Research Project
Javad Jamshidi
Current Appointments
Postdoctoral FellowKey Research Areas
Javad Jamshidi completed his BSc degree in cellular and molecular biology in 2009 and then completed a Master’s degree in human genetics in 2012 in Shahid Beheshti University of Medical Sciences in Tehran. After graduation, he joined Fasa University of Medical Sciences (FUMS) as a lecturer for five years. Besides teaching, he actively continued his research career and collaborations with other researchers which resulted in a number of publications in his fields of interest: human genetics, neurogenetics and psychiatric genetics. Demonstrating excellence in research, Javad was awarded the “Outstanding Researcher Award” by FUMS twice in 2014 and 2017. He is also an investigator on the largest cohort study in Iran, the “PERSIAN Cohort”, a prospective study aiming to recruit 170,000 Iranian participants (35-70 years) to identify the risk factors of the most prevalent chronic diseases. Holding a prestigious UNSW Scientia PhD scholarship awarded by University of New South Wales, he is now a PhD student in NeuRA working on the genetics and neuroscience of wellbeing and resilience.
Publications
2023 May
Negative association between anterior insula activation and resilience during sustained attention: an fMRI twin study
View full journal-article on https://doi.org/10.1017/S0033291721005262
2022 Dec
Wellbeing and brain structure: A comprehensive phenotypic and genetic study of image‐derived phenotypes in the UK Biobank
View full journal-article on https://doi.org/10.1002/hbm.25993
2022, 19 Mar
Phenotypic and genetic analysis of a wellbeing factor score in the UK Biobank and the impact of childhood maltreatment and psychiatric illness
View full journal-article on https://doi.org/10.1038/s41398-022-01874-5
2021, 02 Aug
Associations between mental wellbeing and fMRI neural bases underlying responses to positive emotion in a twin sample
View full journal-article on http://dx.doi.org/10.1017/s0033291721002695
2020 Nov
Diverse phenotypic measurements of wellbeing: Heritability, temporal stability and the variance explained by polygenic scores
View full journal-article on https://doi.org/10.1111/gbb.12694
2020
Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes
View full journal-article on http://www.scopus.com/inward/record.url?eid=2-s2.0-85078077745&partnerID=MN8TOARS
2019 Dec
Genetic analysis of rs11038167, rs11038172 and rs835784 polymorphisms of the TSPAN18 gene in Iranian schizophrenia patients
View full journal-article on http://dx.doi.org/10.1016/j.mgene.2019.100609
2019, 04 May
Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy
View full journal-article on http://dx.doi.org/10.1080/13816810.2019.1622023
2019
Homozygous Mutation in TWNK Cases Ataxia, Sensorineural Hearing Loss and Optic Nerve Atrophy
View full journal-article on http://www.scopus.com/inward/record.url?eid=2-s2.0-85076339219&partnerID=MN8TOARS
2018
A novel c.240_241insGG mutation in NDP gene in a family with Norrie disease
View full journal-article on http://www.scopus.com/inward/record.url?eid=2-s2.0-85030111995&partnerID=MN8TOARS