Fatemeh Bitarafan

9PUBLICATIONS
16CO-AUTHORS
Gene and molecular therapyMetabolic medicineMicro- and nanosystemsEpigenetics (incl. genome methylation and epigenomics)Gene mapping
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Publications (9)

|Jun 18, 2024
Homozygous TREM2 c.549del; p.(Leu184Serfs*5) variant causing Nasu-Hakola disease in three siblings in a consanguineous Iraqi family: Case report and review of literature.

Naser Gilani, Fatemeh Bitarafan, Mehmet Ozaslan

|Apr 27, 2024
Biallelic NDUFA4 Deletion Causes Mitochondrial Complex IV Deficiency in a Patient with Leigh Syndrome.

Doriana Misceo, Petter Strømme, Fatemeh Bitarafan

|Nov 11, 2023
Expanding phenotype heterogeneity of NARS2 by presenting subdural hematoma and parenchymal hemorrhage.

Mehrnoosh Khodaeian, Fatemeh Bitarafan, Fatemeh Garrousi

|Dec 28, 2022
A biallelic variant in POLR2C is associated with congenital hearing loss and male infertility: Case report.

Fatemeh Bitarafan, Ehsan Razmara, Ehsan Jafarinia

|Nov 18, 2020
Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss.

Safoura Zardadi, Ehsan Razmara, Golareh Asgaritarghi

|Sep 01, 2020
Identification of novel variants in Iranian consanguineous pedigrees with nonsyndromic hearing loss by next-generation sequencing.

Fatemeh Bitarafan, Seyed Yousef Seyedena, Mahdi Mahmoudi

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Frequent Collaborators

4 joint publications

Ehsan Razmara

4 joint publications

Masoud Garshasbi

1 joint publications

Shirin Hasani-Ranjbar

1 joint publications

Hanieh-Sadat Ejtahed