Wu-Lin Charng

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 6

Top Topics

Escherichia Coli

Intellectual Disability

Gene Expression

Top Venues

Journal of medical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Wu-Lin Charng, Momchil Nikolov, Isabel Shrestha, Mark A Seeley, Navya Shilpa Josyula, Anne E Justice, Matthew B Dobbs, Christina A Gurnett
Exome sequencing of 1190 non-syndromic clubfoot cases reveals HOXD12 as a novel disease gene. Journal of medical genetics (2024)
Wu-Lin Charng, Momchil Nikolov, Isabel Shrestha, Mark A Seeley, Navya Shilpa Josyula, Anne E Justice, Matthew B Dobbs, Christina A Gurnett
Exome sequencing of 1190 non-syndromic clubfoot cases reveals HOXD12 as a novel disease gene. Journal of medical genetics 61 (7) (2024)
Wu-Lin Charng, Momchil Nikolov, Isabel Shrestha, Mark A Seeley, Navya Shilpa Josyula, Anne E Justice, Matthew B Dobbs, Christina A Gurnett
Exome sequencing of 1190 non-syndromic clubfoot cases reveals HOXD12 as a novel disease gene. Journal of medical genetics 61 (7) (2024)
Wu-Lin Charng, Momchil Nikolov, Isabel Shrestha, Mark A Seeley, Navya Shilpa Josyula, Anne E Justice, Matthew B Dobbs, Christina A Gurnett
Exome sequencing of 1190 non-syndromic clubfoot cases reveals HOXD12 as a novel disease gene. Journal of medical genetics 61 (7) (2024)
Wu-Lin Charng, Momchil Nikolov, Isabel Shrestha, Mark A Seeley, Navya Shilpa Josyula, Anne E Justice, Matthew B Dobbs, Christina A Gurnett
Exome sequencing of 1190 non-syndromic clubfoot cases reveals HOXD12 as a novel disease gene. Journal of medical genetics (2024)
Ximena M Bustamante-Marin, Amjad Horani, Mihaela Stoyanova, Wu-Lin Charng, Mathieu Bottier, Patrick R Sears, Wei-Ning Yin, M Leigh Anne Daniels, Hailey Bowen, Donald F Conrad, Michael R Knowles, Lawrence E Ostrowski, Maimoona A Zariwala, Susan K Dutcher
Mutation of CFAP57, a protein required for the asymmetric targeting of a subset of inner dynein arms in Chlamydomonas, causes primary ciliary dyskinesia. PLoS genetics 16 (8) (2020)