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Cureus|August 1, 2022
A Rare Case of Horseshoe Kidney With Multiple Atrial Myxomas Presenting as Cerebrovascular AccidentAndrea Marin, Ankita Prasad, Sharon Hechter, et al.
The Journal of Biological Chemistry|November 27, 2025
A truncated CDC14A retains catalytic structure and phosphatase activity preserving male fertility but causes nonsyndromic deafnessKanwal Shabbir, Gina Jackisch, Inna A Belyantseva, et al.
BMC Pediatrics|May 2, 2025
Diagnostic accuracy of visual triage checklist in early recognition of COVID-19 cases in the pediatric population: A retrospective cohort studyAyesha Imtiaz, Abdullah Y Akkam, Lulwah H AlThumali, et al.
Plos One|June 20, 2024
Exploring the effects of noise pollution on physiology and ptilochronology of birdsRida Amjad, Tahira Ruby, Kashif Ali, et al.
Clinical Genetics|August 31, 2016
Genetic causes of moderate to severe hearing loss point to modifiersSadaf Naz, Ayesha Imtiaz, Ghulam Mujtaba, et al.
Human Mutation|July 5, 2016
Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human DeafnessAtteeq U Rehman, Jonathan E Bird, Rabia Faridi, et al.
Human Mutation|July 15, 2021
Variants of human CLDN9 cause mild to profound hearing lossMemoona Ramzan, Christophe Philippe, Inna A Belyantseva, et al.
JCI Insight|June 21, 2019
TRIOBP-5 sculpts stereocilia rootlets and stiffens supporting cells enabling hearingTatsuya Katsuno, Inna A Belyantseva, Alexander X Cartagena-Rivera, et al.
Scientific Reports|May 5, 2026
Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from PakistanMemoona Ramzan, Hafiza Idrees, Hina Khan, et al.
Human Mutation|October 11, 2018
Global genetic insight contributed by consanguineous Pakistani families segregating hearing lossElodie M Richard, Regie Lyn P Santos-Cortez, Rabia Faridi, et al.
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