about
Genome-Wide Association of Heroin Dependence in Han ChineseThe prefrontal dysfunction in individuals with Internet gaming disorder: a meta-analysis of functional magnetic resonance imaging studies.Reward pathway dysfunction in gambling disorder: A meta-analysis of functional magnetic resonance imaging studies.Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern Chinese population.Advanced paternal age increases the risk of schizophrenia and obsessive-compulsive disorder in a Chinese Han population.A COMT gene haplotype associated with methamphetamine abuse.Association study of 45 candidate genes in nicotine dependence in Han Chinese.Short-term effects of antipsychotic treatment on cerebral function in drug-naive first-episode schizophrenia revealed by "resting state" functional magnetic resonance imaging.Interaction among genes influencing ethanol metabolism and sex is association with alcohol use disorders in a Tibet population.Allelic association analysis of the dopamine D2, D3, 5-HT2A, and GABA(A)gamma2 receptors and serotonin transporter genes with heroin abuse in Chinese subjects.Association analysis of polymorphisms in the μ opioid gene and heroin abuse in Chinese subjects.Association between apolipoprotein CI HpaI polymorphism and sporadic Alzheimer's disease in Chinese.Mutation screening and association analysis of the parkin gene in Parkinson's disease patients from South-West China.No association between polymorphisms of methylenetetrahydrofolate reductase gene and schizophrenia in both Chinese and Scottish populations.Changes of brain morphometry in first-episode, drug-naïve, non-late-life adult patients with major depression: an optimized voxel-based morphometry study.PRODH gene is associated with executive function in schizophrenic families.Analysis of CAG/CTG repeat size in Chinese subjects with schizophrenia and bipolar affective disorder using the repeat expansion detection method.Ethnic variation in the thymidylate synthase enhancer region polymorphism among Caucasian and Asian populations.Transmission disequilibrium analysis of a triplet repeat within the hKCa3 gene using family trios with schizophrenia.Hair thyroid hormones concentration in patients with depression changes with disease episodes in female Chinese.The role of single nucleotide polymorphism of D2 dopamine receptor gene on major depressive disorder and response to antidepressant treatment.Association of white matter deficits with clinical symptoms in antipsychotic-naive first-episode schizophrenia: an optimized VBM study using 3T.Factor structures of the neurocognitive assessments and familial analysis in first-episode schizophrenia patients, their relatives and controls.A Prospective Twin Registry in Southwestern China (TRiSC): exploring the effects of genetic and environmental factors on cognitive and behavioral development and mental health wellbeing in children and adolescents.Association analysis of the RGS4 gene in Han Chinese and Scottish populations with schizophrenia.The functional MMP-9 microsatellite marker is not associated with episodic memory in humans.Accuracy and sensitivity of DNA pooling with microsatellite repeats using capillary electrophoresis.Affected sibling pair linkage analysis of qualitative and quantitative traits for schizophrenia on chromosome 22 in a Chinese population.Association analysis of polymorphisms in the DRD4 gene and heroin abuse in Chinese subjects.No NRG1 V266L in Chinese patients with schizophreniaReaction time of the Continuous Performance Test is an endophenotypic marker for schizophrenia: A study of first-episode neuroleptic-naive schizophrenia, their non-psychotic first-degree relatives and healthy population controlsIdentifying potential risk haplotypes for schizophrenia at the DTNBP1 locus in Han Chinese and Scottish populationsTransmission disequilibrium analysis of HLA class II DRB1, DQA1, DQB1 and DPB1 polymorphisms in schizophrenia using family trios from a Han Chinese populationFamily-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11Association analysis between dopamine receptor genes and bipolar affective disorderCase-control, haplotype relative risk and transmission disequilibrium analysis of a dopamine D2 receptor functional promoter polymorphism in schizophreniaCatechol-O-methyltransferase Vall58Met polymorphism: frequency analysis in Han Chinese subjects and allelic association of the low activity allele with bipolar affective disorderAllelic functional variation of serotonin transporter expression is a susceptibility factor for late onset Alzheimerʼs diseaseNo association between a promoter polymorphism in the noradrenaline transporter gene and anorexia nervosaAssociation between 5-HT2A gene promoter polymorphism and anorexia nervosa
P50
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P50
description
Chinese neuroscience researcher
@en
name
Li T
@nl
Tao Li
@en
type
label
Li T
@nl
Tao Li
@en
altLabel
Li T
@en
prefLabel
Li T
@nl
Tao Li
@en
P106
P31
P496
0000-0003-3831-901X