about
Association of β-Secretase Functional Polymorphism with Risk of Schizophrenia.A cohort study protocol to analyze the predisposing factors to common chronic non-communicable diseases in rural areas: Fasa Cohort Study.Association of ACE gene D polymorphism with left ventricular hypertrophy in patients with diastolic heart failure: a case-control study.RAB7L1 promoter polymorphism and risk of Parkinson's disease; a case-control study.Biased homozygous haplotypes across the human caveolin 1 upstream purine complex in Parkinson's disease.Omentin Val109Asp polymorphism and risk of coronary artery disease.SNAP-25 gene variations and attention-deficit hyperactivity disorder in Iranian population.Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population.A novel mutation and variable phenotypic expression in a large consanguineous pedigree with Jalili syndrome.Detection of copy number changes in genes associated with Parkinson's disease in Iranian patients.HLA-DRA is associated with Parkinson's disease in Iranian population.A novel c.240_241insGG mutation in NDP gene in a family with Norrie disease.A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations.Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome.A genetic variant in miRNA binding site of glutamate receptor 4, metabotropic (GRM4) is associated with increased risk of major depressive disorder.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.PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism.RIT2 Polymorphisms: Is There a Differential Association?A novel mutation in SMOC1 and variable phenotypic expression in two patients with Waardenburg anophthalmia syndrome.A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder.SIPA1L2, MIR4697, GCH1 and VPS13C loci and risk of Parkinson's diseases in Iranian population: A case-control study.c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness.Analysis of CYP17, CYP19 and CYP1A1 Gene Polymorphisms in Iranian Women with Breast Cancer.Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian populationThe analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson's disease in Iranian populationBioinformatic tools to determine the pathogenicity of a missense mutation in PKHD1 in autosomal recessive polycystic kidney diseaseATP2B1 rs2681472 and STK39 rs35929607 polymorphisms and risk of Hypertension in Iranian PopulationPhenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genesIncomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy
P50
Q30400805-369A5B30-6CFB-4FFF-B7B6-4CE6F0C2D19BQ36166742-ECC5508D-3336-46F8-91B4-626097EC661CQ36602874-1E1E93F1-F8DE-40DD-99E0-BFD9CF074BD4Q38937020-A4FF9215-BB13-45B9-8891-28FD37FEB414Q39156780-55EB682F-793C-42B1-BCBF-846A7D06493FQ40282241-C2F25F40-8396-4009-8B45-E4A2C730ED72Q40522908-17BF4100-7D0F-49D0-B2D2-72BC106B5191Q40540189-BE7B7824-4DE8-4450-AE13-7177F8A2C6C5Q42696184-D3076C5C-7FD0-4342-A410-7B5E7C1C6FFDQ43556322-35CF7FBC-FB45-412C-9CA3-ED4BCD4DC978Q43823053-777983C2-550F-439D-947F-541111BFE438Q47662882-14F1D07B-A730-437E-A0C6-39737D90F6ECQ47871666-F6A07E8C-376A-47DA-AA64-CDBF9648033CQ47962206-52AA85F1-5F3C-43CC-A6F5-CA043CC8F231Q48037794-3BBAD097-2CA6-4AE1-80B4-623592E14EC3Q48132786-336D74BA-560C-438E-B616-216E9C2A557AQ48474330-9CE68E26-A876-4B7B-8667-DB190C628BF7Q50227781-F8E4E6A4-B24D-49FF-B6EB-C100E54D6A90Q50306968-DEE2F8E7-550F-4351-9723-31BAAEC93F3CQ50792441-D360E22F-059F-410A-A5ED-79A26558CC42Q51479145-86869D66-3F5A-43E1-B977-326D319B9E24Q51559893-B21DAA83-76D5-417A-8451-9A518968FD32Q53104132-F1CB4801-147F-4C78-BCF6-2D2320140925Q85370313-40E306CF-94C3-4EF5-8D8A-01B8858F7E53Q87017078-71918299-05AD-4439-BBAF-033D79F6A288Q88265178-ACFA6D74-FD38-4CCF-8610-4D864FDA416FQ91213981-D31C615B-0DCB-4EBB-ABA3-8A3C2F829456Q92860605-AB4B9696-1EE5-4897-B646-8AD1144009D7Q92874003-B6AEFF75-2CBC-4EC3-BEB3-5808338466FB
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Javad Jamshidi
@ast
Javad Jamshidi
@en
Javad Jamshidi
@es
Javad Jamshidi
@nl
Javad Jamshidi
@sl
type
label
Javad Jamshidi
@ast
Javad Jamshidi
@en
Javad Jamshidi
@es
Javad Jamshidi
@nl
Javad Jamshidi
@sl
prefLabel
Javad Jamshidi
@ast
Javad Jamshidi
@en
Javad Jamshidi
@es
Javad Jamshidi
@nl
Javad Jamshidi
@sl
P108
P1053
F-6472-2012
P106
P1153
55667802600
P2798
P31
P3829
P3835
javad-jamshidi2
P496
0000-0002-6607-418X