Lanlan Dai

666 total citations
8 papers, 303 citations indexed

About

Lanlan Dai is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Lanlan Dai has authored 8 papers receiving a total of 303 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Sensory Systems. Recurrent topics in Lanlan Dai's work include Genetic Syndromes and Imprinting (2 papers), Hedgehog Signaling Pathway Studies (2 papers) and Connexins and lens biology (2 papers). Lanlan Dai is often cited by papers focused on Genetic Syndromes and Imprinting (2 papers), Hedgehog Signaling Pathway Studies (2 papers) and Connexins and lens biology (2 papers). Lanlan Dai collaborates with scholars based in China, Sweden and Denmark. Lanlan Dai's co-authors include Xuanzhu Liu, Jianguo Zhang, Wei Li, Lin Yang, Mingrong Zhang, Zhiyong Zhou, Zhe Zhang, Xin He, Yi Wang and Aihua Wei and has published in prestigious journals such as Scientific Reports, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Lanlan Dai

8 papers receiving 300 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Lanlan Dai China	7	221	138	59	54	46	8	303
Khadim Shah Pakistan	10	178 0.8×	32 0.2×	84 1.4×	5 0.1×	16 0.3×	31	267
Lizhu Yang China	13	322 1.5×	53 0.4×	111 1.9×	5 0.1×	184 4.0×	30	377
Hirofumi Aoki Japan	8	57 0.3×	195 1.4×	9 0.2×	66 1.2×	4 0.1×	14	300
Fedor A. Konovalov Russia	11	161 0.7×	29 0.2×	107 1.8×	6 0.1×	10 0.2×	46	374
Eric Souied France	10	213 1.0×	40 0.3×	18 0.3×	6 0.1×	255 5.5×	19	367
Gou Takahashi Japan	8	315 1.4×	17 0.1×	151 2.6×	7 0.1×	10 0.2×	18	360
Zahid Azeem Pakistan	12	226 1.0×	101 0.7×	105 1.8×	11 0.2×	1 0.0×	24	358
Hao Chang United States	12	305 1.4×	149 1.1×	44 0.7×	11 0.2×	1 0.0×	29	434
Demelza Koehn United States	9	116 0.5×	48 0.3×	20 0.3×	4 0.1×	154 3.3×	10	260
Kirsten A. Wunderlich Germany	10	154 0.7×	16 0.1×	21 0.4×	25 0.5×	91 2.0×	12	282

Countries citing papers authored by Lanlan Dai

Since Specialization

Citations

This map shows the geographic impact of Lanlan Dai'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 Lanlan Dai with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lanlan Dai more than expected).

Fields of papers citing papers by Lanlan Dai

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lanlan Dai. 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 Lanlan Dai. The network helps show where Lanlan Dai may publish in the future.

Co-authorship network of co-authors of Lanlan Dai

This figure shows the co-authorship network connecting the top 25 collaborators of Lanlan Dai. A scholar is included among the top collaborators of Lanlan Dai 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 Lanlan Dai. Lanlan Dai is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

1.

Jespersgaard, Cathrine, Mingyan Fang, Mette Bertelsen, et al.. (2019). Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy. Scientific Reports. 9(1). 1219–1219. 86 indexed citations

2.

Wang, Yun, Huaizhou Wang, Chongyi Jiang, et al.. (2017). FBN3gene involved in pathogenesis of a Chinese family with Bardet-Biedl syndrome. Oncotarget. 8(49). 86718–86725. 5 indexed citations

3.

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

4.

Zhang, Feng, Lanlan Dai, Weimin Lin, et al.. (2015). Exome sequencing identified FGF12 as a novel candidate gene for Kashin-Beck disease. Functional & Integrative Genomics. 16(1). 13–17. 13 indexed citations

5.

Wang, Huijun, Xu Cao, Zhimiao Lin, et al.. (2014). Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome. Human Molecular Genetics. 24(1). 243–250. 37 indexed citations

6.

Wei, Aihua, Zhe Zhang, Xuanzhu Liu, et al.. (2013). Exome Sequencing Identifies SLC24A5 as a Candidate Gene for Nonsyndromic Oculocutaneous Albinism. Journal of Investigative Dermatology. 133(7). 1834–1840. 90 indexed citations

7.

Tang, Zhanli, et al.. (2013). Recurrent splice-site mutation in MBTPS2underlying IFAP syndrome with Olmsted syndrome-like features in a Chinese patient. Clinical and Experimental Dermatology. 39(2). 158–161. 17 indexed citations

8.

Lin, Zhimiao, Quan Chen, Lei Shi, et al.. (2012). Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia. The American Journal of Human Genetics. 91(5). 906–911. 47 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.

Explore authors with similar magnitude of impact