Peining Li

2.6k total citations
84 papers, 1.3k citations indexed

About

Peining Li is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Peining Li has authored 84 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Genetics, 30 papers in Molecular Biology and 29 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Peining Li's work include Genomic variations and chromosomal abnormalities (40 papers), Prenatal Screening and Diagnostics (26 papers) and Genomics and Rare Diseases (13 papers). Peining Li is often cited by papers focused on Genomic variations and chromosomal abnormalities (40 papers), Prenatal Screening and Diagnostics (26 papers) and Genomics and Rare Diseases (13 papers). Peining Li collaborates with scholars based in United States, China and Spain. Peining Li's co-authors include Wei Shu, Chenghua Cui, Fang Xu, Jerry N. Thompson, Bixia Xiang, Hongyan Chai, Miguel Reyes‐Múgica, Akihiro Imura, Carol Nelson‐Williams and Yo‐ichi Nabeshima and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Peining Li

76 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peining Li United States 20 657 512 300 152 148 84 1.3k
Marie‐Pierre Audrézet France 26 924 1.4× 794 1.6× 265 0.9× 54 0.4× 116 0.8× 69 2.0k
Jasenka Wagner Croatia 23 209 0.3× 397 0.8× 135 0.5× 28 0.2× 47 0.3× 66 1.4k
Katherine L. Harper United Kingdom 16 301 0.5× 418 0.8× 68 0.2× 52 0.3× 28 0.2× 23 1.0k
Yue‐Qiu Tan China 26 936 1.4× 999 2.0× 540 1.8× 85 0.6× 9 0.1× 139 2.2k
I. White United Kingdom 19 238 0.4× 344 0.7× 81 0.3× 33 0.2× 49 0.3× 39 1.1k
Periklis Makrythanasis Switzerland 18 278 0.4× 402 0.8× 59 0.2× 24 0.2× 24 0.2× 58 798
Silvana Guerneri Italy 17 406 0.6× 357 0.7× 344 1.1× 121 0.8× 15 0.1× 50 902
Deborah Hyink United States 19 290 0.4× 1.1k 2.1× 160 0.5× 7 0.0× 148 1.0× 33 1.3k
William T. Yewdell United States 15 96 0.1× 612 1.2× 29 0.1× 67 0.4× 42 0.3× 23 1.3k
M. Lau United States 16 311 0.5× 461 0.9× 187 0.6× 16 0.1× 11 0.1× 40 1.3k

Countries citing papers authored by Peining Li

Since Specialization
Citations

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

Fields of papers citing papers by Peining Li

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peining Li

This figure shows the co-authorship network connecting the top 25 collaborators of Peining Li. A scholar is included among the top collaborators of Peining Li 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 Peining Li. Peining Li 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.
Liu, Mengjun, et al.. (2025). Superhydrophobic and corrosion resistance behavior of Al-15Si-5Cu-5 Mg-2Mn alloy surface. Surface and Coatings Technology. 512. 132311–132311. 1 indexed citations
3.
Abdelhamed, Zakia, et al.. (2024). P602: Genetic modifiers as a basis for phenotypic variability in mosaic trisomy 8. SHILAP Revista de lepidopterología. 2. 101508–101508.
4.
Chai, Hongyan, Mei Ling Chong, Guilin Wang, et al.. (2024). Patterns of Cytogenomic Findings from a Case Series of Recurrent Pregnancy Loss Provide Insight into the Extent of Genetic Defects Causing Miscarriages. SHILAP Revista de lepidopterología. 11(1). 123–131. 1 indexed citations
5.
Peng, Gang, Qinghua Zhou, Hongyan Chai, et al.. (2023). Estimation on risk of spontaneous abortions by genomic disorders from a meta‐analysis of microarray results on large case series of pregnancy losses. Molecular Genetics & Genomic Medicine. 11(8). e2181–e2181. 7 indexed citations
6.
Ordulu, Zehra, Hongyan Chai, Gang Peng, et al.. (2020). Molecular and clinicopathologic characterization of intravenous leiomyomatosis. Modern Pathology. 33(9). 1844–1860. 21 indexed citations
7.
Chang, Hao, Sean F. Landrette, Sheng Ding, et al.. (2019). Efficient genome-wide first-generation phenotypic screening system in mice using the piggyBac transposon. Proceedings of the National Academy of Sciences. 116(37). 18507–18516. 9 indexed citations
8.
Chai, Hongyan, Fang Xu, Qinghua Zhou, et al.. (2019). A Retrospective Analysis of 10-Year Data Assessed the Diagnostic Accuracy and Efficacy of Cytogenomic Abnormalities in Current Prenatal and Pediatric Settings. Frontiers in Genetics. 10. 1162–1162. 12 indexed citations
9.
Xu, Fang, et al.. (2017). Concomitant 1q42.13-q44 Duplication and 14q32.33 Deletion: A Case Report and Review of Literature. Zenodo (CERN European Organization for Nuclear Research). 10(2).
10.
Li, Peining, Fang Xu, & Wei Shu. (2016). The Spectrum of Cytogenomic Abnormalities in Patients with Developmental Delay and Intellectual Disabilities. North American Journal of Medicine and Science. 8(4). 3 indexed citations
11.
Li, Peining, et al.. (2016). Diagnostic Yield of Cytogenomic Abnormalities in Current Prenatal Diagnosis: A Retrospective Analysis in a Clinical Cytogenetics Laboratory. North American Journal of Medicine and Science. 9(4). 1 indexed citations
12.
13.
14.
Ma, Deqiong, et al.. (2013). Biobanking of Residual Specimens from Diagnostic Genetic Laboratories: Standard Operating Procedures, Ethical and Legal Considerations, and Research Applications. North American Journal of Medicine and Science. 6(4). 3 indexed citations
15.
Xu, Fang, et al.. (2013). Interstitial Duplication and Distal Deletion in a Ring Chromosome 13 with Pulmonary Atresia and Ventricular Septal Defect: A Case Report and Review of Literature. North American Journal of Medicine and Science. 6(4). 5 indexed citations
16.
Li, Peining, et al.. (2013). Progress and Perspective of Professional Training in Medical Genetics and Genomics: A Report of the Association of Chinese Geneticists in America. North American Journal of Medicine and Science. 6(4). 1 indexed citations
17.
Li, Peining, et al.. (2013). Non-Invasive Prenatal Diagnosis: A Comparison of Cell Free Fetal DNA (cffDNA) Based Screening and Fetal Nucleated Red Blood Cell (fnRBC) Initiated Testing. North American Journal of Medicine and Science. 6(4). 194–194. 8 indexed citations
18.
Brownstein, Catherine A., F.T. Adler, Carol Nelson‐Williams, et al.. (2008). A translocation causing increased α-Klotho level results in hypophosphatemic rickets and hyperparathyroidism. Proceedings of the National Academy of Sciences. 105(9). 3455–3460. 165 indexed citations
19.
Li, Peining, Tim Wood, & Jerry N. Thompson. (2002). Diversity of mutations and distribution of single nucleotide polymorphic alleles in the human α-l-iduronidase (IDUA) gene. Genetics in Medicine. 4(6). 420–426. 33 indexed citations
20.
Li, Peining, Jerry N. Thompson, Xiaoyun Wang, & Song Li. (1998). Analysis of common mutations and associated haplotypes in Chinese patients with glucose‐6‐phosphate dehydrogenase deficiency. IUBMB Life. 46(6). 1135–1143. 3 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Marie‐Pierre Audrézet Breakdown of academic impact, for papers by Jasenka Wagner Breakdown of academic impact, for papers by Katherine L. Harper Breakdown of academic impact, for papers by Yue‐Qiu Tan Breakdown of academic impact, for papers by I. White Breakdown of academic impact, for papers by Periklis Makrythanasis Breakdown of academic impact, for papers by Silvana Guerneri Breakdown of academic impact, for papers by Deborah Hyink Breakdown of academic impact, for papers by William T. Yewdell Breakdown of academic impact, for papers by M. Lau
Rankless by CCL
2026