Author

Geng Tian

Binzhou Medical UniversityORCID 0000-0001-9939-7287Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:whole-genome sequencing· 2 Approach:benchmark study· 1 Research Focus:database / resource· 1 Research Focus:fine-mapping· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Hou‐Feng ZhengiD· 3 shared Jianguo TaoiD· 3 shared Mengyuan YangiD· 3 shared Mo-Chang Qiu· 3 shared Peng-Lin GuaniD· 3 shared Pianpian ZhaoiD· 3 shared Saber KhederzadehiD· 3 shared Si-Rui GaiiD· 3 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Hou‐Feng ZhengORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJan 18, 2024

GWAS of ~30,000 samples with bone mineral density at multiple skeletal sites and its clinical relevance on fracture prediction, genetic correlations and prioritization of drug targets

Yu Qian, Jiangwei Xia, Pingyu Wang…·Hou‐Feng Zheng

This study performs GWAS on BMD traits and fracture risk using 30,000 UK Biobank samples, identifies novel loci, and prioritizes drug targets for osteoporosis prevention.

1 citation

humanGWAS summary statistics

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Genetic & Genomic MedicinemedRxivPreprintDec 23, 2023

SEAD: an augmented reference panel with 22,134 haplotypes boosts the rare variants imputation and GWAS analysis in Asian population

Mengyuan Yang, Jia-Dong Zhong, Xin Li…·Hou‐Feng Zheng

The paper introduces SEAD, an Asian reference panel that improves rare variant imputation and GWAS analysis, identifying a novel association between SNTG1 and hip BMD.

1 citation

humanwhole-genome sequencing

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GeneticsbioRxivPreprintFeb 6, 2021

Genomic analyses of 10,376 individuals provides comprehensive map of genetic variations, structure and reference haplotypes for Chinese population

Peikuan Cong, Wei-Yang Bai, Jinchen Li…·Hou‐Feng Zheng

The paper presents genomic analyses of 10,376 Chinese individuals, identifying novel genetic variations and providing a reference haplotype map, along with an imputation server for improved accuracy.

3 citations

humanwhole-genome sequencing

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