Mehri Khatami

597 total citations
58 papers, 438 citations indexed

About

Mehri Khatami is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Mehri Khatami has authored 58 papers receiving a total of 438 indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 11 papers in Cellular and Molecular Neuroscience and 11 papers in Genetics. Recurrent topics in Mehri Khatami's work include Mitochondrial Function and Pathology (13 papers), Congenital heart defects research (10 papers) and Genetic Neurodegenerative Diseases (9 papers). Mehri Khatami is often cited by papers focused on Mitochondrial Function and Pathology (13 papers), Congenital heart defects research (10 papers) and Genetic Neurodegenerative Diseases (9 papers). Mehri Khatami collaborates with scholars based in Iran, Austria and Portugal. Mehri Khatami's co-authors include Mohammad Heidari, Massoud Houshmand, Shahriar Nafissi, Saman Hosseinkhani, Ali Reza Talebi, Barbara Scheiber‐Mojdehkar, Ali Reza Talebi, M. Teresa Moreno, Masood Fereidoonnezhad and Fatemeh Kazeminasab and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and European Journal of Inorganic Chemistry.

In The Last Decade

Mehri Khatami

52 papers receiving 435 citations

Peers

Mehri Khatami

CCM

EPIDE

CMN

GENET

Anna M. Sokòl Germany

Carita Lannér Canada

Catherine Brunel‐Guitton Canada

Zhifang Hao China

Katalin Sümegi Hungary

Lode De Cauwer Belgium

Zheng Wei China

Xiuzhi Duan China

Jing Song China

Tatsuo Shinagawa United States

Anna M. Sokòl Germany

Mehri Khatami

407 ×1.5

50 ×0.8

CCM

41 ×0.7

EPIDE

31 ×0.5

CMN

29 ×0.5

GENET

Citations per year, relative to Mehri Khatami Mehri Khatami (= 1×) peers Anna M. Sokòl

Countries citing papers authored by Mehri Khatami

Since Specialization

Citations

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

Fields of papers citing papers by Mehri Khatami

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mehri Khatami

This figure shows the co-authorship network connecting the top 25 collaborators of Mehri Khatami. A scholar is included among the top collaborators of Mehri Khatami 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 Mehri Khatami. Mehri Khatami is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Heidari, Mohammad, et al.. (2025). New strategy for the design and cloning of novel humanized biparatopic anti-CD52 nanobodies: Tools for targeted drug delivery and therapeutic approaches. Biochemical Engineering Journal. 219. 109736–109736.

Mansoor, Wasat, et al.. (2025). Rare pathogenic NR2F2 (COUP-TFII) variants as potential etiological causes in pediatric patients with congenital heart diseases (CHDs). Hellenic Journal of Cardiology. 1 indexed citations

Salari, Mahdieh & Mehri Khatami. (2025). Simultaneous Application of Electron Beam Irradiation and Freezing as an Effective Method for Shelf Life Extension of Minced Turkey Meat. Food Science & Nutrition. 13(1). e4752–e4752. 1 indexed citations

Khatami, Mehri, et al.. (2024). Evaluation of the expression of LINCOO475 and FOXO1 genes as tumor suppressor genes in breast cancer: Correlation of bioinformatics tools and experimental approaches. Gene Reports. 36. 101980–101980. 1 indexed citations

Khatami, Mehri, et al.. (2024). Mutational analysis and prediction of the potential impact of missense mutations in the HOXA9 gene in B-cell acute lymphoblastic leukemia. Human Gene. 41. 201318–201318.

Heidari, Mohammad, et al.. (2024). CDR grafting and site-directed mutagenesis approach for the generation and affinity maturation of Anti-CD20 nanobody. Molecular Biology Reports. 51(1). 751–751. 5 indexed citations

Heidari, Mohammad, et al.. (2023). Novel nucleotide variations in the thrombomodulin (THBD) gene involved in coagulation pathways can increase the risk of recurrent pregnancy loss (RPL). Gene. 895. 148011–148011. 1 indexed citations

Khatami, Mehri, et al.. (2021). Novel Point Mutations in 3′-Untranslated Region of GATA4 Gene Are Associated with Sporadic Non-syndromic Atrial and Ventricular Septal Defects. Current Medical Science. 42(1). 129–143. 3 indexed citations

Heidari, Mohammad, et al.. (2020). MicroRNAs as a New Molecular Biomarker for Diagnosis and Prognosis of T-cell Acute Lymphoblastic Leukemia (T-ALL): A Systematic Review. 10(3). 184–199. 2 indexed citations

10.

Heidari, Mohammad, et al.. (2020). Novel Point Mutations in Mitochondrial MT-CO2 Gene May Be Risk Factors for Coronary Artery Disease. Applied Biochemistry and Biotechnology. 191(3). 1326–1339. 18 indexed citations

11.

Heidari, Mohammad, et al.. (2020). Association of Pathogenic Missense and Nonsense Mutations in Mitochondrial COII Gene with Familial Adenomatous Polyposis (FAP).. PubMed. 9(4). 255–265.

12.

Heidari, Mohammad, et al.. (2019). The association between TNP2 gene polymorphisms and Iranian infertile men with varicocele: A case-control study. International Journal of Reproductive BioMedicine (IJRM). 17(8). 557–566. 5 indexed citations

13.

Khatami, Mehri, et al.. (2017). Designing and Validation of One-Step T-ARMS-PCR for Genotyping the eNOS rs1799983 SNP. Iranian Journal of Biotechnology. 15(3). 208–212. 4 indexed citations

14.

Khatami, Mehri, et al.. (2017). Novel and heteroplasmic mutations in mitochondrial tRNA genes in Brugada syndrome. Cardiology Journal. 25(1). 113–119. 21 indexed citations

15.

Khatami, Mehri, et al.. (2016). Mitochondrial Mutations in tRNA Glu and Cytochrome b Genes Associated with Iranian Congenial Heart Disease. 10(4).

16.

Khatami, Mehri & Mohammad Heidari. (2016). Common rs5918 (PlA1/A2) polymorphism in the ITGB3 gene and risk of coronary artery disease. Archives of Medical Science - Atherosclerotic Diseases. 1(1). 9–15. 21 indexed citations

17.

Khatami, Mehri, et al.. (2014). Novel Nucleotide Changes in Mitochondrial COXII, Cytochrome B and tRNAGlu Genes in Patients with Brugada Syndrome. SHILAP Revista de lepidopterología.

18.

Khatami, Mehri, et al.. (2011). Increased Prevalence 12308 A > G mutation in Mitochondrial tRNALeu (CUN) Gene Associated with earlier Age of Onset in Friedreich Ataxia. 5(4). 25–31. 3 indexed citations

19.

Khatami, Mehri, et al.. (2009). Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor?. Cardiovascular Pathology. 19(2). e21–e27. 9 indexed citations

20.

Heidari, Mohammad, Massoud Houshmand, Saman Hosseinkhani, et al.. (2008). A Novel Mitochondrial Heteroplasmic C13806A Point Mutation Associated with Iranian Friedreich’s Ataxia. Cellular and Molecular Neurobiology. 29(2). 225–233. 13 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.

Explore authors with similar magnitude of impact