Javad Mohammadi‐Asl

1.3k total citations
117 papers, 1.0k citations indexed

About

Javad Mohammadi‐Asl is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Javad Mohammadi‐Asl has authored 117 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Molecular Biology, 19 papers in Genetics and 16 papers in Genetics. Recurrent topics in Javad Mohammadi‐Asl's work include Hearing, Cochlea, Tinnitus, Genetics (13 papers), Vestibular and auditory disorders (10 papers) and Reproductive Biology and Fertility (8 papers). Javad Mohammadi‐Asl is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (13 papers), Vestibular and auditory disorders (10 papers) and Reproductive Biology and Fertility (8 papers). Javad Mohammadi‐Asl collaborates with scholars based in Iran, Iraq and United States. Javad Mohammadi‐Asl's co-authors include Fatemeh Haidari, Najmaldin Saki, Ali Khodadadi, Masoud Hemadi, Ghasem Saki, Mehrnoosh Zakerkish, Majid Mohammadshahi, Hossein Khadem Haghighian, Parvin Mehdipour and Mohammadreza Gholami and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Investigative Dermatology and Gene.

In The Last Decade

Javad Mohammadi‐Asl

107 papers receiving 1000 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Javad Mohammadi‐Asl Iran 16 435 152 136 129 103 117 1.0k
Aligholi Sobhani Iran 18 310 0.7× 547 3.6× 60 0.4× 417 3.2× 95 0.9× 76 1.1k
Jianda Dong China 18 374 0.9× 112 0.7× 139 1.0× 68 0.5× 62 0.6× 36 946
Junyan Sun China 16 318 0.7× 176 1.2× 127 0.9× 228 1.8× 110 1.1× 26 844
Katarzyna Jarząbek Poland 16 326 0.7× 151 1.0× 105 0.8× 116 0.9× 18 0.2× 37 813
Min‐Ji Kim South Korea 16 431 1.0× 61 0.4× 156 1.1× 98 0.8× 28 0.3× 39 840
Linlin Sun China 20 860 2.0× 40 0.3× 214 1.6× 52 0.4× 55 0.5× 53 1.4k
Che‐Chung Yeh United States 18 604 1.4× 25 0.2× 191 1.4× 30 0.2× 33 0.3× 35 1.1k
Zohreh Mazaheri Iran 14 243 0.6× 175 1.2× 34 0.3× 166 1.3× 64 0.6× 67 634
Hiroyuki Kawagishi Japan 14 391 0.9× 147 1.0× 121 0.9× 197 1.5× 17 0.2× 23 893
Florence Gizard France 24 861 2.0× 71 0.5× 226 1.7× 54 0.4× 19 0.2× 32 1.8k

Countries citing papers authored by Javad Mohammadi‐Asl

Since Specialization
Citations

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

Fields of papers citing papers by Javad Mohammadi‐Asl

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Javad Mohammadi‐Asl. 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 Javad Mohammadi‐Asl. The network helps show where Javad Mohammadi‐Asl may publish in the future.

Co-authorship network of co-authors of Javad Mohammadi‐Asl

This figure shows the co-authorship network connecting the top 25 collaborators of Javad Mohammadi‐Asl. A scholar is included among the top collaborators of Javad Mohammadi‐Asl 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 Javad Mohammadi‐Asl. Javad Mohammadi‐Asl 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.
Tehrani, Mohsen Nader, et al.. (2025). Crosstalk between non-coding RNAs and programmed cell death in colorectal cancer: implications for targeted therapy. Epigenetics & Chromatin. 18(1). 3–3. 10 indexed citations
2.
Mohammadi‐Asl, Javad, et al.. (2024). Identification and characterization of NMNAT1 gene mutations in an Iranian patient with Leber congenital amaurosis 9. SHILAP Revista de lepidopterología. 12(10). e9506–e9506.
3.
Mohammadi‐Asl, Javad, et al.. (2024). Retinitis pigmentosa‐1 due to an RP1 mutation in a consanguineous Iranian family: Report of a novel mutation. SHILAP Revista de lepidopterología. 12(3). e8666–e8666. 2 indexed citations
4.
Mohammadi‐Asl, Javad, et al.. (2022). Exome sequencing identifies a novel GUCY2D mutation in an Iranian family with Leber congenital amaurosis-1: a case report. SHILAP Revista de lepidopterología. 23(1). 1 indexed citations
5.
Mohammadi‐Asl, Javad, et al.. (2021). An intelligent prenatal screening system for the prediction of Trisomy-21. Informatics in Medicine Unlocked. 24. 100625–100625. 9 indexed citations
6.
Malamiri, Reza Azizi, et al.. (2021). Identification of a Novel Stop Loss Mutation in P2RX2 Gene in an Iranian Family with Autosomal Nonsyndromic Hearing Loss. PubMed. 25(5). 368–73. 2 indexed citations
7.
Mohammadi‐Asl, Javad, et al.. (2021). The worldwide molecular spectrum and distribution of thalassaemia: a systematic review. Annals of Human Biology. 48(4). 307–312. 6 indexed citations
8.
Hosseini, Seyed Mohammad, et al.. (2020). Influence of Two DNA Repair Pathway Polymorphisms in Colorectal Cancer Risk in Southwest Iran. Asian Pacific Journal of Cancer Prevention. 21(7). 1919–1924. 2 indexed citations
9.
Saki, Nader, et al.. (2019). Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing. Audiology and Neurotology. 24(1). 25–31. 16 indexed citations
10.
Hajjari, Mohammadreza, et al.. (2019). Exome sequencing found a novel homozygous deletion in ADCK3 gene involved in autosomal recessive spinocerebellar ataxia. Gene. 708. 10–13. 6 indexed citations
11.
Mohammadi‐Asl, Javad, et al.. (2019). Exome sequencing revealed a p.G299R mutation in the COMP gene in an Iranian family suffering from pseudoachondroplasia. The Journal of Gene Medicine. 21(8). e3103–e3103. 1 indexed citations
12.
Tabatabaiefar, Mohammad Amin, et al.. (2017). A novel pathogenic variant in an Iranian Ataxia telangiectasia family revealed by next-generation sequencing followed by in silico analysis. Journal of the Neurological Sciences. 379. 212–216. 9 indexed citations
13.
Mohammadi‐Asl, Javad, et al.. (2017). Next-generation sequencing identifies three novel missense variants in ILDR1 and MYO6 genes in an Iranian family with hearing loss with review of the literature. International Journal of Pediatric Otorhinolaryngology. 103. 103–108. 8 indexed citations
14.
Vahidnezhad, Hassan, Leila Youssefian, Amir Hossein Saeidian, et al.. (2016). Gene-Targeted Next Generation Sequencing Identifies PNPLA1 Mutations in Patients with a Phenotypic Spectrum of Autosomal Recessive Congenital Ichthyosis: The Impact of Consanguinity. Journal of Investigative Dermatology. 137(3). 678–685. 27 indexed citations
15.
Mohammadi‐Asl, Javad, et al.. (2016). Incidence of T315I mutation in BCR/ABL-positive CML and ALL patients. Frontiers in Biology. 11(5). 404–411. 3 indexed citations
16.
Shahjahani, Mohammad, et al.. (2015). Rare cytogenetic abnormalities and alteration of microRNAs in acute myeloid leukemia and response to therapy. Oncology Reviews. 9(1). 261–261. 13 indexed citations
17.
Mohammadi‐Asl, Javad, Hamid Galehdari, Ahmad Ahmadzadeh, et al.. (2014). Characterization of Wild-Type and Mutated RET Proto-Oncogene Associated with Familial Medullary Thyroid Cancer. Asian Pacific Journal of Cancer Prevention. 15(5). 2027–2033. 5 indexed citations
18.
Mohammadi‐Asl, Javad, et al.. (2012). THE EFFECTS OF HYDRO ALCOHOLIC EXTRACT OF JUGLANS REGIA LEAF ON HISTOLOGICAL CHANGES OF LANGERHANS ISLET IN DIABETIC RATS MODEL. SHILAP Revista de lepidopterología. 15(4). 293–302. 9 indexed citations
19.
Nasrollahzadeh, Javad, Fereydoun Siassi, Mahmood Doosti, et al.. (2008). The influence of feeding linoleic, gamma-linolenic and docosahexaenoic acid rich oils on rat brain tumor fatty acids composition and fatty acid binding protein 7 mRNA expression. Lipids in Health and Disease. 7(1). 45–45. 19 indexed citations
20.
Mohammadi‐Asl, Javad, et al.. (2006). Evaluation of chromosomal changes in patients with spontaneous abortion in Khozestan province. Iranian journal of pathology. 1(1). 21–24. 2 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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