Min Pan

1.5k total citations
79 papers, 924 citations indexed

About

Min Pan is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Min Pan has authored 79 papers receiving a total of 924 indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Pediatrics, Perinatology and Child Health, 27 papers in Genetics and 18 papers in Molecular Biology. Recurrent topics in Min Pan's work include Prenatal Screening and Diagnostics (50 papers), Fetal and Pediatric Neurological Disorders (25 papers) and Parvovirus B19 Infection Studies (15 papers). Min Pan is often cited by papers focused on Prenatal Screening and Diagnostics (50 papers), Fetal and Pediatric Neurological Disorders (25 papers) and Parvovirus B19 Infection Studies (15 papers). Min Pan collaborates with scholars based in China, United States and United Kingdom. Min Pan's co-authors include Dong‐Zhi Li, Jin Han, Xin Yang, Zhen Li, Can Liao, Can Liao, Fang Fu, Yongling Zhang, Fatao Li and Xiumei Zhang and has published in prestigious journals such as Scientific Reports, Gene and Journal of Cellular Biochemistry.

In The Last Decade

Min Pan

72 papers receiving 913 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Min Pan China 15 470 281 236 224 155 79 924
Janet I. Vaughan United Kingdom 22 931 2.0× 205 0.7× 132 0.6× 176 0.8× 202 1.3× 37 1.6k
Seyed Alireza Dastgheib Iran 13 189 0.4× 121 0.4× 166 0.7× 109 0.5× 119 0.8× 117 992
Tonia C. Carter United States 20 177 0.4× 185 0.7× 214 0.9× 39 0.2× 117 0.8× 33 762
Stephanie Allen United Kingdom 16 653 1.4× 316 1.1× 325 1.4× 183 0.8× 93 0.6× 43 1.1k
Lin Wai Chan Hong Kong 22 885 1.9× 136 0.5× 135 0.6× 215 1.0× 212 1.4× 62 1.2k
Ilaria Muller Italy 18 116 0.2× 130 0.5× 128 0.5× 193 0.9× 38 0.2× 58 1.2k
L. Bussières France 22 1.1k 2.3× 89 0.3× 146 0.6× 336 1.5× 171 1.1× 75 1.6k
Corinne Hubinont Belgium 22 807 1.7× 97 0.3× 192 0.8× 173 0.8× 322 2.1× 91 1.7k
Rajni Agarwal United States 16 104 0.2× 120 0.4× 119 0.5× 129 0.6× 41 0.3× 47 819
A.M.Z. Chang Hong Kong 17 397 0.8× 68 0.2× 195 0.8× 94 0.4× 96 0.6× 35 923

Countries citing papers authored by Min Pan

Since Specialization
Citations

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

Fields of papers citing papers by Min Pan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Min Pan

This figure shows the co-authorship network connecting the top 25 collaborators of Min Pan. A scholar is included among the top collaborators of Min Pan 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 Min Pan. Min Pan 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.
2.
Fu, Fang, Xin Yang, Ru Li, et al.. (2024). Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygroma. BMC Medical Genomics. 17(1). 96–96. 1 indexed citations
3.
Lei, Tingying, Zhen Li, Xin Yang, et al.. (2023). Prenatal Diagnosis of PPP2R1A-Related Neurodevelopmental Disorders Using Whole Exome Sequencing: Clinical Report and Review of Literature. Genes. 14(1). 126–126. 7 indexed citations
4.
Li, Zhen, Min Pan, Jin Han, et al.. (2022). Prenatal persistent left superior vena cava in low population: Not a benign vascular anomaly. Taiwanese Journal of Obstetrics and Gynecology. 61(3). 459–463. 4 indexed citations
5.
Lei, Tingying, Fang Fu, Zhen Li, et al.. (2022). Prenatal exome sequencing in fetuses with callosal anomalies. Prenatal Diagnosis. 42(6). 744–752. 13 indexed citations
6.
Zhou, Hang, Fang Fu, Ru Li, et al.. (2022). The Genetic and Clinical Outcomes in Fetuses With Isolated Fetal Growth Restriction: A Chinese Single-Center Retrospective Study. Frontiers in Genetics. 13. 856522–856522. 9 indexed citations
7.
Pan, Min, et al.. (2021). Pregnancies with trisomy 2 cells in chorionic villi: Ultrasound determines the outcome. European Journal of Obstetrics & Gynecology and Reproductive Biology. 261. 247–248. 2 indexed citations
8.
Yang, Yu, et al.. (2021). Fetal akinesia: The application of clinical exome sequencing in cases with decreased fetal movement. European Journal of Obstetrics & Gynecology and Reproductive Biology. 260. 59–63. 8 indexed citations
9.
Li, Lushan, Fang Fu, Ru Li, et al.. (2020). Genetic tests aid in counseling of fetuses with cerebellar vermis defects. Prenatal Diagnosis. 40(10). 1228–1238. 14 indexed citations
10.
He, Yi, Min Pan, Jin Han, et al.. (2020). Prenatal genetic diagnosis of cardiac rhabdomyoma: A single-center experience. European Journal of Obstetrics & Gynecology and Reproductive Biology. 249. 7–10. 6 indexed citations
11.
Pan, Min, et al.. (2019). Ultrasound-Guided Percutaneous Release of A1 Pulley by Using a Needle Knife: A Prospective Study of 41 Cases. Frontiers in Pharmacology. 10. 267–267. 35 indexed citations
12.
Yu, Xuen, et al.. (2019). The study of Wilson disease in pregnancy management. BMC Pregnancy and Childbirth. 19(1). 522–522. 11 indexed citations
13.
Pan, Min, et al.. (2018). Prenatal diagnosis of Wolf-Hirschhorn syndrome: Ultrasonography and molecular karyotyping results. European Journal of Obstetrics & Gynecology and Reproductive Biology. 225. 19–21. 9 indexed citations
14.
Yang, Xin, et al.. (2015). Relationship between absent or hypoplastic fetal nasal bone and chromosome abnormalities: analysis of 187 cases. Zhonghua weichan yixue zazhi. 18(5). 339–342. 1 indexed citations
15.
Pan, Min, et al.. (2015). Non-invasive prenatal detection of haemoglobin Bart's disease by cardiothoracic ratio during the first trimester. European Journal of Obstetrics & Gynecology and Reproductive Biology. 193. 92–95. 7 indexed citations
16.
Fu, Fang, Ru Li, Jin Han, et al.. (2014). Prenatal diagnosis of foetuses with congenital abnormalities and duplication of the MECP2 region. Gene. 546(2). 222–225. 13 indexed citations
17.
Han, Jin, et al.. (2014). Chorionic villus sampling for early prenatal diagnosis: Experience at a mainland Chinese hospital. Journal of Obstetrics and Gynaecology. 34(8). 669–672. 5 indexed citations
18.
Pan, Min, Min Chen, Tak Yeung Leung, et al.. (2011). Outcome of monochorionic twin pregnancies with abnormal umbilical artery Doppler between 16 and 20 weeks of gestation. The Journal of Maternal-Fetal & Neonatal Medicine. 25(3). 277–280. 11 indexed citations
19.
Liao, Can, Jin Han, Daljit Singh Sahota, et al.. (2010). Maternal serum ADAM12 in Chinese women undergoing screening for aneuploidy in the first trimester. The Journal of Maternal-Fetal & Neonatal Medicine. 23(11). 1305–1309. 3 indexed citations
20.
Liao, Can, Min Pan, & Dong‐Zhi Li. (2007). Fetal karyotyping and late sonographic abnormality detection in China. International Journal of Gynecology & Obstetrics. 100(2). 183–184. 1 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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