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Xianglan Lu

TitleAsoc,Research
InstitutionUniversity of Oklahoma Health Sciences Center
DepartmentDept of Pediatrics
AddressBSEB 224
941 Stanton L Young Blvd
Oklahoma City OK 73104
Phone405/271-3589
Fax0
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Srinivasan A, Liu M, Parham D, Li M, Wang X, Lu X, Li S, Zhang L, Yu Z. Infantile Epithelioid Sarcoma with Genomic Segmental Amplification of BIRC3/YAP1 as Double Minutes Plus Trisomy 2: A Case Report. Fetal Pediatr Pathol. 2020 Feb; 39(1):51-61. PMID: 31215292.
      Citations: 1     Fields:    Translation:Humans
    2. Liu G, Lu X, Kim YM, Wang X, Li S, Liu Y. Simultaneous involvement of 11q23 translocation resulting in chimeric MLL-AFF1 and a second translocation [t (9;21) (p13; p11.2)] in an infant acute lymphoblastic leukemia patient at relapse: A case report. Medicine (Baltimore). 2018 May; 97(21):e10874. PMID: 29794792.
      Citations:    Fields:    Translation:HumansCells
    3. Harris VM, Sharma R, Cavett J, Kurien BT, Liu K, Koelsch KA, Rasmussen A, Radfar L, Lewis D, Stone DU, Kaufman CE, Li S, Segal B, Wallace DJ, Weisman MH, Venuturupalli S, Kelly JA, Alarcon-Riquelme ME, Pons-Estel B, Jonsson R, Lu X, Gottenberg JE, Anaya JM, Cunninghame-Graham DS, Huang AJW, Brennan MT, Hughes P, Alevizos I, Miceli-Richard C, Keystone EC, Bykerk VP, Hirschfield G, Xie G, Siminovitch KA, Ng WF, Nordmark G, Bucher SM, Eriksson P, Omdal R, Rhodus NL, Rischmueller M, Rohrer M, Wahren-Herlenius M, Witte T, Mariette X, Lessard CJ, Harley JB, Sivils KL, Scofield RH. Corrigendum to "Klinefelter's syndrome (47,XXY) is in excess among men with Sjögren's syndrome" [Clin. Immunol. 168 (2016) 25-29]. Clin Immunol. 2018 02; 187:137-138. PMID: 29195081.
      Citations:    Fields:    
    4. Liu G, Wen Z, Lu X, Kim YM, Wang X, Crew RM, Cherry MA, Li S, Liu Y. Coexistence of t(2;14;11)(p16.1;q32;q23) and t(14;19)(q32;q13.3) chromosome translocations in a patient with chronic lymphocytic leukemia: A case report. Medicine (Baltimore). 2017 Dec; 96(51):e9169. PMID: 29390452.
      Citations:    Fields:    Translation:HumansCells
    5. Sharma R, Harris VM, Cavett J, Kurien BT, Liu K, Koelsch KA, Fayaaz A, Chaudhari KS, Radfar L, Lewis D, Stone DU, Kaufman CE, Li S, Segal B, Wallace DJ, Weisman MH, Venuturupalli S, Kelly JA, Pons-Estel B, Jonsson R, Lu X, Gottenberg JE, Anaya JM, Cunninghame-Graham DS, Huang AJW, Brennan MT, Hughes P, Alevizos I, Miceli-Richard C, Keystone EC, Bykerk VP, Hirschfield G, Nordmark G, Bucher SM, Eriksson P, Omdal R, Rhodus NL, Rischmueller M, Rohrer M, Wahren-Herlenius M, Witte T, Alarcón-Riquelme M, Mariette X, Lessard CJ, Harley JB, Ng WF, Rasmussen A, Sivils KL, Scofield RH. Rare X Chromosome Abnormalities in Systemic Lupus Erythematosus and Sjögren's Syndrome. Arthritis Rheumatol. 2017 11; 69(11):2187-2192. PMID: 28692793.
      Citations: 11     Fields:    Translation:HumansCells
    6. Sun M, Zhang H, Li G, Guy CJ, Wang X, Lu X, Gong F, Lee J, Hassed S, Li S. Molecular characterization of 20 small supernumerary marker chromosome cases using array comparative genomic hybridization and fluorescence in situ hybridization. Sci Rep. 2017 09 04; 7(1):10395. PMID: 28871159.
      Citations: 3     Fields:    Translation:HumansCells
    7. Guy C, Wang X, Lu X, Lu J, Li S. Clinical report: variable phenotypic expression in a large sibling cohort with a deletion of 4p16.1. Clin Case Rep. 2016 Oct; 4(10):913-918. PMID: 27761238.
      Citations:    
    8. Harris VM, Sharma R, Cavett J, Kurien BT, Liu K, Koelsch KA, Rasmussen A, Radfar L, Lewis D, Stone DU, Kaufman CE, Li S, Segal B, Wallace DJ, Weisman MH, Venuturupalli S, Kelly JA, Alarcon-Riquelme ME, Pons-Estel B, Jonsson R, Lu X, Gottenberg JE, Anaya JM, Cunninghame-Graham DS, Huang AJW, Brennan MT, Hughes P, Alevizos I, Miceli-Richard C, Keystone EC, Bykerk VP, Hirschfield G, Xie G, Siminovitch KA, Ng WF, Nordmark G, Bucher SM, Eriksson P, Omdal R, Rhodus NL, Rischmueller M, Rohrer M, Wahren-Herlenius M, Witte T, Mariette X, Lessard CJ, Harley JB, Sivils KL, Scofield RH. Klinefelter's syndrome (47,XXY) is in excess among men with Sjögren's syndrome. Clin Immunol. 2016 07; 168:25-29. PMID: 27109640.
      Citations: 19     Fields:    Translation:HumansCells
    9. Guy C, Wang X, Lu X, Lu J, Li S. Two patients with small chromosome 22q11.21 alterations and central nervous system abnormalities. Mol Cytogenet. 2015; 8:102. PMID: 26719767.
      Citations:    
    10. Zhang R, Kim YM, Wang X, Li Y, Lu X, Sternenberger AR, Li S, Lee JY. Genomic Copy Number Variations in the Myelodysplastic Syndrome and Acute Myeloid Leukemia Patients with del(5q) and/or -7/del(7q). Int J Med Sci. 2015; 12(9):719-26. PMID: 26392809.
      Citations: 1     Fields:    Translation:HumansCells
    11. Gao M, Wang G, Wang X, Kim YM, Lu X, Lu J, Gu Y, Pang H, Lee J, Sternenberger A, Li S. A cryptic submicroscopic deletion of 5' MLF1-3' NPM1 segment on derivative chromosome 3 in a patient with acute myeloid leukemia with t(3;5)(q25;q35). Leuk Lymphoma. 2015; 56(9):2735-8. PMID: 25629988.
      Citations:    Fields:    Translation:HumansCells
    12. Sun M, Zhang H, Li G, Wang X, Lu X, Sternenberger A, Guy C, Li W, Lee J, Zheng L, Li S. 16p13.3 duplication associated with non-syndromic pierre robin sequence with incomplete penetrance. Mol Cytogenet. 2014; 7(1):76. PMID: 25493098.
      Citations:    
    13. Qiu Y, Song J, Lu X, Li Y, Zheng B, Li S, Liu H. Feature selection for the automated detection of metaphase chromosomes: performance comparison using a receiver operating characteristic method. Anal Cell Pathol (Amst). 2014; 2014:565392. PMID: 25763334.
      Citations: 2     Fields:    Translation:HumansCells
    14. Zhang R, Lee JY, Wang X, Xu W, Hu X, Lu X, Niu Y, Tang R, Li S, Li Y. Identification of novel genomic aberrations in AML-M5 in a level of array CGH. PLoS One. 2014; 9(4):e87637. PMID: 24727659.
      Citations: 6     Fields:    Translation:Humans
    15. Lu X, Wang X, Kim Y, Zhang R, Li S, Lee JY. Acquired genomic copy number changes in CML patients with the Philadelphia chromosome (Ph+). Cancer Genet. 2012 Oct; 205(10):513-8. PMID: 23036696.
      Citations: 1     Fields:    Translation:HumansCells
    16. Zhang R, Kim YM, Lu X, Wang X, Pang H, Li Y, Li S, Lee JY. Characterization of a novel t(2;5;11) in a patient with concurrent AML and CLL: a case report and literature review. Cancer Genet. 2011 Jun; 204(6):328-33. PMID: 21763630.
      Citations: 1     Fields:    Translation:HumansCells
    17. Zhang H, Lu X, Beasley J, Mulvihill JJ, Liu R, Li S, Lee JY. Reversed clinical phenotype due to a microduplication of Sotos syndrome region detected by array CGH: microcephaly, developmental delay and delayed bone age. . 2011 Jun; 155A(6):1374-8. PMID: 21567906.
      Citations:    
    18. Linder CE, Lu X, Kim YM, Li S, Pineda J. "Understanding Adam" multiple reciprocal translocations: complex case presentation. J Perinat Neonatal Nurs. 2009 Apr-Jun; 23(2):150-6; quiz 157-8. PMID: 19474586.
      Citations:    Fields:    Translation:HumansCells
    19. Xu W, Lu X, Kim Y, Luo Y, Martin M, Mulvihill JJ, Li S. Deletion of 14q24.1 approximately q24.3 in a patient with acute lymphoblastic leukemia: a hidden chromosomal anomaly detected by array-based comparative genomic hybridization. Cancer Genet Cytogenet. 2008 Aug; 185(1):43-6. PMID: 18656693.
      Citations: 1     Fields:    Translation:HumansCells
    20. Lee J, Lu X, Shin ES, Kern WF, Mulvihill JJ, Li S. A novel subtelomeric translocation t(5;9) and a deletion of the RB1 gene in a patient with acute myeloid leukemia (AML-M0). Cancer Genet Cytogenet. 2008 Feb; 181(1):36-9. PMID: 18262051.
      Citations: 1     Fields:    Translation:HumansCells
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