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Metabolomics in severe traumatic brain injury: a scoping review

BMC neuroscience, 2023-10, Vol.24 (1), p.1-54, Article 54

2023

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Unraveling complex relationships between COVID-19 risk factors using machine learning based models for predicting mortality of hospitalized patients and identification of high-risk group: a large retrospective study

Frontiers in medicine, 2023-05, Vol.10, p.1170331-1170331

2023

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Beta-Thalassemia in Iran : New Insight into the Role of Genetic Admixture and Migration

TheScientificWorld, 2012-01, Vol.2012 (2012), p.1-7

2012

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Metabolomics and Biomarker Discovery in Traumatic Brain Injury

Journal of neurotrauma, 2018-08, Vol.35 (16), p.1831-1848

2018

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Metabolomic Insights into COVID-19 Severity: A Scoping Review

Metabolites, 2024-11, Vol.14 (11), p.617

2024

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Metabolomics: Applications and Promise in Mycobacterial Disease

Annals of the American Thoracic Society, 2015-09, Vol.12 (9), p.1278-1287

2015

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An A10398G mitochondrial DNA alteration is related to increased risk of breast cancer, and associates with Her2 positive receptor

Mitochondrial DNA. Part A. DNA mapping, sequencing, and analysis, 2020-01, Vol.31 (1), p.11-16

2020

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Reply: Metabolomics and Mycobacterial Disease: Don't Forget the Bioinformatics

Annals of the American Thoracic Society, 2016-01, Vol.13 (1), p.142-143

2016

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Plasma metabolomic profile in fibrosing pulmonary sarcoidosis

Sarcoidosis, vasculitis, and diffuse lung diseases, 2016-03, Vol.33 (1), p.29-38

2016

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Association of genetic variations in the mitochondrial D-loop with β-thalassemia

Mitochondrial DNA. Part A. DNA mapping, sequencing, and analysis, 2016-05, Vol.27 (3), p.1693-1696

2016

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Vitamin D receptor homozygote mutant tt and bb are associated with susceptibility to pulmonary tuberculosis in the Iranian population

International journal of infectious diseases, 2010-01, Vol.14 (1), p.e84-e85

2010

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Generation and bioenergetic analysis of cybrids containing mitochondrial DNA from mouse skeletal muscle during aging

Nucleic acids research, 2010-04, Vol.38 (6), p.1913-1921

2010

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Huntington's disease and mitochondrial DNA deletions: event or regular mechanism for mutant huntingtin protein and CAG repeats expansion?

Cellular and molecular neurobiology, 2007-11, Vol.27 (7), p.867-875

2007

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Visfatin level in patients with colorectal adenoma

Medical journal of the Islamic Republic of Iran, 2016, Vol.30, p.320-320

2016

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Investigation of tRNALeu/Lys and ATPase 6 Genes Mutations in Huntington’s Disease

Cellular and molecular neurobiology, 2008-11, Vol.28 (7), p.933-938

2008

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Investigation of tRNA(Leu/Lys) and ATPase 6 genes mutations in Huntington's disease

Cellular and molecular neurobiology, 2008-11, Vol.28 (7), p.933-938

2008

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Mitochondrial tRNALeu/Lys and ATPase 6/8 Gene Variations in Spinocerebellar Ataxias

Neuro-degenerative diseases, 2009-01, Vol.6 (1-2), p.16-22

2009

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Diversity and relationship between Iranian ethnic groups: Human dopamine transporter gene (DAT1) VNTR genotyping

American journal of human biology, 2007-11, Vol.19 (6), p.821-826

2007

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Do mitochondrial DNA haplogroups play a role in susceptibility to tuberculosis?

Respirology (Carlton, Vic.), 2007-11, Vol.12 (6), p.823-827

2007

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Variation of DAT1 VNTR Alleles and Genotypes Among Old Ethnic Groups in Mesopotamia to the Oxus Region

Human biology, 2008-02, Vol.80 (1), p.73-81

2008

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Variation of DAT1 VNTR Alleles and Genotypes Among Old Ethnic Groups in Mesopotamia to the Oxus Region

Human biology, 2008-02, Vol.80 (1), p.73-81

2008

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Variation ofDAT1 VNTR Alleles and Genotypes Among Old Ethnic Groups in Mesopotamia to the Oxus Region

Human biology, 2008-02, Vol.80 (1), p.73-81

2008

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Variation of DAT1 VNTR Alleles and Genotypes Among Old Ethnic Groups in Mesopotamia to the Oxus Region

Human biology, 2008-02, Vol.80 (1), p.73-81

2008

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An A8296G mutation in the MT-TK gene of a patient with epilepsy - a disease-causing mutation or rare polymorphism?

Neurologia i neurochirurgia polska, 2008-05, Vol.42 (3), p.263

2008

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Machine-learning-based COVID-19 mortality prediction model and identification of patients at low and high risk of dying

Critical care (London, England), 2021-09, Vol.25 (1), p.328-328, Article 328

2021

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Metabolomics in severe traumatic brain injury: a scoping review

Unraveling complex relationships between COVID-19 risk factors using machine learning based models for predicting mortality of hospitalized patients and identification of high-risk group: a large retrospective study

Beta-Thalassemia in Iran : New Insight into the Role of Genetic Admixture and Migration

Metabolomics and Biomarker Discovery in Traumatic Brain Injury

Metabolomic Insights into COVID-19 Severity: A Scoping Review

Metabolomics: Applications and Promise in Mycobacterial Disease

An A10398G mitochondrial DNA alteration is related to increased risk of breast cancer, and associates with Her2 positive receptor

Reply: Metabolomics and Mycobacterial Disease: Don't Forget the Bioinformatics

Plasma metabolomic profile in fibrosing pulmonary sarcoidosis

Association of genetic variations in the mitochondrial D-loop with β-thalassemia

Vitamin D receptor homozygote mutant tt and bb are associated with susceptibility to pulmonary tuberculosis in the Iranian population

Generation and bioenergetic analysis of cybrids containing mitochondrial DNA from mouse skeletal muscle during aging

Huntington's disease and mitochondrial DNA deletions: event or regular mechanism for mutant huntingtin protein and CAG repeats expansion?

Visfatin level in patients with colorectal adenoma

Investigation of tRNALeu/Lys and ATPase 6 Genes Mutations in Huntington’s Disease

Investigation of tRNA(Leu/Lys) and ATPase 6 genes mutations in Huntington's disease

Mitochondrial tRNALeu/Lys and ATPase 6/8 Gene Variations in Spinocerebellar Ataxias

Diversity and relationship between Iranian ethnic groups: Human dopamine transporter gene (DAT1) VNTR genotyping

Do mitochondrial DNA haplogroups play a role in susceptibility to tuberculosis?

Variation of DAT1 VNTR Alleles and Genotypes Among Old Ethnic Groups in Mesopotamia to the Oxus Region

Variation of DAT1 VNTR Alleles and Genotypes Among Old Ethnic Groups in Mesopotamia to the Oxus Region

Variation ofDAT1 VNTR Alleles and Genotypes Among Old Ethnic Groups in Mesopotamia to the Oxus Region

Variation of DAT1 VNTR Alleles and Genotypes Among Old Ethnic Groups in Mesopotamia to the Oxus Region

An A8296G mutation in the MT-TK gene of a patient with epilepsy - a disease-causing mutation or rare polymorphism?

Machine-learning-based COVID-19 mortality prediction model and identification of patients at low and high risk of dying

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