Detalhe da pesquisa
1.
Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci.
Childs Nerv Syst
; 37(3): 819-830, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33226468
2.
Mildly compromised tetrahydrobiopterin cofactor biosynthesis due to Pts variants leads to unusual body fat distribution and abdominal obesity in mice.
J Inherit Metab Dis
; 39(2): 309-19, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26830550
3.
BDNF Val66met and 5-HTTLPR polymorphisms predict a human in vivo marker for brain serotonin levels.
Hum Brain Mapp
; 36(1): 313-23, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25220079
4.
Open and Calm--a randomized controlled trial evaluating a public stress reduction program in Denmark.
BMC Public Health
; 15: 1245, 2015 Dec 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-26673225
5.
Autism associated with low 5-hydroxyindolacetic acid in CSF and the heterozygous SLC6A4 gene Gly56Ala plus 5-HTTLPR L/L promoter variants.
Mol Genet Metab
; 102(3): 368-73, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21183371
6.
Implementation of SCID Screening in Denmark.
Int J Neonatal Screen
; 7(3)2021 Aug 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34449527
7.
Development of a Multiplex Real-Time PCR Assay for the Newborn Screening of SCID, SMA, and XLA.
Int J Neonatal Screen
; 5(4): 39, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-33072998
8.
Differences in 5-HT2A and mGlu2 Receptor Expression Levels and Repressive Epigenetic Modifications at the 5-HT2A Promoter Region in the Roman Low- (RLA-I) and High- (RHA-I) Avoidance Rat Strains.
Mol Neurobiol
; 55(3): 1998-2012, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28265857
9.
In vivo quantification of cerebral translocator protein binding in humans using 6-chloro-2-(4'-123I-iodophenyl)-3-(N,N-diethyl)-imidazo[1,2-a]pyridine-3-acetamide SPECT.
J Nucl Med
; 55(12): 1966-72, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25453044
10.
Autism spectrum disorder associated with low serotonin in CSF and mutations in the SLC29A4 plasma membrane monoamine transporter (PMAT) gene.
Mol Autism
; 5: 43, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25802735