Reza Asadollahi
5PUBLICATIONS
67CO-AUTHORS
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Publications (5)
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|Oct 22, 2025
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function.Reza Asadollahi, Aisha Ahmad, Paranchai Boonsawat
|Aug 05, 2020
Severe reaction to radiotherapy provoked by hypomorphic germline mutations in ATM (ataxia-telangiectasia mutated gene).Reza Asadollahi, Christian Britschgi, Pascal Joset
|Mar 01, 2020
Applying Rogers' framework to evaluate public awareness and knowledge of medical genetics in a developing country.Hamid Asadollahi, Mahmoud Vakili, Reza Asadollahi
|Dec 16, 2018
The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study.Sorina M Papuc, Lucia Abela, Katharina Steindl
|Nov 23, 2018
Need for high-resolution Genetic Analysis in iPSC: Results and Lessons from the ForIPS Consortium.Bernt Popp, Mandy Krumbiegel, Janina Grosch
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Frequent Collaborators
3 joint publications
Anita Rauch
1 joint publications
Bernt Popp
1 joint publications
Zacharias Kohl
1 joint publications
Arif B Ekici
1 joint publications
Martin Regensburger
1 joint publications
André Reis
1 joint publications
Anaïs Begemann
1 joint publications
Michelle Seiler
1 joint publications
Detlev Schindler
1 joint publications
Mareike Lohse
