Detalhe da pesquisa
1.
WashU Epigenome Browser update 2019.
Nucleic Acids Res
; 47(W1): W158-W165, 2019 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31165883
2.
Tissue-specific DNA methylation is conserved across human, mouse, and rat, and driven by primary sequence conservation.
BMC Genomics
; 18(1): 724, 2017 Sep 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28899353
3.
An epigenetic signature in peripheral blood associated with the haplotype on 17q21.31, a risk factor for neurodegenerative tauopathy.
PLoS Genet
; 10(3): e1004211, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24603599
4.
Decision tree analysis of genetic risk for clinically heterogeneous Alzheimer's disease.
BMC Neurol
; 15: 47, 2015 Mar 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-25880661
5.
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.
Neurogenetics
; 14(1): 11-22, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23334463
6.
Human placental cytotrophoblast epigenome dynamics over gestation and alterations in placental disease.
Dev Cell
; 56(9): 1238-1252.e5, 2021 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33891899
7.
Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export.
Nat Genet
; 47(6): 579-81, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25938945
8.
A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsy.
JAMA Neurol
; 72(4): 414-22, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25706306
9.
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice.
Nat Genet
; 45(9): 1077-82, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23913003
10.
Epigenomic annotation of genetic variants using the Roadmap Epigenome Browser.
Nat Biotechnol
; 33(4): 345-6, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25690851