Pak Chung Sham
According to our database1,
Pak Chung Sham
authored at least 36 papers
between 2002 and 2024.
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Bibliography
2024
Estimation of causal effects of genes on complex traits using a Bayesian-network-based framework applied to GWAS data.
Nat. Mac. Intell., 2024
2023
Inferring CTCF-binding patterns and anchored loops across human tissues and cell types.
Patterns, August, 2023
2022
VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseases.
Nucleic Acids Res., 2022
2021
A framework to decipher the genetic architecture of combinations of complex diseases: applications in cardiovascular medicine.
Bioinform., November, 2021
2020
QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes.
Nucleic Acids Res., 2020
CAUSALdb: a database for disease/trait causal variants identified using summary statistics of genome-wide association studies.
Nucleic Acids Res., 2020
Briefings Bioinform., 2020
2019
A powerful conditional gene-based association approach implicated functionally important genes for schizophrenia.
Bioinform., 2019
Evaluation of tools for highly variable gene discovery from single-cell RNA-seq data.
Briefings Bioinform., 2019
2018
GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits.
Nucleic Acids Res., 2018
A powerful approach reveals numerous expression quantitative trait haplotypes in multiple tissues.
Bioinform., 2018
2017
mTCTScan: a comprehensive platform for annotation and prioritization of mutations affecting drug sensitivity in cancers.
Nucleic Acids Res., 2017
2016
GWASdb v2: an update database for human genetic variants identified by genome-wide association studies.
Nucleic Acids Res., 2016
Inheritance-mode specific pathogenicity prioritization (ISPP) for human protein coding genes.
Bioinform., 2016
2015
Bioinform., 2015
Exploring the function of genetic variants in the non-coding genomic regions: approaches for identifying human regulatory variants affecting gene expression.
Briefings Bioinform., 2015
2014
Nucleic Acids Res., 2014
2013
GWAS3D: detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications.
Nucleic Acids Res., 2013
2012
GWASdb: a database for human genetic variants identified by genome-wide association studies.
Nucleic Acids Res., 2012
2011
Bioinform., 2011
2010
FastPval: a fast and memory efficient program to calculate very low <i>P</i>-values from empirical distribution.
Bioinform., 2010
2009
IGG3: a tool to rapidly integrate large genotype datasets for whole-genome imputation and individual-level meta-analysis.
Bioinform., 2009
2008
Int. J. Bioinform. Res. Appl., 2008
2007
Comput. Stat. Data Anal., 2007
Combining functional and linkage disequilibrium information in the selection of tag SNPs.
Bioinform., 2007
2006
Proceedings of the Workshops Proceedings of the 6th IEEE International Conference on Data Mining (ICDM 2006), 2006
2005
Bioinform., 2005
2003
Comput. Methods Programs Biomed., 2003
Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits.
Bioinform., 2003
2002
Briefings Bioinform., 2002