Zhimiao Lin (Z Lin)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 22

Top Venues

The British journal of dermatology

Clinical and experimental dermatology

Journal of the European Academy of Dermatology and Venereology : JEADV

Patient preference and adherence

Peking University First Hospital (PHD)

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

Education History

Peking University First Hospital

China

PHD :: Dermatology

Publications

Zhuoqing Gong, Kai Chen, Zhe Xu, Zhou Yang, Huijin Wang, Zhimiao Lin
Skin biopsy findings in megaconial congenital muscular dystrophy with psoriasiform lesions due to variants in CHKB. Journal of the European Academy of Dermatology and Venereology : JEADV (2023)
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)
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)
Juan Liu, Zhiming Chen, Linghan Hu, Zhongya Song, Ran Mo, Lemuel Shui-Lun Tsang, Yihe Liu, Xin Huang, Zhuoqing Gong, Ruiyu Xiang, Zhimiao Lin, Yong Yang
Three new founder mutations in Chinese patients with Nagashima-type palmoplantar keratoderma. The British journal of dermatology 187 (6) (2022)
Xuan Wang, Jun Liu, Junyi Chen, Xueyan Xu, Yadan Zhong, Yingping Xu, Ping Lu, Jia-jian Zhou, Zhimiao Lin, Bin Yang, Chao Yang
Loss-of-function mutations in CST6 cause dry skin, desquamation and abnormal keratosis without hypotrichosis. Clinical genetics (2022)
Juan Liu, Zhiming Chen, Linghan Hu, Zhongya Song, Ran Mo, Lemuel Shui-Lun Tsang, Yihe Liu, Xin Huang, Zhuoqing Gong, Zhimiao Lin, Yong Yang
Investigation of Nagashima-type palmoplantar keratoderma in China: A cross-sectional study of 234 patients. The Journal of dermatology (2022)
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)
Ran Mo, M Lin, M Lee, W Yan, H Wang, Zhimiao Lin
Nonsense mutations in KRT1 caused recessive epidermolytic palmoplantar keratoderma with knuckle pads. Journal of the European Academy of Dermatology and Venereology : JEADV 36 (10) (2022)
Z Gong, H Wang, Zhimiao Lin
Glycine substitution mutation of COL5A1 in classic Ehlers-Danlos syndrome: a case report and literature review. Clinical and experimental dermatology 46 (5) (2021)
Yi Zhao, Gang Wang, Wenqiong Ni, Zhiqiang Song, Kun Chen, Chunlei Zhang, Shoumin Zhang, Yangfeng Ding, Min Zheng, Yulin Shi, Zhimiao Lin, Xiaomin Liu, Xiaofei Zhang, Qintian Zhou, Kazi Deluwar Ahmed
Visit Adherence of Mild to Moderate Psoriasis Patients: A Mobile-Based Randomized Study. Patient preference and adherence 14 (2021)
Z Xu, Zhimiao Lin
Image Gallery: Cutaneous findings in an adult with X-linked reticulate pigmentary disorder. The British journal of dermatology 180 (2) (2020)
Jie Liu, Weilong Zhong, Bo Yu, Zhimiao Lin, Yalei Zheng, Xiaoping Hu
Generalized bullae in a young girl with KRT6A-related pachyonychia congenita. Pediatric dermatology 37 (5) (2020)
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)
X Chen, Y Yang, Zhimiao Lin
Image Gallery: Poikiloderma with neutropenia. The British journal of dermatology 180 (1) (2019)
Ruojun Wang, Zhimiao Lin
Image Gallery: Segmental multiple piloleiomyomas. The British journal of dermatology 179 (6) (2019)
Y Pan, W Zhong, H Wang, Y Yang, Zhimiao Lin
Reticulate acropigmentation of Kitamura with a novel mutation in ADAM10. Clinical and experimental dermatology 44 (6) (2018)
Y Pan, Y Men, Zhimiao Lin
Palmoplantar keratoderma Bothnia type with acrokeratoelastoidosis-like features due to AQP5 mutations. Clinical and experimental dermatology 44 (1) (2018)
W Zhong, Y Pan, Y Shao, Y Yang, B Yu, Zhimiao Lin
Atypical presentation of dyschromatosis universalis hereditaria with a novel ABCB6 mutation. Clinical and experimental dermatology 44 (3) (2018)

Zhimiao Lin.css-eqlu8i{font-size:small;padding-left:4px;} (Z Lin)

Publication Activity (10 Years)

Top Topics

Top Venues

Zhimiao Lin (Z Lin)