Junbin Liang

2.2k total citations
6 papers, 198 citations indexed

About

Junbin Liang is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Junbin Liang has authored 6 papers receiving a total of 198 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Pediatrics, Perinatology and Child Health, 3 papers in Genetics and 2 papers in Molecular Biology. Recurrent topics in Junbin Liang's work include Prenatal Screening and Diagnostics (3 papers), Cancer Genomics and Diagnostics (2 papers) and Acute Myeloid Leukemia Research (2 papers). Junbin Liang is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Cancer Genomics and Diagnostics (2 papers) and Acute Myeloid Leukemia Research (2 papers). Junbin Liang collaborates with scholars based in China, Germany and United Kingdom. Junbin Liang's co-authors include Chongjian Chen, Katia Ancelin, Tao Liu, Rafael Galupa, Édith Heard, Laurène Syx, Maud Borensztein, Emmanuel Barillot, Nicolas Servant and M. Azim Surani and has published in prestigious journals such as Scientific Reports, Nature Structural & Molecular Biology and Oncotarget.

In The Last Decade

Junbin Liang

6 papers receiving 196 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Junbin Liang China	6	121	97	54	38	31	6	198
Sandra Fert‐Ferrer France	7	46 0.4×	39 0.4×	32 0.6×	12 0.3×	30 1.0×	10	117
Jorge F. Sánchez-García Spain	8	117 1.0×	109 1.1×	140 2.6×	28 0.7×	22 0.7×	13	259
Kalin Mayberry United States	7	160 1.3×	48 0.5×	24 0.4×	12 0.3×	46 1.5×	16	227
Elisabet Lloveras Spain	8	58 0.5×	153 1.6×	132 2.4×	7 0.2×	29 0.9×	20	250
Süleyman Aktuna Türkiye	7	146 1.2×	54 0.6×	71 1.3×	9 0.2×	73 2.4×	20	286
Katherine L. Palmerola United States	8	225 1.9×	75 0.8×	125 2.3×	8 0.2×	18 0.6×	22	401
Cristina González-González Spain	10	51 0.4×	93 1.0×	209 3.9×	13 0.3×	20 0.6×	12	253
Laura Kasak Estonia	8	135 1.1×	159 1.6×	91 1.7×	21 0.6×	4 0.1×	12	293
Eshwar Meduri United Kingdom	6	187 1.5×	63 0.6×	16 0.3×	10 0.3×	24 0.8×	11	234
Anne H. Shen China	3	263 2.2×	101 1.0×	12 0.2×	6 0.2×	28 0.9×	3	291

Countries citing papers authored by Junbin Liang

Since Specialization

Citations

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

Fields of papers citing papers by Junbin Liang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Junbin Liang

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

1.

Qi, Hong, Zhaoling Xuan, Yang Du, et al.. (2018). High resolution global chromosomal aberrations from spontaneous miscarriages revealed by low coverage whole genome sequencing. European Journal of Obstetrics & Gynecology and Reproductive Biology. 224. 21–28. 22 indexed citations

2.

Du, Yang, Han Zhang, Zhandong Wang, et al.. (2018). Identification of a de novo fetal variant in osteogenesis imperfecta by targeted sequencing-based noninvasive prenatal testing. Journal of Human Genetics. 63(11). 1129–1137. 14 indexed citations

3.

Zhao, Pan, et al.. (2018). Association of Gene Mutations with Response to Arsenic-Containing Compound Qinghuang Powder (复方青黄散) in Patients with Myelodysplastic Syndromes. Chinese Journal of Integrative Medicine. 25(6). 409–415. 5 indexed citations

4.

Borensztein, Maud, Laurène Syx, Katia Ancelin, et al.. (2017). Xist-dependent imprinted X inactivation and the early developmental consequences of its failure. Nature Structural & Molecular Biology. 24(3). 226–233. 116 indexed citations

5.

Liu, Yangyang, Guangyuan Hou, Lili Wang, et al.. (2016). Mutational spectrum and risk stratification of intermediate-risk acute myeloid leukemia patients based on next-generation sequencing. Oncotarget. 7(22). 32065–32078. 26 indexed citations

6.

Zhao, Yangyu, Jing Song, Hua Yang, et al.. (2015). Statistical Approach to Decreasing the Error Rate of Noninvasive Prenatal Aneuploid Detection caused by Maternal Copy Number Variation. Scientific Reports. 5(1). 16106–16106. 15 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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