Xin Fan

1.1k total citations
51 papers, 587 citations indexed

About

Xin Fan is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Xin Fan has authored 51 papers receiving a total of 587 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 20 papers in Genetics and 11 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Xin Fan's work include Thyroid Disorders and Treatments (9 papers), Congenital heart defects research (8 papers) and Genomic variations and chromosomal abnormalities (7 papers). Xin Fan is often cited by papers focused on Thyroid Disorders and Treatments (9 papers), Congenital heart defects research (8 papers) and Genomic variations and chromosomal abnormalities (7 papers). Xin Fan collaborates with scholars based in China, United States and Hong Kong. Xin Fan's co-authors include Jingsi Luo, Shaoke Chen, Yiping Shen, Chunyun Fu, Jiasun Su, Xuyun Hu, Jin Wang, Shiyu Luo, Bobo Xie and Rongyu Chen and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Gene.

In The Last Decade

Xin Fan

49 papers receiving 575 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Xin Fan China 15 307 243 187 119 56 51 587
Caroline M. McKinnon United Kingdom 8 329 1.1× 160 0.7× 205 1.1× 53 0.4× 58 1.0× 13 602
Liora S. Katz United States 17 331 1.1× 171 0.7× 175 0.9× 38 0.3× 42 0.8× 28 737
S. Ekberg Sweden 12 227 0.7× 337 1.4× 109 0.6× 55 0.5× 35 0.6× 16 718
Sylvie Renouf France 13 200 0.7× 222 0.9× 62 0.3× 33 0.3× 47 0.8× 19 644
Kenji Ohba Japan 16 354 1.2× 377 1.6× 92 0.5× 28 0.2× 58 1.0× 41 833
Mikaela Granvik Belgium 10 398 1.3× 170 0.7× 290 1.6× 62 0.5× 98 1.8× 11 820
Alena Musilová Czechia 15 309 1.0× 125 0.5× 217 1.2× 94 0.8× 18 0.3× 34 768
Éva Dizin Switzerland 15 446 1.5× 61 0.3× 115 0.6× 29 0.2× 48 0.9× 19 768
Mindy A. Kendrick United States 16 489 1.6× 169 0.7× 170 0.9× 27 0.2× 100 1.8× 17 805
Valeria Mannella Italy 9 465 1.5× 57 0.2× 446 2.4× 44 0.4× 25 0.4× 12 752

Countries citing papers authored by Xin Fan

Since Specialization
Citations

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

Fields of papers citing papers by Xin Fan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xin Fan

This figure shows the co-authorship network connecting the top 25 collaborators of Xin Fan. A scholar is included among the top collaborators of Xin Fan 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 Xin Fan. Xin Fan 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.
Xie, Bobo, Yan Huang, Xin Fan, et al.. (2024). Complex genotype–phenotype correlation of MYH11: new insights from monozygotic twins with highly variable expressivity and outcomes. BMC Medical Genomics. 17(1). 135–135.
2.
Gui, Baoheng, et al.. (2022). Phenotypic variability of syndromic craniosynostosis caused by c.833G > T in FGFR2: Clinical and genetic evaluation of eight patients from a five‐generation family. Molecular Genetics & Genomic Medicine. 10(4). e1901–e1901. 3 indexed citations
3.
Liu, Lian, Li‐Ying Sun, Yujun Chen, et al.. (2022). Delineation of dual molecular diagnosis in patients with skeletal deformity. Orphanet Journal of Rare Diseases. 17(1). 139–139. 1 indexed citations
4.
Yang, Qi, Rong Hua, Shang Yi, et al.. (2020). PREPL Deficiency: A Homozygous Splice Site PREPL Mutation in a Patient With Congenital Myasthenic Syndrome and Absence of Ovaries and Hypoplasia of Uterus. Frontiers in Genetics. 11. 198–198. 8 indexed citations
5.
Yang, Qi, et al.. (2020). Case reports: three novel variants in PCCA and PCCB genes in Chinese patients with propionic acidemia. BMC Medical Genetics. 21(1). 72–72. 3 indexed citations
6.
Chen, Fei, Shaoke Chen, Qi Yang, et al.. (2019). Three additional de novo CTCF mutations in Chinese patients help to define an emerging neurodevelopmental disorder. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 181(2). 218–225. 18 indexed citations
7.
Yang, Qi, Mengting Li, Bobo Xie, et al.. (2019). Genetic analyses of oculocutaneous albinism types 1 and 2 with four novel mutations. BMC Medical Genetics. 20(1). 106–106. 18 indexed citations
8.
Meyer, Julia, Jennifer Wambach, Daniel Wegner, et al.. (2018). Gene variants of the phosphatidylcholine synthesis pathway do not contribute to RDS in the Chinese population. World Journal of Pediatrics. 14(1). 52–56. 1 indexed citations
9.
Fu, Chunyun, Shiyu Luo, Qifei Li, et al.. (2018). Newborn screening of glucose-6-phosphate dehydrogenase deficiency in Guangxi, China: determination of optimal cutoff value to identify heterozygous female neonates. Scientific Reports. 8(1). 833–833. 33 indexed citations
10.
Gui, Baoheng, Yanning Song, Xuyun Hu, et al.. (2018). Novel pathogenic RECQL4 variants in Chinese patients with Rothmund-Thomson syndrome. Gene. 654. 110–115. 5 indexed citations
11.
Zhang, Qiang, et al.. (2017). α+-Thalassemia Caused by an 811 bp Deletion in Individuals from Nanning, Guangxi: A Report of Two Cases. Hemoglobin. 41(3). 185–188. 1 indexed citations
12.
Fan, Xin, Chunyun Fu, Yiping Shen, et al.. (2017). Next-generation sequencing analysis of twelve known causative genes in congenital hypothyroidism. Clinica Chimica Acta. 468. 76–80. 41 indexed citations
13.
Hu, Xuyun, Baoheng Gui, Yufei Xu, et al.. (2017). Prenatal and early diagnosis of Chinese 3-M syndrome patients with novel pathogenic variants. Clinica Chimica Acta. 474. 159–164. 11 indexed citations
14.
Fu, Chunyun, Bobo Xie, Shujie Zhang, et al.. (2016). Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism. BMJ Open. 6(5). e010719–e010719. 22 indexed citations
15.
Fu, Chunyun, Shujie Zhang, Yun Chen, et al.. (2016). Mutation screening of the SLC26A4 gene in a cohort of 192 Chinese patients with congenital hypothyroidism. Archives of Endocrinology and Metabolism. 60(4). 323–327. 12 indexed citations
16.
Zhang, Shujie, Jin Wang, Shiyu Luo, et al.. (2016). Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability. Molecular Cytogenetics. 9(1). 66–66. 10 indexed citations
17.
Hu, Xuyun, Rongyu Chen, Chunyun Fu, et al.. (2016). Thyroglobulin gene mutations in Chinese patients with congenital hypothyroidism. Molecular and Cellular Endocrinology. 423. 60–66. 23 indexed citations
18.
Fu, Chunyun, Jin Wang, Shiyu Luo, et al.. (2016). Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients. Clinica Chimica Acta. 462. 127–132. 25 indexed citations
19.
Li, Chuan, Rongyu Chen, Xin Fan, et al.. (2015). EPHA4 haploinsufficiency is responsible for the short stature of a patient with 2q35-q36.2 deletion and Waardenburg syndrome. BMC Medical Genetics. 16(1). 23–23. 4 indexed citations
20.
Chen, Shaoke, Jingsi Luo, Yingfen Qin, et al.. (2011). [Epidemiological study on the association between obesity with metabolic syndrome in obese children and adolescents of Nanning city, Guangxi].. PubMed. 32(10). 969–72. 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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