By Dr Javad Jamshidi

Journal articles

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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