Yi Jiang
Neuroscience · Purdue University West Lafayette
Publications
74
Citations
642
Est. group size
—
Recurring co-author estimate
Active years
34
Publishing since 1992
This publication record appears to combine work from multiple distinct researchers sharing the name Yi Jiang, spanning hearing loss genetics, ear malformations, and prenatal genetic screening, alongside unrelated topics like civil engineering, cancer biology, and agricultural genetics. The genetics-and-hearing-focused strand studies inherited causes of deafness (such as mutations in GJB2 and SLC26A4 genes), inner ear structural abnormalities like enlarged vestibular aqueduct, and methods for prenatal genetic testing. Because the bibliographic data mixes clearly unrelated fields, prospective students should verify which specific publications and topics belong to the PI they are considering.
Publication output over the last decade has fluctuated, with a notable gap in 2023 followed by a peak in 2024, and the 5-year average of about 3.4 papers per year suggests a moderate and somewhat uneven publication pace.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- A Digital Solution for Enhancing Safety and Efficiency in Post-Disaster Restoration Workforce Management
2025
- Reevaluation of Enlarged Vestibular Aqueduct
JAMA Otolaryngology–Head & Neck Surgery · 2025
- Prediction and analysis of expressway tunnels crash based on modified convolutional neural network and Shapley additive explanations
Proceedings of the Institution of Civil Engineers - Transport · 2025
- Sanguinarine suppresses oral squamous cell carcinoma progression by targeting the PKM2/TFEB aix to inhibit autophagic flux
Phytomedicine · 2024
- Reducing amylose content in wheat (<i>Triticum aestivum</i> L.) using a novel <i>Wx</i>‐<scp><i>D1</i></scp> null allele generated by chemical mutagenesis
Journal of the Science of Food and Agriculture · 2024
- Targeted Linked-Read Sequencing for Direct Haplotype Phasing of Parental GJB2/SLC26A4 Alleles
Journal of Molecular Diagnostics · 2024
- A capture‐based method of prenatal cell‐free DNA screening for autosomal recessive non‐syndromic hearing loss
Prenatal Diagnosis · 2024
- Study of Correlation between Fetal Bowel Dilation and Congenital Gastrointestinal Malformation
Children · 2024
- Sanguinarine Suppresses Oral Squamous Cell Carcinoma Progression by Targeting Pkm2/Tfeb Aix to Inhibit Autophagic Flux
SSRN Electronic Journal · 2024
- The Phenotypic and Genomic Landscapes of 2,774 Chinese Patients with the Most Common Inner Ear Malformation: Optimization of Enlarged Vestibular Aqueduct Diagnosis and Prevention
SSRN Electronic Journal · 2024
- [Postoperative effect analysis of different surgical techniques used in facial nerve reconstruction].
PubMed · 2024
- Challenges and recent progress in ursodeoxycholic acid production
Advances in Engineering Technology Research · 2024
- Biallelic p.V37I variant in GJB2 is associated with increasing incidence of hearing loss with age
Genetics in Medicine · 2022
- Evolutionary origin of pathogenic <scp>GJB2</scp> alleles in China
Clinical Genetics · 2022
- Genetic findings of Sanger and nanopore single-molecule sequencing in patients with X-linked hearing loss and incomplete partition type III
Orphanet Journal of Rare Diseases · 2022
- Acta Oto-Laryngologica×3
- Zhonghua xiaoerwaike zazhi×3
- SSRN Electronic Journal×3
- Genetics in Medicine×1
- Phytomedicine×1
- Srikanth Ponneganti
Neuroscience · The Ohio State University
- Soumyajit Das
Neuroscience · Purdue University West Lafayette
- Kevin T. Booth
Neuroscience · Indiana University
- Raymundo Munguia
Neuroscience · Indiana University
- Ursula M. Findlen
Neuroscience · The Ohio State 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