Babak Emamalizadeh

6PUBLICATIONS
2CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Electrochemical energy storage and conversionDevelopmental genetics (incl. sex determination)
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Publications (6)

|Jul 19, 2022
A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis.

Yousef Daneshmandpour, Zahra Bahmanpour, Somayeh Kazeminasab

|May 21, 2021
Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations.

Babak Emamalizadeh, Yousef Daneshmandpour, Somayeh Kazeminasb

|Sep 14, 2020
A novel splice site mutation in the SDCCAG8 gene in an Iranian family with Bardet-Biedl syndrome.

Zahra Bahmanpour, Yousef Daneshmandpour, Somayeh Kazeminasab

|Oct 15, 2019
Tips for improving the quality and quantity of the extracted DNA from exhaled breath condensate samples.

Somayeh Kazeminasab, Babak Emamalizadeh, Vahid Jouyban-Gharamaleki

|Feb 02, 2019
Features, genetics and their correlation in Jalili syndrome: a systematic review.

Yousef Daneshmandpour, Hossein Darvish, Fariba Pashazadeh

|Jun 04, 2018
RIT2: responsible and susceptible gene for neurological and psychiatric disorders.

Yousef Daneshmandpour, Hossein Darvish, Babak Emamalizadeh

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