Detalhe da pesquisa
1.
FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.
Nucleic Acids Res
; 51(D1): D1300-D1311, 2023 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36350676
2.
Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.
Am J Hum Genet
; 108(7): 1350-1355, 2021 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34115965
3.
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
Am J Hum Genet
; 108(5): 874-893, 2021 05 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33887194
4.
CoFeSe2 @DMSA@FA Nanocatalyst for Amplification of Oxidative Stress to Achieve Multimodal Tumor Therapy.
Chembiochem
; 25(2): e202300631, 2024 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37930640
5.
Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program.
Am J Hum Genet
; 105(4): 706-718, 2019 10 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31564435
6.
SAIGEgds-an efficient statistical tool for large-scale PheWAS with mixed models.
Bioinformatics
; 37(5): 728-730, 2021 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32898220
7.
A fully adjusted two-stage procedure for rank-normalization in genetic association studies.
Genet Epidemiol
; 43(3): 263-275, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30653739
8.
A high-resolution HLA imputation system for the Taiwanese population: a study of the Taiwan Biobank.
Pharmacogenomics J
; 20(5): 695-704, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32042094
9.
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
Am J Hum Genet
; 108(6): 1165, 2021 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34087167
10.
Genome-wide minor histocompatibility matching as related to the risk of graft-versus-host disease.
Blood
; 129(6): 791-798, 2017 02 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27872059
11.
A functional FePt@MOFs (MIL-101(Fe)) nano-platform for high efficient colorimetric determination of H2O2.
Analyst
; 144(8): 2716-2724, 2019 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30865189
12.
Capture and separation of circulating tumor cells using functionalized magnetic nanocomposites with simultaneous in situ chemotherapy.
Nanotechnology
; 30(28): 285706, 2019 Jul 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30849773
13.
Characterizing the noncovalent binding behavior of tartrazine to lysozyme: A combined spectroscopic and computational analysis.
J Biochem Mol Toxicol
; 33(3): e22258, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30368991
14.
A facile preparation of FePt-loaded few-layer MoS2 nanosheets nanocomposites (F-MoS2-FePt NCs) and their application for colorimetric detection of H2O2 in living cells.
J Nanobiotechnology
; 17(1): 38, 2019 Mar 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30866971
15.
HLA-DPB1 and HLA class I confer risk of and protection from narcolepsy.
Am J Hum Genet
; 96(1): 136-46, 2015 Jan 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-25574827
16.
SeqArray-a storage-efficient high-performance data format for WGS variant calls.
Bioinformatics
; 33(15): 2251-2257, 2017 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28334390
17.
pH-Responsive, Self-Sacrificial Nanotheranostic Agent for Potential In Vivo and In Vitro Dual Modal MRI/CT Imaging, Real-Time, and In Situ Monitoring of Cancer Therapy.
Bioconjug Chem
; 28(2): 400-409, 2017 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28042941
18.
Phenome-wide association study maps new diseases to the human major histocompatibility complex region.
J Med Genet
; 53(10): 681-9, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27287392
19.
Eigenanalysis of SNP data with an identity by descent interpretation.
Theor Popul Biol
; 107: 65-76, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26482676
20.
Genetic variation associated with circulating monocyte count in the eMERGE Network.
Hum Mol Genet
; 22(10): 2119-27, 2013 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23314186