Detalhe da pesquisa
1.
Gene expression profiling of archived dried blood spot samples from the Danish Neonatal Screening Biobank.
Mol Genet Metab
; 116(3): 119-24, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26212339
2.
CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastoma.
J Neurooncol
; 125(1): 75-8, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26290144
3.
UGT1A1*28 polymorphism and acute lymphoblastic leukemia in children: a Danish case-control study.
Pediatr Res
; 76(5): 459-63, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25105254
4.
Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia.
J Psychiatry Neurosci
; 39(6): 386-96, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24936775
5.
Common variants at VRK2 and TCF4 conferring risk of schizophrenia.
Hum Mol Genet
; 20(20): 4076-81, 2011 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21791550
6.
Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis.
BMC Med Genet
; 12: 22, 2011 Feb 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-21306642
7.
Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source.
BMC Genet
; 12: 58, 2011 Jul 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-21726430
8.
Genome-wide scans using archived neonatal dried blood spot samples.
BMC Genomics
; 10: 297, 2009 Jul 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-19575812
9.
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Nat Genet
; 51(1): 63-75, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30478444
10.
Identification of common genetic risk variants for autism spectrum disorder.
Nat Genet
; 51(3): 431-444, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30804558
11.
Evaluation of whole genome amplified DNA to decrease material expenditure and increase quality.
Mol Genet Metab Rep
; 11: 36-45, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28487825
12.
RNA sequencing of archived neonatal dried blood spots.
Mol Genet Metab Rep
; 10: 33-37, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28053876
13.
Genetic Variation in NFKBIE Is Associated With Increased Risk of Pneumococcal Meningitis in Children.
EBioMedicine
; 3: 93-99, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26870821
14.
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.
Nat Genet
; 48(5): 552-5, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26998691
15.
An epigenetic clock for gestational age at birth based on blood methylation data.
Genome Biol
; 17(1): 206, 2016 10 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27717399
16.
Mannose-Binding Lectin Gene, MBL2, Polymorphisms Do Not Increase Susceptibility to Invasive Meningococcal Disease in a Population of Danish Children.
Open Forum Infect Dis
; 2(4): ofv127, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26464842
17.
Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia: A Danish Population-Based Study and Meta-analysis.
JAMA Psychiatry
; 72(7): 635-41, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25830477
18.
Common variants associated with general and MMR vaccine-related febrile seizures.
Nat Genet
; 46(12): 1274-82, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25344690
19.
Genome-wide association analyses identify variants in developmental genes associated with hypospadias.
Nat Genet
; 46(9): 957-63, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25108383
20.
A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations.
Nat Genet
; 46(1): 51-5, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24241537