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Author Details
Full Name
Hui Zhao
Affiliation
College of Life Sciences, University of Chinese Academy of Sciences
ORCID
Career Start Year
2007
Papers
28
H Index
23
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34980918
Mendelian randomization analyses support causal relationships between blood metabolites and the gut microbiome.
Nat Genet
2022
33662387
Gut Microbiota Perturbation in IgA Deficiency Is Influenced by IgA-Autoantibody Status.
Gastroenterology
2021
32718321
DNA methylation repels binding of hypoxia-inducible transcription factors to maintain tumor immunotolerance.
Genome Biol
2020
31806420
Metagenomic profiling of the pro-inflammatory gut microbiota in ankylosing spondylitis.
J Autoimmun
2020
31084400
Clinical significance of tumor miR-21, miR-221, miR-143, and miR-106a as biomarkers in patients with osteosarcoma.
Int J Biol Markers
2019
30010932
Genome wide analyses uncover allele-specific RNA editing in human and mouse.
Nucleic Acids Res
2018
28024299
The role of fatty acid β-oxidation in lymphangiogenesis.
Nature
2017
29018189
The gut microbiome in atherosclerotic cardiovascular disease.
Nat Commun
2017
26408641
Metagenomic analysis of faecal microbiome as a tool towards targeted non-invasive biomarkers for colorectal cancer.
Gut
2017
26693899
Genetic heterogeneity after first-line chemotherapy in high-grade serous ovarian cancer.
Eur J Cancer
2016
26574572
CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer.
Endocr Relat Cancer
2016
27533040
Tumour hypoxia causes DNA hypermethylation by reducing TET activity.
Nature
2016
27556229
Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus.
PLoS One
2016
27551723
Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent.
PLoS Med
2016
27135401
Five endometrial cancer risk loci identified through genome-wide association analysis.
Nat Genet
2016
26856890
Relief of hypoxia by angiogenesis promotes neural stem cell differentiation by targeting glycolysis.
EMBO J
2016
27106403
Corrigendum to "Genetic heterogeneity after first-line chemotherapy in high-grade serous ovarian cancer" [Eur J Cancer 53 (2016) 51-64].
Eur J Cancer
2016
27053251
Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry.
Cancer Causes Control
2016
25529635
Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1.
Am J Hum Genet
2015
26330482
Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancer.
Endocr Relat Cancer
2015
26349763
DNA methylation profiling of non-small cell lung cancer reveals a COPD-driven immune-related signature.
Thorax
2015
24105373
Exome sequencing reveals HINT1 mutations as a cause of distal hereditary motor neuropathy.
Eur J Hum Genet
2014
25085081
Mismatch repair deficiency endows tumors with a unique mutation signature and sensitivity to DNA double-strand breaks.
Elife
2014
22343411
Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis.
Hum Mol Genet
2012
21856995
Human polymorphisms at long non-coding RNAs (lncRNAs) and association with prostate cancer risk.
Carcinogenesis
2011
22178994
Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing.
Nat Biotechnol
2011
17943122
A second generation human haplotype map of over 3.1 million SNPs.
Nature
2007
17943131
Genome-wide detection and characterization of positive selection in human populations.
Nature
2007
1 - 28 of 28
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Institute of Medical Research, Northwestern Polytechnical University
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Martha J Shrubsole
Vanderbilt University Medical Center
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