Erica Nading

Mutations in SCO2 Are Associated with Autosomal-Dominant High-Grade Myopia

Khanh-Nhat Tran-Viet, Caldwell Powell, Veluchamy A. Barathi et al. · The American Journal of Human Genetics · 2013 · 116 citations · Full text

Medicine, Genetics, Molecular Genetics +13

CYP1B1, MYOC, and LTBP2 Mutations in Primary Congenital Glaucoma Patients in the United States

Sing-Hui Lim, Khanh-Nhat Tran-Viet, Tammy L. Yanovitch et al. · American Journal of Ophthalmology · 2012 · 83 citations · Full text

Medicine, Genetics, Ophthalmology +10

The Global ALPL gene variant classification project: Dedicated to deciphering variants

Mariam R. Farman, Catherine Rehder, Theodora Malli et al. · Bone · 2023 · 59 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes.

Khanh-Nhat Tran-Viet, Vincent Soler, Valencia Quiette et al. · PubMed · 2013 · 19 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Pulmonary outcome measures in long‐term survivors of infantile Pompe disease on enzyme replacement therapy: A case series

Mai K. ElMallah, Ankit K. Desai, Erica Nading et al. · Pediatric Pulmonology · 2020 · 15 citations · Full text

Medicine, Clinical Sciences, Pediatrics +12