Renqian Du

1.0k total citations
13 papers, 304 citations indexed

About

Renqian Du is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Renqian Du has authored 13 papers receiving a total of 304 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 4 papers in Plant Science. Recurrent topics in Renqian Du's work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (4 papers) and Genomics and Rare Diseases (3 papers). Renqian Du is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (4 papers) and Genomics and Rare Diseases (3 papers). Renqian Du collaborates with scholars based in China, United States and Türkiye. Renqian Du's co-authors include Feng Zhang, Jin Li, Shilin Li, James R. Lupski, Zeynep Coban‐Akdemir, Xin Zhang, Xiaofei Song, Hongyan Wang, Ian M. Campbell and Shen Gu and has published in prestigious journals such as Scientific Reports, Genome Research and Human Molecular Genetics.

In The Last Decade

Renqian Du

13 papers receiving 298 citations

Peers

Renqian Du

GENET

RHEUM

H.‐J. Lüdecke Germany

Joyce Andrade Brazil

Milena Simioni Brazil

María Gabriela Obregón Argentina

Chureerat Phokaew Thailand

Mario Bengala Italy

Simone Schiller Germany

Jeannette Connerney United States

Magdalena Socha Poland

Marilena Carmela Di Giacomo Italy

H.‐J. Lüdecke Germany

Renqian Du

180 ×0.9

166 ×1.0

GENET

29 ×0.7

31 ×0.9

42 ×1.8

RHEUM

Citations per year, relative to Renqian Du Renqian Du (= 1×) peers H.‐J. Lüdecke

Countries citing papers authored by Renqian Du

Since Specialization

Citations

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

Fields of papers citing papers by Renqian Du

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renqian Du

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

All Works

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13 of 13 papers shown

Du, Renqian, Kai Kang, Fan Wang, et al.. (2022). A review of pre-implantation genetic testing technologies and applications. Reproductive and Developmental Medicine. 7(1). 20–31. 9 indexed citations

Song, Xiaofei, Christine R. Beck, Renqian Du, et al.. (2018). Predicting human genes susceptible to genomic instability associated with Alu/Alu-mediated rearrangements. Genome Research. 28(8). 1228–1242. 51 indexed citations

Lin, Ge, Aijie Liu, Kai Gao, et al.. (2018). Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy. Scientific Reports. 8(1). 14989–14989. 14 indexed citations

Du, Renqian, Zeynep Coban‐Akdemir, Yavuz Bayram, et al.. (2018). A biallelic ANTXR1 variant expands the anthrax toxin receptor associated phenotype to tooth agenesis. American Journal of Medical Genetics Part A. 176(4). 1015–1022. 10 indexed citations

Du, Renqian, Xiaofei Song, Zeynep Coban‐Akdemir, et al.. (2018). Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis. Human Genetics. 137(9). 689–703. 17 indexed citations

Du, Renqian, Lauren E. Petty, Zeynep Coban‐Akdemir, et al.. (2017). Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis. Journal of Dental Research. 97(1). 49–59. 48 indexed citations

Guan, Jing, Dayong Wang, Wenjian Cao, et al.. (2016). SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans. Journal of Human Genetics. 61(11). 917–922. 11 indexed citations

Zhao, Dandan, Renqian Du, Yuehua Zhang, et al.. (2015). Clinical and molecular genetic analysis of a family with late-onset LAMA2-related muscular dystrophy. Brain and Development. 38(2). 242–249. 10 indexed citations

Zhang, Xin, Renqian Du, Shilin Li, et al.. (2014). Evaluation of copy number variation detection for a SNP array platform. BMC Bioinformatics. 15(1). 50–50. 36 indexed citations

10.

Zhou, Weichen, et al.. (2014). Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genome. Human Molecular Genetics. 24(5). 1225–1233. 11 indexed citations

11.

Du, Renqian, Chuncheng Lu, Zhengwen Jiang, et al.. (2012). Efficient typing of copy number variations in a segmental duplication-mediated rearrangement hotspot using multiplex competitive amplification. Journal of Human Genetics. 57(8). 545–551. 50 indexed citations

12.

Jiang, Yuwu, Yuehua Zhang, Ping Zhang, et al.. (2012). NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy. Human Genetics. 131(7). 1217–1224. 30 indexed citations

13.

Du, Renqian, Jin Li, & Feng Zhang. (2011). Copy number variations in the human genome: their mutational mechanisms and roles in diseases. Hereditas (Beijing). 33(8). 857–869. 7 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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