Fatemeh Bitarafan

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 17

Top Venues

Molecular genetics & genomic medicine

European journal of clinical investigation

Genes

Journal of clinical laboratory analysis

DeNA laboratory

University of Guilan (MSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

DeNA laboratory

Iran

SENIOR MEDICAL GENETICS LABORATORY TECHNICIAN :: Human Molecular Genetics Department

Pars Hospital

Iran

SENIOR MEDICAL GENETICS LABORATORY TECHNICIAN :: Human Molecular Genetics Department

Sarem Women Hospital Laboratory

Iran

MEDICAL GENETICS LABORATORY TECHNICIAN :: Human Molecular Genetics Department

Education History

University of Guilan

Iran

MSC :: Department of Biology

Islamic Azad University Tehran Medical Sciences

Iran

BSC :: Department of Cellular and Molecular Biology

Publications

Naser Gilani, Fatemeh Bitarafan, Mehmet Ozaslan, Sarah Åsheim, Morteza Heidari, Masoud Garshasbi
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. Molecular genetics & genomic medicine 12 (6) (2024)
Naser Gilani, Fatemeh Bitarafan, Mehmet Ozaslan, Sarah Åsheim, Morteza Heidari, Masoud Garshasbi
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. Molecular genetics & genomic medicine 12 (6) (2024)
Doriana Misceo, Petter Strømme, Fatemeh Bitarafan, Maninder Singh Chawla, Ying Sheng, Sandra Monica Bach de Courtade, Lars Eide, Eirik Frengen
Biallelic NDUFA4 Deletion Causes Mitochondrial Complex IV Deficiency in a Patient with Leigh Syndrome. Genes 15 (4) (2024)
Naser Gilani, Fatemeh Bitarafan, Mehmet Ozaslan, Sarah Åsheim, Morteza Heidari, Masoud Garshasbi
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. Molecular genetics & genomic medicine 12 (6) (2024)
Doriana Misceo, Petter Strømme, Fatemeh Bitarafan, Maninder Singh Chawla, Ying Sheng, Sandra Monica Bach de Courtade, Lars Eide, Eirik Frengen
Biallelic NDUFA4 Deletion Causes Mitochondrial Complex IV Deficiency in a Patient with Leigh Syndrome. Genes 15 (4) (2024)
Doriana Misceo, Petter Strømme, Fatemeh Bitarafan, Maninder Singh Chawla, Ying Sheng, Sandra Monica Bach de Courtade, Lars Eide, Eirik Frengen
Biallelic NDUFA4 Deletion Causes Mitochondrial Complex IV Deficiency in a Patient with Leigh Syndrome. Genes 15 (4) (2024)
Doriana Misceo, Petter Strømme, Fatemeh Bitarafan, Maninder Singh Chawla, Ying Sheng, Sandra Monica Bach de Courtade, Lars Eide, Eirik Frengen
Biallelic NDUFA4 Deletion Causes Mitochondrial Complex IV Deficiency in a Patient with Leigh Syndrome. Genes 15 (4) (2024)
Fatemeh Bitarafan, Ehsan Razmara, Ehsan Jafarinia, Navid Almadani, Masoud Garshasbi
A biallelic variant in POLR2C is associated with congenital hearing loss and male infertility: Case report. European journal of clinical investigation 53 (4) (2023)
Mehrnoosh Khodaeian, Fatemeh Bitarafan, Fatemeh Garrousi, Elham Amjadi Sardehie, Neda Pak, Sareh Hosseinpour, Marjan Shakiba, Masoumeh Falah, Masoud Garshasbi, Ali Reza Tavasoli
Expanding phenotype heterogeneity of NARS2 by presenting subdural hematoma and parenchymal hemorrhage. Journal of clinical laboratory analysis (2023)
Fatemeh Bitarafan, Ehsan Razmara, Ehsan Jafarinia, Navid Almadani, Masoud Garshasbi
A biallelic variant in POLR2C is associated with congenital hearing loss and male infertility: Case report. European journal of clinical investigation 53 (4) (2023)
Fatemeh Bitarafan, Ehsan Razmara, Ehsan Jafarinia, Navid Almadani, Masoud Garshasbi
A biallelic variant in POLR2C is associated with congenital hearing loss and male infertility: Case report. European journal of clinical investigation (2022)
Fatemeh Bitarafan, Ehsan Razmara, Ehsan Jafarinia, Navid Almadani, Masoud Garshasbi
A biallelic variant in POLR2C is associated with congenital hearing loss and male infertility: Case report. European journal of clinical investigation (2022)
Fatemeh Bitarafan, Ehsan Razmara, Mehrnoosh Khodaeian, Mohammad Keramatipour, Alireza Kalhor, Ehsan Jafarinia, Masoud Garshasbi
Three Novel Variants identified in FBN1 and TGFBR2 in seven Iranian families with suspected Marfan syndrome. Molecular genetics & genomic medicine 8 (8) (2020)
Fatemeh Bitarafan, Seyed Yousef Seyedena, Mahdi Mahmoudi, Masoud Garshasbi
Identification of novel variants in Iranian consanguineous pedigrees with nonsyndromic hearing loss by next-generation sequencing. Journal of clinical laboratory analysis 34 (12) (2020)
Safoura Zardadi, Ehsan Razmara, Golareh Asgaritarghi, Ehsan Jafarinia, Fatemeh Bitarafan, Sima Rayat, Navid Almadani, Saeid Morovvati, Masoud Garshasbi
Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss. Molecular genetics & genomic medicine 8 (12) (2020)
Afrooz Sepahvand, Ehsan Razmara, Fatemeh Bitarafan, Mohammad Galehdari, Ali Reza Tavasoli, Navid Almadani, Masoud Garshasbi
A homozygote variant in the tRNA splicing endonuclease subunit 54 causes pontocerebellar hypoplasia in a consanguineous Iranian family. Molecular genetics & genomic medicine 8 (10) (2020)
Shirin Hasani-Ranjbar, Hanieh-Sadat Ejtahed, Mahsa M. Amoli, Fatemeh Bitarafan, Mostafa Qorbani, Akbar Soltani, Bahareh Yarjoo
SLC34A3 Intronic Deletion in an Iranian Kindred with Hereditary Hypophosphatemic Rickets with Hypercalciuria Journal of clinical research in pediatric endocrinology 10 (4) (2018)

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Publication Activity (10 Years)

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Fatemeh Bitarafan