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Author Details
Full Name
Yi Wang
Affiliation
the Children's Hospital Affiliated to Xi'an Jiaotong University
ORCID
Career Start Year
2006
Papers
46
H Index
20
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36880243
[Predictive value of Pv-aCO<sub>2</sub>/Ca-vO<sub>2</sub> combined blood lactate concentration for primary peritonitis-related septic shock in children].
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue
2023
34999338
Associations between polygenic risk scores and amplitude of low-frequency fluctuation of inferior frontal gyrus in schizophrenia.
J Psychiatr Res
2022
35499292
Prediction of lung cancer risk in Chinese population with genetic-environment factor using extreme gradient boosting.
Cancer Med
2022
36107107
Electrical activation of the pedunculopontine tegmental nucleus modulates the neuronal activities of the subthalamic nucleus and the substantia nigra pars reticulata in anesthetized rats.
J Neurosci Res
2022
36060302
Exome sequencing identifies rare mutations of <i>LDLR</i> and <i>QTRT1</i> conferring risk for early-onset coronary artery disease in Chinese.
Natl Sci Rev
2022
33966706
[Research Progress of the Effects of Vitamin D Supplementation on Glycemic Control and Adverse Maternal-neonatal Outcomes in Gestational Diabetes Mellitus Patients].
Zhongguo Yi Xue Ke Xue Yuan Xue Bao
2021
36939745
Using Composite Phenotypes to Reveal Hidden Physiological Heterogeneity in High-Altitude Acclimatization in a Chinese Han Longitudinal Cohort.
Phenomics
2021
35048853
Associations between hemispheric asymmetry and schizophrenia-related risk genes in people with schizophrenia and people at a genetic high risk of schizophrenia.
Br J Psychiatry
2021
34416338
The HuaBiao project: whole-exome sequencing of 5000 Han Chinese individuals.
J Genet Genomics
2021
31400761
Trans-acting non-synonymous variant of FOXA1 predisposes to hepatocellular carcinoma through modulating FOXA1-ERα transcriptional program and may have undergone natural selection.
Carcinogenesis
2020
33194084
Effect of <i>ERCC2</i> rs13181 and rs1799793 polymorphisms and environmental factors on the prognosis of patients with lung cancer.
Am J Transl Res
2020
32958750
Polygenic risk for autism spectrum disorder affects left amygdala activity and negative emotion in schizophrenia.
Transl Psychiatry
2020
31024629
Robust Reference Powered Association Test of Genome-Wide Association Studies.
Front Genet
2019
28249201
Genome-wide screening for highly discriminative SNPs for personal identification and their assessment in world populations.
Forensic Sci Int Genet
2017
26832887
Inferring the Dynamics of Effective Population Size Using Autosomal Genomes.
Sci Rep
2016
27498855
MtDNA analysis reveals enriched pathogenic mutations in Tibetan highlanders.
Sci Rep
2016
26368009
HIF2A Variants Were Associated with Different Levels of High-Altitude Hypoxia among Native Tibetans.
PLoS One
2015
25170956
Y chromosomes of 40% Chinese descend from three Neolithic super-grandfathers.
PLoS One
2014
25501874
Two functional loci in the promoter of EPAS1 gene involved in high-altitude adaptation of Tibetans.
Sci Rep
2014
25313938
Influences of APOA5 variants on plasma triglyceride levels in Uyghur population.
PLoS One
2014
25151233
A functional polymorphism affecting the APOA5 gene expression is causally associated with plasma triglyceride levels conferring coronary atherosclerosis risk in Han Chinese Population.
Biochim Biophys Acta
2014
20643764
A polymorphism rs17336700 in the PSMD7 gene is associated with ankylosing spondylitis in Chinese subjects.
Ann Rheum Dis
2011
21998705
Major population expansion of East Asians began before neolithic time: evidence of mtDNA genomes.
PLoS One
2011
21904623
Human migration through bottlenecks from Southeast Asia into East Asia during Last Glacial Maximum revealed by Y chromosomes.
PLoS One
2011
21698238
Replication of putative susceptibility loci from genome-wide association studies associated with coronary atherosclerosis in Chinese Han population.
PLoS One
2011
20485444
Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.
J Hum Genet
2010
20920665
Identification of copy number variation hotspots in human populations.
Am J Hum Genet
2010
18180757
A high-density single-nucleotide polymorphism screen of 23 candidate genes in attention deficit hyperactivity disorder: suggesting multiple susceptibility genes among Chinese Han population.
Mol Psychiatry
2009
19458053
Association of XPD polymorphisms with severe toxicity in non-small cell lung cancer patients in a Chinese population.
Clin Cancer Res
2009
19126779
Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease.
Hum Mol Genet
2009
19238116
Common variants of four bilirubin metabolism genes and their association with serum bilirubin and coronary artery disease in Chinese Han population.
Pharmacogenet Genomics
2009
19262575
Polymorphisms in the interleukin 3 gene show strong association with susceptibility to Graves' disease in Chinese population.
Genes Immun
2009
19284636
Missing call bias in high-throughput genotyping.
BMC Genomics
2009
19243019
Association of polymorphisms in four bilirubin metabolism genes with serum bilirubin in three Asian populations.
Hum Mutat
2009
18818557
Association of human aryl hydrocarbon receptor gene polymorphisms with risk of lung cancer among cigarette smokers in a Chinese population.
Pharmacogenet Genomics
2009
18767114
Association between polymorphisms in the GSTA4 gene and risk of lung cancer: a case-control study in a Southeastern Chinese population.
Mol Carcinog
2009
18692935
Genetic variants in GTF2H1 and risk of lung cancer: a case-control analysis in a Chinese population.
Lung Cancer
2009
17870204
Polymorphisms in hMLH1 and risk of early-onset lung cancer in a southeast Chinese population.
Lung Cancer
2008
18212820
A spatial analysis of genetic structure of human populations in China reveals distinct difference between maternal and paternal lineages.
Eur J Hum Genet
2008
17971837
Exploration of gene-gene interaction effects using entropy-based methods.
Eur J Hum Genet
2008
17157823
Effect of mu-opioid receptor gene polymorphisms on heroin-induced subjective responses in a Chinese population.
Biol Psychiatry
2007
17943131
Genome-wide detection and characterization of positive selection in human populations.
Nature
2007
17943122
A second generation human haplotype map of over 3.1 million SNPs.
Nature
2007
17630283
Dissecting linkage disequilibrium in African-American genomes: roles of markers and individuals.
Mol Biol Evol
2007
16432195
Linkage disequilibrium sharing and haplotype-tagged SNP portability between populations.
Proc Natl Acad Sci U S A
2006
16835333
Polymorphisms in the two helicases ERCC2/XPD and ERCC3/XPB of the transcription factor IIH complex and risk of lung cancer: a case-control analysis in a Chinese population.
Cancer Epidemiol Biomarkers Prev
2006
1 - 46 of 46
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Shanghai Fifth People's Hospital, Institutes of Biomedical Sciences, Fudan University
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Yong Loo Lin School of Medicine, National University of Singapore
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Obstetrics and Gynecology Hospital, Human Phenome Institute, Fudan University
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Shi Yan
Qilu Hospital of Shandong University
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Mark F Leppert
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