A. Parsian

发表

Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.

Aldo Quattrone, Nobutaka Hattori, Mariza de Andrade, 2006, JAMA.

Association of a variation in the promoter region of the brain-derived neurotrophic factor gene with familial Parkinson's disease.

J. Perlmutter, J. Zhao, B. Racette, 2004, Parkinsonism & related disorders.

Alcoholism and Alleles of the Human Dopamine D2 Receptor Locus - Studies of Association and Linkage

T. Reich, B. Suarez, R. Todd, 1991 .

Strong and weak cross-inheritance of substance use disorders in a nationally representative sample

B. Grant, S. P. Chou, D. Goldman, 2021, Molecular Psychiatry.

Association between cholesteryl ester transfer protein TaqIB variants and risk of coronary artery disease and diabetes mellitus in the population of western Iran.

Z. Rahimi, A. Vaisi-Raygani, A. Parsian, 2011, Genetic testing and molecular biomarkers.

Collaborative Analysis of (cid:1) -Synuclein Gene Promoter Variability and Parkinson Disease

J. Ioannidis, M. Farrer, M. Hulihan, 2006 .

Platelet adenylyl cyclase activity in alcoholics and subtypes of alcoholics. WHO/ISBRA Study Clinical Centers.

C. Robert Cloninger, R. Todd, B. Tabakoff, 1996, Alcoholism, clinical and experimental research.

Sickle Cell Disease and Venous Thromboembolism

Z. Rahimi, A. Parsian, 2011, Mediterranean journal of hematology and infectious diseases.

Monoamine oxidases and alcoholism. I. Studies in unrelated alcoholics and normal controls.

C. Robert Cloninger, B. Suarez, B. Tabakoff, 1995, American journal of medical genetics.

Mutation, sequence analysis, and association studies of alpha-synuclein in Parkinson's disease.

A. Goate, M. Rundle, J. Perlmutter, 1998, Neurology.

Association studies of polymorphisms of CYP2E1 gene in alcoholics with cirrhosis, antisocial personality, and normal controls.

C. Robert Cloninger, A. Parsian, Z. H. Zhang, 1998, Alcoholism, clinical and experimental research.

Strong interaction between T allele of endothelial nitric oxide synthase with B1 allele of cholesteryl ester transfer protein TaqIB highly elevates the risk of coronary artery disease and type 2 diabetes mellitus

Z. Rahimi, A. Parsian, Z. Rahimi, 2012, Human Genomics.

Detection of responsible mutations for beta thalassemia in the Kermanshah Province of Iran using PCR-based techniques

Z. Rahimi, A. Parsian, Adriana Muniz, 2009, Molecular Biology Reports.

Preeclampsia and angiotensin converting enzyme (ACE) I/D and angiotensin II type-1 receptor (AT1R) A1166C polymorphisms: association with ACE I/D polymorphism

Z. Rahimi, A. Parsian, H. Mozafari, 2013, Journal of the renin-angiotensin-aldosterone system : JRAAS.

MTHFR C677T and eNOS G894T variants in preeclamptic women: Contribution to lipid peroxidation and oxidative stress.

Z. Rahimi, A. Parsian, Z. Rahimi, 2013, Clinical biochemistry.

Thrombophilic mutations and susceptibility to preeclapmsia in Western Iran

Z. Rahimi, A. Parsian, Z. Rahimi, 2011, Journal of Thrombosis and Thrombolysis.

Concomitant presence of endothelial nitric oxide 894T and angiotensin II‐converting enzyme D alleles are associated with diabetic nephropathy in a Kurdish population from Western Iran

Z. Rahimi, A. Vaisi-Raygani, A. Parsian, 2012, Nephrology.

Butyrylcholinesterase (BChE) activity is associated with the risk of preeclampsia: influence on lipid and lipoprotein metabolism and oxidative stress

Z. Rahimi, A. Vaisi-Raygani, A. Parsian, 2013, Journal of Maternal-Fetal & Neonatal Medicine.

Plasma lipids and lipoproteins in children and young adults with major β-thalassemia from western Iran: influence of genotype

Z. Rahimi, A. Vaisi-Raygani, A. Parsian, 2011, Molecular Biology Reports.

Functional variation in promoter region of monoamine oxidase A and subtypes of alcoholism: Haplotype analysis

C. Robert Cloninger, A. Parsian, R. Sinha, 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Human GABA, Receptor αl and α3 Subunits Genes and Alcoholism.

C. R. Cloninger, A. Parsian, C. Cloninger, 1997, Alcoholism, clinical and experimental research.

Human GABAA receptor alpha 1 and alpha 3 subunits genes and alcoholism.

C. Robert Cloninger, A. Parsian, 1997, Alcoholism, clinical and experimental research.

Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study.

T. Gillis, M. MacDonald, H. Shill, 2006, Archives of neurology.

Comparison of Electron and Light Microscopy of Chromosome Aberration Induced in Human Lymphocytes by Adriamycin and Mitomycin C

A. Parsian, 1986 .

Behavioural features of alcohol-preferring rats: focus on inbred strains.

D. Overstreet, A. Rezvani, A. Parsian, 1999, Alcohol and Alcoholism.

Haplotype analysis of beta thalassemia patients in Western Iran.

Z. Rahimi, A. Vaisi-Raygani, A. Parsian, 2009, Blood cells, molecules & diseases.

Lack of association between MTHFR C677T and A1298C polymorphisms and risk of childhood acute lymphoblastic leukemia in the Kurdish population from Western Iran.

Z. Rahimi, A. Vaisi-Raygani, A. Parsian, 2012, Genetic testing and molecular biomarkers.

Bipolar disorder and the pseudoautosomal region: an association study.

R. Todd, A. Parsian, 1994, American journal of medical genetics.

Human GABA, Receptor cyl and cy3 Subunits Genes and Alcoholism

C. R. Cloninger, A. Parsian, C. Cloninger, 1997 .

No evidence for a schizophrenia susceptibility gene in the vicinity of IL2RB on chromosome 22.

C. Robert Cloninger, B. Suarez, K. Isenberg, 1997, American journal of medical genetics.

Parsing genetically influenced risk pathways: genetic loci impact problematic alcohol use via externalizing and specific risk

Holly E. Poore, Scott F. Saccone, L. Almasy, 2021, Translational Psychiatry.

Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction

Dajiang J. Liu, Holly E. Poore, James W. Madole, 2021, Nature Neuroscience.

Serotonergic pathway genes and subtypes of alcoholism: association studies

C. Robert Cloninger, A. Parsian, 2001, Psychiatric genetics.

Human dopamine transporter gene polymorphism (VNTR) and alcoholism.

A. Parsian, Z. H. Zhang, 1997, American journal of medical genetics.

No association between polymorphisms in the human dopamine D3 and D4 receptors genes and alcoholism.

C. Robert Cloninger, S. Chakraverty, A. Parsian, 1997, American journal of medical genetics.

Possible association between the dopamine D3 receptor gene and bipolar affective disorder.

R. Todd, S. Chakraverty, A. Parsian, 1994, American journal of medical genetics.

Genomic clone OS-2 (D10S20) detects different restriction fragment length polymorphisms in Caucasians and Orientals for both HindIII and TaqI.

E. Devor, A. Parsian, 1991, Human heredity.

Linkage disequilibria at the D2 dopamine receptor locus (DRD2) in alcoholics and controls.

C. Robert Cloninger, T. Reich, B. Suarez, 1994, Genomics.

Alcoholism and alleles of the human D2 dopamine receptor locus. Studies of association and linkage.

C. Robert Cloninger, T. Reich, B. Suarez, 1991, Archives of general psychiatry.

Genetic association between monoamine oxidase and manic-depressive illness: comparison of relative risk and haplotype relative risk data.

R. Todd, A. Parsian, 1997, American journal of medical genetics.

Analysis of-Synuclein Gene Promoter Variability and Parkinson Disease

J. Ioannidis, M. Farrer, M. Hulihan, 2006 .

Further genetic characterization of the fawn-hooded (FH/Wjd) rat, an animal model of comorbid depression and alcoholism

D. Overstreet, A. Rezvani, M. Cleves, 2007, Psychiatric genetics.

Thymidylate synthase and methionine synthase polymorphisms are not associated with susceptibility to childhood acute lymphoblastic leukemia in Kurdish population from Western Iran

Z. Rahimi, A. Vaisi-Raygani, A. Parsian, 2011, Molecular Biology Reports.

Parkinson's disease and apolipoprotein E: possible association with dementia but not age at onset.

J. Perlmutter, B. Racette, A. Parsian, 2002, Genomics.

Monoamine oxidases and alcoholism. II. Studies in alcoholic families.

C. Robert Cloninger, B. Suarez, A. Parsian, 1995, American journal of medical genetics.

Depressive-like behavior and high alcohol drinking co-occur in the FH/WJD rat but appear to be under independent genetic control

D. Overstreet, A. Rezvani, A. Lawrence, 2007, Neuroscience & Biobehavioral Reviews.

Analysis of alcohol-related phenotypes in F2 progeny derived from FH/Wjd and ACI/N rat strains reveals independent measures and sex differences

D. Overstreet, A. Rezvani, M. Cleves, 2007, Behavioural Brain Research.

The Fawn-Hooded (FH/Wjd) rat: a genetic animal model of comorbid depression and alcoholism

D. Overstreet, A. Rezvani, A. Parsian, 2002, Psychiatric genetics.

Linkage disequilibrium and haplotype analysis between serotonin receptor 1B gene variations and subtypes of alcoholism

ASSOCIATION AND LINKAGE STUDIES OF NEW HUMAN DOPAMINE D2 RECEPTOR POLYMORPHISMS (RFLPS) IN ALCOHOLISM

B. Suarez, R. Todd, C. R. Cloninger, 1992 .

A new TaqI RFLP within intron 2 of human dopamine D2 receptor gene (DRD2).

R. Todd, K. O’Malley, A. Parsian, 1991, Nucleic acids research.

Deep venous thrombosis and thrombophilic mutations in western Iran: association with factor V Leiden

Z. Rahimi, A. Ghavamzadeh, K. Mansouri, 2010, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction

Dajiang J. Liu, Holly E. Poore, Scott F. Saccone, 2021, Nature Neuroscience.

Human chromosomes 11p15 and 4p12 and alcohol dependence: possible association with the GABRB1 gene.

A. Parsian, Z. H. Zhang, 1999, American journal of medical genetics.

Association of variations in monoamine oxidases A and B with Parkinson's disease subgroups.

M. Rundle, J. Perlmutter, B. Racette, 2004, Genomics.

Functional variant in the DRD2 receptor promoter region and subtypes of alcoholism.

C. Robert Cloninger, A. Parsian, Z. H. Zhang, 2000, American journal of medical genetics.

Molecular Biology of Parkinson's Disease

A. Parsian, B. Patra, 2009 .

Prevalence of parkin gene mutations and variations in idiopathic Parkinson's disease.

J. Perlmutter, B. Racette, A. Parsian, 2005, Parkinsonism & related disorders.

Sequence analysis of exon 8 of MAO-A gene in alcoholics with antisocial personality and normal controls.

A. Parsian, 1999, Genomics.

Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran

Z. Rahimi, A. Vaisi-Raygani, A. Parsian, 2009, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Z. Rahimi, A. Parsian, Z. Rahimi, 2012, Human Genomics.

Monoamine oxidases and alcoholism: studies in unrelated alcoholics, normal controls and alcoholic families.

C. Robert Cloninger, B. Suarez, B. Tabakoff, 1994, Alcohol and alcoholism (Oxford, Oxfordshire). Supplement.

Thymidylate synthase and methionine synthase polymorphisms are not associated with susceptibility to childhood acute lymphoblastic leukemia in Kurdish population from Western Iran

Z. Rahimi, A. Vaisi-Raygani, A. Parsian, 2012, Molecular Biology Reports.

A rapid technique for preparing human chromosomes for electron microscopy

A. Parsian, D. Buthala, 1985 .

Evaluation of a screening questionnaire for genetic studies of Parkinson's disease.

M. Rundle, J. Perlmutter, B. Racette, 1999, American journal of medical genetics.

Manic-depressive illness and tyrosine hydroxylase markers

E. Lobos, J. R. DePaulo, S. Simpson, 1996, The Lancet.

Concomitant presence of endothelial nitric oxide 894T and angiotensin II‐converting enzyme D alleles are associated with diabetic nephropathy in a Kurdish population from Western Iran

Z. Rahimi, A. Vaisi-Raygani, A. Parsian, 2012, Nephrology.

Association between cholesteryl ester transfer protein TaqIB variants and risk of coronary artery disease and diabetes mellitus in the population of western Iran.

Z. Rahimi, A. Vaisi-Raygani, A. Parsian, 2011, Genetic testing and molecular biomarkers.

Sequence analysis of exon eight of MAO-A gene in alcoholics with antisocial personality and in normal controls

S. Chakraverty, A. Parsian, D. Tribune, 1996 .