EVIDENCE OF A SUSCEPTIBILITY LOCUS FOR BIPOLAR DISORDER ON CHROMOSOME 1p IN THE SARDINIAN POPULATION
BIPOLAR DISORDER GENOME SCREEN, CONDITIONING ON THE PRESENCE OF PSYCHOSIS
THE BIPOLAR AFFECTIVE DISORDER (BPAD) PHENOME DATABASE: A RESOURCE FOR GENETIC STUDIES
COMBINED ANALYSIS FROM ELEVEN LINKAGE STUDIES OF BIPOLAR DISORDER PROVIDES STRONG EVIDENCE FOR SUSCEPTIBILITY LOCI ON CHROMOSOMES 6q AND 8q
NOVEL BIOSTATISTICAL AND BIOINFORMATIC APPROACHES TO IDENTIFYING AND PROFILING DIFFERENTIALLY EXPRESSED GENES IN THE BRAIN IN SCHIZOPHRENIA
CONVERGENT FUNCTIONAL GENOMICS: BIPOLAR DISORDERS AND SCHIZOPHRENIA
GENE EXPRESSION PROFILE OF G PROTEIN COUPLED RECEPTOR AND RELATED SIGNALING PATHWAYS IN MOOD DISORDER
A NOVEL APPROACH TO IDENTIFYING SCHIZOPHRENIA BIOMARKERS PROVIDES CONCURRENT VALIDATION OF SELENBP1 GENE UP-REGULATION IN BLOOD AND BRAIN
SNPS ON CHIPS: A WORD OF CAUTION ON THE HIDDEN GENETIC CODE IN EXPRESSION ARRAYS
novoSNP: AUTOMATED SNP AND MUTATION DISCOVERY SOFTWARE
CLINICAL COVARIATES IN ASSOCIATION ANALYSIS: SEQUENTIAL ADDITION OF CASES
A FLEXIBLE FRAMEWORK FOR DATA MINING AND KNOWLEDGE DISCOVERY IN PSYCHIATRIC GENETICS
STREAMLINED ANALYSIS OF POOLED GENOTYPE DATA IN SNP-BASED ASSOCIATION STUDIES
A NOVEL APPROACH TO THE ANALYSIS OF AUTISM ASSOCIATED CYTOGENETIC REGIONS OF INTEREST USING GENE INTERACTION NETWORKS
PLENARY LECTURE: IMAGING THE ADDICTED BRAIN
TBX1 —A VCFS CANDIDATE WITH RELEVANCE TO AUTISM SPECTRUM DISORDER AND SCHIZOPHRENIA?
GENOME-WIDE SCAN FOR SCHIZOPHRENIA IN THE MOLECULAR GENETICS OF SCHIZOPHRENIA (MGS1) COLLABORATION PEDIGREES SUGGESTS LINKAGE IN 8p23.3-p12 AND 11p11.2-q22.3. RESULTS OF FINE MAPPING
A LINKAGE DISEQUILIBRIUM MAP OF CHROMOSOME 5q IN A LARGE HAN CHINESE SCHIZOPHRENIA COHORT
IDENTIFICATION OF GENES INVOLVED IN PREPULSE INHIBITION OF STARTLE, AN ENDOPHENOTYPE OF SCHIZOPHRENIA, IN MOUSE CHROMOSOME SUBSTITUTION STRAINS
BEYOND POSITIONAL CLONING AND ASSOCIATION: THE SEARCH FOR SCHIZOPHRENIA LIABILITY VARIATION IN THE DTNBP1 GENE IN THE IRISH STUDY OF HIGH DENSITY SCHIZOPHRENIA FAMILIES (ISHDSF)
IDENTIFICATION OF EPISTATIC INTERACTIONS IN TWO EXAMPLES: MYELIN RELATED GENES IN BIPOLAR DISORDER AND GABAA RECEPTOR SUBUNIT GENES IN SCHIZOPHRENIA
ENDOPHENOTYPES FOR MOLECULAR GENETIC STUDIES OF ADHD: DO ALTERNATIVE CONTINUOUS PERFORMANCE TASK ERROR INDICES MEDIATE AND/OR MODERATE PREVIOUSLY OBSERVED ASSOCIATIONS BETWEEN ADHD AND DAT1 AND DRD4?
A PHARMACO-BEHAVIORAL GENETIC STUDY OF THE DOPAMINE TRANSPORTER GENE (SLC6A3) IN CHILDREN WITH ATTENTION DEFICIT HYPERACTIVITY
FAMILY BASED ASSOCIATION ANALYSIS OF A STATISTICALLY DERIVED QUANTITATIVE TRAIT FOR ADHD REVEALS AN ASSOCIATION IN DRD4 WITH INATTENTIVE SYMPTOMS IN ADHD INDIVIDUALS
ANALYSIS OF GENETIC FACTORS, PRENATAL SMOKING AND DRINKING FACTORS, AND THEIR INTERACTIONS ON SUBTYPES OF ADHD
COLLABORATIVE ANALYSIS OF DRD4 AND DAT GENOTYPES IN POPULATION-DEFINED ADHD SUBTYPES
TESTING FOR GENETIC DISSOCIATION BETWEEN TWO DOPAMINE GENES AND MEASURES OF EXECUTIVE FUNCTIONS RELEVANT TO ADHD
EXTRAVERSION AND NEUROTICISM AS INDICES OF GENETIC AND ENVIRONMENTAL RISK FOR SOCIAL PHOBIA
TRANSCRIPTOME ANALYSIS IN A MURINE MODEL OF ANXIETY OVEREXPRESSING THE NEUROTROPHIN-3 RECEPTOR ( NTRK3 )
ASSOCIATION BETWEEN GLUTAMIC ACID DECARBOXYLASE (GAD) GENES AND MOOD AND ANXIETY DISORDERS
INVESTIGATION OF RGS2 AND RGS13 GENE POLYMORPHISMS IN HUMAN PANIC DISORDER
PHENOTYPIC EFFECTS OF KNOCKING OUT THE 5-HT1A RECEPTOR DEPEND ON BACKGROUND STRAIN
GENOME-WIDE LINKAGE SCAN OF OBSESSIVE-COMPULSIVE DISORDER: SIGNIFICANT EVIDENCE FOR SUSCEPTIBILITY LOCI ON CHROMOSOMES 3q21-27
DISC-1 GENETIC VARIATION AND HUMAN BRAIN DEVELOPMENT AND FUNCTION
NEUROIMAGING-BASED PHENOTYPE DELINEATION OF NON-MENDELIAN DISEASES OF THE BRAIN AS A PRELUDE TO GENETIC ASSOCIATION STUDIES
IMAGING GENOMICS: PRINCIPLES AND PRACTICES
sMRI IN MONOZYGOTIC TWINS DISCORDANT FOR ANXIOUS DEPRESSION
PHENOTYPE REFINEMENT IN ANXIOUS/DEPRESSION. A MULTI-INFORMANT, DEVELOPMENTAL, TWIN STUDY FROM AGE 3 TO ADULTHOOD
AN UPDATE ON REPLICATE EDAC LINKAGE STUDIES OF ANXIOUS DEPRESSION: A TWIN FAMILY STUDY FROM AUSTRALIA
ELUCIDATING THE GENES FOR THE SUSCEPTIBILITY TO DEPRESSION AND ANXIETY
MOLECULAR CONSEQUENCES OF PATHOGENIC CREB1 PROMOTER MUTATION IN RE-MDD
ASSOCIATION STUDY OF DEVELOPMENTAL DYSLEXIA AND THE GENES FOR VMP, DCDC2, KIAA0319, TTRAP AND THEM2 ON CHROMOSOME 6p
GENOTYPIC EFFECTS ON EPISODIC MEMORY: RECENT EXPERIENCE FROM BDNF, G72, AND GRM3
GENETIC VARIABILITY OF HUMAN EPISODIC MEMORY
ASSOCIATION ANALYSIS OF DYSLEXIA IN AN AFRIKANER POPULATION
ASSOCIATION BETWEEN GENOTYPE AT AN EXONIC SNP IN DISC1 AND NORMAL COGNITIVE AGING
STRONG EVIDENCE THAT KIAA0319 IS A SUSCEPTIBILITY GENE FOR DEVELOPMENTAL DYSLEXIA ON CHROMOSOME 6p
LINKAGE FINDINGS FROM COGA AND NAG: INDEPENDENT STUDIES SUGGEST A GENE ON CHROMOSOME 2p WITH PLEIOTROPIC EFFECTS ON MULTIPLE PSYCHIATRIC PHENOTYPES
GENETIC VULNERABILITY FOR NICOTINE DEPENDENCE: LINKAGE RESULTS FROM THE NAG (NICOTINE ADDICTION GENETICS) PROJECT
GENETIC VULNERABILITY TO COMORBID ANXIETY ATTACK AND DSM-IV NICOTINE WITHDRAWAL IN AUSTRALIAN FAMLIES: THE NICOTINE ADDICTION GENETICS PROJECT (NAG)
GENOME-WIDE GENETIC LINKAGE ANALYSIS OF A QUANTITATIVE TRAIT IN AN AUSTRALIAN AND FINNISH STUDY OF NICOTINE DEPENDENCE
ASSOCIATION OF THE SEROTONIN TRANSPORTER GENE WITH NICOTINE DEPENDENCE
ASSOCIATION OF DNA POLYMORPHISMS IN THE SYNAPTIC VESICULAR AMINE TRANSPORTER GENE (SLC18A2) WITH ALCOHOL- AND NICOTINE DEPENDENCE
DIFFERENTIAL EFFECTS OF DISC1 AND DTNBP1 RISK GENOTYPES ON COGNITION: NEW EVIDENCE FOR SPECIFICITY
IL-10 RECEPTOR 1: ASSOCIATION STUDY IN MAJOR DEPRESSION
‘GENERALIST GENES’ AND MATHEMATICS
THE RISK FOR ALZHEIMER'S DISEASE IS RELATED TO A CLUSTER OF GENES INVOLVED IN BRAIN CHOLESTEROL METABOLISM
ALTERED BRAIN ACTIVATION IN DORSOLATERAL PREFRONTAL CORTEX IN ADOLESCENTS AND YOUNG ADULTS AT GENETIC RISK FOR SCHIZOPHRENIA: AN FMRI STUDY OF WORKING MEMORY
ALLELOTYPING OVER 10,000 SNPS USING DNA POOLS AND MICROARRAYS NOMINATES FOUR SNPS ASSOCIATED WITH MILD MENTAL IMPAIRMENT
CRITICAL PARAMETERS FOR THE GENETICS OF SCHIZOPHRENIA
MINOR GENOTYPING ERROR CAN RESULT IN SUBSTANTIAL ELEVATION IN TYPE I ERROR RATE IN HAPLOTYPE BASED CASE CONTROL ANALYSIS
GENOME-WIDE ASSOCIATION: PRACTICAL APPLICATION OF CURRENT TECHNOLOGY TO OVERCOME MULTIPLE TESTING
A GENE-BASED APPROACH TO EPISTASIS IN LARGE-SCALE ASSOCIATION STUDIES
THE CONTROL OF FALSE DISCOVERIES IN LARGE SCALE GENETIC STUDIES
A GENOME-WIDE LINKAGE SCAN FOR ILLICIT DRUG PHENOTYPES IN AUSTRALIAN ADULTS FROM THE NICOTINE ADDICTION GENETICS (NAG) PROJECT
SNPs AT THE BRAIN DERIVED NEUROTROPHIC FACTOR (BDNF) GENE SHOW ASSOCIATION WITH OPIOID ADDICTION
LONGITUDINAL MODELING OF MEASURES OF PEER GROUP DEVIANCY (PGD) AND THE GENETIC AND ENVIRONMENTAL SOURCES OF COVARIANCE BETWEEN PGD, DRUG USE, ABUSE AND DEPENDENCE IN ADULT MALE TWINS
WHOLE GENOME LINKAGE SCAN FOR ALCOHOL CONSUMPTION IN A SELECTED SIBLING SAMPLE
CIRCADIAN RHYTHM GENES PER1 AND PER2 REGULATE GENE-ENVIRONMENT INTERACTIONS AND ARE ASSOCIATED WITH ALCOHOL DRINKING BEHAVIOUR IN HUMANS
METHAMPHETAMINE DIFFERENTIALLY REGULATES IMMEDIATE EARLY GENES IN THE PREFRONTAL CORTEX OF HIGH AS COMPARED TO LOW RESPONDERS
A MULTIGENE NEURAL NETWORK BASED PREDICTOR OF LITHIUM RESPONSE
DISCOVERY OF GENETIC MARKERS ASSOCIATED WITH CLOZAPINE INDUCED AGRANULOCYTOSIS
A GENE EXPRESSION STUDY OF CLOZAPINE COMPARED TO HALOPERIDOL AND HOW THESE DRUGS INTERACT WITH GENES IMPLICATED IN SCHIZOPHRENIA
ASSOCIATION OF THE SEROTONIN TRANSPORTER AND OTHER CANDIDATES WITH THERAPEUTIC RESPONSE TO SSRI ANTIDEPRESSANTS IN THE KAISER PERMANENTE STUDY ON GENETICS OF RESPONSE TO ANTIDEPRESSANTS
CHRONIC ANTIPSYCHOTIC ADMINISTRATION ALTERS MESSENGER RNA EDITING
EVIDENCE THAT SSRI RESPONSE IN DEPRESSION IS INFLUENCED BY A FUNCTIONAL HAPLOTYPE IN HTR1B AND THE C-1019G SNP IN HTR1A
GENETIC VARIATION AT OR NEAR COMT INFLUENCES SUSCEPTIBILITY TO A PHENOTYPE CHARACTERIZED BY THE CO-EXISTENCE OF MARKED FEATURES OF MANIA AND PSYCHOSIS
THE BEGINNING OF THE END FOR THE KRAEPELINIAN DICHOTOMY—RESPONSE TO CRADDOCK & OWEN
MOLECULAR GENETIC EVIDENCE FOR OVERLAP BETWEEN BIPOLAR DISORDER AND SCHIZOPHRENIA
AUTOSOMAL GENOME SCANS FOR TWO CLINICAL CONDITIONS (PSYCHOSIS AND MANIC EPISODE) IN MULTIPLEX ASHKENAZI JEWISH PEDIGREES WITH SCHIZOPHRENIA, SCHIZOAFFECTIVE DISORDER AND/OR BIPOLAR I DISORDER
VARIATION AT THE DAOA/G30 LOCUS INFLUENCES SUSCEPTIBILITY TO MAJOR MOOD EPISODES BUT NOT PSYCHOSIS IN PATIENTS WITH SCHIZOPHRENIA AND BIPOLAR DISORDER
COMBINED APPROACH OF MICROARRAY GENE EXPRESSION AND GENETIC ASSOCIATION IN SCHIZOPHRENIA
EVIDENCE FOR ASSOCIATION AND INTERACTION BETWEEN G72 AND DAAO MARKERS IN AN IRISH CASE-CONTROL SCHIZOPHRENIA SAMPLE
APPRAISING NEUROCOGNITIVE ENDOPHENOTYPES FOR SCHIZOPHRENIA
ANALYSIS OF COMT, ProDH AND ZDHHC8 RISK VARIANTS DOES NOT PROVIDE EVIDENCE FOR A SINGLE OR COMBINED-SYNERGISTIC RISK EFFECT OF THESE GENES TO SCHIZOPHRENIA
GENES BEHIND COMPLEX DISEASE IN A SIMPLE POPULATION: SCHIZOPHRENIA SUSCEPTIBILITY GENES IN FINLAND
AN ANIMAL MODEL FOR PSYCHOSIS
POSITIONAL CLONING, ASSOCIATION ANALYSIS, AND EXPRESSION STUDIES PROVIDE CONVERGENT EVIDENCE THAT THE CADHERIN GENE FAT CONTAINS A BIPOLAR DISORDER SUSCEPTIBILITY ALLELE
ASSOCIATION OF GRIK2 HAPLOTYPES WITH BIPOLAR AFFECTIVE DISORDER AND POTENTIAL INTERACTION BETWEEN GRIK2 AND ALPHA-LAMININS
HIGH DENSITY SNP ASSOCIATION STUDY OF 22Q13 IDENTIFIES CACGN2 AS A SUSCEPTIBILITY LOCUS FOR BIPOLAR DISORDER IN TWO INDEPENDENT SAMPLES
VARIATIONS IN THE VESICULAR MONOAMINE TRANSPORTER 1 GENE (VMAT1/SLC18A1) ARE ASSOCIATED WITH BIPOLAR I DISORDER
FURTHER EVIDENCE THAT THE DAOA(G72) GENE IS A RISK FACTOR FOR BIPOLAR DISORDER: RESULTS FROM A FAMILY BASED ASSOCIATION STUDY
FURTHER INVESTIGATION OF ASSOCIATION BETWEEN BIPOLAR DISORDER AND BDNF: CHARACTERIZATION OF POPULATION GENETIC STRUCTURE AND HAPLOTYPE ASSOCIATION STUDIES IN FOUR PATIENT SAMPLES
CHROMOSOME 11-Q24 REGION IN TOURETTE SYNDROME: ASSOCIATION AND LINKAGE DISEQUILIBRIUM STUDY IN THE FRENCH CANADIAN POPULATION
ASSOCIATION BETWEEN THE DOPAMINE D5 RECEPTOR (DRD5) MARKER AND AUTISM
THE IDENTIFICATION OF NOVEL MICRODELETIONS AND MICRODUPLICATIONS CAUSING AUTISM SPECTRUM DISORDER (ASD) USING 1 MB ARRAY-COMPARATIVE GENOMIC HYBRIDIZATION (ARRAY-CGH)
THE EXTENT OF GENETIC INFLUENCES ON PERFORMANCE ON REACTION TIME, INHIBITION AND ‘DELAY AVERSION’ TASKS
A GENOME-WIDE SCAN OF GILLES DE LA TOURETTE SYNDROME
THE CIRCADIAN GENE HPER3 AND NOVELTY SEEKING IN MOOD DISORDERS
GSK3β GENE MAY INFLUENCE SCHIZOTYPAL PERSONALITY TENDENCIES AND DEVELOPMENT OF DELUSIONS
ASSOCIATION BETWEEN TRYPTOPHAN HYDROXYLASE 2 POLYMORPHISMS AND MAJOR DEPRESSIVE DISORDER IN WOMEN
TRYIPTOPHAN HYDROXYLASE GENE (TPH) MAY BE INVOLVED IN SEVERE GASTROINTESTINAL SIDE EFFECTS DURING THE TREATMENT WITH SRIS
IS THE POSTPARTUM ONSET SPECIFIER IN DSM-IV TOO NARROW? EVIDENCE FROM A FAMILY STUDY
STRATIFIED BIPOLAR AND PANIC DISORDER SIB PAIR ANALYSIS OF NIMH WAVE 1-4 PEDIGREES
SEROTONIN TRANSPORTER GENE, STRESSFUL LIFE EVENTS AND THE ONSET OF MOOD DISORDERS
ALLELIC AND HAPLOTYPIC ASSOCIATION WITH BIPOLAR DISORDER IMPLICATES A 300 KILOBASE REGION ON CHROMOSOME 12Q24.3 CONTAINING NOVEL BRAIN EXPRESSED GENE SEQUENCES
GENETIC MODULATION OF ANXIETY RESPONSE IN SSRI TREATED MAJOR DEPRESSION
SEXUAL ENDOPHENOTYPES IN THE MALE RAT
A GENOME WIDE MAPPING APPROACH FOR MOOD DISORDERS SUSCEPTIBILITY LOCI: A PRELIMINARY SIB PAIRS STUDY
SEROTONIN TRANSPORTER PROMOTER GENETIC CHARACTERIZATION: POSSIBLE PHARMACOGENETIC IMPLICATIONS OF RARE ALLELES
NEW HTTLPR AND PER VARIANTS INFLUENCE SSRI RESPONSE AND OTHER FEATURES OF MOOD DISORDERS
ASSOCIATION OF POLYMORPHISMS IN GENES OF THE DOPAMINE AND SEROTONIN SYSTEMS AND HEROIN DEPENDENCE
HAPLOTYPIC ASSOCIATION OF DOPAMINE TRANSPORTER GENE VNTRS AND METHAMPHETAMINE ABUSE
THE ROLE OF CONDUCT DISORDER IN EXPLAINING THE COMORBIDITY BETWEEN ALCOHOL AND ILLICIT SUBSTANCE ABUSE AND DEPENDENCE PROBLEMS
CB1 RECEPTOR GENE CN1 AND DRUG DEPENDENCE: REPLICATION OF ASSOCIATION WITH A 3-MARKER INTRON 2 HAPLOTYPE IN BOTH CAUCASIAN AND AFRICAN-AMERICAN SAMPLES
STUDY OF ASSOCIATION BETWEEN THE CATECHOL-O-METHYLTRANSFERASE (COMT) VAL158MET GENE POLYMORPHISM AND COCAINE DEPENDENCE IN A BRAZILIAN SAMPLE
ELUCIDATING THE COMORBID RELATIONSHIP BETWEEN PANIC DISORDER AND ALCOHOL DEPENDENCE IN VIETNAM ERA MALE TWINS
ASSOCIATION OF SEROTONIN TRANSPORTER GENE WITH TYPE I ALCOHOL DEPENDENCE
FURTHER EVIDENCE IN SUPPORT OF ALLELIC AND HAPLOTYPIC ASSOCIATION OF GABAA RECEPTORS AND ALCOHOL DEPENDENCE IN AN IRISH SAMPLE
ASSOCIATION ANALYSIS OF THE 5-HT2A RECEPTOR AND SEROTONIN AND DOPAMINE TRANSPORTER GENES WITH HEROIN ABUSE IN BULGARIAN SUBJECTS
INFLUENCE OF ALCOHOL METABOLISM GENE VARIANTS ON DRINKING PROBLEMS AND ALCOHOL DEPENDENCE IN EUROPEANS
VARIATION IN THE BDNF GENE CONTRIBUTES TO ALCOHOL CONSUMPTION LEVELS IN THE POPULATION
PREVALENCE OF SUBSTANCE ABUSE AMONG UNIVERSITY STUDENTS IN THE GAZA STRIP
REEXAMINING COMORBIDITY THROUGH STAGE MODELS
IMPLICATION OF THE Al ALLELE OF THE DRD2 IN ALCOHOL CRAVING
IMPACT OF THE Al ALLELE OF THE DRD2 IN MALE ALCOHOL DEPENDENT PATIENTS WITH PATERNAL HISTORY OF ALCOHOLISM
ASSOCIATION/LINKAGE DISEQUILIBRIUM STUDIES OF GLUTAMATE RECEPTOR GRIK3 SER310ALA FUNCTIONAL POLYMORPHISM IN POLISH FAMILIES WITH ALCOHOL DEPENDENCE
A POSSIBLE GENETIC COMPONENT IN THE DEVELOPMENT OF SUBSTANCE USE DISORDER IN EARLY ADULTHOOD WITH A HISTORY OF CHILDHOOD ATTENTION-DEFICIT HYPERACTIVITY DISORDER
ALLELE AND HAPLOTYPE FREQUENCIES OF AN ADDICTION CANDIDATE GENE, CNR1, IN AFRICAN AMERICANS AND EUROPEAN AMERICANS WITH COCAINE DEPENDENCE
STRAIN DIFFERENCES IN RESPONSE ACQUISITION DYNAMICS OF COCAINE SELF-ADMINISTRATION
MISSENSE MUTATION IN A BITTER TASTE RECEPTOR (HTAS2R16) INFLUENCES RISK FOR ALCOHOL DEPENDENCE
ASSOCIATION OF THE PHOSPHATASE AND TENSIN HOMOLOG GENE (PTEN) WITH SMOKING INITIATION AND PROGRESSION TO NICOTINE DEPENDENCE
THE GENE FOR MITOCHONDRIAL CERAMIDASE IS LOCATED IN A REGION LINKED TO MATERNALLY INHERITED LATE ONSET ALZHEIMER'S DISEASE (LOAD) AND IS DOWNREGULATED IN MATERNAL LOAD CASES
APOE ε4 ALLELE AND FMRI ACTIVATION PATTERNS
ASSOCIATION STUDY BETWEEN APOE POLYMORPHISM AND COGNITIVE DECLINE IN AN ELDERLY BRAZILIAN SAMPLE
MEMBERSHIP IN HIGH-RISK GENETIC GROUPS PREDICTS RISK OF ALZHEIMER'S DISEASE
I-ALLELE OF THE ANGIOTENSIN-CONVERTING ENZYME INSERTION DELETION GENE POLYMORPHISM INCREASES RISK FOR ALZHEIMER'S DISEASE IN A GERMAN POPULATION
SAITOHIN GENE SINGLE NUCLEOTIDE POLYMORPHISM AND TAU EXTENDED HAPLOTYPE IN A GERMAN POPULATION, NO ASSOCIATION WITH ALZHEIMER'S DISEASE
FUNCTIONAL ANALYSIS OF IMPAS GENES RELATED TO ALZHEIMER'S DISEASE PRESENILINS
PARSING THE GENETIC HETEROGENEITY ON CHROMOSOME 12q FOR LATE-ONSET ALZHEIMER DISEASE BY FAMILY-BASED ASSOCIATION ANALYSIS
GENETIC SUSCEPTIBILTY FOR ALZHEIMER'S DISEASE AND OTHER DEMENTIAS: THE POSSIBLE ROLE OF SEROTONIN TRANSPORTER AND GLICOGEN SYNTHASE KINASE 3-BETA GENES
HAPLOTYPE ANALYSIS OF α7 NICOTINIC ACETYLCHOLINE RECEPTOR GENE (CHRNA7) AND ASSOCIATIONS WITH ALZHEIMER'S DISEASE
GENETIC INFLUENCES ON THE PSYCHOTIC SYMPTOMATOLOGY OF ALZHEIMER'S DISEASE
APOE POLYMORPHISM IN DEMENTIA
INFLUENCE OF POLYMORPHISMS IN INTERLEUKIN-1 GENE ON AMYLOID AND NON-AMYLOID VASCULAR PATHOLOGIES IN ALZHEIMER'S DISEASE
THE ROLE OF INTERLEUKIN-6 (-174) POLYMORPHISM IN THE AMYLOID PLAQUES AND VASCULAR PATHOLOGY IN ALZHEIMER'S DISEASE
THE INFLUENCE OF POLYMORPHISMS IN OLR1 GENE ON Aß40 LOAD IN CAA THROUGH AN INTERACTION WITH APOE ε4 ALLELE IN ALZHEIMER'S DISEASE
HERITABILITY AND BI-VARIATE ANALYSES OF PTSD, DEPRESSION AND ANXIETY IN A FAMILY STUDY OF SURVIVORS FROM AN ARMENIAN EARTHQUAKE
ITEMS REPORTED BY EXPERTS AS SPECIFIC TO THE O-C PHENOTYPE DEPEND ON EXPERTS’ BACKGROUND. EXPERT-CONSTRUCTED YASR OC SUBSCALE SCORES IN A DUTCH TWIN SAMPLE
EFFECTS OF POLYMORPHISMS OF THE SEROTONERGIC, DOPAMINERGIC AND NORADRENERGIC SYSTEMS ON CLOMIPRAMINE EFFICACY IN THE OBSESSIVE-COMPULSIVE DISORDER TREATMENT
ASSOCIATION TO MARKERS IN THE 19P13 REGION IN PANIC DISORDER SAMPLES FROM THE GENETIC ISOLATE OF FAROE ISLANDS
GENETIC IMPLICATIONS OF THE ENDOCANNABINOID SYSTEM IN ANXIETY DISORDERS VERSUS DEPRESSIVE DISORDERS: IS THERE ANY EVIDENCE FOR THE CONTINUUM HYPOTHESIS?
SIBLING RESEMBLANCE FOR CLINICAL FEATURES OF OBSESSIVE-COMPULSIVE DISORDER
SEVERAL BDNF SNPS, BUT NOT THE VAL66MET FUNCTIONAL VARIANT, SHOW ASSOCIATION WITH PANIC DISORDER
SEQUENCE ANALYSIS OF GABRB3, PREVIOUSLY LINKED TO PANIC DISORDER
SYNDROMAL PANIC ATTACKS ARE POSSIBLY ASSOCIATED WITH POLYMORPHISMS IN THE ANGIOTENSIN CONVERTING ENZYME (ACE) GENE
CHARACTERIZATION OF MULTIGENERATIONAL FAMILIES WITH OCD
GENETIC EPIDEMIOLOGICAL STUDY OF PERSONALITY DISORDER PATIENTS IN HOSPITAL POPULATION
SEROTONIN 2A RECEPTOR (5HT2A) AND OBSESSIVE-COMPULSIVE DISORDER
EPIGENETIC AND GENETIC MODULATION OF BRAIN CATHECHOL-O-METHYLTRANSFERASE (COMT) INFLUENCES RISK FOR SCHIZOPHRENIA AND BIPOLAR DISORDER
HAPLOTYPE ANALYSIS OF THE DRD4 GENE IN MEXICAN PSYCHOTIC PATIENTS
FAMILY BASED ASSOCIATION STUDY BETWEEN COMT GENE AND OBSESSIVE COMPULSIVE DISORDER
ASSOCIATION BETWEEN 5-HTTLPR, DRD2 TAQA1 POLYMORPHISMS AND PERSONALITY RISK FACTORS IN PATHOLOGICAL GAMBLING IN HONG KONG CHINESE
ASSOCIATION ANALYSIS OF THE CHROMOSOME 4P-LOCATED G PROTEIN-COUPLED RECEPTOR 78 (GPR78) GENE IN BIPOLAR AFFECTIVE DISORDER AND SCHIZOPHRENIA
CONFIRMATION OF GENOME-WIDE ASSOCIATION STUDY FOR TREATMENT-EMERGENT WEIGHT GAIN: FINDINGS IN AN OBESITY COHORT
ANGER-RELATED PERSONALITY TRAITS AND VARIATION IN THE COMT VAL158MET POLYMORHISM
DRD4 GENE POLYMORPHISM AND CHILDREN'S ATTACHMENT TO THEIR MOTHER AT 1 AND 6 YEARS OF AGE
SNP-BASED ASSOCIATION STUDY OF THE INTERLEUKIN-12 P40 SUBUNIT LOCATED ON 5Q33 WITH BIPOLAR DISORDER
THE CORTISOL AND ACTH RESPONSE IN THE COMBINED DEX/CRH TEST OF ACUTELY DEPRESSED PATIENTS VARIES SIGNIFICANTLY BETWEEN 5-HT2A RECEPTOR GENOTYPES
NO ASSOCIATION OF HAPLOTYPE-TAGGING SNPS IN TRAR4 WITH SCHIZOPHRENIA IN JAPANESE PATIENTS
POST-PARTUM PSYCHOSES AND SEROTONERGIC GENES: AN ASSOCIATION STUDY
ASSOCIATION OF DRD2 GENE VARIANT WITH SCHIZOPHRENIA
ASSOCIATION BETWEEN MYELIN-RELATED GENES AND THE DEVELOPMENT OF SCHIZOPHRENIA
ASSOCIATION OF TOURETTE SYNDROME AND THE MONOAMINOOXYDASE-A GENE
ASSOCIATION BETWEEN ADRA2A GENOTYPES AND BONE DENSITY IN FEMALE SCHIZOPHRENIC PATIENTS
GENE-BASED HAPLOTYPE ANALYSIS REVEALS GENE VARIANTS STRONGLY ASSOCIATED WITH PSYCHIATRIC DISEASE
NO ASSOCIATION BETWEEN POLYMORPHISMS OF BDNF GENE AND SCHIZOPHRENIA IN A CHINESE POPULATION
QTLS FOR READING DISABILITY AT 7 YEARS: GENOTYPING POOLED DNA ON 100K SNP MICROARRAYS
POSITIVE ASSOCIATION OF BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) POLYMORPHISM WITH COGNITION AND MEMORY RECALL IN A HEALTHY ELDERLY POPULATION
ROLE OF ALLELIC VARIANTS OF DOPAMINE RECEPTOR GENES IN PERSONALITY TRAITS: A FINNISH POPULATION-BASED BIRTH COHORT STUDY
BEYOND CYTOGENETICS: ASSESSING THE WIDER CONTRIBUTION OF DISRUPTED GENES TO SCHIZOPHRENIA AND AFFECTIVE DISORDERS THROUGH ASSOCIATION STUDIES
REPLICATION OF ASSOCIATION BETWEEN TOURETTE SYNDROME AND 17Q25 IN THE FRENCH CANADIAN POPULATION
EVIDENCE FOR ASSOCIATION BETWEEN THE DYSBINDIN (DTNBP1) GENE AND SCHIZOPHRENIA: A CASE-CONTROL STUDY FROM THE JAPANESE POPULATION
ASSOCIATION BETWEEN LOW AMPLITUDE P3 AND DRD4 POLYMORPHISMS IN 8-YEARS OLD CHILDREN
#88. FAMILY-BASED ASSOCIATION STUDY BETWEEN BRAIN-DERIVED NEUROTROPHIC FACTOR GENE POLYMORPHISMS AND ATTENTION DEFICIT HYPERACTIVITY DISORDER
TRYPTOPHAN HYDROXYLASE (TPH) 1 AND SEROTONIN TRANSPORTER (5-HTT) GENE VARIANTS ASSOCIATE WITH A GROUP OF SUICIDAL BORDERLINE WOMEN
THE EFFECT OF GENDER ON THE SIBLING RISK RATIO FOR COMBINED TYPE ATTENTION DEFICIT HYPERACTIVITY DISORDER
THE DOPAMINE D4 GENE AND ADHD: ASSOCIATION WITH DIAGNOSIS AND ENDOPHENOTYPIC MEASURES
A COMMON HAPLOTYPE OF THE DOPAMINE TRANSPORTER GENE IS ASSOCIATED WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER AND INTERACTS WITH PRENATAL EXPOSURE TO ALCOHOL
SUGGESTIVE ASSOCIATION OF FATTY ACID METABOLISM GENES WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER.
ASSOCIATION OF THE NMDA RECEPTOR SUBUNIT GENE GRIN2B WITH ATTENTION-DEFICIT/ HYPERACTIVITY DISORDER (ADHD)
ASSOCIATION STUDY OF GLUTAMATE RECEPTOR SUBUNIT GENES AND CHILDHOOD-ONSET MOOD DISORDERS (COMD)
ADHD AND DEVELOPMENTAL COORDINATION DISORDER
ADHD IN ADULTS AND DOPAMINE NEUROTRANSMISSION: A CANDIDATE GENE-BASED ASSOCIATION STUDY
PHARMACOGENETIC RESPONSE PREDICTION IN ADULTS WITH ADHD
POLYMORPHISMS IN THE DOPAMINE D4 AND D2 RECEPTOR GENE AND ATTENTION DEFICIT HYPERACTIVITY DISORDER IN HAN CHINESE POPULATION
PREFERENTIAL TRANSMISSION OF PATERNAL ALLELES AT RISK GENES IN ADHD
MOVEMENT VARIABILITY IN CHILDREN WITH ADHD
ANALYSIS OF THE ALPHA ADRENERGIC RECEPTOR GENE 2A (ADRA2A) IN PATIENTS WITH TOURETTE'S SYNDROME AND ATTENTION-DEFICIT/ HYPERACTIVITY DISORDER
ASSOCIATION BETWEEN SNAP-25 WITH ADHD WITH COMORBID MAJOR DEPRESSIVE DISORDER
A STUDY OF HOW SOCIOECONOMIC STATUS MODERATES THE RELATIONSHIP BETWEEN SNPS ENCOMPASSING BDNF AND ADHD SYMPTOM COUNTS IN ADHD FAMILIES
ASSOCIATION ANALYSIS OF POLYMORPHISMS IN THE A-SUBUNIT OF THE OLFACTORY G-PROTEIN G(OLF) IN ATTENTION-DEFICIT/ HYPERACTIVITY DISORDER
ASSOCIATION STUDY OF THE NICOTINIC ACETYLCHOLINE RECEPTOR A4 SUBUNIT POLYMORPHISM WITH ATTENTION DEFICIT/ HYPERACTIVITY DISORDER
ASSOCIATION BETWEEN SEROTONIN GENE AND ATTENTION DEFICIT HYPERACTIVITY DISORDER IN CHINESE HAN SUBJECTS
PHENOTYPE:GENOTYPE ANALYSIS OF DRD4, DRD5 AND SNAP-25 IN AN IRISH ADHD SAMPLE
INVESTIGATING THE GENETIC RELATIONSHIP BETWEEN THE MAJOR DOMAINS OF THE ADHD PHENOTYPE: RESULTS FROM A POPULATION BASED TWIN STUDY
ASSOCIATION OF DRD4 EXON III POLYMORPHISM WITH FAMILIAL RISK OF ADHD IN CHILDREN WITH BIPOLAR DISORDER
GENETIC POLYMORPHISMS PREDICT VARIATIONIIN INTELLIGENCE AND ADULT PROGNOSIS AMONG CHILDREN WITH ATTENTION-DEFICIT HYPERACTIVITY DISORDER
HOME AND FAMILY ENVIRONMENT IN ADHD
SYMPTOMS OF AUTISM IN ATTENTION DEFICIT HYPERACTIVITY DISORDER
INTERACTION BETWEEN ADVERSE LIFE EVENTS AND SEROTONIN AND NOREPINEPHRINE TRANSPORTER GENE VARIANTS IN ADULT ADHD
AUTISTIC TRAITS IN HERITABLE ADHD SUBTYPES
FAMILY BASED AND CONTROL ANALYSES OF DOPAMINERGIC AND NORADRENERGIC GENES IN ATTENTION-DEFICIT/HYPERACTIVITY DISORDER—INATTENTIVE TYPE IN BRAZIL
A CASE-CONTROL STUDY OF ATTENTION-DEFICIT/ HYPERACTIVITY DISORDER—INATTENTIVE TYPE AND PRE-NATAL EXPOSURE TO MATERNAL TOBACCO SMOKING IN BRAZILIAN YOUTHS
ALCOHOL AND RETROSPECTIVELY ASSESSED ADHD IN A SAMPLE OF MIDDLE AGED VETERANS
ASSOCIATION STUDY BETWEEN TRYPTOPHAN HYDROXYLASE 1 (TPH1) GENE POLYMORPHISMS AND ADHD
TRYPTOPHAN HYDROXYLASE 2 (TPH2) GENE VARIANTS ASSOCIATED WITH ADHD
A CONTROLLED FAMILY STUDY OF ADHD AND TOURETTE'S DISORDER
DOPAMINE TRANSPORT GENE POLYMORPHISMS AND ADULT ADHD
REPLICATION AND VALIDATION OF POPULATION DERIVED ADHD PHENOTYPES
POSSIBLE ASSOCIATION OF THE ALPHA-2A-ADRENERGIC RECEPTOR GENE (ADRA2A) WITH SYMPTOMS OF ATTENTION-DEFICIT/ HYPERACTIVITY DISORDER
ASSOCIATION OF NOREPINEPHRINE TRANSPORTER GENE AND MONOAMINE OXIDASE A GENE WITH METHYLPHENIDATE RESPONSE
ASSOCIATION ANALYSIS OF DOPAMINE BETA-HYDROXYLASE GENE AND ATTENTION DEFICIT HYPERACTIVITY DISORDER IN THE CHINESE HAN POPULATION
ASSOCIATION STUDY BETWEEN THREE POLYMORPHISMS OF MAOA GENE AND ATTENTION DEFICIT HYPERACTIVITY DISORDER AMONG THE CHINESE HAN ETHNICITY
THE GLUTAMATE DECARBOXYLASE GENE 1 AS A POTENTIAL CANDIDATE GENE FOR AUTISM
FOXP2 POLYMORPHISMS IN INDIVIDUALS WITH AUTISM AND PROMINENT ABNORMALITIES OF SPEECH AND LANGUAGE
CHROMOSOME 15 ABNORMALITIES AND AUTISTIC SYMPTOMATOLOGY: CASE—CONTROL INVESTIGATIONS
ALTERED SOCIAL COMMUNICATION IN MICE WITH DISRUPTION IN THE FOXP2 GENE
ASSOCIATION OF AUTISM WITH SEROTONIN-RELATED GENES
FUNCTIONAL VARIANTS IN THE C-MET RECEPTOR ASSOCIATED WITH AUTISM
AN ASSOCIATION STUDY AND MUTATION SCREEN OF NLGN3 AND NLGN4X IN AN IRISH POPULATION SUFFERING AUTISM
MATERNAL RECURRENT MOOD DISORDERS AND HIGH-FUNCTIONING AUTISM
FURTHER EVIDENCE SUPPORTING THE ROLE OF ITGA4 AS A CANDIDATE GENE FOR AUTISM
REFINING THE REPETITIVE BEHAVIOR PHENOTYPE IN AUTISM
AN ASSOCIATION ANALYSIS OF GABRB3, A CANDIDATE GENE OF THE GABAA RECEPTOR COMPLEX ON CHROMOSOME 15Q AND AUTISM SPECTRUM DISORDER
CONFIRMATION OF ASSOCIATION BETWEEN ARGININE VASOPRESSIN 1A RECEPTOR (AVPR1A) AND AUTISM IN A FAMILY-BASED STUDY
IDENTIFICATION OF AUTISM SUSCEPTIBILITY GENES ON CHROMOSOME 16P AND 5Q
EXAMINATION OF SEROTONIN RELATED GENES IN AUTISM
ASSOCIATION STUDIES AND MUTATION SCREENING IN THE GERMAN SAMPLE OF PATIENTS WITH AUTISM SPECTRUM DISORDERS
THE XQ/YQ PSEUDOAUTOSOMAL REGION (PAR2) IS A SUSCEPTIBILITY LOCUS FOR AUTISM
ASSOCIATION FINDINGS FOR FOUR AUTISM CANDIDATE GENES BELONGING TO THE “NEUROBEACHIN PATHWAY” IN THE ASPERGER SYNDROME
EVIDENCE FOR AUTISM LOCI, IN ADDITION TO AGC1, IN THE CHROMOSOME 2q24-q33 REGION
AUTISM, ASPERGER'S, AND SCHIZOPHRENIA: COMMON ENDOPHENOTYPIC AND GENETIC CHARACTERISTICS OF NEGATIVE SYMPTOM SPECTRUM DISORDERS
ABSENCE OF MUTATIONS R451C AND D396TER (1186 INST) IN THE NEUROLIGINS NOS. 3 AND 4, GENES, RESPECTIVELY, IN 140 ITALIAN PATIENTS WITH AUTISM SPECTRUM DISORDERS
INVESTIGATING OVERLAP IN THE ‘TRIAD OF IMPAIRMENTS’ THAT DEFINE AUTISM SPECTRUM CONDITIONS: EVIDENCE FOR GENETIC HETEROGENEITY AT THE EXTREME
HAPLOTYPE ANALYSIS AND ASSOCIATION STUDIES IN AUTISM CANDIDATE GENES.
REPLICATION OF GENETIC ASSOCIATION BETWEEN AUTISM AND THE SLC25A12 GENE ON CHROMOSOME 2Q
EXCESS OF STRUCTURAL VARIANTS IN THE NEUREXIN 1ß GENE IN PATIENTS WITH AUTISM
MUTATION ANALYSIS OF THE RETT SYNDROME GENE (MECP2) EXON 1 IN AUTISM AND MENTAL RETARDATION, AND GENETIC STUDIES OF THE DISTAL PORTION OF CHROMOSOME XQ
ALLELIC HETEROGENEITY AT THE SEROTONIN TRANSPORTER GENE CONFERS RISK FOR AUTISM AND RIGID-COMPULSIVE BEHAVIORS
AN INVERSION INV (4) (P12-P15.3) ASSOCIATED WITH AUTISM IMPLICATES THE 4P GABA RECEPTOR GENE CLUSTER
BREAKPOINT MAPPING OF A COMPLEX REARRANGEMENT OF CHROMOSOME 13 IN A CHILD WITH AUTISM
RELATIONSHIPS BETWEEN VARIATION IN ITGB3, SEROTONIN LEVEL, EXPRESSION LEVEL, SLC6A4 AND AUTISM SUSCEPTIBILITY
GENOME-WIDE SCAN FOR AUTISM IN AN EXTENDED PEDIGREE FROM A REGIONAL SUBISOLATE IN FINLAND
LSMATCHMAKER: AN INTEGRATED ENVIRONMENT FOR ASSOCIATION ANALYSIS
PROTEIN EXPRESSION PROFILING OF POSTMORTEM BRAIN IN SCHIZOPHRENIA
GENES AS MODIFIERS OF ENVIRONMENTAL INPUT—CONVERGING EVIDENCE FROM EPIDEMIOLOGY AND SYSTEMS BIOLOGY
DEVELOPMENT OF DATA MANAGEMENT SYSTEM FOR GENETIC ASSOCIATION STUDIES
A MODEL OF PARTNERSHIP FOR THE PROTECTION OF CONFIDENTIALITY IN PSYCHIATRIC GENETIC RESEARCH
SCHIZOPHRENIA IS LINKED TO DNA CHANGES AT MULTIPLE FRAGILE SITES
LINKAGE DISEQUILIBRIUM MAPPING AT THE DAOA (G72) LOCUS
ASSOCIATION BETWEEN G72 HAPLOTYPES AND BIPOLAR DISORDER IN A NORDIC SAMPLE
EVIDENCE OF ALLELIC ASSOCIATION OF BIPOLAR DISORDER WITH TWO GENES P2RX7 AND AY070435 6 MB APART ON 12Q24
NO EVIDENCE FOR ASSOCIATION OF NEUREGULIN 1 WITH BIPOLAR DISORDER IN IRISH FAMILIES
A WHOLE GENOME SCAN FOR LINKAGE IN 62 IRISH PEDIGREES WITH BIPOLAR DISORDER
IDENTIFICATION OF NOVEL VALPROATE REGULATED GENES IN THE MOUSE BRAIN
NO ASSOCIATION BETWEEN SEROTONIN TRANSPORTER PROMOTER POLYMORPHISM (5-HTTLPR) AND SUICIDAL BEHAVIOR IN PATIENTS WITH BIPOLAR AFFECTIVE DISORDER
DOCK9, A CANDIDATE GENE FOR BIPOLAR DISORDER (BPAD) ON CHROMOSOME 13Q32.3
CO-TRANSMISSION OF BIPOLAR DISORDER AND A QUANTITATIVE DEVELOPMENTAL ENDOPHENOTYPE
LACK OF ASSOCIATION BETWEEN PHOSPHOLIPASE A2 GENE AND BIPOLAR MOOD DISORDER IN A MULTICENTRE EUROPEAN SAMPLE
NOREPINEPHRINE TRANSPORTER GENE POLYMORPHISMS AND THE PHENOTYPIC EXPRESSION OF BIPOLAR DISORDER
HAPLOTYPE AND ALLELE SHARING ANALYSIS OF CHROMOSOME 4P LINKED FAMILIES WITH BIPOLAR AFFECTIVE DISORDER
META-ANALYSIS REVEALS ASSOCIATION BETWEEN TRYPTOPHAN HYDROXYLASE GENE (TPH1) A218C POLYMORPHISM AND BIPOLAR DISORDER
NO EVIDENCE FOR ASSOCIATION BETWEEN POLYMORPHISMS IN P2X7 AND BIPOLAR DISORDER
DIFFERENTIAL LINKAGE TO BIPOLAR DISORDER RESULTING FROM CLASSIFICATION BY THE EXISTENCE OF COMORBID DIAGNOSES
THE BREAKPOINT CLUSTER REGION (BCR) GENE ON CHROMOSOME 22Q11 IS ASSOCIATED WITH BIPOLAR DISORDER
T(4;12) TRANSLOCATION AN A PATIENT WITH BIPOLAR AFFECTIVE DISORDER
POLARITY AT ONSET IS A FAMILIAL FEATURE OF BIPOLAR AFFECTIVE DISORDER
ASSOCIATION OF DISC1 WITH BIPOLAR DISORDER IN TWO SAMPLE SETS
RESEQUENCING AND FINE MAP ASSOCIATION STUDY OF G72/G30 REGION IN BIPOLAR DISORDER
FUNCTIONAL SIGNIFICANCE OF CONSERVED POLYGLUTAMINE MOTIF IN CIRCADIAN GENES: A HYPOTHESIS
GENOME-WIDE SCAN OF BIPOLAR DISORDER IN FAMILIES WITH MULTIPLE CASES OF ALCOHOLISM
MOOD STABILISING DRUGS ALTER GENE EXPRESSION IN NEURAL CELL LINES
ASSOCIATION ANALYSIS OF CANDIDATE GENES ON 16P12 IN FINNISH BIPOLAR DISORDER FAMILIES
THE DYSBINDIN GENE IS ASSOCIATED WITH BIPOLAR AFFECTIVE DISORDER
AUDITORY P300 AND DURATION MISMATCH NEGATIVITY (MMN) AS ENDOPHENOTYPES IN PSYCHOTIC BIPOLAR DISORDER (BP)
PATERNAL AGE AFTER 35 YEARS REDUCES THE AGE OF ONSET OF BIPOLAR DISORDER ONLY IN FEMALES
ASSOCIATION STUDY OF P2RX7 POLYMORPHISMS IN BIPOLAR DISORDER
SEQUENCE ANALYSIS OF A SEX-SPECIFIC ASSOCIATION BETWEEN BIPOLAR AFFECTIVE DISORDER IN WOMEN AND GPR50
EVIDENCE FOR THE INVOLVEMENT OF DAO AND G72/G30 IN THE SUSCEPTIBILITY OF BIPOLAR DISORDER IN THE NORTHERN SWEDISH POPULATION
A CANDIDATE GENE STUDY OF THE DOPAMINE RECEPTOR D1 (DRD1) IN OCD INCLUDING NEUROIMAGING PHENOTYPES
A GLUTAMINE TO ARGININE MUTATION IN THE C-TERMINAL DOMAIN OF P2RX7 DETERMINES THE RISK FOR MOOD DISORDERS
CATECHOL-O-METHYL TRANSFERASE GENE AND TOURETTE SYNDROME: PRELIMINARY RESULTS FROM A PEDIATRIC SAMPLE
THE PROTOCADHERIN X AND Y GENE PAIR AND DOMINANCE FOR LANGUAGE: THE EVIDENCE AND CASE FOR EPIGENETIC VARIATION
DOES COMT PROMOTER METHYLATION REGULATE GENE EXPRESSION?
THE -1019C/G 5-HT1A POLYMORPHISM: ASSOCATION WITH DECREASED PREFRONTAL CORTEX ACTIVATION MEASURED WITH 3T FMRI IN PANIC DISORDER
EXTENSIVE GENE CONVERSION SHAPES THE DNA SEQUENCE VARIABILITY OF HBII-52 SMALL NUCLEOLAR RNA CLUSTER AND LEADS TO RARE HAPLOTYPES WITH POTENTIAL LINK TO EATING DISORDERS
LARGE CANDIDATE GENE SCREEN FOR BIPOLAR OR SCHIZOPHRENIA SUSCEPTIBILITY AMONG ASHKENAZI JEWISH CASE-PARENT TRIOS INCLUSION OF COVARIATES
ASSOCIATION ANALYSIS OF THE TRYPTOPHAN HYDROXYLASE GENE IN RUSSIAN SUICIDE ATTEMPTERS
ABSENCE OF SEQUENCE VARIATION IN THE PCDH11X/Y GENE-PAIR IN RELATION TO RIGHT AND LEFT HANDEDNESS
OVERVIEW OF CANDIDATE GENE STUDIES IN THE NIMH CHILDHOOD-ONSET SCHIZOPHRENIA SAMPLE
A DOPAMINE TRANSPORTER GENE FUNCTIONAL VARIANT ASSOCIATED WITH COCAINE ABUSE IN A BRAZILIAN SAMPLE
A GTP1 FUNCTION VARIANT ASSOCIATED WITH COCAINE ABUSE IN THE BRAZILIAN POPULATION
SMALL-MOLECULE SCREENING USING NEURONAL CELLS TO ASSESS CANDIDATE GENES RELEVANT TO PSYCHIATRIC DISEASE
GENE EXPRESSION AND PATHWAY MAPPING OF THE PONTO-GENICULO-OCCIPITAL (PGO) NETWORK: COMPUTATIONAL, MOLECULAR, CELLULAR, AND BEHAVIORAL SYSTEMS
ASSOCIATIONS BETWEEN THE SEROTONIN TRANSPORTER GENE LINKED PROMOTER REGION POLYMORPHISM (5HTTLPR) AND CHILDHOOD DEPRESSION AND ANXIETY DISORDER SYMPTOMS
ANALYSIS OF PI4KIIβ, A CANDIDATE GENE FROM THE BIPOLAR SUSCEPTIBILITY LOCUS ON CHROMOSOME 4P15-16
NOVEL MUTATION IDENTIFICATION OF THE HUMAN NOREPINEPHRINE TRANSPORTER PROMOTER
ASSESSING THE EFFECT OF DRD4 PROMOTER POLYMORPHISMS ON GENE EXPRESSION USING PROMOTER HAPLOTYPES
NR2E1 VARIANTS ARE UNLIKELY TO CONTRIBUTE TO THE MICROCEPHALY, MICROPHTHALMIA, ECTRODACTYLY, AND PROGNATHISM (MMEP) PHENOTYPE
ANALYSIS OF POLYMORPHISMS IN AT-RICH DOMAINS OF NEUREGULIN 1 GENE IN SCHIZOPHRENIA
GENETIC VARIATION IN ION CHANNELS AND HUMAN BEHAVIOR
MALIC ENZYME 2 AND SUSCEPTIBILITY TO SCHIZOPHRENIA
THE ANGIOTENSINOGEN GENE CONTRIBUTES TO THE GENETIC VARIANCE OF DEPRESSION SYMPTOMATOLOGY
N-METHYL-D-ASPARTATE RECEPTOR NRL SUBUNIT GENE (GRIN1): EXPRESSION LEVEL IN SCHIZOPHRENIA AND BIPOLAR DISORDER
GENE X ENVIRONMENT INTERACTION AND SMOKING TRAJECTORY IN THE NEW ENGLAND FAMILY STUDY: 5-HTT, HOUSING DENSITY AND MOTHERS' AGE AT BIRTH
RARE VARIANTS OF THE POTASSIUM-CHLORIDE CO-TRANSPORTER 3 GENE PROMOTER, ASSOCIATED WITH BIPOLAR DISORDER, ARE METHYLATED IN VIVO
METHYLATION ANALYSIS OF A NGF1-A TRANSCRIPTION FACTOR BINDING-SITE IN THE PROMOTER REGION OF THE HUMAN GLUCOCORTICOID RECEPTOR GENE (NR3C1)
NO EVIDENCE FOR ASSOCIATION BETWEEN POLYMORPHISMS IN GRM3 AND SCHIZOPHRENIA
DOPAMINE TRANSPORTER (SLC6A3) POLYMORPHISM ASSOCIATED WITH EXTRAVERSION AND IMMEDIATE RECALL IN A NON-DEMENTED ELDERLY POPULATION
GENETIC AND ENVIRONMENTAL CONTRIBUTIONS TO ANTISOCIAL BEHAVIOURAL OUTCOMES IN A LARGE AUSTRALIAN COMMUNITY SURVEY
ASSOCIATION BETWEEN THE NEUROGRANIN GENE AND SCHIZOPHRENIA IN MALES
SEARCHING FOR NEW INTERMEDIATE PHENOTYPES: AGGRESSION-RELATED GENES IN SUICIDAL BEHAVIOR
ASSESSMENT OF SCHIZOPHRENIA GENOMES FOR DNA COPY NUMBER ALTERATIONS
SELECTIVE ERRORS IN DECLARATIVE MEMORY AND HIPPOCAMPAL FUNCTION ASSOCIATED WITH BRAIN DERIVED NEUROTROPHIC FACTOR POLYMORPHISM
VARIANTS AT THE DAOA/G30 LOCUS ARE ASSOCIATED WITH SCHIZOPHRENIA, BIPOLAR AFFECTIVE DISORDER, PANIC DISORDER, AND UNIPOLAR DEPRESSION
5-HTTLPR AND ANXIETY-RELATED PERSONALITY TRAITS META ANALYSIS REVISITED
ASSOCIATION ANALYSIS SUGGESTING GPR24 AS A SHARED SUSCEPTIBILITY GENE FOR BIPOLAR AFFECTIVE DISORDER AND SCHIZOPHRENIA
LOW GENETIC DIVERSITY AND STRONG PURIFYING SELECTION AT HUMAN NR2E1: IMPLICATIONS FOR BRAIN-BEHAVIOR DISEASE AND EVOLUTION
CANDIDATE GENE STUDY OF BIPOLAR FAMILY SAMPLE: SNP VARIATION IN COMT, NRG1 AND DTNBP1 GENES
THE ROLE OF THE DOPAMINE D4 RECEPTOR GENE POLYMORPHISM IN MAINTAINING FOCUSED ATTENTION ACROSS TIME
REVISITING AN OLD STORY: REPLICATED ASSOCIATIONS OF SNPs SPANNING DRD3 IN TWO INDEPENDENT SAMPLES MAY RESOLVE CONTROVERSIAL SER9GLY ASSOCIATION WITH SCHIZOPHRENIA
ASSOCIATION OF AKT1 WITH SCHIZOPHRENIA CONFIRMED IN THE IRISH STUDY OF HIGH DENSITY SCHIZOPHRENIA FAMILIES (ISHDSF)
ASSOCIATION ANALYSIS OF THREE SCHIZOPHRENIA CANDIDATE GENES IN FINNISH FAMILY SAMPLE: AKT1, DYSBINDIN AND NEUREGULIN 1
ASSOCIATION ANALYSES OF THE NEUREGULIN 1 GENE WITH SCHIZOPHRENIA AND MANIC PSYCHOSIS IN A HISPANIC POPULATION
ASSOCIATION BETWEEN REPEAT POLYMORPHISMS IN THE ANDROGEN RECEPTOR GENE AND PERSONALITY TRAITS IN MEN
FINDING QUANTITATIVE TRAIT GENES THAT INFLUENCE MOUSE BEHAVIOUR—AND INVESTIGATING THEIR ROLE IN HUMAN PSYCHOPATHOLOGY
THE P-5 PROMOTER VARIANT IN THE GRK3 GENE ALTERS BINDING TO SP1 FAMILY TRANSCRIPTION FACTORS AND IS ASSOCIATED WITH BIPOLAR DISORDER
TDT ANALYSES SUGGEST TWO DISTINCT HAPLOTYES IN G PROTEIN RECEPTOR KINASE-3 (GRK3) ARE ASSOCIATED WITH BIPOLAR DISORDER
EPISTASIS BETWEEN ARGININE VASOPRESSIN RECEPTOR 1A (AVPR1A) AND SEROTONIN TRANSPORTER (SLC6A4) POLYMORPHISMS CONFER RISK FOR ANOREXIA NERVOSA AND SMOKING
PATTERNS OF BDNF/NTRK2 DNA VARIANTS AND BDNF PROTEIN BLOOD LEVELS IN EATING DISORDERS
INCREASED BLOOD LEVELS OF BDNF IN PATIENTS WITH EATING DISORDERS ARE INDEPENDENT OF THE VAL66MET VARIANT AND ARE ASSOCIATED WITH THE -270C/T VARIANT
ALLELES AT THE SEROTONIN RECEPTOR 5HT2C ARE ASSOCIATED WITH EATING DISORDERS AND RELATED PSYCHOPATHOLOGICAL TRAITS
ROLE OF THE BRAIN-DERIVED NEUROTROPHIC FACTOR GENE (BDNF) IN BULIMIA NERVOSA AND SEASONAL AFFECTIVE DISORDER
A MODEL FOR INTERNATIONAL COLLABORATION: INDO-US TRAINING GRANT FOR PSYCHIATRIC GENETICS IN INDIA
PUBLIC POLICY, ADVOCACY AND EDUCATION
ASSOCIATIONS BETWEEN GENETIC RISK ESTIMATION, REPRODUCTIVE DECISIONS, AND VIEWS ABOUT PREDICTIVE GENETIC TESTING AMONGST THE UNAFFECTED RELATIVES OF INDIVIDUALS WITH PSYCHOTIC DISORDERS
ATTITUDES TOWARDS PSYCHIATRIC GENETICS IN DIFFERENT PROFESIONAL GROUPS
GENETIC COUNSELLING SCENARIOS FOR OFFSPRING OF DUAL MATING PSYCHIATRIC PATIENTS: A NATIONAL DANISH SAMPLE FOLLOWED-UP AND EXPANDED
GENETIC COUNSELORS IN PSYCHIATRY; THE INDICATION OF SCHIZOPHRENIA
ATTITUDES TOWARDS PSYCHIATRIC GENETIC RESEARCH AND TESTING: FEARS, HOPES, AND INTENTIONS
GENETIC COUNSELING AND SCHIZOPHRENIA
PSYCHIATRIC ILLNESS: NATURE? NUTURE? BOTH? NEITHER?
WHOLE GENOME ANALYSIS OF DNA COPY NUMBER VARIATION USING AFFYMETRIX AND BAC MICROARRAYS
THE PONTO-GENICULO-OCCIPITAL (PGO) NETWORK: A BEHAVIORAL BENCHMARK FOR GENE EXPRESSION PROFILING
SINAPSE: SINGLE-PCR, EFFICIENT SNP DETECTION ON STANDARD DNA SEQUENCING EQUIPMENT
SNPLEX GENOTYPING OF THE BDNF GENE IN ANOREXIA NERVOSA AND BULIMIA NERVOSA
TAILING-PATH BAC MICROARRAYS O HUMAN CHROMOSOMES 15 AND 22 FR TE ANALYSIS O LARGE COPY VARIANTS, GENOMIC MUTATIONS AND PSYCHIATRIC DISORDERS
BIOCHEMICAL CHARACTERIZATION OF MUTANT AROMATIC AMINO ACID HYDROXYLASES IMPLICATED IN PSYCHIATRIC DISORDERS.
WILL WHOLE GENOME AMPLIFICATION PROVE RELIABLE FR LARGE-SCALE ASSOCIATION STUDIES?
RIGIDITY IN FAMILIES OFPATIENTS WTH NONPSYCHOTIC MENTAL DISORDERS
COMORBIDITIES BETWEEN READING DISABILITIES, LANGUAGE IMPAIRMENTS AND ADHD SYMPTOMS IN EARLY CHILDHOOD: A ‘BEHAVIORAL GENOMIC’ ANALYSIS USING A READING DISABILITY ‘SNP-SET’
CORRELATIONS BETWEEN GENE EXPRESSION OF GAP JUNCTIONS AND ACQUISITION AND PERFORMANCE SCORES OF WATER MAZE IN RATS
LINKAGE ANALYSES OF IQ IN THE COLLABORATIVE STUDY ON THE GENETICS OF ALCOHOLISM (COGA) SAMPLE5
IDENTIFICATION OF SUSCEPTIBILITY LOCI FOR ALCOHOL-RELATED TRAITS IN THE IRISH AFFECTED SIB PAIR STUDY OF ALCOHOL DEPENDENCE
THE FOLLOW-UP LINKAGE ANALYSIS OF ALCOHOL DEPENDENCE SYMPTOMS ON CHROMOSOME 4 IN THE IRISH AFFECTED SIB PAIR STUDY
FINE MAPPING OF A SCHIZOPHRENIA-RELATED LOCUS ON CHROMOSOME 15Q14-15Q15.1
A PARTIAL GENOME SCAN TO IDENTIFY SUSCEPTIBILITY LOCI FOR MAJOR PSYCHOSES: A PRELIMINARY REPORT
COMBINED WHOLE GENOME LINKAGE ANALYSIS OF EXTRAVERSION
SCANNING SUSCEPTIBILITY REGIONS FOR BIPOLAR DISORDER IN A LARGE SOUTH INDIAN PEDIGREE.
A GENOME SCAN FOR CSF LEVELS OF SEROTONIN, DOPAMINE AND NOREPINEPHRINE METABOLITES IN BABOONS (PAPIO HAMADRYAS)
MAPPING SUSCEPTIBILITY LOCI FOR AFFECTIVE DISORDER IN THE NORTHERN SWEDISH POPULATION
“KINDLING” RECONSIDERED
INFLUENCE OF THE DIFFERENT SUBTYPES OF THE SERTPR POLYMORPHISM ON PSYCHIC AND SOMATIC ANXIETY RESPONSE TO ANTIDEPRESSANTS IN MDD PATIENTS
CHARACTERISTICS OF RECURRENT MAJOR DEPRESSION IN A LARGE PEDIGREE FROM A RURAL COMMUNITY IN PAKISTAN
SEROTONIN TRANSPORTER PROMOTER POLYMORPHISM: EXPRESSION AND GENE-ENVIRONMENT STUDIES IN LYMPHOBLAST CELL LINES FROM A MAJOR DEPRESSION SAMPLE
THE GEM INTERACTING PROTEIN (GMIP) GENE IS ASSOCIATED WITH MAJOR DEPRESSIVE DISORDER
DOPAMINE B-HYDROXYLASE AND PSYCHOTIC DEPRESSION
GENOTYPIC PREDICTORS TO DEPRESSION TREATMENT OUTCOME
ASSOCIATION STUDY OF INFLAMMATION-RELATED GENES IN CHILDHOOD-ONSET MOOD DISORDERS
LIFE EVENTS, FIRST DEPRESSION ONSET, AND THE SEROTONIN TRANSPORTER GENE
ANGER ENDOPHENOTYPES AND SINGLE NUCLEOTIDE POLYMORPHISMS IN cAMP RESPONSE ELEMENT BINDING PROTEIN (CREB) IN MAJOR DEPRESSIVE DISORDER
GLOBAL GENE EXPRESSION PROFILING IN THE HIPPOCAMPUS AND FRONTAL CORTEX OF ESCITALOPRAM-TREATED LEARNED HELPLESSNESS RATS
MAJOR DEPRESSIVE DISORDER: IDENTIFYING PHENOTYPIC SUBTYPES FOR GENETIC STUDIES.
DECREASED CAMP LEVELS IN LEUKOCYTES OF HIBERNATING BEARS, DUE TO METABOLIC DEPRESSION, EXPLAINS SIMILAR FINDING SUGGESTING HYPOMETABOLISM IN MAJOR DEPRESSION
GENOMIC EXPRESSION PROFILE OF MAJOR DEPRESSION IN PERIPHERAL LEUKOCYTES
A TRIALLELIC SEROTONIN TRANSPORTER GENE PROMOTER POLYMORPHISM (5-HTTLPR), STRESSFUL LIFE EVENTS AND SEVERITY OF DEPRESSION
A DEVELOPMENTAL APPROACH TO UNDERSTANDING FRAGILE X SYNDROME: THE INFLUENCE OF ENVIRONMENTAL AND GENETIC FACTORS ON BEHAVIOR PROBLEMS IN PATIENTS WITH FRAGILE X SYNDROME
BEHAVIOURAL PHENOTYPES IN GENETIC SYNDROMES: A WINDOW TO THE BIOLOGY OF BEHAVIOUR
ADVANCES IN RESEARCH ON THE FRAGILE X SYNDROME: ANALYZING GENE-BRAIN-BEHAVIOR RELATIONSHIPS IN NEURODEVELOPMENTAL EFFECTS
THE BEHAVIOURAL NEUROGENETICS OF FRAGILE X SYNDROME
BRAIN: BEHAVIOR ASSOCIATIONS IN VELOCARDIOFACIAL SYNDROME (22Q11.2 DELETION SYNDROME)
VISUOSPATIAL WORKING MEMORY IN CHILDREN AND ADOLESCENTS WITH VELO-CARDIO-FACIAL SYNDROME; AN FMRI STUDY
THE GENETICS OF NEUROCOGNITIVE DYSFUNCTION IN SCHIZOPHRENIA
FAMILIAL AGGREGATION OF ADHD SYMPTOMS AND NEUROPSYCHOLOGICAL FUNCTIONS
MOLECULAR GENETIC ARCHITECTURE OF HUMAN PREPULSE INHIBITION
ASSOCIATION STUDY OF THE COMT GENE VAL158MET POLYMORPHISM WITH AUDITORY P300 AND PERFORMANCE ON NEUROCOGNITIVE TESTS IN PATIENTS WITH SCHIZOPHRENIA AND THEIR RELATIVES
THE MULTIDIMENSIONAL STRUCTURE OF THE PSYCHOSIS CONSTRUCT: BOTTOM-UP SYMPTOM FACTORING APPROACH AND RESULTING FACTORS' HERITABILITIES
POLYMORPHISM FOR NEUROPSYCHIATRIC DISORDERS IN WILSON DISEASE PATIENTS IN THE VOLGA-URAL POPULATION
DOPAMINE SYSTEM GENES AND P300 AMPLITUDE
TEN YEARS OF PERSONALITY GENETICS
META-ANALYSIS OF GENETIC ASSOCIATION STUDIES: LIMITATIONS, AND DIRECTIONS FOR FUTURE RESEARCH
SEROTONIN TRANSPORTER POLYMORPHISM ASSOCIATED WITH BORDERLINE AND ANTISOCIAL FEATURES
CLUSTERING OF PHENOTYPIC FEATURES IN FAMILIAL SCHIZOPHRENIA
PERSONALITY AND THE GENETIC RISK FOR COMORBID INTERNALIZING AND EXTERNALIZING BEHAVIOR IN ADOLESCENTS
ASSOCIATIONS BETWEEN A POLYMORPHISM IN THE SEROTONIN TRANSPORTER GENE AND MULTIPLE MEASURES OF CHILD TEMPERAMENT
EFFECT OF A COMT POLYMORPHISM ON THE NEURAL CORRELATES OF WORKING MEMORY IN VELOCARDIOFACIAL SYNDROME (22Q11 DELETION SYNDROME)
POLYMORPHISMS IN FKBP5 ARE ASSOCIATED WITH PERI-TRAUMATIC DISSOCIATION IN MEDICALLY INJURED CHILDREN
INDEPENDENT EVIDENCE FOR THE VMP/DCDC2/KAAG1 GENE LOCUS ON CHROMOSOMAL REGION 6P22 AS SUSCEPTIBILITY FACTOR FOR DYSLEXIA
PSYCHIATRIC PROFILE OF CHILDREN WITH VELO-CARDIO-FACIAL SYNDROME (VCFS)
EFFECT OF DOPAMINE GENES ON TOURETTE'S SYNDROME
THE ASSOCIATION OF DRD4 AND NOVELTY SEEKING IS REPLICATED IN A NONHUMAN PRIMATE MODEL
THE ROLE OF DOPAMINE IN REWARD AND PLEASURE BEHAVIOR—REVIEW OF DATA FROM PRECLINICAL RESEARCH
NEUREGULIN (NRG1): SUSCEPTIBILITY HAPLOTYPES AND NEURODEVELOPMENT IN CHILDHOOD ONSET SCHIZOPHRENIA
HISTONE METHYLATION IN CHROMATIN SURROUNDING GAD1/GAD67 (2Q31.1) IN HUMAN PREFRONTAL CORTEX
‘THEORY OF MIND’ AND FACIAL AFFECT RECOGNITION IN UNAFFECTED RELATIVES OF PATIENTS WITH SCHIZOPHRENIA
A GENOME-WIDE SEARCH FOR SHARED ALLELES AND HAPLOTYPES IN DISTANTLY RELATED PATIENTS WITH BIPOLAR AFFECTIVE DISORDER OR SCHIZOPHRENIA FROM THE FAROE ISLANDS
CHARACTERIZATION OF A CO-FAMILIAL TRAIT OF SCHIZOPHRENIA: THE ROLE OF CONTRAST IN VELOCITY DISCRIMINATION DEFICITS IN RELATIVES OF SCHIZOPHRENIA PATIENTS
GENETIC INFLUENCES ON BRAIN PHYSIOLOGY IN SCHIZOPHRENIA
THE EFFECT OF DELETION 22Q11 ON BRAIN ANATOMY AND BEHAVIOUR: A STRUCTURAL IMAGING STUDY OF CHILDREN WITH VELO-CARDIO-FACIAL SYNDROME (VCFS)
REFINEMENT OF A SCHIZOPHRENIA LINKAGE REGION AT 17P11.2-Q25.1
NO ASSOCIATION BETWEEN HOMOZIGOSITY FOR DOPAMINE D3 RECEPTOR GENE SER9GLY POLYMORPHISM AND SCHIZOPHRENIA
A FAMILY BASED AND CASE-CONTROL STUDY OF THE SYNAPSIN III GENE AND SCHIZOPHRENIA
TRAIT VS STATE MARKERS FOR SCHIZOPHRENIA: THE CASE OF VISUAL MOTION PROCESSING
GENETIC ASSOCIATION AND GENE EXPRESSION STUDIES IMPLICATE THE CHROMOSOME 11Q23.3 GENE FXYD2 IN SUSCEPTIBILITY TO SCHIZOPHRENIA
IDENTIFYING POTENTIAL RISK HAPLOTYPES FOR SCHIZOPHRENIA AT THE DTNBP1 LOCUS IN HAN CHINESE AND SCOTTISH POPULATIONS
FAMILIALITY OF SANS-SAPS SYMPTOM DIMENSIONS IN A HISPANIC POPULATION
RISK REGIONS FOR SCHIZOPHRENIA SITUATED ON CHROMOSOMES 6, 8 AND 10
NEUREGULIN AND DYSBINDIN? ARE THESE REALLY GENES FOR SCHIZOPHRENIA?
DETECTION OF POTENTIAL AETIOLOGICAL BASE PAIR CHANGES CAUSING GENETIC SUSCEPTIBILITY TO SCHIZOPHRENIA IN THE PERICENTRIOLAR MATERIAL 1 (PCM1) GENE ON CHROMOSOME 8P22 SUPPORTS EVIDENCE FROM ALLELIC ASSOCIATION
ASSOCIATION STUDY BETWEEN POLYMORPHISM OF THE HUMAN CYCLIC GMP—DEPENDENT PROTEIN KINASE GENE AND ANTIPSYCHOTIC-INDUCED WEIGHT GAIN
THE ROLE OF ESTROGEN SIGNALING IN SCHIZOPHRENIA
EVIDENCE THAT DYSBINDIN-1 IS ASSOCIATED WITH POORER SPATIAL WORKING MEMORY PERFORMANCE IN SCHIZOPHRENIA.
EVIDENCE THAT G72 AND DAAO INFLUENCE NEUROCOGNITIVE PERFORMANCE IN PATIENTS WITH SCHIZOPHRENIA
IDENTIFICATION OF GENES ASSOCIATED WITH SCHIZOPHRENIA USING GENE EXPRESSION ANALYSIS OF AN ANIMAL MODEL OF ANTIPSYCHOTIC DRUG ACTION
EVIDENCE FOR CAPON AFFECTING RISK FOR SCHIZOPHRENIA
GENOME SCAN OF LATENT CLASSES OF PSYCHOTIC ILLNESS
ASSOCIATION STUDY AND META-ANALYSIS OF -308 A/G FUNCTIONAL POLYMORPHISM IN TNFα GENE WITH SCHIZOPHRENIA
GENETIC ANALYSIS OF THE HYPOTHESIS OF ALTERED OLIGODENDROCYTE FUNCTION IN SCHIZOPHRENIA
BIOLOGICAL CORRELATIVES IN FAMILIES OF PATIENTS WITH SCHIZOPHRENIA
P300 AND DURATION MISMATCH NEGATIVITY IN SCHIZOPHRENIC TWINS
CANDIDATE GENES FOR SCHIZOPHRENIA ON CHROMOSOMES 1 & 2 IN A LARGE HAN CHINESE COHORT
TWO BIOLOGICALLY INTERACTING GENES, DISC1 AND NDE1, ASSOCIATE WITH SCHIZOPHRENIA AND VISUAL WORKING MEMORY FUNCTIONS
THE RELATION OF MYELIN-RELATED GENES TO BRAIN MORPHOLOGY IN SCHIZOPHRENIA
SNP FINE MAPPING OF CHROMOSOME 6P24-23 REVEALS TWO POTENTIAL CANDIDATE GENES FOR SCHIZOPHRENIA, BMP6 AND TXNDC5
XBP1 FUNCTIONAL PROMOTER VARIANT AND SCHIZOPHRENIA: A CASE-CONTROL STUDY
BRAIN-DERIVED NEUROTROPHIC FACTOR GENE ( BDNF ) VARIANTS, SCHIZOPHRENIA, AND RELATED TRAITS: AN ASSOCIATION STUDY
AN ASSOCIATION STUDY OF SCHIZOPHRENIA WITH ERBB3
GENETIC TRANSMISSION IN PSYCHOSIS
DRD2 PROMOTER REGION VARIATION PREDICTS SUSTAINED RESPONSE TO ANTIPSYCHOTICS IN FIRST EPISODE SCHIZOPHRENIA
DIMENSIONS OF PSYCHOTIC ILLNESS IN SCHIZOPHRENIA PEDIGREES
FAMILIAL CORRELATION IN SKIN FLUSH RESPONSE TO NIACIN PATCH BETWEEN SCHIZOPHRENIC PATIENTS AND THEIR FIRST-DEGREE RELATIVES
SNP FINE MAPPING OF CHROMOSOME 8P21-12 REVEALS FOUR POTENTIAL CANDIDATE GENES FOR SCHIZOPHRENIA, DPYSL2, TRIM35, PTK2B, AND CHRNA2
SNP FINE MAPPING OF CHROMOSOME 22Q12 REVEALS THE NOVEL VULNERABILITY GENE FOR SCHIZOPHRENIA, CACNG2: ASSOCIATION WITH IMPAIRMENT OF SUSTAINED ATTENTION AND EXECUTIVE FUNCTION
FAILURE TO SUPPORT BOTH AKT-1 AND ZDHHC8 AS CANDIDATE GENES FOR SCHIZOPHRENIA IN THE COHORT OF TAIWAN
DYNAMIC REGULATION OF DISC1-PDE4 COMPLEXES MAY LINK cAMP SIGNALLING TO NEURONAL PATHWAYS RELEVANT TO PSYCHIATRIC ILLNESS
PHARMACOGENETIC PREDICTION OF ZIPRASIDONE RESPONSE IN SCHIZOPHRENIC PATIENTS
SCREENING OF DNA SAMPLES FOR COMPLEMENT C2 AND C4 COMPONENTS NONSENSE MUTATIONS: HEALTHY VOLUNTEERS VERSUS SCHIZOPHRENIC PATIENTS WITH POSITIVE FAMILY HISTORY OF THE DISEASE
ASSOCIATION STUDY OF THREE OXIDATIVE STRESS GENES PUTATIVELY INVOLVED IN THE PATHOGENESIS OF SCHIZOPHRENIA IN A LARGE IRISH CASE-CONTROL SAMPLE.
LIMB TRUNCAL DYSKINESIA IS ASSOCIATED WITH SERINE ALLELE OF DRD3 IN MALES
MOLECULAR ANALYSIS OF THE PROXIMAL AND DISTAL BREAKPOINTS OF A 4Q INVERSION SEGREGATING IN A LARGE SCHIZOPHRENIA KINDRED FROM HONG KONG
DETECTION OF SIGNIFICANT LINKAGE TO CHROMOSOME 18Q IN PORTUGUESE FAMILIES WITH SCHIZOPHRENIA AND DISSOCIATION FROM 5Q LINKAGE BASED ON MODE OF INHERITANCE AND NUMBER OF AFFECTEDS PER FAMILY
EXCLUSION OF AMINO ACID TRANSPORTER A2 (ATA2) GENE IN RELATION TO THE ATTENUATED TYROSINE TRANSPORT IN SCHIZOPHRENIA
PSYCHOSIS IN VELO-CARDIO-FACIAL (22Q11 DELETION) SYNDROME
SEARCH OF SUSCEPTIBILITY SNP FOR SCHIZOPHRENIA IN THE PAEL-R GENE
ASSOCIATION ANALYSES OF THE BLOC-1 GENES SUGGEST THE INVOLVEMENT OF BLOC-1 IN SCHIZOPHRENIA ETIOLOGY
EARLY PSYCHOSIS IN A HIGH RISK POPULATION ISOLATE
GENETIC-EPIDEMIOLOGY, CONSANGUINITY AND PATTERNS OF INHERITANCE OF SCHIZOPHRENIA IN HOSPITAL POPULATION
MYH16 INITIALLY SHOWS FAVORABLE ASSOCIATION TO SCHIZOPHRENIA PSEUDOGENE OR FUNCTIONAL LINK TO SCHIZOPHRENIA?
THE INVOLVEMENT OF ERBB4 WITH SCHIZOPHRENIA: ASSOCIATION AND EXPRESSION STUDIES
EVIDENCE FOR STATISTICAL EPISTASIS BETWEEN (COMT) VAL158MET POLYMORPHISM AND MULTIPLE PUTATIVE SCHIZOPHRENIA SUSCEPTIBILITY GENES
ASSOCIATION OF THE 5HT2C GENE POLYMORPHISM AND ANTIPSYCHOTIC-INDUCED WEIGHT GAIN
ASSOCIATION BETWEEN A POLYMORPHISM IN THE GRM7 GENE AND SCHIZOPHRENIA IN A JAPANESE POPULATION
LARGE-SCALE TRANSCRIPTOME ANALYSES OF SCHIZOPHRENIC BRAINS USING SERIAL ANALYSIS OF GENE EXPRESSION (SAGE)
TESTING FOR ASSOCIATION OF REGIONAL CANDIDATE GENES ON 7Q22 IN FINNISH SCHIZOPHRENIA FAMILIES
CELL AND MOUSE MODELS OF INDUCIBLE EXPRESSION OF MUTANT HUMAN DISC1
DISRUPTED IN SCHIZOPHRENIA 1 AND PHOSPHODIESTERASE 4B ARE GENETIC FACTORS IN SCHIZOPHRENIA THAT INTERACT TO REGULATE cAMP SIGNALLING
FAILURE TO CONFIRM ASSOCIATION BETWEEN SCHIZOPHRENIA AND MARKERS ON CHROMOSOME 1Q23.3 AT THE RGS4 AND CAPON GENES
CANDIDATE GENE STUDY ON CHROMOSOME 1Q32 IN FINNISH SCHIZOPHRENIA FAMILIES
POLYMORPHISM IN THE PROMOTER REGION OF SERINE RACEMASE GENE IN SCHIZOPHRENIA
COGNITIVE ENDOPHENOTYPES FOR MOLECULAR GENETIC STUDIES IN SCHIZOPHRENIA
A FRAMESHIFT MUTATION IN DISRUPTED IN SCHIZOPHRENIA 1 IN AN AMERICAN FAMILY WITH SCHIZOPHRENIA AND SCHIZOAFFECTIVE DISORDER
MECHANISTIC AND POSITIONAL CANDIDATE GENES FOR SCHIZOPHRENIA IN A LARGE HAN CHINESE COHORT
NEUREGULIN 1 (NRG1) AND SCHIZOPHRENIA: ANALYSIS OF A US FAMILY SAMPLE AND THE EVIDENCE IN THE BALANCE
PRODUCTION OF DISC1 TRANSGENIC AND KNOCKOUT MICE
ADDITIONAL SUPPORT FOR POSSIBLE SCHIZOPHRENIA LINKAGE TO CHROMOSOME 3Q29
SHARED GENETIC VULNERABILITY IN SCHIZOPHRENIA, SCHIZOAFFECTIVE DISORDER AND BIPOLAR ILLNESS H.H.
THE CONSORTIUM ON THE GENETICS OF SCHIZOPHRENIA (COGS): PRELIMINARY FINDINGS OF IMPAIRED LEARNING AND MEMORY ON A LISTLEARNING TEST IN SUBJECTS WITH SCHIZOPHRENIA IN A MULTI-SITE STUDY
DETECTION OF DYSBINDIN (DTNBP1) EFFECTS ON CLINICAL AND COGNITIVE PHENOTYPES CAN BE HIGHLY DEPENDENT ON VARIATION IN COMT
MUTED, A PROTEIN THAT BINDS TO DYSBINDIN (DTNBP1), IS ASSOCIATED WITH SCHIZOPHRENIA
BIOINFORMATIC TOOLS FOR SCHIZOPHRENIA GENETIC RESEARCH
COMT POLYMORPHISMS, CLINICAL STATUS, AND NEUROCOGNITIVE FUNCTIONING IN THE CATIE TRIAL OF SCHIZOPHRENIA
SIGNIFICANT ASSOCIATION BETWEEN CHROMOGRANIN A GENE POLYMORPHISMAND SCHIZOPHRENIA IN THE JAPANESE POPULATION
AN FMRI STUDY OF VERBAL ENCODING SHOWING ALTERED BRAIN ACTIVATION IN THE PARAHIPPOCAMPUS IN ADOLESCENTS AND YOUNG ADULTS AT GENETIC RISK FOR SCHIZOPHRENIA
ASSOCIATION BETWEEN BDNF, NRG1 AND DTNBP1 AND OUTCOME MEASURES IN AN ITALIAN COHORT OF PATIENTS WITH SCHIZOPHRENIA
RISK OF SCHIZOPHRENIA AND THE GLUTATHIONE RELATED GENES
A NOVEL APPROACH TO IDENTIFYING SCHIZOPHRENIA BIOMARKERS PROVIDES CONCURRENT VALIDATION OF SELENBP1 GENE UP-REGULATION IN BLOOD AND BRAIN
SCREENINGS OF DE NOVO TRANSPOSON-INSERTION SITES IN SCHIZOPHRENIA USING DNA WALKING PCR
APPLICATION OF ULTRA-HIGH RESOLUTION FINE-TILING ARRAY CGH (FT-CGH) TO THE ANALYSIS OF 22Q11 DELETION SYNDROME
A 8Q21 DELETION IN A PATIENT WITH A CO-MORBID PSYCHOSIS AND MENTAL RETARDATION
EFFECTS OF A FUNCTIONAL COMT POLYMORPHISM ON BRAIN ANATOMY IN PEOPLE WITH VELO-CARDIO-FACIAL SYNDROME
DOPAMINE RECEPTOR TYPE 2 ASSOCIATION WITH SCHIZOPHRENIA AND TREATMENT RESPONSE IN SOUTH INDIAN PATIENTS
TRACE AMINE RECEPTOR 4 (TRAR4) GENE IS ASSOCIATED WITH SCHIZOPHRENIA IN THE IRISH STUDY OF HIGH DENSITY SCHIZOPHRENIA FAMILIES
SUSTAINED ATTENTION DEFICITS IN FIRST-DEGREE RELATIVES OF SCHIZOPHRENIC PATIENTS AND DRUG NAIVE FIRST-ONSET SCHIZOPHRENIC PATIENTS: AN ENDOPHENOTYPES FOR GENETIC SUSCEPTIBILITY TO SCHIZOPHRENIA
VARIATION IN PPP1R1B PREDICTS RISK FOR SCHIZOPHRENIA, COGNITIVE FUNCTION, AND GENE EXPRESSION IN BRAIN
EVIDENCE FOR ASSOCIATION OF DNA VARIANTS IN THE AKT-1 GENE WITH SCHIZOPHRENIA IN A CAUCASIAN FAMILY SAMPLE
GENOME-WIDE SEARCH FOR SCHIZOPHRENIA SUSCEPTIBILITY GENES IN CONSANGUINEOUS FAMILIES FROM LOCALIZED POPULATION OF TUNISIA
GENOME-WIDE ASSOCIATION STUDY OF TRIO SAMPLES ON 100K SNPCHIP IN JAPANESE SCHIZOPHRENIC PEDIGREES
TEMPERAMENT IN INDIVIDUALS AT HIGH RISK FOR SCHIZOPHRENIA AND THE RELATIONSHIP WITH CHARACTER TO SCHIZOTYPY MULTIDIMENSIONALITY
ASSOCIATION STUDY OF 12 MARKERS ACROSS DRD2 IN TARDIVE DYSKINESIA
GENETIC AND FUNCTIONAL STUDY OF DISRUPTED-IN-SCHIZOPHRENIA 1 (DISC1)
ASSOCIATION STUDY BETWEEN ENDOPHENOTYPES FOR SCHIZOPHRENIA AND SNPS IN THE DYSBINDIN GENE
ANTICIPATION IN SCHIZOPHRENIA: FACTOR ANALYSIS APPROACH
GENETIC RISKS FOR SUICIDE IN SCHIZOPHRENIA
SEMI-PARAMETRIC REGRESSION REVEALS LINKAGE AND ASSOCIATION ON CHROMOSOME 4 FOR EXTERNALIZING SYMPTOMS IN COGA
A GEE-BASED REGRESSION MODEL ON GENETIC VARIABILITY OF ENDOPHENOTYPES IN SCHIZOPHRENIC FAMILIES
THE EFFECT OF LINKAGE DISEQUILIBRIUM ON MULTIPOINT LINKAGE ANALYSIS
EVO-LD: A MODEL DISCOVERY STRATEGY FOR LINKAGE DISEQUILIBRIUM STUDIES WITH LARGE DATABASES
SHESIS, A POWERFUL SOFTWARE PLATFORM FOR ANALYSES OF LINKAGE DISEQUILIBRIUM, HAPLOTYPE CONSTRUCTION, AND GENETIC ASSOCIATION AT POLYMORPHISM LOCI
MULTIVARIATE ADAPTIVE REGRESSION SPLINES: A POWERFUL METHOD FOR DETECTING GENOTYPE-ENVIRONMENT INTERACTION
AN ACCURATE AND EFFICIENT APPROXIMATION FOR PEARSON'S STATISTIC IN TWO-STAGE GENETIC CASE-CONTROL STUDIES WHERE DATA ARE POOLED
SIMULATION BASED POWER OF ASSOCIATION ANALYSIS IN AN ISOLATED POPULATION
CAA INSERTION AND TATA DELETION POLYMORPHISMS IN THE RETICULON 4 GENE ARE ASSOCIATED WITH CHRONIC SCHIZOPHRENIA IN FEMALES
CRITERIA FOR EVALUATING THE VALIDITY AND UTILITY OF ENDOPHENOTYPES FOR CANDIDATE GENE STUDIES: APPLICATION TO EXECUTIVE FUNCTION MEASURES AND ADHD
SYSTEMATIC SELECTION OF CANDIDATE GENES BY MODEL-BASED INTEGRATION OF BIOLOGICAL DATABASES
IMPROVING THE MENTAL HEALTH ENVIRONMENT: STIGMA AND MOBILIZATION
GENETIC RESEARCH: WHAT MATTERS TO CONSUMER ADVOCATES?
RESEARCHER-ADVOCACY PARTNERSHIPS: ADVANCING TREATMENT AND REDUCING STIGMA FOR BORDERLINE PERSONALITY DISORDER
BEHAVIORAL TRAITS IN JUVENILE VERVET MONKEYS: HERITABILITY OF SOCIAL FACTORS AND REACTIVITY
THE GENETIC AND ENVIRONMENTAL STRUCTURE OF EXTERNALIZING BEHAVIORS
ANTIDEPRESSANT DRUGS BUT NOT MOOD-STABILIZERS INDUCE SREBP-MEDIATED ACTIVATION OF CHOLESTEROL- AND FATTY ACID BIOSYNTESIS IN HUMAN GLIAL CELLS
A ROLE FOR SEX CHROMOSOME GENES IN SEXUALLY DIMORPHIC BEHAVIORS
METHYLOMICS IN PSYCHIATRY: THE POTENTIAL ROLE OF EPIGENETIC REGULATION IN SCHIZOPHRENIA
GENE EXPRESSION ANALYSES OF A MOUSE FIBROBLAST CELL LINE AFTER ANTIDEPRESSANT TREATMENT