Kimia Kahrizi

24PUBLICATIONS
55CO-AUTHORS
Genetic immunologyCircuits and systemsEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesCell and nuclear division
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Publications (24)

|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

|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

|Feb 26, 2025
A Novel Candidate Gene MACF1 is Associated with Autosomal Dominant Non-syndromic Hearing Loss in an Iranian Family.

Niloofar Bazazzadegan, Mojgan Babanejad, Susan Banihashemi

|Feb 19, 2025
Unraveling the Genetic Landscape of Hearing Loss: A Comprehensive Study of Azeri Families in Ardabil, Iran.

Marzieh Mohseni, Farzane Zare Ashrafi, Ehsan Abbaspour Rodbaneh

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Frequent Collaborators

20 joint publications

Hossein Najmabadi

7 joint publications

Marzieh Mohseni

4 joint publications

Kevin Ta Booth

4 joint publications

Richard Jh Smith