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M. Estiar · SciRah

Researcher profile · Semantic Scholar

M. Estiar

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M. Estiar — researcher profile on SciRah

h-index: 21
Works: 85
Citations: 1,362

Most-cited papers

Carbon nanotubes part II: a remarkable carrier for drug and gene delivery
M. Karimi, Navid Solati, A. Ghasemi, M. Estiar +10 more
2015Expert Opinion on Drug Delivery146 citations Open access
Semantic Scholar
Carbon nanotubes part I: preparation of a novel and versatile drug-delivery vehicle
M. Karimi, Navid Solati, M. Amiri, H. Mirshekari +10 more
2015Expert Opinion on Drug Delivery113 citations Open access
Semantic Scholar
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects
L. Krohn, K. Heilbron, C. Blauwendraat, R. Reynolds +102 more
2022Nature Communications84 citations Open access
Semantic Scholar
Enrichment of SARM1 alleles encoding variants with constitutively hyperactive NADase in patients with ALS and other motor nerve disorders
J. Gilley, O. Jackson, M. Pipis, M. Estiar +18 more
2021medRxiv66 citations Open access
Semantic Scholar
Fine mapping of the HLA locus in Parkinson’s disease in Europeans
E. Yu, A. Ambati, Maren Stolp Andersen, L. Krohn +15 more
2020medRxiv60 citations Open access
Semantic Scholar
Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease
E. Yu, Uladzislau Rudakou, L. Krohn, K. Mufti +16 more
2020medRxiv46 citations Open access
Semantic Scholar
Effects of zinc supplementation on antioxidant status and lipid peroxidation in hemodialysis patients.
M. Mazani, H. Argani, N. Rashtchizadeh, A. Ghorbanihaghjo +3 more
2013Journal of renal nutrition45 citations
Semantic Scholar
siRNA-mediated silencing of survivin inhibits proliferation and enhances etoposide chemosensitivity in acute myeloid leukemia cells.
Hadi Karami, B. Baradaran, A. Esfahani, M. Estiar +3 more
2013Asian Pacific Journal of Cancer Prevention45 citations Open access
Semantic Scholar
siRNA-mediated silencing of MDR1 reverses the resistance to oxaliplatin in SW480/OxR colon cancer cells.
N. Montazami, M. K. Andish, J. Majidi, M. Yousefi +8 more
2015Cellular and Molecular Biology40 citations
Semantic Scholar
Deregulated expression of HDAC3 in colorectal cancer and its clinical significance.
M. Nemati, N. Ajami, M. Estiar, S. Rezapour +4 more
2018Advances in Clinical and Experimental Medicine38 citations Open access
Semantic Scholar
Assessment of the role of non-coding RNAs in the pathophysiology of Parkinson's disease.
Omidvar Rezaei, S. Nateghinia, M. Estiar, M. Taheri +1 more
2021European Journal of Pharmacology32 citations
Semantic Scholar
ATM in breast and brain tumors: a comprehensive review
M. Estiar, P. Mehdipour
2018Cancer Biology and Medicine31 citations Open access
Semantic Scholar
Detection of aberrant methylated SEPT9 and NTRK3 genes in sporadic colorectal cancer patients as a potential diagnostic biomarker.
Shahin Behrouz Sharif, S. Hashemzadeh, Reza Mousavi Ardehaie, A. Eftekharsadat +5 more
2016Oncology Letters28 citations Open access
Semantic Scholar
Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype
M. Estiar, Etienne Leveille, D. Spiegelman, N. Dupré +3 more
2020Molecular Genetics & Genomic Medicine27 citations Open access
Semantic Scholar
Vitamin D receptor gene polymorphisms in Iranian Azary patients with Behçet’s disease
S. Kolahi, A. Khabbazi, H. Khodadadi, M. Estiar +3 more
2015Scandinavian Journal of Rheumatology27 citations
Semantic Scholar
Evidence for Non‐Mendelian Inheritance in Spastic Paraplegia 7
M. Estiar, E. Yu, Ikhlass Haj Salem, J. Ross +16 more
2020medRxiv26 citations Open access
Semantic Scholar
Genetic, structural and clinical analysis of spastic paraplegia 4
P. Varghaei, M. Estiar, S. Ashtiani, S. Veyron +13 more
2021medRxiv25 citations Open access
Semantic Scholar
A Single Nucleotide Polymorphism in the FOXP3 Gene Associated with Behçet's Disease in an Iranian Population.
A. Hosseini, D. Shanehbandi, M. Estiar, S. Gholizadeh +4 more
2015Clinical Laboratory25 citations
Semantic Scholar
Assessing non-Mendelian Inheritance in Inherited Axonopathies
Dana M. Bis-Brewer, Z. Gan-or, P. Sleiman, Aixa Rodriguez +62 more
2020Genetics in Medicine24 citations Open access
Semantic Scholar
BiP inactivation due to loss of the deAMPylation function of FICD causes a motor neuron disease.
A. Rebelo, Ariel Ruiz, M. Dohrn, Melanie Wayand +15 more
2022Genetics in Medicine23 citations Open access
Semantic Scholar
HER2 gene amplification in patients with prostate cancer: Evaluating a CISH-based method.
Nazanin Sharifi, Arash Salmaninejad, Samira Ferdosi, Abolfazl Nesaei Bajestani +5 more
2016Oncology Letters23 citations Open access
Semantic Scholar
Variants in GNPTAB, GNPTG and NAGPA genes are associated with stutterers.
Nima Kazemi, M. Estiar, Hassan Fazilaty, E. Sakhinia
2018Gene21 citations
Semantic Scholar
STC1 and NF-κB p65 (Rel A) is Constitutively Activated in Colorectal Cancer.
S. Rezapour, Tayyeb Bahrami, S. Hashemzadeh, M. Estiar +7 more
2016Clinical Laboratory21 citations
Semantic Scholar
Inhibitor of Aurora Kinase B Induces Differentially Cell Death and Polyploidy via DNA Damage Response Pathways in Neurological Malignancy: Shedding New Light on the Challenge of Resistance to AZD1152-HQPA
A. Zekri, S. H. Ghaffari, Marjan Yaghmaie, M. Estiar +3 more
2016Molecular Neurobiology19 citations
Semantic Scholar
SPTAN1 variants as a potential cause for autosomal recessive hereditary spastic paraplegia
Etienne Leveille, M. Estiar, L. Krohn, D. Spiegelman +5 more
2019Journal of Human Genetics18 citations Open access
Semantic Scholar
TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions.
H. Hijazi, Linda M. Reis, D. Pehlivan, Jonathan A. Bernstein +34 more
2022American Journal of Human Genetics17 citations Open access
Semantic Scholar
Expression Analysis of MicroRNA-222 in Breast Cancer.
S. Amini, Atefe Abak, M. Estiar, V. Montazeri +2 more
2018Clinical Laboratory17 citations
Semantic Scholar
Clinical utility of measuring expression levels of Stanniocalcin 2 in patients with colorectal cancer
S. Hashemzadeh, A. Arabzadeh, M. Estiar, Masoud Sakhinia +4 more
2014Medical Oncology16 citations
Semantic Scholar
High expression of CEACAM19, a new member of carcinoembryonic antigen gene family, in patients with breast cancer
M. Estiar, R. Esmaeili, A. Zare, L. Farahmand +4 more
2017Clinical and Experimental Medicine (Testo stampato)14 citations
Semantic Scholar
Clinical significance of NDRG3 in patients with breast cancer.
M. Estiar, A. Zare, R. Esmaeili, L. Farahmand +4 more
2017Future Oncology14 citations
Semantic Scholar
Hereditary spastic paraplegia initially diagnosed as cerebral palsy
O. Suchowersky, S. Ashtiani, P. Au, Scott A McLeod +3 more
2021Clinical Parkinsonism & Related Disorders13 citations Open access
Semantic Scholar
Analysis of miRNA-221 Expression Level in Tumors and Marginal Biopsies from Patients with Breast Cancer (Cross-Sectional Observational Study).
Atefe Abak, S. Amini, M. Estiar, V. Montazeri +2 more
2018Clinical Laboratory13 citations
Semantic Scholar
Analysis of the Association between MDM4 rs4245739 Single Nucleotide Polymorphism and Breast Cancer Susceptibility.
Negar Pedram, N. Pouladi, M. Feizi, V. Montazeri +2 more
2016Clinical Laboratory13 citations
Semantic Scholar
Bcl-2 gene expression in human breast cancers in iran.
Leila Rostamizadeh, A. Fakhrjou, V. Montazeri, M. Estiar +4 more
2013Asian Pacific Journal of Cancer Prevention13 citations Open access
Semantic Scholar
GCH1 mutations in hereditary spastic paraplegia
P. Varghaei, G. Yoon, M. Estiar, S. Veyron +5 more
2021medRxiv12 citations Open access
Semantic Scholar
Evaluation of DNA methylation status of toll‐like receptors 2 and 4 promoters in Behcet's disease
S. Kolahi, N. Rashtchizadeh, A. M. Mahdavi, Jafar Farhadi +6 more
2020Journal of Gene Medicine12 citations
Semantic Scholar
Expression Analysis of Aurora-C and Survivin, Two Testis-Specific Genes, in Patients with Colorectal Cancer.
S. Hosseini, S. Hashemzadeh, M. Estiar, R. Ebrahimzadeh +5 more
2015Clinical Laboratory12 citations
Semantic Scholar
Lack of Causal Effects or Genetic Correlation between Restless Legs Syndrome and Parkinson’s Disease
M. Estiar, K. Senkevich, E. Yu, P. Varghaei +5 more
2021medRxiv11 citations Open access
Semantic Scholar
Genetic and Epidemiological Study of Adult Ataxia and Spastic Paraplegia in Eastern Quebec
Ikhlass Haj Salem, M. Beaudin, Monica Stumpf, M. Estiar +7 more
2021Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques11 citations Open access
Semantic Scholar
Prognostic significance of MYCN gene amplification and protein expression in primary brain tumors: Astrocytoma and meningioma
M. Estiar, F. Javan, A. Zekri, M. Mehrazin +1 more
2017Cancer Biomarkers11 citations Open access
Semantic Scholar
Molecular Characterization of KRAS, BRAF, and EGFR Genes in Cases with Prostatic Adenocarcinoma; Reporting Bioinformatics Description and Recurrent Mutations.
Arash Salmaninejad, S. Ghadami, M. Z. Dizaji, Zahra Golchehre +5 more
2015Clinical Laboratory11 citations
Semantic Scholar
Isolation and Characterization of Dental Pulp Stem Cells from Primary and Permanent Teeth
M. Samiei, Marziyeh Aghazadeh, A. Movassaghpour, A. Fallah +7 more
201311 citations
Semantic Scholar
Molecular Analysis of IGH and Incomplete IGH D-J Clonality Gene Rearrangements in Hodgkin Lymphoma Malignancies.
S. Ghorbian, I. Jahanzad, M. Estiar, Jamal Eivazi Ziae +4 more
2015Clinical Laboratory10 citations
Semantic Scholar
Fine mapping of the HLA locus in Parkinson’s disease in Europeans
E. Yu, A. Ambati, Maren Stolp Andersen, L. Krohn +15 more
2021npj Parkinson's Disease8 citations Open access
Semantic Scholar
Expression Analysis of p16, c-Myc, and mSin3A in Non-small Cell Lung Cancer by Computer Aided Scoring and Analysis (CASA).
Arash Salmaninejad, M. Estiar, R. Gill, J. Shih +6 more
2015Clinical Laboratory8 citations
Semantic Scholar
Genome-wide association study of REM sleep behavior disorder identifies novel loci with distinct polygenic and brain expression effects
L. Krohn, K. Heilbron, C. Blauwendraat, R. Reynolds +54 more
2021medRxiv6 citations Open access
Semantic Scholar
A Case of Tuberous Sclerosis Without Multiorgan Involvement
Parisa Falsafi, Ali Taghavi-Zenouz, Reza Khorshidi-Khiyavi, N. Nezami +1 more
2015Global Journal of Health Science6 citations Open access
Semantic Scholar
EEFSEC deficiency: A selenopathy with early-onset neurodegeneration
L. Laugwitz, R. Buchert, P. Olguín, M. Estiar +46 more
2025American Journal of Human Genetics5 citations Open access
Semantic Scholar
From spastic paraplegia to infantile neurodegenerative disorder: Expanding the phenotypic spectrum associated with biallelic SPAST variants
M. Degoutin, C. Angelini, C. Bar, Wahiba Amer El Khedoud +16 more
2024European Journal of Neurology5 citations Open access
Semantic Scholar
Rare PSAP Variants and Possible Interaction with GBA in REM Sleep Behavior Disorder
Y. Sosero, E. Yu, M. Estiar, L. Krohn +45 more
2021medRxiv5 citations Open access
Semantic Scholar

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