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Afsaneh Taghipour‐Sheshdeh

Observed names: A. Taghipour-Sheshdeh, Afsaneh Taghipour Sheshdeh, Afsaneh Taghipour-Sheshdeh, Afsaneh taghipour, Taghipour Sheshdeh, Afsaneh
Institution: Griffith University
ORCID: 0000-0002-0195-6085
Observed ORCID: 0000-0002-0195-6085
OpenAlex ID: A5047093264
Expanding the molecular and clinical phenotypes of FUT8‐CDG
2020 · Bobby G. Ng, Hassan Dastsooz, et al. · Journal of Inherited Metabolic Disease · 33
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Genomic prediction for growth using a low-density SNP panel in dromedary camels
2021 · Morteza Bitaraf Sani, Javad Zare Harofte, et al. · Scientific Reports · 24
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Genetic Testing in Various Neurodevelopmental Disorders Which Manifest as Cerebral Palsy: A Case Study From Iran
2021 · Marzieh Nejabat, Soroor Inaloo, et al. · Frontiers in Pediatrics · 20
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Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing
2019 · Narges Zarepour, Mahbobeh Koohiyan, et al. · Audiology and Neurotology · 16
Identification of Candidate Genes for Pigmentation in Camels Using Genotyping-by-Sequencing
2022 · Morteza Bitaraf Sani, Javad Zare Harofte, et al. · Animals · 13
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A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family
2018 · Afsaneh Taghipour-Sheshdeh, Fatemeh Nemati-Zargaran, et al. · Genomics · 11
Investigating the association between common DRD2/ANKK1 genetic polymorphisms and schizophrenia: a meta-analysis
2021 · Parham Habibzadeh, Azim Nemati, et al. · Journal of Genetics · 9
Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder
2021 · Daniel L. Polla, Mohammad Ali Farazi Fard, et al. · Genetics in Medicine · 9
Genome-Wide Diversity, Population Structure and Demographic History of Dromedaries in the Central Desert of Iran
2020 · Morteza Bitaraf Sani, Javad Zare Harofte, et al. · Genes · 7
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SMN1 variants identified by false-positive SMA newborn screening tests: Therapeutic hurdles and functional and epidemiological solutions
2026 · Brunhilde Wirth, Joyosmita Das, et al. · The American Journal of Human Genetics · 5
Clinical relevance of zebrafish for gene variants testing. Proof-of-principle with SMN1/SMA
2025 · Brett W Stringer, Yougang Zhang, et al. · EMBO Molecular Medicine · 4
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A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family
2019 · Azam Pourahmadiyan, Paria Alipour, et al. · International Journal of Audiology · 3
Genetic analysis of Usher syndrome associated genes in Iranian pedigrees: The prominent role of MYO7A gene
2019 · Fatemeh Sadat Tabei, Seyed Sajjad Tabei, et al. · Gene Reports · 1
536PFalse-positive results in 5q-SMA newborn screening: SMN1 VUS studies in zebrafish support therapeutic decision
2025 · H. Kölbel, B. Wirth, et al. · Neuromuscular Disorders
Genetic linkage analysis of DFNB39 locus in families with autosomal recessive non-syndromic hearing loss (ARNSHL) from Khuzestan province
2017 · Narges Zarepour, Mohammad Amin Tabatabaiefar, et al. · Journal of Shahrekord University of Medical Sciences
Genetic linkage analysis of the DFNB48 and DFNB98 loci in families with Autosomal Recessive Non-Syndromic Hearing Loss (ARNSHL) from Khouzestan province
2017 · Afsaneh Taghipour Sheshdeh, Mohammad Amin Tabatabaiefar, et al. · Journal of Shahrekord University of Medical Sciences
Works count: 17
Citation count: 155
H-index: 8
I10-index: 6
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