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Yirou Wang

Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette

Established · publishing since 1987

Publications

73

Citations

441

Est. group size

Recurring co-author estimate

Active years

40

Publishing since 1987

Research summary
AI-generated

Yirou Wang studies rare pediatric genetic conditions in China, focusing on describing the clinical features and underlying gene variants of syndromes such as Cornelia de Lange syndrome, Kabuki syndrome, Turner syndrome, and various developmental and endocrine disorders. Much of this work involves large single-center patient cohorts that connect specific genetic mutations to observed physical and health traits (genotype-phenotype correlation), aiming to improve diagnosis and understanding of these conditions. This research is relevant to students interested in clinical genetics, pediatric rare disease research, and molecular diagnostics.

Rare pediatric genetic syndromesGenotype-phenotype correlationClinical genetics of developmental disordersPediatric endocrinology and metabolic conditionsCase reports on novel gene variants

Publication output has remained fairly steady over the last decade, rising from 2018-2020, dipping slightly around 2021-2022, and continuing at a moderate, consistent pace through 2025.

Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026

Publication cadence
Publications per year over the last 10 years — averaging 5.4/year recently
172018: 3 publications182019: 8 publications192020: 9 publications9202021: 6 publications212022: 5 publications222023: 7 publications232024: 5 publications242025: 7 publications252026: 3 publications26
Recent publications
Publishes in
  • PubMed×6
  • Orphanet Journal of Rare Diseases×3
  • BMC Pediatrics×3
  • Research Square×3
  • Frontiers in Endocrinology×2
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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 20, 2026.

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