Wanqing Shao

Boston Children's Hospital — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

12h-index1.1kcitations38works3.72yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

RNA Research and Splicing(13), RNA modifications and cancer(10), Genomics and Chromatin Dynamics(9), Chromosomal and Genetic Variations(6), RNA and protein synthesis mechanisms(5)

Publications36 total

Cross-tissue molecular responses in the liver and blood after toxicant exposures
2025Open Access
Toxicogenomic Insights into Environmental Toxicant Exposures: The TaRGET II Resource
2025Open Access
Comprehensive Transcriptomic and Epigenomic Insights into Environmental Toxicant Exposures: The TaRGET II Resource
2025· 2 citedOpen Access
The impact of environmental exposures on the epigenomic and transcriptomic landscape of transposable elements
2025Open Access
O52: Diagnostic benefits of long-read genome sequencing for short-read negative rare disease cases
Genetics in Medicine Open·2025Open Access
P648: Automated reanalysis of clinical genomic data in undiagnosed patients
Genetics in Medicine Open·2025Open Access
Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomes
npj Genomic Medicine·2024· 7 citedOpen Access
Genome Sequencing After Exome Sequencing in Pediatric Epilepsy
JAMA Neurology·2024· 4 citedOpen Access
473P Using RNAseq analysis in a cohort of undiagnosed congenital myopathy patients
Neuromuscular Disorders·2024
Long-Read Sequencing Increases Diagnostic Yield for Pediatric Sensorineural Hearing Loss
2024Open Access
Utility of Genome Sequencing After Nondiagnostic Exome Sequencing in Unexplained Pediatric Epilepsy
2024· 2 citedOpen Access
Zebrafish models of candidate human epilepsy-associated genes provide evidence of hyperexcitability
iScience·2024· 13 citedOpen Access
Zebrafish models of candidate human epilepsy-associated genes provide evidence of hyperexcitability
2024· 5 citedOpen Access
Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental features
Human Genetics and Genomics Advances·2024· 3 citedOpen Access
P645: Utility of RNAseq in a cohort of undiagnosed congenital myopathy patients: A case series
Genetics in Medicine Open·2024Open Access
Zebrafish Models of Candidate Human Epilepsy-Associated Genes Provide Evidence of Hyperexcitability
SSRN Electronic Journal·2024Open Access
Heterozygous loss-of-function <i>SMC3</i> variants are associated with variable and incompletely penetrant growth and developmental features
2023Open Access
Utility of Exome Sequencing for Diagnosis in Unexplained Pediatric-Onset Epilepsy
JAMA Network Open·2023· 37 citedOpen Access
Spatial transcriptomics reveals a cnidarian segment polarity program in Nematostella vectensis
Current Biology·2023· 24 cited
Spatial transcriptomics reveals a conserved segment polarity program that governs muscle patterning in <i>Nematostella vectensis</i>
2023Open Access
page 1 of 2Next →

Frequent Co-authors

Julia Zeitlinger(11), Shira Rockowitz(10), Ting Wang(9), Annapurna Poduri(7), Hyun Yong Koh(6), Courtney E. French(6), Shiyuan Chen(4), Alissa M. D’Gama(4), Piotr Sliz(4), Alexander Rotenberg(4), Sergio G-M Alcantara(4), Bo Zhang(4), Benpeng Miao(4), Shuhua Fu(4), Cristian Coarfa(4), Sandra L. Grimm(4), Daofeng Li(4), Shaopeng Liu(4), Heather B. Patisaul(4), Dana C. Dolinoy(4)