Wen Jiang, M.D.

Bio

Dr. Wen Jiang is a board-certified, fellowship-trained pediatric otolaryngologist at Rady Children's Hospital-San Diego and a clinical professor of surgery at UC San Diego School of Medicine.

Her practice is dedicated solely to the treatment of children with a variety of ear, nose and throat complaints.

Specializing in voice disorders in children, she currently co-directs the Speech and Voice Endoscopy Clinic, a multidisciplinary voice and speech team that works closely with Rady Children's Speech-Language Pathology Department. This team provides comprehensive service to children with speech-related disorders such as vocal nodules, hypernasality and/or velopharyngeal incompetence.

Dr. Jiang has extensive training and experience in surgeries of the head and neck, treating both benign and malignant tumors. A major focus of her surgical practice is the treatment of thyroid neoplasm in children. She and Dr. Phillips from the Division of Endocrinology/Diabetes have created a multidisciplinary thyroid tumor board that meets on a bimonthly to discuss the management of patients with thyroid pathology.

Publications

Pediatric thyroid surgery and management of thyroid nodules - an institutional experience over a 10-year period
Jiang W, Newbury RO, Newfield RS

Mutational Analysis in Pediatric Thyroid Cancer and Correlations with Age, Ethnicity, and Clinical Presentation
Nikita ME, Jiang W, Cheng SM, Hantash FM, McPhaul MJ, Newbury RO, Phillips SA, Reitz RE, Waldman FM, Newfield RS

Pathology Quiz Case 1. Diagnosis: Carcinoid Tumor of the Middle Ear
Jiang W, Hill DA, Lieu JE

Pathology Forum: Quiz Case 4. Diagnosis: Synovial Chondromatosis of the TMJ
Jiang W, Mishra S, Francis HW

Paternal Origin of FGFR2 Mutations in Sporadic Cases of Crouzon Syndrome and Pfeiffer Syndrome
Glaser RL, Jiang W, Boyadjiev SA, Tran AK, Zachary AA, Van Maldergem L, Johnson D, Walsh S, Oldridge M, Wall SA, Wilkie AO, Jabs EW

Combination Surgery and Nonviral Interleukin 2 Gene Therapy for Head and Neck Cancer
Li D, Jiang W, Bishop JS, Ralston R, O'Malley BW Jr.

A Novel Skeletal Dysplasia with Developmental Delay and Acanthosis Nigricans is Caused by a Lys650Met Mutation in the Fibroblast Growth Factor Receptor 3 Gene
Tavormina PL, Bellus GA, Webster MK, Bamshad MJ, Fraley AE, McIntosh I, Szabo J, Jiang W, Jabs EW, Wilcox WR, Wasmuth JJ, Donoghue DJ, Thompson LM, Francomano CA

De Novo Alu-Element Insertions in FGFR2 Identify a Distinct Pathological Basis for Alpert Syndrome
Oldridge M, Zackai EH, McDonald-McGinn DM, Iseki S, MOrriss-Kay GM, Twigg SR, Johnson D, Wall SA, Jiang W, Theda C, Jabs EW, Wilkie AO

Prenatal Ultrasonographic and Molecular Diagnosis of Alpert Syndrome
Filkins K, Russo JF, Boehmer S, Camous M, Przlepa KA, Jiang W, Jabs EW

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