Morteza Oladnabi

33.6k total citations
40 papers, 229 citations indexed

About

Morteza Oladnabi is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Morteza Oladnabi has authored 40 papers receiving a total of 229 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 5 papers in Genetics and 5 papers in Immunology. Recurrent topics in Morteza Oladnabi's work include Amino Acid Enzymes and Metabolism (3 papers), Metabolism and Genetic Disorders (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (3 papers). Morteza Oladnabi is often cited by papers focused on Amino Acid Enzymes and Metabolism (3 papers), Metabolism and Genetic Disorders (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (3 papers). Morteza Oladnabi collaborates with scholars based in Iran, Germany and Türkiye. Morteza Oladnabi's co-authors include Anvarsadat Kianmehr, Abbas Azadmehr, Abouzar Bagheri, Mina Ohadi, Hossein Darvish, Saghar Ghasemi Firouzabadi, Ayyoob Khosravi, Mozhgan Rezaei Kanavi, Hossein Najmabadi and Moein Shirzad and has published in prestigious journals such as SHILAP Revista de lepidopterología, Biochemical and Biophysical Research Communications and Frontiers in Immunology.

In The Last Decade

Morteza Oladnabi

37 papers receiving 229 citations

Peers

Morteza Oladnabi

GENET

ONCOL

CMN

Mingwei Zhu China

Rossella Rispoli Italy

Gina P. Kwon United States

Ponnalagu Murugeswari India

Carla J. Ramos United States

Julian Schumacher Germany

Christiane Kummer Germany

Duah Alkam United States

Faisal Hayat Nazir Sweden

Zhongliang Liu China

Mingwei Zhu China

Morteza Oladnabi

147 ×1.4

25 ×0.8

GENET

30 ×1.2

ONCOL

57 ×2.6

33 ×1.8

CMN

Citations per year, relative to Morteza Oladnabi Morteza Oladnabi (= 1×) peers Mingwei Zhu

Countries citing papers authored by Morteza Oladnabi

Since Specialization

Citations

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

Fields of papers citing papers by Morteza Oladnabi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Morteza Oladnabi

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

All Works

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20 of 20 papers shown

Oladnabi, Morteza, et al.. (2024). Hearing Loss Among Families with 2 and More Affected Members in Golestan Province, Iran: A Cross-Sectional Study of 320 Families. The Journal of International Advanced Otology. 20(1). 44–49. 1 indexed citations

Samaei, Nader Mansour, et al.. (2024). Identification of novel and known genetic variants associated with hereditary hearing loss in iranian families using whole exome sequencing. Molecular Biology Reports. 51(1). 662–662.

Oladnabi, Morteza, et al.. (2024). A novel biallelic 19-bp deletion in the IL10RB gene caused infant-onset inflammatory bowel disease in a consanguineous family: a molecular docking simulation study and literature review. Molecular Biology Reports. 51(1). 223–223. 1 indexed citations

Khosravi, Ayyoob, et al.. (2023). Impact of umbelliprenin-containing niosome nanoparticles on VEGF-A and CTGF genes expression in retinal pigment epithelium cells. International Journal of Ophthalmology. 17(1). 7–15. 3 indexed citations

Oladnabi, Morteza, et al.. (2022). Molecular insight of dyskeratosis congenita: Defects in telomere length homeostasis. Journal of Clinical and Translational Research. 8(1). 20–30. 5 indexed citations

Pormohammad, Ali, Emad Behboudi, Ali Ramezani, et al.. (2022). Global Study of Viral Meningitis: A Systematic Review and Meta-analysis. SHILAP Revista de lepidopterología. 1 indexed citations

Behboudi, Emad, et al.. (2021). The effects of fasting in Ramadan on the risk factors of COVID-19 in adolescents: a brief review. International Journal of Pediatrics. 9(1). 12835–12842. 2 indexed citations

Oladnabi, Morteza, et al.. (2021). In silico drug repurposing for the treatment of heart diseases using gene expression data and molecular docking techniques. Biochemical and Biophysical Research Communications. 572. 138–144. 5 indexed citations

Oladnabi, Morteza, et al.. (2020). A review on the genetics of autosomal recessive primary microcephaly. SHILAP Revista de lepidopterología. 1 indexed citations

10.

Hashemi‐Soteh, Mohammad Bagher, et al.. (2020). Genetic Counseling for Families with Sporadic Intellectual Disability in North of Iran: A Retrospective Study. International Journal of Pediatrics. 8(8). 11709–11718.

11.

Oladnabi, Morteza, et al.. (2020). Detection of the Duplication in Exons 56-63 of Duchenne Muscular Dystrophy Patients with MLPA. International Journal of Pediatrics. 8(79). 11617–11623. 2 indexed citations

12.

Oladnabi, Morteza, et al.. (2020). Transfusion Related Adverse Effects on Beta-Thalassemia Major and New Therapeutic Approaches: A Review Study. International Journal of Pediatrics. 8(7). 11651–11661. 2 indexed citations

13.

Oladnabi, Morteza, et al.. (2019). Hereditary Hearing Loss and Consanguinity in Turkmen Population of Iran: A Retrospective Study. International journal of pediatrics. 7(11). 10323–10334. 1 indexed citations

14.

Tahamtan, Alireza, et al.. (2019). Cannabinoid CB2 Receptor Functional Variation (Q63R) Is Associated with Multiple Sclerosis in Iranian Subjects. Journal of Molecular Neuroscience. 70(1). 26–31. 12 indexed citations

15.

Kianmehr, Anvarsadat, et al.. (2018). Enzymatic characterization of a NADH-dependent diaphorase from Lysinibacillus sp. strain PAD-91. Protein Expression and Purification. 146. 1–7. 2 indexed citations

16.

Oladnabi, Morteza, et al.. (2017). Fibrodysplasia ossificans progressive: A case report. SHILAP Revista de lepidopterología.

17.

Kianmehr, Anvarsadat, Abdolkarim Mahrooz, Morteza Oladnabi, et al.. (2016). Purification and Characterization of Recombinant Darbepoetin Alfa from Leishmania tarentolae. Molecular Biotechnology. 58(8-9). 566–572. 2 indexed citations

18.

Kianmehr, Anvarsadat, et al.. (2015). Cloning and expression of codon-optimized recombinant darbepoetin alfa in Leishmania tarentolae T7-TR. Protein Expression and Purification. 118. 120–125. 6 indexed citations

19.

Ohadi, Mina, Arash Mirabzadeh, Maryam Rezazadeh, et al.. (2012). Novel evidence of the involvement of calreticulin in major psychiatric disorders. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 37(2). 276–281. 17 indexed citations

20.

Heidari, Asieh, Ziba Nariman‐Saleh‐Fam, Mehdi Banan, et al.. (2011). Core promoter STRs: Novel mechanism for inter-individual variation in gene expression in humans. Gene. 492(1). 195–198. 23 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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