Huijun Wang (H Wang, Huijin Wang)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 23

Top Topics

Dna Methylation

Chronic Myeloid Leukemia

Top Venues

The British journal of dermatology

Clinical and experimental dermatology

Journal of the European Academy of Dermatology and Venereology : JEADV

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

Publications

Xingyuan Jiang, Chao Yang, Zhaoyang Wang, Lina Liang, Zhuoqing Gong, Shimiao Huang, Zigang Xu, Bin Zhang, Xiaoping Pei, Liangqi Cai, Huijun Wang, Zhimiao Lin
Loss-of-function variants in GLMN are associated with generalized skin hyperpigmentation with or without glomuvenous malformation. The British journal of dermatology 191 (1) (2024)
Xingyuan Jiang, Chao Yang, Zhaoyang Wang, Lina Liang, Zhuoqing Gong, Shimiao Huang, Zigang Xu, Bin Zhang, Xiaoping Pei, Liangqi Cai, Huijun Wang, Zhimiao Lin
Loss-of-function variants in GLMN are associated with generalized skin hyperpigmentation with or without glomuvenous malformation. The British journal of dermatology 191 (1) (2024)
Lina Liang, Sha Peng, Shimiao Huang, Huijun Wang, Zhimiao Lin
Progressive hyperpigmentation and lentigines due to KIT variants improving with imatinib. The British journal of dermatology 191 (1) (2024)
Xingyuan Jiang, Chao Yang, Zhaoyang Wang, Lina Liang, Zhuoqing Gong, Shimiao Huang, Zigang Xu, Bin Zhang, Xiaoping Pei, Liangqi Cai, Huijun Wang, Zhimiao Lin
Loss-of-function variants in GLMN are associated with generalized skin hyperpigmentation with or without glomuvenous malformation. The British journal of dermatology (2024)
Xingyuan Jiang, Chao Yang, Zhaoyang Wang, Lina Liang, Zhuoqing Gong, Shimiao Huang, Zigang Xu, Bin Zhang, Xiaoping Pei, Liangqi Cai, Huijun Wang, Zhimiao Lin
Loss-of-function variants in GLMN are associated with generalized skin hyperpigmentation with or without glomuvenous malformation. The British journal of dermatology 191 (1) (2024)
Huijun Wang, Yuan Wu, Jennifer A Bassetti, Zhaoyang Wang, Vikash S Oza, Sneha A Rangu, Bobbi McGivern, Sha Peng, Lina Liang, Shimiao Huang, Zhuoqing Gong, Zigang Xu, Zhimiao Lin
A gain-of-function variant in SREBF1 causes generalized skin hyperpigmentation with congenital cataracts. The British journal of dermatology (2024)
Lina Liang, Sha Peng, Shimiao Huang, Huijun Wang, Zhimiao Lin
Progressive hyperpigmentation and lentigines due to KIT variants improving with imatinib. The British journal of dermatology 191 (1) (2024)
Lina Liang, Sha Peng, Shimiao Huang, Huijun Wang, Zhimiao Lin
Progressive hyperpigmentation and lentigines due to KIT variants improving with imatinib. The British journal of dermatology (2024)
Lina Liang, Sha Peng, Shimiao Huang, Huijun Wang, Zhimiao Lin
Progressive hyperpigmentation and lentigines due to KIT variants improving with imatinib. The British journal of dermatology 191 (1) (2024)
Xingyuan Jiang, Chao Yang, Zhaoyang Wang, Lina Liang, Zhuoqing Gong, Shimiao Huang, Zigang Xu, Bin Zhang, Xiaoping Pei, Liangqi Cai, Huijun Wang, Zhimiao Lin
Loss-of-function variants in GLMN are associated with generalized skin hyperpigmentation with or without glomuvenous malformation. The British journal of dermatology (2024)
Xingyuan Jiang, Chao Yang, Zhaoyang Wang, Lina Liang, Zhuoqing Gong, Shimiao Huang, Zigang Xu, Bin Zhang, Xiaoping Pei, Liangqi Cai, Huijun Wang, Zhimiao Lin
Loss-of-function variants in GLMN are associated with generalized skin hyperpigmentation with or without glomuvenous malformation. The British journal of dermatology 191 (1) (2024)
Xingyuan Jiang, Chao Yang, Zhaoyang Wang, Lina Liang, Zhuoqing Gong, Shimiao Huang, Zigang Xu, Bin Zhang, Xiaoping Pei, Liangqi Cai, Huijun Wang, Zhimiao Lin
Loss-of-function variants in GLMN are associated with generalized skin hyperpigmentation with or without glomuvenous malformation. The British journal of dermatology (2024)
Zijuan Wang, Zeqiao Zhang, Jun Liu, Huijun Wang, Zhimiao Lin
A loss-of-function variant in KLF4 affecting zinc finger motifs causes progressive symmetric erythrokeratodermia. The British journal of dermatology (2024)
Ruzeng Xue, Qing Cheng, Ming Li, Sha Peng, Lina Liang, Mao-Ying Lin, Huijun Wang, Zhimiao Lin
A case of familial Flegel's disease caused by a novel splicing variant in SPTLC1. Clinical and experimental dermatology (2023)
Huijun Wang, Zhimiao Lin
Identification of the underlying gene for Flegel disease: another 'two-hit' genodermatosis? The British journal of dermatology 188 (1) (2023)
Huijun Wang, Zhimiao Lin
Identification of the underlying gene for Flegel disease: another 'two-hit' genodermatosis? The British journal of dermatology 188 (1) (2023)
Liangqi Cai, Zhimiao Lin, Huijun Wang
A novel CLDN1 variant identified in a case of ILVAC syndrome with sparse curly hair. Clinical and experimental dermatology (2023)
Bin Hu, Zhuoqing Gong, Sha Peng, Huijun Wang, Liuqing Chen, Zhimiao Lin
PLACK syndrome caused by novel pathogenic variants in CAST: a case report and literature review. Clinical and experimental dermatology (2023)
Zhuoqing Gong, Shangzhi Dai, Xingyuan Jiang, Mingyang Lee, Xuejun Zhu, Huijun Wang, Zhimiao Lin
Variants in KLK11, affecting signal peptide cleavage of kallikrein-related peptidase 11, cause an autosomal-dominant cornification disorder. The British journal of dermatology 188 (1) (2023)
Qing Cheng, Fang Yang, Ruzeng Xue, Huijun Wang, Zhimiao Lin
Postzygotic gain-of-function variants in FGFR2 in two patients with hair follicle nevus. The British journal of dermatology (2023)
Sai Wang, Qianqian Bai, Mingyang Lee, Zhimiao Lin, Liangqi Cai, Huijun Wang
A novel KRT16 frameshift variant causing pachyonychia congenita by re-initiation of translation. Journal of the European Academy of Dermatology and Venereology : JEADV (2022)
X Jiang, Zhimiao Lin, Huijun Wang
Multiple lentigines and cutaneous hyperpigmentation caused by a KIT mutation. The British journal of dermatology 183 (5) (2020)
S Dai, Z Sun, M Lee, Huijun Wang, Y Yang, Zhimiao Lin
Olmsted syndrome with alopecia universalis caused by heterozygous mutation in PERP. The British journal of dermatology 182 (1) (2019)