Detalhe da pesquisa
1.
Analysis of genes within the schizophrenia-linked 22q11.2 deletion identifies interaction of night owl/LZTR1 and NF1 in GABAergic sleep control.
PLoS Genet
; 16(4): e1008727, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32339168
2.
AMPK signaling linked to the schizophrenia-associated 1q21.1 deletion is required for neuronal and sleep maintenance.
PLoS Genet
; 14(12): e1007623, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30566533
3.
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.
PLoS Genet
; 12(5): e1005993, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27153221
4.
Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome: a study in male mice.
J Psychiatry Neurosci
; 42(1): 48-58, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27391101
5.
Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.
Am J Hum Genet
; 92(3): 439-47, 2013 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23453669
6.
Quetiapine versus aripiprazole in children and adolescents with psychosis--protocol for the randomised, blinded clinical Tolerability and Efficacy of Antipsychotics (TEA) trial.
BMC Psychiatry
; 14: 199, 2014 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-25015535
7.
Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder.
Nat Genet
; 56(2): 234-244, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38036780
8.
Quantifying the Relative Importance of Genetics and Environment on the Comorbidity between Mental- and Cardiometabolic Disorders: A Comprehensive Analysis of National Register Data from 17 million Scandinavians.
medRxiv
; 2024 Feb 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38464139
9.
The genetic background of hydrocephalus in a population-based cohort: implication of ciliary involvement.
Brain Commun
; 5(1): fcad004, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36694575
10.
Genetic regulation of spermine oxidase activity and cancer risk: a Mendelian randomization study.
Sci Rep
; 11(1): 17463, 2021 08 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-34465810
11.
Interactive effects between hemizygous 15q13.3 microdeletion and peripubertal stress on adult behavioral functions.
Neuropsychopharmacology
; 44(4): 703-710, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30188511
12.
Shared Molecular Neuropathology Across Major Psychiatric Disorders Parallels Polygenic Overlap.
Focus (Am Psychiatr Publ)
; 17(1): 66-72, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32015716
13.
Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants.
Nat Neurosci
; 22(12): 1961-1965, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31768057
14.
Association of a dopamine beta-hydroxylase gene variant with depression in elderly women possibly reflecting noradrenergic dysfunction.
J Affect Disord
; 106(1-2): 169-72, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17698206
15.
Heritability of Schizophrenia and Schizophrenia Spectrum Based on the Nationwide Danish Twin Register.
Biol Psychiatry
; 83(6): 492-498, 2018 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28987712
16.
Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap.
Science
; 359(6376): 693-697, 2018 02 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29439242
17.
Complex spatio-temporal distribution and genomic ancestry of mitochondrial DNA haplogroups in 24,216 Danes.
PLoS One
; 13(12): e0208829, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30543675
18.
Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease.
PLoS One
; 13(12): e0208828, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30532134
19.
The Anorexia Nervosa Genetics Initiative (ANGI): Overview and methods.
Contemp Clin Trials
; 74: 61-69, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30287268
20.
Novel procedure for genotyping of the human serotonin transporter gene-linked polymorphic region (5-HTTLPR)--a region with a high level of allele diversity.
Psychiatr Genet
; 17(5): 287-91, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17728667