Alireza Pasdar

Research output

Research output per year 2002 2017 2019 2020 2021 2023

• 88 Article
• 14 Review article
• 8 Abstract
• 5 Other
• 1 More
  • 1 Chapter

Research output per year

Research output per year

Search results

• 2023

  Association between the rs2241883 polymorphism of the fatty acid-binding protein-1 (FABP1) gene and obesity in a population of MASHAD study cohort

  Valizadeh, M., Aghasizadeh, M., Shaghi, F., Moradi, A., Afshari, H. S. T., Zare-Feyzabadi, R., Saberi-Karimian, M., Hashemi, M., Doust, F. N. S., Nematy, M., Bahre, E. A., Aghaei-Bakhtiari, S. H., Ghazizadeh, H., Safarian-Bana, H., Shabani, N., Esmaily, H., Ferns, G. A., Pasdar, A. & Ghayour-Mobarhan, M., Jul 2023, In: Molecular Genetics and Genomic Medicine. 11, 7, 8 p., e2173.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • Fatty Acid-Binding Proteins 100%
  • Heart Diseases 62%
  • Obesity 53%
  • Stroke 52%
  • Cohort Studies 52%
  1 Downloads (Pure)

• Genetic architecture of mammographic density as a risk factor for breast cancer: a systematic review

  Khorshid Shamshiri, A., Alidoust, M., Hemmati Nokandei, M., Pasdar, A. & Afzaljavan, F., 1 Jun 2023, In: Clinical and Translational Oncology. 25, 6, p. 1729-1747 19 p.

  Research output: Contribution to journal › Review article › peer-review

  • Breast Density 100%
  • Systematic Reviews 53%
  • Breast Neoplasms 46%
  • Genes 29%
  • Mammography 22%
  1 Citation (Scopus)

• The association of paraoxonase 1 activities, serum mRNA expression and polymorphisms with in-stent coronary restenosis; a case-control study

  Soflaei, S. S., Baktashian, M., Saberi-Karimian, M., Esmaily, H., Moohebati, M., Ebrahimi, M., Gholoobi, A., Hashemi, S. M., Ghazizadeh, H., Ferns, G. A., Salehi, M., Pasdar, A. & Ghayour-Mobarhan, M., Jun 2023, In: Gene Reports. 31, 101773.

  Research output: Contribution to journal › Article › peer-review

  • Coronary Restenosis 100%
  • Aryldialkylphosphatase 90%
  • Stents 58%
  • Case-Control Studies 54%
  • Messenger RNA 38%

• Genetic contribution of caspase-8 variants and haplotypes to breast cancer risk and prognosis: a case-control study in Iran

  Afzaljavan, F., Vahednia, E., Barati Bagherabad, M., Vakili, F., Moezzi, A., Hosseini, A., Homaei Shandiz, F., Kooshyar, M. M., Nassiri, M. & Pasdar, A., 4 Apr 2023, In: BMC Medical Genomics. 16, 1, 72.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • Caspase 8 100%
  • Iran 84%
  • Haplotypes 81%
  • Case-Control Studies 69%
  • Breast Neoplasms 55%
  1 Citation (Scopus)

• A novel electrochemical biosensor based on signal amplification of Au HFGNs/PnBA-MXene nanocomposite for the detection of miRNA-122 as a biomarker of breast cancer

  Ranjbari, S., Rezayi, M., Arefinia, R., Aghaee-Bakhtiari, S. H., Hatamluyi, B. & Pasdar, A., 1 Apr 2023, In: Talanta. 255, 124247.

  Research output: Contribution to journal › Article › peer-review

  • Biological Marker 100%
  • Nanocomposite 72%
  • MicroRNA 34%
  • Single-Stranded DNA 29%
  • Acrylate 12%
  14 Citations (Scopus)

• Evaluation of osteogenic induction potency of miR-27a-3p in adipose tissue-derived human mesenchymal stem cells (AD-hMSCs)

  Arab, F., Aghaee Bakhtiari, S. H., Pasdar, A. & Saburi, E., Feb 2023, In: Molecular Biology Reports. 50, 2, p. 1281-1291 11 p.

  Research output: Contribution to journal › Article › peer-review

  • Mesenchymal Stem Cells 100%
  • Bone and Bones 66%
  • Osteocalcin 52%
  • Osteonectin 46%
  • Osteoblasts 30%
  4 Citations (Scopus)

• Investigating the inflammatory status in the patients candidate for second angiography after coronary stent implantation

  Soflaei, S. S., Saberi-Karimian, M., Baktashian, M., Tajfard, M., Alimi, H., Tayefi, M., Moohebati, M., Ebrahimi, M., Kosari, N., Dehghani, M., Esmaily, H., Hashemi, S. M., Ferns, G. A., Salehi, M., Pasdar, A. & Ghayour-Mobarhan, M., 2023, In: Acta Cardiologica. 78, 1, p. 80-85 6 p.

  Research output: Contribution to journal › Article › peer-review

  • Coronary Angiography 100%
  • Stents 87%
  • Coronary Artery Disease 67%
  • C-Reactive Protein 53%
  • Intercellular Signaling Peptides and Proteins 49%
  2 Citations (Scopus)
• 2022

  Genetic Basis of Stroke in Iran: A Systematic Review and meta-analysis

  Afzaljavan, F., Khorshid Shamshiri, A., Eslami, A., Ashari, R. & Pasdar, A., 1 Dec 2022, In: Human Gene. 34, 11 p., 201126.

  Research output: Contribution to journal › Review article › peer-review

  • Iran 100%
  • Meta-Analysis 76%
  • Systematic Reviews 75%
  • Stroke 70%
  • Genetic Markers 11%

• A novel causative functional mutation in GATA6 gene is responsible for familial dilated cardiomyopathy as supported by in silico functional analysis

  Khazamipour, A., Gholampour-Faroji, N., Zeraati, T., Vakilian, F., Haddad-Mashadrizeh, A., Ghayour Mobarhan, M. & Pasdar, A., Dec 2022, In: Scientific Reports. 12, 13 p., 13752.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • Familial dilated cardiomyopathy 100%
  • Computer Simulation 56%
  • Mutation 33%
  • Genes 24%
  • Pedigree 21%

• Association of SMAD7 genetic markers and haplotypes with colorectal cancer risk

  Alidoust, M., Hamzehzadeh, L., Khorshid Shamshiri, A., Afzaljavan, F., Kerachian, M. A., Fanipakdel, A., Aledavood, S. A., Allahyari, A., Bari, A., Moosanen Mozaffari, H., Goshayeshi, L. & Pasdar, A., Dec 2022, In: BMC Medical Genomics. 15, 1, 9 p., 8.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • Genetic Markers 100%
  • Haplotypes 89%
  • Colorectal Neoplasms 75%
  • Single Nucleotide Polymorphism 16%
  • Genes 15%
  8 Citations (Scopus)

• The relationship between genetic variants associated with primary ovarian insufficiency and lipid profile in women recruited from MASHAD cohort study

  Mirinezhad, M. R., Ghazizadeh, H., Aghsizadeh, M., Zamiri Bidary, M., Naghipour, A., Hasanzadeh, E., Yaghooti-Khorasani, M., Ebrahimi Dabagh, A., Moghadam, M. R. S. F., Sheikh Andalibi, N., Naseri Far, Z., Esmaily, H., Ferns, G. A., Hamzehloei, T., Pasdar, A. & Ghayour-Mobarhan, M., Dec 2022, In: BMC Women's Health. 22, 12 p., 2.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • Primary Ovarian Insufficiency 100%
  • Cohort Studies 50%
  • Lipids 48%
  • Genotype 33%
  • Single Nucleotide Polymorphism 23%
  1 Citation (Scopus)

• Associação do Genótipo e Fenótipo da Paraoxonase-1 com Angiografia Positiva para Doença Arterial Coronariana

  Translated title of the contribution: Association of Paraoxonase-1 Genotype and Phenotype with Angiogram Positive Coronary Artery DiseaseSoflaei, S. S., Baktashian, M., Moghaddam, K. H., Saberi-Karimian, M., Kosari, N., Hashemi, S. M., Mouhebati, M., Amini, M., Dehghani, M., Esmaily, H., Ebrahimi, M., Falsoleiman, H., Nosrati-Tirkani, A., Sadabadi, F., Ferns, G. A., Salehi, M., Pasdar, A. & Ghayour-Mobarhan, M., 29 Aug 2022, In: Arquivos Brasileiros de Cardiologia. 119, 4, p. 593-601 9 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • Aryldialkylphosphatase 100%
  • Coronary Artery Disease 62%
  • Angiography 60%
  • Genotype 54%
  • Single Nucleotide Polymorphism 52%
  5 Citations (Scopus)

• 2q35-rs13387042 variant and the risk of breast cancer: a case–control study

  Nesaei, A., Naderi Ghale-noie, Z., Khorshid Shamshiri, A., Afzaljavan, F., Rivandi, M., Tajbakhsh, A., Homaei Shandiz, F. & Pasdar, A., 20 Apr 2022, In: Molecular Biology Reports. 49, 5, p. 3549-3557 9 p.

  Research output: Contribution to journal › Article › peer-review

  • Breast Neoplasms 100%
  • Genotype 56%
  • Genetic Background 27%
  • Genetic Markers 27%
  • Genome-Wide Association Study 27%
  1 Citation (Scopus)

• The association between a variant of the cyclin-dependent kinase inhibitor 2A/B gene and risk of cardiovascular disease

  Sadegh-Khorrami, M., Hatami, H., Bakhshani, A., Bagherikashouk, S., Sadabadi, F., Ghazizadeh, H., Amerizadeh, F., Esmaeily, H., Moohebati, M., Heidari-Bakavoli, A., Ferns, G. A., Pasdar, A., Ghayour-Mobarhan, M. & Avan, A., Mar 2022, In: Gene Reports. 26, 101480.

  Research output: Contribution to journal › Article › peer-review

  • Cyclin-Dependent Kinase Inhibitor p16 100%
  • Cardiovascular Diseases 49%
  • Genotype 29%
  • Genes 27%
  • Heart Diseases 22%

• SARS-CoV-2 Liability: The Hidden Mystery Behind Its Presentation in Children

  Esfehani, R. J., Aelami, M. H., Kalat, A. R., Soleimanpour, S., Pasdar, Z., Khazaei, M., Pasdar, A. & Avan, A., 8 Feb 2022, Advances in Experimental Medicine and Biology. Springer, Vol. 1353. p. 225-241 17 p. (Advances in experimental medicine and biology).

  Research output: Chapter in Book/Report/Conference proceeding › Chapter

  • SARS Virus 100%
  • Coronavirus 85%
  • Child 29%
  • Pediatrics 21%
  • Disease Susceptibility 15%

• A Genetic Variant in Proline and Serine Rich Coiled-Coil 1 Gene Is Associated with the Risk of Cardiovascular Disease

  Khorrami, M. S., Sadabadi, F., Pasdar, A., Safarian-Bana, H., Amerizadeh, F., Esmaeily, H., Moohebati, M., Heidari-Bakavoli, A., Ferns, G., Ghayour-Mobarhan, M. & Avan, A., 7 Feb 2022, In: Reports of Biochemistry and Molecular Biology. 10, 4, p. 653-663 11 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • Proline 100%
  • Serine 91%
  • Low-Density Lipoprotein Cholesterol 74%
  • Cardiovascular Diseases 68%
  • Genotype 67%
• 2021

  Whole exome sequencing in 17 consanguineous Iranian pedigrees expands the mutational spectrum of inherited retinal dystrophies

  Rehman, A. U., Sepahi, N., Bedoni, N., Ravesh, Z., Salmaninejad, A., Cancellieri, F., Peter, V. G., Quinodoz, M., Mojarrad, M., Pasdar, A., Asad, A. G., Ghalamkari, S., Piran, M., Piran, M., Superti-Furga, A. & Rivolta, C., 1 Dec 2021, In: Scientific Reports. 11, 1, 9 p., 19332.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • Retinal Dystrophies 100%
  • Whole Exome Sequencing 83%
  • Pedigree 76%
  • Inheritance Patterns 22%
  • High-Throughput Nucleotide Sequencing 16%
  2 Citations (Scopus)

  3 Downloads (Pure)

• The significant role of a functional polymorphism in the NF-κB1 gene in breast cancer: evidence from an Iranian cohort

  Alidoust, M., Shamshiri, A. K., Tajbakhsh, A., Gheibihayat, S. M., Mazloom, S. M., Alizadeh, F. & Pasdar, A., Dec 2021, In: Future Oncology. 17, 35, p. 4895-4905 11 p.

  Research output: Contribution to journal › Article › peer-review

  • Breast Neoplasms 100%
  • Genes 63%
  • Genome-Wide Association Study 27%
  • Genetic Predisposition to Disease 26%
  • Iran 25%
  2 Citations (Scopus)

• Secondary findings from whole-exome sequencing data in families with familial combined hyperlipidemia (FCHL)

  Zakeri, M., Safaiee, M. S., Taheri, F., Taghizadeh, E., Ferns, G. A., Mobarhan, M. G. & Pasdar, A., 2 Nov 2021, In: Egyptian Journal of Medical Human Genetics. 22, 5 p., 79.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • Familial Combined Hyperlipidemia 100%
  • Whole Exome Sequencing 73%
  • Pedigree 11%
  • Genes 8%
  • Genome 7%
  6 Downloads (Pure)

• Association of macro-and micro-nutrients dietary intakes with rs2241883 genetic variants of FABP 1 gene in MASHAD study population

  Valizadeh, M., Aghasizadeh, M., Saberi-Karimian, M., Safari, M., Rohban, M., Bana, H. S., Zare-Feyzabadi, R., Tavakkol Afshari, H. S., Moradi, A., Ahangari, N., Hashemi, M., Nematy, M., Bahre, E. A., Aghaei-Bakhtiari, S. H., Ghazizadeh, H., Esmaily, H., Ferns, G. A., Pasdar, A. & Ghayour-Mobarhan, M., 2 Sept 2021, In: Clinical nutrition ESPEN. 45, p. 262-266 5 p.

  Research output: Contribution to journal › Article › peer-review

  • Dyslipidemias 100%
  • Nutrients 87%
  • Heart Diseases 82%
  • Stroke 69%
  • Genetic Models 45%

• A Novel Splice Site Variant in the LDLRAP1 Gene Causes Familial Hypercholesterolemia

  Ahangari, N., Sahebkar, A., Azimi-Nezhad, M., Ghazizadeh, H., Moohebati, M., Ebrahim, M., Esmaeili, H., Ferns, G. A., Pasdar, A. & Ghayour Mobarhan, M., 1 Sept 2021, In: Iranian biomedical journal. 25, 5, p. 374-379 6 p.

  Research output: Contribution to journal › Article › peer-review

  • Pravastatin 100%
  • Simvastatin 89%
  • Hyperlipoproteinemia Type II 75%
  • Disorder 52%
  • Pharmacological Metabolism 47%

• The association between a Fatty Acid Binding Protein 1 (FABP1) gene polymorphism and serum lipid abnormalities in the MASHAD cohort study

  Valizadeh, M., Aghasizadeh, M., Nemati, M., Hashemi, M., Aghaee-Bakhtiari, S. H., Zare-Feyzabadi, R., Esmaily, H., Ghazizdaeh, H., Sahebi, R., Ahangari, N., Ferns, G. A., Pasdar, A. & Ghayour-Mobarhan, M., 1 Sept 2021, In: Prostaglandins Leukotrienes and Essential Fatty Acids. 172, 6 p., 102324.

  Research output: Contribution to journal › Article › peer-review

  • Fatty Acid-Binding Proteins 100%
  • Dyslipidemias 75%
  • Fatty Acid 61%
  • Lipid 52%
  • Cohort Studies 52%
  14 Citations (Scopus)

• The impact of CYP19A1 variants and haplotypes on breast cancer risk, clinicopathological features and prognosis

  Alwan, A. M., Afzaljavan, F., Tavakol Afshari, J., Homaei Shandiz, F., Barati Bagherabad, M., Vahednia, E., Kheradmand, N. & Pasdar, A., 20 May 2021, In: Molecular genetics & genomic medicine. p. e1705 10 p., e1705.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Haplotypes 100%
  • Breast Neoplasms 67%
  • Alleles 46%
  • Menarche 25%
  • Linkage Disequilibrium 24%
  6 Citations (Scopus)

• Clinical significance of circulating tumor cell related markers in patients with epithelial ovarian cancer before and after adjuvant chemotherapy

  Yousefi, M., Rajaie, S., Keyvani, V., Bolandi, S., Hasanzadeh, M. & Pasdar, A., 18 May 2021, In: Scientific Reports. 11, 1, 10 p., 10524.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • Circulating Neoplastic Cells 100%
  • Ovarian Epithelial Carcinoma 93%
  • Adjuvant Chemotherapy 81%
  • Messenger RNA 46%
  • CA-125 Antigen 43%
  6 Citations (Scopus)

  2 Downloads (Pure)

• Age-related variation in expression of breast cancer tumour markers in Iranian patients

  Homaei Shandiz, F., Afzaljavan, F., Tajbakhsh, A., Rivadeh, M., Sharifi, N., Taghi Shakeri, M. & Pasdar, A., 1 Apr 2021, In: Middle East Journal of Cancer. 12, 2, p. 269-275 7 p.

  Research output: Contribution to journal › Article › peer-review

  • Tumor Biomarkers 100%
  • Breast Neoplasms 65%
  • human ERBB2 protein 62%
  • Progesterone Receptors 35%
  • Estrogen Receptors 31%

• Association of Interleukin-10 –592 C > A gene polymorphism with coronary artery disease: A case-control study and meta-analysis

  Ghalandari, M., Jamialahmadi, K., Nik, M. M., Pirhoushiaran, M., Mirhafez, S. R., Rooki, H., Avan, A., Ghazizadeh, H., Moohebati, M., Nohtani, M., Zaimkohan, H., Ferns, G. A., Pasdar, A. & Ghayour-Mobarhan, M., 1 Mar 2021, In: Cytokine. 139, 9 p., 155403.

  Research output: Contribution to journal › Article › peer-review

  • Interleukin-10 100%
  • Marker 98%
  • Coronary Artery Disease 92%
  • Case-Control Studies 90%
  • Meta-Analysis 83%
  1 Citation (Scopus)

• Evaluating the association between ccr5delta32 polymorphism (Rs333) and the risk of breast cancer in a cohort of Iranian population

  Tajbakhsh, A., Farjami, Z., Nesaei-Bajestani, A., Afzaljavan, F., Rivandi, M., Moezzi, A., Abedini, S., Asghari, M., Kooshyar, M. M., Homaei Shandiz, F. & Pasdar, A., 1 Mar 2021, In: Iranian Journal of Public Health. 50, 3, p. 583-591 9 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • cancer 100%
  • CCR5 Receptors 82%
  • Genotype 78%
  • Breast Neoplasms 70%
  • Population 43%
  3 Citations (Scopus)

  8 Downloads (Pure)

• Association of PICK1 and BDNF variations with increased risk of methamphetamine dependence among Iranian population: a case–control study

  Tajbakhsh, A., Alimardani, M., Asghari, M., Abedini, S., Saghafi Khadem, S., Nesaei Bajestani, A., Alipoor, F., Alidoust, M., Savardashtaki, A., Hashemian, P. & Pasdar, A., 26 Jan 2021, In: BMC Medical Genomics. 14, 1, 10 p., 27.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • Methamphetamine 100%
  • Brain-Derived Neurotrophic Factor 89%
  • Phosphotransferases 65%
  • Haplotypes 39%
  • Population 33%
  2 Citations (Scopus)

  2 Downloads (Pure)

• AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data

  Quinodoz, M., Peter, V. G., Bedoni, N., Royer Bertrand, B., Cisarova, K., Salmaninejad, A., Sepahi, N., Rodrigues, R., Piran, M., Mojarrad, M., Pasdar, A., Ghanbari Asad, A., Sousa, A. B., Coutinho Santos, L., Superti-Furga, A. & Rivolta, C., 22 Jan 2021, In: Nature Communications. 12, 1, 7 p., 518.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • sequencing 100%
  • Whole Exome Sequencing 87%
  • High-Throughput Nucleotide Sequencing 70%
  • Medical Genetics 66%
  • Marker 64%
  65 Citations (Scopus)

  3 Downloads (Pure)

• GATA3 somatic mutations are associated with clinicopathological features and expression profile in TCGA breast cancer patients

  Afzaljavan, F., Sadr, A. S., Savas, S. & Pasdar, A., 18 Jan 2021, In: Scientific Reports. 11, 1, 13 p., 1679.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • Breast Neoplasms 100%
  • Mutation 87%
  • Survival 43%
  • Neoplasms 42%
  • Interleukin-6 40%
  15 Citations (Scopus)

  3 Downloads (Pure)

• Genetic determinants of premature menopause in A Mashhad population cohort

  Mirinezhad, M. R., Khosroabadi, N., Rahpeyma, M., Khayami, R., Hashemi, S. R., Ghazizadeh, H., Ferns, G. A., Pasdar, A., Ghayour-Mobarhan, M. & Hamzehloei, T., 1 Jan 2021, In: International Journal of Fertility and Sterility. 15, 1, p. 26-33 8 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • Premature Menopause 100%
  • Alleles 26%
  • Population 24%
  • Single Nucleotide Polymorphism 22%
  • Primary Ovarian Insufficiency 12%
  6 Citations (Scopus)

  5 Downloads (Pure)
• 2020

  AutoMap: High performance homozygosity mapping using sequencing data

  Quinodoz, M., Peter, V., Bedoni, N., Bertrand, B. R., Cisarova, K., Salmaninejad, A., Sepahi, N., Rodrigues, R., Piran, M., Mojarrad, M., Pasdar, A., Asad, A., Sousa, A., Coutinho-Santos, L., Superti-Furga, A. & Rivolta, C., Dec 2020, In: European Journal of Human Genetics. 28, SUPPL 1, p. 657-657 1 p.

  Research output: Contribution to journal › Abstract › peer-review

  • Exome 100%
  • Sensitivity and Specificity 41%
  • Whole Genome Sequencing 32%
  • Information Storage and Retrieval 25%
  • Mutation 15%
  4 Citations (Scopus)

• MiR-492 as an important biomarker for early diagnosis and targeted treatment in different cancers

  Taghizadeh, E., Taheri, F., Rostami, D., Renani, P. G., Ferns, G. A., Pasdar, A. & Mobarhan, M. G., 20 Nov 2020, In: Current Cancer Therapy Reviews. 16, 4, p. 269-275 7 p.

  Research output: Contribution to journal › Review article › peer-review

  • Early Diagnosis 100%
  • Biomarkers 80%
  • Pseudogenes 78%
  • Breast Neoplasms 78%
  • Retinoblastoma 73%
  2 Citations (Scopus)

• Personalised medicine in hypercholesterolaemia: the role of pharmacogenetics in statin therapy

  Ahangari, N., Doosti, M., Mobarhan, M. G., Sahebkar, A., Ferns, G. A. & Pasdar, A., 16 Nov 2020, In: Annals of Medicine. 52, 8, p. 462-470 9 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Pharmacogenetics 100%
  • Precision Medicine 94%
  • Hypercholesterolemia 87%
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors 85%
  • Genes 35%
  14 Citations (Scopus)

• Whole exome sequencing and homozygosity mapping reveals genetic defects in consanguineous Iranian families with inherited retinal dystrophies

  Salmaninejad, A., Bedoni, N., Ravesh, Z., Quinodoz, M., Shoeibi, N., Mojarrad, M., Pasdar, A. & Rivolta, C., 10 Nov 2020, In: Scientific Reports. 10, 7 p., 19413.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • Retinal Dystrophies 100%
  • Whole Exome Sequencing 83%
  • Iran 45%
  • c-Mer Tyrosine Kinase 42%
  • Genetic Heterogeneity 27%
  9 Citations (Scopus)

  3 Downloads (Pure)

• ESR1 gene variants, haplotypes and diplotypes may influence the risk of breast cancer and mammographic density

  Shamshiri, A. K., Afzaljavan, F., Alidoust, M., Taherian, V., Vakili, F., Moezzi, A., Shandiz, F. H., Farrokh, D. & Pasdar, A., Nov 2020, In: Molecular Biology Reports. 47, p. 8367-8375 9 p.

  Research output: Contribution to journal › Article › peer-review

  • Breast Density 100%
  • Estrogen Receptor alpha 84%
  • Haplotypes 68%
  • Breast Neoplasms 46%
  • Genes 29%
  6 Citations (Scopus)

• Predictive and prognostic value of LSP1 rs3817198 in sporadic breast cancer in northeastern population of Iran

  Afzaljavan, F., Moezzi, A., Vahednia, E., Khorshid Shamshiri, A., Vakili, F., Homaei Shandiz, F. & Pasdar, A., 31 Oct 2020, In: Experimental and molecular pathology. 116, 8 p., 104514.

  Research output: Contribution to journal › Article › peer-review

  • Iran 100%
  • Breast Neoplasms 65%
  • Population 40%
  • Epigenomics 29%
  • Therapeutics 11%
  4 Citations (Scopus)

• The Dilemma of TP53 Codon 72 Polymorphism (rs1042522) and Breast Cancer Risk: A Case-Control Study and Meta-Analysis in The Iranian Population

  Afzaljavan, F., Tehrani, N. C., Rivandi, M., Ghasemian, S. Z., Vahednia, E., Khayami, R., Abavisani, M. & Pasdar, A., Sept 2020, In: Cell journal. 22, 2, p. 185-192 8 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File

  • Proline 100%
  • Arginine 97%
  • Codon 95%
  • Chain Reaction 95%
  • Mutation 82%
  5 Citations (Scopus)

  4 Downloads (Pure)

• A comparison of dietary intake between personnel of a gas processing company and a sample population of public employees from Mashhad

  Ardabili, H. M., Sheikh Andalibi, M. S., Safari, M., Khakpour, S., Tayefi, M., Moallem, S. R., Fayaz, M., Zarifian, A., Saberi-Karimian, M., Khorasanchi, Z., Pasdar, A., Ferns, G. A. & Ghayour-Mobarhan, M., 31 Aug 2020, In: Clinical nutrition ESPEN. 38, p. 124-128 5 p.

  Research output: Contribution to journal › Article › peer-review

  • Gases 100%
  • Occupational Groups 85%
  • Nutrients 80%
  • Vitamin B 6 59%
  • Niacin 58%
  2 Citations (Scopus)

• Current insights into the metastasis of epithelial ovarian cancer - hopes and hurdles

  Yousefi, M., Dehghani, S., Nosrati, R., Ghanei, M., Salmaninejad, A., Rajaie, S., Hasanzadeh, M. & Pasdar, A., Aug 2020, In: Cellular Oncology. 43, p. 515–538 24 p.

  Research output: Contribution to journal › Article › peer-review

  • Ovarian Epithelial Carcinoma 100%
  • Neoplasm Metastasis 53%
  • Ovarian Neoplasms 26%
  • Circulating Neoplastic Cells 17%
  • Neoplasms 16%
  72 Citations (Scopus)

• Genetic Testing Identifies Known and Unknown Mutations in Iranian Families with Hereditary Retinal Diseases

  Ravesh, Z., Salmaninejad, A., Sepahi, N., Rehman, A. U., Bedoni, N., Pasdar, A., Quinodoz, M., Peter, V. G., Mojarrad, M., Asad, A. G., Piran, M., Ghalamkari, S. & Rivolta, C., 30 Jun 2020, In: Investigative Ophthalmology & Visual Science. 61, 7, p. 2384 1 p.

  Research output: Contribution to journal › Abstract › peer-review

  Open Access

  • Retinal Diseases 100%
  • Genetic Testing 83%
  • Inborn Genetic Diseases 74%
  • Consanguinity 69%
  • c-Mer Tyrosine Kinase 48%

• A novel mutation in USF1 gene is associated with familial combined hyperlipidemia

  Taghizadeh, E., Mirzaei, F., Jalilian, N., Mobarhan, M. G., Ferns, G. A. & Pasdar, A., 30 Apr 2020, In: IUBMB life. 72, 4, p. 616-623 8 p.

  Research output: Contribution to journal › Article › peer-review

  • Familial Combined Hyperlipidemia 100%
  • Triglyceride 65%
  • Arginine 62%
  • Tryptophan 57%
  • Cholesterol 55%
  5 Citations (Scopus)

• Prognostic Factors Associating with Pro-oxidant-antioxidant Balance; Neutrophils to Lymphocytes Ratio, Vitamin D, Heat Shock Protein 27, and Red Cell Distribution Width

  Ghazizadeh, H., Mirinezhad, M. R., Seyedi, S. M. R., Sadabadi, F., Ahmadnezhad, M., Jaberi, N., Pasdar, A., Ferns, G. A., Esmaily, H. & Ghayour-Mobarhan, M., 3 Apr 2020, In: Archives of medical research. 51, 3, p. 261-267 7 p.

  Research output: Contribution to journal › Article › peer-review

  • HSP27 Heat-Shock Proteins 100%
  • Erythrocyte Indices 84%
  • Vitamin D 65%
  • Reactive Oxygen Species 56%
  • Neutrophils 55%
  16 Citations (Scopus)

• Association between serum cell adhesion molecules with hs-CRP, uric acid and VEGF genetic polymorphisms in subjects with metabolic syndrome

  Ghazizadeh, H., Rezaei, M., Avan, A., Fazilati, M., Pasdar, A., Tavallaie, S., Kazemi, E., Seyedi, S. M. R., Ferns, G. A., Azimi-Nezhad, M. & Ghayour-Mobarhan, M., 28 Feb 2020, In: Molecular Biology Reports. 47, 2, p. 867-875 9 p.

  Research output: Contribution to journal › Article › peer-review

  • Cell Adhesion Molecules 100%
  • Genetic Polymorphisms 94%
  • Uric Acid 91%
  • Metabolic Syndrome 82%
  • Vascular Endothelial Growth Factor A 77%
  16 Citations (Scopus)

• A novel variant in LPL gene is associated with familial combined hyperlipidemia

  Taghizadeh, E., Ghayour‐Mobarhan, M., Ferns, G. A. & Pasdar, A., 10 Jan 2020, In: BioFactors. 46, 1, p. 94-99 6 p.

  Research output: Contribution to journal › Article › peer-review

  • Familial Combined Hyperlipidemia 100%
  • Dideoxynucleotide DNA Sequencing 53%
  • Substitution Reaction 39%
  • Apolipoprotein 38%
  • Asparagine 36%
  10 Citations (Scopus)
• 2019

  Circulating exosomal miRNAs in cardiovascular disease pathogenesis: New emerging hopes

  Aghabozorgi, A. S., Ahangari, N., Eftekhaari, T. E., Torbati, P. N., Bahiraee, A., Ebrahimi, R. & Pasdar, A., Dec 2019, In: Journal of Cellular Physiology. 234, 12, p. 21796-21809

  Research output: Contribution to journal › Article › peer-review

  • Circulating MicroRNA 100%
  • MicroRNA 87%
  • Cardiovascular Diseases 51%
  • MicroRNAs 50%
  • Exosomes 42%
  48 Citations (Scopus)

• Association of caspase 8 promoter variants and haplotypes with the risk of breast cancer and its molecular profile in an Iranian population: A case‐control study

  Bagherabad, M. B., Afzaljavan, F., Vahednia, E., Rivandi, M., Vakili, F., Sadr, S. S. H., Shandiz, F. H. & Pasdar, A., Oct 2019, In: Journal of Cellular Biochemistry. 120, 10, p. 16435-16444 10 p.

  Research output: Contribution to journal › Article › peer-review

  • Caspase 8 100%
  • Apoptotic 99%
  • Cell Death 92%
  • Haplotypes 81%
  • Protective 71%
  8 Citations (Scopus)

• PD-1/PD-L1 pathway: Basic biology and role in cancer immunotherapy

  Salmaninejad, A., Valilou, S. F., Shabgah, A. G., Aslani, S., Alimardani, M., Pasdar, A. & Sahebkar, A., Oct 2019, In: Journal of Cellular Physiology. 234, 10, p. 16824-16837 14 p.

  Research output: Contribution to journal › Review article › peer-review

  • Cell Death 100%
  • Antitumor 86%
  • Biological Marker 84%
  • Immunotherapy 82%
  • Regulatory T-Lymphocytes 46%
  266 Citations (Scopus)

• The Impact of CASP8 rs10931936 and rs1045485 Polymorphisms as well as the Haplotypes on Breast Cancer Risk: A Case-Control Study

  Vahednia, E., Shandiz, F. H., Bagherabad, M. B., Moezzi, A., Afzaljavan, F., Tajbakhsh, A., Kooshyar, M. M. & Pasdar, A., Oct 2019, In: Clinical Breast Cancer. 19, 5, p. E563-E577 15 p.

  Research output: Contribution to journal › Article › peer-review

  • Caspase 8 100%
  • Haplotypes 81%
  • Case-Control Studies 69%
  • Breast Neoplasms 55%
  • Genotype 36%
  6 Citations (Scopus)

• Familial combined hyperlipidemia: An overview of the underlying molecular mechanisms and therapeutic strategies

  Taghizadeh, E., Esfehani, R. J., Sahebkar, A., Parizadeh, S. M., Rostami, D., Mirinezhad, M., Poursheikhani, A., Mobarhan, M. G. & Pasdar, A., Sept 2019, In: IUBMB life. 71, 9, p. 1221–1229 9 p.

  Research output: Contribution to journal › Article › peer-review

  • Familial Combined Hyperlipidemia 100%
  • Lipoprotein 68%
  • Clearance 50%
  • Metabolic 37%
  • Lipoproteins 29%
  30 Citations (Scopus)