Hua Wang

ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 5

Top Venues

Journal of medical genetics

Molecular genetics & genomic medicine

European journal of human genetics : EJHG

Clinical genetics

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

Publications

Juan Li, Shiyue Mei, Xiao Mao, Lily Wan, Hua Wang, Bo Xiao, Yanmin Song, Weiyue Gu, Yan Liu, Lili Long
De novo variants in KCNJ3 are associated with early-onset epilepsy. Journal of medical genetics (2023)
Qi Tian, Li Shu, Chuqiang Shu, Hui Xi, Na Ma, Xiao Mao, Hua Wang
Compound heterozygous variants in MAN2B2 identified in a Chinese child with congenital disorders of glycosylation. European journal of human genetics : EJHG (2022)
Shanyu Pi, Xiao Mao, Hong-Yu Long, Hua Wang
A de novo inframe deletion variant in CAPZA2 tentacle domain with global developmental delay and secondary microcephaly. Clinical genetics 102 (4) (2022)
Alka Malhotra, Alban Ziegler, Li Shu, Renee Perrier, Louise Amlie-Wolf, Elizabeth Wohler, Nara Lygia de Macena Sobreira, Estelle Colin, Adeline Vanderver, Omar Sherbini, Katrien Stouffs, Emmanuel Scalais, Alessandro Serretti, Magalie Barth, Benjamin Navet, Paul Rollier, Hui Xi, Hua Wang, Hainan Zhang, Denise L Perry, Alessandra Ferrarini, Roberto Colombo, Alexander Pepler, Adele Schneider, Kiyotaka Tomiwa, Nobuhiko Okamoto, Naomichi Matsumoto, Noriko Miyake, Ryan Taft, Xiao Mao, Dominique Bonneau
De novo missense variants in LMBRD2 are associated with developmental and motor delays, brain structure abnormalities and dysmorphic features. Journal of medical genetics 58 (10) (2020)
Yanghui Zhang, Haoxian Li, Jing Liu, Huiming Yan, Qin Liu, Xianda Wei, Hui Xi, Zhengjun Jia, Lingqian Wu, Hua Wang
Molecular investigation in Chinese patients with primary carnitine deficiency. Molecular genetics & genomic medicine 7 (9) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Hua Wang