09/26/2026