Sirous Zeinali

2.5k total citations
101 papers, 1.4k citations indexed

About

Sirous Zeinali is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Sirous Zeinali has authored 101 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 35 papers in Hematology and 30 papers in Genetics. Recurrent topics in Sirous Zeinali's work include Hemoglobinopathies and Related Disorders (28 papers), Iron Metabolism and Disorders (17 papers) and Skin and Cellular Biology Research (11 papers). Sirous Zeinali is often cited by papers focused on Hemoglobinopathies and Related Disorders (28 papers), Iron Metabolism and Disorders (17 papers) and Skin and Cellular Biology Research (11 papers). Sirous Zeinali collaborates with scholars based in Iran, United States and France. Sirous Zeinali's co-authors include Morteza Karimipoor, Hamid Reza Heidari, Houman Kahroba, Ali Sadeghinia, Ommoleila Molavi, Jouni Uitto, Hassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian and Nejat Mahdieh and has published in prestigious journals such as SHILAP Revista de lepidopterología, Clinical Infectious Diseases and Scientific Reports.

In The Last Decade

Sirous Zeinali

95 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sirous Zeinali Iran 18 543 406 373 217 192 101 1.4k
Karl X. Chai United States 24 796 1.5× 336 0.8× 212 0.6× 125 0.6× 79 0.4× 48 1.6k
Irina Golovleva Sweden 25 927 1.7× 153 0.4× 355 1.0× 146 0.7× 284 1.5× 78 1.9k
FS Collins United States 25 1.1k 2.0× 372 0.9× 405 1.1× 106 0.5× 349 1.8× 50 2.2k
Sirous Zeinali Iran 18 794 1.5× 151 0.4× 115 0.3× 63 0.3× 202 1.1× 112 1.3k
Güven Lüleci Türkiye 21 750 1.4× 166 0.4× 112 0.3× 55 0.3× 808 4.2× 110 1.7k
Kenneth S. Zuckerman United States 24 598 1.1× 330 0.8× 469 1.3× 72 0.3× 98 0.5× 67 1.5k
Daniel S. Wechsler United States 23 833 1.5× 198 0.5× 210 0.6× 168 0.8× 146 0.8× 66 1.8k
Véronique David France 19 523 1.0× 348 0.9× 408 1.1× 45 0.2× 406 2.1× 40 1.6k
D. Wade Clapp United States 29 1.2k 2.2× 380 0.9× 961 2.6× 170 0.8× 352 1.8× 64 3.1k
David George United States 20 697 1.3× 189 0.5× 176 0.5× 166 0.8× 119 0.6× 28 1.2k

Countries citing papers authored by Sirous Zeinali

Since Specialization
Citations

This map shows the geographic impact of Sirous Zeinali'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 Sirous Zeinali with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sirous Zeinali more than expected).

Fields of papers citing papers by Sirous Zeinali

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sirous Zeinali. 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 Sirous Zeinali. The network helps show where Sirous Zeinali may publish in the future.

Co-authorship network of co-authors of Sirous Zeinali

This figure shows the co-authorship network connecting the top 25 collaborators of Sirous Zeinali. A scholar is included among the top collaborators of Sirous Zeinali 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 Sirous Zeinali. Sirous Zeinali 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
1.
2.
Khosravi, Mohammad, et al.. (2022). Lentiviral vector containing beta-globin gene for beta thalassemia gene therapy. Gene Reports. 27. 101615–101615. 3 indexed citations
3.
Youssefian, Leila, Amir Hossein Saeidian, Ali Reza Tavasoli, et al.. (2022). Recalcitrant Cutaneous Warts in a Family with Inherited ICOS Deficiency. Journal of Investigative Dermatology. 142(9). 2435–2445. 4 indexed citations
4.
Vahidnezhad, Hassan, Leila Youssefian, Ali Reza Tavasoli, et al.. (2022). Mutation update: The spectra of PLEC sequence variants and related plectinopathies. Human Mutation. 43(12). 1706–1731. 8 indexed citations
5.
Youssefian, Leila, Fateme Rajabi, Fahimeh Abdollahimajd, et al.. (2022). Ichthyosis follicularis syndromes in patients with mutations in GJB2. Clinical and Experimental Dermatology. 47(8). 1561–1566. 2 indexed citations
6.
Ghafari, Mahan, Majid Heydari, Sirous Zeinali, et al.. (2021). Lessons for preparedness and reasons for concern from the early COVID-19 epidemic in Iran. Epidemics. 36. 100472–100472. 17 indexed citations
7.
Vahidnezhad, Hassan, et al.. (2021). Very-Early-Onset Inflammatory Bowel Disease in a Patient With Junctional Epidermolysis Bullosa With a Homozygous Mutation in the α6 Integrin Gene (ITGA6). Inflammatory Bowel Diseases. 27(11). 1865–1869. 1 indexed citations
8.
Youssefian, Leila, Sadegh Khodavaisy, Amir Hossein Saeidian, et al.. (2021). Ichthyosis, psoriasiform dermatitis, and recurrent fungal infections in patients with biallelic mutations in PERP. Journal of the European Academy of Dermatology and Venereology. 36(3). 472–479. 2 indexed citations
9.
Bayat, Elham, et al.. (2021). Targeted integration into pseudo attP sites of CHO cells using CRISPR/Cas9. Journal of Biotechnology. 337. 1–7. 10 indexed citations
10.
Mansouri, Parvin, Hamidreza Mahmoudi, Leila Youssefian, et al.. (2020). Keratitis‐ichthyosis‐deafness syndrome: Phenotypic heterogeneity and treatment perspective of patients with p. Asp50Asn GJB2 mutation. Dermatologic Therapy. 33(6). e14493–e14493. 4 indexed citations
11.
12.
Youssefian, Leila, Hassan Vahidnezhad, Amir Hossein Saeidian, et al.. (2018). Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families. Human Mutation. 40(3). 288–298. 39 indexed citations
13.
Zeinali, Sirous, et al.. (2017). History of Leukemia: Diagnosis and Treatment from Beginning to Now. Galen Medical Journal. 6(1). 4 indexed citations
14.
Kadivar, Mehdi, Behrooz Johari, Majid Lotfinia, et al.. (2016). Transduction of an optimized recombinant lentivirus expressing E-cadherin shRNA resulted in stable downregulation of CDH1 gene and obvious cell morphological change in the human colorectal cancer cell line HT29. International Journal of Medical Research & Health Sciences. 5(11). 87–93. 7 indexed citations
15.
Tavakkoly‐Bazzaz, Javad, et al.. (2015). NPM1 Mutation Detection in Acute Myeloid Leukemia: A Method Comparison Study. Genetic Testing and Molecular Biomarkers. 20(2). 63–66. 4 indexed citations
16.
Zeinali, Sirous, et al.. (2011). β-Thalassemia Mutations Found During 1 Year of Prenatal Diagnoses in Fars Province, Iran. Hemoglobin. 35(4). 331–337. 6 indexed citations
17.
Mahdieh, Nejat, et al.. (2011). Impact of Consanguineous Marriages in GJB2 -Related Hearing Loss in the Iranian Population: A Report of a Novel Variant. Genetic Testing and Molecular Biomarkers. 15(7-8). 489–493. 29 indexed citations
18.
Hamid, Mohammad, et al.. (2011). RELATIONSHIP BETWEEN DNA POLYMORPHISMS AT THE BCL11A AND HBS1L-MYB LOCI IN β- THALASSEMIA PATIENTS WITH INCREASED FETAL HEMOGLOBIN LEVELS. Scientific Journal of Iran Blood Transfus Organ. 8(332). 149–157. 2 indexed citations
19.
Mortazavi, Yousef, et al.. (2008). CHARACTERIZATION OF BETA GLOBIN GENE MUTATIONS IN ZANJAN PROVINCE: AN INTRODUCTION TO PRENATAL DIAGNOSIS OF THALASSEMIA. Journal of Advances in Medical and Biomedical Research. 16(63). 1–10. 4 indexed citations
20.
Abolghasemi, Hassan, Ali Amid, Sirous Zeinali, et al.. (2007). Thalassemia in Iran. Journal of Pediatric Hematology/Oncology. 29(4). 233–238. 185 indexed citations

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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