X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (17) 17
index medicus (17) 17
female (15) 15
polymorphism (15) 15
iran (13) 13
male (13) 13
parkinson's disease (12) 12
genetic aspects (10) 10
middle aged (10) 10
neurosciences (10) 10
parkinson disease - genetics (9) 9
risk factors (9) 9
gene frequency (8) 8
genes (8) 8
genetic research (8) 8
genotype (8) 8
parkinson’s disease (8) 8
aged (7) 7
association (7) 7
genetic predisposition to disease - genetics (7) 7
genetics & heredity (7) 7
neurology (7) 7
polymorphism, single nucleotide - genetics (7) 7
clinical neurology (6) 6
iranian (6) 6
susceptibility (6) 6
adult (5) 5
case-control studies (5) 5
iranian population (5) 5
mutation (5) 5
protein (5) 5
schizophrenia (5) 5
bipolar disorder (4) 4
genetic association studies (4) 4
genome-wide association (4) 4
medical genetics (4) 4
medicine, general & internal (4) 4
mental disorders (4) 4
polymorphism, single nucleotide (4) 4
rab7l1 (4) 4
snca (4) 4
3′utr (3) 3
adhd (3) 3
analysis (3) 3
breast cancer (3) 3
disease susceptibility (3) 3
gene (3) 3
genetic polymorphisms (3) 3
genomics (3) 3
medical research (3) 3
medicine, experimental (3) 3
membrane proteins - genetics (3) 3
metaanalysis (3) 3
mlpa (3) 3
monomeric gtp-binding proteins - genetics (3) 3
mutations (3) 3
parkinsons-disease (3) 3
promoter (3) 3
rit2 (3) 3
single nucleotide polymorphisms (3) 3
variants (3) 3
alleles (2) 2
animal genetics and genomics (2) 2
asian continental ancestry group (2) 2
asian continental ancestry group - genetics (2) 2
autism (2) 2
biochemistry & molecular biology (2) 2
biomedicine (2) 2
bipolar disorder - genetics (2) 2
brca1 (2) 2
breast neoplasms - genetics (2) 2
candidate gene (2) 2
cell biology (2) 2
chi-square distribution (2) 2
children (2) 2
cone-rod dystrophy (2) 2
csmd1 (2) 2
deficit/hyperactivity disorder (2) 2
early-onset parkinsonism (2) 2
expression (2) 2
families (2) 2
genetic predisposition to disease (2) 2
genetics (2) 2
genome-wide association study (2) 2
genomes (2) 2
huseyo (2) 2
identification (2) 2
iran - epidemiology (2) 2
life sciences (2) 2
medicine & public health (2) 2
methylphenidate (2) 2
microbial genetics and genomics (2) 2
movement disorders (2) 2
nervous system diseases (2) 2
neurobiology (2) 2
neurodegenerative diseases (2) 2
neurological disorders (2) 2
ophthalmology (2) 2
original (2) 2
original article (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Medical Genetics, ISSN 0022-2593, 2019, Volume 56, Issue 6, pp. 358 - 369
Jalili syndrome is a rare genetic disorder first identified by Jalili in Gaza. Amelogenesis imperfecta and cone-rode dystrophy are simultaneously seen in... 
cone-rode dystrophy | jalili syndrome | cnnm4 | photoreceptor dystrophies | amelogenesis imperfecta | PROTEIN | CONE-ROD DYSTROPHY | MOLECULAR DIAGNOSIS | FAMILIES | GENETICS & HEREDITY | MUTATIONS | IDENTIFICATION | RECESSIVE AMELOGENESIS IMPERFECTA | DELETION
Journal Article
Meta Gene, ISSN 2214-5400, 12/2019, Volume 22
Schizophrenia is a debilitating psychiatric disorder. In a recent GWA study, three single nucleotide polymorphisms (SNPs) within the intronic region of gene,... 
Association | TSPAN18 | Schizophrenia | Single nucleotide polymorphism
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 4/2018, Volume 55, Issue 4, pp. 3477 - 3489
Journal Article
Clinical and Experimental Optometry, ISSN 0816-4622, 03/2018, Volume 101, Issue 2, pp. 255 - 259
Background: Norrie disease (ND) is a rare, X-linked recessive disorder with the main characteristic of early childhood blindness. The aim of the present study... 
mutation | Iranian | pseudoglioma | Norrie disease | blindness | EXUDATIVE VITREORETINOPATHY | FZD4 | OPHTHALMOLOGY | CANDIDATE GENE | Genetic research | Genetic aspects | Codon | Genes | Blindness | NDP gene | Frameshift mutation | Insertion | Stop codon | Children | Mutation | Males | Hereditary diseases | Index Medicus
Journal Article
Neurological Research, ISSN 0161-6412, 05/2017, Volume 39, Issue 5, pp. 468 - 471
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 4/2017, Volume 54, Issue 3, pp. 2234 - 2240
Journal Article
Iranian Red Crescent Medical Journal, ISSN 2074-1804, 01/2017, Volume 19, Issue 1, p. 1
Background: Multiple sclerosis (MS) is an autoimmune disease that affects the central nervous system (CNS). MS is one of the most common cause of neurological... 
Multiple sclerosis | Autoimmune diseases | FOXP3 | Genetic polymorphisms | Multiple Sclerosis | MEDICINE, GENERAL & INTERNAL | TARGET GENES | STIMULATION | Autoimmune Diseases | TRANSCRIPTION FACTOR FOXP3 | REGULATORY T-CELLS | SUPPRESSOR FUNCTION | PREECLAMPSIA | POLYMORPHISM | Genetic Polymorphisms
Journal Article
Asian Pacific Journal of Cancer Prevention, ISSN 1513-7368, 2016, Volume 17, pp. 23 - 26
Journal Article
Basal Ganglia, ISSN 2210-5336, 11/2017, Volume 10, pp. 4 - 7
Objectives Parkinson's disease (PD) is a complex disorder influenced by genetic and environmental factors. One of the several genes indicated to be important... 
Promoter | Parkinson's disease | 3′UTR | Polymorphism | SNCA | Iranians | Genetic aspects | Research | Health aspects | Genetic polymorphisms | Risk factors
Journal Article
Basal Ganglia, ISSN 2210-5336, 11/2017, Volume 10, pp. 4 - 7
Parkinson’s disease (PD) is a complex disorder influenced by genetic and environmental factors. One of the several genes indicated to be important in the... 
Promoter | 3′UTR | Parkinson’s disease | SNCA | Polymorphism
Journal Article
Asian Pacific Journal of Cancer Prevention, ISSN 1513-7368, 06/2016, Volume 17, Issue sup3, pp. 23 - 26
Journal Article
Pakistan Journal of Medical Sciences, ISSN 1682-024X, 2015, Volume 31, Issue 5, pp. 1162 - 1166
Background & Objectives: Attention deficit hyperactivity disorder (ADHD) is a common heritable psychiatric disorder with a worldwide prevalence of 5%. The... 
DISC1 gene | ADHD | Association | Iran | Polymorphisms | Hyperactivity | NO ASSOCIATION | MEDICINE, GENERAL & INTERNAL | VARIANTS | polymorphisms | IN-SCHIZOPHRENIA 1 | BRAIN | CHILDREN | Genetic aspects | Single nucleotide polymorphisms | Analysis | Attention-deficit hyperactivity disorder | Original
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.