Embed

Academic

Authors

Mohammad Taghi Akbari

Mohammad Taghi Akbari,Tarbiat Modares University,Genetics & Genealogy,Physiology,Oncology

Edit

Mohammad Taghi Akbari

Tarbiat Modares University

Publications: 22 | Citations: 38

Fields: Genetics & Genealogy, Physiology, Oncology

Collaborated with 78 co-authors from 2003 to 2012 | Cited by 141 authors

Cumulative Annual

Sort by:

Publications (22)

BibTeX | RIS | RefWorks Download

Clinical Features, DYT1 Mutation Screening and Genotype-Phenotype Correlation in Patients with Dystonia from Iran

, , ,

Journal: Medical Principles and Practice - MED PRINCIP PRACT , vol. 21, pp. 462-466, 2012

Mutation spectrum of phenylketonuria in Iranian population (Citations: 1)

, , , , , ,

Journal: Molecular Genetics and Metabolism - MOL GENET METAB , vol. 102, no. 1, pp. 29-32, 2011

Determination of exon 7 SMN1 deletion in Iranian patients and heterozygous carriers by quantitative real-time PCR

, , ,

Journal: Journal of Genetics - J GENET , vol. 90, no. 1, pp. 133-136, 2011

RB1 gene mutations in Iranian patients with retinoblastoma: report of four novel mutations

, , ,

Journal: Cancer Letters - CANCER LETT , vol. 204, no. 6, pp. 316-322, 2011

Identification of rare hemoglobin variant (Hb Fairfax) causing dominant β-thalassemia phenotype in an Iranian family

, ,

Journal: Annals of Hematology - ANN HEMATOL , vol. 90, no. 3, pp. 349-351, 2011

Sort by:

Citations (38 times by 34 publications)

Plasma lipids and lipoproteins in children and young adults with major β-thalassemia from western Iran: influence of genotype (Citations: 1)

, , , , , , , , ,

Journal: Molecular Biology Reports - MOL BIOL REP , vol. 38, no. 4, pp. 2573-2578, 2011

Identification of rare hemoglobin variant (Hb Fairfax) causing dominant β-thalassemia phenotype in an Iranian family

, ,

Journal: Annals of Hematology - ANN HEMATOL , vol. 90, no. 3, pp. 349-351, 2011

A 13-bp Deletion in the 3′ Untranslated Region of the β-Globin Gene Causes β-Thalassemia Major in Compound Heterozygosity with IVSII-1 Mutation

Journal: Medical Principles and Practice - MED PRINCIP PRACT , vol. 20, pp. 488-490, 2011

Frequency of Positive XmnI Gγ polymorphism and coinheritance of common alpha thalassemia mutations do not show statistically significant difference between thalassemia major and intermedia cases with homozygous IVSII-1 mutation (Citations: 6)

, ,

Journal: Blood Cells Molecules and Diseases - BLOOD CELLS MOLECULES DIS , vol. 44, no. 2, pp. 95-99, 2010

Detection of responsible mutations for beta thalassemia in the Kermanshah Province of Iran using PCR-based techniques (Citations: 2)

, ,

Journal: Molecular Biology Reports - MOL BIOL REP , vol. 37, no. 1, pp. 149-154, 2010

Comments

Co-authors (78)

Journals (13)

Keywords (58)

Mohammad Taghi Akbari,Tarbiat Modares University,Genetics & Genealogy,Physiology,Oncology

Publications (22)

BibTeX | RIS | RefWorks Download

Clinical Features, DYT1 Mutation Screening and Genotype-Phenotype Correlation in Patients with Dystonia from Iran

Mutation spectrum of phenylketonuria in Iranian population (Citations: 1)

Determination of exon 7 SMN1 deletion in Iranian patients and heterozygous carriers by quantitative real-time PCR

RB1 gene mutations in Iranian patients with retinoblastoma: report of four novel mutations

Identification of rare hemoglobin variant (Hb Fairfax) causing dominant β-thalassemia phenotype in an Iranian family

Citations (38 times by 34 publications)

Plasma lipids and lipoproteins in children and young adults with major β-thalassemia from western Iran: influence of genotype (Citations: 1)

Identification of rare hemoglobin variant (Hb Fairfax) causing dominant β-thalassemia phenotype in an Iranian family

A 13-bp Deletion in the 3′ Untranslated Region of the β-Globin Gene Causes β-Thalassemia Major in Compound Heterozygosity with IVSII-1 Mutation

Frequency of Positive XmnI Gγ polymorphism and coinheritance of common alpha thalassemia mutations do not show statistically significant difference between thalassemia major and intermedia cases with homozygous IVSII-1 mutation (Citations: 6)

Detection of responsible mutations for beta thalassemia in the Kermanshah Province of Iran using PCR-based techniques (Citations: 2)


	View FAQ about top research areas and Fields of study

Mohammad Taghi Akbari,Tarbiat Modares University,Genetics & Genealogy,Physiology,Oncology

Publications (22) BibTeX | RIS | RefWorks Download

Mutation spectrum of phenylketonuria in Iranian population (Citations: 1)

Plasma lipids and lipoproteins in children and young adults with major β-thalassemia from western Iran: influence of genotype (Citations: 1)

Frequency of Positive XmnI Gγ polymorphism and coinheritance of common alpha thalassemia mutations do not show statistically significant difference between thalassemia major and intermedia cases with homozygous IVSII-1 mutation (Citations: 6)

Detection of responsible mutations for beta thalassemia in the Kermanshah Province of Iran using PCR-based techniques (Citations: 2)

Publications (22)

BibTeX | RIS | RefWorks Download