Asan

6.7k total citations
31 papers, 1.2k citations indexed

About

Asan is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Asan has authored 31 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 16 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Asan's work include Connective tissue disorders research (8 papers), Prenatal Screening and Diagnostics (6 papers) and Renal and related cancers (4 papers). Asan is often cited by papers focused on Connective tissue disorders research (8 papers), Prenatal Screening and Diagnostics (6 papers) and Renal and related cancers (4 papers). Asan collaborates with scholars based in China, United Kingdom and United States. Asan's co-authors include Xiuqing Zhang, Nicholas Caruccio, Jay Shendure, Xun Xu, Jacob O. Kitzman, Alexandra P MacKenzie, Andrew C. Adey, Emily H. Turner, Hilary G. Morrison and Bethany Stackhouse and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Current Biology.

In The Last Decade

Asan

29 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Asan China 18 689 538 164 160 116 31 1.2k
Emmelien Aten Netherlands 13 573 0.8× 333 0.6× 71 0.4× 70 0.4× 95 0.8× 17 1.0k
Juan Du China 23 732 1.1× 690 1.3× 78 0.5× 70 0.4× 188 1.6× 110 1.6k
Steven A. Vokes United States 22 1.8k 2.6× 443 0.8× 54 0.3× 126 0.8× 50 0.4× 37 2.1k
Graham McVicker United States 13 1.5k 2.2× 948 1.8× 183 1.1× 236 1.5× 45 0.4× 23 2.2k
Michał Witt Poland 25 690 1.0× 671 1.2× 93 0.6× 172 1.1× 158 1.4× 87 1.7k
Shinji Kondo Japan 19 1.5k 2.2× 390 0.7× 148 0.9× 362 2.3× 36 0.3× 41 1.9k
Sabine Guth Switzerland 16 1.7k 2.4× 431 0.8× 100 0.6× 544 3.4× 67 0.6× 23 2.2k
A M Giusti United States 15 882 1.3× 969 1.8× 83 0.5× 67 0.4× 68 0.6× 19 1.7k
Tomas Fitzgerald United Kingdom 20 911 1.3× 906 1.7× 248 1.5× 240 1.5× 153 1.3× 43 1.6k
Patricia A. Martin‐DeLeon United States 29 1.0k 1.5× 439 0.8× 119 0.7× 144 0.9× 78 0.7× 85 2.0k

Countries citing papers authored by Asan

Since Specialization
Citations

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

Fields of papers citing papers by Asan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Asan

This figure shows the co-authorship network connecting the top 25 collaborators of Asan. A scholar is included among the top collaborators of Asan 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 Asan. Asan 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.
Zhao, Yanping, Jiandong Li, Gongsang Quzhen, et al.. (2022). Echinococcus spp. and genotypes infecting humans in Tibet Autonomous Region of China: a molecular investigation with near-complete/complete mitochondrial sequences. Parasites & Vectors. 15(1). 75–75. 10 indexed citations
2.
Li, Ang, Ying‐Xia Cui, Jianhong Liu, et al.. (2018). Three Novel Heterozygous<b><i> COL4A4</i></b> Mutations Result in Three Different Collagen Type IV Kidney Disease Phenotypes. Cytogenetic and Genome Research. 154(1). 30–36.
3.
Ye, Jun, Chao Chen, Yuan Yuan, et al.. (2018). Haplotype-based Noninvasive Prenatal Diagnosis of Hyperphenylalaninemia through Targeted Sequencing of Maternal Plasma. Scientific Reports. 8(1). 161–161. 16 indexed citations
4.
Asan, Dexuan Ma, Fang Lv, et al.. (2017). Gene mutation spectrum and genotype-phenotype correlation in a cohort of Chinese osteogenesis imperfecta patients revealed by targeted next generation sequencing. Osteoporosis International. 28(10). 2985–2995. 63 indexed citations
5.
Lv, Fang, Xiaojie Xu, Yuwen Song, et al.. (2017). Novel Mutations in PLOD2 Cause Rare Bruck Syndrome. Calcified Tissue International. 102(3). 296–309. 19 indexed citations
6.
Qi, Xuan, Qianqian Pang, Jiawei Wang, et al.. (2017). Familial Early-Onset Paget’s Disease of Bone Associated with a Novel hnRNPA2B1 Mutation. Calcified Tissue International. 101(2). 159–169. 25 indexed citations
7.
Hackinger, Sophie, Thirsa Kraaijenbrink, Yali Xue, et al.. (2016). Wide distribution and altitude correlation of an archaic high-altitude-adaptive EPAS1 haplotype in the Himalayas. Human Genetics. 135(4). 393–402. 31 indexed citations
8.
Yi, Yuting, Hong Yao, Huamei Hu, et al.. (2016). Targeted next-generation sequencing identification of mutations in patients with disorders of sex development. BMC Medical Genetics. 17(1). 23–23. 51 indexed citations
9.
Xu, Xiaojie, Fang Lv, Yi Liu, et al.. (2016). A cryptic balanced translocation involving COL1A2 gene disruption cause a rare type of osteogenesis imperfecta. Clinica Chimica Acta. 460. 33–39. 4 indexed citations
10.
Liu, Yi, Lijie Song, Fang Lv, et al.. (2016). Genotype-phenotype analysis of a rare type of osteogenesis imperfecta in four Chinese families with WNT1 mutations. Clinica Chimica Acta. 461. 172–180. 20 indexed citations
11.
Shan, Dan, Yuan Yuan, Yaoshen Wang, et al.. (2016). Non-Invasive Prenatal Diagnosis of Lethal Skeletal Dysplasia by Targeted Capture Sequencing of Maternal Plasma. PLoS ONE. 11(7). e0159355–e0159355. 14 indexed citations
12.
Sun, Jun, Jason Pinner, Zhihui Yan, et al.. (2016). Diaphragmatic Eventration in Sisters with Asparagine Synthetase Deficiency: A Novel Homozygous ASNS Mutation and Expanded Phenotype. JIMD Reports. 34. 1–9. 23 indexed citations
13.
Lv, Fang, Xiaojie Xu, Jianyi Wang, et al.. (2016). Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfecta. Journal of Human Genetics. 61(6). 539–545. 32 indexed citations
14.
Xu, Xiaojie, Fang Lv, Yi Liu, et al.. (2016). Novel mutations in FKBP10 in Chinese patients with osteogenesis imperfecta and their treatment with zoledronic acid. Journal of Human Genetics. 62(2). 205–211. 15 indexed citations
15.
Asan, Zhihui Yan, Huifeng Jiang, et al.. (2016). Targeted Genes Sequencing Identified a Novel 15 bp Deletion on GJA8 in a Chinese Family with Autosomal Dominant Congenital Cataracts. Chinese Medical Journal. 129(7). 860–867. 8 indexed citations
16.
Liu, Jiawei, Asan, Jun Sun, et al.. (2015). Differential Diagnosis of Two Chinese Families with Dyschromatoses by Targeted Gene Sequencing. Chinese Medical Journal. 129(1). 33–38. 6 indexed citations
17.
Martín, Julio, Asan, Yuting Yi, et al.. (2015). Comprehensive carrier genetic test using next-generation deoxyribonucleic acid sequencing in infertile couples wishing to conceive through assisted reproductive technology. Fertility and Sterility. 104(5). 1286–1293. 49 indexed citations
18.
Kim, Jaebum, Denis M. Larkin, Qingle Cai, et al.. (2013). Reference-assisted chromosome assembly. Proceedings of the National Academy of Sciences. 110(5). 1785–1790. 86 indexed citations
19.
Adey, Andrew C., Hilary G. Morrison, Asan, et al.. (2010). Rapid, low-input, low-bias construction of shotgun fragment libraries by high-density in vitro transposition. Genome biology. 11(12). R119–R119. 410 indexed citations
20.
Xu, Yang, Yali Xue, Asan, et al.. (2008). Variation of the oxytocin/neurophysin I (OXT) gene in four human populations. Journal of Human Genetics. 53(7). 637–643. 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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