LabCompass

Manyan Huang

Biochemistry, Genetics and Molecular Biology · Indiana University

OpenAlex ORCID
Congenital heart defects researchCongenital Heart Disease StudiesGenetic Associations and EpidemiologyGenomics and Rare DiseasesCardiovascular Function and Risk Factors

Publications

16

Citations

146

Est. group size

—

Recurring co-author estimate

Active years

12

Publishing since 2015

Research summary
AI-generated

Manyan Huang works in statistical genetics and genomics, developing and applying methods to find genes and molecular markers linked to congenital heart defects (heart abnormalities present at birth). Much of the research uses large birth-defect study datasets and novel statistical techniques, such as "random field" methods, to identify genetic and epigenetic (DNA methylation) factors associated with disease risk.

Statistical genetics of congenital heart defectsGene-based and genome-wide association testingMethylation quantitative trait loci (epigenetics)Maternal–fetal genotype interactionsGenetic epidemiology methods development

Publication activity has been irregular, with a peak in 2021 followed by a lower, intermittent output through 2026, averaging under two papers per year over the last five years.

Generated by claude-opus-4-8 from public bibliographic data · Jul 11, 2026

Publication cadence
Publications per year over the last 10 years — averaging 1.6/year recently
17182019: 1 publication19202021: 6 publications6212022: 2 publications222023: 4 publications232024: 1 publication24252026: 1 publication26
Recent publications
Publishes in
  • Figshare×4
  • Journal of Chromatography A×1
  • Journal of the American Heart Association×1
  • The Journal of Pediatrics×1
  • BMC Genomic Data×1

This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.

Last updated Jul 11, 2026.

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