Qingbo S. Wang

Broad Institute — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

27h-index17.1kcitations62works14.62yr avg
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Research Topics

Genomics and Rare Diseases(19), Genetic Associations and Epidemiology(11), Bioinformatics and Genomic Networks(9), CRISPR and Genetic Engineering(8), Single-cell and spatial transcriptomics(8)

Publications57 total

Identification and replication of sex-dimorphic protein quantitative trait loci across multiple ancestries and their associations with diseases
Scientific Reports·2025· 1 citedOpen Access
Deciphering state-dependent immune features from multi-layer omics data at single-cell resolution
Nature Genetics·2025· 4 citedOpen Access
The effect of LRRK2 loss-of-function variants in humans
UNC Libraries·2025Open Access
Author Correction: The effect of LRRK2 loss-of-function variants in humans
UNC Libraries·2025Open Access
JOB: Japan Omics Browser provides integrative visualization of multi-omics data
BMC Genomics·2025Open Access
Unraveling the COVID-19 Severity Hubs and Interplays in Inflammatory-Related RNA–Protein Networks
International Journal of Molecular Sciences·2025Open Access
Germline variants and mosaic chromosomal alterations affect COVID-19 vaccine immunogenicity
Cell Genomics·2025· 5 citedOpen Access
Platform-dependent effects of genetic variants on plasma APOL1
2025· 3 citedOpen Access
Blood DNA virome associates with autoimmune diseases and COVID-19
Nature Genetics·2025· 15 citedOpen Access
Publisher Correction: Statistically and functionally fine-mapped blood eQTLs and pQTLs from 1,405 humans reveal distinct regulation patterns and disease relevance
Nature Genetics·2024· 1 citedOpen Access
Statistically and functionally fine-mapped blood eQTLs and pQTLs from 1,405 humans reveal distinct regulation patterns and disease relevance
Nature Genetics·2024· 27 citedOpen Access
Spinal cord motor neuron phenotypes and polygenic risk scores in sporadic amyotrophic lateral sclerosis: deciphering the disease pathology and therapeutic potential of ropinirole hydrochloride
Journal of Neurology Neurosurgery & Psychiatry·2024· 1 citedOpen Access
Quantification of escape from X chromosome inactivation with single-cell omics data reveals heterogeneity across cell types and tissues
Cell Genomics·2024· 16 citedOpen Access
Functional dissection of complex and molecular trait variants at single nucleotide resolution
2024· 26 citedOpen Access
Spinal Cord Motor Neuron Phenotypes and Polygenic Risk Scores in Sporadic Amyotrophic Lateral Sclerosis: Deciphering the Disease Pathology and Therapeutic Potential of Ropinirole Hydrochloride
2024Open Access
Author Correction: A genomic mutational constraint map using variation in 76,156 human genomes
Nature·2024· 157 citedOpen Access
A genomic mutational constraint map using variation in 76,156 human genomes
Nature·2023· 1.1k citedOpen Access
Clonal Hematopoiesis Is Associated with Severe COVID-19 Enhancing Inflammatory Responses in Myeloid Cells
Blood·2023Open Access
Quantification of the escape from X chromosome inactivation with the million cell-scale human single-cell omics datasets reveals heterogeneity of escape across cell types and tissues
2023· 6 citedOpen Access
Estimating gene-level false discovery probability improves eQTL statistical fine-mapping precision
NAR Genomics and Bioinformatics·2023· 1 citedOpen Access
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Frequent Co-authors

Laurent C. Francioli(22), Beryl B. Cummings(20), Jessica Alföldi(19), Laura D. Gauthier(19), Nicholas A. Watts(19), Anne O’Donnell‐Luria(19), Ryan L. Collins(18), Konrad J. Karczewski(17), Kristen M. Laricchia(17), Matthew Solomonson(17), Mark J. Daly(17), Masahiro Kanai(17), Timothy Poterba(16), Irina M. Armean(16), Ruchi Munshi(16), Valentín Ruano-Rubio(16), Grace Tiao(15), Yossi Farjoun(15), Eric Banks(15), Christopher Vittal(15)