Detalhe da pesquisa
1.
Coding mutations in NUS1 contribute to Parkinson's disease.
Proc Natl Acad Sci U S A
; 115(45): 11567-11572, 2018 11 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30348779
2.
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.
Am J Hum Genet
; 93(2): 249-63, 2013 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-23849776
3.
Whole-genome Sequencing Reveals Autooctoploidy in Chinese Sturgeon and Its Evolutionary Trajectories.
Genomics Proteomics Bioinformatics
; 22(1)2024 May 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38862424
4.
The first high-quality chromosome-level genome of the Sipuncula Sipunculus nudus using HiFi and Hi-C data.
Sci Data
; 10(1): 317, 2023 05 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37231051
5.
Microbiota-mediated shaping of mouse spleen structure and immune function characterized by scRNA-seq and Stereo-seq.
J Genet Genomics
; 50(9): 688-701, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37156441
6.
Single-cell and spatiotemporal transcriptomic analyses reveal the effects of microorganisms on immunity and metabolism in the mouse liver.
Comput Struct Biotechnol J
; 21: 3466-3477, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38152123
7.
Low-frequency and rare coding variants of NUS1 contribute to susceptibility and phenotype of Parkinson's disease.
Neurobiol Aging
; 110: 106-112, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34635350
8.
Nutrigenomics reveals potential genetic underpinning of diverse taste preference of Chinese men.
Genes Genomics
; 43(6): 689-699, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33843022
9.
Genome-Wide Association Study of Smoking Behavior Traits in a Chinese Han Population.
Front Psychiatry
; 11: 564239, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33033484
10.
High-throughput sequencing reveals the diversity of TCR ß chain CDR3 repertoire in patients with severe acne.
Mol Immunol
; 120: 23-31, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32045771
11.
GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control study.
Transl Neurodegener
; 9(1): 31, 2020 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32746945
12.
Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing.
J Genet Genomics
; 45(10): 527-538, 2018 10 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-30392784
13.
Identification of MicroRNA Targets of Capsicum spp. Using MiRTrans-a Trans-Omics Approach.
Front Plant Sci
; 8: 495, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28443105
14.
PEAR1 gene polymorphism in a Chinese pedigree with pulmonary thromboembolism.
Medicine (Baltimore)
; 95(51): e5687, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28002340
15.
Deep sequencing of the MHC region in the Chinese population contributes to studies of complex disease.
Nat Genet
; 48(7): 740-6, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27213287
16.
Whole-exome sequencing implicates UBE3D in age-related macular degeneration in East Asian populations.
Nat Commun
; 6: 6687, 2015 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25872646
17.
Genetic diagnosis of two dopa-responsive dystonia families by exome sequencing.
PLoS One
; 9(9): e106388, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25181484
18.
A large-scale screen for coding variants predisposing to psoriasis.
Nat Genet
; 46(1): 45-50, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24212883
19.
Sequencing-based approach identified three new susceptibility loci for psoriasis.
Nat Commun
; 5: 4331, 2014 Jul 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-25006012