Christina M. Hultman
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Swedish professor
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Computer Science
Christina M. Hultman's Degrees
- Masters Computer Science Uppsala University
- Bachelors Computer Science Uppsala University
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(Suggest an Edit or Addition)Christina M. Hultman's Published Works
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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Biological Insights From 108 Schizophrenia-Associated Genetic Loci (2014) (6445)
- Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence. (2014) (2344)
- Synaptic, transcriptional, and chromatin genes disrupted in autism (2014) (2080)
- Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (2013) (2011)
- Genome-wide association study identifies five new schizophrenia loci (2011) (1680)
- Rare chromosomal deletions and duplications increase risk of schizophrenia (2008) (1506)
- Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia (2013) (1455)
- A polygenic burden of rare disruptive mutations in schizophrenia (2014) (1371)
- Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study (2009) (1190)
- Identification of common genetic risk variants for autism spectrum disorder (2019) (1140)
- A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) (1125)
- Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2018) (1064)
- Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
- Most genetic risk for autism resides with common variation (2014) (995)
- Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 (2011) (929)
- The familial risk of autism. (2014) (895)
- Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2016) (736)
- Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders (2019) (724)
- Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma (2015) (690)
- Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
- Perinatal Risk Factors for Infantile Autism (2002) (577)
- Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
- Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (2014) (510)
- Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. (2012) (496)
- Exome sequencing and the genetic basis of complex traits (2012) (409)
- A structural variation reference for medical and population genetics (2020) (394)
- The Heritability of Autism Spectrum Disorder (2017) (392)
- Advancing paternal age and risk of autism: new evidence from a population-based study and a meta-analysis of epidemiological studies (2011) (391)
- Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia (2016) (381)
- Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders (2016) (363)
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) (361)
- Quantifying prion disease penetrance using large population control cohorts (2016) (352)
- Prenatal and perinatal risk factors for schizophrenia, affective psychosis, and reactive psychosis of early onset: case-control study. (1999) (338)
- Preterm birth and psychiatric disorders in young adult life. (2012) (330)
- Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia (2013) (325)
- Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia (2017) (301)
- Parental Psychiatric Disorders Associated With Autism Spectrum Disorders in the Offspring (2008) (290)
- Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder (2011) (280)
- Advancing maternal age is associated with increasing risk for autism: a review and meta-analysis. (2012) (270)
- Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort. (2019) (267)
- Excellent school performance at age 16 and risk of adult bipolar disorder: national cohort study (2010) (267)
- Increased neutrophil extracellular trap formation promotes thrombosis in myeloproliferative neoplasms (2018) (255)
- Creativity and mental disorder: Family study of 300 000 people with severe mental disorder (2011) (251)
- An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation (2016) (249)
- Family history of schizophrenia and bipolar disorder as risk factors for autism. (2012) (247)
- Copy number variation in schizophrenia in Sweden (2014) (245)
- Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) (240)
- Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder (2012) (232)
- The increasing prevalence of reported diagnoses of childhood psychiatric disorders: a descriptive multinational comparison (2015) (222)
- Mental illness, suicide and creativity: 40-year prospective total population study. (2013) (221)
- Methylome-wide association study of schizophrenia: identifying blood biomarker signatures of environmental insults. (2014) (221)
- The risk factors for postpartum depression: A population‐based study (2017) (220)
- Extremely low-coverage sequencing and imputation increases power for genome-wide association studies (2012) (217)
- zCall: a rare variant caller for array-based genotyping: Genetics and population analysis (2012) (209)
- Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
- Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
- Autism risk associated with parental age and with increasing difference in age between the parents (2015) (200)
- Can Association Between Preterm Birth and Autism be Explained by Maternal or Neonatal Morbidity? (2009) (194)
- Advancing paternal age and bipolar disorder. (2008) (191)
- The Promises and Pitfalls of Genoeconomics* (2012) (187)
- Rates, Distribution, and Implications of Post-zygotic Mosaic Mutations in Autism Spectrum Disorder (2017) (187)
- The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability (2017) (182)
- Very preterm birth, birth trauma, and the risk of anorexia nervosa among girls. (1999) (182)
- Incidence of hospitalization for postpartum psychotic and bipolar episodes in women with and without prior prepregnancy or prenatal psychiatric hospitalizations. (2007) (179)
- Validity of bipolar disorder hospital discharge diagnoses: file review and multiple register linkage in Sweden (2011) (174)
- Recurrence risks for schizophrenia in a Swedish National Cohort (2006) (165)
- Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia (2011) (165)
- Women with schizophrenia: pregnancy outcome and infant death among their offspring (2002) (163)
- Autism and mental retardation among offspring born after in vitro fertilization. (2013) (160)
- Offspring psychopathology following preconception, prenatal and postnatal maternal bereavement stress (2013) (158)
- Parental Autoimmune Diseases Associated With Autism Spectrum Disorders in Offspring (2010) (155)
- Rare coding variants in ten genes confer substantial risk for schizophrenia (2022) (154)
- Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder. (2016) (153)
- A methylome-wide study of aging using massively parallel sequencing of the methyl-CpG-enriched genomic fraction from blood in over 700 subjects. (2014) (149)
- A comprehensive family-based replication study of schizophrenia genes. (2013) (144)
- Autism risk across generations: a population-based study of advancing grandpaternal and paternal age. (2013) (142)
- Clinical Diagnosis of Mental Disorders Immediately Before and After Cancer Diagnosis: A Nationwide Matched Cohort Study in Sweden. (2016) (138)
- Birth weight and attention-deficit/hyperactivity symptoms in childhood and early adolescence: a prospective Swedish twin study. (2007) (136)
- Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder (2017) (136)
- Evidence that duplications of 22q11.2 protect against schizophrenia (2013) (130)
- Maternal effects for preterm birth: a genetic epidemiologic study of 630,000 families. (2009) (129)
- Prenatal and neonatal risk factors for schizophrenia (1997) (127)
- Maternal Smoking During Pregnancy and School Performance at Age 15 (2006) (125)
- Exome Aggregation Consortium (2016) (125)
- Sequencing and de novo assembly of 150 genomes from Denmark as a population reference (2017) (118)
- Relationships between social support, social coping and life events in the relapse of schizophrenic patients. (1997) (117)
- Psychotic Illness in First-Time Mothers with No Previous Psychiatric Hospitalizations: A Population-Based Study (2009) (117)
- Familial confounding of the association between maternal smoking during pregnancy and offspring criminality: a population-based study in Sweden. (2010) (111)
- Genetic correlation between amyotrophic lateral sclerosis and schizophrenia (2017) (107)
- Scholastic achievement at age 16 and risk of schizophrenia and other psychoses: a national cohort study (2007) (106)
- Common risk variants identified in autism spectrum disorder (2017) (106)
- Dietary intake of fish, omega-3, omega-6 polyunsaturated fatty acids and vitamin D and the prevalence of psychotic-like symptoms in a cohort of 33 000 women from the general population (2010) (103)
- High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction (2015) (101)
- Specific glial functions contribute to schizophrenia susceptibility. (2014) (100)
- Polygenic overlap between schizophrenia risk and antipsychotic response: a genomic medicine approach. (2016) (99)
- The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls (2018) (99)
- Estimation of SNP heritability from dense genotype data. (2013) (94)
- MBD-seq as a cost-effective approach for methylome-wide association studies: demonstration in 1500 case--control samples. (2012) (92)
- Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
- Exome Sequencing of Familial Bipolar Disorder. (2016) (91)
- Transcript expression-aware annotation improves rare variant interpretation (2020) (89)
- Social support moderates posttraumatic stress and general distress after disaster. (2012) (88)
- Evaluating drug targets through human loss-of-function genetic variation (2019) (86)
- Trajectories leading to autism spectrum disorders are affected by paternal age: findings from two nationally representative twin studies. (2010) (85)
- At issue: siblings of patients with schizophrenia: sibling bond, coping patterns, and fear of possible schizophrenia heredity. (2004) (84)
- Suicide among patients with amyotrophic lateral sclerosis. (2008) (83)
- GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia (2011) (83)
- CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 (2013) (83)
- A quasi-experimental study of maternal smoking during pregnancy and offspring academic achievement. (2010) (81)
- Ultra-rare disruptive and damaging mutations influence educational attainment in the general population (2016) (79)
- A nationwide study of the association between celiac disease and the risk of autistic spectrum disorders. (2013) (78)
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) (78)
- "Selfish spermatogonial selection": a novel mechanism for the association between advanced paternal age and neurodevelopmental disorders. (2013) (76)
- Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum. (2018) (76)
- Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders (2017) (73)
- Advanced paternal and grandpaternal age and schizophrenia: A three-generation perspective (2011) (73)
- The Genetic Structure of the Swedish Population (2011) (73)
- Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia (2014) (70)
- The effect of LRRK2 loss-of-function variants in humans (2020) (69)
- The effect of LRRK2 loss-of-function variants in humans (2020) (69)
- Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder (2015) (68)
- Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder (2015) (68)
- Adverse pregnancy outcomes in mothers with affective psychosis. (2007) (67)
- Maternal smoking during pregnancy and intellectual performance in young adult Swedish male offspring. (2010) (66)
- Implication of a rare deletion at distal 16p11.2 in schizophrenia. (2013) (66)
- A population-based heritability estimate of bipolar disorder – In a Swedish twin sample (2019) (63)
- A genome-wide association study of kynurenic acid in cerebrospinal fluid: implications for psychosis and cognitive impairment in bipolar disorder (2015) (62)
- A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts (2020) (60)
- Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility (2014) (60)
- New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. (2015) (58)
- Fine mapping of ZNF 804 A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder (2011) (57)
- Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk (2018) (55)
- Autism and epilepsy (2016) (55)
- The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders (2017) (54)
- Fertility of first-degree relatives of patients with schizophrenia: A three generation perspective (2007) (54)
- The effect of traumatic bereavement on tsunami-exposed survivors. (2009) (52)
- Schizophrenia and offspring's risk for adverse pregnancy outcomes and infant death (2008) (52)
- Fetal growth restriction and schizophrenia: a Swedish twin study. (2005) (52)
- Familial factors confound the association between maternal smoking during pregnancy and young adult offspring overweight. (2010) (50)
- Traumatic bereavement, acute dissociation, and posttraumatic stress: 14 years after the MS Estonia disaster. (2011) (50)
- Nationwide Genomic Study in Denmark Reveals Remarkable Population Homogeneity (2016) (49)
- Multiple sclerosis and psychiatric disorders: Comorbidity and sibling risk in a nationwide Swedish cohort (2014) (48)
- Integrating evolutionary and regulatory information with a multispecies approach implicates genes and pathways in obsessive-compulsive disorder (2017) (48)
- Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia (2020) (47)
- The Association Between Familial Risk and Brain Abnormalities Is Disease Specific: An ENIGMA-Relatives Study of Schizophrenia and Bipolar Disorder (2019) (47)
- Prevalence and predictors of anxiety and depression among esophageal cancer patients prior to surgery. (2016) (45)
- Autism and mental retardation among offspring born after in vitro fertilization (2014) (44)
- Genetic Differences between Five European Populations (2010) (43)
- Tsunami-affected Scandinavian tourists: Disaster exposure and post-traumatic stress symptoms (2011) (43)
- Undiagnosed cardiovascular disease prior to cardiovascular death in individuals with severe mental illness (2019) (42)
- Impact of Exposure to Trauma on Posttraumatic Stress Disorder Symptomatology in Swedish Tourist Tsunami Survivors (2009) (41)
- Tsunami-exposed Tourist Survivors: Signs of Recovery in a 3-year Perspective (2011) (41)
- Recurrence Risk of Autism in Siblings and Cousins: A Multi-National, Population-Based Study. (2019) (39)
- DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia (2021) (38)
- Psychiatric disorders and suicide attempts in Swedish survivors of the 2004 southeast Asia tsunami: a 5 year matched cohort study. (2015) (38)
- The International Collaboration for Autism Registry Epidemiology (iCARE): Multinational Registry-Based Investigations of Autism Risk Factors and Trends (2013) (37)
- A longitudinal assessment of psychological distress after oesophageal cancer surgery (2017) (37)
- An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis (2014) (36)
- Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases (2018) (36)
- Niacin skin-flush response and electrodermal activity in patients with schizophrenia and healthy controls. (2006) (36)
- Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden (2017) (35)
- Implication of LRRC4C and DPP6 in neurodevelopmental disorders (2017) (33)
- Total and cause-specific standardized mortality ratios in patients with schizophrenia and/or substance use disorder (2018) (33)
- Social Class, Social Mobility and Risk of Psychiatric Disorder - A Population-Based Longitudinal Study (2013) (32)
- Multidimensional assessment of impulsivity in schizophrenia, bipolar disorder, and major depressive disorder: testing for shared endophenotypes (2016) (32)
- A genome-wide association study of kynurenic acid in cerebrospinal fluid: implications for psychosis and cognitive impairment in bipolar disorder (2013) (32)
- Familial aggregation of schizophrenia: The moderating effect of age at onset, parental immigration, paternal age and season of birth (2012) (32)
- Prolonged grief among traumatically bereaved relatives exposed and not exposed to a tsunami. (2011) (31)
- A polygenic resilience score moderates the genetic risk for schizophrenia (2019) (31)
- Enhanced neurocognitive functioning and positive temperament in twins discordant for bipolar disorder. (2014) (31)
- Erratum: Parental psychiatric disorders associated with autism spectrum disorders in the offspring (Pediatrics (2008) 121:5 (e1357-e1362)) (2008) (30)
- Prevalences of autoimmune diseases in schizophrenia, bipolar I and II disorder, and controls (2017) (29)
- A Loss-of-Function Variant in a Minor Isoform of ANK3 Protects Against Bipolar Disorder and Schizophrenia (2016) (29)
- Combining data from 2 nested case-control studies of overlapping cohorts to improve efficiency. (2008) (28)
- Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression (2019) (27)
- Aspects of emotional functioning following oesophageal cancer surgery in a population‐based cohort study (2015) (27)
- Complement Gene Expression Correlates with Superior Frontal Cortical Thickness in Humans (2017) (26)
- Poor school performance in offspring of patients with schizophrenia: what are the mechanisms? (2011) (25)
- Complement genes contribute sex-biased vulnerability in diverse disorders (2020) (25)
- Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample (2013) (25)
- Genetic risk scores and family history as predictors of schizophrenia in Nordic registers (2017) (24)
- Waiting time for cancer treatment and mental health among patients with newly diagnosed esophageal or gastric cancer: a nationwide cohort study (2017) (24)
- Fifteen years after a ferry disaster: clinical interviews and survivors’ self-assessment of their experience (2013) (23)
- Parental and Perinatal Risk Factors for Autism (2013) (23)
- Microparticles and microscopic structures in three fractions of fresh cerebrospinal fluid in schizophrenia: Case report of twins (2013) (23)
- Genome-wide association study identifies 30 loci associated with bipolar disorder (2019) (22)
- Regulatory variants explain much more heritability than coding variants across 11 common diseases (2014) (22)
- Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder (2018) (22)
- No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia (2014) (21)
- Examining the role of common and rare mitochondrial variants in schizophrenia (2018) (21)
- Correcting for cell-type effects in DNA methylation studies: reference-based method outperforms latent variable approaches in empirical studies (2017) (21)
- Refinement of schizophrenia GWAS loci using methylome-wide association data (2014) (20)
- Genetic variation associated with euphorigenic effects of d-amphetamine is associated with diminished risk for schizophrenia and attention deficit hyperactivity disorder (2014) (20)
- Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder (2016) (20)
- Perinatal risk factors in offenders with severe personality disorder: a population-based investigation. (2012) (20)
- Cognitive endophenotypes inform genome-wide expression profiling in schizophrenia. (2016) (20)
- A shared genetic contribution to breast cancer and schizophrenia (2020) (19)
- Electrodermal activity and social network as predictors of outcome of episodes in schizophrenia. (1996) (19)
- Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis (2015) (19)
- Mediterranean diet and depression: a population-based cohort study (2021) (18)
- MethylPCA: a toolkit to control for confounders in methylome-wide association studies (2013) (18)
- Dimensions of psychotic experiences among women in the general population (2014) (18)
- Comprehensive analysis of copy number variation in monozygotic twins discordant for bipolar disorder or schizophrenia (2013) (18)
- Benchmarking the HLA typing performance of Polysolver and Optitype in 50 Danish parental trios (2018) (17)
- Increased schizophrenia family history burden and reduced premorbid IQ in treatment-resistant schizophrenia: a Swedish National Register and Genomic Study (2019) (17)
- Social problem-solving in high-functioning schizophrenia: Specific deficits in sending skills (2009) (17)
- Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia (2017) (17)
- Inherited DNA Repair Gene Mutations in Men with Lethal Prostate Cancer (2020) (17)
- School achievements and schizophrenia: a case–control study (2003) (17)
- Combined Whole Methylome and Genomewide Association Study Implicates CNTN4 in Alcohol Use. (2015) (17)
- Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (2021) (16)
- Diagnostic tests and treatment procedures performed prior to cardiovascular death in individuals with severe mental illness (2020) (16)
- Cerebrospinal fluid microglia and neurodegenerative markers in twins concordant and discordant for psychotic disorders (2016) (16)
- Mosaic copy number variation in schizophrenia (2013) (15)
- Human loss-of-function variants suggest that partial LRRK2 inhibition is a safe therapeutic strategy for Parkinson’s disease (2019) (15)
- Pregnancy outcomes in women with autism: a nationwide population-based cohort study (2018) (15)
- How rare and common risk variation jointly affect liability for autism spectrum disorder (2020) (14)
- Evidence for cerebello-thalamo-cortical hyperconnectivity as a heritable trait for schizophrenia (2019) (14)
- Psychiatric disorder and work life: A longitudinal study of intra-generational social mobility (2016) (14)
- CNV analysis in a large schizophrenia sample implicates deletions at 16 p 12 . 1 and SLC 1 A 1 and duplications at 1 p 36 . 33 and CGNL 1 (2014) (13)
- After the flood: Resilience among tsunami-afflicted adolescents (2014) (13)
- Maternal Effects as Causes of Risk for Obsessive-Compulsive Disorder (2020) (13)
- Characterization of Single Gene Copy Number Variants in Schizophrenia (2019) (13)
- Cognition and autonomic function in schizophrenia: Inferior cognitive test performance in electrodermal and niacin skin flush non-responders (2015) (13)
- Covariance component models for multivariate binary traits in family data analysis (2008) (13)
- Coping Styles in Twins Discordant for Schizophrenia, Bipolar Disorder, and Depression (2016) (12)
- Kynurenic acid and psychotic symptoms and personality traits in twins with psychiatric morbidity (2017) (12)
- Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance. (2016) (12)
- Independent Methylome-Wide Association Studies of Schizophrenia Detect Consistent Case-Control Differences. (2020) (12)
- Autism—prenatal insults or an epiphenomenon of a strongly genetic disorder? (2004) (12)
- Video-based assessment of interpersonal problem solving skills in patients with schizophrenia, their siblings and non-psychiatric controls. (2007) (12)
- Initiating therapy with antidepressants after discontinuation of hormone therapy (2012) (12)
- Prenatal Ultrasound Scanning and the Risk of Schizophrenia and Other Psychoses (2007) (12)
- Intelligence, educational attainment, and brain structure in those at familial high‐risk for schizophrenia or bipolar disorder (2020) (12)
- Perinatal characteristics and schizophrenia : electrodermal activity as a mediating link in a vulnerability-stress perspective (1998) (11)
- Multivariate Pattern Analysis of Genotype–Phenotype Relationships in Schizophrenia (2018) (11)
- Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder (2021) (11)
- The schizophrenia and bipolar twin study in Sweden (STAR) (2019) (11)
- Test-retest stability of the oral niacin test and electrodermal activity in patients with schizophrenia. (2009) (11)
- Age at fatherhood: heritability and associations with psychiatric disorders (2016) (10)
- Cohort profile: Epidemiology and Genetics of Obsessive–compulsive disorder and chronic tic disorders in Sweden (EGOS) (2020) (10)
- Lack of Support for the Genes by Early Environment Interaction Hypothesis in the Pathogenesis of Schizophrenia (2021) (10)
- Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1 (2017) (9)
- Systematic review and meta-analysis: relationships between attention-deficit/hyperactivity disorder and urinary symptoms in children (2020) (9)
- Mortality and major disease risk among migrants of the 1991–2001 Balkan wars to Sweden: A register-based cohort study (2020) (9)
- Electrodermal activity and obstetric complications in schizophrenia. (1998) (9)
- Genetic variation in 117 myelination-related genes in schizophrenia: Replication of association to lipid biosynthesis genes (2018) (9)
- Risk of suicide among operated and non-operated patients hospitalised for peptic ulcers (2009) (8)
- Erratum: Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder (2017) (8)
- The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia (2021) (8)
- Microscopic Particles in Two Fractions of Fresh Cerebrospinal Fluid in Twins with Schizophrenia or Bipolar Disorder and in Healthy Controls (2012) (8)
- Genetic Variants in the 9p21.3 Locus Associated with Glioma Risk in Children, Adolescents, and Young Adults: A Case–Control Study (2019) (8)
- The Weighting is the Hardest Part: On the Behavior of the Likelihood Ratio Test and the Score Test Under a Data-Driven Weighting Scheme in Sequenced Samples (2017) (7)
- Genome-wide association study identifies new locus associated with OCD (2021) (7)
- The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum. (2021) (7)
- Ethical Issues in Cancer Register Follow-Up of Hormone Treatment in Adolescence (2009) (7)
- Schizophrenia susceptibility and age of diagnosis — A frailty approach (2013) (6)
- Systematic review and meta‐analysis identify significant relationships between clinical anxiety and lower urinary tract symptoms (2021) (6)
- Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility (2014) (6)
- Utilizing Twins as Controls for Non-Twin Case-Materials in Genome Wide Association Studies (2013) (5)
- the Offspring Parental Psychiatric Disorders Associated With Autism Spectrum Disorders in (2008) (5)
- P.1.k.021 Multiple sclerosis and psychiatric disorders: comorbidity and sibling risk in a nationwide Swedish cohort (2014) (4)
- Academic achievement at age 16 has contrasting effects on risk of later bipolar disorder and schizophrenia (2006) (4)
- Chronicity and Sex Affect Genetic Risk Prediction in Schizophrenia (2020) (4)
- Fetal Growth Restriction and Schizophrenia: A Swedish Twin Study (2005) (4)
- Risk of neurological, eye and ear disease in offspring to parents with schizophrenia or depression compared with offspring to healthy parents (2018) (4)
- The genetic architecture of obsessive-compulsive disorder: alleles across the frequency spectrum contribute liability to OCD (2021) (4)
- Early parental death: relation to electrodermal orienting response and gender in schizophrenia (1992) (4)
- Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans (2021) (3)
- Evacuation of Swedish survivors after the 2004 Southeast Asian tsunami: The survivors’ perspective and symptoms of post-traumatic stress (2019) (3)
- The offspring of women with severe mental disorder (2009) (3)
- The Neuroscience of Autism Spectrum Disorders (2013) (3)
- ADVANCED PATERNAL AND GRANDPATERNAL AGE AS A RISK FACTOR FOR PSYCHIATRIC DISORDERS (2012) (3)
- Neurodevelopmental Outcomes of Preterm Birth: Preterm birth and fetal growth in relation to adult psychopathology (2010) (3)
- Twin study shows association between monocyte chemoattractant protein-1 and kynurenic acid in cerebrospinal fluid (2019) (3)
- Svensson et al. respond to "Maternal genes and environment in preterm birth". (2009) (2)
- Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (2)
- Phenotypic Impact of Rare Potentially Damaging Copy Number Variation in Obsessive-Compulsive Disorder and Chronic Tic Disorders (2022) (2)
- Author Correction: Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2021) (1)
- Autism in children born after in vitro fertilization--reply. (2013) (1)
- Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia (2022) (1)
- Aberrations in intra-unterine growth as independent risk factors for schizophrenia (1998) (1)
- Transcript expression-aware annotation improves rare variant interpretation (2020) (1)
- An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation (2016) (1)
- 103 – Preterm birth and psychiatric outcome in adolescence and early adulthood: A study using the Swedish National Registers (2008) (1)
- The impact of educational attainment, intelligence and intellectual disability on schizophrenia: a Swedish population-based register and genetic study (2022) (1)
- The weighting is the hardest part: on the behavior of the likelihood ratio test and score test under weight misspecification in rare variant association studies (2015) (1)
- Analysis of 62 hybrid assembled human Y chromosomes exposes rapid structural changes and high rates of gene conversion (2017) (1)
- OCD symptom severity and comorbid psychiatric diagnoses in a Swedish genetic epidemiological obsessive-compulsive disorder cohort (2021) (1)
- Obstetric complications, electrodermal activity and psychosocial factors within a vulnerability-stress model of schizophrenia (1996) (1)
- Increased risk for psychiatric disorders immediately before and after cancer diagnosis: A nationwide matched cohort study in Sweden (2015) (1)
- Large-scale analysis of DNA methylation identifies cellular alterations in blood from psychosis patients and molecular biomarkers of treatment-resistant schizophrenia (2020) (1)
- POLYGENIC RISK AND BODY MASS INDEX IN THE SWEDEN SCHIZOPHRENIA STUDY (2022) (0)
- Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder (2018) (0)
- Author Correction: Transcript expression-aware annotation improves rare variant interpretation (2021) (0)
- MethylPCA: a toolkit to control for confounders in methylome-wide association studies (2013) (0)
- Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans (2021) (0)
- Correcting for cell-type effects in DNA methylation studies: reference-based method outperforms latent variable approaches in empirical studies (2017) (0)
- The effect of LRRK2 loss-of-function variants in humans (2020) (0)
- The effect of LRRK2 loss-of-function variants in humans (2020) (0)
- TU77. THE IMPACT OF EDUCATIONAL ATTAINMENT, INTELLIGENCE AND INTELLECTUAL DISABILITY ON SCHIZOPHRENIA: A SWEDISH POPULATION-BASED REGISTER AND GENETIC STUDY (2021) (0)
- Intra-uterine growth and risk of schizophrenia, effective psychosis, reactive psychosis, infantile autism and anorexia nervosa (2000) (0)
- Elevated risk of pregnancy and delivery complications in births to mothers with affective psychosis (2004) (0)
- Fetal Programming and Future Mental Health (2007) (0)
- 190: Incidence of Postpartum Psychosis in Women with and Without Pre-Pregnancy Psychiatric Hospitalizations (2005) (0)
- Association of Anxiety Disorders and Attention Deficit Hyperactivity Disorders With Lower Urinary Tract Symptoms (2020) (0)
- 2D-1 Adverse pregnancy outcomes in mothers with schizophrenia: maternal and paternal influences (2007) (0)
- Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (2021) (0)
- Birthweight and Attention-deficit Hyperactivity Disorder in Childhood and Early Adolescence: A Prospective Swedish Twin Study - Session: Language Development (2004) (0)
- Interpersonal problem solving skills and electrodermal activity in schizophrenia (2003) (0)
- Evolutionary and functional data power search for obsessive-compulsive disorder genes (2017) (0)
- Title : Genetic maternal effects contributes to the risk of Tourette ' s disorder (2020) (0)
- VKučinskas-2001-2016 (2016) (0)
- Author Correction: The effect of LRRK2 loss-of-function variants in humans (2021) (0)
- Autism andMental Retardation AmongOffspring Born After In Vitro Fertilization (2013) (0)
- Benchmarking the HLA typing performance of Polysolver and Optitype in 50 Danish parental trios (2018) (0)
- Prevalence and Phenotypic Impact of Rare Likely Pathogenic Variants in Autism Spectrum Disorder (2020) (0)
- University of Groningen Fine mapping of ZNF 804 A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder (2017) (0)
- Direct additive genetics and maternal effect contribute to the risk of Tourette disorder (2023) (0)
- Prospective longitudinal long-term studies 14-20 years after three disasters (2011) (0)
- Can a Natural Disaster Lead to Suicide Attempts and Psychiatric Disorders in Adults? A 5-Year Matched Cohort Study (2015) (0)
- The International Collaboration for Autism Registry Epidemiology (iCARE): Multinational Registry-Based Investigations of Autism Risk Factors and Trends (2013) (0)
- Systematic Review and Meta-Analysis Identifies Significant Relationships Between Anxiety Disorders and Daytime Lower Urinary Tract Symptoms (2020) (0)
- Adult Sibling Response to Chronic Mental Illness Interview (2012) (0)
- T63GENETIC AND ENVIRONMENTAL FACTORS AND RISK OF OBSESSIVE-COMPULSIVE DISORDER (2019) (0)
- Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum (2017) (0)
- Author response: DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia (2020) (0)
- School achievements, prenatal factors and age of onseet in schizophrenia (2001) (0)
- Supplementary Information for Extremely low-coverage sequencing and imputation increases power for genome-wide association studies (2012) (0)
- Genetic maternal effects contributes to the risk of Tourette's disorder (2020) (0)
- Maternal smoking during pregnancy and offspring overweight: the role of familiar factors (abstract) (2009) (0)
- Still birth, infant death, preterm birth and low birth weight among offspring of women with schizophrenia (2001) (0)
- Traumatic bereavement and complicated grief among tsunami-exposed and home-staying relatives (2010) (0)
- Early risk factors for infantile autism (2001) (0)
- O7.5. EVIDENCE FOR CEREBELLO-THALAMO-CORTICAL HYPERCONNECTIVITY AS A HERITABLE TRAIT FOR SCHIZOPHRENIA (2019) (0)
- Low Birthweight and Schizophrenia - a Swedish Twin Study, Session: Poster (2004) (0)
- Psychometric properties of the Swedish translation of the Obsessive–Compulsive Inventory-Revised and the population characteristics of the symptom dimensions of OCD (2022) (0)
- 5.45 RECURRENT AND LARGE COPY NUMBER VARIATION IN OCD RISK: RESULTS FROM THE EGOS STUDY (2019) (0)
- Registration and definitions of mental disorders in Swedish survivors of the 2004 southeast Asia tsunami--Authors' response. (2015) (0)
- Rates of clinically confirmed stress-related psychiatric disorders among Swedish tsunami survivors: 9-year follow-up. (2021) (0)
- T198. Evidence for Cerebello-Thalamo-Cortical Hyperconnectivity as a Heritable Trait for Schizophrenia (2019) (0)
- Genome-wide study of CSF kynurenic acid in bipolar disorder implicates a molecular pathway underlying psychosis (2012) (0)
- Bayesian Integrated Analysis Of Multiple Types Of Rare Variants To Infer Risk Genes For Schizophrenia And Other Neurodevelopmental Disorders (2017) (0)
- Fetal growth impairment – the relevance to psychiatric outcome (2002) (0)
- Supervision and equality in medical research - Obstacles due to gender? (1995) (0)
- P.1.b.002 Microscopic particles in fresh cerebrospinal fluid in twins with schizophrenia and bipolar disorder and in healthy subjects (2012) (0)
- [Instruction and equality in medical research. Sex-related obstacles after equal education]. (1995) (0)
- Large-scale genetic studies of rare and common variation in schizophrenia risk (2010) (0)
- Tsunami-exposed survivors - signs of recovery in a three-year perspective (2010) (0)
- Edinburgh Research Explorer Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder (2017) (0)
- Integrating evolutionary and regulatory information with a multispecies approach implicates genes and pathways in obsessive-compulsive disorder (2017) (0)
- A longitudinal study of posttraumatic stress : from 3 months to 14 years after the m/s Estonia disaster (2009) (0)
- Author Correction: A structural variation reference for medical and population genetics (2021) (0)
- Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (0)
- Trajectoriesand rates of recovery in Swedish survivors of the 2004 tsunami (2011) (0)
- Waiting time for cancer treatment and mental health among patients with newly diagnosed esophageal or gastric cancer: a nationwide cohort study (2017) (0)
- EXOME SEQUENCING IN SCHIZOPHRENIA TO MAP DISEASE VARIANTS, GENES AND NETWORKS (2012) (0)
- Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia (2022) (0)
- NEXT GENERATION GENOME-WIDE ASSOCIATION STUDY OF SCHIZOPHRENIA FROM SWEDEN (2022) (0)
- Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia (2020) (0)
- Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders (2017) (0)
- 82. INCREASED BURDEN OF RARE TANDEM REPEAT EXPANSIONS IN SCHIZOPHRENIA (2021) (0)
- Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1 (2016) (0)
- M91 INCREASED SCHIZOPHRENIA FAMILY HISTORY BURDEN AND REDUCED PREMORBID IQ IN TREATMENT-RESISTANT SCHIZOPHRENIA: A SWEDISH NATIONAL REGISTER AND GENOMIC STUDY (2019) (0)
- A structural variation reference for medical and population genetics (2020) (0)
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2020) (0)
- Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia (2022) (0)
- Evaluating drug targets through human loss-of-function genetic variation (2020) (0)
- M16 IDENTICAL BUT NOT THE SAME - WHOLE GENOME SEQUENCING OF MONOZYGOTIC TWINS DISCORDANT FOR PSYCHIATRIC ILLNESS (2019) (0)
- Cover Image, Volume 173A, Number 2, February 2017. (2017) (0)
- Refinement of schizophrenia GWAS loci using methylome-wide association data (2014) (0)
- High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction (2015) (0)
- The mutational constraint spectrum quantified from variation in 141,456 humans (2020) (0)
- Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder (2020) (0)
- Sibling bond and coping with heredity in schizophrenia (2003) (0)
- Higher Maternal Age Predicts Risk of Autism (2012) (0)
- The association between family history and genomic burden with schizophrenia mortality: a Swedish population-based register and genetic sample study (2021) (0)
- ' s response to reviews Title : Dietary intake of fish , omega-3 , omega-6 polyunsaturated fatty acids and vitamin D and risk of psychotic-like symptoms in a cohort of 33 000 women from the general population (2010) (0)
- Identification of common genetic risk variants for autism spectrum disorder (2019) (0)
- ' s response to reviews Title : Dietary intake of fish , omega-3 , omega-6 polyunsaturated fatty acids and vitamin D and risk of psychotic-like symptoms in a cohort of 33 000 women from the general population (2010) (0)
- T117. POLYGENIC RISK SCORES AND CONCORDANCE FOR SCHIZOPHRENIA AND BIPOLAR DISORDER IN SWEDISH MONOZYGOTIC AND DIZYGOTIC TWINS (2022) (0)
- Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis (2015) (0)
- Autism Sequencing Consortium (ASC) iPSYCH-BROAD Consortium Broad Institute Center for Common Disease Genomics (Broad-CCDG) (2021) (0)
- Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2020) (0)
- Genes implicated by a methylome-wide schizophrenia study in neonatal blood show differential expression in adult brain samples. (2023) (0)
- Author Correction: Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2021) (0)
- Genetic variation in 117 myelination-related genes in schizophrenia: Replication of association to lipid biosynthesis genes (2018) (0)
- Author Correction: Evaluating drug targets through human loss-of-function genetic variation (2021) (0)
- Ultra-Rare Protein-Altering Variants Among 4,877 Swedish Individuals with Schizophrenia (2017) (0)
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What Schools Are Affiliated With Christina M. Hultman?
Christina M. Hultman is affiliated with the following schools:
