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Letter to the Editor Re: How to Estimate Allele Frequencies and Make Statistical Comparisons in Case-Control Studies of Polymorphic X-Linked Loci

Turk oftalmoloji gazetesi, 2024-07, Vol.54 (4), p.246-247

Saadat, Mostafa

2024

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Association between null Genotypes of glutathione S-transferase M1 and T1 and susceptibility to systemic lupus erythematosus: A meta-analysis

Scripta Medica (English Edition), 2024, Vol.55 (1), p.97-105

Saadat, Mostafa

2024

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Evaluation of associations of GSTM1/GSTT1 null genotypes with the susceptibility to age-related macular degeneration: A meta-analysis

Scripta Medica (English Edition), 2021, Vol.52 (1), p.38-41

Saadat, Mostafa

2021

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Introducing a new index for selecting genetic polymorphisms for association studies

EXCLI journal, 2022-06, Vol.21, p.814-817

2022

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Association between Alu insertion/deletion polymorphism in intron 8 of human tissue plasminogen activator gene (PLAT) and risk of age-related macular degeneration

Scripta Medica (English Edition), 2023-01, Vol.54 (3), p.285-288

2023

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Estimation of allelic frequencies for ABO and Rh blood groups

The Egyptian journal of medical human genetics, 2015-04, Vol.16 (2), p.205-206

Saadat, Mostafa

2015

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Hardy–Weinberg equilibrium and association study of insertion/deletion polymorphism of ACE gene and Alzheimer’s disease in Egyptian patients

The Egyptian journal of medical human genetics, 2014-10, Vol.15 (4), p.405-406

Saadat, Mostafa

2014

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COVID-19 prevalence and mortality is associated with the allele frequency of CCR5-Δ32

Croatian medical journal, 2021-06, Vol.62 (3), p.303-304

Saadat, Mostafa

2021

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Comments on: rs3761548 polymorphisms of Foxp3 gene in Iranian patients with migraine

The Egyptian journal of medical human genetics, 2023-12, Vol.24 (1)

Saadat, Mostafa

2023

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COVID-19 prevalence and mortality is associated with the allele frequency of CCR5-[DELTA]32

Croatian medical journal, 2021-06, Vol.62 (3), p.303

Saadat, Mostafa

2021

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Chromosomal Distribution of Ankylosing Spondylitis Susceptibility Loci

Mediterranean journal of rheumatology, 2023-06, Vol.34 (2), p.159

Saadat, Mostafa

2023

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Association between consanguinity and survival of marriages

The Egyptian journal of medical human genetics, 2015-01, Vol.16 (1), p.67-70

Saadat, Mostafa

2015

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Association between 15 Insertion/Deletion Polymorphisms and the Risk of Type 1 Bipolar Disorder

Gene expression, 2024-07

2024

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Sex ratio at birth in COVID-19 era

EXCLI journal, 2021-10, Vol.20, p.1499-1501

Mostafa Saadat

2021

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Study of liver function and expression of some detoxification genes in the male rats exposed to methyl-tertiary butyl ether

The Egyptian journal of medical human genetics, 2016-10, Vol.17 (4), p.325-329

2016

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Extremely low frequency electromagnetic field in combination with β-Lapachone up-regulates the genes of non-homologous end joining

The Egyptian journal of medical human genetics, 2017-10, Vol.18 (4), p.389-392

2017

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The morbidity and mortality of COVID-19 are associated with ABO and Rh blood groups

European journal of preventive cardiology, 2021-09, Vol.28 (11), p.e26-e28

2021

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DNA repair gene XRCC7 G6721T variant and susceptibility to colorectal cancer

The Egyptian journal of medical human genetics, 2016-10, Vol.17 (4), p.373-376

2016

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Association Study of Glutathione S-transferases Gene Polymorphisms (GSTM1 and GSTT1) with Ulcerative Colitis and Crohn's Disease in the South of Iran

Advanced biomedical research, 2017-01, Vol.6 (1), p.67-67

2017

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Evaluation of Association Between Q192R and L55M Genetic Polymorphisms of PON1 and Serum Paraoxonase-1 Activity in Healthy Individuals, a Meta-Analysis

Romanian Journal of Diabetes Nutrition and Metabolic Diseases, 2018-06, Vol.25 (2), p.171-180

Saadat, Mostafa

2018

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Allelic prevalence of intron 3 insertion/deletion genetic polymorphism of DNA double-strand break repair gene XRCC4 in four healthy Iranian populations

The Egyptian journal of medical human genetics, 2015-07, Vol.16 (3), p.215-218

2015

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Susceptibility to methamphetamine dependence associated with high transcriptional activity alleles of VNTR polymorphism in the promoter region of monoamine oxidase A (MAOA)

The Egyptian journal of medical human genetics, 2016-01, Vol.17 (1), p.111-114

2016

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Distribution of genetic polymorphism of CAT C-262T in three Iranian populations / Üç İran popülasyonunda CAT C-262T genetik polimorfizminin dağılımı

Turkish Journal of Biochemistry, 2015-10, Vol.40 (5), p.386-389

2015

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Evaluation of chromosomal aberrations induced by hydralazine in Chinese hamster ovary cells

The Egyptian journal of medical human genetics, 2014-10, Vol.15 (4), p.343-346

2014

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Distributions of susceptibility loci to late onset Alzheimer's disease on human chromosomes

EXCLI journal, 2016-06, Vol.15, p.403-405

Saadat, Mostafa

2016

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Letter to the Editor Re: How to Estimate Allele Frequencies and Make Statistical Comparisons in Case-Control Studies of Polymorphic X-Linked Loci

Association between null Genotypes of glutathione S-transferase M1 and T1 and susceptibility to systemic lupus erythematosus: A meta-analysis

Evaluation of associations of GSTM1/GSTT1 null genotypes with the susceptibility to age-related macular degeneration: A meta-analysis

Introducing a new index for selecting genetic polymorphisms for association studies

Association between Alu insertion/deletion polymorphism in intron 8 of human tissue plasminogen activator gene (PLAT) and risk of age-related macular degeneration

Estimation of allelic frequencies for ABO and Rh blood groups

Hardy–Weinberg equilibrium and association study of insertion/deletion polymorphism of ACE gene and Alzheimer’s disease in Egyptian patients

COVID-19 prevalence and mortality is associated with the allele frequency of CCR5-Δ32

Comments on: rs3761548 polymorphisms of Foxp3 gene in Iranian patients with migraine

COVID-19 prevalence and mortality is associated with the allele frequency of CCR5-[DELTA]32

Chromosomal Distribution of Ankylosing Spondylitis Susceptibility Loci

Association between consanguinity and survival of marriages

Association between 15 Insertion/Deletion Polymorphisms and the Risk of Type 1 Bipolar Disorder

Sex ratio at birth in COVID-19 era

Study of liver function and expression of some detoxification genes in the male rats exposed to methyl-tertiary butyl ether

Extremely low frequency electromagnetic field in combination with β-Lapachone up-regulates the genes of non-homologous end joining

The morbidity and mortality of COVID-19 are associated with ABO and Rh blood groups

DNA repair gene XRCC7 G6721T variant and susceptibility to colorectal cancer

Association Study of Glutathione S-transferases Gene Polymorphisms (GSTM1 and GSTT1) with Ulcerative Colitis and Crohn's Disease in the South of Iran

Evaluation of Association Between Q192R and L55M Genetic Polymorphisms of PON1 and Serum Paraoxonase-1 Activity in Healthy Individuals, a Meta-Analysis

Allelic prevalence of intron 3 insertion/deletion genetic polymorphism of DNA double-strand break repair gene XRCC4 in four healthy Iranian populations

Susceptibility to methamphetamine dependence associated with high transcriptional activity alleles of VNTR polymorphism in the promoter region of monoamine oxidase A (MAOA)

Distribution of genetic polymorphism of CAT C-262T in three Iranian populations / Üç İran popülasyonunda CAT C-262T genetik polimorfizminin dağılımı

Evaluation of chromosomal aberrations induced by hydralazine in Chinese hamster ovary cells

Distributions of susceptibility loci to late onset Alzheimer's disease on human chromosomes

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