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C. Hultman · SciRah

Researcher profile · Semantic Scholar

C. Hultman

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C. Hultman — researcher profile on SciRah

h-index: 92
Works: 278
Citations: 61K

Most-cited papers

Mapping genomic loci implicates genes and synaptic biology in schizophrenia
V. Trubetskoy, A. Pardiñas, Ting Qi, G. Panagiotaropoulou +430 more
2022Nature2,385 citations Open access
Semantic Scholar
Identification of common genetic risk variants for autism spectrum disorder
J. Grove, S. Ripke, T. Als, M. Mattheisen +272 more
2019Nature Genetics2,146 citations Open access
Semantic Scholar
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Satterstrom, Jack A. Kosmicki, Jiebiao Wang, M. Breen +186 more
2019Cell2,103 citations Open access
Semantic Scholar
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
C. Marshall, D. Howrigan, D. Merico, B. Thiruvahindrapuram +265 more
2016bioRxiv1,294 citations Open access
Semantic Scholar
Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology
N. Mullins, A. Forstner, K. O’Connell, B. Coombes +313 more
2021Nature Genetics1,030 citations Open access
Semantic Scholar
Rare coding variants in 10 genes confer substantial risk for schizophrenia
T. Singh, T. Poterba, D. Curtis, H. Akil +107 more
2022Nature687 citations Open access
Semantic Scholar
Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes
D. Ruderfer, S. Ripke, A. McQuillin, J. Boocock +496 more
2018Cell675 citations Open access
Semantic Scholar
The Heritability of Autism Spectrum Disorder
S. Sandin, P. Lichtenstein, R. Kuja-Halkola, C. Hultman +2 more
2017Journal of the American Medical Association (JAMA)657 citations Open access
Semantic Scholar
Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort.
Dan Bai, B. Yip, G. Windham, A. Sourander +18 more
2019JAMA psychiatry521 citations Open access
Semantic Scholar
The Risk Factors for Postpartum Depression: A Population Based Study
M. Silverman, A. Reichenberg, David A. Savitz, S. Cnattingius +4 more
2017Depression and Anxiety392 citations Open access
Semantic Scholar
Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders
T. Singh, M. Kurki, D. Curtis, S. Purcell +58 more
2016bioRxiv263 citations Open access
Semantic Scholar
The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability
T. Singh, J. Walters, M. Johnstone, D. Curtis +19 more
2017Nature Genetics232 citations Open access
Semantic Scholar
Clinical Diagnosis of Mental Disorders Immediately Before and After Cancer Diagnosis: A Nationwide Matched Cohort Study in Sweden.
D. Lu, T. Andersson, K. Fall, C. Hultman +3 more
2016JAMA Oncology217 citations Open access
Semantic Scholar
Sequencing and de novo assembly of 150 genomes from Denmark as a population reference
L. Maretty, J. M. Jensen, Bent Petersen, J. Sibbesen +55 more
2017Nature148 citations Open access
Semantic Scholar
Mediterranean diet and depression: a population-based cohort study
Wei-Yao Yin, M. Löf, Ruo-Qing Chen, C. Hultman +2 more
2021International Journal of Behavioral Nutrition and Physical Activity130 citations Open access
Semantic Scholar
Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression
A. Forstner, S. Awasthi, C. Wolf, E. Maron +71 more
2019Molecular Psychiatry119 citations Open access
Semantic Scholar
Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum
A. Ganna, Kyle F. Satterstrom, S. Zekavat, I. Das +40 more
2017bioRxiv117 citations Open access
Semantic Scholar
DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia
E. Hannon, E. Dempster, G. Mansell, J. Burrage +42 more
2021eLife114 citations Open access
Semantic Scholar
Polygenic overlap between schizophrenia risk and antipsychotic response: a genomic medicine approach
D. Ruderfer, A. Charney, B. Readhead, B. Kidd +10 more
2016Lancet psychiatry114 citations Open access
Semantic Scholar
The effect of LRRK2 loss-of-function variants in humans
N. Whiffin, I. Armean, A. Kleinman, Jamie L. Marshall +36 more
2020Nature Medicine111 citations Open access
Semantic Scholar
A population-based heritability estimate of bipolar disorder - In a Swedish twin sample.
Viktoria Johansson, R. Kuja-Halkola, Tyrone D. Cannon, C. Hultman +1 more
2019Psychiatry Research107 citations
Semantic Scholar
Common risk variants identified in autism spectrum disorder
J. Grove, S. Ripke, T. Als, M. Mattheisen +71 more
2017bioRxiv105 citations Open access
Semantic Scholar
Recurrence risk of autism in siblings and cousins: a multi-national, population-based study
S. N. Hansen, D. Schendel, R. Francis, G. Windham +16 more
2019Journal of the American Academy of Child and Adolescent Psychiatry98 citations Open access
Semantic Scholar
Ultra-rare disruptive and damaging mutations influence educational attainment in the general population
A. Ganna, G. Genovese, D. Howrigan, Andrea E. Byrnes +28 more
2016Nature Neuroscience98 citations Open access
Semantic Scholar
Undiagnosed cardiovascular disease prior to cardiovascular death in individuals with severe mental illness
I. H. Heiberg, B. K. Jacobsen, L. Balteskard, J. G. Bramness +6 more
2019Acta Psychiatrica Scandinavica81 citations Open access
Semantic Scholar
Prevalence and predictors of anxiety and depression among esophageal cancer patients prior to surgery.
Y. Hellstadius, J. Lagergren, J. Zylstra, J. Gossage +4 more
2016Diseases of the esophagus77 citations
Semantic Scholar
Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia
M. Halvorsen, Ruth Huh, N. Oskolkov, Jia Wen +16 more
2020Nature Communications76 citations Open access
Semantic Scholar
Total and cause-specific standardized mortality ratios in patients with schizophrenia and/or substance use disorder
Ina H. Heiberg, B. Jacobsen, R. Nesvåg, J. Bramness +5 more
2018PLoS ONE68 citations Open access
Semantic Scholar
Integrating evolutionary and regulatory information with a multispecies approach implicates genes and pathways in obsessive-compulsive disorder
H. J. Noh, R. Tang, J. Flannick, C. O'Dushlaine +28 more
2017Nature Communications62 citations Open access
Semantic Scholar
Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases
A. Charney, E. Stahl, E. Green, Chia-Yen Chen +42 more
2018bioRxiv60 citations Open access
Semantic Scholar
Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk
F. Satterstrom, Jack A. Kosmicki, Jiebiao Wang, M. Breen +153 more
2018bioRxiv60 citations Open access
Semantic Scholar
A longitudinal assessment of psychological distress after oesophageal cancer surgery
Y. Hellstadius, J. Lagergren, J. Zylstra, J. Gossage +4 more
2017Acta oncologica60 citations Open access
Semantic Scholar
The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia
R. Nehme, O. Pietiläinen, M. Artomov, M. Tegtmeyer +41 more
2021Nature Communications54 citations Open access
Semantic Scholar
How rare and common risk variation jointly affect liability for autism spectrum disorder
L. Klei, L. McClain, B. Mahjani, K. Panayidou +12 more
2020Molecular Autism48 citations Open access
Semantic Scholar
Prevalences of autoimmune diseases in schizophrenia, bipolar I and II disorder, and controls.
L. Cremaschi, M. Kardell, Viktoria Johansson, A. Isgren +4 more
2017Psychiatry Research47 citations
Semantic Scholar
A shared genetic contribution to breast cancer and schizophrenia
D. Lu, Jie Song, Yi Lu, K. Fall +8 more
2020Nature Communications45 citations Open access
Semantic Scholar
Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden
B. Yip, Dan Bai, B. Mahjani, L. Klei +8 more
2017Biological Psychiatry44 citations Open access
Semantic Scholar
Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder
B. Mahjani, S. de Rubeis, Christina Gustavsson Mahjani, Maureen S. Mulhern +12 more
2021Molecular Autism41 citations Open access
Semantic Scholar
Increased schizophrenia family history burden and reduced premorbid IQ in treatment-resistant schizophrenia: a Swedish National Register and Genomic Study
K. Kowalec, Yi Lu, A. Sariaslan, Jie Song +6 more
2019Molecular Psychiatry41 citations Open access
Semantic Scholar
Genome-wide association study of over 40,000 bipolar disorder cases provides novel biological insights
N. Mullins, A. Forstner, K. O’Connell, B. Coombes +309 more
2020medRxiv38 citations Open access
Semantic Scholar
Complement Gene Expression Correlates with Superior Frontal Cortical Thickness in Humans
D. Allswede, A. Zheutlin, Yoonho Chung, K. Anderson +3 more
2017Neuropsychopharmacology38 citations Open access
Semantic Scholar
Waiting time for cancer treatment and mental health among patients with newly diagnosed esophageal or gastric cancer: a nationwide cohort study
Huan Song, F. Fang, U. Valdimarsdóttir, D. Lu +7 more
2017BMC Cancer37 citations Open access
Semantic Scholar
Benchmarking the HLA typing performance of Polysolver and Optitype in 50 Danish parental trios
M. Matey-Hernandez, L. Maretty, J. M. Jensen, Bent Petersen +55 more
2018BMC Bioinformatics36 citations Open access
Semantic Scholar
Maternal Effects as Causes of Risk for Obsessive-Compulsive Disorder
B. Mahjani, L. Klei, C. Hultman, H. Larsson +4 more
2020Biological Psychiatry35 citations Open access
Semantic Scholar
Evidence for cerebello-thalamo-cortical hyperconnectivity as a heritable trait for schizophrenia
Heng-Yi Cao, M. Ingvar, C. Hultman, T. Cannon
2019Translational Psychiatry35 citations Open access
Semantic Scholar
Pregnancy outcomes in women with autism: a nationwide population-based cohort study
H. Sundelin, O. Stephansson, C. Hultman, J. Ludvigsson
2018Clinical Epidemiology34 citations Open access
Semantic Scholar
The genetic architecture of obsessive-compulsive disorder: alleles across the frequency spectrum contribute liability to OCD.
B. Mahjani, L. Klei, M. Mattheisen, M. Halvorsen +16 more
2021American Journal of Psychiatry33 citations Open access
Semantic Scholar
Systematic review and meta‐analysis identify significant relationships between clinical anxiety and lower urinary tract symptoms
B. Mahjani, L. R. Koskela, A. Batuure, Christina Gustavsson Mahjani +6 more
2021Brain and Behavior33 citations Open access
Semantic Scholar
Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder
T. Hughes, I. Sønderby, T. Polushina, Lars Hansson +20 more
2018Translational Psychiatry31 citations Open access
Semantic Scholar
Intelligence, educational attainment, and brain structure in those at familial high‐risk for schizophrenia or bipolar disorder
S. D. de Zwarte, R. Brouwer, I. Agartz, M. Alda +98 more
2020Human Brain Mapping30 citations Open access
Semantic Scholar

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