Author

Hongyu Luo

BGI GenomicsPrimary ORCID profile (0000-0002-1734-4585 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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Hongyu LuoiD1 paper · Baidu (China)

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Jiale XiangiD· 2 shared Zhiyu PengiD· 2 shared Bing HaniD· 1 shared Chengbin Yan· 1 shared Chunming Cui· 1 shared Cui SongiD· 1 shared Cynthia Casson MortoniD· 1 shared Dayong Wang· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Jiale XiangORCID

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2 papers

Recent·Most cited

Molecular diagnosis of non-syndromic hearing loss patients using a stepwise approach

Jing Wang, Jiale Xiang, Lisha Chen, Hongyu Luo, Xiuhua Xu, Nan Li, Chunming Cui, Jing-Jing Xu, Nana Song, Jiguang Peng, Zhiyu Peng

This study uses a stepwise approach combining multiplex PCR and exome sequencing to diagnose 64% of non-syndromic hearing loss patients, identifying 59 molecular diagnoses from 92 unrelated cases.

Scientific Reports · Feb 17, 2021Peer-reviewedGenetic & Genomic Medicine

Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China

Qiuju Wang, Jiale Xiang, Junwei Sun, Yun Sik Yang, Jing Guan, Dayong Wang, Cui Song, Ling Guo, Hongyang Wang, Yaqiu Chen, Junhong Leng, Xiaman Wang, Junqing Zhang, Bing Han, Jing Zou, , Zhiyu Peng

This study shows that adding genetic screening to newborn hearing tests in China improves detection and reduces loss-to-follow-up, with significant benefits for identifying preventable hearing loss.

Genetics in Medicine · Mar 19, 2019Peer-reviewedGenetics