Author

Shadi Vakili

OpenAlex ID: A5000189486

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

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

Novel Mutations Responsible for α-Thalassemia in Iranian Families

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

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

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

Works count: 10

Citation count: 87

H-index: 6

I10-index: 3