Yao‐Shan Fan

1.3k total citations
39 papers, 913 citations indexed

About

Yao‐Shan Fan is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Yao‐Shan Fan has authored 39 papers receiving a total of 913 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 12 papers in Molecular Biology and 12 papers in Plant Science. Recurrent topics in Yao‐Shan Fan's work include Genomic variations and chromosomal abnormalities (19 papers), Chromosomal and Genetic Variations (12 papers) and Chronic Lymphocytic Leukemia Research (6 papers). Yao‐Shan Fan is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Chromosomal and Genetic Variations (12 papers) and Chronic Lymphocytic Leukemia Research (6 papers). Yao‐Shan Fan collaborates with scholars based in United States, Canada and United Kingdom. Yao‐Shan Fan's co-authors include Victoria Mok Siu, Jack H. Jung, Sandra A. Farrell, Kamilia Rizkalla, Shaohua Li, Lawrence H. Chow, Stephen M. Sims, J. Geoffrey Pickering, Eric van der Veer and Hongbo Zhu and has published in prestigious journals such as Circulation Research, International Journal of Molecular Sciences and Molecular Endocrinology.

In The Last Decade

Yao‐Shan Fan

39 papers receiving 874 citations

Peers

Yao‐Shan Fan
Caroline Astbury United States
Kosuke Izumi United States
Jeroen Knijnenburg Netherlands
Yves Lacassie United States
Sung‐Hae Kang United States
Anas M. Alazami Saudi Arabia
Greg B. Peters Australia
Caroline Astbury United States
Yao‐Shan Fan
Citations per year, relative to Yao‐Shan Fan Yao‐Shan Fan (= 1×) peers Caroline Astbury

Countries citing papers authored by Yao‐Shan Fan

Since Specialization
Citations

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

Fields of papers citing papers by Yao‐Shan Fan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yao‐Shan Fan. 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 Yao‐Shan Fan. The network helps show where Yao‐Shan Fan may publish in the future.

Co-authorship network of co-authors of Yao‐Shan Fan

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

All Works

20 of 20 papers shown
1.
Chapman, Jennifer R., Julia T. Geyer, Yao‐Shan Fan, et al.. (2017). Myeloid neoplasms with features intermediate between primary myelofibrosis and chronic myelomonocytic leukemia. Modern Pathology. 31(3). 429–441. 10 indexed citations
2.
Fan, Yao‐Shan, Jennifer R. Chapman, Offiong F. Ikpatt, et al.. (2016). HER2 FISH classification of equivocal HER2 IHC breast cancers with use of the 2013 ASCO/CAP practice guideline. Breast Cancer Research and Treatment. 155(3). 457–462. 31 indexed citations
3.
Pinto, André, Vânia Nosé, Claudia Rojas, Yao‐Shan Fan, & Carmen Gomez‐Fernandez. (2013). Searching for mammary analog secretory carcinoma of salivary gland among its mimics. Modern Pathology. 27(1). 30–37. 70 indexed citations
4.
Fan, Yao‐Shan. (2013). Companion Diagnostic Testing for Targeted Cancer Therapies: An Overview. Genetic Testing and Molecular Biomarkers. 17(7). 515–523. 11 indexed citations
5.
Fan, Yao‐Shan, Xiaomei Ouyang, Mustafa Tekin, et al.. (2013). Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarray. Molecular Cytogenetics. 6(1). 38–38. 25 indexed citations
6.
Li, Deling, Mustafa Tekin, Maria Buch, & Yao‐Shan Fan. (2012). Co-existence of other copy number variations with 22q11.2 deletion or duplication: a modifier for variable phenotypes of the syndrome?. Molecular Cytogenetics. 5(1). 18–18. 9 indexed citations
7.
Ruivenkamp, Claudia, Johan Staaf, Hongbo Zhu, et al.. (2008). Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platforms. European Journal of Human Genetics. 16(7). 786–792. 26 indexed citations
8.
Quadrelli, Roberto, et al.. (2007). A Girl with del(4)(q33) And Occipital Encephalocele: Clinical Description And Molecular Genetic Characterization of A Rare Patient. Genetic Testing. 11(1). 4–10. 11 indexed citations
9.
Fan, Yao‐Shan, Parul Jayakar, Hongbo Zhu, et al.. (2007). Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization. Human Mutation. 28(11). 1124–1132. 93 indexed citations
10.
Zhang, Yang, et al.. (2006). Breakpoint Associated with a novel 2.3 Mb deletion in the VCFS region of 22q11 and the role of Alu (SINE) in recurring microdeletions. BMC Medical Genetics. 7(1). 18–18. 23 indexed citations
11.
Fan, Yao‐Shan & Kamilia Rizkalla. (2003). Comprehensive cytogenetic analysis including multicolor spectral karyotyping and interphase fluorescence in situ hybridization in lymphoma diagnosis. Cancer Genetics and Cytogenetics. 143(1). 73–79. 21 indexed citations
12.
Fan, Yao‐Shan, Victoria Mok Siu, Jack H. Jung, & Jie Xu. (2000). Sensitivity of Multiple Color Spectral Karyotyping in Detecting Small Interchromosomal Rearrangements. Genetic Testing. 4(1). 9–14. 33 indexed citations
13.
Fan, Yao‐Shan, et al.. (2000). Jumping Translocations of 11q in Acute Myeloid Leukemia and 1q in Follicular Lymphoma. Cancer Genetics and Cytogenetics. 118(1). 35–41. 20 indexed citations
14.
Fan, Yao‐Shan, et al.. (1999). Small terminal deletion of 1p and duplication of 1q: Cytogenetics, FISH studies, and clinical observations at newborn and at age 16 years. American Journal of Medical Genetics. 86(2). 118–123. 18 indexed citations
15.
Fan, Yao‐Shan, et al.. (1996). Endoreduplication and telomeric association in a choroid plexus carcinoma. Cancer Genetics and Cytogenetics. 87(1). 7–10. 17 indexed citations
16.
Farrell, Sandra A. & Yao‐Shan Fan. (1995). Balanced nonacrocentric whole‐arm reciprocal translocations: A de novo case and literature review. American Journal of Medical Genetics. 55(4). 423–426. 19 indexed citations
17.
Fan, Yao‐Shan, et al.. (1993). Correction of Mucolipidosis III in Vitro by Gene Transfer. Genomics. 18(2). 236–243. 1 indexed citations
18.
Nishi, Masahiro, Tokio Sanke, Susumu Seino, et al.. (1989). Human Islet Amyloid Polypeptide Gene: Complete Nucleotide Sequence, Chromosomal Localization, and Evolutionary History. Molecular Endocrinology. 3(11). 1775–1781. 79 indexed citations
19.
Fan, Yao‐Shan, Maria R. Baer, Sheila N.J. Sait, et al.. (1988). An acquired robertsonian translocation dic(14;14)(p11;p11) in a patient with a myelodysplastic syndrome following treatment of multiple myeloma. Cancer Genetics and Cytogenetics. 30(1). 133–137. 5 indexed citations
20.
Fan, Yao‐Shan, Jacob M. Rowe, Paola Dal Cin, & Avery A. Sandberg. (1988). A translocation t(9;11)(p11;q23) in T-cell acute lymphoblastic leukemia (FAB-L2). Cancer Genetics and Cytogenetics. 31(2). 263–269. 5 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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