Javad Jamshidi

1.0k total citations
57 papers, 582 citations indexed

About

Javad Jamshidi is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Javad Jamshidi has authored 57 papers receiving a total of 582 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 21 papers in Genetics and 9 papers in Cognitive Neuroscience. Recurrent topics in Javad Jamshidi's work include Genetics and Neurodevelopmental Disorders (8 papers), Parkinson's Disease Mechanisms and Treatments (7 papers) and Autism Spectrum Disorder Research (6 papers). Javad Jamshidi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Parkinson's Disease Mechanisms and Treatments (7 papers) and Autism Spectrum Disorder Research (6 papers). Javad Jamshidi collaborates with scholars based in Iran, Australia and United States. Javad Jamshidi's co-authors include Hossein Darvish, Ehsan Bahramali, Farkhondeh Pouresmaeili, Eznollah Azargashb, Babak Emamalizadeh, Abbas Tafakhori, Justine M. Gatt, Alireza Askari, Hossein Poustchi and Hossein Bahrami and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Biological Psychiatry.

In The Last Decade

Javad Jamshidi

55 papers receiving 577 citations

Peers

Javad Jamshidi
Brecht A. G. Willems Netherlands
Omar A. Mesarwi United States
Michael L. Pucci United States
Kyan James Allahdadi Brazil
Harm de Wit Netherlands
Rebecca Persky United States
Enrico D’Ambrosio Italy
Zarazuela Zolkipli United Kingdom
Alexandra F. Trollope Australia
Anita Devlin United Kingdom
Brecht A. G. Willems Netherlands
Javad Jamshidi
Citations per year, relative to Javad Jamshidi Javad Jamshidi (= 1×) peers Brecht A. G. Willems

Countries citing papers authored by Javad Jamshidi

Since Specialization
Citations

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

Fields of papers citing papers by Javad Jamshidi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Javad Jamshidi

This figure shows the co-authorship network connecting the top 25 collaborators of Javad Jamshidi. A scholar is included among the top collaborators of Javad Jamshidi 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 Jamshidi. Javad Jamshidi 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
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Jamshidi, Javad, et al.. (2022). Wellbeing and brain structure: A comprehensive phenotypic and genetic study of image‐derived phenotypes in the UK Biobank. Human Brain Mapping. 43(17). 5180–5193. 8 indexed citations
3.
Jamshidi, Javad, Peter R. Schofield, Justine M. Gatt, & Janice M. Fullerton. (2022). Phenotypic and genetic analysis of a wellbeing factor score in the UK Biobank and the impact of childhood maltreatment and psychiatric illness. Translational Psychiatry. 12(1). 113–113. 15 indexed citations
4.
Park, Haeme R. P., Leanne M. Williams, Mayuresh S. Korgaonkar, et al.. (2022). Negative association between anterior insula activation and resilience during sustained attention: an fMRI twin study. Psychological Medicine. 53(7). 3187–3199. 6 indexed citations
5.
Park, Haeme R. P., et al.. (2021). Associations between mental wellbeing and fMRI neural bases underlying responses to positive emotion in a twin sample. Psychological Medicine. 53(4). 1215–1223. 8 indexed citations
6.
Jamshidi, Javad, Leanne M. Williams, Peter R. Schofield, et al.. (2020). Diverse phenotypic measurements of wellbeing: Heritability, temporal stability and the variance explained by polygenic scores. Genes Brain & Behavior. 19(8). e12694–e12694. 20 indexed citations
7.
Darvish, Hossein, Luís Azcona, Abbas Tafakhori, et al.. (2020). Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes. Scientific Reports. 10(1). 968–968. 11 indexed citations
8.
9.
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
10.
Jamshidi, Javad, Ehsan Esmaili Shandiz, Reza Mirfakhraie, et al.. (2017). Association of β-Secretase Functional Polymorphism with Risk of Schizophrenia. Genetic Testing and Molecular Biomarkers. 21(4). 248–251. 3 indexed citations
11.
Bahramali, Ehsan, et al.. (2016). Association of ACE gene D polymorphism with left ventricular hypertrophy in patients with diastolic heart failure: a case–control study. BMJ Open. 6(2). e010282–e010282. 31 indexed citations
12.
Lima, Behnam Safarpour, Hamid Ghaedi, Narsis Daftarian, et al.. (2016). c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness. European Journal of Medical Genetics. 59(2). 65–69. 6 indexed citations
13.
Khaniani, Mahmoud Shekari, Ehsan Esmaili Shandiz, Hormoz Ayromlou, et al.. (2016). Genetic Analysis of the ZNF512B , SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population. Genetic Testing and Molecular Biomarkers. 20(10). 629–632. 13 indexed citations
14.
Jamshidi, Javad, et al.. (2016). SNAP-25gene variations and attention-deficit hyperactivity disorder in Iranian population. Neurological Research. 38(11). 959–964. 1 indexed citations
15.
Daftarian, Narsis, Hamid Ahmadieh, Babak Emamalizadeh, et al.. (2016). A novel mutation and variable phenotypic expression in a large consanguineous pedigree with Jalili syndrome. Eye. 30(11). 1424–1432. 9 indexed citations
16.
Firouzabadi, Saghar Ghasemi, Roxana Kariminejad, Roshanak Vameghi, et al.. (2016). Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome. Molecular Neurobiology. 54(9). 7019–7027. 19 indexed citations
17.
Farzaneh, Farah, et al.. (2016). Analysis of CYP17, CYP19 and CYP1A1 Gene Polymorphisms in Iranian Women with Breast Cancer. Asian Pacific Journal of Cancer Prevention. 17(sup3). 23–26. 8 indexed citations
18.
Jamshidi, Javad, Farkhondeh Pouresmaeili, Hossein Darvish, et al.. (2014). FABP9 Mutations Are Not Detected in Cases of Infertility due to Sperm Morphological Defects in Iranian Men. SHILAP Revista de lepidopterología. 2 indexed citations
19.
Pouresmaeili, Farkhondeh, et al.. (2013). Association between Vitamin D Receptor Gene BsmI\nPolymorphism and Bone Mineral Density in A Population\nof 146 Iranian Women. SHILAP Revista de lepidopterología. 23 indexed citations
20.
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

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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