Hu Tan

503 total citations
30 papers, 304 citations indexed

About

Hu Tan is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hu Tan has authored 30 papers receiving a total of 304 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 9 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hu Tan's work include Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (4 papers) and Connective tissue disorders research (4 papers). Hu Tan is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (4 papers) and Connective tissue disorders research (4 papers). Hu Tan collaborates with scholars based in China, Malaysia and Australia. Hu Tan's co-authors include Lingqian Wu, Siyuan Linpeng, Hongmin Zhu, David S. Cram, Yu Zhang, Hua Wang, Yingdi Liu, Fuli Yu, Huaiyu Sun and Feng Tian and has published in prestigious journals such as Gene, Clinica Chimica Acta and Genetics in Medicine.

In The Last Decade

Hu Tan

28 papers receiving 302 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hu Tan China 8 184 148 74 51 30 30 304
Siyuan Linpeng China 8 197 1.1× 131 0.9× 116 1.6× 58 1.1× 25 0.8× 26 319
Elizabeth Scotchman United Kingdom 9 255 1.4× 166 1.1× 104 1.4× 31 0.6× 35 1.2× 12 335
Tamar Goldwaser United States 6 147 0.8× 116 0.8× 56 0.8× 23 0.5× 30 1.0× 7 297
Fucheng Li China 9 77 0.4× 52 0.4× 69 0.9× 30 0.6× 31 1.0× 35 216
Tingying Lei China 10 157 0.9× 128 0.9× 148 2.0× 24 0.5× 47 1.6× 39 314
Jiansheng Xie China 10 65 0.4× 71 0.5× 155 2.1× 20 0.4× 42 1.4× 31 318
George Rebello South Africa 10 106 0.6× 67 0.5× 158 2.1× 25 0.5× 62 2.1× 25 316
Erica Sanford Kobayashi United States 10 31 0.2× 183 1.2× 95 1.3× 29 0.6× 30 1.0× 22 293
Irina Banzola Italy 11 192 1.0× 17 0.1× 86 1.2× 52 1.0× 25 0.8× 21 363
Chunyu Luo China 8 82 0.4× 61 0.4× 138 1.9× 16 0.3× 40 1.3× 35 258

Countries citing papers authored by Hu Tan

Since Specialization
Citations

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

Fields of papers citing papers by Hu Tan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hu Tan

This figure shows the co-authorship network connecting the top 25 collaborators of Hu Tan. A scholar is included among the top collaborators of Hu Tan 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 Hu Tan. Hu Tan 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
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Zhang, Hongyun, Xin Chen, Hu Tan, et al.. (2022). The exploration of genetic aetiology and diagnostic strategy for 321 Chinese individuals with intellectual disability. Clinica Chimica Acta. 538. 94–103. 1 indexed citations
4.
Liu, Xi, Xu G. Yu, Xijing Zhang, et al.. (2020). Epidemiological and clinical characteristics of 47 corona virus disease 2019 non-survivors in Huoshenshan Hospital. Jiefangjun yixue zazhi. 45(5). 475–480. 2 indexed citations
5.
Tan, Hu, et al.. (2020). Novel and recurrent variants identified in fetuses with central nervous system abnormalities by trios-medical exome sequencing. Clinica Chimica Acta. 510. 599–604. 14 indexed citations
6.
Liu, Yingdi, Zhuo Li, Siyuan Linpeng, et al.. (2020). A novel GJB1 mutation associated with X‐linked Charcot–Marie–Tooth disease in a large Chinese family pedigree. Molecular Genetics & Genomic Medicine. 8(3). e1127–e1127. 3 indexed citations
7.
Luo, Dan, et al.. (2019). Molecular genetic study of 59 Chinese Oculocutaneous albinism families. European Journal of Medical Genetics. 62(10). 103709–103709. 5 indexed citations
8.
Cram, David S., Hu Tan, Siyuan Linpeng, et al.. (2019). Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes. Genetics in Medicine. 21(9). 1998–2006. 167 indexed citations
9.
Lv, Weigang, et al.. (2019). Development and validation of a haplotype‐free technique for non‐invasive prenatal diagnosis of spinal muscular atrophy. Journal of Clinical Laboratory Analysis. 34(2). e23046–e23046. 10 indexed citations
10.
Tan, Hu, Xin Chen, Weigang Lv, et al.. (2018). Truncating mutations of HIBCH tend to cause severe phenotypes in cases with HIBCH deficiency: a case report and brief literature review. Journal of Human Genetics. 63(7). 851–855. 10 indexed citations
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Tan, Hu, et al.. (2018). Three Novel Mutations in <i>FBN1</i> and <i>TGFBR2</i> in Patients with the Syndromic Form of Thoracic Aortic Aneurysms and Dissections. International Heart Journal. 59(5). 1059–1068. 6 indexed citations
13.
Luo, Xiaomei, Yongyi Zou, Yue Zhang, et al.. (2017). Novel GATAD2B loss-of-function mutations cause intellectual disability in two unrelated cases. Journal of Human Genetics. 62(4). 513–516. 12 indexed citations
14.
Tan, Hu, Pu Yang, Yanru Huang, et al.. (2017). A lesson from a reported pathogenic variant in Peutz-Jeghers syndrome: a case report. Familial Cancer. 16(3). 417–422. 2 indexed citations
15.
Huang, Yanru, Weigang Lv, Haoxian Li, et al.. (2016). Targeted exome sequencing identifies novel compound heterozygous mutations in P3H1 in a fetus with osteogenesis imperfecta type VIII. Clinica Chimica Acta. 464. 170–175. 4 indexed citations
16.
Tan, Hu, Yanru Huang, Pu Yang, et al.. (2016). Three novel mutations of STK11 gene in Chinese patients with Peutz–Jeghers syndrome. BMC Medical Genetics. 17(1). 77–77. 7 indexed citations
17.
Yang, Pu, Hu Tan, Yan Xia, et al.. (2016). De novo exonic deletion of KDM6A in a Chinese girl with Kabuki syndrome: A case report and brief literature review. American Journal of Medical Genetics Part A. 170(6). 1613–1621. 13 indexed citations
18.
Tan, Hu, Pu Yang, Haoxian Li, et al.. (2015). A novel FOXL2 mutation in a Chinese family with blepharophimosis, ptosis, epicanthus inversus syndrome. Human Genome Variation. 2(1). 15008–15008. 1 indexed citations
19.
Li, Haoxian, Yanghui Zhang, Ying Peng, et al.. (2015). Rare intracranial cholesterol deposition and a homozygous mutation of LDLR in a familial hypercholesterolemia patient. Gene. 569(2). 313–317. 5 indexed citations
20.
Huang, Yanru, Qian Pan, Hu Tan, et al.. (2015). Novel de novo nonsense mutation of the PHEX gene (p.Lys50Ter) in a Chinese patient with hypophosphatemic rickets. Gene. 565(1). 150–154. 4 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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