Tara Lynn Wenger MD PhD
Medical Genetics
Assistant Professor, Seattle Children's Hospital
Join to View Full Profile
34th & Civic Center BlvdChildren's Hospital Of PhiladelphiaPhiladelphia, PA 19104
Phone+1 215-590-1000
Dr. Wenger is on Doximity
As a Doximity member you'll join over two million verified healthcare professionals in a private, secure network.
- Gain access to free telehealth tools, such as our “call shielding” and one-way patient texting.
- Connect with colleagues in the same hospital or clinic.
- Read the latest clinical news, personalized to your specialty.
Education & Training
Children's Hospital of PhiladelphiaResidency, Pediatrics/Medical Genetics and Genomics, 2008 - 2014
University of Rochester School of Medicine and DentistryClass of 2008
Certifications & Licensure
WA State Medical License 2014 - 2027
PA State Medical License 2008 - 2014
American Board of Pediatrics Pediatrics
American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Publications & Presentations
PubMed
- Management and Outcomes of Neonates with Treacher Collins and Nager Syndromes.Tara L Wenger, K Taylor Wild, Isabella Zaniletti, Elaine H Zackai, Janet Lioy
The Journal of Pediatrics. 2025-08-01 - Treatment of PDGFRB-Related Penttinen Syndrome With Imatinib in a Young Child.Molly McPheron, Katelyn Burns, Tara L Wenger
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 2025-07-31 - Implementation of First-Line Rapid Genome Sequencing in Non-Critical Care Pediatric Wards.Alexandra C Keefe, Abbey A Scott, Lukas Kruidenier, Jessie Conta, Darci Sternen
The Journal of Pediatrics. 2025-06-23
Journal Articles
- Nonreentrant Atrial Tachycardia Occurs Independently of Hypertrophic Cardiomyopathy in RASopathy PatientsKaren W Gripp, Rosemarie Smith, Stephanie M Ware, Paula Goldenberg, Kathryn C Chatfield, Mark D Levin, Richard J Czosek, Elaine H Zackai, Angela E Lin, Tara L Wenger, ..., American Journal of Medical Genetics Part A
- A Genotype-Specific Surgical Approach for Patients with Pfeiffer Syndrome Due to W290C Pathogenic Variant in FGFR2 Is Associated with Improved Developmental Outcomes a...Tara Wenger, MD, Nature
Press Mentions
GeneDx Announces Publication of SeqFirst Study Demonstrating Need for First Tier Rapid Genomic Testing for Non-Critical Care Pediatric Inpatients in the Journal of PediatricsJune 25th, 2025- Q&A: ‘We Are Not as Good as We Think’ at Identifying Genetic Conditions in BabiesMarch 10th, 2025
- Landmark Seqfirst-Neo Study Showcases the Significant Impact of Genomic Testing in the NICU, Revealing Gaps in Current ProtocolsFebruary 24th, 2025
- Join now to see all
Viewing the full profile is available to verified healthcare professionals only.
Find your profile and take control of your online presence:
