Shaobin Lin

783 citations
50 papers · 623 · h-index 15

Impact in

Papers in

    • Prenatal Screening and Diagnostics 25
    • Fetal and Pediatric Neurological Disorders 2
    • Genomic variations and chromosomal abnormalities 15
    • Forensic and Genetic Research 4
    • Genomics and Rare Diseases 3
    • Hemoglobinopathies and Related Disorders 2

Shaobin Lin

47 papers receiving 608 citations

Peers

Shaobin Lin
Comparison fields: 5 of 49
  • Pediatrics, Perinatology and Child Health 225
  • Health, Toxicology and Mutagenesis 147
  • Genetics 162
  • Developmental Neuroscience 13
  • Pollution 26
Replace Hannah E. Laue with:
Hannah E. Laue United States
Mounir Ajina Tunisia
Thomas J. G. Chambers United Kingdom
Janet M. Ferrell United States
Kenji Tawara Japan
Nadia Soledad Bourguignon Argentina
Anne‐Maarit Haavisto Finland
Kenneth A. Faber United States
Taiza Stumpp Brazil
Theresa A. Fico United States
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Citations per field
00.5×5×10×14.7×
Hannah E. Laue · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Shaobin Lin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Shaobin Lin Line = papers co-authored together Shaobin Lin links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 50 papers — load more, or switch the sort, to bring in the rest.

#Work
1 201487
2
Distributions of heavy metals in maternal and cord blood and the association with infant birth weight in China.
201574
3 201467
4 201637
5 201722
6 201921
7 201719
8 201518
9 201818
10 202018
11 201517
12 201616
13 201816
14
[Meta-analysis on the association of ACE/ID polymorphism and essential hypertension in Chinese population].
200115
15 201715
16 201713
17 201713
18 201913
19 201412
20 201810

About Shaobin Lin

Shaobin Lin is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Health, Toxicology and Mutagenesis, Genetics and Developmental Neuroscience, having authored 50 papers that have together received 623 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (25 papers), Genomic variations and chromosomal abnormalities (15 papers), Forensic and Genetic Research (4 papers), Genomics and Rare Diseases (3 papers), Pesticide Exposure and Toxicity (2 papers), Fetal and Pediatric Neurological Disorders (2 papers), Hemoglobinopathies and Related Disorders (2 papers) and Toxic Organic Pollutants Impact (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (225 citations), Health, Toxicology and Mutagenesis (147 citations), Genetics (162 citations), Developmental Neuroscience (13 citations) and Pollution (26 citations). Shaobin Lin has collaborated with scholars based in China, United States and Denmark. Frequent co-authors include Yanmin Luo, Linhuan Huang, Qun Fang, Zhiming He, Yibin Cheng, Yonghong Li, Yinlong Jin, Yi Yuan Zhou, Shanshan Shi and 欧雪玲. Their work appears in journals such as Prenatal Diagnosis, Electrophoresis, Molecular Cytogenetics, Transfusion and Frontiers in Genetics.

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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