Hossein Najmabadi

37PUBLICATIONS
70CO-AUTHORS
Genetic immunologyCircuits and systemsEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesAnthropological genetics
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Publications (37)

|Jul 02, 2026
Diagnostic Yield of Genome Sequencing in an Iranian Exome-Negative Autosomal-Recessive Intellectual Disability Cohort.

|Jan 09, 2026
Identification of Two Rare Variants in Iranian Families With Familial Sudden Cardiac Death.

Mahsa Tahmasebivand, Sepideh Mehvari, Fatemeh Ghodratpour

|Dec 26, 2025
Biallelic Variant in NRDC Gene in Two Siblings With Developmental Delay and Seizures.

Fatemeh Fatehi, Zeinab Ghorbanoghli, Mahdieh Kooshki

|Aug 31, 2025
Investigation of the Clinical and Genetic Spectrum of PMM2-CDG: Insights from a Family with a Novel Variant and Previous Studies.

Parnian Alagha, Tara Akhtarkhavari, Ebrahim Shokouhian

|Aug 28, 2025
FSCN1 as a Candidate Gene for Syndromic Intellectual Disability? Evidence From a Recurrent Variant in an Iranian Cohort.

Hossein Najmabadi, Tara Akhtarkhavari, Ebrahim Shokouhian

|May 18, 2025
First Iranian Family with a Novel Missense Variant in MYO9B Gene Causing Charcot-Marie-Tooth Disease.

Maryam Beheshtian, Maryam Mozaffarpour Nouri, Fatemeh Ahangari

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Frequent Collaborators

20 joint publications

Kimia Kahrizi

9 joint publications

Marzieh Mohseni

4 joint publications

Kevin Ta Booth

4 joint publications

Richard Jh Smith