Detalhe da pesquisa
1.
Analysis of protein-coding genetic variation in 60,706 humans.
Nature
; 536(7616): 285-91, 2016 08 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-27535533
2.
De novo mutations in schizophrenia implicate synaptic networks.
Nature
; 506(7487): 179-84, 2014 Feb 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-24463507
3.
A polygenic burden of rare disruptive mutations in schizophrenia.
Nature
; 506(7487): 185-90, 2014 Feb 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-24463508
4.
Synaptic, transcriptional and chromatin genes disrupted in autism.
Nature
; 515(7526): 209-15, 2014 Nov 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-25363760
5.
Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Nature
; 485(7397): 242-5, 2012 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-22495311
6.
Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence.
N Engl J Med
; 371(26): 2477-87, 2014 Dec 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-25426838
7.
Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder.
Am J Hum Genet
; 93(4): 607-19, 2013 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24094742
8.
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data.
Circ Res
; 115(10): 884-896, 2014 Oct 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-25205790
9.
Genomic aberrations in cervical adenocarcinomas in Hong Kong Chinese women.
Int J Cancer
; 137(4): 776-83, 2015 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25626421
10.
Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth.
Am J Hum Genet
; 91(4): 597-607, 2012 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23040492
11.
zCall: a rare variant caller for array-based genotyping: genetics and population analysis.
Bioinformatics
; 28(19): 2543-5, 2012 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22843986
12.
Recovering key biological constituents through sparse representation of gene expression.
Bioinformatics
; 27(5): 655-61, 2011 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21258061
13.
PANDORA: analysis of protein and peptide sets through the hierarchical integration of annotations.
Nucleic Acids Res
; 38(Web Server issue): W84-9, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20444873
14.
Exposing the co-adaptive potential of protein-protein interfaces through computational sequence design.
Bioinformatics
; 26(18): 2266-72, 2010 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20679332
15.
SPRINT: side-chain prediction inference toolbox for multistate protein design.
Bioinformatics
; 26(19): 2466-7, 2010 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20685957
16.
A holistic approach for suppression of COVID-19 spread in workplaces and universities.
PLoS One
; 16(8): e0254798, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34383766
17.
Toward a Mobile Platform for Real-world Digital Measurement of Depression: User-Centered Design, Data Quality, and Behavioral and Clinical Modeling.
JMIR Ment Health
; 8(8): e27589, 2021 Aug 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34383685
18.
Design of multispecific protein sequences using probabilistic graphical modeling.
Proteins
; 78(3): 530-47, 2010 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19842166
19.
Viral adaptation to host: a proteome-based analysis of codon usage and amino acid preferences.
Mol Syst Biol
; 5: 311, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19888206
20.
Tradeoff between stability and multispecificity in the design of promiscuous proteins.
PLoS Comput Biol
; 5(12): e1000627, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20041208