Xinyan Lu

2.6k total citations
58 papers, 969 citations indexed

About

Xinyan Lu is a scholar working on Hematology, Oncology and Genetics. According to data from OpenAlex, Xinyan Lu has authored 58 papers receiving a total of 969 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Hematology, 21 papers in Oncology and 19 papers in Genetics. Recurrent topics in Xinyan Lu's work include Acute Myeloid Leukemia Research (20 papers), Lymphoma Diagnosis and Treatment (14 papers) and Chronic Lymphocytic Leukemia Research (12 papers). Xinyan Lu is often cited by papers focused on Acute Myeloid Leukemia Research (20 papers), Lymphoma Diagnosis and Treatment (14 papers) and Chronic Lymphocytic Leukemia Research (12 papers). Xinyan Lu collaborates with scholars based in United States, China and Australia. Xinyan Lu's co-authors include L. Jeffrey Medeiros, Shimin Hu, Wei Wang, Guilin Tang, Pei Lin, Joseph D. Khoury, Sa A. Wang, Keyur P. Patel, Ken H. Young and Zhenya Tang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Xinyan Lu

58 papers receiving 957 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Xinyan Lu United States	20	375	313	292	280	271	58	969
Maher Albitar United States	14	305 0.8×	287 0.9×	213 0.7×	321 1.1×	197 0.7×	48	783
Alicja Gruszka Italy	20	274 0.7×	378 1.2×	259 0.9×	395 1.4×	380 1.4×	36	945
Teresa Flores Spain	19	255 0.7×	285 0.9×	492 1.7×	539 1.9×	414 1.5×	25	1.3k
Rocío Benito Spain	17	260 0.7×	289 0.9×	128 0.4×	295 1.1×	134 0.5×	59	745
Tobias Berg Canada	19	402 1.1×	231 0.7×	211 0.7×	856 3.1×	189 0.7×	60	1.3k
Jacques Vargaftig France	12	439 1.2×	249 0.8×	174 0.6×	309 1.1×	202 0.7×	23	887
Debra Saxe United States	20	458 1.2×	244 0.8×	300 1.0×	578 2.1×	170 0.6×	45	1.4k
Kimberly Hayes United States	19	833 2.2×	753 2.4×	337 1.2×	428 1.5×	394 1.5×	38	1.5k
Nathalie Gachard France	18	401 1.1×	354 1.1×	463 1.6×	311 1.1×	565 2.1×	57	1.3k
Maria Kleppe United States	13	361 1.0×	302 1.0×	230 0.8×	459 1.6×	72 0.3×	24	947

Countries citing papers authored by Xinyan Lu

Since Specialization

Citations

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

Fields of papers citing papers by Xinyan Lu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xinyan Lu

This figure shows the co-authorship network connecting the top 25 collaborators of Xinyan Lu. A scholar is included among the top collaborators of Xinyan 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 Xinyan Lu. Xinyan 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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20 of 20 papers shown

Lu, Xinyan, Dongshi Chen, Min Wang, et al.. (2025). Depletion of oxysterol-binding proteins by OSW-1 triggers RIP1/RIP3-independent necroptosis and sensitization to cancer immunotherapy. Cell Death and Differentiation. 32(11). 2038–2052. 2 indexed citations

Segal, Jeremy, Sandeep Gurbuxani, Irene Helenowski, et al.. (2022). Therapy‐related myeloid neoplasms with normal karyotype show distinct genomic and clinical characteristics compared to their counterparts with abnormal karyotype. British Journal of Haematology. 197(6). 736–744. 8 indexed citations

Zhang, Jingxin, Yijie Liu, Xu Han, et al.. (2019). Rats provide a superior model of human stress erythropoiesis. Experimental Hematology. 78. 21–34.e3. 19 indexed citations

Gu, Jun, Rashmi Kanagal‐Shamanna, Zhenya Tang, et al.. (2019). Clinical implications of cytogenetic heterogeneity in Philadelphia chromosome positive (Ph+) adult B cell acute lymphoblastic leukemia following tyrosine kinase inhibitors and chemotherapy regimens. Leukemia Research. 84. 106176–106176. 6 indexed citations

Tang, Zhenya, Guilin Tang, Shimin Hu, et al.. (2019). Deciphering the complexities of MECOM rearrangement-driven chromosomal aberrations. Cancer Genetics. 233-234. 21–31. 15 indexed citations

Medeiros, L. Jeffrey, Wei Wang, Tariq Muzzafar, et al.. (2018). Clinicopathologic and molecular features in hairy cell leukemia-variant: single institutional experience. Modern Pathology. 31(11). 1717–1732. 32 indexed citations

Medeiros, L. Jeffrey, Jatin J. Shah, Donna M. Weber, et al.. (2017). Additional–structural–chromosomal aberrations are associated with inferior clinical outcome in patients with hyperdiploid multiple myeloma: a single-institution experience. Modern Pathology. 30(6). 843–853. 11 indexed citations

Hao, Suyang, Pei Lin, L. Jeffrey Medeiros, et al.. (2017). Clinical implications of cytogenetic heterogeneity in multiple myeloma patients with TP53 deletion. Modern Pathology. 30(10). 1378–1386. 9 indexed citations

Miranda, Roberto N., Guilin Tang, Sa A. Wang, et al.. (2017). Myeloproliferative neoplasms with t(8;22)(p11.2;q11.2)/ BCR-FGFR1 : a meta-analysis of 20 cases shows cytogenetic progression with B-lymphoid blast phase. Human Pathology. 65. 147–156. 25 indexed citations

10.

Tang, Zhenya, Jianjun Zhang, Xinyan Lu, et al.. (2017). Coexistent genetic alterations involving ALK, RET, ROS1 or MET in 15 cases of lung adenocarcinoma. Modern Pathology. 31(2). 307–312. 25 indexed citations

11.

Tang, Zhenya, Yan Li, Sa A. Wang, et al.. (2016). Clinical significance of acquired loss of the X chromosome in bone marrow. Leukemia Research. 47. 109–113. 8 indexed citations

12.

Singh, Rajesh R., Meenakshi Mehrotra, Hui Chen, et al.. (2016). Comprehensive Screening of Gene Copy Number Aberrations in Formalin-Fixed, Paraffin-Embedded Solid Tumors Using Molecular Inversion Probe–Based Single-Nucleotide Polymorphism Array. Journal of Molecular Diagnostics. 18(5). 676–687. 9 indexed citations

13.

Tang, Zhenya, L. Jeffrey Medeiros, C. Cameron Yin, et al.. (2016). Sex chromosome loss after allogeneic hematopoietic stem cell transplant in patients with hematologic neoplasms: a diagnostic dilemma for clinical cytogeneticists. Molecular Cytogenetics. 9(1). 62–62. 4 indexed citations

14.

Hong, Ming, Suyang Hao, Keyur P. Patel, et al.. (2016). Whole-arm translocation of der(5;17)(p10;q10) with concurrent TP53 mutations in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS): A unique molecular-cytogenetic subgroup. Cancer Genetics. 209(5). 205–214. 7 indexed citations

15.

Liu, Houfu, Na Yu, Sijie Lu, et al.. (2015). Solute Carrier Family of the Organic Anion-Transporting Polypeptides 1A2– Madin-Darby Canine Kidney II: A Promising In Vitro System to Understand the Role of Organic Anion-Transporting Polypeptide 1A2 in Blood-Brain Barrier Drug Penetration. Drug Metabolism and Disposition. 43(7). 1008–1018. 37 indexed citations

16.

Fang, Min, Pamela S. Becker, Michael Linenberger, et al.. (2015). Adult Low-Hypodiploid Acute B-Lymphoblastic Leukemia WithIKZF3Deletion andTP53Mutation. American Journal of Clinical Pathology. 144(2). 263–270. 10 indexed citations

17.

Gu, Jun, Keyur P. Patel, Bing Bai, et al.. (2015). Double inv(3)(q21q26.2) in acute myeloid leukemia is resulted from an acquired copy neutral loss of heterozygosity of chromosome 3q and associated with disease progression. Molecular Cytogenetics. 8(1). 68–68. 4 indexed citations

18.

Oran, Betül, Piyanuch Kongtim, Uday Popat, et al.. (2014). Cytogenetics, Donor Type, and Use of Hypomethylating Agents in Myelodysplastic Syndrome with Allogeneic Stem Cell Transplantation. Biology of Blood and Marrow Transplantation. 20(10). 1618–1625. 36 indexed citations

19.

Singh, Rajesh R., Keyur P. Patel, Mark J. Routbort, et al.. (2014). Clinical massively parallel next-generation sequencing analysis of 409 cancer-related genes for mutations and copy number variations in solid tumours. British Journal of Cancer. 111(10). 2014–2023. 65 indexed citations

20.

Gu, Heng, et al.. (2013). A Familial Cri-du-Chat/5p Deletion Syndrome Resulted from Rare Maternal Complex Chromosomal Rearrangements (CCRs) and/or Possible Chromosome 5p Chromothripsis. PLoS ONE. 8(10). e76985–e76985. 28 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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