I. Sønderby

Linking obesity with white matter microstructure highlights the importance of brainstem tracts and sex differences.
20260 citationsauthor #10
Gene dosage effects of 22q11.2 copy number variants on in-vivo measures of white matter axonal density and dispersion.
20260 citationsauthor #18
Genetic liability to addiction underlies comorbid bipolar and substance use disorders
20260 citationsauthor #6
Genome-wide study of somatic symptom and related disorders identifies novel genomic loci and map genetic architecture
20250 citationsauthor #25
Gene dosage effects of 22q11.2 copy number variants on in-vivo measures of white matter axonal density and dispersion
20250 citationsauthor #18
FEMA-Long: Modeling unstructured covariances for discovery of time-dependent effects in large-scale longitudinal datasets
20250 citationsauthor #9
The role of rare copy number variants in early-onset depression
20251 citationsauthor #2
Penetrance of neurodevelopmental copy number variants is associated with variations in cortical morphology.
20252 citationsauthor #2
A cross-disorder analysis of CNVs finds novel loci and dose-dependent relationships of genes to psychiatric traits
20255 citationsauthor #12
T2. MULTIMODAL HAZARD SCORE INTEGRATES GENETICS, METABOLOMICS, AND MENTAL HEALTH-RELATED RISK FACTORS TO IMPROVE CARDIOVASCULAR DISEASE RISK PREDICTION
20250 citationsauthor #7
Pleiotropic and sex-specific genetic mechanisms of circulating metabolic markers
20255 citationsauthor #9
Youth psychotic experiences: psychometric evaluation and diagnostic associations of the CAPE‐16 in adolescents from the Norwegian Mother, Father and Child Cohort
20250 citationsauthor #13
Psychiatric disorders converge on common pathways but diverge in cellular context, spatial distribution, and directionality of genetic effects
20253 citationsauthor #24
Mapping obesity-related traits with regional white matter microstructure highlights the importance of brainstem tracts and sex-related differences.
20250 citationsauthor #10
Abstracts for Presentation at the SSBP 27th International Research Symposium and Educational Day, Amsterdam, the Netherlands.
20250 citationsauthor #129
Associations of Genetic Liability to Six Psychiatric Disorders With Cardiometabolic Diseases
20250 citationsauthor #14
Cortical differences across psychiatric disorders and associated common and rare genetic variants
20251 citationsauthor #28
Multimodal Prediction of Psychosis in the Prospective MoBa Birth Cohort
20250 citationsauthor #15
Mapping Cerebellar Morphology in 15q11.2 CNV Carriers Using Normative Modeling
20250 citationsauthor #11
5. Discordant Cortical Patterns Between Psychiatric Disorders and Corresponding Common and Rare Genetic Risks
20250 citationsauthor #15
Shared genetic architecture between autism spectrum disorder, loneliness, and social isolation reveals novel genetic loci
20251 citationsauthor #6
Atlas of plasma metabolic markers linked to human brain morphology
20251 citationsauthor #9
Recommendations for defining treatment outcomes in major psychiatric disorders using real-world data.
20257 citationsauthor #10
F15. IMMUNOMETABOLIC FACTORS UNDERLYING MAJOR DEPRESSIVE DISORDER AND ITS ASSOCIATION WITH CARDIOVASCULAR DISEASE
20240 citationsauthor #4
META-ANALYSIS OF RARE CNV GENOME-WIDE ASSOCIATION STUDIES ACROSS MAJOR PSYCHIATRIC DISORDERS IN EUR, AFR/AFAM, AND ASN/ASAM POPULATIONS
20240 citationsauthor #11
400. Polygenic Architecture of Metabolic Markers Reveals Distinct Patterns of Overlap With Psychiatric Disorders
20240 citationsauthor #6
How real-world data can facilitate the development of precision medicine treatment in psychiatry.
202429 citationsauthor #22
COSGAP: COntainerized Statistical Genetics Analysis Pipelines
20249 citationsauthor #12
Poor muscle health and cardiometabolic risks associated with antidepressant treatment
20243 citationsauthor #4
Elevated levels of peripheral and central nervous system immune markers reflect innate immune dysregulation in autism spectrum disorder.
20245 citationsauthor #5
Linking sarcopenia, brain structure and cognitive performance: a large-scale UK Biobank study
202417 citationsauthor #8
Divergent patterns of genetic overlap between severe mental disorders and metabolic markers
20243 citationsauthor #9
Author Correction: Using rare genetic mutations to revisit structural brain asymmetry
20240 citationsauthor #23
Unraveling the link between CNVs, cognition and individual neuroimaging deviation scores from a population-based reference cohort
20244 citationsauthor #2
Youth Psychotic Experiences: Diagnostic Associations and Evaluation of the CAPE-16
20241 citationsauthor #13
Using rare genetic mutations to revisit structural brain asymmetry
20244 citationsauthor #23
Gene-based burden tests of rare germline variants identify six cancer susceptibility genes
202410 citationsauthor #35
Association of complex traits with common genetic variation across genomic regions containing pathogenic copy number variations
20241 citationsauthor #4
Large-scale brainstem neuroimaging and genetic analyses provide new insights into the neuronal mechanisms of hypertension
20231 citationsauthor #10
W90. GENOME-WIDE ANALYSIS OF SELF-REPORTED PSYCHOTIC EXPERIENCES IN THE NORWEGIAN MOTHER, FATHER, AND CHILD STUDY
20230 citationsauthor #9
Dissecting unique and common variance across body and brain health indicators using age prediction
20237 citationsauthor #17
69. GENOME-WIDE ASSOCIATION OF COPY NUMBER VARIANTS ACROSS SIX MAJOR PSYCHIATRIC DISORDERS REVEALS GENOTYPE-PHENOTYPE RELATIONSHIPS OF RARE VARIANTS
20230 citationsauthor #9
Beyond the Global Brain Differences: Intra-individual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers
20234 citationsauthor #116
Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence
202321 citationsauthor #26
Using rare genetic mutations to revisit structural brain asymmetry
20233 citationsauthor #23
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
202314 citationsauthor #26
Subcortical Brain Alterations in Carriers of Genomic Copy Number Variants.
202312 citationsauthor #33
Subcortical brain alterations in carriers of genomic copy number variants
20232 citationsauthor #34
T48. CNVS AND DIAGNOSIS LINKAGE IN 220,000 INDIVIDUALS FROM THE NORWEGIAN MOTHER, FATHER, AND CHILD STUDY, MOBA
20230 citationsauthor #1
Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
20230 citationsauthor #26
No signs of neurodegenerative effects in 15q11.2 BP1-BP2 copy number variant carriers in the UK Biobank
20233 citationsauthor #9
Unraveling the Link between CNVs, General Cognition, and Individual Neuroimaging Deviation Scores from a Reference Cohort
20230 citationsauthor #2
The role of liver fat in cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition
20220 citationsauthor #3
A family study of symbolic learning and synaptic plasticity in autism spectrum disorder
20222 citationsauthor #6
P87. No Signs of Neurodegenerative Effects in 15q11.2 BP1-BP2 Copy Number Variant Carriers
20220 citationsauthor #9
COGEDAP: A COmprehensive GEnomic Data Analysis Platform
20222 citationsauthor #12
P86. The Structure of Brain Stem Subregions and Blood Pressure in 32,731 Individuals
20220 citationsauthor #7
T91. LARGE-SCALE ANALYSIS WITH SOFTWARE CONTAINERS IN ENIGMA-CNV – AN INTERNATIONAL WORKING GROUP TO STUDY RECURRENT COPY NUMBER VARIANTS AND BRAIN MEASURES
20220 citationsauthor #6
Rare CNVs and phenome-wide profiling: a tale of brain-structural divergence and phenotypical convergence
20221 citationsauthor #26
The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition
202213 citationsauthor #3
34. A GENOME-WIDE ASSOCIATION STUDY OF COPY NUMBER VARIATION ACROSS MAJOR PSYCHIATRIC DISORDERS IN 500,000 INDIVIDUALS
20220 citationsauthor #9
Efficient meta-analysis of multivariate genome-wide association studies with Meta-MOSTest
20221 citationsauthor #6
HOW DO INDIVIDUALS WITH RARE PSYCHIATRIC-ASSOCIATED GENETIC VARIANTS AGE?
20220 citationsauthor #9
COPY NUMBER VARIANTS AND DIAGNOSIS LINKAGE IN 220,000 INDIVIDUALS FROM THE NORWEGIAN MOTHER, FATHER AND CHILD STUDY, MOBA
20220 citationsauthor #1
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans
202136 citationsauthor #1
Lessons Learned From Neuroimaging Studies of Copy Number Variants: A Systematic Review.
202131 citationsauthor #7
Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs
202155 citationsauthor #1
Population-based body–brain mapping links brain morphology with anthropometrics and body composition
202130 citationsauthor #13
Population-based body-brain mapping links brain morphology and body composition
20203 citationsauthor #13
University of Birmingham ENIGMA and global neuroscience
20200 citationsauthor #84
Erratum: Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (Molecular psychiatry (2020) 25 3 (584-602)) : Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
20202 citationsauthor #1
The genetic architecture of the human cerebral cortex
2020722 citationsauthor #125
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.
202076 citationsauthor #2
Association between complement component 4A expression, cognitive performance and brain imaging measures in UK Biobank
202022 citationsauthor #2
Planar cell polarity pathway and development of the human visual cortex
20193 citationsauthor #160
ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries
2019536 citationsauthor #150
Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder
2019108 citationsauthor #7
THE 16P11.2 DISTAL COPY NUMBER VARIANT CONVEYS DOSE-RESPONSE EFFECTS ON INTRACRANIAL VOLUME AND STRUCTURES OF THE BASAL GANGLIA: A MEGA-ANALYSIS FROM THE ENIGMA-CNV WORKING GROUP
20190 citationsauthor #1
Enigma-CNV: Unraveling the Effects on Brain Structure of Rare Copy Number Variants Involved in Autism and Other Neurodevelopmental Diseases
20190 citationsauthor #1
15POSITIVE DOSE RESPONSE OF THE 1Q21.1 DISTAL CNV ON ICV THROUGH AN EFFECT ON CORTICAL SURFACE AREA
20190 citationsauthor #1
188. ENIGMA-CNV: Unraveling the Effects of Rare Copy Number Variants on Brain Structure
20192 citationsauthor #1
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
20192 citationsauthor #1
Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder
201828 citationsauthor #2
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes
2018119 citationsauthor #10
Genetic variation in 117 myelination-related genes in schizophrenia: Replication of association to lipid biosynthesis genes
201814 citationsauthor #3
Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium
201826 citationsauthor #209
Genetic control of variability in subcortical and intracranial volumes
20187 citationsauthor #37
Assessing Genetic Control Over Brain Morphology Variance In Psychosis: A Genome-Wide Variance-Controling Qtl (Vqtl) Neuroimaging Study
20170 citationsauthor #8
Association of Subcortical Brain Volumes with CNVS: A Mega-Analysis From The Enigma-CNV Working Group
20172 citationsauthor #1
Effects of autozygosity and schizophrenia polygenic risk on cognitive and brain developmental trajectories
201712 citationsauthor #10
A Loss-of-Function Variant in a Minor Isoform of ANK3 Protects Against Bipolar Disorder and Schizophrenia.
201634 citationsauthor #3
MicroRNAs enrichment in GWAS of complex human phenotypes
20150 citationsauthor #3
Genome-wide association study identifies common variants associated with pharmacokinetics of psychotropic drugs
201511 citationsauthor #5
Genome-Wide Analysis of Attention Deficit Hyperactivity Disorder in Norway
201583 citationsauthor #3
Investigation of the genetic interaction between BDNF and DRD3 genes in suicidical behaviour in psychiatric disorders
201517 citationsauthor #3
MicroRNAs enrichment in GWAS of complex human phenotypes
201522 citationsauthor #3
Association analysis between suicidal behaviour and candidate genes of bipolar disorder and schizophrenia.
201432 citationsauthor #2
No evidence for association between bipolar disorder risk gene variants and brain structural phenotypes.
201345 citationsauthor #3
Pathway analysis of genetic markers associated with a functional MRI faces paradigm implicates polymorphisms in calcium responsive pathways
201316 citationsauthor #4
TCF4 sequence variants and mRNA levels are associated with neurodevelopmental characteristics in psychotic disorders
201279 citationsauthor #3

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