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Maryam Neishabury
Observed name:
M.R. Neishabury
Institution:
University of Social Welfare and Rehabilitation Sciences
Observed institutions:
Swansea University,
University of Tabriz,
University of Social Welfare and Rehabilitation Sciences,
University of Wales
ORCID:
0000-0002-0315-529X
Observed ORCID:
0000-0002-0315-529X
OpenAlex ID:
A5069238172
Mycorrhizal colonization improves onion (Allium cepa L.) yield and water use efficiency under water deficit condition
2007
·
S. Bolandnazar
, N. Aliasgarzad
, et al.
·
Scientia Horticulturae
·
76
Spontaneous mutation, oxidative DNA damage, and the roles of base and nucleotide excision repair in the yeast Saccharomyces cerevisiae
1999
·
Andrew D. Scott
, Maryam Neishabury
, et al.
·
Yeast
·
56
PDF
Rare and unexpected mutations among Iranian beta-thalassemia patients and prenatal samples discovered by reverse-hybridization and DNA sequencing.
2002
·
Hossein Najmabadi
, Ali A Pourfathollah
, et al.
·
PubMed
·
42
The XmnI andBCL11ASingle Nucleotide Polymorphisms May Help Predict Hydroxyurea Response in Iranian β-Thalassemia Patients
2012
·
Mehdi Banan
, Hadi Bayat
, et al.
·
Hemoglobin
·
41
The Iranian Human Mutation Gene Bank: A data and sample resource for worldwide collaborative genetics research
2003
·
Hossein Najmabadi
, Maryam Neishabury
, et al.
·
Human Mutation
·
33
PDF
alpha-globin gene deletion and point mutation analysis among in Iranian patients with microcytic hypochromic anemia.
2003
·
Masoud Garshasbi
, Christian Oberkanins
, et al.
·
PubMed
·
30
Molecular Mechanisms Underlying Thalassemia Intermedia in Iran
2008
·
Maryam Neishabury
, Azita Azarkeivan
, et al.
·
Genetic Testing
·
24
High Prevalence of the −α3.7Deletion Among Thalassemia Patients in Iran
2003
·
Maryam Neishabury
, Christian Oberkanins
, et al.
·
Hemoglobin
·
24
Frequency of Positive XmnI Gγ polymorphism and coinheritance of common alpha thalassemia mutations do not show statistically significant difference between thalassemia major and intermedia cases with homozygous IVSII-1 mutation
2009
·
Maryam Neishabury
, Azita Azarkeivan
, et al.
·
Blood Cells Molecules and Diseases
·
22
The influence of the BCL11A polymorphism on the phenotype of patients with beta thalassemia could be affected by the beta globin locus control region and/or the Xmn1-HBG2 genotypic background
2013
·
Maryam Neishabury
, Fahimeh Zamani
, et al.
·
Blood Cells Molecules and Diseases
·
15
The modifying effect of Xmn1-HBG2 on thalassemic phenotype is associated with its linked elements in the beta globin locus control region, including the palindromic site at 5′HS4
2011
·
Maryam Neishabury
, Shahbaz Zamani
, et al.
·
Blood Cells Molecules and Diseases
·
14
Novel mutations in mitochondrial carrier family gene SLC25A38, causing congenital sideroblastic anemia in Iranian families, identified by whole exome sequencing
2018
·
Maghsood Mehri
, Maryam Zarin
, et al.
·
Blood Cells Molecules and Diseases
·
10
The First Case of BENTA Disease (B Cell Expansion with NF-κB and T Cell Anergy) from Iran
2021
·
Maryam Neishabury
, Azita Azarkeivan
, et al.
·
Journal of Clinical Immunology
·
7
PDF
Novel variants in Iranian individuals suspected to have inherited red blood cell disorders, including bone marrow failure syndromes
2019
·
Maryam Neishabury
, Maghsood Mehri
, et al.
·
Haematologica
·
7
PDF
A Report of 8 Cases With Hemoglobin H Disease in an Iranian Family
2010
·
Azarkeivan Azita
, Maryam Neishabury
, et al.
·
Pediatric Hematology and Oncology
·
4
Analyzing 5′HS3 and 5′HS4 LCR core regions and NF-E2 in Iranian thalassemia intermedia patients with normal or carrier status for beta-globin mutations
2011
·
Maryam Neishabury
, Azita Azarkeivan
, et al.
·
Blood Cells Molecules and Diseases
·
3
Genetic Diagnosis of Pyruvate Kinase Deficiency in Undiagnosed Iranian Patients with Severe Hemolytic Anemia, using Whole Exome Sequencing
2022
·
Jafar Mehrabi Sisakht
, Maghsood Mehri
, et al.
·
Archives of Iranian Medicine
·
2
PDF
The Impact ofXmnI-HBG2, BCL11Aand HBS1L-MYB Single Nucleotide Polymorphisms on Hb F Variation of Hematologically Normal Iranian Individuals
2016
·
Elaheh Keyhani
, Mahjoobeh Jafari Vesiehsari
, et al.
·
Hemoglobin
·
2
The Spectrum of HBB Mutations among 2315 Beta Thalassemia Patients of a Reference Clinic in Tehran-Iran
2023
·
Niloofar Bazazzadegan
, Seyedeh Sedigheh Abedini
, et al.
·
Hemoglobin
·
1
Electromobility Shift Assay Reveals Evidence in Favor of Allele-Specific Binding of RUNX1 to the 5′ Hypersensitive Site 4-Locus Control Region
2016
·
Hossein Dehghani
, Sepideh Ghobakhloo
, et al.
·
Hemoglobin
·
1
Pyruvate Kinase Deficiency: An Underdiagnosed Cause of Severe Hemolytic Anemia in Iranian Population: Insights From Whole Exome Sequencing of Four Families and Screening of a Population‐Specific Database
2025
·
Milad Rafat
, Yassin Bouraqi
, et al.
·
International Journal of Laboratory Hematology
HFE and Non- HFE Hereditary Hemochromatosis Based on Screening of 854 Individuals: 12 Years of an Iranian Experience
2024
·
Razieh Zarifian Yeganeh
, Masoumeh Akbari Kelishomi
, et al.
·
Genetic Testing and Molecular Biomarkers
Contributions of nucleotide and base excision repair to the repair of DNA oxidative base damage in Saccharomyces cerevisiae
1998
·
Maryam Neishabury
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Works count:
23
Citation count:
413
H-index:
11
I10-index:
12
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