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Author Details

Christina M Hultman
Karolinska Institutet
1992
239
74
PMIDPaper TitleJournal TitlePublished Year
36380236Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia.Mol Psychiatry2023
36380236Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia.Mol Psychiatry2023
37106120Genes implicated by a methylome-wide schizophrenia study in neonatal blood show differential expression in adult brain samples.Mol Psychiatry2023
37100590Direct additive genetics and maternal effect contribute to the risk of Tourette disorder.J Neurol Neurosurg Psychiatry2023
37106120Genes implicated by a methylome-wide schizophrenia study in neonatal blood show differential expression in adult brain samples.Mol Psychiatry2023
37100590Direct additive genetics and maternal effect contribute to the risk of Tourette disorder.J Neurol Neurosurg Psychiatry2023
33027543Intelligence, educational attainment, and brain structure in those at familial high-risk for schizophrenia or bipolar disorder.Hum Brain Mapp2022
35396580Mapping genomic loci implicates genes and synaptic biology in schizophrenia.Nature2022
35396579Rare coding variants in ten genes confer substantial risk for schizophrenia.Nature2022
36292681Phenotypic Impact of Rare Potentially Damaging Copy Number Variation in Obsessive-Compulsive Disorder and Chronic Tic Disorders.Genes (Basel)2022
35760976The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia.Nat Commun2022
35379910The impact of educational attainment, intelligence and intellectual disability on schizophrenia: a Swedish population-based register and genetic study.Mol Psychiatry2022
33635440Systematic review and meta-analysis: relationships between attention-deficit/hyperactivity disorder and urinary symptoms in children.Eur Child Adolesc Psychiatry2022
33987677Lack of Support for the Genes by Early Environment Interaction Hypothesis in the Pathogenesis of Schizophrenia.Schizophr Bull2022
33027543Intelligence, educational attainment, and brain structure in those at familial high-risk for schizophrenia or bipolar disorder.Hum Brain Mapp2022
35064790Psychometric properties of the Swedish translation of the Obsessive-Compulsive Inventory-Revised and the population characteristics of the symptom dimensions of OCD.Soc Psychiatry Psychiatr Epidemiol2022
34987162Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia.Nat Commun2022
34799476Rates of Clinically Confirmed Stress-related Psychiatric Disorders Among Swedish Tsunami Survivors: 9-year Follow-up.Epidemiology2022
34789012The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum.Am J Psychiatry2022
35379910The impact of educational attainment, intelligence and intellectual disability on schizophrenia: a Swedish population-based register and genetic study.Mol Psychiatry2022
35396580Mapping genomic loci implicates genes and synaptic biology in schizophrenia.Nature2022
35760976The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia.Nat Commun2022
35396579Rare coding variants in ten genes confer substantial risk for schizophrenia.Nature2022
36292681Phenotypic Impact of Rare Potentially Damaging Copy Number Variation in Obsessive-Compulsive Disorder and Chronic Tic Disorders.Genes (Basel)2022
33635440Systematic review and meta-analysis: relationships between attention-deficit/hyperactivity disorder and urinary symptoms in children.Eur Child Adolesc Psychiatry2022
35064790Psychometric properties of the Swedish translation of the Obsessive-Compulsive Inventory-Revised and the population characteristics of the symptom dimensions of OCD.Soc Psychiatry Psychiatr Epidemiol2022
34987162Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia.Nat Commun2022
34789012The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum.Am J Psychiatry2022
34799476Rates of Clinically Confirmed Stress-related Psychiatric Disorders Among Swedish Tsunami Survivors: 9-year Follow-up.Epidemiology2022
33987677Lack of Support for the Genes by Early Environment Interaction Hypothesis in the Pathogenesis of Schizophrenia.Schizophr Bull2022
31712719Increased schizophrenia family history burden and reduced premorbid IQ in treatment-resistant schizophrenia: a Swedish National Register and Genomic Study.Mol Psychiatry2021
31712720Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression.Mol Psychiatry2021
31712719Increased schizophrenia family history burden and reduced premorbid IQ in treatment-resistant schizophrenia: a Swedish National Register and Genomic Study.Mol Psychiatry2021
34002096Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.Nat Genet2021
33674754Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.Mol Psychiatry2021
33723211The association between family history and genomic burden with schizophrenia mortality: a Swedish population-based register and genetic sample study.Transl Psychiatry2021
33646943DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia.Elife2021
34402598Systematic review and meta-analysis identify significant relationships between clinical anxiety and lower urinary tract symptoms.Brain Behav2021
34615535Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder.Mol Autism2021
34615521How rare and common risk variation jointly affect liability for autism spectrum disorder.Mol Autism2021
34838037Mediterranean diet and depression: a population-based cohort study.Int J Behav Nutr Phys Act2021
33674754Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.Mol Psychiatry2021
33646943DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia.Elife2021
33723211The association between family history and genomic burden with schizophrenia mortality: a Swedish population-based register and genetic sample study.Transl Psychiatry2021
34615535Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder.Mol Autism2021
34615521How rare and common risk variation jointly affect liability for autism spectrum disorder.Mol Autism2021
34402598Systematic review and meta-analysis identify significant relationships between clinical anxiety and lower urinary tract symptoms.Brain Behav2021
34838037Mediterranean diet and depression: a population-based cohort study.Int J Behav Nutr Phys Act2021
34002096Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.Nat Genet2021
31712720Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression.Mol Psychiatry2021
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Co-authored papers 38
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Abraham Reichenberg
Co-authored papers 34
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Co-authored papers 28
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Markus M N??then
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Kimberly Chambert
Co-authored papers 15
Michele T Pato
Co-authored papers 15
Giulio Genovese
Co-authored papers 15
Mark J Daly
Massachusetts General Hospital
Co-authored papers 15
Michael Gill
Co-authored papers 15
Kenneth S Kendler
Virginia Commonwealth University
Co-authored papers 14
Stephan Ripke
Massachusetts General Hospital and Harvard Medical School
Co-authored papers 14
Release 1.2