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Plos Genetics|September 30, 2024
Prioritizing disease-related rare variants by integrating gene expression dataHanmin Guo, Alexander Eckehart Urban, Wing Hung WongBiorxiv : the Preprint Server for Biology|April 2, 2024
Prioritizing disease-related rare variants by integrating gene expression dataHanmin Guo, Alexander Eckehart Urban, Wing Hung WongResearch Square|May 20, 2024
Prioritizing disease-related rare variants by integrating gene expression dataHanmin Guo, Alexander Eckehart Urban, Wing Hung WongProceedings of the National Academy of Sciences of the United States of America|June 12, 2025
Improving polygenic prediction from whole-genome sequencing data by leveraging predicted epigenomic featuresWanwen Zeng, Hanmin Guo, Qiao Liu, et al.Nature Communications|April 2, 2021
Detecting local genetic correlations with scan statisticsHanmin Guo, James J Li, Qiongshi Lu, et al.Nature Communications|February 14, 2023
Quantifying portable genetic effects and improving cross-ancestry genetic prediction with GWAS summary statisticsJiacheng Miao, Hanmin Guo, Gefei Song, et al.Elife|June 6, 2022
Quantifying concordant genetic effects of de novo mutations on multiple disordersHanmin Guo, Lin Hou, Yu Shi, et al.Proceedings of the National Academy of Sciences of the United States of America|May 11, 2026
Peripheral complement C4 protein in schizophrenia: Association with gene copy number and immune cell subtypesAgnieszka Kalinowski, Claudia Macaubas, Hanmin Guo, et al.Proceedings of the National Academy of Sciences of the United States of America|July 23, 2024
Resolving the 22q11.2 deletion using CTLR-Seq reveals chromosomal rearrangement mechanisms and individual variance in breakpointsBo Zhou, Carolin Purmann, Hanmin Guo, et al.Cell|October 1, 2024
Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disordersBo Zhou, Joseph G Arthur, Hanmin Guo, et al.Pageof 1