Mina Ohadi

1.6k total citations
73 papers, 1.0k citations indexed

About

Mina Ohadi is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Mina Ohadi has authored 73 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 24 papers in Genetics and 19 papers in Cellular and Molecular Neuroscience. Recurrent topics in Mina Ohadi's work include RNA Research and Splicing (18 papers), RNA and protein synthesis mechanisms (17 papers) and Genetics and Neurodevelopmental Disorders (14 papers). Mina Ohadi is often cited by papers focused on RNA Research and Splicing (18 papers), RNA and protein synthesis mechanisms (17 papers) and Genetics and Neurodevelopmental Disorders (14 papers). Mina Ohadi collaborates with scholars based in Iran, United Kingdom and Netherlands. Mina Ohadi's co-authors include Hossein Najmabadi, Hossein Darvish, Akbar Biglarian, Koorosh Kamali, Arash Mirabzadeh, Jinghua Zhao, Caroline Shiach, Pak C. Sham, Sally E. Kinsey and D. Mark Layton and has published in prestigious journals such as Scientific Reports, Brain Research and The American Journal of Human Genetics.

In The Last Decade

Mina Ohadi

70 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mina Ohadi Iran 18 525 270 197 143 121 73 1.0k
Koen L.I. van Gassen Netherlands 22 564 1.1× 407 1.5× 319 1.6× 29 0.2× 96 0.8× 42 1.3k
Ruma Raha‐Chowdhury United Kingdom 21 303 0.6× 67 0.2× 234 1.2× 483 3.4× 123 1.0× 40 1.4k
Carol Guy United Kingdom 16 522 1.0× 257 1.0× 169 0.9× 92 0.6× 25 0.2× 25 910
M. Pineda Spain 22 618 1.2× 398 1.5× 165 0.8× 125 0.9× 49 0.4× 51 1.7k
J.L. Haines United States 15 247 0.5× 319 1.2× 120 0.6× 27 0.2× 112 0.9× 20 853
J. Michael Andresen United States 17 1.2k 2.3× 170 0.6× 552 2.8× 171 1.2× 53 0.4× 21 1.6k
Susan B. Olson United States 12 672 1.3× 90 0.3× 356 1.8× 197 1.4× 43 0.4× 20 1.2k
Kathryn A. Helmin United States 14 827 1.6× 101 0.4× 317 1.6× 25 0.2× 329 2.7× 22 1.4k
Noemi Morello Italy 11 470 0.9× 310 1.1× 159 0.8× 45 0.3× 37 0.3× 15 795
Jami Dwyer United States 14 597 1.1× 194 0.7× 265 1.3× 26 0.2× 379 3.1× 15 1.3k

Countries citing papers authored by Mina Ohadi

Since Specialization
Citations

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

Fields of papers citing papers by Mina Ohadi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mina Ohadi

This figure shows the co-authorship network connecting the top 25 collaborators of Mina Ohadi. A scholar is included among the top collaborators of Mina Ohadi 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 Mina Ohadi. Mina Ohadi 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.
Ohadi, Mina, Safoura Khamse, Samira Alizadeh, et al.. (2024). Novel crossover and recombination hotspots massively spread across primate genomes. Biology Direct. 19(1). 70–70.
2.
Salesi, Mahmood, et al.. (2022). Global abundance of short tandem repeats is non-random in rodents and primates. BMC Genomic Data. 23(1). 77–77. 4 indexed citations
3.
Emamalizadeh, Babak, et al.. (2020). Analysis of polymorphism and function of GA repeat in RIT2 gene promoterAnalysis of polymorphism and function of GA repeat in RIT2 gene promoter in Parkinson’s disease. Research in Medicine. 44(4). 526–531. 1 indexed citations
4.
Kalhor, Naser, Reza Najafipour, Mahshid Foroughan, et al.. (2020). Natural Selection at the NHLH2 Core Promoter Exceptionally Long CA-Repeat in Human and Disease-Only Genotypes in Late-Onset Neurocognitive Disorder. Gerontology. 66(5). 514–522. 10 indexed citations
5.
6.
Ohadi, Mina, et al.. (2019). Genome-wide prediction and prioritization of human aging genes by data fusion: a machine learning approach. BMC Genomics. 20(1). 832–832. 12 indexed citations
7.
Alehabib, Elham, Ehsan Esmaili Shandiz, Javad Jamshidi, et al.. (2017). Support for “Disease-Only” Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in Schizophrenia. Genetic Testing and Molecular Biomarkers. 21(8). 485–490. 14 indexed citations
8.
Aghajanirefah, Ali, Luan N. Nguyen, & Mina Ohadi. (2015). BEND3 is involved in the human-specific repression of calreticulin: Implication for the evolution of higher brain functions in human. Gene. 576(1). 577–580. 8 indexed citations
9.
Nikkhah, M Javan, Maryam Rezazadeh, Hamid Reza Khorram Khorshid, Akbar Biglarian, & Mina Ohadi. (2015). An exceptionally long CA-repeat in the core promoter of SCGB2B2 links with the evolution of apes and Old World monkeys. Gene. 576(1). 109–114. 18 indexed citations
10.
Farashi, Samaneh, Mina Ohadi, Saman Hosseinkhani, Hossein Darvish, & Arash Mirabzadeh. (2015). Decreased gene expression activity as a result of a mutation in the calreticulin gene promoter in a family case of schizoaffective disorder. Cognitive Neurodynamics. 10(3). 269–274. 2 indexed citations
11.
Darvish, Hossein, Abolfazl Heidari, Saman Hosseinkhani, et al.. (2013). Biased Homozygous Haplotypes Across the Human Caveolin 1 Upstream Purine Complex in Parkinson’s Disease. Journal of Molecular Neuroscience. 51(2). 389–393. 19 indexed citations
12.
Heidari, Asieh, Mehrdad Behmanesh, Mohammad Ali Sahraian, et al.. (2011). The human caveolin 1 gene upstream purine complex and neurodegeneration—A common signature. Journal of Neuroimmunology. 236(1-2). 106–110. 7 indexed citations
13.
Darvish, Hossein, Saghar Ghasemi Firouzabadi, Masoud Karimlou, et al.. (2011). Exceptional human core promoter nucleotide compositions. Gene. 475(2). 79–86. 17 indexed citations
14.
Mirabzadeh, Arash, et al.. (2010). Reversion of the human calreticulin gene promoter to the ancestral type as a result of a novel psychosis-associated mutation. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 35(2). 541–544. 17 indexed citations
15.
Nunes, Ana F., Mina Ohadi, Alireza Rahimi, et al.. (2008). A mutation in the calreticulin gene promoter in a family case of schizoaffective disorder leads to its aberrant transcriptional activation. Brain Research. 1239. 36–41. 8 indexed citations
16.
Heshmati, Yaser, Arash Mirabzadeh, Koorosh Kamali, et al.. (2008). A novel polymorphic purine complex at the 1.5 kb upstream region of the human caveolin‐1 gene and risk of Alzheimer's disease; Extra‐short alleles and accumulated allele homozygosity. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(2). 248–253. 16 indexed citations
17.
Ohadi, Mina, et al.. (2007). Gender dimorphism in the DAT1 − 67 T-allele homozygosity and predisposition to bipolar disorder. Brain Research. 1144. 142–145. 14 indexed citations
18.
Ohadi, Mina, et al.. (2006). Attention-deficit/hyperactivity disorder (ADHD) association with the DAT1 core promoter −67 T allele. Brain Research. 1101(1). 1–4. 15 indexed citations
19.
Ohadi, Mina, et al.. (2005). Association between the DRD2 A1 allele and opium addiction in the Iranian population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 134B(1). 39–41. 32 indexed citations
20.
Ohadi, Mina, M. R. A. LALLOZ, Pak C. Sham, et al.. (1999). Localization of a Gene for Familial Hemophagocytic Lymphohistiocytosis at Chromosome 9q21.3-22 by Homozygosity Mapping. The American Journal of Human Genetics. 64(1). 165–171. 138 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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