Maryam Sobhani

I am Dr. Maryam Sobhani, a graduate of Medical Genetics from Tehran University of Medical Sciences, and I have published quite a lot of articles in this field in international journals and presented some of them in international and domestic congresses. In the international book titled The Neurobiology, Physiology, and Behavior of Pain under the supervision of Professor Timothy Bennett, I collaborated and wrote the chapter on the genetic basis of pain. Currently, I am a member of EFI European Federation for Immunogenetics and EACR European Association for Cancer Research, and I was responsible for refereeing and editing several articles. My motivation to pursue genetics and bioinformatics came from my experience in different Genetics labs, so I learned the importance of collaboration and conflict management and decided to apply to university and nurture bigger career dreams.

Living in : Iran

Gender : FemaleRace : White

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Educations

Medical Genetics And GenomicsPhDTehran University of Medical Sciences2013-08-15 Iran

Supervisor's name :Mohamad.Reza Noori-Daloii

Title :

Study of molecular genetics and genetic linkage (WFS1 and WFS2 genes) in Iranian patients with Wolfram syndrome.

Work Experiences

Management of Genetic Dep

at Iranian Blood Transfusion

I am currently working in this role

Genetic counselor

at Rooyesh Institute. infert

Start : 28-Feb-2021

End : 28-Feb-2023

Conferences

Your Presentation Title :

USERN Workshop

Conference Name :The Transition from Genetics t

Iran

2017

Journal Publications

Publication Title :

Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report.First author

Journal :

BMC Medical Genomics

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Publication Title :

Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome. First author

Journal :

Endocrine

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Publication Title :

Homozygosity mapping and direct sequencing identify a novel pathogenic variant in the CISD2 gene in an Iranian Wolfram syndrome familySecond author

Journal :

Acta Diabetologica

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Publication Title :

The first case report of a patient with trisomy 4p and monosomy 10qFirst author

Journal :

Archives of Iranian Medicine

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Publication Title :

A new mutation in NTRK1 gene is associated with congenital insensitivity to pain without anhidrosisThird author

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Publication Title :

Significant expressivity of Wolfram syndrome: report of a novel mutation and phenotypic assessment of two known mutations in the WFS1 gene in the Iranian patients.First author

Journal :

Molecular Biology Reports

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Research Keywords

Genetics

molecular

Awards

First Rank Student in UniversityPHD

References

Mohamad Reza Noori-Daloii

nooridaloii@sina.tums.ac.ir

Abdol-Mohammad Kajbafzadeh

kajbafzd@sina.tums.ac.ir

Hassan Vahidnezhad

hxv006@jefferson.edu