Mahsa Mohammad Amoli

24PUBLICATIONS
62CO-AUTHORS
Neurology and neuromuscular diseasesMedical biochemistry - proteins and peptides (incl. medical proteomics)Peripheral nervous systemGene mappingEpigenetics (incl. genome methylation and epigenomics)
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Publications (24)

|Dec 22, 2025
DYNC1H1 in Spinal Muscular Atrophy: Diagnostic Findings From Two Families and a Comprehensive Review of Its Role in Neuromuscular and Neurodevelopmental Disorders.

Maryam Namdari, Behnaz Ansari, Keivan Basiri

|Jul 15, 2025
High Occurrence of a Missense Variant (c.471C>A) in the FGF23 Gene Related to Hyperostosis-Hyperphosphatemia Syndrome With a Possible Founder Effect.

Maryam Sedghi, Elika Esmaeilzadeh Gharehdaghi, Vahid Ziaee

|Apr 16, 2025
Complete Loss of PAX4 causes Transient Neonatal Diabetes in Humans.

James Russ-Silsby, Yunkyeong Lee, Varsha Rajesh

|Dec 23, 2024
Whole exome sequencing revealed new variants and haplotypes associated with monogenic obesity.

Morteza Gholami, Armita Kakavand Hamidi, Zeinab Naghshband

|Nov 29, 2024
Genetic research in Immunogenetics Group of Endocrinology and Metabolism Research Institute.

Saeedeh Asgarbeik, Mahsa M Amoli, Aida Vahidi

|Jul 06, 2024
Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: Unveiling 58 distinct variants in 14 genes.

Hamidreza Mianesaz, Safoura Ghalamkari, Farzaneh Abbasi

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Frequent Collaborators

4 joint publications

Mojgan Asadi

4 joint publications

Zeynab Nickhah Klashami

2 joint publications

Bagher Larijani

2 joint publications

Majid Gholamzadeh Roudbordeh