Shaobin Lin

783 total citations
52 papers, 569 citations indexed

About

Shaobin Lin is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Shaobin Lin has authored 52 papers receiving a total of 569 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Pediatrics, Perinatology and Child Health, 25 papers in Genetics and 19 papers in Molecular Biology. Recurrent topics in Shaobin Lin's work include Prenatal Screening and Diagnostics (26 papers), Genomic variations and chromosomal abnormalities (17 papers) and Fetal and Pediatric Neurological Disorders (9 papers). Shaobin Lin is often cited by papers focused on Prenatal Screening and Diagnostics (26 papers), Genomic variations and chromosomal abnormalities (17 papers) and Fetal and Pediatric Neurological Disorders (9 papers). Shaobin Lin collaborates with scholars based in China, United States and Denmark. Shaobin Lin's co-authors include Yanmin Luo, Linhuan Huang, Qun Fang, Zhiming He, Yibin Cheng, Yonghong Li, Yinlong Jin, Yi Zhou, Shanshan Shi and Baojiang Chen and has published in prestigious journals such as Chemosphere, Environmental Research and Electrophoresis.

In The Last Decade

Shaobin Lin

49 papers receiving 559 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Shaobin Lin China	14	243	177	159	127	39	52	569
Amita Bansal United States	15	254 1.0×	105 0.6×	389 2.4×	267 2.1×	83 2.1×	28	931
Panagiotis Filis United Kingdom	14	195 0.8×	111 0.6×	151 0.9×	206 1.6×	23 0.6×	25	623
Johanna Bodin Norway	15	95 0.4×	89 0.5×	411 2.6×	76 0.6×	63 1.6×	25	688
Karen Kilcoyne United Kingdom	12	111 0.5×	153 0.9×	173 1.1×	228 1.8×	73 1.9×	15	618
Stephanie E. King United States	11	146 0.6×	82 0.5×	137 0.9×	298 2.3×	14 0.4×	19	584
Guimin Hao China	19	268 1.1×	54 0.3×	129 0.8×	139 1.1×	26 0.7×	73	975
Qiuqin Tang China	18	113 0.5×	98 0.6×	157 1.0×	311 2.4×	21 0.5×	42	820
Cristián Sobarzo Argentina	14	71 0.3×	43 0.2×	112 0.7×	126 1.0×	47 1.2×	32	552
Frances Xin United States	10	142 0.6×	66 0.4×	390 2.5×	151 1.2×	16 0.4×	13	612
Marina Trevizan Guerra Brazil	14	100 0.4×	45 0.3×	276 1.7×	64 0.5×	27 0.7×	28	475

Countries citing papers authored by Shaobin Lin

Since Specialization

Citations

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

Fields of papers citing papers by Shaobin Lin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shaobin Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Shaobin Lin. A scholar is included among the top collaborators of Shaobin Lin 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 Shaobin Lin. Shaobin Lin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Lin, Shaobin, et al.. (2025). Prenatal diagnosis of geleophysic dysplasia with ADAMTSL2 mutations. Taiwanese Journal of Obstetrics and Gynecology. 64(3). 528–530.

Liu, Jingyu, et al.. (2023). Prenatal evaluation of genetic variants in fetuses with small head circumference: A single-center retrospective study. European Journal of Obstetrics & Gynecology and Reproductive Biology. 293. 57–66. 2 indexed citations

Zhang, Nan, Shanshan Shi, Shaobin Lin, et al.. (2023). Application of SNPs with low minor allele frequencies in missing person identification (MPI) through kinship analysis of DNA mixtures. Electrophoresis. 44(19-20). 1569–1578. 1 indexed citations

Lin, Shaobin, Weiqiang Liu, Guo Li, et al.. (2022). [A consensus on prenatal diagnosis and genetic counseling for chromosomal mosaicism].. PubMed. 39(8). 797–802. 3 indexed citations

Lin, Shaobin, Zhiming He, Linhuan Huang, et al.. (2021). Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese Family. Frontiers in Genetics. 12. 640992–640992. 2 indexed citations

Lin, Shaobin, Shufang Huang, Xueling Ou, et al.. (2021). Mosaic duplication of 8q24.1q24.3 detected by chromosomal microarray but not karyotyping in two unrelated fetuses with cardiac defects. Molecular Cytogenetics. 14(1). 26–26. 1 indexed citations

Liu, Weiqiang, Jian Lu, Jun Zhang, et al.. (2020). [A consensus recommendation for the interpretation and reporting of copy number variation and regions of homozygosity in prenatal genetic diagnosis].. PubMed. 37(7). 701–708. 5 indexed citations

Zhang, Yan, Weiqiang Liu, Jun Zhang, et al.. (2020). [A consensus recommendation for the interpretation and reporting of exome sequencing in prenatal genetic diagnosis].. PubMed. 37(11). 1205–1212. 2 indexed citations

Zhao, Hu, Shaobin Lin, Linhuan Huang, et al.. (2020). Evaluation of a Microhaplotype-Based Noninvasive Prenatal Test in Twin Gestations: Determination of Paternity, Zygosity, and Fetal Fraction. Genes. 12(1). 26–26. 16 indexed citations

10.

Hu, Liqin, et al.. (2020). A child with a novel DDX3X variant mimicking cerebral palsy: a case report. The Italian Journal of Pediatrics/Italian journal of pediatrics. 46(1). 88–88. 6 indexed citations

11.

Shi, Shanshan, et al.. (2020). Discordance of cardiovascular abnormalities in a monozygotic twin pair carrying a class II 1q21.1 microdeletion. Taiwanese Journal of Obstetrics and Gynecology. 59(1). 123–126. 3 indexed citations

12.

Lin, Shaobin, Shanshan Shi, Linhuan Huang, et al.. (2019). Is an analysis of copy number variants necessary for various types of kidney ultrasound anomalies in fetuses?. Molecular Cytogenetics. 12(1). 31–31. 10 indexed citations

13.

Li, Lin, Linhuan Huang, Xuan Huang, et al.. (2018). Prenatal diagnosis of Pallister‐Killian syndrome in one twin. Clinical Case Reports. 6(8). 1470–1473. 2 indexed citations

14.

Shi, Shanshan, Shaobin Lin, Baojiang Chen, & Yi Zhou. (2017). Isolated chromosome 8p23.2-pter deletion: Novel evidence for developmental delay, intellectual disability, microcephaly and neurobehavioral disorders. Molecular Medicine Reports. 16(5). 6837–6845. 20 indexed citations

15.

Lin, Shaobin, et al.. (2016). Chromosome 10q26 deletion syndrome: Two new cases and a review of the literature. Molecular Medicine Reports. 14(6). 5134–5140. 13 indexed citations

16.

Lin, Shaobin, Yingjun Xie, Yi Zhou, et al.. (2015). Improved assay performance of single nucleotide polymorphism array over conventional karyotyping in analyzing products of conception. Journal of the Chinese Medical Association. 78(7). 408–413. 14 indexed citations

17.

Li, Lin, Linhuan Huang, Yanmin Luo, et al.. (2015). Differing Microdeletion Sizes and Breakpoints in Chromosome 7q11.23 in Williams-Beuren Syndrome Detected by Chromosomal Microarray Analysis. Molecular Syndromology. 6(6). 268–275. 17 indexed citations

18.

Chen, Qiong, Tongzhang Zheng, Bryan A. Bassig, et al.. (2014). Prenatal Exposure to Polycyclic Aromatic Hydrocarbons and Birth Weight in China. 3(4). 100–110. 12 indexed citations

19.

Guo, Huan, Yinlong Jin, Yibin Cheng, et al.. (2014). Prenatal exposure to organochlorine pesticides and infant birth weight in China. Chemosphere. 110. 1–7. 78 indexed citations

20.

Su, Liqin, et al.. (2008). [Study on the relationship between GSTM1, GSTT1 gene polymorphisms and arsenic methylation level].. PubMed. 37(4). 432–4. 2 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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