Zhili Lin

1.2k total citations
13 papers, 403 citations indexed

About

Zhili Lin is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Zhili Lin has authored 13 papers receiving a total of 403 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Pediatrics, Perinatology and Child Health and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Zhili Lin's work include Neonatal Health and Biochemistry (4 papers), Methemoglobinemia and Tumor Lysis Syndrome (3 papers) and Metabolism and Genetic Disorders (3 papers). Zhili Lin is often cited by papers focused on Neonatal Health and Biochemistry (4 papers), Methemoglobinemia and Tumor Lysis Syndrome (3 papers) and Metabolism and Genetic Disorders (3 papers). Zhili Lin collaborates with scholars based in United States and China. Zhili Lin's co-authors include Jon F. Watchko, Gael Carney, William B. Rizzo, Edwin W. Naylor, Reese H. Clark, Alan R. Spitzer, M. Whit Walker, Joseph Suzow, Jennifer M. Puck and Diana Hu and has published in prestigious journals such as PEDIATRICS, The American Journal of Human Genetics and Chemico-Biological Interactions.

In The Last Decade

Zhili Lin

13 papers receiving 394 citations

Peers

Zhili Lin
Emily C. Lisi United States
Margaret C. Chetty United Kingdom
Alina Khromykh United States
Chin-To Fong United States
Kristen Wigby United States
H H Kazazian United States
Vrunda Sheth United States
Zhili Lin
Citations per year, relative to Zhili Lin Zhili Lin (= 1×) peers G. Biolcati

Countries citing papers authored by Zhili Lin

Since Specialization
Citations

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

Fields of papers citing papers by Zhili Lin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zhili Lin

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

All Works

13 of 13 papers shown
1.
Lin, Zhili, et al.. (2020). The dynamics mechanism of islet inflammation during type 2 diabetes progress. Chinese Science Bulletin (Chinese Version). 65(35). 4139–4148. 3 indexed citations
2.
Kwan, Antonia, Diana Hu, Diana González‐Espinosa, et al.. (2015). Successful newborn screening for SCID in the Navajo Nation. Clinical Immunology. 158(1). 29–34. 38 indexed citations
3.
Wang, Huijun, Yuchen Han, Jian‐Hua Zhao, et al.. (2014). Lipoid Proteinosis Resulting from a Large Homozygous Deletion Affecting Part of the ECM1 Gene and Adjacent Long Non-coding RNA. Acta Dermato Venereologica. 95(5). 608–610. 9 indexed citations
4.
Clark, Reese H., et al.. (2013). Utility of Genetic Testing for the Detection of Late-Onset Hearing Loss in Neonates. American Journal of Audiology. 22(2). 209–215. 9 indexed citations
5.
Watchko, Jon F. & Zhili Lin. (2009). Exploring the genetic architecture of neonatal hyperbilirubinemia. Seminars in Fetal and Neonatal Medicine. 15(3). 169–175. 56 indexed citations
6.
Watchko, Jon F., et al.. (2009). Complex Multifactorial Nature of Significant Hyperbilirubinemia in Neonates. PEDIATRICS. 124(5). e868–e877. 57 indexed citations
7.
Lin, Zhili, et al.. (2008). Coexpression of Gene Polymorphisms Involved in Bilirubin Production and Metabolism. PEDIATRICS. 122(1). e156–e162. 37 indexed citations
8.
Lin, Zhili, et al.. (2005). Alternative DNA-based newborn screening for glucose-6-phosphate dehydrogenase deficiency. Molecular Genetics and Metabolism. 86(1-2). 212–219. 37 indexed citations
9.
Lin, Zhili, et al.. (2005). A Simple Automated DNA Extraction Method for Dried Blood Specimens Collected on Filter Paper. JALA Journal of the Association for Laboratory Automation. 10(5). 310–314. 11 indexed citations
10.
Lin, Zhili, et al.. (2004). A high throughput β-globin genotyping method by multiplexed melting temperature analysis. Molecular Genetics and Metabolism. 81(3). 237–243. 13 indexed citations
11.
Rizzo, William B., Zhili Lin, & Gael Carney. (2001). Fatty aldehyde dehydrogenase: genomic structure, expression and mutation analysis in Sjögren–Larsson syndrome. Chemico-Biological Interactions. 130-132(1-3). 297–307. 25 indexed citations
12.
Lin, Zhili, Gael Carney, & William B. Rizzo. (2000). Genomic Organization, Expression, and Alternate Splicing of the Mouse Fatty Aldehyde Dehydrogenase Gene. Molecular Genetics and Metabolism. 71(3). 496–505. 19 indexed citations
13.
Rizzo, William B., Gael Carney, & Zhili Lin. (1999). The Molecular Basis of Sjögren-Larsson Syndrome: Mutation Analysis of the Fatty Aldehyde Dehydrogenase Gene. The American Journal of Human Genetics. 65(6). 1547–1560. 89 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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