Pak Chung Sham

According to our database1, Pak Chung Sham authored at least 36 papers between 2002 and 2024.

Collaborative distances:
  • Dijkstra number2 of four.
  • Erdős number3 of four.

Timeline

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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

vSampler: fast and annotation-based matched variant sampling tool.
Bioinform., 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

Methods and resources to access mutation-dependent effects on cancer drug treatment.
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

Predicting regulatory variants with composite statistic.
Bioinform., 2016

Inheritance-mode specific pathogenicity prioritization (ISPP) for human protein coding genes.
Bioinform., 2016

2015
MGAS: a powerful tool for multivariate gene-based genome-wide association analysis.
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
dbPSHP: a database of recent positive selection across human populations.
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
Correlated evolution of transcription factors and their binding sites.
Bioinform., 2011

2010
SKM-SNP: SNP markers detection method.
J. Biomed. Informatics, 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
Unidimensional nonnegative scaling for genome-wide Linkage Disequilibrium maps.
Int. J. Bioinform. Res. Appl., 2008

2007
Constrained unidimensional scaling with application to genomics.
Comput. Stat. Data Anal., 2007

Combining functional and linkage disequilibrium information in the selection of tag SNPs.
Bioinform., 2007

WHAP: haplotype-based association analysis.
Bioinform., 2007

IGG: A tool to integrate GeneChips for genetic studies.
Bioinform., 2007

2006
Clustering of SNP Data with Application to Genomics.
Proceedings of the Workshops Proceedings of the 6th IEEE International Conference on Data Mining (ICDM 2006), 2006

2005
CLUSTAG: hierarchical clustering and graph methods for selecting tag SNPs.
Bioinform., 2005

2003
Generic number systems and haplotype analysis.
Comput. Methods Programs Biomed., 2003

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits.
Bioinform., 2003

2002
GENECOUNTING: haplotype analysis with missing genotypes.
Bioinform., 2002

Analytic approaches to twin data using structural equation models.
Briefings Bioinform., 2002


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