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Tara L. Wenger

Seattle Children's

39

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374

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42. Laboratory and clinician collaboration yields results: Development of a comprehensive craniosynostosis genetic testing panel with a high diagnostic rate

2021 Cancer Genetics and Cytogenetics
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Targeted long-read sequencing identifies missing disease-causing variation

2021 American Journal of Human Genetics
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Table 1. [Distinguishing Characteristics of FGFR Craniosynostosis Syndromes].

2020
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A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants

2020 medRxiv
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Muenke syndrome: Medical and surgical comorbidities and long‐term management

2019 American Journal of Medical Genetics Part A
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A genotype-specific surgical approach for patients with Pfeiffer syndrome due to W290C pathogenic variant in FGFR2 is associated with improved developmental outcomes and reduced mortality

2019 Genetics in Medicine
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Table 1. [Molecular Genetic Testing Used in Apert Syndrome].

2019
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Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients

2018
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“It’s Not the Shunt”: An Algorithm for the Assessment of Other Medically Actionable Causes of Vomiting in Children With Craniofacial Malformations

2018 The Cleft Palate-Craniofacial Journal
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Expanding the phenotypic spectrum of TP63-related disorders including the first set of monozygotic twins

2018 American Journal of Medical Genetics Part A
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