Yirou Wang
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
Publications
73
Citations
441
Est. group size
—
Recurring co-author estimate
Active years
40
Publishing since 1987
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.
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
- Clinical delineation and genotype–phenotype correlation of 84 pediatric patients with Cornelia de Lange syndrome: insights from a single-center Chinese study
European Journal of Pediatrics · 2026
- [Combined analysis of epigenetic and transcriptomic data from children with Wiedemann-Steiner syndrome due to variants of KMT2A gene].
PubMed · 2026
- Clinical delineation and genotype–phenotype correlation in 104 children with kabuki syndrome: A single-center, cross-sectional and follow-up study in China
European Journal of Pediatrics · 2025
- Focusing on Rare Variants Related to Maturity‐Onset Diabetes of the Young in Children
Pediatric Diabetes · 2025
- Clinical delineation and genotype-phenotype correlation in 104 pediatric patients with kabuki syndrome: a large longitudinal cohort from a single center in china
Endocrine Abstracts · 2025
- Two Chinese patients with Basilicata-Akhtar syndrome caused by novel MSL3 variants: a case report and literature review
Translational Pediatrics · 2025
- Cardiovascular phenotypes of children and adolescents with Turner syndrome from a single-center cohort study
Orphanet Journal of Rare Diseases · 2025
- D-arginine-loaded pH-responsive mesoporous silica nanoparticles enhances the efficacy of water jet therapy in decontaminating biofilm-coated titanium surface
Journal of Controlled Release · 2024
- Behavior, attitude, perception, and knowledge regarding fertility preservation among Chinese pediatric oncologists: a survey in China
Journal of Assisted Reproduction and Genetics · 2024
- A de novo variant in ZBTB18 gene caused autosomal dominant non-syndromic intellectual disability 22 syndrome: A case report and literature review
Medicine · 2024
- Sex-specific difference in phenotype of Kabuki syndrome type 2 patients: a matched case-control study
BMC Pediatrics · 2024
- Clinical characteristics and genetic expansion of 46,XY disorders of sex development children in a Chinese prospective study
Endocrine Connections · 2023
- Genotypic and phenotypic features of dyslipidemia in a sample of pediatric patients in China
BMC Pediatrics · 2023
- Effect Analysis of Different Environmental Disinfection Methods on Reducing Contamination of Surfaces by the Omicron BA.2.2 Variant of SARS-CoV-2 and the Characteristics of Fomite Contamination in the Fever Clinic in the Out-Broken of Shanghai
Food and Environmental Virology · 2023
- Molecular and phenotypic spectrum of cardio-facio-cutaneous syndrome in Chinese patients
Orphanet Journal of Rare Diseases · 2023
- PubMed×6
- Orphanet Journal of Rare Diseases×3
- BMC Pediatrics×3
- Research Square×3
- Frontiers in Endocrinology×2
- Kayla Treat
Biochemistry, Genetics and Molecular Biology · Indiana University
- Bimal P. Chaudhari
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Alex H. Wagner
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Amy Siemon
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Benjamin M. Helm
Biochemistry, Genetics and Molecular Biology · Indiana University
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.
Claim or correct this profile