Christina M Hultman


Ontology type: schema:Person     


Person Info

NAME

Christina M

SURNAME

Hultman

Publications in SciGraph latest 50 shown

  • 2018-12 Genetic variation in 117 myelination-related genes in schizophrenia: Replication of association to lipid biosynthesis genes in SCIENTIFIC REPORTS
  • 2018-12 Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder in TRANSLATIONAL PSYCHIATRY
  • 2018-02 The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders in MOLECULAR PSYCHIATRY
  • 2018-02 Complement Gene Expression Correlates with Superior Frontal Cortical Thickness in Humans in NEUROPSYCHOPHARMACOLOGY
  • 2017-12 Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders in GENOME MEDICINE
  • 2017-12 Correcting for cell-type effects in DNA methylation studies: reference-based method outperforms latent variable approaches in empirical studies in GENOME BIOLOGY
  • 2017-12 Waiting time for cancer treatment and mental health among patients with newly diagnosed esophageal or gastric cancer: a nationwide cohort study in BMC CANCER
  • 2017-09 Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1 in MOLECULAR NEUROBIOLOGY
  • 2017-09 Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder in NATURE NEUROSCIENCE
  • 2017-08 Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder in MOLECULAR PSYCHIATRY
  • 2017-08 Cerebrospinal fluid microglia and neurodegenerative markers in twins concordant and discordant for psychotic disorders in EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE
  • 2017-08 The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability in NATURE GENETICS
  • 2017-03-21 Genetic correlation between amyotrophic lateral sclerosis and schizophrenia in NATURE COMMUNICATIONS
  • 2017-01 Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder in TRANSLATIONAL PSYCHIATRY
  • 2017-01 Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects in NATURE GENETICS
  • 2016-12 An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation in GENOME BIOLOGY
  • 2016-12 Ultra-rare disruptive and damaging mutations influence educational attainment in the general population in NATURE NEUROSCIENCE
  • 2016-12 Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis in MOLECULAR NEUROBIOLOGY
  • 2016-11 Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia in NATURE NEUROSCIENCE
  • 2016-10 A genome-wide association study of kynurenic acid in cerebrospinal fluid: implications for psychosis and cognitive impairment in bipolar disorder in MOLECULAR PSYCHIATRY
  • 2016-09 Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder in MOLECULAR PSYCHIATRY
  • 2016-08 Analysis of protein-coding genetic variation in 60,706 humans in NATURE
  • 2016-05 Autism risk associated with parental age and with increasing difference in age between the parents in MOLECULAR PSYCHIATRY
  • 2016-04 Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders in NATURE NEUROSCIENCE
  • 2015-12 High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction in GENOME BIOLOGY
  • 2015-12 Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma in NATURE COMMUNICATIONS
  • 2015-04 No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-02 The increasing prevalence of reported diagnoses of childhood psychiatric disorders: a descriptive multinational comparison in EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
  • 2015-02 Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways in NATURE NEUROSCIENCE
  • 2015-01 Refinement of schizophrenia GWAS loci using methylome-wide association data in HUMAN GENETICS
  • 2014-09 Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia in MOLECULAR PSYCHIATRY
  • 2014-08 Most genetic risk for autism resides with common variation in NATURE GENETICS
  • 2014-07 Copy number variation in schizophrenia in Sweden in MOLECULAR PSYCHIATRY
  • 2014-07 Biological insights from 108 schizophrenia-associated genetic loci in NATURE
  • 2014-04 Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility in MOLECULAR PSYCHIATRY
  • 2014-03 The KMO allele encoding Arg452 is associated with psychotic features in bipolar disorder type 1, and with increased CSF KYNA level and reduced KMO expression in MOLECULAR PSYCHIATRY
  • 2014-02 A polygenic burden of rare disruptive mutations in schizophrenia in NATURE
  • 2014-01 Evidence that duplications of 22q11.2 protect against schizophrenia in MOLECULAR PSYCHIATRY
  • 2013-12 MethylPCA: a toolkit to control for confounders in methylome-wide association studies in BMC BIOINFORMATICS
  • 2013-11 The International Collaboration for Autism Registry Epidemiology (iCARE): Multinational Registry-Based Investigations of Autism Risk Factors and Trends in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2013-11 Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample in MOLECULAR PSYCHIATRY
  • 2013-09 Mosaic copy number variation in schizophrenia in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2012-10 Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia in MOLECULAR PSYCHIATRY
  • 2012-09 Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder in MOLECULAR PSYCHIATRY
  • 2012-06 Exome sequencing and the genetic basis of complex traits in NATURE GENETICS
  • 2012-06 Extremely low-coverage sequencing and imputation increases power for genome-wide association studies in NATURE GENETICS
  • 2011-12 Advancing paternal age and risk of autism: new evidence from a population-based study and a meta-analysis of epidemiological studies in MOLECULAR PSYCHIATRY
  • 2011-11 GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia in MOLECULAR PSYCHIATRY
  • 2011-10 Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 in NATURE GENETICS
  • 2011-10 Genome-wide association study identifies five new schizophrenia loci in NATURE GENETICS
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