Author details

Full Name

Bingshan Li

Affiliation

ORCID

Career Start Year

2003

Papers

106

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36750564	Multi-ancestry and multi-trait genome-wide association meta-analyses inform clinical risk prediction for systemic lupus erythematosus.		2023
36350676	FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.	Nucleic Acids Res	2023
35012639	Artificial intelligence framework identifies candidate targets for drug repurposing in Alzheimer's disease.	Alzheimers Res Ther	2022
35396981	Evaluating breast cancer predisposition genes in women of African ancestry.	Genet Med	2022
35459094	A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritization.	BMC Bioinformatics	2022
35649341	A computational framework to unify orthogonal information in DNA methylation and copy number aberrations in cell-free DNA for early cancer detection.	Briefings in Bioinformatics	2022
36356581	Genome- and transcriptome-wide association studies of 386,000 Asian and European-ancestry women provide new insights into breast cancer genetics.	Am J Hum Genet	2022
36075150	Risperidone-induced changes in DNA methylation in peripheral blood from first-episode schizophrenia patients parallel changes in neuroimaging and cognitive phenotypes.	Psychiatry Res	2022
35740538	Genomic Aberrations in Circulating Tumor DNAs from Palbociclib-Treated Metastatic Breast Cancer Patients Reveal a Novel Resistance Mechanism.	Cancers (Basel)	2022
35311964	Incorporating Polygenic Risk Scores and Nongenetic Risk Factors for Breast Cancer Risk Prediction Among Asian Women.	JAMA Netw Open	2022
35205424	Leveraging Gene-Level Prediction as Informative Covariate in Hypothesis Weighting Improves Power for Rare Variant Association Studies.	Genes	2022
35013250	Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension.	Nat Commun	2022
34582791	Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.	Am J Hum Genet	2021
34078304	Integration of circulating tumor cell and neutrophil-lymphocyte ratio to identify high-risk metastatic castration-resistant prostate cancer patients.	BMC Cancer	2021
34075047	Whole-exome sequencing identifies somatic mutations and intratumor heterogeneity in inflammatory breast cancer.	NPJ Breast Cancer	2021
33745745	Race disparities in genetic alterations within Wilms tumor specimens.	Journal of Pediatric Surgery	2021
33739539	Incorporating European GWAS findings improve polygenic risk prediction accuracy of breast cancer among East Asians.	Genetic Epidemiology	2021
33450815	Improved Prognostic Stratification Using Circulating Tumor Cell Clusters in Patients with Metastatic Castration-Resistant Prostate Cancer.	Cancers (Basel)	2021
33712848	DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions.	J Am Med Inform Assoc	2021
33190990	Blunted PTH response to vitamin D insufficiency/deficiency and colorectal neoplasia risk.	Clin Nutr	2021
34497089	Integrating Genome and Methylome Data to Identify Candidate DNA Methylation Biomarkers for Pancreatic Cancer Risk.	Cancer Epidemiology Biomarkers and Prevention	2021
31143935	Genetically Predicted Levels of DNA Methylation Biomarkers and Breast Cancer Risk: Data From 228â¿¿951 Women of European Descent.	J Natl Cancer Inst	2020
32139696	Identification of novel breast cancer susceptibility loci in meta-analyses conducted among Asian and European descendants.	Nat Commun	2020
32367460	Prognostic value of HER2 status on circulating tumor cells in advanced-stage breast cancer patients with HER2-negative tumors.	Breast Cancer Res Treat	2020
32356724	A big-data approach to understanding metabolic rate and response to obesity in laboratory mice.	eLife	2020
32296164	Electronic health record phenotypes associated with genetically regulated expression of CFTR and application to cystic fibrosis.	Genet Med	2020
31883642	Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts.	Am J Hum Genet	2020
31826910	Identification of Novel Loci and New Risk Variant in Known Loci for Colorectal Cancer Risk in East Asians.	Cancer Epidemiol Biomarkers Prev	2020
31932796	Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies.	Nat Med	2020
32282793	DRAMS: A tool to detect and re-align mixed-up samples for integrative studies of multi-omics data.	PLoS Comput Biol	2020
32280092	Ca:Mg Ratio, APOE Cytosine Modifications, and Cognitive Function: Results from a Randomized Trial.	J Alzheimers Dis	2020
32596635	Evaluating the Utility of Polygenic Risk Scores in Identifying High-Risk Individuals for Eight Common Cancers.	JNCI Cancer Spectr	2020
32984537	INCIDENTAL PULMONARY METASTASES REVEALING SUBCENTIMETER PAPILLARY THYROID CARCINOMA.	AACE Clinical Case Reports	2020
32847609	PSCAN: Spatial scan tests guided by protein structures improve complex disease gene discovery and signal variant detection.	Genome Biol	2020
32888493	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Cell	2020
30988527	A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data.	Nat Neurosci	2019
31629678	Re-evaluating genetic variants identified in candidate gene studies of breast cancer risk using data from nearly 280,000 women of Asian and European ancestry.	EBioMedicine	2019
30307499	Whole genome sequence association with E-selectin levels reveals loss-of-function variant in African Americans.	Hum Mol Genet	2019
30256891	De novo pattern discovery enables robust assessment of functional consequences of non-coding variants.	Bioinformatics	2019
30529582	Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer.	Gastroenterology	2019
30528798	Association of clinical outcomes in metastatic breast cancer patients with circulating tumour cell and circulating cell-free DNA.	Eur J Cancer	2019
29848177	Transcriptome-Wide Association Study Identifies Susceptibility Loci and Genes for Age at Natural Menopause.	Reprod Sci	2019
30683671	Insight into the Etiology of Undifferentiated Soft Tissue Sarcomas from a Novel Mouse Model.	Molecular Cancer Research	2019
30849219	Methods for the Analysis and Interpretation for Rare Variants Associated with Complex Traits.	Current Protocols in Human Genetics	2019
29727689	A Comprehensive cis-eQTL Analysis Revealed Target Genes in Breast Cancer Susceptibility Loci Identified in Genome-wide Association Studies.	Am J Hum Genet	2018
30155617	Molecular and epidemiologic characterization of Wilms tumor from Baghdad, Iraq.	World Journal of Pediatrics	2018
29915430	A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer.	Nat Genet	2018
30054336	A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk.	Cancer Res	2018
30323088	A Routine Laboratory Data-Based Model for Predicting Recurrence After Curative Resection of Stage II Colorectal Cancer.	J Natl Compr Canc Netw	2018
29764838	A common TCN1 loss-of-function variant is associated with lower vitamin B12 concentration in African Americans.	Blood	2018