Mr Javad Jamshidi

Conjoint Lecturer
Medicine & Health
School of Clinical Medicine
  • Journal articles | 2024
    Ramshe SM; Zardadi S; Alehabib E; Nourinia R; Jamshidi J; Soosanabadi M; Darvish H, 2024, 'A Novel Ornithine Aminotransferase Splice Site Mutation Causes Vitamin B6-Responsive Gyrate Atrophy', Journal of Ophthalmic and Vision Research, 19, pp. 118 - 132, http://dx.doi.org/10.18502/jovr.v19i1.15446
    Journal articles | 2023
    Montalto A; Park HRP; Williams LM; Korgaonkar MS; Chilver MR; Jamshidi J; Schofield PR; Gatt JM, 2023, 'Negative association between anterior insula activation and resilience during sustained attention: An fMRI twin study', Psychological Medicine, 53, pp. 3187 - 3199, http://dx.doi.org/10.1017/S0033291721005262
    Journal articles | 2023
    Park HRP; Chilver MR; Montalto A; Jamshidi J; Schofield PR; Williams LM; Gatt JM, 2023, 'Associations between mental wellbeing and fMRI neural bases underlying responses to positive emotion in a twin sample', Psychological Medicine, 53, pp. 1215 - 1223, http://dx.doi.org/10.1017/S0033291721002695
    Journal articles | 2022
    Jamshidi J; Park HRP; Montalto A; Fullerton JM; Gatt JM, 2022, 'Wellbeing and brain structure: A comprehensive phenotypic and genetic study of image-derived phenotypes in the UK Biobank', Human Brain Mapping, 43, pp. 5180 - 5193, http://dx.doi.org/10.1002/hbm.25993
    Journal articles | 2022
    Jamshidi J; Schofield PR; Gatt JM; Fullerton JM, 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, pp. 113, http://dx.doi.org/10.1038/s41398-022-01874-5
    Journal articles | 2022
    Shourian M; Jamshidi J, 2022, 'Hedging rule-based optimized reservoir operation using metaheuristic algorithms', E3S Web of Conferences, 346, pp. 02011 - 02011, http://dx.doi.org/10.1051/e3sconf/202234602011
    Journal articles | 2021
    Gatt J; Chilver M; Champaigne-Klassen E; Park H; Jamshidi J; Montalto A; Schofield P; Williams LM, 2021, 'Predictors of Wellbeing and Wellbeing Change Over a 12-Month Period in 1,327 Twins', Biological Psychiatry, 89, pp. S315 - S316, http://dx.doi.org/10.1016/j.biopsych.2021.02.787
    Journal articles | 2021
    Kalani M; Kouhpayeh SA; Shamsdin SA; Jamshidi J; Choopanizadeh M; Keighobadi G; Moravej A, 2021, 'Association of interleukin-17 A gene variants and susceptibility to H. pylori related gastric diseases', Meta Gene, 28, http://dx.doi.org/10.1016/j.mgene.2021.100885
    Journal articles | 2021
    Kalani M; Shams SR; Namdarnia S; Choopanizadeh M; Jamshidi J; Moravej A, 2021, 'Interleukine-22 gene variants are associated with susceptibility to visceral leishmaniasis', Experimental Parasitology, 226-227, http://dx.doi.org/10.1016/j.exppara.2021.108122
    Journal articles | 2021
    Montalto A; Park HRP; Williams LM; Korgaonkar MS; Chilver MR; Jamshidi J; Schofield P; Gatt JM, 2021, 'Negative Association Between the Bilateral Anterior Insula and Resilience During a Continuous Performance Task: An fMRI Twin Study', BIOLOGICAL PSYCHIATRY, 89, pp. S175 - S176, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000645683800423&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
    Journal articles | 2020
    Abolghasemi M; Daneshmandpour Y; Poursaei E; Jamshidi J; Baradaran B; Shanehbandi D; Kazeminasab S; Emamalizadeh B, 2020, 'MMP9 (RS20544) and ADCY2 (RS58502974) as susceptibility factors for schizophrenia in Iranian population', Meta Gene, 26, http://dx.doi.org/10.1016/j.mgene.2020.100810
    Journal articles | 2020
    Chilver MR; Keller AS; Park HRP; Jamshidi J; Montalto A; Schofield PR; Clark CR; Harmon-Jones E; Williams LM; Gatt JM, 2020, 'Electroencephalography profiles as a biomarker of wellbeing: A twin study', Journal of Psychiatric Research, 126, pp. 114 - 121, http://dx.doi.org/10.1016/j.jpsychires.2020.04.010
    Journal articles | 2020
    Darvish H; Azcona LJ; Tafakhori A; Mesias R; Ahmadifard A; Sanchez E; Habibi A; Alehabib E; Johari AH; Emamalizadeh B; Jamali F; Chapi M; Jamshidi J; Kajiwara Y; Paisán-Ruiz C, 2020, 'Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes', Scientific Reports, 10, http://dx.doi.org/10.1038/s41598-020-57929-4
    Journal articles | 2020
    Jamshidi J; Williams LM; Schofield PR; Park HRP; Montalto A; Chilver MR; Bryant RA; Toma C; Fullerton JM; Gatt JM, 2020, 'Diverse phenotypic measurements of wellbeing: Heritability, temporal stability and the variance explained by polygenic scores', Genes, Brain and Behavior, 19, pp. e12694, http://dx.doi.org/10.1111/gbb.12694
    Journal articles | 2020
    Poursaei E; Daneshmandpour Y; Aghaei Moghadam E; Abolghasemi M; Jamshidi J; Baradaran B; Asadi M; Kazeminasab S; Emamalizadeh B, 2020, 'LRP8 (rs5177) and CEP85L (rs11756438) are contributed to schizophrenia susceptibility in Iranian population', Psychiatric Genetics, 30, pp. 162 - 165, http://dx.doi.org/10.1097/YPG.0000000000000266
    Journal articles | 2019
    Chapi M; Sabbaghi H; Suri F; Alehabib E; Rahimi-Aliabadi S; Jamali F; Jamshidi J; Emamalizadeh B; Darvish H; Mirrahimi M; Ahmadieh H; Daftarian N, 2019, 'Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy', Ophthalmic Genetics, 40, pp. 259 - 266, http://dx.doi.org/10.1080/13816810.2019.1622023
    Journal articles | 2019
    Jamali F; Ghaedi H; Tafakhori A; Alehabib E; Chapi M; Daftarian N; Darvish H; Jamshidi J, 2019, 'Homozygous Mutation in TWNK Cases Ataxia, Sensorineural Hearing Loss and Optic Nerve Atrophy', Archives of Iranian medicine, 22, pp. 728 - 730
    Journal articles | 2019
    Jamshidi J; Shourian M, 2019, 'Hedging Rules-Based Optimal Reservoir Operation Using Bat Algorithm', Water Resources Management, 33, pp. 4525 - 4538, http://dx.doi.org/10.1007/s11269-019-02402-9
    Journal articles | 2019
    Shokraeian P; Daneshmandpour Y; Jamshidi J; Emamalizadeh B; Darvish H, 2019, 'Genetic analysis of rs11038167, rs11038172 and rs835784 polymorphisms of the TSPAN18 gene in Iranian schizophrenia patients', Meta Gene, 22, http://dx.doi.org/10.1016/j.mgene.2019.100609
    Journal articles | 2018
    Andarva M; Jamshidi J; Ghaedi H; Daftarian N; Emamalizadeh B; Alehabib E; Taghavi S; Pouriran R; Darvish H, 2018, 'A novel c.240_241insGG mutation in NDP gene in a family with Norrie disease', Clinical and Experimental Optometry, 101, pp. 255 - 259, http://dx.doi.org/10.1111/cxo.12599
    Journal articles | 2018
    Jamshidi J; Asnaashari A; Alipoor R; Mohammadi S; Roostaei S; Samadian MM; Aliabadi SH; Bahramali E, 2018, 'ATP2B1 rs2681472 and STK39 rs35929607 polymorphisms and risk of Hypertension in Iranian Population', Medical Journal of the Islamic Republic of Iran, 32, pp. 78 - 82, http://dx.doi.org/10.14196/MJIRI.32.14
    Journal articles | 2018
    Taghavi S; Chaouni R; Tafakhori A; Azcona LJ; Firouzabadi SG; Omrani MD; Jamshidi J; Emamalizadeh B; Shahidi GA; Ahmadi M; Habibi SAH; Ahmadifard A; Fazeli A; Motallebi M; Petramfar P; Askarpour S; Askarpour S; Shahmohammadibeni HA; Shahmohammadibeni N; Eftekhari H; Shafiei Zarneh AE; Mohammadihosseinabad S; Khorrami M; Najmi S; Chitsaz A; Shokraeian P; Ehsanbakhsh H; Rezaeidian J; Ebrahimi Rad R; Madadi F; Andarva M; Alehabib E; Atakhorrami M; Mortazavi SE; Azimzadeh Z; Bayat M; Besharati AM; Harati-Ghavi MA; Omidvari S; Dehghani-Tafti Z; Mohammadi F; Mohammad Hossein Pour B; Noorollahi Moghaddam H; Esmaili Shandiz E; Habibi A; Taherian-Esfahani Z; Darvish H; Paisán-Ruiz C, 2018, 'A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations', Molecular Neurobiology, 55, pp. 3477 - 3489, http://dx.doi.org/10.1007/s12035-017-0535-1
    Journal articles | 2017
    Alehabib E; Jamshidi J; Ghaedi H; Askarian F; Mahmoudieh L; Johari AH; Darvish H, 2017, 'Bioinformatic tools to determine the pathogenicity of a missense mutation in PKHD1 in autosomal recessive polycystic kidney disease', Nephrology, 22, pp. 330 - 331, http://dx.doi.org/10.1111/nep.12919
    Journal articles | 2017
    Alehabib E; Jamshidi J; Ghaedi H; Emamalizadeh B; Andarva M; Daftarian N; Kanavi MR; Torbati PM; Espandar G; Alinaghi S; Johari AH; Saghally M; Mohajerani F; Darvish H, 2017, 'Novel mutations in TACSTD2 gene in families with gelatinous drop-like corneal dystrophy (GDLD)', International Journal of Molecular and Cellular Medicine, 6
    Journal articles | 2017
    Bahramali E; Firouzabadi N; Rajabi M; Manafi A; Zarghami M; Mousavi SM; Jamshidi J, 2017, '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', Clinical and Experimental Hypertension, 39, pp. 371 - 376, http://dx.doi.org/10.1080/10641963.2016.1267196
    Journal articles | 2017
    Dadkhah T; Rahimi-Aliabadi S; Jamshidi J; Ghaedi H; Taghavi S; Shokraeian P; Akhavan-Niaki H; Tafakhori A; Ohadi M; Darvish H, 2017, 'A genetic variant in miRNA binding site of glutamate receptor 4, metabotropic (GRM4) is associated with increased risk of major depressive disorder', Journal of Affective Disorders, 208, pp. 218 - 222, http://dx.doi.org/10.1016/j.jad.2016.10.008
    Journal articles | 2017
    Emamalizadeh B; Jamshidi J; Movafagh A; Ohadi M; khaniani MS; Kazeminasab S; Biglarian A; Taghavi S; Motallebi M; Fazeli A; Ahmadifard A; Shahidi GA; Petramfar P; Shahmohammadibeni N; Dadkhah T; Khademi E; Tafakhori A; Khaligh A; Safaralizadeh T; Kowsari A; Mirabzadeh A; Zarneh AES; Khorrami M; Shokraeian P; Banavandi MJS; Lima BS; Andarva M; Alehabib E; Atakhorrami M; Darvish H, 2017, 'RIT2 Polymorphisms: Is There a Differential Association?', Molecular Neurobiology, 54, pp. 2234 - 2240, http://dx.doi.org/10.1007/s12035-016-9815-4
    Journal articles | 2017
    Firouzabadi SG; Kariminejad R; Vameghi R; Darvish H; Ghaedi H; Banihashemi S; Firouzkouhi Moghaddam M; Jamali P; Mofidi Tehrani HF; Dehghani H; Narooie-Nejad M; Jamshidi J; Tafakhori A; Sadabadi S; Najmabadi H; Behjati F, 2017, 'Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome', Molecular Neurobiology, 54, pp. 7019 - 7027, http://dx.doi.org/10.1007/s12035-016-0202-y
    Journal articles | 2017
    Gholami M; Darvish H; Ahmadi H; Rahimi-Aliabadi S; Emamalizadeh B; Amirabadi MRE; Jamshidi J; Movafagh A, 2017, 'Functional genetic variants of FOXP3 and risk of multiple sclerosis', Iranian Red Crescent Medical Journal, 19, http://dx.doi.org/10.5812/ircmj.34597
    Journal articles | 2017
    Jamshidi J; Abdollahi S; Ghaedi H; Alehabib E; Tafakhori A; Alinaghi S; Chapi M; Johari AH; Darvish H, 2017, 'A novel mutation in SMOC1 and variable phenotypic expression in two patients with Waardenburg anophthalmia syndrome', European Journal of Medical Genetics, 60, pp. 578 - 582, http://dx.doi.org/10.1016/j.ejmg.2017.08.006
    Journal articles | 2017
    Jamshidi J; Ghanbari M; Asnaashari A; Jafari N; Valizadeh GA, 2017, 'Omentin Val109Asp polymorphism and risk of coronary artery disease', Asian Cardiovascular and Thoracic Annals, 25, pp. 199 - 203, http://dx.doi.org/10.1177/0218492317699752
    Journal articles | 2017
    Khademi E; Alehabib E; Shandiz EE; Ahmadifard A; Andarva M; Jamshidi J; Rahimi-Aliabadi S; Pouriran R; Nejad FR; Mansoori N; Shahmohammadibeni N; Taghavi S; Shokraeian P; Akhavan-Niaki H; Paisán-Ruiz C; Darvish H; Ohadi M, 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, pp. 485 - 490, http://dx.doi.org/10.1089/gtmb.2016.0422
    Journal articles | 2017
    Khaligh A; Goudarzian M; Moslem A; Mehrtash A; Jamshidi J; Darvish H; Emamalizadeh B, 2017, 'RAB7L1 promoter polymorphism and risk of Parkinson’s disease; a case-control study', Neurological Research, 39, pp. 468 - 471, http://dx.doi.org/10.1080/01616412.2017.1297558
    Journal articles | 2017
    Khodadadi H; Azcona LJ; Aghamollaii V; Omrani MD; Garshasbi M; Taghavi S; Tafakhori A; Shahidi GA; Jamshidi J; Darvish H; Paisán-Ruiz C, 2017, 'PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism', Movement Disorders, 32, pp. 287 - 291, http://dx.doi.org/10.1002/mds.26824
    Journal articles | 2017
    Rahimi M; Akbari M; Jamshidi J; Tafakhori A; Emamalizadeh B; Darvish H, 2017, 'Genetic analysis of SNCA gene polymorphisms in Parkinson's disease in an Iranian population', Basal Ganglia, 10, pp. 4 - 7, http://dx.doi.org/10.1016/j.baga.2017.08.001
    Journal articles | 2017
    Rahimi-Aliabadi S; Shahmohammadibeni N; Jamshidi J; Shandiz EE; Mirfakhraie R; Ohadi M; Nejad FR; Mansoori N; Taheri M; Gholipour F; Moudi S; Tayebi G; Divsalar S; Darvish H; Movafagh A, 2017, 'Association of β-secretase functional polymorphism with risk of schizophrenia', Genetic Testing and Molecular Biomarkers, 21, pp. 248 - 251, http://dx.doi.org/10.1089/gtmb.2016.0262
    Journal articles | 2016
    Ahmadifard A; Jamshidi J; Tafakhori A; Mollazadeh R; Falsafi Z; Darvish H, 2016, 'Emery-Dreifuss muscular dystrophy: A report of a large family with 11 affected individuals', International Journal of Molecular and Cellular Medicine, 5, pp. 196 - 198
    Journal articles | 2016
    Atakhorrami M; Rahimi-Aliabadi S; Jamshidi J; Moslemi E; Movafagh A; Ohadi M; Mirabzadeh A; Emamalizadeh B; Ghaedi H; Gholipour F; Fazeli A; Motallebi M; Taghavi S; Ahmadifard A; Mohammadihosseinabad S; Shafiei Zarneh AE; Shahmohammadibeni N; Madadi F; Andarva M; Darvish H, 2016, 'A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder', Journal of Neural Transmission, 123, pp. 323 - 328, http://dx.doi.org/10.1007/s00702-015-1456-7
    Journal articles | 2016
    Bahramali E; Rajabi M; Jamshidi J; Mousavi SM; Zarghami M; Manafi A; Firouzabadi N, 2016, 'Association of ACE gene D polymorphism with left ventricular hypertrophy in patients with diastolic heart failure: A case-control study', BMJ Open, 6, http://dx.doi.org/10.1136/bmjopen-2015-010282
    Journal articles | 2016
    Farjam M; Askari A; Hoseinipour A; Homayounfar R; Jamshidi J; Khodabakhshi F; Zakeri H, 2016, 'A cohort study protocol of low back pain in rural area inhabitants: Fasa low back pain cohort study (FABPACS)', Galen Medical Journal, 5, pp. 225 - 229
    Journal articles | 2016
    Farjam M; Bahrami H; Bahramali E; Jamshidi J; Askari A; Zakeri H; Homayounfar R; Poustchi H; Malekzadeh R, 2016, 'A cohort study protocol to analyze the predisposing factors to common chronic non-communicable diseases in rural areas: Fasa Cohort Study', BMC Public Health, 16, pp. 1 - 8, http://dx.doi.org/10.1186/s12889-016-3760-z
    Journal articles | 2016
    Farzaneh F; Noghabaei G; Barouti E; Pouresmaili F; Jamshidi J; Fazeli A; Taghavi S; Emamalizadeh B; Darvish H, 2016, 'Analysis of CYP17, CYP19 and CYP1A1 gene polymorphisms in Iranian women with breast cancer', Asian Pacific Journal of Cancer Prevention, 17, pp. 23 - 26, http://dx.doi.org/10.7314/APJCP.2016.17
    Journal articles | 2016
    Fazeli A; Motallebi M; Jamshidi J; Movafagh A; Ghaedi H; Emamalizadeh B; Kashani K; Darvish H, 2016, 'Vitamin D receptor gene rs4334089 polymorphism and Parkinson's disease in Iranian population', Basal Ganglia, 6, pp. 157 - 160, http://dx.doi.org/10.1016/j.baga.2016.04.001
    Journal articles | 2016
    Firouzabadi SG; Vameghi R; Kariminejad R; Darvish H; Banihashemi S; Moghaddam MF; Jamali P; Tehrani HFM; Dehghani H; Raeisoon MR; Narooie-Nejad M; Jamshidi J; Tafakhori A; Sadabadi S; Behjati F, 2016, '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, 5, pp. 236 - 245, http://dx.doi.org/10.22088/acadpub.BUMS.5.4.236
    Journal articles | 2016
    Jamshidi J; Naderi H; Taghavi S; Emamalizadeh B; Darvish H, 2016, 'A Novel PKD1 Mutation in a Patient with Autosomal Dominant Polycystic Kidney Disease', International Journal of Molecular and Cellular Medicine, 5, pp. 123 - 124
    Journal articles | 2016
    Madadi F; Khaniani MS; Shandiz EE; Ayromlou H; Najmi S; Emamalizadeh B; Taghavi S; Jamshidi J; Tafakhori A; Shahidi GA; Darvish H, 2016, 'Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population', Genetic Testing and Molecular Biomarkers, 20, pp. 629 - 632, http://dx.doi.org/10.1089/gtmb.2016.0133
    Journal articles | 2016
    Rahimi-Aliabadi S; Daftarian N; Ahmadieh H; Emamalizadeh B; Jamshidi J; Tafakhori A; Ghaedi H; Noroozi R; Taghavi S; Ahmadifard A; Alehabib E; Andarva M; Shokraeian P; Atakhorrami M; Darvish H, 2016, 'A novel mutation and variable phenotypic expression in a large consanguineous pedigree with Jalili syndrome', Eye (Basingstoke), 30, pp. 1424 - 1432, http://dx.doi.org/10.1038/eye.2016.137
    Journal articles | 2016
    Safaralizadeh T; Jamshidi J; Esmaili Shandiz E; Movafagh A; Fazeli A; Emamalizadeh B; Manafi N; Taghavi S; Tafakhori A; Darvish H, 2016, 'SIPA1L2, MIR4697, GCH1 and VPS13C loci and risk of Parkinson's diseases in Iranian population: A case-control study', Journal of the Neurological Sciences, 369, pp. 1 - 4, http://dx.doi.org/10.1016/j.jns.2016.08.001
    Journal articles | 2016
    Safaralizadeh T; Jamshidi J; Shandiz EE; Movafagh A; Fazeli A; Emamalizadeh B; Manafi N; Taghavi S; Tafakhori A; Darvish H, 2016, 'SIPA1L2, MIR4697, GCH1 and VPS13C loci and risk of Parkinson's diseases in Iranian population: A case -control study', JOURNAL OF THE NEUROLOGICAL SCIENCES, 369, pp. 1 - 4, http://dx.doi.org/10.1016/jjns.2016.08.001
    Journal articles | 2016
    Safarpour Lima B; Ghaedi H; Daftarian N; Ahmadieh H; Jamshidi J; Khorrami M; Noroozi R; Sohrabifar N; Assarzadegan F; Hesami O; Taghavi S; Ahmadifard A; Atakhorrami M; Rahimi-Aliabadi S; Shahmohammadibeni N; Alehabib E; Andarva M; Darvish H; Emamalizadeh B, 2016, 'C.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness', European Journal of Medical Genetics, 59, pp. 65 - 69, http://dx.doi.org/10.1016/j.ejmg.2016.01.001
    Journal articles | 2016
    Shahmohammadibeni N; Rahimi-Aliabadi S; Jamshidi J; Emamalizadeh B; Shahmohammadibeni HA; Zare Bidoki A; Akhavan-Niaki H; Eftekhari H; Abdollahi S; Shekari Khaniani M; Shahmohammadibeni M; Fazeli A; Motallebi M; Taghavi S; Ahmadifard A; Shafiei Zarneh AE; Andarva M; Dadkhah T; Khademi E; Alehabib E; Rahimi M; Tafakhori A; Atakhorrami M; Darvish H, 2016, 'The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson’s disease in Iranian population', Neurological Sciences, 37, pp. 731 - 736, http://dx.doi.org/10.1007/s10072-015-2420-x
    Journal articles | 2016
    Zarrabi Alhosseini M; Jamshidi J; Zare Bidoki A; Ganji S; Eslami Amirabadi MR; Emamalizadeh B; Taghavi S; Shokraeian P; Mohajerani F; Darvish H, 2016, 'SNAP-25 gene variations and attention-deficit hyperactivity disorder in Iranian population', Neurological Research, 38, pp. 959 - 964, http://dx.doi.org/10.1080/01616412.2016.1232548
    Journal articles | 2015
    Haghnejad L; Emamalizadeh B; Jamshidi J; Bidoki AZ; Ghaedi H; Ahmadi E; Abdollahi S; Shahmohammadibeni N; Taghavi S; Fazeli A; Motallebi M; Zarneh AES; Mohammadihosseinabad S; Abbaszadegan MR; Torkamandi S; Gavenaroudi MA; Pedram N; Shahidi GA; Tafakhori A; Darvish H; Movafagh A, 2015, '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, 355, pp. 72 - 74, http://dx.doi.org/10.1016/j.jns.2015.05.020
    Journal articles | 2014
    Jamshidi J; Movafagh A; Emamalizadeh B; Zare Bidoki A; Manafi A; Ghasemi Firouzabadi S; Shahidi GA; Kazeminasab S; Petramfar P; Fazeli A; Motallebi M; Mortazavi-Tabatabaei SA; Kowsari A; Jafarian Z; Darvish H, 2014, 'HLA-DRA is associated with Parkinson's disease in Iranian population', International Journal of Immunogenetics, 41, pp. 508 - 511, http://dx.doi.org/10.1111/iji.12151
    Journal articles | 2014
    Jamshidi J; Pouresmaeili F; Darvish H; Omrani MD; Azargashb E; Sadeghi MR; Lakpour N, 2014, 'FABP9 mutations are not detected in cases of infertility due to sperm morphological defects in Iranian Men', International Journal of Fertility and Sterility, 7, pp. 275 - 280
    Journal articles | 2013
    Darvish H; Heidari A; Hosseinkhani S; Movafagh A; Khaligh A; Jamshidi J; Noorollahi-Moghaddam H; Heidari-Rostami HR; Karkheiran S; Shahidi GA; Togha M; Paknejad SMH; Ashrafian H; Abdi S; Firouzabadi SG; Jamaldini SH; Ohadi M, 2013, 'Biased homozygous haplotypes across the human caveolin 1 upstream purine complex in Parkinson's disease', Journal of Molecular Neuroscience, 51, pp. 389 - 393, http://dx.doi.org/10.1007/s12031-013-0021-9
    Journal articles | 2013
    Darvish H; Movafagh A; Omrani MD; Firouzabadi SG; Azargashb E; Jamshidi J; Khaligh A; Haghnejad L; Naeini NS; Talebi A; Heidari-Rostami HR; Noorollahi-Moghaddam H; Karkheiran S; Shahidi GA; Paknejad SMH; Ashrafian H; Abdi S; Kayyal M; Akbari M; Pedram N; Emamalizadeh B, 2013, 'Detection of copy number changes in genes associated with Parkinson's disease in Iranian patients', Neuroscience Letters, 551, pp. 75 - 78, http://dx.doi.org/10.1016/j.neulet.2013.07.013
    Journal articles | 2013
    Pouresmaeili F; Jamshidi J; Azargashb E; Samangouee S, 2013, 'Association between vitamin D receptor gene BsmI polymorphism and bone mineral density in a population of 146 Iranian women', Cell Journal, 15, pp. 75 - 82
  • Conference Abstracts | 2021
    Chilver M; Keller AS; Park H; Jamshidi J; Montalto A; Schofield P; Clark R; Harmon-Jones E; Williams L; Gatt J, 2021, 'Distinct Electrophysiological Markers of Mental Wellbeing and Mental Illness Symptoms in 422 Healthy Adults', in BIOLOGICAL PSYCHIATRY, ELSEVIER SCIENCE INC, Vol. 89, pp. S163 - S164, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000645683800394&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
    Conference Papers | 2021
    Jamshidi J; Schofield PR; Gatt JM; Fullerton JM, 2021, 'Phenotypic and Genetic Study of a Wellbeing Factor Score in the UK Biobank and the Impact of Childhood Maltreatment', in BEHAVIOR GENETICS, SPRINGER, pp. 712 - 713, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000709342700075&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
    Conference Abstracts | 2019
    Gatt J; Chilver M; Jamshidi J; Montalto A; Schofield P; Williams L, 2019, 'Neuropsychological correlates of wellbeing using a twin design', in Behavior Genetics, Springer (part of Springer Nature), Stockholm, Vol. 49, pp. 509 - 510, presented at Behavior Genetics Association, Stockholm
    Conference Abstracts | 2019
    Jamshidi J; Montalto A; Chilver M; Toma C; Schofield PR; Williams L; Fullerton J; Gatt J, 2019, 'Genetic factors influencing quantitative measures of subjective and psychological wellbeing using the COMPAS-W scale in a healthy Australian twin cohort', in Behavior Genetics, Stockholm, Vol. 49, pp. 511 - 511, presented at Behavior Genetics Association, Stockholm
    Conference Papers | 2015
    Zarebidoki A; Jamshidi J; Golchin N; Darvish H, 2015, 'HLA-DRA IS ASSOCIATED WITH PARKINSON'S DISEASE IN IRANIAN POPULATION', in TISSUE ANTIGENS, WILEY, SWITZERLAND, Geneva, pp. 370 - 370, presented at 29th European Immunogenetics and Histocompatibility Conference, SWITZERLAND, Geneva, 26 April 2015 - 29 April 2015, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000352907000189&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
    Conference Papers | 2013
    Jamshidi J, 2013, 'Synthesis of 2-arylbenzimidazoles catalyzed by transition metal nitrates', in ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, AMER CHEMICAL SOC, IN, Indianapolis, presented at 246th National Meeting of the American-Chemical-Society (ACS), IN, Indianapolis, 08 September 2013 - 12 September 2013, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000329618405417&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1