Detalhe da pesquisa
1.
Enhancer release and retargeting activates disease-susceptibility genes.
Nature
; 595(7869): 735-740, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34040254
2.
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia.
Mol Psychiatry
; 28(5): 2071-2080, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-36869225
3.
HEDD: Human Enhancer Disease Database.
Nucleic Acids Res
; 46(D1): D113-D120, 2018 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29077884
4.
Integrated rare variant-based risk gene prioritization in disease case-control sequencing studies.
PLoS Genet
; 13(12): e1007142, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29281626
5.
PGA: post-GWAS analysis for disease gene identification.
Bioinformatics
; 34(10): 1786-1788, 2018 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29300829
6.
Cyclin C regulates adipogenesis by stimulating transcriptional activity of CCAAT/enhancer-binding protein α.
J Biol Chem
; 292(21): 8918-8932, 2017 05 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-28351837
7.
Systems-level analysis of human aging genes shed new light on mechanisms of aging.
Hum Mol Genet
; 25(14): 2934-2947, 2016 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27179790
8.
INK4 locus of the tumor-resistant rodent, the naked mole rat, expresses a functional p15/p16 hybrid isoform.
Proc Natl Acad Sci U S A
; 112(4): 1053-8, 2015 Jan 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-25550505
9.
Transcriptomic dynamics of breast cancer progression in the MMTV-PyMT mouse model.
BMC Genomics
; 18(1): 185, 2017 02 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-28212608
10.
Mapping copy number variation by population-scale genome sequencing.
Nature
; 470(7332): 59-65, 2011 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-21293372
11.
MicroRNA expression and gene regulation drive breast cancer progression and metastasis in PyMT mice.
Breast Cancer Res
; 18(1): 75, 2016 07 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-27449149
12.
The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes.
Genome Res
; 23(5): 749-61, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23478400
13.
Naked mole-rat has increased translational fidelity compared with the mouse, as well as a unique 28S ribosomal RNA cleavage.
Proc Natl Acad Sci U S A
; 110(43): 17350-5, 2013 Oct 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-24082110
14.
SubNet: a Java application for subnetwork extraction.
Bioinformatics
; 29(19): 2509-11, 2013 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23946504
15.
Rare genetic coding variants associated with age-related episodic memory decline implicate distinct memory pathologies in the hippocampus.
medRxiv
; 2024 May 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38826255
16.
Polygenic prediction of human longevity on the supposition of pervasive pleiotropy.
medRxiv
; 2023 Dec 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38168353
17.
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS.
NPJ Genom Med
; 8(1): 17, 2023 Jul 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37463940
18.
Protocol for gene annotation, prediction, and validation of genomic gene expansion.
STAR Protoc
; 3(4): 101692, 2022 12 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36125934
19.
Substance abuse and the risk of severe COVID-19: Mendelian randomization confirms the causal role of opioids but hints a negative causal effect for cannabinoids.
Front Genet
; 13: 1070428, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36583016
20.
Identification of genomic indels and structural variations using split reads.
BMC Genomics
; 12: 375, 2011 Jul 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-21787423