Author details

Full Name

Gao Wang

Affiliation

ORCID

Career Start Year

2010

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37425935	Fast and flexible joint fine-mapping of multiple traits via the Sum of Single Effects model.	bioRxiv	2024
36788145	Rare-variant association analysis reveals known and new age-related hearing loss genes.	Eur J Hum Genet	2023
37418505	A flexible empirical Bayes approach to multivariate multiple regression, and its improved accuracy in predicting multi-tissue gene expression from genotypes.	PLoS Genet	2023
36896235	The genetic contribution of the X chromosome in age-related hearing loss.	Front Genet	2023
37377600	Variants in <i>JAZF1</i> are associated with asthma, type 2 diabetes, and height in the United Kingdom biobank population.	Front Genet	2023
35853082	Fine-mapping from summary data with the "Sum of Single Effects" model.	PLoS Genet	2022
36183486	Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology.	EBioMedicine	2022
33499903	Exploiting the GTEx resources to decipher the mechanisms at GWAS loci.	Genome Biol	2021
32732423	Allele-specific open chromatin in human iPSC neurons elucidates functional disease variants.	Science	2020
37220626	A simple new approach to variable selection in regression, with application to genetic fine mapping.	J R Stat Soc Series B Stat Methodol	2020
32601472	Genetic analyses support the contribution of mRNA N<sup>6</sup>-methyladenosine (m<sup>6</sup>A) modification to human disease heritability.	Nat Genet	2020
32964524	Fine-mapping and QTL tissue-sharing information improves the reliability of causal gene identification.	Genetic Epidemiology	2020
32913075	Cell type-specific genetic regulation of gene expression across human tissues.	Science	2020
32740652	A quantitative trait rare variant nonparametric linkage method with application to age-at-onset of Alzheimer's disease.	Eur J Hum Genet	2020
30811390	Script of Scripts: A pragmatic workflow system for daily computational research.	PLoS Computational Biology	2019
31585107	A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data.	Am J Hum Genet	2019
30478440	Flexible statistical methods for estimating and testing effects in genomic studies with multiple conditions.	Nat Genet	2019
29790910	SoS Notebook: an interactive multi-language data analysis environment.	Bioinformatics	2018
28157542	Erratum: The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data.	Am J Hum Genet	2017
28669402	SEQSpark: A Complete Analysis Tool for Large-Scale Rare Variant Association Studies Using Whole-Genome and Exome Sequence Data.	Am J Hum Genet	2017
28065470	The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data.	Am J Hum Genet	2017
27666372	Guidelines for Large-Scale Sequence-Based Complex Trait Association Studies: Lessons Learned from the NHLBI Exome Sequencing Project.	Am J Hum Genet	2016
26757982	Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project.	Eur J Hum Genet	2016
27418160	Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms.	J Am Heart Assoc	2016
26121085	Rare A2ML1 variants confer susceptibility to otitis media.	Nat Genet	2015
25873013	Collapsed haplotype pattern method for linkage analysis of next-generation sequence data.	Eur J Hum Genet	2015
25491636	Challenges and solutions for gene identification in the presence of familial locus heterogeneity.	Eur J Hum Genet	2015
26177964	Generation of sequence-based data for pedigree-segregating Mendelian or Complex traits.	Bioinformatics	2015
24778108	Power analysis and sample size estimation for sequence-based association studies.	Bioinformatics	2014
25278557	RNF213 rare variants in an ethnically diverse population with Moyamoya disease.	Stroke	2014
24360806	Rare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data.	Am J Hum Genet	2014
24336645	PhenoMan: phenotypic data exploration, selection, management and quality control for association studies of rare and common variants.	Bioinformatics	2014
24791902	Variant association tools for quality control and analysis of large-scale sequence and genotyping array data.	Am J Hum Genet	2014
23757187	Testing for rare variant associations in the presence of missing data.	Genet Epidemiol	2013
23810381	TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.	Am J Hum Genet	2013
22138362	Integrated annotation and analysis of genetic variants from next-generation sequencing studies with variant tools.	Bioinformatics	2012
22914216	SimRare: a program to generate and analyze sequence-based data for association studies of quantitative and qualitative traits.	Bioinformatics	2012
22865616	A fast and noise-resilient approach to detect rare-variant associations with deep sequencing data for complex disorders.	Genet Epidemiol	2012
20413980	Genome-wide conditional search for epistatic disease-predisposing variants in human association studies.	Human Heredity	2010