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Publications by Saima Riazuddin

Actin-Bundling Protein TRIOBP Forms Resilient Rootlets of Hair Cell Stereocilia Essential for Hearing

Cell
BiochemistryGeneticsMolecular Biology
2010English

FUT2 Variants Confer Susceptibility to Familial Otitis Media

American Journal of Human Genetics
Genetics
2018English

Variants in PUS7 Cause Intellectual Disability With Speech Delay, Microcephaly, Short Stature, and Aggressive Behavior

American Journal of Human Genetics
Genetics
2018English

Tricellulin Deficiency Affects Tight Junction Architecture and Cochlear Hair Cells

Journal of Clinical Investigation
Medicine
2013English

Biallelic Variants in LINGO1 Are Associated With Autosomal Recessive Intellectual Disability, Microcephaly, Speech and Motor Delay

Genetics in Medicine
MedicineGenetics
2017English

Novel and Recurrent CIB2 Variants, Associated With Nonsyndromic Deafness, Do Not Affect Calcium Buffering and Localization in Hair Cells

European Journal of Human Genetics
Genetics
2015English

Noncoding Mutations of HGF Are Associated With Nonsyndromic Hearing Loss, DFNB39

American Journal of Human Genetics
Genetics
2009English

Some Deafness-Causing Mutations Can Be Silenced With the Appropriate Gene Partner

The Scientific World Journal
BiochemistryMedicineGeneticsMolecular BiologyEnvironmental Science
2001English

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