Ruobing Zou

581 total citations
5 papers, 221 citations indexed

About

Ruobing Zou is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Surgery. According to data from OpenAlex, Ruobing Zou has authored 5 papers receiving a total of 221 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Cellular and Molecular Neuroscience and 1 paper in Surgery. Recurrent topics in Ruobing Zou's work include Genomics and Rare Diseases (1 paper), Ion channel regulation and function (1 paper) and Mitochondrial Function and Pathology (1 paper). Ruobing Zou is often cited by papers focused on Genomics and Rare Diseases (1 paper), Ion channel regulation and function (1 paper) and Mitochondrial Function and Pathology (1 paper). Ruobing Zou collaborates with scholars based in Canada, Australia and Saudi Arabia. Ruobing Zou's co-authors include Dennis E. Bulman, Kym M. Boycott, Lemuel Racacho, Fengxia Xiao, David A. Grimes, Fabin Han, Michel Panisset, Melissa T. Carter, Jeremy Schwartzentruber and Peter W. Schofield and has published in prestigious journals such as Arteriosclerosis Thrombosis and Vascular Biology, Movement Disorders and Orphanet Journal of Rare Diseases.

In The Last Decade

Ruobing Zou

5 papers receiving 219 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ruobing Zou Canada	5	146	131	40	40	20	5	221
Christopher Elzinga United States	5	58 0.4×	106 0.8×	32 0.8×	37 0.9×	50 2.5×	5	186
Florian Harmuth Germany	8	120 0.8×	117 0.9×	58 1.4×	49 1.2×	52 2.6×	11	235
Claire Guissart France	12	174 1.2×	76 0.6×	65 1.6×	73 1.8×	35 1.8×	22	301
Kaisu Nikali Finland	7	290 2.0×	150 1.1×	33 0.8×	87 2.2×	32 1.6×	10	388
Heliane Guerra Serra Brazil	5	302 2.1×	308 2.4×	62 1.6×	30 0.8×	18 0.9×	7	368
Yvonne L. Clarkson United Kingdom	11	304 2.1×	232 1.8×	26 0.7×	29 0.7×	29 1.4×	11	486
Vukasin M. Jovanovic United States	8	184 1.3×	51 0.4×	21 0.5×	29 0.7×	10 0.5×	13	274
Anna Walczak Poland	11	174 1.2×	79 0.6×	22 0.6×	68 1.7×	30 1.5×	19	271
Tania Cruz Mariño Canada	9	185 1.3×	209 1.6×	113 2.8×	53 1.3×	26 1.3×	27	289
Gertrud Strobl‐Wildemann Germany	6	97 0.7×	75 0.6×	18 0.5×	74 1.9×	27 1.4×	7	215

Countries citing papers authored by Ruobing Zou

Since Specialization

Citations

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

Fields of papers citing papers by Ruobing Zou

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruobing Zou

This figure shows the co-authorship network connecting the top 25 collaborators of Ruobing Zou. A scholar is included among the top collaborators of Ruobing Zou 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 Ruobing Zou. Ruobing Zou 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:

5 of 5 papers shown

1.

Lemire, Gabrielle, Bixia Zheng, Ruobing Zou, et al.. (2021). Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasia. American Journal of Medical Genetics Part A. 185(10). 3005–3011. 4 indexed citations

2.

Brown, Alison, Martine Tétreault, David A. Dyment, et al.. (2016). Concordance between whole‐exome sequencing and clinical Sanger sequencing: implications for patient care. Molecular Genetics & Genomic Medicine. 4(5). 504–512. 25 indexed citations

3.

Huang, Lijia, Jodi Warman‐Chardon, Melissa T. Carter, et al.. (2012). Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia. Orphanet Journal of Rare Diseases. 7(1). 67–67. 104 indexed citations

4.

Grimes, David A., Fabin Han, Michel Panisset, et al.. (2006). Translated mutation in the Nurr1 gene as a cause for Parkinson's disease. Movement Disorders. 21(7). 906–909. 80 indexed citations

5.

McNicol, Archibald, Michael R. Sutherland, Ruobing Zou, & Jeanne Drouin. (1996). Defective Thrombin-Induced Calcium Changes and Aggregation of Bernard-Soulier Platelets Are Not Associated With Deficient Moderate-Affinity Receptors. Arteriosclerosis Thrombosis and Vascular Biology. 16(5). 628–632. 8 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