Majid Kheirollahi

857 total citations
66 papers, 613 citations indexed

About

Majid Kheirollahi is a scholar working on Molecular Biology, Physiology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Majid Kheirollahi has authored 66 papers receiving a total of 613 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 13 papers in Physiology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Majid Kheirollahi's work include Prenatal Screening and Diagnostics (6 papers), Folate and B Vitamins Research (6 papers) and Telomeres, Telomerase, and Senescence (6 papers). Majid Kheirollahi is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Folate and B Vitamins Research (6 papers) and Telomeres, Telomerase, and Senescence (6 papers). Majid Kheirollahi collaborates with scholars based in Iran, Pakistan and France. Majid Kheirollahi's co-authors include Mohammad Kazemi, Mansoor Salehi, Parvin Mehdipour, Elahe Kazemi, Sepideh Dashti, Fariborz Khorvash, Javad Mohammadi‐Asl, Manijeh Mahdavi, Parvin Mahzouni and Maryam Derakhshan and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Analytical Biochemistry.

In The Last Decade

Majid Kheirollahi

63 papers receiving 601 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Majid Kheirollahi Iran 13 256 77 75 61 55 66 613
Xiaowei Xing China 17 385 1.5× 94 1.2× 62 0.8× 102 1.7× 61 1.1× 53 724
Vien Nguyen United States 14 324 1.3× 86 1.1× 50 0.7× 78 1.3× 26 0.5× 30 696
Keiko Yanagihara Japan 18 246 1.0× 100 1.3× 59 0.8× 122 2.0× 23 0.4× 68 792
Ju Gao China 14 335 1.3× 122 1.6× 66 0.9× 60 1.0× 61 1.1× 67 797
Antigoni Manousopoulou United Kingdom 17 361 1.4× 76 1.0× 82 1.1× 89 1.5× 103 1.9× 40 910
John Hoon Rim South Korea 18 322 1.3× 168 2.2× 57 0.8× 31 0.5× 31 0.6× 66 796
Lin Zou China 19 509 2.0× 96 1.2× 92 1.2× 96 1.6× 48 0.9× 73 1.1k
Zhou Jiang China 14 302 1.2× 81 1.1× 42 0.6× 41 0.7× 18 0.3× 43 663
Rachel Dakin United Kingdom 12 375 1.5× 109 1.4× 45 0.6× 206 3.4× 21 0.4× 17 751

Countries citing papers authored by Majid Kheirollahi

Since Specialization
Citations

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

Fields of papers citing papers by Majid Kheirollahi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Majid Kheirollahi

This figure shows the co-authorship network connecting the top 25 collaborators of Majid Kheirollahi. A scholar is included among the top collaborators of Majid Kheirollahi 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 Majid Kheirollahi. Majid Kheirollahi 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.
Yaghini, Omid, et al.. (2023). Griscelli syndrome type 1: a novel pathogenic variant, and review of literature. Molecular Genetics and Genomics. 298(2). 485–493. 1 indexed citations
2.
3.
Tabatabaiefar, Mohammad Amin, et al.. (2021). Homozygous TFG gene variants expanding the mutational and clinical spectrum of hereditary spastic paraplegia 57 and a review of literature. Journal of Human Genetics. 66(10). 973–981. 4 indexed citations
4.
Yaghini, Omid, et al.. (2021). Identification of a Missense Variant in the EIF2B3 Gene Causing Vanishing White Matter Disease with Antenatal-Onset but Mild Symptoms and Long-Term Survival. Journal of Molecular Neuroscience. 71(11). 2405–2414. 7 indexed citations
5.
Kheirollahi, Majid, et al.. (2020). New Variants in the CDH1 Gene in Iranian Families with Hereditary Diffuse Gastric Cancer. SHILAP Revista de lepidopterología. 11(4). 493–501. 1 indexed citations
6.
Hosseini, Seyed Younes, Jamal Sarvari, Fatemeh Rahbarizadeh, et al.. (2020). Gene Delivery by Pei-Nanocomplex Into Breast andColorectal Tumor Cell Lines, The Impacts Of N/P Ratio, Sizeand Type of The Cell. 45(1). 19–27. 1 indexed citations
7.
Kheirollahi, Majid, et al.. (2020). Effect of Donepezil and Hyoscyamoside on Improving Spatial Memory in Rats With Alzheimer's Disease. SHILAP Revista de lepidopterología. 23(4). 524–539. 2 indexed citations
8.
Moridnia, Abbas, et al.. (2018). Novel Variants and Copy Number Variation in CDH1 Gene in Iranian Patients with Sporadic Diffuse Gastric Cancer. Journal of Gastrointestinal Cancer. 50(3). 420–427. 6 indexed citations
9.
Kheirollahi, Majid, et al.. (2017). A Novel Mutation in SLC7A9 Gene in Cystinuria.. PubMed. 11(2). 138–141. 5 indexed citations
10.
Kazemi, Mohammad, Mansoor Salehi, & Majid Kheirollahi. (2016). Down Syndrome: Current Status, Challenges and Future Perspectives.. PubMed. 5(3). 125–133. 100 indexed citations
11.
12.
Sichani, Mehrdad Mohammadi, et al.. (2015). Mutation analysis of SLC3A1 and SLC7A9 genes in patients with cystinuria. Urolithiasis. 43(5). 447–453. 11 indexed citations
13.
Kheirollahi, Majid, et al.. (2014). Brain tumors: Special characters for research and banking. SHILAP Revista de lepidopterología. 4(1). 4–4. 32 indexed citations
14.
Kheirollahi, Majid, et al.. (2013). The Role of Telomere in Cell; Telomere Dysfunction and Tumorigenesis. SHILAP Revista de lepidopterología. 1 indexed citations
15.
Kheirollahi, Majid, et al.. (2012). Telomere Structure and Its Role in DNA Damage and Genetic Disorders. SHILAP Revista de lepidopterología. 1 indexed citations
16.
Mojarrad, Majid, et al.. (2011). Use of siRNA in knocking down of dopamine receptors, a possible therapeutic option in neuropsychiatric disorders. Molecular Biology Reports. 39(2). 2003–2010. 11 indexed citations
17.
Noori–Daloii, Mohammad Reza, et al.. (2010). Alpha- and Beta-Synucleins mRNA Expression in Lymphocytes of Schizophrenia Patients. Genetic Testing and Molecular Biomarkers. 14(5). 725–729. 10 indexed citations
18.
Kheirollahi, Majid, et al.. (2010). Expression of cyclin D2, P53, Rb and ATM cell cycle genes in brain tumors. Medical Oncology. 28(1). 7–14. 24 indexed citations
19.
Mehdipour, Parvin, Saeed Pirouzpanah, Majid Kheirollahi, & Morteza Atri. (2010). Androgen Receptor Gene CAG Repeat Polymorphism and Breast Cancer Risk in Iranian Women: A Case-Control Study. The Breast Journal. 17(1). 39–46. 15 indexed citations
20.
Heidari, Maryam, et al.. (2008). The Spectrum of β -thalassemia Mutations in Isfahan Province of Iran. SHILAP Revista de lepidopterología. 37(2). 106–111. 14 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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