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Medical Genetics, Neurogenetics, Behavioral Genetics
Australia, Iran

Activities

Employment (5)

Neuroscience Research Australia: Sydney, NSW, AU

2022-10-04 to present | Postdoctoral Fellow
Employment
Source: Self-asserted source
Javad Jamshidi

Neuroscience Research Australia: Sydney, NSW, AU

2018-06-04 to 2022-10-07 | PhD Student
Employment
Source: Self-asserted source
Javad Jamshidi

Journal of Fasa University of Medical Sciences: Fasa, IR

2012-10-07 to 2018-05-01 | Executive Manager
Employment
Source: Self-asserted source
Javad Jamshidi

Fasa University of Medical Sciences: Fasa, Fars, IR

2012 to 2018-05-01 | Lecturer
Employment
Source: Self-asserted source
Javad Jamshidi

Fasa University of Medical Science: Fasa, Fars, IR

2015 to 2018 | Researcher (Noncommunicable Diseases Research Center)
Employment
Source: Self-asserted source
Javad Jamshidi

Education and qualifications (3)

University of New South Wales: Sydney, NSW, AU

2018-06-04 to 2022-06-03 | PhD
Education
Source: Self-asserted source
Javad Jamshidi

Shahid Beheshti University of Medical Sciences School of Medicine: Tehran, Tehran, IR

2008 to 2011 | Master of Science (MSc), Human Genetics (Medical Genetics)
Education
Source: Self-asserted source
Javad Jamshidi

Shahid Chamran University Faculty of Science: Ahwaz, Khuzestan, IR

2004 to 2008 | Bachelor's degree, Genetics (Biology)
Education
Source: Self-asserted source
Javad Jamshidi

Professional activities (1)

Behavior Genetics Association: Boulder, Colorado, US

2019-03-29 to present
Membership
Source: Self-asserted source
Javad Jamshidi

Works (48)

Negative association between anterior insula activation and resilience during sustained attention: an fMRI twin study

Psychological Medicine
2023-05 | Journal article
Contributors: Arthur Montalto; Haeme R. P. Park; Leanne M. Williams; Mayuresh S. Korgaonkar; Miranda R. Chilver; Javad Jamshidi; Peter R. Schofield; Justine M. Gatt
Source: check_circle
Crossref

Wellbeing and brain structure: A comprehensive phenotypic and genetic study of image‐derived phenotypes in the UK Biobank

Human Brain Mapping
2022-12 | Journal article
Contributors: Javad Jamshidi; Haeme R. P. Park; Arthur Montalto; Janice M. Fullerton; Justine M. Gatt
Source: check_circle
Crossref

Phenotypic and genetic analysis of a wellbeing factor score in the UK Biobank and the impact of childhood maltreatment and psychiatric illness

Translational Psychiatry
2022-03-19 | Journal article
Contributors: Javad Jamshidi; Peter R. Schofield; Justine M. Gatt; Janice M. Fullerton
Source: check_circle
Crossref

Associations between mental wellbeing and fMRI neural bases underlying responses to positive emotion in a twin sample

Psychological Medicine
2021-08-02 | Journal article
Part of ISSN: 0033-2917
Part of ISSN: 1469-8978
Source: Self-asserted source
Javad Jamshidi

Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes

Scientific Reports
2020 | Journal article
EID:

2-s2.0-85078077745

Contributors: Darvish, H.; Azcona, L.J.; Tafakhori, A.; Mesias, R.; Ahmadifard, A.; Sanchez, E.; Habibi, A.; Alehabib, E.; Johari, A.H.; Emamalizadeh, B. et al.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

Diverse phenotypic measurements of wellbeing: Heritability, temporal stability and the variance explained by polygenic scores

Genes, Brain and Behavior
2020-11 | Journal article
Contributors: Javad Jamshidi; Leanne M. Williams; Peter R. Schofield; Haeme R. P. Park; Arthur Montalto; Miranda R. Chilver; Richard A. Bryant; Claudio Toma; Janice M. Fullerton; Justine M. Gatt
Source: check_circle
Crossref

Homozygous Mutation in TWNK Cases Ataxia, Sensorineural Hearing Loss and Optic Nerve Atrophy

Archives of Iranian medicine
2019 | Journal article
EID:

2-s2.0-85076339219

Contributors: Jamali, F.; Ghaedi, H.; Tafakhori, A.; Alehabib, E.; Chapi, M.; Daftarian, N.; Darvish, H.; Jamshidi, J.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

Genetic analysis of rs11038167, rs11038172 and rs835784 polymorphisms of the TSPAN18 gene in Iranian schizophrenia patients

Meta Gene
2019-12 | Journal article
Part of ISSN: 2214-5400
Source: Self-asserted source
Javad Jamshidi
grade
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Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy

Ophthalmic Genetics
2019-05-04 | Journal article
Part of ISSN: 1381-6810
Part of ISSN: 1744-5094
Source: Self-asserted source
Javad Jamshidi
grade
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A novel c.240_241insGG mutation in NDP gene in a family with Norrie disease

Clinical and Experimental Optometry
2018 | Journal article
EID:

2-s2.0-85030111995

Contributors: Andarva, M.; Jamshidi, J.; Ghaedi, H.; Daftarian, N.; Emamalizadeh, B.; Alehabib, E.; Taghavi, S.; Pouriran, R.; Darvish, H.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

ATP2B1 rs2681472 and STK39 rs35929607 polymorphisms and risk of Hypertension in Iranian Population

Medical Journal of the Islamic Republic of Iran
2018 | Journal article
EID:

2-s2.0-85062338126

Contributors: Jamshidi, J.; Asnaashari, A.; Alipoor, R.; Mohammadi, S.; Roostaei, S.; Samadian, M.M.; Aliabadi, S.H.; Bahramali, E.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome

Molecular Neurobiology
2017 | Journal article
EID:

2-s2.0-84992718242

Contributors: Firouzabadi, S.G.; Kariminejad, R.; Vameghi, R.; Darvish, H.; Ghaedi, H.; Banihashemi, S.; Firouzkouhi Moghaddam, M.; Jamali, P.; Mofidi Tehrani, H.F.; Dehghani, H. et al.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

Functional genetic variants of FOXP3 and risk of multiple sclerosis

Iranian Red Crescent Medical Journal
2017 | Journal article
EID:

2-s2.0-85011888143

Contributors: Gholami, M.; Darvish, H.; Ahmadi, H.; Rahimi-Aliabadi, S.; Emamalizadeh, B.; Amirabadi, M.R.E.; Jamshidi, J.; Movafagh, A.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

Novel mutations in TACSTD2 gene in families with gelatinous drop-like corneal dystrophy (GDLD)

International Journal of Molecular and Cellular Medicine
2017 | Journal article
EID:

2-s2.0-85042388828

Contributors: Alehabib, E.; Jamshidi, J.; Ghaedi, H.; Emamalizadeh, B.; Andarva, M.; Daftarian, N.; Kanavi, M.R.; Torbati, P.M.; Espandar, G.; Alinaghi, S. et al.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

RIT2 Polymorphisms: Is There a Differential Association?

Molecular Neurobiology
2017 | Journal article
EID:

2-s2.0-84960091450

Contributors: Emamalizadeh, B.; Jamshidi, J.; Movafagh, A.; Ohadi, M.; khaniani, M.S.; Kazeminasab, S.; Biglarian, A.; Taghavi, S.; Motallebi, M.; Fazeli, A. et al.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

A novel mutation in SMOC1 and variable phenotypic expression in two patients with Waardenburg anophthalmia syndrome

European Journal of Medical Genetics
2017-08 | Journal article
Contributors: Javad Jamshidi; Shokoufeh Abdollahi; Hamid Ghaedi; Elham Alehabib; Abbas Tafakhori; Somayeh Alinaghi; Marjan Chapi; Amir Hossein Johari; Hossein Darvish
Source: Self-asserted source
Javad Jamshidi via Crossref Metadata Search
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Genetic analysis of SNCA gene polymorphisms in Parkinson’s disease in an Iranian population

Basal Ganglia
2017-08 | Journal article
Contributors: Mahnoosh Rahimi; Mojdeh Akbari; Javad Jamshidi; Abbas Tafakhori; Babak Emamalizadeh; Hossein Darvish
Source: Self-asserted source
Javad Jamshidi via Crossref Metadata Search
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Support for “Disease-Only” Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in Schizophrenia

Genetic Testing and Molecular Biomarkers
2017-08 | Journal article
Contributors: Ehteram Khademi; Elham Alehabib; Ehsan Esmaili Shandiz; Azadeh Ahmadifard; Monavvar Andarva; Javad Jamshidi; Simin Rahimi-Aliabadi; Ramin Pouriran; Farhad Ramezani Nejad; Nader Mansoori et al.
Source: Self-asserted source
Javad Jamshidi via Crossref Metadata Search
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A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations.

2017-05 | Journal article
Contributors: Taghavi S; Chaouni R; Tafakhori A; Azcona LJ; Firouzabadi SG; Omrani MD; Jamshidi J; Emamalizadeh B; Shahidi GA; Ahmadi M et al.
Source: Self-asserted source
Javad Jamshidi via Europe PubMed Central
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Association of renin-angiotensin-aldosterone system gene polymorphisms with left ventricular hypertrophy in patients with heart failure with preserved ejection fraction: A case-control study.

2017-05 | Journal article
Contributors: Bahramali E; Firouzabadi N; Rajabi M; Manafi A; Zarghami M; Mousavi SM; Jamshidi J
Source: Self-asserted source
Javad Jamshidi via Europe PubMed Central
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Association of β-Secretase Functional Polymorphism with Risk of Schizophrenia

Genetic Testing and Molecular Biomarkers
2017-04 | Journal article
Contributors: Simin Rahimi-Aliabadi; Neda Shahmohammadibeni; Javad Jamshidi; Ehsan Esmaili Shandiz; Reza Mirfakhraie; Mina Ohadi; Farhad Ramezani Nejad; Nader Mansoori; Mohammad Taheri; Fatemeh Gholipour et al.
Source: Self-asserted source
Javad Jamshidi via Crossref Metadata Search
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Omentin Val109Asp polymorphism and risk of coronary artery disease

Asian Cardiovascular and Thoracic Annals
2017-03 | Journal article
Contributors: Javad Jamshidi; Mehrdad Ghanbari; Ali Asnaashari; Nosaybeh Jafari; Gholam Abbas Valizadeh
Source: Self-asserted source
Javad Jamshidi via Crossref Metadata Search
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RAB7L1 promoter polymorphism and risk of Parkinson's disease; a case-control study.

2017-02 | Journal article
Contributors: Khaligh A; Goudarzian M; Moslem A; Mehrtash A; Jamshidi J; Darvish H; Emamalizadeh B
Source: Self-asserted source
Javad Jamshidi via Europe PubMed Central
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A cohort study protocol of low back pain in rural area inhabitants: Fasa low back pain cohort study (FABPACS)

Galen Medical Journal
2016 | Journal article
EID:

2-s2.0-85043556097

Contributors: Farjam, M.; Askari, A.; Hoseinipour, A.; Homayounfar, R.; Jamshidi, J.; Khodabakhshi, F.; Zakeri, H.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

A cohort study protocol to analyze the predisposing factors to common chronic non-communicable diseases in rural areas: Fasa Cohort Study

BMC Public Health
2016 | Journal article
EID:

2-s2.0-84992362154

Contributors: Farjam, M.; Bahrami, H.; Bahramali, E.; Jamshidi, J.; Askari, A.; Zakeri, H.; Homayounfar, R.; Poustchi, H.; Malekzadeh, R.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder

Journal of Neural Transmission
2016 | Journal article
EID:

2-s2.0-84959101406

Contributors: Atakhorrami, M.; Rahimi-Aliabadi, S.; Jamshidi, J.; Moslemi, E.; Movafagh, A.; Ohadi, M.; Mirabzadeh, A.; Emamalizadeh, B.; Ghaedi, H.; Gholipour, F. et al.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

A Novel PKD1 Mutation in a Patient with Autosomal Dominant Polycystic Kidney Disease

International Journal of Molecular and Cellular Medicine
2016 | Journal article
EID:

2-s2.0-85016605393

Contributors: Jamshidi, J.; Naderi, H.; Taghavi, S.; Emamalizadeh, B.; Darvish, H.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

Analysis of copy number variations in patients with autism using cytogenetic and MLPA techniques: Report of 16p13.1p13.3 and 10q26.3 duplications

International Journal of Molecular and Cellular Medicine
2016 | Journal article
EID:

2-s2.0-85021856276

Contributors: Firouzabadi, S.G.; Vameghi, R.; Kariminejad, R.; Darvish, H.; Banihashemi, S.; Moghaddam, M.F.; Jamali, P.; Tehrani, H.F.M.; Dehghani, H.; Raeisoon, M.R. et al.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

Analysis of CYP17, CYP19 and CYP1A1 gene polymorphisms in Iranian women with breast cancer

Asian Pacific Journal of Cancer Prevention
2016 | Journal article
EID:

2-s2.0-85010447623

Contributors: Farzaneh, F.; Noghabaei, G.; Barouti, E.; Pouresmaili, F.; Jamshidi, J.; Fazeli, A.; Taghavi, S.; Emamalizadeh, B.; Darvish, H.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

Emery-Dreifuss muscular dystrophy: A report of a large family with 11 affected individuals

International Journal of Molecular and Cellular Medicine
2016 | Journal article
EID:

2-s2.0-85021957031

Contributors: Ahmadifard, A.; Jamshidi, J.; Tafakhori, A.; Mollazadeh, R.; Falsafi, Z.; Darvish, H.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population

Genetic Testing and Molecular Biomarkers
2016 | Journal article
EID:

2-s2.0-84992166060

Contributors: Madadi, F.; Khaniani, M.S.; Shandiz, E.E.; Ayromlou, H.; Najmi, S.; Emamalizadeh, B.; Taghavi, S.; Jamshidi, J.; Tafakhori, A.; Shahidi, G.-A. et al.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson’s disease in Iranian population

Neurological Sciences
2016 | Journal article
EID:

2-s2.0-84953303593

Contributors: Shahmohammadibeni, N.; Rahimi-Aliabadi, S.; Jamshidi, J.; Emamalizadeh, B.; Shahmohammadibeni, H.A.; Zare Bidoki, A.; Akhavan-Niaki, H.; Eftekhari, H.; Abdollahi, S.; Shekari Khaniani, M. et al.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

Vitamin D receptor gene rs4334089 polymorphism and Parkinson's disease in Iranian population

Basal Ganglia
2016 | Journal article
EID:

2-s2.0-84969790762

Contributors: Fazeli, A.; Motallebi, M.; Jamshidi, J.; Movafagh, A.; Ghaedi, H.; Emamalizadeh, B.; Kashani, K.; Darvish, H.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

A genetic variant in miRNA binding site of glutamate receptor 4, metabotropic (GRM4) is associated with increased risk of major depressive disorder.

2016-10 | Journal article
Contributors: Dadkhah T; Rahimi-Aliabadi S; Jamshidi J; Ghaedi H; Taghavi S; Shokraeian P; Akhavan-Niaki H; Tafakhori A; Ohadi M; Darvish H
Source: Self-asserted source
Javad Jamshidi via Europe PubMed Central
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PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism.

2016-10 | Journal article
Contributors: Khodadadi H; Azcona LJ; Aghamollaii V; Omrani MD; Garshasbi M; Taghavi S; Tafakhori A; Shahidi GA; Jamshidi J; Darvish H et al.
Source: Self-asserted source
Javad Jamshidi via Europe PubMed Central
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SIPA1L2, MIR4697, GCH1 and VPS13C loci and risk of Parkinson's diseases in Iranian population: A case-control study

Journal of the Neurological Sciences
2016-10 | Journal article
Contributors: Tannaz Safaralizadeh; Javad Jamshidi; Ehsan Esmaili Shandiz; Abolfazl Movafagh; Atena Fazeli; Babak Emamalizadeh; Navid Manafi; Shaghayegh Taghavi; Abbas Tafakhori; Hossein Darvish
Source: Self-asserted source
Javad Jamshidi via Crossref Metadata Search
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Bioinformatic tools to determine the pathogenicity of a missense mutation in PKHD1 in autosomal recessive polycystic kidney disease.

2016-09 | Journal article
Contributors: Alehabib E; Jamshidi J; Ghaedi H; Askarian F; Mahmoudieh L; Johari AH; Darvish H
Source: Self-asserted source
Javad Jamshidi via Europe PubMed Central
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SNAP-25 gene variations and attention-deficit hyperactivity disorder in Iranian population.

2016-09 | Journal article
Contributors: Zarrabi Alhosseini M; Jamshidi J; Zare Bidoki A; Ganji S; Eslami Amirabadi MR; Emamalizadeh B; Taghavi S; Shokraeian P; Mohajerani F; Darvish H
Source: Self-asserted source
Javad Jamshidi via Europe PubMed Central
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A novel mutation and variable phenotypic expression in a large consanguineous pedigree with Jalili syndrome.

2016-07 | Journal article
Contributors: Rahimi-Aliabadi S; Daftarian N; Ahmadieh H; Emamalizadeh B; Jamshidi J; Tafakhori A; Ghaedi H; Noroozi R; Taghavi S; Ahmadifard A et al.
Source: Self-asserted source
Javad Jamshidi via Europe PubMed Central
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Association of ACE gene D polymorphism with left ventricular hypertrophy in patients with diastolic heart failure: a case–control study

BMJ Open
2016-02 | Journal article
Contributors: Ehsan Bahramali; Mona Rajabi; Javad Jamshidi; Seyyed Mohammad Mousavi; Mehrdad Zarghami; Alireza Manafi; Negar Firouzabadi
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Crossref
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c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness

European Journal of Medical Genetics
2016-02 | Journal article
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Crossref
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Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian population

Journal of the Neurological Sciences
2015-05 | Journal article
Contributors: Leyla Haghnejad; Babak Emamalizadeh; Javad Jamshidi; Alireza Zare Bidoki; Hamid Ghaedi; Ehsan Ahmadi; Shokoufeh Abdollahi; Neda Shahmohammadibeni; Shaghayegh Taghavi; Atena Fazeli et al.
Source: Self-asserted source
Javad Jamshidi via Crossref Metadata Search
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FABP9 mutations are not detected in cases of infertility due to sperm morphological defects in Iranian Men

International Journal of Fertility and Sterility
2014 | Journal article
EID:

2-s2.0-84891055109

Contributors: Jamshidi, J.; Pouresmaeili, F.; Darvish, H.; Omrani, M.D.; Azargashb, E.; Sadeghi, M.R.; Lakpour, N.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

HLA-DRA is associated with Parkinson's disease in Iranian population

Int J Immunogenet
2014 | Journal article
Contributors: Jamshidi, J.; Movafagh, A.; Emamalizadeh, B.; Zare Bidoki, A.; Manafi, A.; Ghasemi Firouzabadi, S.; Shahidi, G. A.; Kazeminasab, S.; Petramfar, P.; Fazeli, A. et al.
Source: Self-asserted source
Javad Jamshidi via ResearcherID
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Gene Family: Structure, Organization and Evolution

Journal of Fasa Univeristy of Medical Sciences
2014-09-13 | Journal article
Source: Self-asserted source
Javad Jamshidi

Association between vitamin D receptor gene BsmI polymorphism and bone mineral density in a population of 146 Iranian women

Cell Journal
2013 | Journal article
EID:

2-s2.0-84877303244

Contributors: Pouresmaeili, F.; Jamshidi, J.; Azargashb, E.; Samangouee, S.
Source: Self-asserted source
Javad Jamshidi via Scopus - Elsevier

Biased homozygous haplotypes across the human caveolin 1 upstream purine complex in Parkinson's disease

J Mol Neurosci
2013 | Journal article
Contributors: Darvish, H.; Heidari, A.; Hosseinkhani, S.; Movafagh, A.; Khaligh, A.; Jamshidi, J.; Noorollahi-Moghaddam, H.; Heidari-Rostami, H. R.; Karkheiran, S.; Shahidi, G. A. et al.
Source: Self-asserted source
Javad Jamshidi via ResearcherID
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Detection of Copy Number Changes in Genes Associated with Parkinson's Disease in Iranian Patients

Neurosci Lett
2013 | Journal article
Contributors: Darvish, H.; Movafagh, A.; Omrani, M. D.; Firouzabadi, S. G.; Azargashb, E.; Jamshidi, J.; Khaligh, A.; Haghnejad, L.; Naeini, N. S.; Talebi, A. et al.
Source: Self-asserted source
Javad Jamshidi via ResearcherID
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