|
| 36380236 | Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia. | Mol Psychiatry | 2023 |
| 36380236 | Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia. | Mol Psychiatry | 2023 |
| 36824788 | DeepGWAS: Enhance GWAS Signals for Neuropsychiatric Disorders via Deep Neural Network. | Res Sq | 2023 |
| 36454006 | Increased Prevalence of Rare Copy Number Variants in Treatment-Resistant Psychosis. | Schizophr Bull | 2023 |
| 36824788 | DeepGWAS: Enhance GWAS Signals for Neuropsychiatric Disorders via Deep Neural Network. | Res Sq | 2023 |
| 36454006 | Increased Prevalence of Rare Copy Number Variants in Treatment-Resistant Psychosis. | Schizophr Bull | 2023 |
| 34987162 | Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia. | Nat Commun | 2022 |
| 35396580 | Mapping genomic loci implicates genes and synaptic biology in schizophrenia. | Nature | 2022 |
| 35379910 | The impact of educational attainment, intelligence and intellectual disability on schizophrenia: a Swedish population-based register and genetic study. | Mol Psychiatry | 2022 |
| 34987162 | Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia. | Nat Commun | 2022 |
| 35379910 | The impact of educational attainment, intelligence and intellectual disability on schizophrenia: a Swedish population-based register and genetic study. | Mol Psychiatry | 2022 |
| 35396580 | Mapping genomic loci implicates genes and synaptic biology in schizophrenia. | Nature | 2022 |
| 32064741 | Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. | Addict Biol | 2021 |
| 32064741 | Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. | Addict Biol | 2021 |
| 31548576 | Correction: Common-variant associations with fragile X syndrome. | Mol Psychiatry | 2020 |
| 32365089 | Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis. | PLoS Comput Biol | 2020 |
| 32066678 | Treatment-resistant psychotic symptoms and the 15q11.2 BP1-BP2 (Burnside-Butler) deletion syndrome: case report and review of the literature. | Transl Psychiatry | 2020 |
| 32296054 | Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia. | Nat Commun | 2020 |
| 31767120 | Characterization of Single Gene Copy Number Variants in Schizophrenia. | Biol Psychiatry | 2020 |
| 32943312 | Treatment-resistant psychotic symptoms and early-onset dementia: A case report of the 3q29 deletion syndrome. | Schizophr Res | 2020 |
| 31548576 | Correction: Common-variant associations with fragile X syndrome. | Mol Psychiatry | 2020 |
| 31767120 | Characterization of Single Gene Copy Number Variants in Schizophrenia. | Biol Psychiatry | 2020 |
| 32066678 | Treatment-resistant psychotic symptoms and the 15q11.2 BP1-BP2 (Burnside-Butler) deletion syndrome: case report and review of the literature. | Transl Psychiatry | 2020 |
| 32943312 | Treatment-resistant psychotic symptoms and early-onset dementia: A case report of the 3q29 deletion syndrome. | Schizophr Res | 2020 |
| 32365089 | Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis. | PLoS Comput Biol | 2020 |
| 32296054 | Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia. | Nat Commun | 2020 |
| 30531935 | Common-variant associations with fragile X syndrome. | Mol Psychiatry | 2019 |
| 30531935 | Common-variant associations with fragile X syndrome. | Mol Psychiatry | 2019 |
| 30718465 | The genomics of major psychiatric disorders in a large pedigree from Northern Sweden. | Transl Psychiatry | 2019 |
| 30718465 | The genomics of major psychiatric disorders in a large pedigree from Northern Sweden. | Transl Psychiatry | 2019 |
| 29712475 | Developmental Delay, Treatment-Resistant Psychosis, and Early-Onset Dementia in a Man With 22q11 Deletion Syndrome and Huntington's Disease. | Am J Psychiatry | 2018 |
| 29930110 | Analysis of shared heritability in common disorders of the brain. | Science | 2018 |
| 29490610 | A randomized approach to speed up the analysis of large-scale read-count data in the application of CNV detection. | BMC Bioinformatics | 2018 |
| 29712475 | Developmental Delay, Treatment-Resistant Psychosis, and Early-Onset Dementia in a Man With 22q11 Deletion Syndrome and Huntington's Disease. | Am J Psychiatry | 2018 |
| 29930110 | Analysis of shared heritability in common disorders of the brain. | Science | 2018 |
| 29490610 | A randomized approach to speed up the analysis of large-scale read-count data in the application of CNV detection. | BMC Bioinformatics | 2018 |
| 27869829 | Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. | Nat Genet | 2017 |
| 28763065 | Genome-wide association analysis identifies common variants influencing infant brain volumes. | Transl Psychiatry | 2017 |
| 28368970 | Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa. | Psychiatr Genet | 2017 |
| 27759917 | Implication of LRRC4C and DPP6 in neurodevelopmental disorders. | Am J Med Genet A | 2017 |
| 27869829 | Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. | Nat Genet | 2017 |
| 28368970 | Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa. | Psychiatr Genet | 2017 |
| 28763065 | Genome-wide association analysis identifies common variants influencing infant brain volumes. | Transl Psychiatry | 2017 |
| 27759917 | Implication of LRRC4C and DPP6 in neurodevelopmental disorders. | Am J Med Genet A | 2017 |
| 26899349 | One CNV Discordance in NRXN1 Observed Upon Genome-wide Screening in 38 Pairs of Adult Healthy Monozygotic Twins. | Twin Res Hum Genet | 2016 |
| 26899349 | One CNV Discordance in NRXN1 Observed Upon Genome-wide Screening in 38 Pairs of Adult Healthy Monozygotic Twins. | Twin Res Hum Genet | 2016 |
| 25883151 | Allele-specific copy-number discovery from whole-genome and whole-exome sequencing. | Nucleic Acids Res | 2015 |
| 25883151 | Allele-specific copy-number discovery from whole-genome and whole-exome sequencing. | Nucleic Acids Res | 2015 |
| 26431523 | A New Method for Detecting Associations with Rare Copy-Number Variants. | PLoS Genet | 2015 |
| 26431523 | A New Method for Detecting Associations with Rare Copy-Number Variants. | PLoS Genet | 2015 |