Zhimiao Lin

2.5k total citations
62 papers, 857 citations indexed

About

Zhimiao Lin is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Zhimiao Lin has authored 62 papers receiving a total of 857 indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 24 papers in Cell Biology and 12 papers in Genetics. Recurrent topics in Zhimiao Lin's work include Skin and Cellular Biology Research (21 papers), Pain Mechanisms and Treatments (7 papers) and Hair Growth and Disorders (6 papers). Zhimiao Lin is often cited by papers focused on Skin and Cellular Biology Research (21 papers), Pain Mechanisms and Treatments (7 papers) and Hair Growth and Disorders (6 papers). Zhimiao Lin collaborates with scholars based in China, United States and Hong Kong. Zhimiao Lin's co-authors include Yong Yang, Huijun Wang, Lynda Tyrrell, Stephen G. Waxman, Sulayman D. Dib‐Hajj, Michael A. Gomez, James C. Carrington, Nigel J. Taylor, Brian J. Staskawicz and Luke Hayden and has published in prestigious journals such as New England Journal of Medicine, Cell and SHILAP Revista de lepidopterología.

In The Last Decade

Zhimiao Lin

57 papers receiving 844 citations

Peers

Zhimiao Lin

PHYSI

CMN

Yanli Zhu China

Xuyang Liu China

Ye Tao China

Julia F. Doerner Germany

Xuechao Feng China

Miwako Matsuki-Fukushima Japan

David B. West United States

Helen M. Brereton Australia

M. Wolff Germany

Tariq Zaman Pakistan

Yanli Zhu China

Zhimiao Lin

486 ×0.9

111 ×0.5

PHYSI

67 ×0.3

80 ×0.7

CMN

12 ×0.1

Citations per year, relative to Zhimiao Lin Zhimiao Lin (= 1×) peers Yanli Zhu

Countries citing papers authored by Zhimiao Lin

Since Specialization

Citations

This map shows the geographic impact of Zhimiao Lin's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Zhimiao Lin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Zhimiao Lin more than expected).

Fields of papers citing papers by Zhimiao Lin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Zhimiao Lin. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Zhimiao Lin. The network helps show where Zhimiao Lin may publish in the future.

Co-authorship network of co-authors of Zhimiao Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Zhimiao Lin. A scholar is included among the top collaborators of Zhimiao Lin based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Zhimiao Lin. Zhimiao Lin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Wang, Huijun, Yuan Wu, Jennifer A. Bassetti, et al.. (2024). A gain-of-function variant in SREBF1 causes generalized skin hyperpigmentation with congenital cataracts. British Journal of Dermatology. 191(5). 805–815. 1 indexed citations

Yang, Chao, Zhaoyang Wang, Zigang Xu, et al.. (2024). Loss-of-function variants in GLMN are associated with generalized skin hyperpigmentation with or without glomuvenous malformation. British Journal of Dermatology. 191(1). 107–116. 2 indexed citations

Wang, Huijun, et al.. (2024). Dermatopathological features and successful treatment with topical antioxidant for ichthyosiform lesions in Mitchell syndrome caused by an ACOX1 variant. The Journal of Dermatology. 52(3). 445–451. 2 indexed citations

Yang, Jianqiu, et al.. (2023). Biallelic mutations in LSS in autosomal‐recessive mutilating palmoplantar keratoderma. Experimental Dermatology. 32(5). 699–706. 2 indexed citations

Zhang, Bin, Zigang Xu, Wei Li, et al.. (2023). Somatic mutation spectrum of a Chinese cohort of pediatrics with vascular malformations. Orphanet Journal of Rare Diseases. 18(1). 261–261. 3 indexed citations

Yang, Fang, et al.. (2023). Postzygotic gain-of-function variants in FGFR2 in two patients with hair follicle naevus. British Journal of Dermatology. 189(5). 641–643.

Chen, Wei, Jiayu Wang, Wenlong Yang, et al.. (2023). Detection of low-frequency mutations in clinical samples by increasing mutation abundance via the excision of wild-type sequences. Nature Biomedical Engineering. 7(12). 1602–1613. 23 indexed citations

Wang, Huijun, et al.. (2023). PLACK syndrome caused by novel pathogenic variants in CAST: a case report and literature review. Clinical and Experimental Dermatology. 48(9). 1052–1055. 2 indexed citations

Yang, Fang, Ming-Yang Lee, Zhengren Xu, et al.. (2022). Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2. Journal of Investigative Dermatology. 142(10). 2687–2694.e2. 8 indexed citations

10.

Lee, Ming-Yang, et al.. (2022). Variants in KLK11, affecting signal peptide cleavage of kallikrein-related peptidase 11, cause an autosomal-dominant cornification disorder. British Journal of Dermatology. 188(1). 100–111. 6 indexed citations

11.

Liu, Jun, Yingping Xu, Ping Lü, et al.. (2022). Loss‐of‐function mutations in CST6 cause dry skin, desquamation and abnormal keratosis without hypotrichosis. Clinical Genetics. 103(3). 301–309. 2 indexed citations

12.

Wang, Chu, et al.. (2022). KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia. Journal of Investigative Dermatology. 142(8). 2079–2087.e8. 9 indexed citations

13.

Hu, Linghan, et al.. (2022). Investigation of Nagashima‐type palmoplantar keratoderma in China: A cross‐sectional study of 234 patients. The Journal of Dermatology. 50(3). 375–382. 6 indexed citations

14.

Chen, Xi, Vesna Stanić, Zhimiao Lin, et al.. (2021). Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes. Journal of Investigative Dermatology. 141(8). 1964–1974. 25 indexed citations

15.

Liu, Jie, et al.. (2020). Generalized bullae in a young girl with KRT6A‐related pachyonychia congenita. Pediatric Dermatology. 37(5). 974–976. 1 indexed citations

16.

Gomez, Michael A., Zhimiao Lin, Raj Deepika Chauhan, et al.. (2018). Simultaneous CRISPR /Cas9‐mediated editing of cassava eIF 4E isoforms nCBP ‐1 and nCBP ‐2 reduces cassava brown streak disease symptom severity and incidence. Plant Biotechnology Journal. 17(2). 421–434. 213 indexed citations

17.

Duo, Lina, Huijun Wang, & Zhimiao Lin. (2016). Mutation analysis of the SERPINB7 gene in two patients with Nagashima-type palmoplantar keratoderma. Chinese Journal of Dermatology. 49(3). 180–182. 1 indexed citations

18.

Su, Zhonglan, Kan Xing Wu, Hao Song, et al.. (2016). Hutchinson-Gilford progeria syndrome. International Journal of Dermatology and Venereology. 42(2). 65–67. 1 indexed citations

19.

Lin, Zhimiao, et al.. (2015). HABP2 Mutation and Nonmedullary Thyroid Cancer.. New England Journal of Medicine. 373(21). 2084–2085. 16 indexed citations

20.

Zhang, Jie, Lina Duo, Zhimiao Lin, et al.. (2015). Exome sequencing reveals novel BCS1L mutations in siblings with hearing loss and hypotrichosis. Gene. 566(1). 84–88. 8 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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