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List of works by Hanan M Fathy

A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome

scientific article

ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling

scientific article published on 8 July 2013

Exome sequencing reveals cubilin mutation as a single-gene cause of proteinuria

scientific article

IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype.

scientific article

Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome ⬇️

article

Mutations of IFT81, encoding an IFT-B core protein, as a rare cause of a ciliopathy.

scientific article published on 13 July 2015

Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis

scientific article published on 8 September 2017

Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies

scientific article

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