Chanjuan Hao

1.5k total citations
61 papers, 1.0k citations indexed

About

Chanjuan Hao is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Chanjuan Hao has authored 61 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 15 papers in Genetics and 9 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Chanjuan Hao's work include Genomics and Rare Diseases (8 papers), Effects and risks of endocrine disrupting chemicals (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Chanjuan Hao is often cited by papers focused on Genomics and Rare Diseases (8 papers), Effects and risks of endocrine disrupting chemicals (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Chanjuan Hao collaborates with scholars based in China, United States and United Kingdom. Chanjuan Hao's co-authors include Hong‐Fei Xia, Xu Ma, Ruolan Guo, Yi Hu, Xu Ma, Wei Li, Jun Guo, Xiaoli Guo, Xuyun Hu and Wei Li and has published in prestigious journals such as Nature Communications, The Journal of Cell Biology and Biochemical and Biophysical Research Communications.

In The Last Decade

Chanjuan Hao

54 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chanjuan Hao China	18	370	339	152	151	127	61	1.0k
Andrea Reyna‐Neyra United States	17	490 1.3×	167 0.5×	204 1.3×	82 0.5×	98 0.8×	25	1.3k
Mafalda Cacciottolo United States	17	480 1.3×	447 1.3×	62 0.4×	108 0.7×	327 2.6×	29	1.4k
Minhan Ka South Korea	21	588 1.6×	104 0.3×	233 1.5×	101 0.7×	81 0.6×	43	1.1k
Haiyan Guan Canada	22	268 0.7×	277 0.8×	98 0.6×	79 0.5×	223 1.8×	33	1.3k
Robert N. Wine United States	18	441 1.2×	214 0.6×	88 0.6×	101 0.7×	67 0.5×	31	1.1k
Magnus R. Dias‐da‐Silva Brazil	22	865 2.3×	282 0.8×	302 2.0×	113 0.7×	39 0.3×	100	1.8k
Amy McCurley United States	14	521 1.4×	77 0.2×	142 0.9×	113 0.7×	128 1.0×	15	1.7k
Bryce A. Mendelsohn United States	16	561 1.5×	69 0.2×	184 1.2×	62 0.4×	106 0.8×	28	1.0k
Laure Bernard France	13	298 0.8×	257 0.8×	145 1.0×	46 0.3×	89 0.7×	17	798
Daniel B. Martinez–Arguelles Canada	20	333 0.9×	644 1.9×	170 1.1×	101 0.7×	54 0.4×	27	1.2k

Countries citing papers authored by Chanjuan Hao

Since Specialization

Citations

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

Fields of papers citing papers by Chanjuan Hao

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chanjuan Hao

This figure shows the co-authorship network connecting the top 25 collaborators of Chanjuan Hao. A scholar is included among the top collaborators of Chanjuan Hao 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 Chanjuan Hao. Chanjuan Hao 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:

20 of 20 papers shown

He, Huan, et al.. (2025). Sex-based differences in mitochondrial activity and cellular calcium signaling in isolated mice cardiomyocytes intervened by doxorubicin. Biochemical and Biophysical Research Communications. 778. 152328–152328.

Sun, Qiqing, et al.. (2024). Cardiomyopathy in children: a single-centre, retrospective study of genetic and clinical characteristics. BMJ Paediatrics Open. 8(1). e002024–e002024.

Fan, Chaonan, et al.. (2024). Clinical and genetic characteristics of RANBP2 mutations in children with acute necrotizing encephalopathy. Neurological Sciences. 46(4). 1817–1826. 1 indexed citations

Leng, Fei, Song Mei, Xiaolin Zhou, et al.. (2023). DVsc: An Automated Framework for Efficiently Detecting Viral Infection from Single-cell Transcriptomics Data. Genomics Proteomics & Bioinformatics. 22(2).

Wang, Qiaochu, Yizhen Wang, Zhan Qi, et al.. (2023). A gain-of-function TPC2 variant R210C increases affinity to PI(3,5)P2 and causes lysosome acidification and hypopigmentation. Nature Communications. 14(1). 226–226. 17 indexed citations

Liu, Xuanshi, Wenjian Xu, Fei Leng, et al.. (2023). NeuroCNVscore: a tissue-specific framework to prioritise the pathogenicity of CNVs in neurodevelopmental disorders. BMJ Paediatrics Open. 7(1). e001966–e001966. 3 indexed citations

Zhang, Yue, Ying Li, Ruolan Guo, et al.. (2023). Genetic diagnostic yields of 354 Chinese ASD children with rare mutations by a pipeline of genomic tests. Frontiers in Genetics. 14. 1108440–1108440. 3 indexed citations

Zhang, Wenyan, Ruolan Guo, Zhan Qi, et al.. (2022). Newborn Genetic Screening Revealed Increased Levels of Biochemical Indicators in Carriers of Heterozygous Variants. Genetic Testing and Molecular Biomarkers. 26(12). 573–581.

Chen, Yuanying, Qiqing Sun, Chanjuan Hao, et al.. (2022). Identification of a novel variant in N-cadherin associated with dilated cardiomyopathy. Frontiers in Medicine. 9. 944950–944950. 3 indexed citations

10.

Zhang, Wenyan, Ruolan Guo, Shuang Zhao, et al.. (2022). Molecular identification of T-box transcription factor 6 and prognostic assessment in patients with congenital scoliosis: A single-center study. Frontiers in Medicine. 9. 941468–941468.

11.

Hao, Chanjuan, Ruolan Guo, Jun Liu, et al.. (2021). Exome sequencing as the first‐tier test for pediatric respiratory diseases: A single‐center study. Human Mutation. 42(7). 891–900. 2 indexed citations

12.

Su, Yan, et al.. (2021). Case Report : Li-Fraumeni Syndrome with Central Nervous System Tumors in Two Siblings. BMC Pediatrics. 21(1). 588–588. 6 indexed citations

13.

Tang, Xiaolei, et al.. (2021). Clinical and Genetic Spectrum of Children With Primary Ciliary Dyskinesia in China. CHEST Journal. 159(5). 1768–1781. 50 indexed citations

14.

Hu, Xuyun, Ruolan Guo, Jun Guo, et al.. (2020). Parallel Tests of Whole Exome Sequencing and Copy Number Variant Sequencing Increase the Diagnosis Yields of Rare Pediatric Disorders. Frontiers in Genetics. 11. 473–473. 12 indexed citations

15.

Liu, Jun, Xuyun Hu, Ruolan Guo, et al.. (2019). Compound heterozygous LPIN2 pathogenic variants in a patient with Majeed syndrome with recurrent fever and severe neutropenia: case report. BMC Medical Genetics. 20(1). 11 indexed citations

16.

Guo, Jun, Zheng Li, Chanjuan Hao, et al.. (2019). A novel de novo CASZ1 heterozygous frameshift variant causes dilated cardiomyopathy and left ventricular noncompaction cardiomyopathy. Molecular Genetics & Genomic Medicine. 7(8). e828–e828. 20 indexed citations

17.

Hu, Xuyun, Jun Liu, Ruolan Guo, et al.. (2019). A novel 14q13.1–21.1 deletion identified by CNV-Seq in a patient with brain-lung-thyroid syndrome, tooth agenesis and immunodeficiency. Molecular Cytogenetics. 12(1). 51–51. 5 indexed citations

18.

Hao, Chanjuan. (2012). Perinatal exposure to diethyl-hexyl-phthalate induces obesity in mice. Frontiers in Bioscience-Elite. E5(2). 725–733. 83 indexed citations

19.

Hao, Chanjuan, et al.. (2012). The Endocrine Disruptor 4-Nonylphenol Promotes Adipocyte Differentiation and Induces Obesity in Mice. Cellular Physiology and Biochemistry. 30(2). 382–394. 56 indexed citations

20.

Hu, Yi, Chunmei Liu, Lu Qi, et al.. (2011). Two common SNPs in pri-miR-125a alter the mature miRNA expression and associate with recurrent pregnancy loss in a Han-Chinese population. RNA Biology. 8(5). 861–872. 95 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