Detalhe da pesquisa
1.
Genes implicated by a methylome-wide schizophrenia study in neonatal blood show differential expression in adult brain samples.
Mol Psychiatry
; 28(5): 2088-2094, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-37106120
2.
Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia.
Mol Psychiatry
; 28(1): 475-482, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36380236
3.
Direct additive genetics and maternal effect contribute to the risk of Tourette disorder.
J Neurol Neurosurg Psychiatry
; 94(8): 638-642, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37100590
4.
The impact of educational attainment, intelligence and intellectual disability on schizophrenia: a Swedish population-based register and genetic study.
Mol Psychiatry
; 27(5): 2439-2447, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35379910
5.
Sequencing and de novo assembly of 150 genomes from Denmark as a population reference.
Nature
; 548(7665): 87-91, 2017 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28746312
6.
Intelligence, educational attainment, and brain structure in those at familial high-risk for schizophrenia or bipolar disorder.
Hum Brain Mapp
; 43(1): 414-430, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33027543
7.
Increased schizophrenia family history burden and reduced premorbid IQ in treatment-resistant schizophrenia: a Swedish National Register and Genomic Study.
Mol Psychiatry
; 26(8): 4487-4495, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31712719
8.
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.
Mol Psychiatry
; 26(9): 5239-5250, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33483695
9.
Psychometric properties of the Swedish translation of the Obsessive-Compulsive Inventory-Revised and the population characteristics of the symptom dimensions of OCD.
Soc Psychiatry Psychiatr Epidemiol
; 57(10): 2147-2155, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-35064790
10.
Systematic review and meta-analysis: relationships between attention-deficit/hyperactivity disorder and urinary symptoms in children.
Eur Child Adolesc Psychiatry
; 31(4): 663-670, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33635440
11.
Mediterranean diet and depression: a population-based cohort study.
Int J Behav Nutr Phys Act
; 18(1): 153, 2021 11 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-34838037
12.
Mortality and major disease risk among migrants of the 1991-2001 Balkan wars to Sweden: A register-based cohort study.
PLoS Med
; 17(12): e1003392, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33259494
13.
Twin study shows association between monocyte chemoattractant protein-1 and kynurenic acid in cerebrospinal fluid.
Eur Arch Psychiatry Clin Neurosci
; 270(7): 933-938, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31302732
14.
A polygenic burden of rare disruptive mutations in schizophrenia.
Nature
; 506(7487): 185-90, 2014 Feb 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-24463508
15.
Cohort profile: Epidemiology and Genetics of Obsessive-compulsive disorder and chronic tic disorders in Sweden (EGOS).
Soc Psychiatry Psychiatr Epidemiol
; 55(10): 1383-1393, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31907560
16.
Evacuation of Swedish survivors after the 2004 Southeast Asian tsunami: The survivors' perspective and symptoms of post-traumatic stress.
Scand J Public Health
; 47(2): 260-268, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29708026
17.
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.
Hum Mol Genet
; 25(15): 3383-3394, 2016 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27329760
18.
Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder.
Am J Hum Genet
; 96(2): 283-94, 2015 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25640677
19.
Risk of neurological, eye and ear disease in offspring to parents with schizophrenia or depression compared with offspring to healthy parents.
Psychol Med
; 48(16): 2710-2716, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29669615
20.
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.
Am J Hum Genet
; 95(5): 535-52, 2014 Nov 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-25439723