Tara Wenger

Targeted long-read sequencing identifies missing disease-causing variation

Danny E. Miller, Arvis Sulovari, Tianyun Wang et al. · The American Journal of Human Genetics · 2021 · 239 citations · Full text

Life Sciences, Bioinformatics, Genetics +14

ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor

Dong Li, Michael March, Álvaro Gutiérrez-Uzquiza et al. · Nature Medicine · 2019 · 219 citations

Medicine, Cell Biology, Molecular Medicine +11

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

Samuel J. R. A. Chawner, Joanne Doherty, Richard Anney et al. · American Journal of Psychiatry · 2021 · 102 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening

Tara Wenger, Judith S. Miller, Lauren M. DePolo et al. · Molecular Autism · 2016 · 100 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly

Dong Li, Tara Wenger, Christoph Seiler et al. · Human Molecular Genetics · 2018 · 100 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13