Jingsi Luo

936 total citations
65 papers, 556 citations indexed

About

Jingsi Luo is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Jingsi Luo has authored 65 papers receiving a total of 556 indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 29 papers in Genetics and 13 papers in Clinical Biochemistry. Recurrent topics in Jingsi Luo's work include RNA modifications and cancer (14 papers), Metabolism and Genetic Disorders (13 papers) and Genetics and Neurodevelopmental Disorders (11 papers). Jingsi Luo is often cited by papers focused on RNA modifications and cancer (14 papers), Metabolism and Genetic Disorders (13 papers) and Genetics and Neurodevelopmental Disorders (11 papers). Jingsi Luo collaborates with scholars based in China, United States and Hong Kong. Jingsi Luo's co-authors include Xin Fan, Shaoke Chen, Jiasun Su, Yiping Shen, Chunyun Fu, Jin Wang, Xuyun Hu, Shiyu Luo, Bobo Xie and Rongyu Chen and has published in prestigious journals such as Scientific Reports, Gene and Clinica Chimica Acta.

In The Last Decade

Jingsi Luo

59 papers receiving 544 citations

Peers

Jingsi Luo

EDM

GENET

PPCH

Bobo Xie China

L Duprez Belgium

Dinane Samara‐Boustani France

Anne Lienhardt-Roussie France

Mouna Mnif Tunisia

Katsumi Goji Japan

Florence Roucher‐Boulez France

Johannes Weigel Germany

T Sunthornthepvarakul Thailand

Sara Roos Sweden

Bobo Xie China

Jingsi Luo

178 ×0.6

134 ×0.6

EDM

106 ×0.5

GENET

91 ×0.6

PPCH

36 ×0.6

Citations per year, relative to Jingsi Luo Jingsi Luo (= 1×) peers Bobo Xie

Countries citing papers authored by Jingsi Luo

Since Specialization

Citations

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

Fields of papers citing papers by Jingsi Luo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jingsi Luo

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

Zhang, Qiang, Shujie Zhang, Lin Li, et al.. (2024). Whole-exome sequencing identified a novel heterozygous variant in UBAP2L in a Chinese family with neurodevelopmental disorder characterized by impaired language, behavioral abnormalities, and dysmorphic facies. Frontiers in Genetics. 15. 1503048–1503048. 1 indexed citations

Zhang, Qiang, et al.. (2024). Clinical and genetic analysis of trichohepatoneurodevelopmental syndrome caused by a CCDC47 variant. Heliyon. 10(6). e27955–e27955.

Luo, Jingsi, et al.. (2023). Detection of gonosomal mosaicism by ultra‐deep sequencing and droplet digital PCR in patients with Emery–Dreifuss muscular dystrophy. Molecular Genetics & Genomic Medicine. 11(6). e2161–e2161. 1 indexed citations

Qin, Zailong, Junjie Chen, Shang Yi, et al.. (2023). Early onset horizontal gaze palsy and progressive scoliosis due to a noncanonical splicing‐site variant and a missense variant in the ROBO3 gene. Molecular Genetics & Genomic Medicine. 11(9). e2215–e2215. 4 indexed citations

Zhang, Qiang, et al.. (2022). Characteristics of Allan-Herndon-Dudley Syndrome in Chinese children: Identification of two novel pathogenic variants of the SLC16A2 gene. Frontiers in Pediatrics. 10. 1050023–1050023. 3 indexed citations

Yang, Qi, et al.. (2022). De Novo CSNK2B Mutations in Five Cases of Poirier–Bienvenu Neurodevelopmental Syndrome. Frontiers in Neurology. 13. 811092–811092. 7 indexed citations

Li, Mengting, Qi Yang, Fei Chen, et al.. (2022). Novel and recurrent ASPM mutations of founder effect in Chinese population. Brain and Development. 44(8). 540–545. 2 indexed citations

Wang, Jin, Qi Yang, Shang Yi, et al.. (2022). Clinical and genetic analysis of combined oxidative phosphorylation defificiency-10 caused by MTO1 mutation. Clinica Chimica Acta. 526. 74–80. 5 indexed citations

Yang, Qi, Rong Hua, Shang Yi, et al.. (2020). PREPL Deficiency: A Homozygous Splice Site PREPL Mutation in a Patient With Congenital Myasthenic Syndrome and Absence of Ovaries and Hypoplasia of Uterus. Frontiers in Genetics. 11. 198–198. 8 indexed citations

10.

Yang, Qi, et al.. (2020). Case reports: three novel variants in PCCA and PCCB genes in Chinese patients with propionic acidemia. BMC Medical Genetics. 21(1). 72–72. 3 indexed citations

11.

Fu, Chunyun, Shiyu Luo, Qifei Li, et al.. (2018). Newborn screening of glucose-6-phosphate dehydrogenase deficiency in Guangxi, China: determination of optimal cutoff value to identify heterozygous female neonates. Scientific Reports. 8(1). 833–833. 33 indexed citations

12.

Hu, Xuyun, Baoheng Gui, Yufei Xu, et al.. (2017). Prenatal and early diagnosis of Chinese 3-M syndrome patients with novel pathogenic variants. Clinica Chimica Acta. 474. 159–164. 11 indexed citations

13.

Su, Jiasun, Jin Wang, Xin Fan, et al.. (2017). Mosaic UPD(7q)mat in a patient with silver Russell syndrome. Molecular Cytogenetics. 10(1). 36–36. 8 indexed citations

14.

Fu, Chunyun, Bobo Xie, Shujie Zhang, et al.. (2016). Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism. BMJ Open. 6(5). e010719–e010719. 22 indexed citations

15.

Fu, Chunyun, Jin Wang, Shiyu Luo, et al.. (2016). Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients. Clinica Chimica Acta. 462. 127–132. 25 indexed citations

16.

Xie, Bobo, Xin Fan, Rongyu Chen, et al.. (2016). A novel de novo microdeletion at 17q11.2 adjacent to NF1 gene associated with developmental delay, short stature, microcephaly and dysmorphic features. Molecular Cytogenetics. 9(1). 41–41. 12 indexed citations

17.

Wang, Jin, Chunyun Fu, Shujie Zhang, et al.. (2016). A rare occurrence of two large de novo duplications on 1q42-q44 and 9q21.12-q21.33. Gene. 594(1). 59–65. 3 indexed citations

18.

Hu, Xuyun, Rongyu Chen, Chunyun Fu, et al.. (2016). Thyroglobulin gene mutations in Chinese patients with congenital hypothyroidism. Molecular and Cellular Endocrinology. 423. 60–66. 23 indexed citations

19.

Fu, Chunyun, Shiyu Luo, Shujie Zhang, et al.. (2016). Next-generation sequencing analysis of DUOX2 in 192 Chinese subclinical congenital hypothyroidism (SCH) and CH patients. Clinica Chimica Acta. 458. 30–34. 48 indexed citations

20.

Chen, Shaoke, Jingsi Luo, Yingfen Qin, et al.. (2011). [Epidemiological study on the association between obesity with metabolic syndrome in obese children and adolescents of Nanning city, Guangxi].. PubMed. 32(10). 969–72. 4 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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