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Journal of Affective Disorders|October 30, 2016
A genetic variant in miRNA binding site of glutamate receptor 4, metabotropic (GRM4) is associated with increased risk of major depressive disorderTahereh Dadkhah, Simin Rahimi-Aliabadi, Javad Jamshidi, et al.Psychological Medicine|July 14, 2023
Negative association between anterior insula activation and resilience during sustained attention: an fMRI twin studyArthur Montalto, Haeme R P Park, Leanne M Williams, et al.Neurological Research|September 16, 2016
SNAP-25 gene variations and attention-deficit hyperactivity disorder in Iranian populationMahjoubeh Zarrabi Alhosseini, Javad Jamshidi, Alireza Zare Bidoki, et al.Ophthalmic Genetics|June 20, 2019
Incomplete penetrance of <i>CRX</i> gene for autosomal dominant form of cone-rod dystrophyMarjan Chapi, Hamideh Sabbaghi, Fatemeh Suri, et al.Genetic Testing and Molecular Biomarkers|September 10, 2016
Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian PopulationFaranak Madadi, Mahmoud Shekari Khaniani, Ehsan Esmaili Shandiz, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 19, 2016
PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonismHamidreza Khodadadi, Luis J Azcona, Vajiheh Aghamollaii, et al.Genes, Brain, and Behavior|August 14, 2020
Diverse phenotypic measurements of wellbeing: Heritability, temporal stability and the variance explained by polygenic scoresJavad Jamshidi, Leanne M Williams, Peter R Schofield, et al.Journal of Psychiatric Research|May 26, 2020
Electroencephalography profiles as a biomarker of wellbeing: A twin studyMiranda R Chilver, Arielle S Keller, Haeme R P Park, et al.International Journal of Molecular and Cellular Medicine|July 11, 2018
Novel Mutations in <i>TACSTD2</i> Gene in Families with Gelatinous Drop-like Corneal Dystrophy (GDLD)Elham Alehabib, Javad Jamshidi, Hamid Ghaedi, et al.Genetic Testing and Molecular Biomarkers|April 7, 2017
Association of β-Secretase Functional Polymorphism with Risk of SchizophreniaSimin Rahimi-Aliabadi, Neda Shahmohammadibeni, Javad Jamshidi, et al.Pageof 5