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M

Mahsa M. Amoli

tehran university of medical sciences

31H指数
256论文数
3.6K被引数
收录论文 36
发表时间
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DYNC1H1 in Spinal Muscular Atrophy: Diagnostic Findings From Two Families and a Comprehensive Review of Its Role in Neuromuscular and Neurodevelopmental DisordersDYNC1H1基因在脊髓性肌萎缩症中的诊断发现：来自两个家庭的病例及对其在神经肌肉和神经发育障碍中作用的全面综述
errMolecular Genetics & Genomic Medicine
IF1.6
err2025-12-22
err0
errOAAI
errNamdari, Maryam; Ansari, Behnaz; Basiri, Keivan; Azimi, Elham Sadat; Hosseinzadeh, Majid; Bahreini, Amir; Nouri, Narges; Sedghi, Maryam; Fattahpur, Shirin; Amoli, Mahsa M.; Tajsharghi, Homa
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Applications of Danio rerio as a model for studying NAFLD and NASH斑马鱼（Danio rerio）作为研究非酒精性脂肪肝（NAFLD）和非酒精性脂肪性肝炎（NASH）的模型应用
errJournal of Diabetes and Metabolic Disorders
IF1.6
err2025-12-20
err0
PREAI
errRafizadeh, Melika; Khazaei-Poul, Yalda; Mohammadi, Hassan; Khorramizadeh, Mohammadreza; M.Amoli, Mahsa; Larijani, Bagher; Ziai, Seyed Ali
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Neonatal diabetes mellitus is a significant feature of COXPD-24 caused by recessive NARS2 variants新生儿糖尿病是因隐性NARS2变异引起的COXPD-24的一个显著特征。
errDiabetic Medicine
IF3.4
err2025-08-31
err0
errOAAI
errRussell Donis; Matthew N. Wakeling; Nicola Jeffery; Molly Govier; Matthew B. Johnson; Samar Sabir Hassan; Mohammed Ahmed Abdullah; Khadiga Yehia Elsayed Eltonbary; Nima Parvaneh; Mahsa M. Amoli; Farzaneh Abbasi; Selin Elmaoğulları; Semra Çetinkaya; Kubra Gunes; Meltem Tayfun; Hanieh Yaghootkar; Andrew T. Hattersley; Sarah E. Flanagan; Elisa De Franco
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Complete loss of PAX4 causes transient neonatal diabetes in humansPAX4的完全缺失会导致人类一过性新生儿糖尿病
errMolecular Metabolism
IF6.6
err2025-07-02
err0
errOAAI
errJames Russ-Silsby; Yunkyeong Lee; Varsha Rajesh; Mahsa Amoli; Nasser Ali Mirhosseini; Tushar Godbole; Matthew B. Johnson; D. Evelyn Ibarra; Han Sun; Nicole A.J. Krentz; Matthew N. Wakeling; Sarah E. Flanagan; Andrew T. Hattersley; Anna L. Gloyn; Elisa De Franco
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High Occurrence of a Missense Variant (c.471C>A) in the FGF23 Gene Related to Hyperostosis-Hyperphosphatemia Syndrome With a Possible Founder Effect
errHUMAN MUTATION
IF3.7
err2025-02-17
err0
errOAAI
errSedghi, Maryam; Gharehdaghi, Elika Esmaeilzadeh; Ziaee, Vahid; Abbasi, Farzaneh; Meybodi, Hamid Reza Aghaei; Smailey, Elina; Mehdizadeh, Mehrzad; Raeeskarami, Seyyed Reza; Aslani, Nahid; Shiran, Sahar Naderi; Vafadar, Mehdi; Amoli, Mahsa M.
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A homozygous TARS2 variant is a novel cause of syndromic neonatal diabetes纯合子TARS2变异是新生儿糖尿病综合征的新原因
errDIABETIC MEDICINE
IF3.4
err2024-11-07
err0
errOAAI
errDonis, Russell; Patel, Kashyap A.; Wakeling, Matthew N.; Johnson, Matthew B.; Amoli, Masha M.; Yildiz, Melek; Akcay, Teoman; Aspi, Irani; Yong, James; Yaghootkar, Hanieh; Weedon, Michael N.; Hattersley, Andrew T.; Flanagan, Sarah E.; De Franco, Elisa
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Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: Unveiling 58 distinct variants in 14 genes
errJOURNAL OF DIABETES INVESTIGATION
IF3
err2024-07-06
err0
errOAAI
errMianesaz, Hamidreza; Ghalamkari, Safoura; Abbasi, Farzaneh; Razzaghy-Azar, Maryam; Sayarifard, Fatemeh; Vakili, Rahim; Sedghi, Maryam; Asl, Samaneh Noroozi; Hosseini, Sousan; Amoli, Mahsa M.; Yaghootkar, Hanieh
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PTEN promoter methylation and expression in endometrial cancer tissues
errEPIGENOMICS
IF2.6
err2023-06-21
err4
PREAI
errKhatami, Fatemeh; Shahriari, Shadab; Aminimoghaddam, Soheila; Klashami, Zeynab Nickhah; Farahani, Maryam Shahrabi; Teimoori-Toolabi, Ladan; Amoli, Mahsa M.; Asadi, Mojgan; Rashidi, Batool Hossein
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Metformin and long non-coding RNAs in breast cancer
errJOURNAL OF TRANSLATIONAL MEDICINE
IF7.5
err2023-02-27
err11
errOAAI
errGholami, Morteza; Klashami, Zeynab Nickhah; Ebrahimi, Pirooz; Mahboobipour, Amir Ali; Farid, Amir Salehi; Vahidi, Aida; Zoughi, Marziyeh; Asadi, Mojgan; Amoli, Mahsa M.
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Haplotypic variants of COVID-19 related genes are associated with blood pressure and metabolites levels
errJOURNAL OF MEDICAL VIROLOGY
IF4.6
err2022-12-08
err1
errOAAI
errGholami, Morteza; Zoughi, Marziyeh; Hasanzad, Mandana; Larijani, Bagher; Amoli, Mahsa M.
err分享
err收藏
The role of inflammatory miRNA-mRNA interactions in PBMCs of colorectal cancer and obesity patients
errIMMUNITY INFLAMMATION AND DISEASE
IF2.7
err2022-10-27
err2
errOAAI
errGholami, Morteza; Zoughi, Marziyeh; Larijani, Bagher; Abdollahzadeh, Rasoul; Taslimi, Reza; Rahmani, Zeinab; Kazemeini, Alireza; Behboo, Roobic; Razi, Farideh; Bastami, Milad; Hasani-Ranjbar, Shirin; Amoli, Mahsa M.
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Role of genetic polymorphisms in recurrent aphthous stomatitis: A systematic review and meta-analysis
errCYTOKINE
IF3.7
err2022-05-01
err4
PREAI
errYousefi, Hila; Gholami, Morteza; Zoughi, Marziyeh; Rezaei, Nima; Chuppani, Aria; Nikfar, Shekoufeh; Amoli, Mahsa M.
err分享
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Differentially expressed miR-152, a potential biomarker for in-stent restenosis (ISR) in peripheral blood mononuclear cells (PBMCs) of coronary artery disease (CAD) patients
errNUTRITION METABOLISM AND CARDIOVASCULAR DISEASES
IF3.7
err2021-04-01
err8
PREAI
errMaheronnaghsh, M.; Niktab, I.; Enayati, S.; Amoli, M. M.; Hosseini, S. K.; Tavakkoly-Bazzaz, J.
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Letter to the editor: Association between α-adducin rs4961 polymorphism and hypertension: A meta-analysis based on 40 432 subjects
errJOURNAL OF CELLULAR BIOCHEMISTRY
IF2.8
err2020-01-13
err0
PREAI
errGholami, Morteza; Amoli, Mahsa M.; Sharifi, Farshad
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err收藏
Comments on and assessments of 'Associations between FCGR polymorphisms and immune thrombocytopenia: A meta-analysis'
errSCANDINAVIAN JOURNAL OF IMMUNOLOGY
IF1.6
err2019-11-19
err2
errOAAI
errGholami, Morteza; Amoli, Mahsa M.; Sharifi, Farshad
err分享
err收藏
Comments on and assessments of 'Associations between endothelial nitric oxide synthase gene polymorphisms and the risk of coronary artery disease: A systematic review and meta-analysis of 132 case-control studies'
errEUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY
IF7.5
err2019-08-06
err1
errOAAI
errGholami, Morteza; Amoli, Mahsa M.; Sharifi, Farshad; Khoshnevisan, Kamyar
err分享
err收藏
Overall corrections and assessments of Correlations between TLR polymorphisms and inflammatory bowel disease: a meta-analysis of 49 case-control studies
errIMMUNOLOGIC RESEARCH
IF3.1
err2019-07-27
err3
PREAI
errGholami, Morteza; Amoli, Mahsa M.; Sharifi, Farshad
err分享
err收藏
Type 1 diabetes genetic risk score discriminates between monogenic and Type 1 diabetes in children diagnosed at the age of <5 years in the Iranian population
errDIABETIC MEDICINE
IF3.4
err2019-07-25
err14
errOAAI
errYaghootkar, H.; Abbasi, F.; Ghaemi, N.; Rabbani, A.; Wakeling, M. N.; Eshraghi, P.; Enayati, S.; Vakili, S.; Heidari, S.; Patel, K.; Sayarifard, F.; Borhan-Dayani, S.; McDonald, T. J.; Ellard, S.; Hattersley, A. T.; Amoli, M. M.; Vakili, R.; Colclough, K.
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MIF 173 G > C variation was associated with depressive disorder in type 2 diabetes in an Iranian population
errPSYCHONEUROENDOCRINOLOGY
IF3.6
err2019-06-01
err10
PREAI
errHamidi, Armita Kakavand; Arzaghi, Seyed Masoud; Qorbani, Mostafa; Khatami, Fatemeh; Ebrahimi, Mehdi; Bandarian, Fatemeh; Enayati, Samaneh; Amolia, Mahsa M.
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Circulating ctDNA methylation quantification of two DNA methyl transferases in papillary thyroid carcinoma
errJOURNAL OF CELLULAR BIOCHEMISTRY
IF2.8
err2019-05-24
err12
PREAI
errKhatami, Fatemeh; Teimoori-Toolabi, Ladan; Heshmat, Ramin; Nasiri, Shirzad; Saffar, Hiva; Mohammadamoli, Mahsa; Aghdam, Mohammad Haddadi; Larijani, Bagher; Tavangar, Seyed Mohammad
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研究方向

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合作学者
合作期刊
A
Andrew T. Hattersley
H 指数: 161 · 论文数: 1.3K
S
Sian Ellard
H 指数: 118 · 论文数: 918
N
Nima Rezaei
H 指数: 116 · 论文数: 2.2K
B
Bagher Larijani
H 指数: 105 · 论文数: 2.1K
M
Margitta Worm
H 指数: 99 · 论文数: 1.1K
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