S. Yu

697 total citations
9 papers, 564 citations indexed

About

S. Yu is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, S. Yu has authored 9 papers receiving a total of 564 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Plant Science. Recurrent topics in S. Yu's work include Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (3 papers) and Prenatal Screening and Diagnostics (2 papers). S. Yu is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (3 papers) and Prenatal Screening and Diagnostics (2 papers). S. Yu collaborates with scholars based in United States, Australia and China. S. Yu's co-authors include Sherif Tawfic, Russell A. Faust, Khalil Ahmed, Alan T. Davis, G.R. Sutherland, W. Graf, Annemarie Poustka, Harriet L. Robinson, Bella Gross and Emma K. Baker and has published in prestigious journals such as Nature Genetics, Journal of Medical Genetics and Cytogenetic and Genome Research.

In The Last Decade

S. Yu

9 papers receiving 550 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
S. Yu United States	7	430	278	83	69	59	9	564
Jelle Verbeeck Belgium	12	346 0.8×	170 0.6×	39 0.5×	50 0.7×	30 0.5×	16	469
Kiyotaka Oshikawa Japan	9	465 1.1×	119 0.4×	40 0.5×	197 2.9×	33 0.6×	13	668
Barbara A. Boggs United States	12	691 1.6×	391 1.4×	11 0.1×	35 0.5×	100 1.7×	16	817
Szabolcs Soeroes Germany	10	780 1.8×	132 0.5×	9 0.1×	28 0.4×	56 0.9×	11	858
Alicia Subtil‐Rodríguez Spain	8	374 0.9×	200 0.7×	31 0.4×	139 2.0×	19 0.3×	10	540
Karen T. Smith United States	9	501 1.2×	143 0.5×	27 0.3×	59 0.9×	13 0.2×	9	578
Lynne Hobson Australia	9	563 1.3×	372 1.3×	8 0.1×	42 0.6×	52 0.9×	11	684
Moises Serrano United States	9	289 0.7×	79 0.3×	17 0.2×	119 1.7×	17 0.3×	17	410
Alison Hanson United States	9	485 1.1×	38 0.1×	17 0.2×	124 1.8×	27 0.5×	14	622
Ewald Münstermann Germany	10	387 0.9×	84 0.3×	45 0.5×	49 0.7×	18 0.3×	11	511

Countries citing papers authored by S. Yu

Since Specialization

Citations

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

Fields of papers citing papers by S. Yu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Yu

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

9 of 9 papers shown

1.

Yu, S., et al.. (2011). Characterizing Small Supernumerary Marker Chromosomes with Combination of Multiple Techniques. Cytogenetic and Genome Research. 136(1). 6–14. 19 indexed citations

2.

Yu, S., W. Graf, Arivudainambi Ramalingam, et al.. (2011). Identification of Copy Number Variants on Human Chromosome 22 in Patients with a Variety of Clinical Findings. Cytogenetic and Genome Research. 134(4). 260–268. 10 indexed citations

3.

Yu, S. & W. Graf. (2010). Telomere Capture as a Frequent Mechanism for Stabilization of the Terminal Chromosomal Deletion Associated with Inverted Duplication. Cytogenetic and Genome Research. 129(4). 265–274. 32 indexed citations

4.

Talseth‐Palmer, Bente A., Nikola A. Bowden, Cliff Meldrum, et al.. (2009). A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology. Cytogenetic and Genome Research. 124(1). 94–101. 6 indexed citations

5.

Bittel, Douglas C., et al.. (2009). Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH. Cytogenetic and Genome Research. 124(2). 113–120. 54 indexed citations

6.

Yu, S., Deborah Barbouth, P.J. Benke, Peter E. Warburton, & Ying Fan. (2007). Characterization of a neocentric supernumerary marker chromosome originating from the Xp distal region by FISH, CENP-C staining, and array CGH. Cytogenetic and Genome Research. 116(1-2). 141–145. 6 indexed citations

7.

Tawfic, Sherif, et al.. (2001). Protein kinase CK2 signal in neoplasia.. PubMed. 16(2). 573–82. 230 indexed citations

8.

Narahara, Kouji, Yuji Yokoyama, S. Yu, et al.. (1997). Localisation of a 10q breakpoint within the PAX2 gene in a patient with a de novo t(10;13) translocation and optic nerve coloboma-renal disease.. Journal of Medical Genetics. 34(3). 213–216. 40 indexed citations

9.

Gedeon, Ági K., Emma K. Baker, Harriet L. Robinson, et al.. (1992). Fragile X syndrome without CCG amplification has an FMR1 deletion. Nature Genetics. 1(5). 341–344. 167 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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