TaraLynnWengerMDPhD

PubMed

• 4 citations
  POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies.
  Kelly Smallwood, Kristin E N Watt, Satoru Ide, Kristina Baltrunaite, Chad Brunswick, Katherine Inskeep, Corrine Capannari, Margaret P Adam, Amber Begtrup, Debora R Ber...> ;American Journal of Human Genetics. 2023 May 4
• 2 citations
  Primary targeted medical therapy for management of bilateral head and neck lymphatic malformations in infants.
  Clare M Richardson, Jonathan N Perkins, Kaitlyn Zenner, Catherine Bull, Erika Lutsky, Dana M Jensen, Victoria Dmyterko, James T Bennett, Tara L Wenger, John P Dahl, Ju...> ;International Journal of Pediatric Otorhinolaryngology. 2023 Jan 1
• 9 citations
  Alpelisib for the treatment of PIK3CA-related head and neck lymphatic malformations and overgrowth.
  Tara L Wenger, Sheila Ganti, Catherine Bull, Erika Lutsky, James T Bennett, Kaitlyn Zenner, Dana M Jensen, Victoria Dmyterko, Ezgi Mercan, Giri M Shivaram, Seth D Frie...> ;Genetics in Medicine. 2022 Nov 1
• 84 citations
  Targeted long-read sequencing identifies missing disease-causing variation
  Danny E. Miller, Arvis Sulovari, Tianyun Wang, Hailey Loucks, Kendra Hoekzema, Katherine M. Munson, Alexandra P. Lewis, Edith P Almanza Fuerte, Catherine R Paschal, Th...> ;American Journal of Human Genetics. 2021 Aug 5
• 1 citations
  Cleft palate morphology, genetic etiology, and risk of mortality in infants with Robin sequence.
  Tara L. Wenger, Jonathan A. Perkins, Julia Parish-Morris, Anne Hing, Maida Lynn Chen, Christopher M. Cielo, Dong Li, Elizabeth J. Bhoj, Hakon Hakonarson, Elaine H. Zac...> ;American Journal of Medical Genetics. Part A. 2021 Jul 22
• 1 citations
  Complex Airway Management in Patients with Tracheal Cartilaginous Sleeves.
  Anisha R Noble, Michael L. Cunningham, Austin S. Lam, Tara L. Wenger, Kathleen C.Y. Sie, Jonathan A. Perkins, John P. Dahl> ;The Laryngoscope. 2021 Jun 16
• Case 2: Seizures in a Neonate.
  Danny E. Miller, Jason N. Wright, Randall A. Bly, Elliott Mark Weiss, Srinivas M. Susarla, Tara L. Wenger> ;Neoreviews. 2021 May 1
• 5 citations
  Perspectives from the Society for Pediatric Research: advice on sustaining science and mentoring during COVID-19.
  Catherine S Forster, Suong T Nguyen, Weston T. Powell, Daniel J. Moore, Jacqueline Ho, Melvin B. Heyman, Tara L. Wenger, Fernando F. Gonzalez, Margaret K. Hostetter, A...> ;Pediatric Research. 2021 Jan 19
• Risk Factors and Inadequacy of Screening for Sleep-Disordered Breathing in Children with Marfan Syndrome.
  E MacKintosh, Maida Lynn Chen, Tara L. Wenger, Kristen Carlin, Luciana Young> ;Pediatric Cardiology. 2021 Jan 4
• 46 citations
  A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants.
  Samuel J.R.A. Chawner, Joanne L. Doherty, Richard Anney, Kevin M. Antshel, Carrie E. Bearden, Raphael Bernier, Wendy K Chung, Caitlin C. Clements, Sarah R Curran, Gora...> ;The American Journal of Psychiatry. 2021 Jan 1
• 20 citations
  Activating variants in PDGFRB result in a spectrum of disorders responsive to imatinib monotherapy.
  Tara L. Wenger, Randall A. Bly, Natalie Wu, Catherine M. Albert, Julie Park, Joseph T. Shieh, Jirat Chenbhanich, Carrie L. Heike, Margaret P. Adam, Irene Chang, Angela...> ;American Journal of Medical Genetics. Part A. 2020 Jul 1
• 10 citations
  Fixing the leaky pipeline: identifying solutions for improving pediatrician-scientist training during pediatric residency.
  Heyman, M. B., Audrea M. Burns, Kate G. Ackerman, Satid Thammasitboon, Caroline E. Rassbach, Mark A. Ward, Rebecca Blankenburg, Catherine S. Forster, Heather McPhillip...> ;Pediatric Research. 2020 Mar 16
• 1 citations
  Catel-Manzke syndrome without Manzke dysostosis.
  Danny E. Miller, Penny Chow, Emily R. Gallagher, Jonathan A. Perkins, Tara L. Wenger> ;American Journal of Medical Genetics. Part A. 2020 Mar 1
• 1 citations
  Muenke syndrome: Medical and surgical comorbidities and long-term management.
  Chaya N. Murali, Donna M. McDonald-McGinn, Tara L. Wenger, Carey McDougall, Bridget M. Stroup, Sarah E Sheppard, Jesse A. Taylor, Scott P. Bartlett, Elizabeth J. Bhoj,...> ;American Journal of Medical Genetics. Part A. 2019 Aug 1
• 108 citations
  ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor
  Dong Li, Michael E. March, Alvaro Gutierrez-Uzquiza, Charlly Kao, Christoph Seiler, Erin Pinto, Leticia S. Matsuoka, Mark R Battig, Elizabeth J. Bhoj, Tara L. Wenger, ...> ;Nature Medicine. 2019 Jul 1
• "It's Not the Shunt": An Algorithm for the Assessment of Other Medically Actionable Causes of Vomiting in Children With Craniofacial Malformations.
  Dawn M. Maxey, Amy Lee, Tara L. Wenger> ;The Cleft Palate-Craniofacial Journal. 2019 Jul 1
• 1 citations
  An Algorithm for the Assessment of Facial Asymmetry in Children With Focus on Etiology and Treatment
  Tara L. Wenger, Emily R. Gallagher, Elizabeth J. Bhoj> ;The Cleft Palate-Craniofacial Journal. 2019 Mar 1
• 8 citations
  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 L. Wenger, Richard A. Hopper, Anna Rosén, Hannah M. Tully, Michael L. Cunningham, Amy Lee> ;Genetics in Medicine. 2019 Feb 1
• 53 citations
  Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly.
  Dong Li, Tara L. Wenger, Christoph Seiler, Michael E. March, Alvaro Gutierrez-Uzquiza, Charlly Kao, Elizabeth J. Bhoj, Lifeng Tian, Misha Rosenbach, Yichuan Liu, Nora ...> ;Human Molecular Genetics. 2018 Sep 15
• 17 citations
  Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients.
  Mark D. Levin, Karen W. Gripp, Tara L. Wenger, Jaya Ganesh, Jennifer M. Kalish, Michael R. Epstein, Rosemarie Smith, Richard J. Czosek, Stephanie M. Ware, Paula Golden...> ;American Journal of Medical Genetics. Part A. 2018 Aug 1
• 4 citations
  Delayed Subaponeurotic Fluid Collections of Infancy.
  Jonathan J Lee, Tara L. Wenger> ;The Journal of Pediatrics. 2018 Mar 15
• 8 citations
  Expanding the phenotypic spectrum of TP63-related disorders including the first set of monozygotic twins
  Tara L. Wenger, Dong Li, Margaret Harr, Wen-Hann Tan, Renata Pellegrino, Zornitza Stark, Hakon Hakonarson, Elizabeth J. Bhoj> ;American Journal of Medical Genetics. Part A. 2018 Jan 1
• 34 citations
  Critical region within 22q11.2 linked to higher rate of autism spectrum disorder.
  Caitlin C. Clements, Tara L. Wenger, Alisa R. Zoltowski, Jennifer R. Bertollo, Judith Miller, Ashley de Marchena, Lauren Mitteer, John C. Carey, Benjamin E. Yerys, Ela...> ;Molecular Autism. 2017 Oct 27
• 14 citations
  Defining and Correcting Asymmetry in Isolated Unilateral Frontosphenoidal Synostosis: Differences in Orbital Shape, Facial Scoliosis, and Skullbase Twist Compared to U...
  Gerhard S. Mundinger, Rachel Skladman, Tara L. Wenger, Craig C. Birgfeld, Joseph S. Gruss, Amy Lee, Richard G. Ellenbogen, Richard A. Hopper> ;The Journal of Craniofacial Surgery. 2017 Oct 1
• 61 citations
  Phenotypes and genotypes in individuals with SMC1A variants
  Sylvia A. Huisman, Paul A. Mulder, Egbert J.W. Redeker, Ingrid Bader, Anne Marie Bisgaard, Alice S. Brooks, Anna Cereda, Constanza Cinca, Dinah Clark, Valérie Cormier-...> ;American Journal of Medical Genetics. Part A. 2017 Aug 1
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Journal Articles

• Nonreentrant Atrial Tachycardia Occurs Independently of Hypertrophic Cardiomyopathy in RASopathy Patients  
  Karen 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