Omid Aryani

418 total citations
42 papers, 307 citations indexed

About

Omid Aryani is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Omid Aryani has authored 42 papers receiving a total of 307 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 11 papers in Physiology and 10 papers in Genetics. Recurrent topics in Omid Aryani's work include Lysosomal Storage Disorders Research (8 papers), Mitochondrial Function and Pathology (6 papers) and Genomics and Rare Diseases (5 papers). Omid Aryani is often cited by papers focused on Lysosomal Storage Disorders Research (8 papers), Mitochondrial Function and Pathology (6 papers) and Genomics and Rare Diseases (5 papers). Omid Aryani collaborates with scholars based in Iran, Malaysia and United States. Omid Aryani's co-authors include Massoud Houshmand, Behnam Kamalıdehghan, Majid Sadeghizadeh, Yong Meng Goh, Zahra‐Soheila Soheili, Fatemeh Ahmadipour, Shahriar Nafissi, Lip Yong Chung, Mahmoud Reza Ashrafi and Maryam Sedghi and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Omid Aryani

41 papers receiving 305 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Omid Aryani Iran 10 186 86 58 42 36 42 307
Linda Manwaring United States 8 136 0.7× 175 2.0× 83 1.4× 75 1.8× 33 0.9× 15 374
Ana Kolicheski United States 11 105 0.6× 60 0.7× 100 1.7× 48 1.1× 33 0.9× 18 343
Shinobu Fukumura Japan 11 149 0.8× 55 0.6× 53 0.9× 43 1.0× 11 0.3× 29 272
Mathilde Nizon France 13 239 1.3× 153 1.8× 23 0.4× 26 0.6× 22 0.6× 26 387
Lenka Mrázová Czechia 12 181 1.0× 39 0.5× 93 1.6× 81 1.9× 16 0.4× 33 308
Imen Dorboz France 14 492 2.6× 94 1.1× 36 0.6× 67 1.6× 24 0.7× 30 650
Giulia Massaro United Kingdom 10 189 1.0× 86 1.0× 163 2.8× 80 1.9× 13 0.4× 17 391
Emmanuelle Ranza Switzerland 12 137 0.7× 103 1.2× 20 0.3× 19 0.5× 15 0.4× 22 295
Erin Knock Canada 11 188 1.0× 50 0.6× 46 0.8× 19 0.5× 79 2.2× 15 307
Takuya Hiraide Japan 12 271 1.5× 185 2.2× 26 0.4× 56 1.3× 17 0.5× 34 441

Countries citing papers authored by Omid Aryani

Since Specialization
Citations

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

Fields of papers citing papers by Omid Aryani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Omid Aryani

This figure shows the co-authorship network connecting the top 25 collaborators of Omid Aryani. A scholar is included among the top collaborators of Omid Aryani 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 Omid Aryani. Omid Aryani 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.
Aryani, Omid, et al.. (2022). P. Ala278Val mutation might cause a pathogenic defect in HEXB folding leading to the Sandhoff disease. Metabolic Brain Disease. 37(8). 2669–2675. 1 indexed citations
2.
Smith, Laurie D., Omid Aryani, Claudia Castiglioni, et al.. (2021). Novel bi-allelic variants expand the SPTBN4-related genetic and phenotypic spectrum. European Journal of Human Genetics. 29(7). 1121–1128. 10 indexed citations
3.
Habibi, Seyed Amir Hassan, et al.. (2019). A novel homozygous variation in the PANK2 gene in two Persian siblings with atypical pantothenate kinase associated neurodegeneration. Neurology International. 11(1). 7959–7959. 4 indexed citations
4.
Kamalıdehghan, Behnam, et al.. (2017). Four novel ARSA gene mutations with pathogenic impacts on metachromatic leukodystrophy: a bioinformatics approach to predict pathogenic mutations. SHILAP Revista de lepidopterología. 1 indexed citations
5.
Sailani, M. Reza, James Chappell, Jingga Inlora, et al.. (2017). WISP3 mutation associated with pseudorheumatoid dysplasia. Molecular Case Studies. 4(1). a001990–a001990. 15 indexed citations
6.
Damme, Tim Van, Alain Colige, Delfien Syx, et al.. (2016). Expanding the clinical and mutational spectrum of the Ehlers–Danlos syndrome, dermatosparaxis type. Genetics in Medicine. 18(9). 882–891. 34 indexed citations
7.
Kamalıdehghan, Behnam, et al.. (2016). Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas. Therapeutics and Clinical Risk Management. Volume 13. 15–19. 2 indexed citations
8.
Tonekaboni, Seyed Hassan, Omid Aryani, Parvaneh Karimzadeh, et al.. (2015). Clinical and Molecular Study of NPC in Iran: Report of 5 Novel Mutations. 9(4). 8–9. 1 indexed citations
9.
Kamalıdehghan, Behnam, et al.. (2014). Two Novel Tyrosinase (TYR) Gene Mutations with Pathogenic Impact on Oculocutaneous Albinism Type 1 (OCA1). PLoS ONE. 9(9). e106656–e106656. 31 indexed citations
10.
Kamalıdehghan, Behnam, Massoud Houshmand, Yong Meng Goh, et al.. (2014). Gene Expression Profiling of Mitochondrial Oxidative Phosphorylation (OXPHOS) Complex I in Friedreich Ataxia (FRDA) Patients. PLoS ONE. 9(4). e94069–e94069. 33 indexed citations
11.
Aryani, Omid, et al.. (2014). Detection of Intragenic SMN1 Mutations in Spinal Muscular Atrophy Patients With a Single Copy of SMN1. Journal of Child Neurology. 30(5). 558–562. 6 indexed citations
12.
Mousavizadeh‬, Kazem, et al.. (2013). Association of human mtDNA mutations with autism in Iranian patients. SHILAP Revista de lepidopterología. 3 indexed citations
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15.
Soheili, Zahra‐Soheila, et al.. (2012). Investigation of the Mitochondrial ATPase 6/8 and tRNALys Genes Mutations in Autism. SHILAP Revista de lepidopterología. 14 indexed citations
16.
Parivar, Kazem, et al.. (2012). Investigation of Exon 1 in FXN Gene in Patients with Clinical Symptomatic of Friedreich Ataxia. SHILAP Revista de lepidopterología. 2 indexed citations
17.
18.
Aryani, Omid, et al.. (2012). Novel Mutations in Sandhoff Disease: A Molecular Analysis Among Iranian Cohort of Infantile Patients. SHILAP Revista de lepidopterología. 3 indexed citations
19.
Aryani, Omid, Massoud Houshmand, & Farzad Fatehi. (2012). A novel PANK2 gene mutation in a Persian boy: The first report from Iran. Clinical Neurology and Neurosurgery. 115(7). 1170–1172. 4 indexed citations
20.
Aryani, Omid, et al.. (2005). Harlequin Ichthyosis: A report of two cases. 8(2). 149–154. 1 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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