Bobo Xie

767 total citations
38 papers, 366 citations indexed

About

Bobo Xie is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Bobo Xie has authored 38 papers receiving a total of 366 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 18 papers in Genetics and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Bobo Xie's work include Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Metabolism and Genetic Disorders (5 papers). Bobo Xie is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Metabolism and Genetic Disorders (5 papers). Bobo Xie collaborates with scholars based in China, United States and Philippines. Bobo Xie's co-authors include Shaoke Chen, Xin Fan, Jingsi Luo, Jin Wang, Chunyun Fu, Shiyu Luo, Jiasun Su, Yiping Shen, Xuyun Hu and Rongyu Chen and has published in prestigious journals such as PLoS ONE, Scientific Reports and Gene.

In The Last Decade

Bobo Xie

33 papers receiving 356 citations

Peers

Bobo Xie

EDM

GENET

PPCH

Jingsi Luo China

Chunyun Fu China

Jiasun Su China

Dana Kostiner United States

Celsa Quinteiro Spain

Yucheng Liao China

Ricardo Gracía Spain

Betty C. Villafuerte United States

Fengxia Yao China

L Duprez Belgium

Jingsi Luo China

Bobo Xie

290 ×1.6

243 ×1.8

EDM

197 ×1.9

GENET

156 ×1.7

PPCH

62 ×1.7

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

Countries citing papers authored by Bobo Xie

Since Specialization

Citations

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

Fields of papers citing papers by Bobo Xie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bobo Xie

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

Huang, Yiyun, Chunyi Peng, Chuan Li, et al.. (2025). Genetic skeletal disorders: phenotypic-genotypic characteristics and RhGH therapy responses of a pediatric cohort. Scientific Reports. 15(1). 20717–20717. 1 indexed citations

Xie, Bobo, Xiaoyun Lei, Shaoke Chen, et al.. (2024). The cryptic complex rearrangements involving the DMD gene: etiologic clues about phenotypical differences revealed by optical genome mapping. Human Genomics. 18(1). 103–103. 1 indexed citations

Xie, Bobo, Yan Huang, Xin Fan, et al.. (2024). Complex genotype–phenotype correlation of MYH11: new insights from monozygotic twins with highly variable expressivity and outcomes. BMC Medical Genomics. 17(1). 135–135.

Lin, Yunting, Xiaohong Chen, Bobo Xie, et al.. (2023). Novel variants and phenotypic heterogeneity in a cohort of 11 Chinese children with Wiedemann-Steiner syndrome. Frontiers in Genetics. 14. 1085210–1085210. 2 indexed citations

Li, Qifei, Lifang Wang, Jiasun Su, et al.. (2019). Etiology and Outcome of non-immune Hydrops Fetalis in Southern China: report of 1004 cases. Scientific Reports. 9(1). 10726–10726. 11 indexed citations

Yang, Qi, Mengting Li, Bobo Xie, et al.. (2019). Genetic analyses of oculocutaneous albinism types 1 and 2 with four novel mutations. BMC Medical Genetics. 20(1). 106–106. 18 indexed citations

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

Luo, Shiyu, Qifei Li, Yuhua Chen, et al.. (2018). Genetic Testing and Pregnancy Outcome Analysis of 362 Fetuses with Congenital Heart Disease Identified by Prenatal Ultrasound. Arquivos Brasileiros de Cardiologia. 111(4). 571–577. 12 indexed citations

Qiu, Lihua, Chao Zhao, Pengfei Wang, et al.. (2018). Genomic structure, expression, and functional characterization of checkpoint kinase 1 from Penaeus monodon. PLoS ONE. 13(5). e0198036–e0198036. 4 indexed citations

10.

Fu, Chunyun, Shiyu Luo, Yingfeng Li, et al.. (2017). Mutation screening of the GLIS3 gene in a cohort of 592 Chinese patients with congenital hypothyroidism. Clinica Chimica Acta. 476. 38–43. 16 indexed citations

11.

Xie, Bobo, Pengfei Wang, Chao Zhao, & Lihua Qiu. (2017). Genomic structure, expression pattern, and functional characterization of transcription factor E2F-2 from black tiger shrimp (Penaeus monodon). PLoS ONE. 12(5). e0177420–e0177420. 5 indexed citations

12.

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

13.

Zhang, Shujie, Jin Wang, Shiyu Luo, et al.. (2016). Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability. Molecular Cytogenetics. 9(1). 66–66. 10 indexed citations

14.

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

15.

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

16.

Xie, Bobo, et al.. (2016). Cloning, characterization, and expression of the macrophage migration inhibitory factor gene from the black tiger shrimp ( Penaeus monodon ). Fish & Shellfish Immunology. 56. 489–495. 19 indexed citations

17.

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

18.

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

19.

Li, Chuan, Rongyu Chen, Xin Fan, et al.. (2015). EPHA4 haploinsufficiency is responsible for the short stature of a patient with 2q35-q36.2 deletion and Waardenburg syndrome. BMC Medical Genetics. 16(1). 23–23. 4 indexed citations

20.

Chen, Rongyu, Chuan Li, Bobo Xie, et al.. (2014). Clinical and molecular evaluations of siblings with “pure” 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3). Molecular Cytogenetics. 7(1). 101–101. 6 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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