Author

Hashem Imanian

OpenAlex ID: A5083642847

Interaction of anα-Globin Gene Triplication withβ-Globin Gene Mutations in Iranian Patients withβ-Thalassemia Intermedia

2015 · Samaneh Farashi, Nooshin Bayat, et al. · Hemoglobin · 30

Genotype-Phenotype Correlation In Iranian Patients With Hb H Disease

2011 · Saedieh Ebrahimkhani, Azita Azarkeivan, et al. · Hemoglobin · 20

Copy number variations of six and seven α-globin genes in a family with intermedia and major thalassemia phenotypes

2015 · Samaneh Farashi, Shadi Vakili, et al. · Expert Review of Hematology · 14

Gene Panel Testing in Hereditary Breast Cancer.

2020 · Parvin Rostami, Kazem Zendehdel, et al. · PubMed · 11

Novel Mutations Responsible for α-Thalassemia in Iranian Families

2013 · Nooshin Bayat, Samaneh Farashi, et al. · Hemoglobin · 11

The Spectrum ofα-Thalassemia Mutations in the Kurdish Population of Northeastern Iraq

2012 · Nasir A.S. Al-Allawi, Sana D. Jalal, et al. · Hemoglobin · 11

Prenatal Screening for Aneuploidies Using QF-PCR and Karyotyping: A Comprehensive Study in Iranian Population.

2015 · Parvin Rostami, Sahar Valizadegan, et al. · PubMed · 10

Point mutations which should not be overlooked in Hb H disease

2015 · Samaneh Farashi, Nooshin Bayat, et al. · Expert Review of Hematology · 7

Hb Dartmouth ( HBA2 : c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient

2015 · Samaneh Farashi, Negin Faramarzi Garous, et al. · Hemoglobin · 7

Homozygosity for the AATAAA > AATA- - Polyadenylation Site Mutation on the α2-Globin Gene Causing Transfusion-Dependent Hb H Disease in an Iranian Patient: A Case Report.

2015 · Samaneh Farashi, Negin F Garous, et al. · PubMed · 7

First Report of a Dominantly Inherited β-Thalassemia Caused by a Novel Elongated β-Globin Chain

2016 · Samaneh Farashi, Fariba Rad, et al. · Hemoglobin · 6

Screening of Iranian Thalassemic Families for the Most Common Deletions of the β-Globin Gene Cluster

2007 · Fatemehsadat Esteghamat, Hashem Imanian, et al. · Hemoglobin · 5

Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on theHBA1Gene

2015 · Samaneh Farashi, Shadi Vakili, et al. · Hemoglobin · 4

Mutations on theα2-Globin Gene That May Triggerα+-Thalassemia

2015 · Samaneh Farashi, Shadi Vakili, et al. · Hemoglobin · 3

A 21 Nucleotide Duplication on theα1- andα2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease

2015 · Samaneh Farashi, Negin Faramarzi Garous, et al. · Hemoglobin · 3

Characterization of Homozygous Hb Setif (HBA2: c.283G>T) in the Iranian Population

2015 · Samaneh Farashi, Negin F. Garous, et al. · Hemoglobin · 1

Prenatal Screening for Aneuploidy in Iranian Families Using QF-PCR

2011 · Parvin Rostami, Najafi Roshanak, et al. · Zhinitīk dar hizārah-i sivvum

Study of Prothrombin G20210A polymorphism as a genetic risk factor for cardiovascular disease in the Iranian population

2010 · Hossein Najmabadi, Maryam Rostami, et al. · Zhinitīk dar hizārah-i sivvum

Study of MTHFR A1298C polymorphism as a genetic risk factor for cardiovascular disease in the Iranian population.

2010 · Hashem Imanian, Valeh Hadavi, et al. · Zhinitīk dar hizārah-i sivvum

A Case of Hemoglobin Lepore Combined With Beta Thalassemia (heterozygote Form)

2007 · Ali Keyvan, Hossein Najmabadi, et al. · Scientific Journal of Iran Blood Transfus Organ

Works count: 20

Citation count: 150

H-index: 7

I10-index: 7