Detalhe da pesquisa
1.
The Splicing Code Goes Deep.
Cell
; 176(3): 414-416, 2019 01 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-30682368
2.
Modeling RNA-Binding Protein Specificity In Vivo by Precisely Registering Protein-RNA Crosslink Sites.
Mol Cell
; 74(6): 1189-1204.e6, 2019 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-31226278
3.
Integrated analysis of mRNA-seq and miRNA-seq for host susceptibilities to influenza A (H7N9) infection in inbred mouse lines.
Funct Integr Genomics
; 18(4): 411-424, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29564647
4.
Predicting mendelian disease-causing non-synonymous single nucleotide variants in exome sequencing studies.
PLoS Genet
; 9(1): e1003143, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23341771
5.
A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases.
Nucleic Acids Res
; 40(7): e53, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22241780
6.
Reference-informed prediction of alternative splicing and splicing-altering mutations from sequences.
bioRxiv
; 2024 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38586002
7.
Prioritizing genes responsible for host resistance to influenza using network approaches.
BMC Genomics
; 14: 816, 2013 Nov 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-24261899
8.
Systematic dissection of coordinated stromal remodeling identifies Sox10+ glial cells as a therapeutic target in myelofibrosis.
Cell Stem Cell
; 30(6): 832-850.e6, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37267917
9.
Rare coding variants in CHRNB2 reduce the likelihood of smoking.
Nat Genet
; 55(7): 1138-1148, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37308787
10.
A deep catalog of protein-coding variation in 985,830 individuals.
bioRxiv
; 2023 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37214792
11.
WITHDRAWN: Evaluation of next-generation sequencing software in mapping and assembly.
J Hum Genet
; 2011 Jun 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-21677664
12.
Evaluation of next-generation sequencing software in mapping and assembly.
J Hum Genet
; 56(6): 406-14, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21525877
13.
A graph model based study on regulatory impacts of transcription factors of Drosophila melanogaster and comparison across species.
Biochem Biophys Res Commun
; 386(4): 559-62, 2009 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-19538943
14.
Stage-specific requirement for Mettl3-dependent m6A mRNA methylation during haematopoietic stem cell differentiation.
Nat Cell Biol
; 21(6): 700-709, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31061465
15.
A rare variant in MLKL confers susceptibility to ApoE É4-negative Alzheimer's disease in Hong Kong Chinese population.
Neurobiol Aging
; 68: 160.e1-160.e7, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29656768
16.
Mutations in Hnrnpa1 cause congenital heart defects.
JCI Insight
; 3(2)2018 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-29367466
17.
PTPN21 exerts pro-neuronal survival and neuritic elongation via ErbB4/NRG3 signaling.
Int J Biochem Cell Biol
; 61: 53-62, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25681686
18.
Short read mapping for exome sequencing.
Methods Mol Biol
; 1038: 93-111, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23872971