Detalhe da pesquisa
1.
A Diagnosis for All Rare Genetic Diseases: The Horizon and the Next Frontiers.
Cell
; 177(1): 32-37, 2019 03 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-30901545
2.
An atlas of combinatorial transcriptional regulation in mouse and man.
Cell
; 140(5): 744-52, 2010 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-20211142
3.
SAMStat 2: quality control for next generation sequencing data.
Bioinformatics
; 39(1)2023 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36637208
4.
Comparative transcriptomics of primary cells in vertebrates.
Genome Res
; 30(7): 951-961, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32718981
5.
An atlas of human long non-coding RNAs with accurate 5' ends.
Nature
; 543(7644): 199-204, 2017 03 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28241135
6.
An expanded phenotype centric benchmark of variant prioritisation tools.
Hum Mutat
; 43(5): 539-546, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35224813
7.
Zika Virus Changes Methylation of Genes Involved in Immune Response and Neural Development in Brazilian Babies Born With Congenital Microcephaly.
J Infect Dis
; 223(3): 435-440, 2021 02 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-32614431
8.
Common and Rare Genetic Variants That Could Contribute to Severe Otitis Media in an Australian Aboriginal Population.
Clin Infect Dis
; 73(10): 1860-1870, 2021 11 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-33693626
9.
Kalign 3: multiple sequence alignment of large data sets.
Bioinformatics
; 2019 Oct 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-31665271
10.
Systematic analysis of transcription start sites in avian development.
PLoS Biol
; 15(9): e2002887, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28873399
11.
A promoter-level mammalian expression atlas.
Nature
; 507(7493): 462-70, 2014 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-24670764
12.
An atlas of active enhancers across human cell types and tissues.
Nature
; 507(7493): 455-461, 2014 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-24670763
13.
Integration of genetics and miRNA-target gene network identified disease biology implicated in tissue specificity.
Nucleic Acids Res
; 46(22): 11898-11909, 2018 12 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30407537
14.
Analysis of the human monocyte-derived macrophage transcriptome and response to lipopolysaccharide provides new insights into genetic aetiology of inflammatory bowel disease.
PLoS Genet
; 13(3): e1006641, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28263993
15.
Identification of novel cerebellar developmental transcriptional regulators with motif activity analysis.
BMC Genomics
; 20(1): 718, 2019 Sep 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-31533632
16.
Shared activity patterns arising at genetic susceptibility loci reveal underlying genomic and cellular architecture of human disease.
PLoS Comput Biol
; 14(3): e1005934, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29494619
17.
Correction to: Relatively frequent switching of transcription start sites during cerebellar development.
BMC Genomics
; 19(1): 39, 2018 01 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29325522
18.
DeepCAGE transcriptomics identify HOXD10 as a transcription factor regulating lymphatic endothelial responses to VEGF-C.
J Cell Sci
; 129(13): 2573-85, 2016 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27199372
19.
The frequent evolutionary birth and death of functional promoters in mouse and human.
Genome Res
; 25(10): 1546-57, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26228054
20.
Discovery of Transcription Factors Novel to Mouse Cerebellar Granule Cell Development Through Laser-Capture Microdissection.
Cerebellum
; 17(3): 308-325, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29307116