Weihua Lin

456 total citations
39 papers, 298 citations indexed

About

Weihua Lin is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Weihua Lin has authored 39 papers receiving a total of 298 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Clinical Biochemistry, 19 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Weihua Lin's work include Metabolism and Genetic Disorders (20 papers), Mitochondrial Function and Pathology (10 papers) and Neonatal Health and Biochemistry (7 papers). Weihua Lin is often cited by papers focused on Metabolism and Genetic Disorders (20 papers), Mitochondrial Function and Pathology (10 papers) and Neonatal Health and Biochemistry (7 papers). Weihua Lin collaborates with scholars based in China, Saudi Arabia and Taiwan. Weihua Lin's co-authors include Yiming Lin, Zhenzhu Zheng, Yeyang Li, Gang Li, Chunmei Lin, Weilin Peng, Dongmei Chen, Yanru Chen, Mengyi Jiang and Min Li and has published in prestigious journals such as SHILAP Revista de lepidopterología, Clinica Chimica Acta and Laboratory Investigation.

In The Last Decade

Weihua Lin

36 papers receiving 280 citations

Peers

Weihua Lin

RHEUM

PPCH

GENET

Elizabeth G. Ames United States

Keiichi Hara Japan

Nithiwat Vatanavicharn Thailand

Emmanuel Benayoun France

Kai Muru Estonia

Engela Honey South Africa

G. Biolcati Italy

Manuel Méndez Spain

Yuanchang Zhu China

Lina Ghaloul‐Gonzalez United States

Elizabeth G. Ames United States

Weihua Lin

26 ×0.2

129 ×0.8

13 ×0.2

RHEUM

25 ×0.4

PPCH

39 ×1.1

GENET

Citations per year, relative to Weihua Lin Weihua Lin (= 1×) peers Elizabeth G. Ames

Countries citing papers authored by Weihua Lin

Since Specialization

Citations

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

Fields of papers citing papers by Weihua Lin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Weihua Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Weihua Lin. A scholar is included among the top collaborators of Weihua 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 Weihua Lin. Weihua 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

Qiu, Yanhua, Weihua Lin, Jiaming Lin, et al.. (2025). Combination of artificial intelligence and chest computed tomography to assess bone mineral density. Skeletal Radiology. 55(3). 671–680.

Lin, Yiming, Zhenzhu Zheng, Weihua Lin, & Weilin Peng. (2024). Incorporating Next‐Generation Sequencing as a Second‐Tier Test for Primary Carnitine Deficiency. Molecular Genetics & Genomic Medicine. 12(9). 1 indexed citations

Li, Yimin, et al.. (2024). Myocardial strain analysis by feature tracking cardiac magnetic resonance to identify subclinical cardiac dysfunction in patients with MINOCA. Journal of Cardiothoracic Surgery. 19(1). 602–602.

Lin, Weihua, et al.. (2024). Newborn screening and genetic diagnosis of 3-methylcrotonyl-CoA carboxylase deficiency in Quanzhou,China. Molecular Genetics and Metabolism Reports. 40. 101127–101127. 1 indexed citations

Lin, Weihua, et al.. (2023). Clinical and genetic analysis of 26 Chinese patients with neonatal intrahepatic cholestasis due to citrin deficiency. Clinica Chimica Acta. 552. 117617–117617. 4 indexed citations

Lin, Yiming, Chunmei Lin, Zhenzhu Zheng, et al.. (2023). Newborn screening for fatty acid oxidation disorders in a southern Chinese population. Heliyon. 10(1). e23671–e23671. 2 indexed citations

Huang, Qingwen, et al.. (2022). Accuracy and image quality of wide-detector revolution CT angiography combined with prospective ECG-triggered CT angiography in the diagnosis of congenital aortic arch anomalies in Chinese children. Frontiers in Pediatrics. 10. 1017428–1017428. 1 indexed citations

Lin, Yiming, et al.. (2022). Newborn screening and genetic features of patients with hyperphenylalaninemia in a southern Chinese population. Clinica Chimica Acta. 535. 13–18. 6 indexed citations

Lin, Yiming, Dongmei Chen, Weilin Peng, et al.. (2020). Newborn screening for isovaleric acidemia in Quanzhou, China. Clinica Chimica Acta. 509. 25–29. 8 indexed citations

10.

Lin, Yiming, et al.. (2020). Combined primary carnitine deficiency with neonatal intrahepatic cholestasis caused by citrin deficiency in a Chinese newborn. BMC Pediatrics. 20(1). 478–478. 5 indexed citations

11.

Lin, Weihua, Zhenzhu Zheng, Yanru Chen, et al.. (2020). Newborn screening for primary carnitine deficiency in Quanzhou, China. Clinica Chimica Acta. 512. 166–171. 10 indexed citations

12.

Lin, Yiming, Hongzhi Gao, Bin Lü, et al.. (2019). Citrullinemia type I is associated with a novel splicing variant, c.773 + 4A > C, in ASS1: a case report and literature review. BMC Medical Genetics. 20(1). 110–110. 6 indexed citations

13.

Lin, Yiming, et al.. (2018). Mild clinical features of isolated methylmalonic acidemia associated with a novel variant in the MMAA gene in two Chinese siblings. BMC Medical Genetics. 19(1). 114–114. 6 indexed citations

14.

Lin, Yiming, Weilin Peng, Mengyi Jiang, et al.. (2018). Clinical, biochemical and genetic analysis of Chinese patients with isobutyryl-CoA dehydrogenase deficiency. Clinica Chimica Acta. 487. 133–138. 20 indexed citations

15.

Li, Gang, et al.. (2016). ILK–PI3K/AKT pathway participates in cutaneous wound contraction by regulating fibroblast migration and differentiation to myofibroblast. Laboratory Investigation. 96(7). 741–751. 65 indexed citations

16.

Lin, Weihua, et al.. (2015). Clinical application of Ranibizumab in the therapy of diabetic cataract. SHILAP Revista de lepidopterología. 1 indexed citations

17.

Lin, Weihua, et al.. (2014). [Study of the effects of integrin-linked kinase on proliferation and differentiation of fibroblast in hypertrophic scar].. PubMed. 30(1). 45–9. 1 indexed citations

18.

Li, Yeyang, et al.. (2011). [Expression of integrin-linked kinase in human hypertrophic scar and its relationship with angiogenesis].. PubMed. 27(6). 411–5. 1 indexed citations

19.

Mi, Lan, et al.. (2011). [The effect of integrin-linked kinase on VEGF expression in fibroblasts from human hypertrophic scar].. PubMed. 27(4). 289–93. 2 indexed citations

20.

Lin, Weihua, et al.. (2010). Experimental study on the effect of high fat diet on hyperlipidemia in rats.. Zhongguo redai yixue. 10(3). 324–325. 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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