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 · 227 citations · Full text

Long-read Sequencing, Long-read Sequencing Identifies, Next-generation Sequencing +4

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 · 213 citations

Lymphoid Neoplasia, Autoimmune Disease, Immunodeficiencies +13

Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly

Dong Li, Tara Wenger, Christoph Seiler et al. · Human Molecular Genetics · 2018 · 98 citations · Full text

Ephb4 Mutation, Genetics, Mtorc1 Activity +21

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 · 96 citations · Full text

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 · 95 citations · Full text