Detalhe da pesquisa
1.
Transmission from vaccinated individuals in a large SARS-CoV-2 Delta variant outbreak.
Cell
; 185(3): 485-492.e10, 2022 02 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35051367
2.
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.
Nat Genet
; 40(9): 1056-8, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18711365
3.
Blended Genome Exome (BGE) as a Cost Efficient Alternative to Deep Whole Genomes or Arrays.
bioRxiv
; 2024 Apr 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38645052
4.
A second generation human haplotype map of over 3.1 million SNPs.
Nature
; 449(7164): 851-61, 2007 Oct 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-17943122
5.
Genome-wide detection and characterization of positive selection in human populations.
Nature
; 449(7164): 913-8, 2007 Oct 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-17943131
6.
Evidence of transmission from fully vaccinated individuals in a large outbreak of the SARS-CoV-2 Delta variant in Provincetown, Massachusetts.
medRxiv
; 2021 Oct 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34704102
7.
Sensitive Detection of Minimal Residual Disease in Patients Treated for Early-Stage Breast Cancer.
Clin Cancer Res
; 26(11): 2556-2564, 2020 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32170028
8.
Development and Validation of a Mass Spectrometry-Based Assay for the Molecular Diagnosis of Mucin-1 Kidney Disease.
J Mol Diagn
; 18(4): 566-71, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27157321
9.
The genomic landscape of pediatric Ewing sarcoma.
Cancer Discov
; 4(11): 1326-41, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25186949
10.
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.
Nat Genet
; 45(3): 299-303, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23396133
11.
DGAT1 mutation is linked to a congenital diarrheal disorder.
J Clin Invest
; 122(12): 4680-4, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23114594
12.
High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing.
Cancer Discov
; 2(1): 82-93, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22585170
13.
Targeted exon sequencing by in-solution hybrid selection.
Curr Protoc Hum Genet
; Chapter 18: Unit 18.4, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20582916
14.
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.
Science
; 316(5829): 1331-6, 2007 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17463246
15.
The structure of haplotype blocks in the human genome.
Science
; 296(5576): 2225-9, 2002 Jun 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-12029063