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Mohammad-Reza Ghasemi
Mohammad-Reza Ghasemi
PhD of Medical Genetics
在 sbmu.ac.ir 的电子邮件经过验证
标题
引用次数
引用次数
年份
Global burden of cardiovascular diseases and risks, 1990-2022
GA Mensah, V Fuster, CJL Murray, GA Roth, ...
Journal of the American College of Cardiology 82 (25), 2350-2473, 2023
2102023
Global, regional, and national burden of disorders affecting the nervous system, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021
JD Steinmetz, KM Seeher, N Schiess, E Nichols, B Cao, C Servili, ...
The Lancet Neurology 23 (4), 344-381, 2024
1162024
Global burden of 288 causes of death and life expectancy decomposition in 204 countries and territories and 811 subnational locations, 1990–2021: a systematic analysis for the …
M Naghavi, KL Ong, A Aali, HS Ababneh, YH Abate, C Abbafati, ...
The Lancet 403 (10440), 2100-2132, 2024
1052024
Global age-sex-specific mortality, life expectancy, and population estimates in 204 countries and territories and 811 subnational locations, 1950–2021, and the impact of the …
AE Schumacher, HH Kyu, A Aali, C Abbafati, J Abbas, ...
The Lancet 403 (10440), 1989-2056, 2024
942024
Global incidence, prevalence, years lived with disability (YLDs), disability-adjusted life-years (DALYs), and healthy life expectancy (HALE) for 371 diseases and injuries in …
AJ Ferrari, DF Santomauro, A Aali, YH Abate, C Abbafati, H Abbastabar, ...
The Lancet 403 (10440), 2133-2161, 2024
752024
Global burden and strength of evidence for 88 risk factors in 204 countries and 811 subnational locations, 1990–2021: a systematic analysis for the Global Burden of Disease …
M Brauer, GA Roth, AY Aravkin, P Zheng, KH Abate, YH Abate, C Abbafati, ...
The Lancet 403 (10440), 2162-2203, 2024
692024
Burden of disease scenarios for 204 countries and territories, 2022–2050: a forecasting analysis for the Global Burden of Disease Study 2021
SE Vollset, HS Ababneh, YH Abate, C Abbafati, R Abbasgholizadeh, ...
The Lancet 403 (10440), 2204-2256, 2024
292024
Global fertility in 204 countries and territories, 1950–2021, with forecasts to 2100: a comprehensive demographic analysis for the Global Burden of Disease Study 2021
NV Bhattacharjee, AE Schumacher, A Aali, YH Abate, R Abbasgholizadeh, ...
The Lancet 403 (10440), 2057-2099, 2024
242024
Global, regional, and national incidence of six major immune-mediated inflammatory diseases: findings from the global burden of disease study 2019
D Wu, Y Jin, Y Xing, MD Abate, M Abbasian, M Abbasi-Kangevari, ...
EClinicalMedicine 64, 2023
222023
The association of coagulation factor V (Leiden) and factor II (prothrombin) mutations with stroke
M Pirhoushiaran, MR Ghasemi, J Hami, P Zargari, PS Nezhad, ...
Iranian Red Crescent Medical Journal 16 (11), 2014
142014
Autophagy ATG16L1 rs2241880 impacts the colorectal cancer risk: a case‐control study
L Jamali, H Sadeghi, MR Ghasemi, R Mohseni, ...
Journal of Clinical Laboratory Analysis 36 (1), e24169, 2022
82022
Correlated downregulation of VDR and CYP3A4 in colorectal cancer
H Sadeghi, V Hashemnia, E Nazemalhosseini-Mojarad, MR Ghasemi, ...
Molecular Biology Reports 50 (2), 1385-1391, 2023
62023
CREB-binding protein (CREBBP) and preeclampsia: a new promising target gene
H Sadeghi, S Esmkhani, R Pirjani, M Amin-Beidokhti, M Gholami, ...
Molecular Biology Reports 48 (3), 2117-2122, 2021
62021
Temporal patterns of cancer burden in Asia, 1990–2019: a systematic examination for the Global Burden of Disease 2019 study
R Sharma, H Abbastabar, DM Abdulah, H Abidi, H Abolhassani, ...
The Lancet Regional Health-Southeast Asia 21, 2024
52024
Identification of a novel de novo mutation in the CTNNB1 gene in an Iranian patient with intellectual disability
S Dashti, S Salehpour, MR Ghasemi, H Sadeghi, M Rostami, ...
Neurological Sciences 43 (4), 2859-2863, 2022
42022
Renin-Angiotensin A1166C Polymorphism and the Rrisk of Stroke
P Zargari, MR Ghasemi, M Pirhoushiaran, V Vakili, J Hami, MT Farzadfard, ...
Journal of Cell and Molecular Research 7 (1), 32-37, 2015
22015
Extending and outlining the genotypic and phenotypic spectrum of novel mutations of NALCN gene in IHPRF1 syndrome: identifying recurrent urinary tract infection
S Tehrani Fateh, S Bagheri, H Sadeghi, S Salehpour, ...
Neurological Sciences 44 (12), 4491-4498, 2023
12023
Alopecia areata-like pattern of baldness: the most recent update and the expansion of novel phenotype and genotype in the CTNNB1 gene
A Moeinafshar, S Tehrani Fateh, H Sadeghi, P Karimzadeh, R Mirfakhraie, ...
Neurological Sciences 44 (11), 4041-4048, 2023
12023
Heterogeneous Inheritance in Autism Genes Shared Across Neurodevelopmental and Neuromuscular Disorders in Consanguineous Singlets
MR Ghasemi, H Sadeghi, F Hashemi-Gorji, R Mirfakhraie, V Gupta, ...
12022
Expanding genetic and clinical aspects of Schwartz-Jampel syndrome: A report of two cases with literature review
IE Vahed, ST Fateh, M Kamali, F Hashemi-Gorji, Z Esmaeilzadeh, ...
Molecular Genetics and Metabolism Reports 40, 101125, 2024
2024
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