Missing a beat: assessment of circadian rhythm abnormalities in bipolar disorder in the genomic era
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000215
Genetic risk factors and gene–environment interactions in adult and childhood attention-deficit/hyperactivity disorder
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000220
Cross-species models of attention-deficit/hyperactivity disorder and autism spectrum disorder: lessons from CNTNAP2, ADGRL3, and PARK2
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000211
In-silico investigation of coding variants potentially affecting the functioning of the glutamatergic N-methyl-D-aspartate receptor in schizophrenia
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000216
Schizophrenia in a genomic era: a review from the pathogenesis, genetic and environmental etiology to diagnosis and treatment insights
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000245
Genomics of human aggression: current state of genome-wide studies and an automated systematic review tool.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000239
Offspring of parents with schizophrenia, bipolar disorder, and depression: a review of familial high-risk and molecular genetics studies.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000240
Familial association of attention-deficit hyperactivity disorder with autoimmune diseases in the population of Sweden
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000212
The emerging pattern of shared polygenic architecture of psychiatric disorders, conceptual and methodological challenges.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000234
Brain-derived neurotrophic factor and schizophrenia.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000237
Endophenotypes of executive functions in obsessive compulsive disorder? A meta-analysis in unaffected relatives.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000241
Anorexia nervosa is associated with Neuronatin variants.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000224
Zinc finger proteins in psychiatric disorders and response to psychotropic medications.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000231
Understanding the schizophrenia phenotype in the first patient with the full SCN2A phenotypic spectrum
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000219
The interaction between estradiol change and the serotonin transporter gene (5-HTTLPR) polymorphism is associated with postpartum depressive symptoms.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000222
Buspirone for the treatment of anxiety-related symptoms in Angelman syndrome: a case series
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000218
Association of CamK2A genetic variants with transition time from occasional to regular heroin use in a sample of heroin-dependent individuals
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000208
New insights and perspectives on the genetics of obsessive-compulsive disorder.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000230
Common variants in SATB2 are associated with schizophrenia in Uygur Chinese population.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000229
A case of intellectual disability reveals a novel mutation in IQSEC2 gene by whole exome sequencing.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000232
Association of polymorphisms in HTR2A, TPH1, and TPH2 genes with attempted suicide in rural China
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000221
Determining population stratification and subgroup effects in association studies of rare genetic variants for nicotine dependence
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000227
Association between RELN polymorphisms and schizophrenia in a Han population from Northeast China.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000235
Decreased serum complement component 4 levels in patients with schizophrenia.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000226
Autism spectrum disorder in a patient with a genomic rearrangement that only involves the EPHA5 gene
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000217
Gene knockout animal models of depression, anxiety and obsessive compulsive disorders.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000238
Catechol-O-methyltransferase gene expression in stress-induced and non-stress induced schizophrenia
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000243
Genotype-phenotype feasibility studies on khat abuse, traumatic experiences and psychosis in Ethiopia.
来源期刊:Psychiatric geneticsDOI:10.1097/ypg.0000000000000242
Schizophrenia in microcephalic osteodysplastic primordial dwarfism type II syndrome: supporting evidence for an association between the PCNT gene and schizophrenia.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000214
No association between CYP2C19 genetic polymorphism with treatment remission to antidepressant venlafaxine in Han Chinese population
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000246
Association study of the PDE4D gene and obsessive-compulsive disorder in a Chinese Han population.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000236
Corpus callosum metrics predict severity of visuospatial and neuromotor dysfuntions in ARID1B mutations with Coffin-Siris syndrome.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000225
A preliminary exome sequence in three patients with tardive dystonia
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000248
Modification of the association between paroxetine serum concentration and SERT-occupancy by ABCB1 (P-glycoprotein) polymorphisms in major depressive disorder
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000244
Clinical association to FKBP5 rs1360780 in patients with depression.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000228
Does 5-HTTLPR moderate the effect of the quality of environmental context on maternal sensitivity? Testing the differential susceptibility hypothesis
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000247