Hongchuan Nie

895 total citations
24 papers, 560 citations indexed

About

Hongchuan Nie is a scholar working on Reproductive Medicine, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Hongchuan Nie has authored 24 papers receiving a total of 560 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Reproductive Medicine, 14 papers in Genetics and 13 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Hongchuan Nie's work include Sperm and Testicular Function (15 papers), Reproductive Biology and Fertility (13 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers). Hongchuan Nie is often cited by papers focused on Sperm and Testicular Function (15 papers), Reproductive Biology and Fertility (13 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers). Hongchuan Nie collaborates with scholars based in China and United States. Hongchuan Nie's co-authors include Lanlan Meng, Yue‐Qiu Tan, Chaofeng Tu, Juan Du, Ge Lin, Guangxiu Lu, Liqing Fan, Wenbing Zhu, Weili Wang and Shi‐Min Yuan and has published in prestigious journals such as Scientific Reports, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Hongchuan Nie

22 papers receiving 549 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hongchuan Nie China 14 350 267 257 161 67 24 560
Filipe Tenório Lira Neto Brazil 7 365 1.0× 223 0.8× 152 0.6× 208 1.3× 43 0.6× 15 577
Paula Intasqui Brazil 16 508 1.5× 274 1.0× 102 0.4× 150 0.9× 29 0.4× 30 657
Vertika Singh India 14 252 0.7× 153 0.6× 138 0.5× 205 1.3× 98 1.5× 20 526
Manjit K. Gill‐Sharma India 9 211 0.6× 128 0.5× 156 0.6× 119 0.7× 41 0.6× 13 418
Paul Gassner Australia 10 295 0.8× 160 0.6× 71 0.3× 144 0.9× 69 1.0× 18 512
Ricardo Pommer Chile 16 395 1.1× 268 1.0× 135 0.5× 135 0.8× 151 2.3× 31 669
Shaobin Lin China 9 152 0.4× 122 0.5× 168 0.7× 99 0.6× 38 0.6× 11 296
Marta Olszewska Poland 13 347 1.0× 206 0.8× 273 1.1× 310 1.9× 92 1.4× 38 635
Margot J. Wyrwoll Germany 10 228 0.7× 143 0.5× 197 0.8× 232 1.4× 47 0.7× 22 452
Sofia Boeg Winge Denmark 13 173 0.5× 73 0.3× 124 0.5× 168 1.0× 42 0.6× 22 449

Countries citing papers authored by Hongchuan Nie

Since Specialization
Citations

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

Fields of papers citing papers by Hongchuan Nie

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hongchuan Nie

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

All Works

20 of 20 papers shown
1.
Xu, Yue‐Ping, Hongchuan Nie, Hui Zhang, et al.. (2025). In vitro induction and characterization of octaploid Schizachyrium scoparium, an ornamental grass. Plant Cell Tissue and Organ Culture (PCTOC). 160(2).
2.
Lu, Wen‐Qing, Yong Li, Lanlan Meng, et al.. (2024). Novel SPEF2 variants cause male infertility and likely primary ciliary dyskinesia. Journal of Assisted Reproduction and Genetics. 41(6). 1485–1498. 1 indexed citations
3.
Meng, Lanlan, Chen Tan, Wenbin He, et al.. (2023). Novel homozygous variants in TTC12 cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella. Frontiers in Cell and Developmental Biology. 11. 1184331–1184331. 7 indexed citations
4.
Li, Yunhao, Yong Li, Ying Wang, et al.. (2022). Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility. Journal of Assisted Reproduction and Genetics. 40(1). 41–51. 7 indexed citations
5.
Wang, Yurong, Ling Liu, Chen Tan, et al.. (2022). Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia. Frontiers in Genetics. 13. 936264–936264. 13 indexed citations
6.
Huang, Chuan, et al.. (2022). Genetic testing of sperm donors at a human sperm bank in China. Frontiers in Endocrinology. 13. 942447–942447.
7.
Wang, Weili, Lanlan Meng, Jiaxin He, et al.. (2022). Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice. Molecular Human Reproduction. 28(6). 9 indexed citations
8.
Wang, Weili, Hongchuan Nie, Chaofeng Tu, et al.. (2021). CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis. Human Molecular Genetics. 30(23). 2240–2254. 33 indexed citations
9.
Tan, Chen, Lanlan Meng, Mingrong Lv, et al.. (2021). Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice. The American Journal of Human Genetics. 109(1). 157–171. 32 indexed citations
10.
Tu, Chaofeng, Ying Wang, Hongchuan Nie, et al.. (2020). An M1AP homozygous splice‐site mutation associated with severe oligozoospermia in a consanguineous family. Clinical Genetics. 97(5). 741–746. 17 indexed citations
11.
Li, Yong, Weili Wang, Chaofeng Tu, et al.. (2020). A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans. Asian Journal of Andrology. 23(2). 197–204. 18 indexed citations
12.
Tu, Chaofeng, Hongchuan Nie, Lanlan Meng, et al.. (2020). Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD. Human Genetics. 139(2). 257–271. 57 indexed citations
13.
Wang, Ying, Chaofeng Tu, Hongchuan Nie, et al.. (2020). Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia. Journal of Assisted Reproduction and Genetics. 37(4). 811–820. 16 indexed citations
14.
Wang, Xingming, Ruixue Li, Zhizhong Liu, et al.. (2020). Improving native human sperm freezing protection by using a modified vitrification method. Asian Journal of Andrology. 23(1). 91–96. 13 indexed citations
15.
Tu, Chaofeng, Lanlan Meng, Hongchuan Nie, et al.. (2020). A homozygous RPL10L missense mutation associated with male factor infertility and severe oligozoospermia. Fertility and Sterility. 113(3). 561–568. 17 indexed citations
16.
Wang, Weili, Chaofeng Tu, Hongchuan Nie, et al.. (2019). Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations. Journal of Medical Genetics. 56(11). 750–757. 70 indexed citations
17.
Wang, Xingming, Zhizhong Liu, Zeng‐Hui Huang, et al.. (2019). The expression characteristics of FBXW7 in human testis suggest its function is different from that in mice. Tissue and Cell. 62. 101315–101315. 13 indexed citations
18.
Tu, Chaofeng, Hongchuan Nie, Lanlan Meng, et al.. (2019). Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella. Scientific Reports. 9(1). 15864–15864. 51 indexed citations
19.
Huang, Chuan, Baishun Li, Dan Liu, et al.. (2016). Decline in semen quality among 30,636 young Chinese men from 2001 to 2015. Fertility and Sterility. 107(1). 83–88.e2. 138 indexed citations
20.
Nie, Hongchuan & Guangxiu Lu. (2010). Long Y chromosome is not a fetal loss risk. Journal of Assisted Reproduction and Genetics. 28(2). 151–156. 6 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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