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29. EPIGENOME-WIDE ASSOCIATION META-ANALYSIS OF ADULT ATTENTION-DEFICIT/HYPERACTIVITY DISORDER
European neuropsychopharmacology, 2022-10, Vol.63, p.e61
2022
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44. META-ANALYSIS OF GENOME-WIDE DNA METHYLATION IN SCHIZOPHRENIA: DOES SEX STRATIFICATION IMPROVE DISCOVERY?
European neuropsychopharmacology, 2023-10, Vol.75, p.S79-S80
2023
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74 GENETICS OF ADHD DIMENSIONS: BIOLOGICAL AND CLINICAL IMPLICATIONS FOR ADHD
European neuropsychopharmacology, 2019-10, Vol.29, p.S101-S101
2019
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76 GENETIC ARCHITECTURE OF PERSISTENT ATTENTION DEFICIT/HYPERACTIVITY DISORDER
European neuropsychopharmacology, 2019-10, Vol.29, p.S102-S103
2019
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87. EXPLORATION OF BRAIN-HERITABLE METHYLATION IN SCHIZOPHRENIA CASES AND CONTROLS
European neuropsychopharmacology, 2022-10, Vol.63, p.e92
2022
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89 CROSS-DISORDER META-ANALYSIS OF GENOMEWIDE ASSOCIATION STUDIES SHEDS LIGHT INTO POTENTIALLY SHARED NEUROBIOLOGY ACROSS ADHD, ASD, OCD, AND TS
European neuropsychopharmacology, 2019-10, Vol.29, p.S109-S109
2019
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A CONTRIBUTION OF RARE COPY NUMBER VARIATIONS TO THE DEVELOPMENT OF ATTENTION DEFICIT HYPERACTIVITY DISORDER: GENOME-WIDE META-ANALYSES IN 12548 INDIVIDUALS
European neuropsychopharmacology, 2019, Vol.29, p.S1042-S1042
2019
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A DNA METHYLATION STUDY OF THE ANTIPSYCHOTIC QUETIAPINE (SEROQUEL): TREATMENT EFFECTS IN SCHIZOPHRENIA AND BIPOLAR DISORDER
European neuropsychopharmacology, 2022-10, Vol.63, p.e131-e132
2022
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F6GENETICS OF TREATMENT RESPONSE FOR ATOMOXETINE IN ADHD
European neuropsychopharmacology, 2019, Vol.29, p.S1113-S1113
2019
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F80. A DNA METHYLATION STUDY OF COMMON AND SPECIFIC TREATMENT EFFECTS OF THREE ANTIPSYCHOTICS IN THE TREATMENT OF PSYCHOSIS
European neuropsychopharmacology, 2023-10, Vol.75, p.S262-S263
2023
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FIVE NOVEL LOCI ASSOCIATED WITH ATTENTION-DEFICIT/HYPERACTIVITY DISORDER ARE REVEALED BY LEVERAGING POLYGENIC OVERLAP WITH EDUCATIONAL ATTAINMENT
European neuropsychopharmacology, 2019, Vol.29, p.S954-S955
2019
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GENETIC PROFILE OF THE NORWEGIAN MOTHER, FATHER, AND CHILD COHORT STUDY (MOBA): RESULTS FROM THE MOBAPSYCHGEN PIPELINE
European neuropsychopharmacology, 2022-10, Vol.63, p.e292-e293
2022
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GENETICALLY INFORMED EARLY IDENTIFICATION OF ATTENTION DEFICIT HYPERACTIVITY DISORDER SYMPTOMS IN THE NORWEGIAN MOTHER, FATHER AND CHILD COHORT STUDY (MOBA)
European neuropsychopharmacology, 2023-10, Vol.75, p.S22-S23
2023
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GENETICS OF ADHD AND ITS UTILITY IN SCIENCE AND CLINIC
European neuropsychopharmacology, 2023-10, Vol.75, p.S20-S21
2023
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Genetics of Adhd Dimensions
European neuropsychopharmacology, 2019, Vol.29, p.S759-S760
2019
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GENOME-WIDE EXAMINATION OF PARENT-OF-ORIGIN EFFECTS IN CHILDREN WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER
European neuropsychopharmacology, 2019, Vol.29, p.S888-S889
2019
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INSIGHTS FROM >80 LOCI ASSOCIATED WITH ATTENTION-DEFICIT/HYPERACTIVITY DISORDER
European neuropsychopharmacology, 2023-10, Vol.75, p.S21-S21
2023
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M1 - FIVE NOVEL LOCI ASSOCIATED WITH ATTENTION-DEFICIT/HYPERACTIVITY DISORDER ARE REVEALED BY LEVERAGING POLYGENIC OVERLAP WITH EDUCATIONAL ATTAINMENT
European neuropsychopharmacology, 2019, Vol.29, p.S954-S955
2019
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M2 THE ROLE OF LOW FREQUENCY VARIANTS ON ATTENTION-DEFICIT/HYPERACTIVITY DISORDER AND AUTISM SPECTRUM DISORDERS
European neuropsychopharmacology, 2019-10, Vol.29, p.S167-S167
2019
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Meta-analysis of the DRD5 VNTR in persistent ADHD
European neuropsychopharmacology, 2016-09, Vol.26 (9), p.1527-1532
2016
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PARENT-OF-ORIGIN EFFECTS IN CHILDHOOD AGGRESSION
European neuropsychopharmacology, 2022-10, Vol.63, p.e281
2022
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S1PARENT-OF-ORIGIN AND MATERNAL EFFECTS IN ATTENTION DEFICIT HYPERACTIVITY DISORDER
European neuropsychopharmacology, 2019-10, Vol.29, p.S114-S114
2019
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S5INVESTIGATION OF SHARED GENETIC RISK BETWEEN CARDIOMETABOLIC MORBIDITY AND ATTENTION DEFICIT HYPERACTIVITY DISORDER IN A NORWEGIAN FAMILY COHORT USING POLYGENIC TRANSMISSION DISEQUILIBRIUM TEST
European neuropsychopharmacology, 2019-10, Vol.29, p.S116-S117
2019
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SA4GENOME-WIDE ASSOCIATION META-ANALYSES OF ADHD SYMPTOMATOLOGY: INATTENTION AND HYPERACTIVITY/IMPULSIVITY
European neuropsychopharmacology, 2019, Vol.29, p.S1190-S1190
2019
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SU4 - GENOME-WIDE EXAMINATION OF PARENT-OF-ORIGIN EFFECTS IN CHILDREN WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER
European neuropsychopharmacology, 2019, Vol.29, p.S888-S889
2019
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