Ali Rashidi-Nezhad

5PUBLICATIONS
10CO-AUTHORS
NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Cellular nervous system
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Publications (5)

|May 25, 2026
Identification of a putative founder effect involving the HACE1:c.1396C>T variant in two Iranian families and review of reported cases.

|Jan 26, 2024
Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies.

Parisa Vaseghi, Laleh Habibi, Julie A Neidich

|Oct 12, 2023
The challenges in the interpretation of genetic variants detected by genomics techniques in patients with congenital anomalies.

Hajar Vaseghi, Seyed Mohammad Akrami, Ali Rashidi-Nezhad

|Sep 20, 2022
Exploring the genetic etiology of drug-resistant epilepsy: incorporation of exome sequencing into practice.

Mojdeh Mahdiannasser, Ali Rashidi-Nezhad, Reza Shervin Badv

|Apr 01, 2022
CEP104 gene may involve in the pathogenesis of a new developmental disorder other than joubert syndrome.

Reza Shervin Badv, Mojdeh Mahdiannasser, Maryam Rasoulinezhad

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Frequent Collaborators

2 joint publications

Reza Shervin Badv

2 joint publications

Mojdeh Mahdiannasser

2 joint publications

Seyed Mohammad Akrami

1 joint publications

Maryam Rasoulinezhad