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Association between tobacco smoking and opioid use: A meta-analysis

Addictive behaviors, 2019-05, Vol.92, p.225-235

2019

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Alport Syndrome: Clinical Spectrum and Therapeutic Advances

Kidney medicine, 2023-05, Vol.5 (5), p.100631-100631, Article 100631

2023

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Cigarette Smoking Behavior a Gateway to Opium Use Disorder: A Mendelian Randomization Analysis

Behavior genetics, 2021-07, Vol.51 (4), p.385-393

2021

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High detection rate for disease-causing variants in a cohort of 30 Iranian pediatric steroid resistant nephrotic syndrome cases

Frontiers in pediatrics, 2022-09, Vol.10, p.974840-974840

2022

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Rectal Thiopental versus Intramuscular Ketamine in Pediatric Procedural Sedation and Analgesia; a Randomized Clinical Trial

Emergency (Tehran, Iran), 2015-01, Vol.3 (1), p.22-26

2015

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The effects of omega-3 and vitamin E co-supplementation on parameters of mental health and gene expression related to insulin and inflammation in subjects with polycystic ovary syndrome

Journal of affective disorders, 2018-03, Vol.229, p.41-47

2018

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New Report of a Different Clinical Presentation of CD151 Splicing Mutation (c.351+2T>C): Could TSPAN11 be Considered as a Potential Modifier Gene for CD151?

Molecular syndromology, 2022-05, Vol.13 (3), p.212-220

2022

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Evaluation of gene expression level of GPRC6A, E.cadherin and ZEB1 in prostate cancer in comparison to benign tissues

Majallah-i Danishkadah-'i Pizishki, 2019-05, Vol.77 (2), p.69-75

2019

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The association between polymorphism of the BDNF gene and cigarette smoking in the Iranian population

The journal of gene medicine, 2018-10, Vol.20 (10-11), p.e3052-n/a

2018

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Molecular Genetic Analysis of Steroid Resistant Nephrotic Syndrome, Detection of a Novel Mutation

Iranian journal of kidney diseases, 2019-05, Vol.13 (3), p.165

2019

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Rectal Thiopental versus Intramuscular Ketamine in Pediatric Procedural Sedation and Analgesia; a Randomized Clinical Trial

Archives of academic emergency medicine, 2018-12, Vol.3 (1)

2018

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Rebuilding Communities after Displacement: Sustainable and Resilience Approaches

MECW: The Middle East in the Contemporary World, 2023

1, 2023

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Complex Alleles of CYP21A2 Are the Most Frequent Causes of Congenital Adrenal Hyperplasia in Iranian Population

Majallah-ʼi bīmārīhā-yi kūdakān-i Īrān = Iranian journal of pediatrics, 2019-12, Vol.In Press (In Press)

2019

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Mutation analysis of Phenylalanine hydroxylase gene in Iranian patients with Phenylketonuria

Medical journal of the Islamic Republic of Iran, 2018, Vol.32 (1), p.21-123

2018

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Mutation analysis of androgen receptor gene: Multiple uses for a single test

Gene, 2014-12, Vol.552 (2), p.234-238

2014

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Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: Phenotypic and genotypic findings

Gene, 2013-03, Vol.517 (1), p.137-145

2013

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Association of homeobox B13 (HOXB13) gene variants with prostate cancer risk in an Iranian population

Medical journal of the Islamic Republic of Iran, 2018, Vol.32, p.97-565

2018

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Genetic Screening of Iranian Patients with 46,XY Disorders of Sex Development

Reports of biochemistry and molecular biology, 2017-10, Vol.6 (1), p.59-65

2017

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Novel nucleotide changes in mutational analysis of mitochondrial 12SrRNA gene in patients with nonsyndromic and aminoglycoside-induced hearing loss

Molecular biology reports, 2013-03, Vol.40 (3), p.2689-2695

2013

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Forced Displacement Following Reconstruction Approaches After 2005 Zarand Earthquake, Iran

Rebuilding Communities After Displacement, 2023, p.217-244

2023

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Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization

Indian journal of human genetics, 2013-10, Vol.19 (4), p.443

2013

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New Report of a Different Clinical Presentation of CD151 Splicing Mutation (c.351+2T>C): Could TSPAN11 be Considered as a Potential Modifier Gene for CD151?

Molecular syndromology, 2022, Vol.13 (3), p.212-220

2022

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Investigation of RBC Indices and HbA2 Levels in Parents of Beta-Thalassemia Patients: Impacts on Premarital Genetic Counseling

Journal of family & reproductive health, 2007-06, Vol.1 (2)

2007

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A homozygous loss-of-function mutation in PTPN14 causes a syndrome of bilateral choanal atresia and early infantile-onset lymphedema

Meta Gene, 2017-12, Vol.14, p.53-58

2017

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Novel human mitochondrial tRNAphe mutation in a patient with hearing impairment: A case study

Mitochondrial DNA, 2013-04, Vol.24 (2), p.132-136

2013

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Association between tobacco smoking and opioid use: A meta-analysis

Alport Syndrome: Clinical Spectrum and Therapeutic Advances

Cigarette Smoking Behavior a Gateway to Opium Use Disorder: A Mendelian Randomization Analysis

High detection rate for disease-causing variants in a cohort of 30 Iranian pediatric steroid resistant nephrotic syndrome cases

Rectal Thiopental versus Intramuscular Ketamine in Pediatric Procedural Sedation and Analgesia; a Randomized Clinical Trial

The effects of omega-3 and vitamin E co-supplementation on parameters of mental health and gene expression related to insulin and inflammation in subjects with polycystic ovary syndrome

New Report of a Different Clinical Presentation of CD151 Splicing Mutation (c.351+2T>C): Could TSPAN11 be Considered as a Potential Modifier Gene for CD151?

Evaluation of gene expression level of GPRC6A, E.cadherin and ZEB1 in prostate cancer in comparison to benign tissues

The association between polymorphism of the BDNF gene and cigarette smoking in the Iranian population

Molecular Genetic Analysis of Steroid Resistant Nephrotic Syndrome, Detection of a Novel Mutation

Rectal Thiopental versus Intramuscular Ketamine in Pediatric Procedural Sedation and Analgesia; a Randomized Clinical Trial

Rebuilding Communities after Displacement: Sustainable and Resilience Approaches

Complex Alleles of CYP21A2 Are the Most Frequent Causes of Congenital Adrenal Hyperplasia in Iranian Population

Mutation analysis of Phenylalanine hydroxylase gene in Iranian patients with Phenylketonuria

Mutation analysis of androgen receptor gene: Multiple uses for a single test

Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: Phenotypic and genotypic findings

Association of homeobox B13 (HOXB13) gene variants with prostate cancer risk in an Iranian population

Genetic Screening of Iranian Patients with 46,XY Disorders of Sex Development

Novel nucleotide changes in mutational analysis of mitochondrial 12SrRNA gene in patients with nonsyndromic and aminoglycoside-induced hearing loss

Forced Displacement Following Reconstruction Approaches After 2005 Zarand Earthquake, Iran

Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization

New Report of a Different Clinical Presentation of CD151 Splicing Mutation (c.351+2T>C): Could TSPAN11 be Considered as a Potential Modifier Gene for CD151?

Investigation of RBC Indices and HbA2 Levels in Parents of Beta-Thalassemia Patients: Impacts on Premarital Genetic Counseling

A homozygous loss-of-function mutation in PTPN14 causes a syndrome of bilateral choanal atresia and early infantile-onset lymphedema

Novel human mitochondrial tRNAphe mutation in a patient with hearing impairment: A case study

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