Author details

Full Name

Yao Hu

Affiliation

ORCID

Career Start Year

2015

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
37601974	Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries.	Cell Genom	2023
37648373	Ancestral diversity in lipoprotein(a) studies helps address evidence gaps.	Open Heart	2023
35263625	Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits.	Am J Hum Genet	2022
35394225	Renal functional and interstitial fibrotic assessment with non-Gaussian diffusion kurtosis imaging.	Insights into Imaging	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
36330478	Bosniak classification of cystic renal masses, version 2019: Is it helpful to incorporate the diffusion weighted imaging characteristic of lesions into the guideline?	Frontiers in Oncology	2022
34727735	Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project.	Stroke	2022
34553764	Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.	Hum Mol Genet	2022
34951656	Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study.	Diabetologia	2022
34875531	NFI, a clinical scoring tool for predicting non-alcoholic fatty liver in the Chinese population.	Public Health	2022
34517814	Correction to: Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) Study.	BMC Genomics	2021
34107879	Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.	BMC Genomics	2021
34047475	A genome-wide association study identifies novel association between genetic variants in GGT7 and LINC00944 and hypertension.	Clinical and Translational Medicine	2021
33887194	Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.	Am J Hum Genet	2021
34087167	Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.	Am J Hum Genet	2021
34337551	BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion.	HGG Adv	2021
31484043	Assessment of renal fibrosis in a rat model of unilateral ureteral obstruction with diffusion kurtosis imaging: Comparison with Î±-SMA expression and <sup>18</sup>F-FDG PET.	Magn Reson Imaging	2020
32323504	Role of Chemical Exchange Saturation Transfer and Magnetization Transfer MRI in Detecting Metabolic and Structural Changes of Renal Fibrosis in an Animal Model at 3T.	Korean J Radiol	2020
32226016	Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.	PLoS Genet	2020
31217584	Genetic analyses of diverse populations improves discovery for complex traits.	Nature	2019
31564435	Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program.	Am J Hum Genet	2019
30552288	Erythrocyte PUFAs, circulating acylcarnitines, and metabolic syndrome risk: a prospective study in Chinese.	Journal of Lipid Research	2019
30240758	Whole-tumor histogram analysis of non-Gaussian distribution DWI parameters to differentiation of pancreatic neuroendocrine tumors from pancreatic ductal adenocarcinomas.	Magnetic Resonance Imaging	2019
30087067	Whole-Tumor Quantitative Apparent Diffusion Coefficient Histogram and Texture Analysis to Differentiation of Minimal Fat Angiomyolipoma from Clear Cell Renal Cell Carcinoma.	Academic Radiology	2019
30277628	Volumetric Apparent Diffusion Coefficient Histogram Analysis in Differentiating Intrahepatic Mass-Forming Cholangiocarcinoma From Hepatocellular Carcinoma.	Journal of Magnetic Resonance Imaging	2019
29273807	Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
30151864	Differentiation of atypical pancreatic neuroendocrine tumors from pancreatic ductal adenocarcinomas: Using whole-tumor CT texture analysis as quantitative biomarkers.	Cancer Med	2018
29764838	A common TCN1 loss-of-function variant is associated with lower vitamin B12 concentration in African Americans.	Blood	2018
29549330	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29549329	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29733515	Assessment of different mathematical models for diffusion-weighted imaging as quantitative biomarkers for differentiating benign from malignant solid hepatic lesions.	Cancer Medicine	2018
29632382	Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.	Nat Genet	2018
29812980	Subtype Differentiation of Small (â¿¤ 4 cm) Solid Renal Mass Using Volumetric Histogram Analysis of DWI at 3-T MRI.	American Journal of Roentgenology	2018
27768857	Effects of Genetic and Nongenetic Factors on Total and Bioavailable 25(OH)D Responses to Vitamin D Supplementation.	Journal of Clinical Endocrinology and Metabolism	2017
28348047	Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians.	Circ Cardiovasc Genet	2017
28898252	Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.	PLoS Med	2017
28334899	Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.	Hum Mol 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
26932504	Meta-analysis of genome-wide association studies identifies three novel loci for saturated fatty acids in East Asians.	European Journal of Nutrition	2017
27859853	Monoexponential, biexponential, and stretched exponential diffusion-weighted imaging models: Quantitative biomarkers for differentiating renal clear cell carcinoma and minimal fat angiomyolipoma.	Journal of Magnetic Resonance Imaging	2017
28298293	Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations.	J Lipid Res	2017
27516387	Coding-sequence variants are associated with blood lipid levels in 14,473 Chinese.	Human Molecular Genetics	2016
25694350	A dose-response study of vitamin D3 supplementation in healthy Chinese: a 5-arm randomized, placebo-controlled trial.	European Journal of Nutrition	2016
27388475	Early Prediction of Developing Type 2 Diabetes by Plasma Acylcarnitines: A Population-Based Study.	Diabetes Care	2016
26744325	Genome-wide meta-analyses identify novel loci associated with n-3 and n-6 polyunsaturated fatty acid levels in Chinese and European-ancestry populations.	Human Molecular Genetics	2016
26590599	Elevated plasma tumor necrosis factor-Î± receptor 2 and resistin are associated with increased incidence of kidney function decline in Chinese adults.	Endocrine	2016
27577511	Adrenal and nephrogenic hypertension: an image quality study of low tube voltage, low-concentration contrast media combined with adaptive statistical iterative reconstruction.	International Journal of Clinical Practice	2016
26535628	Mutational analysis of BRCA1/2 gene and pathologic characteristics from Kazakh population with sporadic breast cancer in northwestern China.	Genetics and Molecular Research	2015
26813132	[Association of single nucleotide polymorphisms of IL-6 gene with longevity in Uyghurs in Xinjiang].	National Medical Journal of China	2015