Xin-Yan Lu

1.0k total citations
7 papers, 594 citations indexed

About

Xin-Yan Lu is a scholar working on Cancer Research, Molecular Biology and Genetics. According to data from OpenAlex, Xin-Yan Lu has authored 7 papers receiving a total of 594 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Cancer Research, 3 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Xin-Yan Lu's work include Genomic variations and chromosomal abnormalities (3 papers), Sarcoma Diagnosis and Treatment (2 papers) and Cancer-related molecular mechanisms research (2 papers). Xin-Yan Lu is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Sarcoma Diagnosis and Treatment (2 papers) and Cancer-related molecular mechanisms research (2 papers). Xin-Yan Lu collaborates with scholars based in United States, Germany and Colombia. Xin-Yan Lu's co-authors include Pulivarthi H. Rao, Richard Görlick, Marc Ladanyi, Charles P. Harris, Michael Overholtzer, Reyna Favis, Michael B. Elowitz, Francis Barany, Arnold J. Levine and Vundavalli V. Murty and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PEDIATRICS and Oncogene.

In The Last Decade

Xin-Yan Lu

7 papers receiving 580 citations

Peers

Countries citing papers authored by Xin-Yan Lu

Since Specialization

Citations

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

Fields of papers citing papers by Xin-Yan Lu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Xin-Yan Lu. 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 Xin-Yan Lu. The network helps show where Xin-Yan Lu may publish in the future.

Co-authorship network of co-authors of Xin-Yan Lu

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

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Integrated multimodal genetic testing of Ewing sarcoma—a single-institution experience 2013 ·Human Pathology ·Mikako Warren, (unknown), (unknown), (unknown), Adriana Reyes, Keita Terashima, Pulivarthi H. Rao, Murali Chintagumpala, John Hicks, Dolores López‐Terrada, Xin-Yan Lu	5
2	Genomic profiling of plasmablastic lymphoma using array comparative genomic hybridization (aCGH): revealing significant overlapping genomic lesions with diffuse large B-cell lymphoma 2009 ·Journal of Hematology & Oncology ·Chung-Che Chang, Xiaobo Zhou, (unknown), Wan‐Ting Huang, Xianwen Ren, Federico A. Monzon, Yongdong Feng, Pulivarthi H. Rao, Xin-Yan Lu, (unknown), Susan G. Hilsenbeck, Chad J. Creighton, Elaine S. Jaffe, Ching‐Ching Lau	53
3	Genomic Imbalances in Neonates With Birth Defects: High Detection Rates by Using Chromosomal Microarray Analysis 2008 ·PEDIATRICS ·Xin-Yan Lu, (unknown), Chad A. Shaw, (unknown), Sarah Neil‐Sztramko, Ankita Patel, Trilochan Sahoo, Carlos A. Bacino, Paweł Stankiewicz, Sung-Hae L. Kang, Seema R. Lalani, A. Craig Chinault, James R. Lupski, Sau Wai Cheung, Arthur L. Beaudet	104
4	Chromosomal amplifications, 3q gain and deletions of 2q33-q37 are the frequent genetic changes in cervical carcinoma 2004 ·BMC Cancer ·Pulivarthi H. Rao, Hugo Arias‐Pulido, Xin-Yan Lu, Charles P. Harris, Hernán Vargas, (unknown), Gopeshwar Narayan, Achim Schneider, Mary Beth Terry, Vundavalli V. Murty	104
5	Genome-wide array comparative genomic hybridization analysis reveals distinct amplifications in osteosarcoma 2004 ·BMC Cancer ·Tsz‐Kwong Man, Xin-Yan Lu, (unknown), László Perlaky, Charles P. Harris, Shishir K. Shah, Marc Ladanyi, Richard Görlick, Ching C. Lau, Pulivarthi H. Rao	115
6	The presence of p53 mutations in human osteosarcomas correlates with high levels of genomic instability 2003 ·Proceedings of the National Academy of Sciences ·Michael Overholtzer, Pulivarthi H. Rao, Reyna Favis, Xin-Yan Lu, Michael B. Elowitz, Francis Barany, Marc Ladanyi, Richard Görlick, Arnold J. Levine	151
7	Genetic analysis identifies putative tumor suppressor sites at 2q35–q36.1 and 2q36.3–q37.1 involved in cervical cancer progression 2003 ·Oncogene ·Gopeshwar Narayan, Hugo Arias‐Pulido, Sanjay Koul, Xin-Yan Lu, Charles P. Harris, (unknown), Hernán Vargas, Héctor Posso, Mary Beth Terry, Lutz Gissmann, Achim Schneider, Mahesh Mansukhani, Pulivarthi H. Rao, Vundavalli V. Murty	62

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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