Publications by authors named "Tara Wenger"

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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, Tara L Wenger

J Pediatr· November 2025

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Expanding implementation of pediatric whole-genome sequencing: Insights from SeqFirst providers to inform equitable access to a precise genetic diagnosis.
Joon-Ho Yu, Katherine E MacDuffie, Olivia Sommerland, Tesla Theoryn, Priyanka Murali, Tara Wenger

HGG Adv· October 2025

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Commentary: Interventional Genetics.
Tara L Wenger, Margaret P Adam

Am J Med Genet C Semin Med Genet· September 2025

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Management and Outcomes of Neonates with Treacher Collins and Nager Syndromes.
Tara L Wenger, K Taylor Wild, Isabella Zaniletti, Elaine H Zackai, Janet Lioy

J Pediatr· August 2025

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Treatment of PDGFRB-Related Penttinen Syndrome With Imatinib in a Young Child.
Molly McPheron, Katelyn Burns, Tara L Wenger

Am J Med Genet C Semin Med Genet· July 2025

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Incidence and Factors Associated With Spontaneous Regression in Head and Neck Lymphatic Malformations.
Juliana Bonilla-Velez, Carrie L Heike, Larry G Kessler, Xing Wang, Tara L Wenger

JAMA Otolaryngol Head Neck Surg· May 2025

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Standardized Classification of Infants With Robin Sequence Using MicroNAPS: The Impact of Syndromes and Comorbidities.
Cory M Resnick, Jody E Heffernan, Snigdha Jindal, Zaara Mehra, Irfan Ahmad, Tara L Wenger

Plast Reconstr Surg Glob Open· May 2025

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SeqFirst: Building equity access to a precise genetic diagnosis in critically ill newborns.
Tara L Wenger, Abbey Scott, Lukas Kruidenier, Megan Sikes, Alexandra Keefe

Am J Hum Genet· March 2025

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A plot TWIST.
Sophia R Meyer, Tara L Wenger

Am J Med Genet C Semin Med Genet· November 2024

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Novel insights into the phenotypic spectrum and pathogenesis of Hardikar syndrome.
Alanna Strong, Michael E March, Christopher J Cardinale, Yichuan Liu, Mark R Battig, Tara Wenger

Genet Med· October 2024

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Case report: Artificial thymic organoids facilitate clinical decisions for a patient with a variant and severe persistent T cell lymphopenia.
Alevtina Gall, Marita Bosticardo, Stacey Ma, Karin Chen, Kayla Amini, Tara Wenger

Front Immunol· October 2024

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Clinical RNA sequencing clarifies variants of uncertain significance identified by prior testing.
Jonathan Marquez, Jennifer N Cech, Cate R Paschal, Bri Dingmann, Anna I Scott, Tara L Wenger

Genet Med Open· August 2024

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Ethical and Legal Issues Surrounding Genetic Testing in the NICU.
Katharine P Callahan, Ellen W Clayton, Amy A Lemke, Bimal P Chaudhari, Tara L Wenger

Neoreviews· March 2024

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The spectrum of heart defects in the -related multiple congenital anomalies-intellectual disability syndrome.
Elise Pisan, Chiara De Luca, Francesco Brancati, Rossana Sanchez Russo, Dong Li, Tara Wenger

Proc Natl Acad Sci U S A· March 2024

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Spectrum of Disease in Hospitalized Newborns with Congenital Micrognathia: A Cohort of 3,236 Infants at North American Tertiary-Care Intensive Care Units.
Michael A Padula, Khatija Naing, Tara L Wenger, Irfan Ahmad, Carl H Coghill

J Pediatr· February 2024

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3-hour genome sequencing and targeted analysis to rapidly assess genetic risk.
Miranda Pg Zalusky, Jonas A Gustafson, Stephanie C Bohaczuk, Ben Mallory, Paxton Reed, Tara Wenger

Genet Med Open· February 2024

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POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies.
Kelly Smallwood, Kristin E N Watt, Satoru Ide, Kristina Baltrunaite, Chad Brunswick, Tara Wenger

Am J Hum Genet· May 2023

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De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis.
Andrew T Timberlake, Stephen McGee, Garrett Allington, Emre Kiziltug, Erin M Wolfe, Tara L Wenger

Am J Hum Genet· May 2023

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Perspectives on the future of dysmorphology.
Benjamin D Solomon, Margaret P Adam, Chin-To Fong, Katta M Girisha, Judith G Hall, Tara L Wenger

Am J Med Genet A· March 2023

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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, Tara L Wenger

Int J Pediatr Otorhinolaryngol· January 2023

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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

Genet Med· November 2022

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Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract.
Johannes Münch, Marie Engesser, Ria Schönauer, J Austin Hamm, Christin Hartig, Tara Wenger

Kidney Int· May 2022

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Avoidance of surgery for head and neck infantile myofibromatosis using imatinib monotherapy.
Prasanth Pattisapu, Tara L Wenger, John P Dahl, Randall A Bly, Juliana Bonilla-Velez

Clin Case Rep· February 2022

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Cleft palate morphology, genetic etiology, and risk of mortality in infants with Robin sequence.
Tara L Wenger, Jonathan Perkins, Julia Parish-Morris, Anne V Hing, Maida L Chen

Am J Med Genet A· December 2021

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Mesenteric Plexiform Neurofibroma as a Cause of Weight Loss and Chronic Diarrhea in a Patient with Variant.
Irina Gorbounova, Arthur Lenahan, Tara Lynn Wenger, Erin Rudzinski, Elizabeth Ren-Yee Tang

JPGN Rep· August 2021

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