Pegah Ghandil

2.6k total citations
30 papers, 352 citations indexed

About

Pegah Ghandil is a scholar working on Immunology, Genetics and Molecular Biology. According to data from OpenAlex, Pegah Ghandil has authored 30 papers receiving a total of 352 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Immunology, 12 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in Pegah Ghandil's work include Diabetes and associated disorders (4 papers), Immune Response and Inflammation (4 papers) and NF-κB Signaling Pathways (4 papers). Pegah Ghandil is often cited by papers focused on Diabetes and associated disorders (4 papers), Immune Response and Inflammation (4 papers) and NF-κB Signaling Pathways (4 papers). Pegah Ghandil collaborates with scholars based in Iran, France and United States. Pegah Ghandil's co-authors include Mehrnoosh Zakerkish, Meysam Alipour, Bahman Cheraghian, Anne Puel, Seyed Ahmad Hosseini, Ata Ghadiri, Jean‐Laurent Casanova, Sophie Caillat‐Zucman, Capucine Pïcard and Danièle Dubois‐Laforgue and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Nature Immunology.

In The Last Decade

Pegah Ghandil

29 papers receiving 338 citations

Peers

Pegah Ghandil
Tracy S. Tylee United States
Peter Švec Slovakia
Ulrich Züegel Germany
Izumi Kusuki Japan
Karol Charkiewicz Poland
Faruk Buyru Türkiye
Kathryn Zavala United States
Sebastian Franik Netherlands
Kadri Haller‐Kikkatalo Estonia
Zaynab Alourfi Syria
Tracy S. Tylee United States
Pegah Ghandil
Citations per year, relative to Pegah Ghandil Pegah Ghandil (= 1×) peers Tracy S. Tylee

Countries citing papers authored by Pegah Ghandil

Since Specialization
Citations

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

Fields of papers citing papers by Pegah Ghandil

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pegah Ghandil

This figure shows the co-authorship network connecting the top 25 collaborators of Pegah Ghandil. A scholar is included among the top collaborators of Pegah Ghandil 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 Pegah Ghandil. Pegah Ghandil 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.
Aminzadeh, Majid, et al.. (2024). Association Study of Polymorphisms in Folate Metabolism and Mothers of Down Syndrome Offsprings in the Southwest of Iran. Jundishapur Journal of Chronic Disease Care. 13(2).
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Mohamadian, Malihe, et al.. (2021). Clinical and Molecular Spectrum of Muscular Dystrophies (MDs) with Intellectual Disability (ID): a Comprehensive Overview. Journal of Molecular Neuroscience. 72(1). 9–23. 10 indexed citations
5.
Aminzadeh, Majid, et al.. (2021). Molecular diagnosis of maturity onset diabetes of the young in Iranian patients: improving management. Journal of Diabetes & Metabolic Disorders. 20(2). 1369–1374. 1 indexed citations
6.
Ghandil, Pegah, et al.. (2021). Genetic association study of CTLA4 and FCεRIα polymorphisms in asthmatic patients in the southwestern region of Iran. Nucleosides Nucleotides & Nucleic Acids. 40(9). 914–925. 2 indexed citations
7.
Nikbakht, Roshan, et al.. (2021). Utilization of Whole Exome Sequencing in Non-Syndromic Premature Ovarian Failure: Ficolin-3 Gene Mutation in an Iranian Family. Iranian Biomedical Journal. 25(6). 441–446. 3 indexed citations
8.
Abolnezhadian, Farhad, Meysam Alipour, Mehrnoosh Zakerkish, et al.. (2020). Association Metabolic Obesity Phenotypes with Cardiometabolic Index, Atherogenic Index of Plasma and Novel Anthropometric Indices: A Link of FTO-rs9939609 Polymorphism. SHILAP Revista de lepidopterología. 6 indexed citations
9.
Abolnezhadian, Farhad, Seyed Ahmad Hosseini, Meysam Alipour, et al.. (2020). <p>Association Metabolic Obesity Phenotypes with Cardiometabolic Index, Atherogenic Index of Plasma and Novel Anthropometric Indices: A Link of FTO-rs9939609 Polymorphism</p>. Vascular Health and Risk Management. Volume 16. 249–256. 35 indexed citations
10.
Birgani, Maryam Tahmasebi, et al.. (2020). Identification of thePRM1gene mutations in oligoasthenoteratozoospermic men. Andrologia. 52(11). e13872–e13872. 4 indexed citations
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Aminzadeh, Majid, et al.. (2018). Clinical features and tubulin folding cofactor E gene analysis in Iranian patients with Sanjad–Sakati syndrome. Jornal de Pediatria. 96(1). 60–65. 4 indexed citations
14.
De, Saurav, Leah Cushing, Lih-Ling Lin, et al.. (2018). Mechanism of dysfunction of human variants of the IRAK4 kinase and a role for its kinase activity in interleukin-1 receptor signaling. Journal of Biological Chemistry. 293(39). 15208–15220. 30 indexed citations
15.
Hintermeyer, Mary, Bertrand Boisson, Maya Chrabieh, et al.. (2017). IRAK4 Deficiency in a Patient with Recurrent Pneumococcal Infections: Case Report and Review of the Literature. Frontiers in Pediatrics. 5. 83–83. 20 indexed citations
16.
Alsina, Laia, Elisabeth Israelsson, Matthew C. Altman, et al.. (2014). A narrow repertoire of transcriptional modules responsive to pyogenic bacteria is impaired in patients carrying loss-of-function mutations in MYD88 or IRAK4. Nature Immunology. 15(12). 1134–1142. 42 indexed citations
17.
Krause, Jens C., Pegah Ghandil, Maya Chrabieh, et al.. (2009). Very Late‐Onset Group BStreptococcusMeningitis, Sepsis, and Systemic Shigellosis due to Interleukin‐1 Receptor–Associated Kinase‐4 Deficiency. Clinical Infectious Diseases. 49(9). 1393–1396. 19 indexed citations
18.
Ghadiri, Ata, et al.. (2008). A polymorphism in the CCL2 chemokine gene is associated with asthma risk: a case–control and a family study in Tunisia. Genes and Immunity. 9(7). 575–581. 15 indexed citations
19.
Ghandil, Pegah, Claude Chelala, Danièle Dubois‐Laforgue, et al.. (2005). Crohn’s disease associated CARD15 (NOD2) variants are not involved in the susceptibility to type 1 diabetes. Molecular Genetics and Metabolism. 86(3). 379–383. 12 indexed citations
20.
Ghandil, Pegah, Ata Ghadiri, D.D. Farhud, & Sirous Zeinali. (2004). Allele frequencies of two polymorphisms associated with the factor IX gene in Iranian population. Thrombosis Research. 113(5). 289–293. 3 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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