Author

Hongzhi Cao

BGI Group (China)ORCID 0009-0007-2454-1003Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Hongzhi Cao1 paper · Ocean University of China

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Approach:benchmark study· 1 Research Focus:differential expression· 1 Research Focus:fine-mapping· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Abdel AbdellaouiiD· 1 shared Albert Hofman DiD· 1 shared Alexandros KanterakisiD· 1 shared Anne BolandiD· 1 shared Anton J.M. de CraeniD· 1 shared Artem KimiD· 1 shared Arthur KoiD· 1 shared Barbera D. C. van SchaikiD· 1 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Abdel AbdellaouiORCID

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2 papers

Recent·Most cited

GeneticsAnnals of the Rheumatic DiseasesPeer-reviewedApr 1, 2019

Sequencing of the MHC region defines HLA-DQA1 as the major independent risk for anti-citrullinated protein antibodies (ACPA)-positive rheumatoid arthritis in Han population

Jianping Guo, Tao Zhang, Hongzhi Cao…·Zhanguo Li

This study identifies HLA-DQA1 as the major independent genetic risk for ACPA-positive RA in Han population through MHC region sequencing and HLA-typing.

39 citationstop 5%

humanwhole-genome sequencing

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GeneticsBrainPeer-reviewedOct 29, 2018

Integrated Clinical and Omics Approach to Rare Diseases: Novel Genes and Oligogenic Inheritance in Holoprosencephaly

Artem Kim, Clara Savary, Christèle Dubourg…·Tania Attié‐Bitach

This study identifies novel HPE genes and oligogenic inheritance patterns in holoprosencephaly by integrating clinical data with exome sequencing and gene prioritization.

62 citationstop 2%

humanwhole-exome sequencing

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