Detalhe da pesquisa
1.
Identifying and Interpreting Apparent Neanderthal Ancestry in African Individuals.
Cell
; 180(4): 677-687.e16, 2020 02 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32004458
2.
Evolutionary history and adaptation from high-coverage whole-genome sequences of diverse African hunter-gatherers.
Cell
; 150(3): 457-69, 2012 Aug 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-22840920
3.
Deep sequencing of 1320 genes reveals the landscape of protein-truncating variants and their contribution to psoriasis in 19,973 Chinese individuals.
Genome Res
; 31(7): 1150-1158, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-34155038
4.
Spatially Resolved Metabolomics Based on Air-Flow-Assisted Desorption Electrospray Ionization-Mass Spectrometry Imaging Reveals Region-Specific Metabolic Alterations in Diabetic Encephalopathy.
J Proteome Res
; 20(7): 3567-3579, 2021 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34137614
5.
Robust Inference of Identity by Descent from Exome-Sequencing Data.
Am J Hum Genet
; 99(5): 1106-1116, 2016 Nov 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27745837
6.
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants.
Nature
; 493(7431): 216-20, 2013 Jan 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-23201682
7.
Human RECQ Helicase Pathogenic Variants, Population Variation and "Missing" Diseases.
Hum Mutat
; 38(2): 193-203, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27859906
8.
Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genome.
Hum Mol Genet
; 24(5): 1225-33, 2015 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25324539
9.
Characteristics of neutral and deleterious protein-coding variation among individuals and populations.
Am J Hum Genet
; 95(4): 421-36, 2014 Oct 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25279984
10.
Rare variation facilitates inferences of fine-scale population structure in humans.
Mol Biol Evol
; 32(3): 653-60, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25415970
11.
Global and disease-associated genetic variation in the human Fanconi anemia gene family.
Hum Mol Genet
; 23(25): 6815-25, 2014 Dec 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-25104853
12.
Selection and adaptation in the human genome.
Annu Rev Genomics Hum Genet
; 14: 467-89, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23834317
13.
Identification of Key Genes of Fruit Shape Variation in Jujube with Integrating Elliptic Fourier Descriptors and Transcriptome.
Plants (Basel)
; 13(9)2024 May 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38732489
14.
Identification of copy number variation hotspots in human populations.
Am J Hum Genet
; 87(4): 494-504, 2010 Oct 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-20920665
15.
Genomic dissection of population substructure of Han Chinese and its implication in association studies.
Am J Hum Genet
; 85(6): 762-74, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19944404
16.
Present Y chromosomes reveal the ancestry of Emperor CAO Cao of 1800 years ago.
J Hum Genet
; 57(3): 216-8, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22189622
17.
Association of polymorphisms in the solute carrier organic anion transporter family member 1B1 gene with essential hypertension in the Uyghur population.
Ann Hum Genet
; 75(2): 305-11, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21309757
18.
Kinetic cellular phenotypic profiling: prediction, identification, and analysis of bioactive natural products.
Anal Chem
; 83(17): 6518-26, 2011 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21793491
19.
Association of a BLVRA common polymorphism with essential hypertension and blood pressure in Kazaks.
Clin Exp Hypertens
; 33(5): 294-8, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21721974
20.
Spatial-resolved metabolomics reveals tissue-specific metabolic reprogramming in diabetic nephropathy by using mass spectrometry imaging.
Acta Pharm Sin B
; 11(11): 3665-3677, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34900545