Author details

Full Name

He Zhang

Affiliation

ORCID

Career Start Year

2008

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37208378	Novel start codons introduce novel coding sequences in the human genomes.	Sci Rep	2023
37553261	Target-directed microRNA degradation regulates developmental microRNA expression and embryonic growth in mammals.		2023
36575369	Genome-wide association study reveals the genetic determinism of serum biochemical indicators in ducks.		2022
35589130	RBM33 directs the nuclear export of transcripts containing GC-rich elements.	Genes and Development	2022
36777998	The HUNT study: A population-based cohort for genetic research.	Cell Genom	2022
34608135	Determinants of renal cell carcinoma invasion and metastatic competence.	Nat Commun	2021
33693786	An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population.	Hum Mol Genet	2021
33727701	Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2021
33506979	Serial genomic analysis of endometrium supports the existence of histologically indistinct endometrial cancer precursors.	Journal of Pathology	2021
32668236	Ribosome Recycling by ABCE1 Links Lysosomal Function and Iron Homeostasis to 3' UTR-Directed Regulation and Nonsense-Mediated Decay.	Cell Reports	2020
32699191	A PoleP286R mouse model of endometrial cancer recapitulates high mutational burden and immunotherapy response.	JCI insight	2020
33184234	A ubiquitin ligase mediates target-directed microRNA decay independently of tailing and trimming.	Science	2020
33230300	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2020
32908981	The immune vulnerability landscape of the 2019 Novel Coronavirus, SARS-CoV-2.	bioRxiv	2020
33339817	Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.	Nat Commun	2020
30735131	PUMILIO hyperactivity drives premature aging of <i>Norad</i>-deficient mice.	Elife	2019
31801078	Suppression of Ribosomal Pausing by eIF5A Is Necessary to Maintain the Fidelity of Start Codon Selection.	Cell Reports	2019
31772025	Fbxw7 is a driver of uterine carcinosarcoma by promoting epithelial-mesenchymal transition.	Proc Natl Acad Sci U S A	2019
31488578	miR-26 suppresses adipocyte progenitor differentiation and fat production by targeting .	Genes and Development	2019
30860569	DEFOR: depth- and frequency-based somatic copy number alteration detector.	Bioinformatics	2019
29950491	Loss of <i>Dis3l2</i> partially phenocopies Perlman syndrome in mice and results in up-regulation of <i>Igf2</i> in nephron progenitor cells.	Genes Dev	2018
30124468	Polymerase-mediated ultramutagenesis in mice produces diverse cancers with high mutational load.	Journal of Clinical Investigation	2018
29884728	An Empirical Approach Leveraging Tumorgrafts to Dissect the Tumor Microenvironment in Renal Cell Carcinoma Identifies Missing Link to Prognostic Inflammatory Factors.	Cancer Discov	2018
28209224	Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated WithÂ Coronary ArteryÂ Disease.	J Am Coll Cardiol	2017
28861891	Improving power of association tests using multiple sets of imputed genotypes from distributed reference panels.	Genet Epidemiol	2017
29030403	New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475â¿¿000 Individuals.	Circ Cardiovasc Genet	2017
29083408	Exome-wide association study of plasma lipids in >300,000 individuals.	Nat Genet	2017
29083407	Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease.	Nat Genet	2017
27548312	A reference panel of 64,976 haplotypes for genotype imputation.	Nat Genet	2016
26934567	Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.	N Engl J Med	2016
27618447	Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.	Nat Genet	2016
27595394	Targeting renal cell carcinoma with a HIF-2 antagonist.	Nature	2016
26690388	Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese.	Nat Commun	2015
25740221	Methods for association analysis and meta-analysis of rare variants in families.	Genet Epidemiol	2015
26448296	Kinase Identification with Supervised Laplacian Regularized Least Squares.	PLoS ONE	2015
24507775	Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.	Am J Hum Genet	2014
24336170	Meta-analysis of gene-level tests for rare variant association.	Nat Genet	2014
24728188	No large-effect low-frequency coding variation found for myocardial infarction.	Hum Mol Genet	2014
24633158	Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk.	Nat Genet	2014
24941081	Loss-of-function mutations in APOC3, triglycerides, and coronary disease.	N Engl J Med	2014
24975945	Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations.	Am J Hum Genet	2014
20406677	Analysis of floral transcription factors from Lycoris longituba.	Genomics	2010
18371837	The interaction mechanisms between Saccharomyces cerevisiae and menadione and its application in toxicology study.	Talanta	2008
18191621	The inhibition of Saccharomyces cerevisiae cells by acetic acid quantified by electrochemistry and fluorescence.	Bioelectrochemistry	2008