Hassan Vahidnezhad

30PUBLICATIONS
143CO-AUTHORS
NeurogeneticsInfant and child healthGene expression (incl. microarray and other genome-wide approaches)Innate immunityMedical genetics (excl. cancer genetics)
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Publications (30)

|Sep 19, 2026
Zygosity-Dependent Phenotypic Spectrum of RELN-Related Disorders: 10 New Patients and Genotype-Phenotype Correlations Across 48 Kindreds.

|Aug 02, 2026
Systemic Comorbidities of Keloid and Hypertrophic Scars: A Phenome-Wide Association Study in a Multiethnic U.S. Pediatric Cohort.

|Jun 30, 2026
Longest surviving patient with a homozygous splice-altering EGFR pathogenic variant presenting with skin autoinflammation and a Bartter-like salt-losing tubulopathy.

|Feb 27, 2026
Human LFA-1 governs T cell immune surveillance of the skin.

Ahmad Yatim, Leila Youssefian, Aida Idani

|Mar 18, 2025
Clinicogenetic characterisation of SLC29A3-related syndromes: a case series, tracing ancestral variants and molecular dynamics simulation.

Sajjad Biglari, Mohammad Shahrooei, Fatemeh Vahidnezhad

|Nov 03, 2022
Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis.

Masato Ogishi, Rui Yang, Rémy Rodriguez

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Frequent Collaborators

16 joint publications

Leila Youssefian

15 joint publications

Jouni Uitto

7 joint publications

Amir Hossein Saeidian

4 joint publications

Hamidreza Mahmoudi