Get started
Author

Fatemeh Ghodratpour

ORCID: 0000-0001-7895-4128
Observed ORCID: 0000-0001-7895-4128
OpenAlex ID: A5003742828
SARS‐CoV‐2 outbreak in Iran: The dynamics of the epidemic and evidence on two independent introductions
2021 · Zohreh Fattahi, Marzieh Mohseni, et al. · Transboundary and Emerging Diseases · 24
PDF
Evaluation of Metastasis Suppressor Genes Expression and In Vitro Anti-Cancer Effects of Zinc Oxide Nanoparticles in Human Breast Cancer Cell Lines MCF-7 and T47D
2020 · Seyed Ataollah Sadat Shandiz, Faryad Sharifian, et al. · Avicenna Journal of Medical Biotechnology · 18
Disease Waves of SARS-CoV-2 in Iran Closely Mirror Global Pandemic Trends
2022 · Zohreh Fattahi, Marzieh Mohseni, et al. · Archives of Iranian Medicine · 14
PDF
Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran
2021 · Marzieh Mohseni, Mojgan Babanejad, et al. · Clinical Genetics · 13
Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients
2024 · Sepideh Mehvari, Nahid Karimian Fathi, et al. · Clinical Genetics · 6
An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene
2023 · Marzieh Mohseni, Yusuf Mohammadi, et al. · Archives of Iranian Medicine · 6
PDF
When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS)
2020 · Marzieh Mohseni, Mojdeh Akbari, et al. · Journal of Human Genetics · 6
Improved Diagnostic Yield in Recessive Intellectual Disability Utilizing Systematic Whole Exome Sequencing Data Reanalysis
2025 · Zohreh Fattahi, Ebrahim Shokouhian, et al. · Clinical Genetics · 5
Investigation of the Clinical and Genetic Spectrum of PMM2-CDG: Insights from a Family with a Novel Variant and Previous Studies
2025 · Parnian Alagha, Tara Akhtarkhavari, et al. · Archives of Iranian Medicine · 1
PDF
Genetic Analysis of 27 Y-STR Haplotypes in 11 Iranian Ethnic Groups
2024 · Somayeh Alinaghi, Marzieh Mohseni, et al. · Archives of Iranian Medicine · 1
PDF
Implementation of an In-House Platform for Rapid Screening of SARS-CoV-2 Genome Variations
2023 · Farzane Zare Ashrafi, Marzieh Mohseni, et al. · Archives of Iranian Medicine · 1
PDF
Cytotoxic effects of Zn oxide nanoparticles against breast cancer T47D cells and NM23 gene expression
2019 · Fatemeh Ghodratpour, Fahimeh Baghbani-Arani, et al. · DOAJ (DOAJ: Directory of Open Access Journals) · 1
Genetic contributors to premature coronary artery disease identified by whole-exome sequencing
2026 · Mahsa Tahmasebivand, Kaveh Hosseini, et al. · Scientific Reports
PDF
Identification of Two Rare Variants in Iranian Families With Familial Sudden Cardiac Death
2026 · Mahsa Tahmasebivand, Sepideh Mehvari, et al. · International Journal of Genomics
PDF
Diagnostic Yield of Genome Sequencing in an Iranian Exome‐Negative Autosomal‐Recessive Intellectual Disability Cohort
2026 · Ebrahim Shokouhian, Masoumeh Moslemi, et al. · Human Mutation
Author response for "Improved Diagnostic Yield in Recessive Intellectual Disability Utilizing Systematic Whole Exome Sequencing Data Reanalysis"
2024 · Zohreh Fattahi, Ebrahim Shokouhian, et al.
Author response for "Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran"
2021 · Marzieh Mohseni, Mojgan Babanejad, et al.
Author response for "Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran"
2021 · Marzieh Mohseni, Mojgan Babanejad, et al.
Author response for "Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran"
2020 · Marzieh Mohseni, Mojgan Babanejad, et al.
Works count: 19
Citation count: 96
H-index: 6
I10-index: 4
Year
Topic
Type