Detalhe da pesquisa
1.
The genetic architecture of type 2 diabetes.
Nature
; 536(7614): 41-47, 2016 08 04.
Artigo
Inglês
| MEDLINE | ID: mdl-27398621
2.
Association of Patient Characteristics and Tumor Genomics With Clinical Outcomes Among Patients With Non-Small Cell Lung Cancer Using a Clinicogenomic Database.
JAMA
; 321(14): 1391-1399, 2019 04 09.
Artigo
Inglês
| MEDLINE | ID: mdl-30964529
3.
The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease.
PLoS Genet
; 11(4): e1005165, 2015 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-25906071
4.
Association of Broad-Based Genomic Sequencing With Survival Among Patients With Advanced Non-Small Cell Lung Cancer in the Community Oncology Setting.
JAMA
; 320(5): 469-477, 2018 08 07.
Artigo
Inglês
| MEDLINE | ID: mdl-30088010
5.
Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland.
Am J Hum Genet
; 94(5): 710-20, 2014 May 01.
Artigo
Inglês
| MEDLINE | ID: mdl-24768551
6.
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy.
Am J Hum Genet
; 88(2): 183-92, 2011 Feb 11.
Artigo
Inglês
| MEDLINE | ID: mdl-21310275
7.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Nat Genet
; 53(2): 185-194, 2021 02.
Artigo
Inglês
| MEDLINE | ID: mdl-33462484
8.
Real-World Evidence In Support Of Precision Medicine: Clinico-Genomic Cancer Data As A Case Study.
Health Aff (Millwood)
; 37(5): 765-772, 2018 05.
Artigo
Inglês
| MEDLINE | ID: mdl-29733723
9.
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
Sci Data
; 5: 180002, 2018 01 23.
Artigo
Inglês
| MEDLINE | ID: mdl-29360107
10.
A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes.
Diabetes
; 66(11): 2903-2914, 2017 11.
Artigo
Inglês
| MEDLINE | ID: mdl-28838971
11.
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
Sci Data
; 4: 170179, 2017 12 19.
Artigo
Inglês
| MEDLINE | ID: mdl-29257133
12.
Author Correction: Genetics of 35 blood and urine biomarkers in the UK Biobank.
Nat Genet
; 53(11): 1622, 2021 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-34608296
13.
Implementing an Electronic End-of-Life Chemotherapy Utilization Measure.
J Oncol Pract
; 15(4): 220-223, 2019 04.
Artigo
Inglês
| MEDLINE | ID: mdl-30883256
14.
Disparities in broad-based genomic sequencing for patients with advanced non-small cell lung cancer.
J Geriatr Oncol
; 10(4): 669-672, 2019 07.
Artigo
Inglês
| MEDLINE | ID: mdl-30718180
15.
Evaluating empirical bounds on complex disease genetic architecture.
Nat Genet
; 45(12): 1418-27, 2013 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-24141362
16.
Genome engineering using the CRISPR-Cas9 system.
Nat Protoc
; 8(11): 2281-2308, 2013 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-24157548
17.
DNA targeting specificity of RNA-guided Cas9 nucleases.
Nat Biotechnol
; 31(9): 827-32, 2013 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-23873081
18.
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes.
Nat Genet
; 45(11): 1380-5, 2013 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-24097065
19.
Three-dimensional genome architecture influences partner selection for chromosomal translocations in human disease.
PLoS One
; 7(9): e44196, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-23028501
20.
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction.
Nat Genet
; 43(8): 801-5, 2011 Jul 24.
Artigo
Inglês
| MEDLINE | ID: mdl-21775993