Hamid Galehdari

2.9k total citations
177 papers, 1.4k citations indexed

About

Hamid Galehdari is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Hamid Galehdari has authored 177 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 86 papers in Molecular Biology, 43 papers in Genetics and 32 papers in Genetics. Recurrent topics in Hamid Galehdari's work include Hemoglobinopathies and Related Disorders (22 papers), Iron Metabolism and Disorders (17 papers) and Blood groups and transfusion (9 papers). Hamid Galehdari is often cited by papers focused on Hemoglobinopathies and Related Disorders (22 papers), Iron Metabolism and Disorders (17 papers) and Blood groups and transfusion (9 papers). Hamid Galehdari collaborates with scholars based in Iran, United Kingdom and Germany. Hamid Galehdari's co-authors include Stephan A. Hahn, Wolff Schmiegel, Irmgard Schwarte‐Waldhoff, Gholamreza Shariati, Mahnaz Kesmati, Doris Henne‐Bruns, Annette Ramaswamy, Verena Bröcker, Detlef K. Bartsch and Zahra Karimi and has published in prestigious journals such as SHILAP Revista de lepidopterología, Oncogene and Scientific Reports.

In The Last Decade

Hamid Galehdari

161 papers receiving 1.4k citations

Peers

Hamid Galehdari
Comparison fields: 5 of 117
  • Molecular Biology 641
  • Oncology 392
  • Genetics 198
  • Cancer Research 194
  • Surgery 172
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Citations per field, relative to Hamid Galehdari
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Citations per year, relative to Hamid Galehdari
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Countries citing papers authored by Hamid Galehdari

Since Specialization
Citations

This map shows the geographic impact of Hamid Galehdari's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Hamid Galehdari with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hamid Galehdari more than expected).

Fields of papers citing papers by Hamid Galehdari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hamid Galehdari. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Hamid Galehdari. The network helps show where Hamid Galehdari may publish in the future.

Co-authorship network of co-authors of Hamid Galehdari

This figure shows the co-authorship network connecting the top 25 collaborators of Hamid Galehdari. A scholar is included among the top collaborators of Hamid Galehdari based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Hamid Galehdari. Hamid Galehdari is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
# Work Indexed citations
1 0
2 3
3 0
4 1
5 1
6 1
7 4
8
Identification of a Novel HADHB Gene Mutation in an Iranian Patient with Mitochondrial Trifunctional Protein Deficiency.
3
9
A Unique Profile of Adenomatous Polyposis Coli Gene Mutations in Iranian Patients Suffering Sporadic Colorectal Cancer
4
10
Prevalence of Co-Inheritance of Alpha-Thalassemia with Beta-Thalassemia and Beta-Hemoglobinopathy in Ahvaz City
1
11 2
12
SMN1 and NAIP Genes Deletions in Different Types of Spinal Muscular Atrophy in Khuzestan Province, Iran
0
13
The first survey of distribution of inherited deafness patterns in individuals referred to genetic center of Ahvaz welfare organization, Southern Iran
1
14
Wide Spectrum of Mutations in the Beta-Globin Gene Causing Beta-Thalassemia Major in Southwest Iran
4
15
CLONING OF POLY (3-HYDROXYBUTYRATE) SYNTHESIS GENES FROM AZOTOBACTER VINELANDII INTO ESCHERICHIA COLI
6
16
MOLECULAR ANALYSIS OF MICROSATELLITE INSTABILITY IN HEREDITARY NON POLYPOSIS COLON CARCINOMA PATIENTS FROM NORTH-EAST IRAN
2
17
MULTIPLEX TETRA-PRIMER AMPLIFICATION REFRACTORY MUTATION SYSTEM POLYMERASE CHAIN REACTION TO GENOTYPE SNP8NRG221533 OF NEUREGULIN-1 GENE
3
18
Cloning and Expression of Thermus aquaticus DNA polymerase in Escherichia coli
7
19 2
20
Cloning and expression of VP2 gene of Infectious bursal disease virus in eukaryotic cells
1

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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