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Shibo Li

TitleProf
InstitutionUniversity of Oklahoma Health Sciences Center
DepartmentDept of Pediatrics
Address1122 NE 13th St
Oklahoma City OK 73117-1039
Phone405/271-3589
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    Collapse Bibliographic 
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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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    1. Williams KM, Holter-Chakrabarty J, Lindenberg L, Duong Q, Vesely SK, Nguyen CT, Havlicek JP, Kurdziel K, Gea-Banacloche J, Lin FI, Avila DN, Selby G, Kanakry CG, Li S, Scordino T, Adler S, Bollard CM, Choyke P, Gress RE. Imaging of subclinical haemopoiesis after stem-cell transplantation in patients with haematological malignancies: a prospective pilot study. Lancet Haematol. 2018 Jan; 5(1):e44-e52. PMID: 29248669.
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    2. 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 Feb; 187:137-138. PMID: 29195081.
      View in: PubMed
    3. 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.
      View in: PubMed
    4. Chen Y, Wang X, Lu S, Wang H, Li S, Chen R. An Array-based Comparative Genomic Hybridization Platform for Efficient Detection of Copy Number Variations in Fast Neutron-induced Medicago truncatula Mutants. J Vis Exp. 2017 11 08; (129). PMID: 29155794.
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    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.
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    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 Sep 04; 7(1):10395. PMID: 28871159.
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    7. Liu L, Li Y, Yang Q, Li S, Yin J. Asymmetric Crying Facies with Multiple Congenital Malformations: a Case Report. Chin Med Sci J. 2017 Jun 10; 32(2):129-1. PMID: 28693695.
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    8. Li J, Roy S, Kim YM, Li S, Zhang B, Love C, Reddy A, Rajagopalan D, Dave S, Diehl AM, Zhuang Y. Id2 Collaborates with Id3 To Suppress Invariant NKT and Innate-like Tumors. J Immunol. 2017 04 15; 198(8):3136-3148. PMID: 28258199.
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    9. Hassed S, Li S, Mulvihill J, Aston C, Palmer S. Adams-Oliver syndrome review of the literature: Refining the diagnostic phenotype. Am J Med Genet A. 2017 Mar; 173(3):790-800. PMID: 28160419.
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    10. Hassed SJ, Li S, Xu W, Taylor AC. A Novel Mutation in PITX2 in a Patient with Axenfeld-Rieger Syndrome. Mol Syndromol. 2017 Mar; 8(2):107-109. PMID: 28611552.
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    11. Sun M, Ning J, Xu W, Zhang H, Zhao K, Li W, Li G, Li S. Genetic heterogeneity in patients with Bartter syndrome type 1. Mol Med Rep. 2017 Feb; 15(2):581-590. PMID: 28000888.
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    12. Hu X, Moon JW, Li S, Xu W, Wang X, Liu Y, Lee JY. Amplification and overexpression of CTTN and CCND1 at chromosome 11q13 in Esophagus squamous cell carcinoma (ESCC) of North Eastern Chinese Population. Int J Med Sci. 2016; 13(11):868-874. PMID: 27877079.
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    13. 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.
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    14. Liu K, Kurien BT, Zimmerman SL, Kaufman KM, Taft DH, Kottyan LC, Lazaro S, Weaver CA, Ice JA, Adler AJ, Chodosh J, Radfar L, Rasmussen A, Stone DU, Lewis DM, Li S, Koelsch KA, Igoe A, Talsania M, Kumar J, Maier-Moore JS, Harris VM, Gopalakrishnan R, Jonsson R, Lessard JA, Lu X, Gottenberg JE, Anaya JM, Cunninghame-Graham DS, Huang AJW, Brennan MT, Hughes P, Illei GG, Miceli-Richard C, Keystone EC, Bykerk VP, Hirschfield G, Xie G, Ng WF, Nordmark G, Eriksson P, Omdal R, Rhodus NL, Rischmueller M, Rohrer M, Segal BM, Vyse TJ, Wahren-Herlenius M, Witte T, Pons-Estel B, Alarcon-Riquelme ME, Guthridge JM, James JA, Lessard CJ, Kelly JA, Thompson SD, Gaffney PM, Montgomery CG, Edberg JC, Kimberly RP, Alarcón GS, Langefeld CL, Gilkeson GS, Kamen DL, Tsao BP, McCune WJ, Salmon JE, Merrill JT, Weisman MH, Wallace DJ, Utset TO, Bottinger EP, Amos CI, Siminovitch KA, Mariette X, Sivils KL, Harley JB, Scofield RH. X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome. Arthritis Rheumatol. 2016 05; 68(5):1290-1300. PMID: 26713507; PMCID: PMC5019501 [Available on 05/01/17].
    15. 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, 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; PMCID: PMC4940221 [Available on 07/01/17].
    16. 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; PMCID: PMC4696335.
    17. 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; PMCID: PMC4571549.
    18. Lee E, Moon JW, Wang X, Kim C, Li S, Shin BK, Jung W, Kim HK, Kim HK, Lee JY. Genomic Copy Number Signatures Uncovered a Genetically Distinct Group from Adenocarcinoma and Squamous Cell Carcinoma in Non-Small Cell Lung Cancer. Hum Pathol. 2015 Aug; 46(8):1111-20. PMID: 26003479.
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    19. 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.
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    20. VandenHeuvel KA, Al-Rohil RN, Stevenson ME, Qian J, Gross NL, McNall-Knapp R, Li S, Wartchow EP, Mierau GW, Fung KM. Primary intracranial Ewing's sarcoma with unusual features. Int J Clin Exp Pathol. 2015; 8(1):260-74. PMID: 25755713; PMCID: PMC4348914.
    21. 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; PMCID: PMC4260201.
    22. Khawandanah M, Gehrs B, Li S, Holter Chakrabarty J, Cherry M. A Case of Acute Myeloid Leukemia with a Previously Unreported Translocation (14; 15) (q32; q13). Case Rep Genet. 2014; 2014:921240. PMID: 25436161; PMCID: PMC4243475.
    23. 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; PMCID: PMC4334018.
    24. Magro CM, Abraham RM, Guo R, Li S, Wang X, Proper S, Crowson AN, Mihm M. Deep penetrating nevus-like borderline tumors: A unique subset of ambiguous melanocytic tumors with malignant potential and normal cytogenetics. Eur J Dermatol. 2014 Sep-Oct; 24(5):594-602. PMID: 25118781.
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    25. Zhang R, Kim YM, Wang X, Li Y, Pang H, Lee JY, Li S. Coexistence of t(15;17) and t(15;16;17) detected by fluorescence in situ hybridization in a patient with acute promyelocytic leukemia: A case report and literature review. Oncol Lett. 2014 Sep; 8(3):1001-1008. PMID: 25120648.
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    26. Xu W, Yang X, Hu X, Li S. Fifty-four novel mutations in the NF1 gene and integrated analyses of the mutations that modulate splicing. Int J Mol Med. 2014 Jul; 34(1):53-60. PMID: 24789688; PMCID: PMC4072343.
    27. 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; PMCID: PMC3984075.
    28. Guo R, Wang X, Chen J, Gillies E, Fung KM, Li S, Hassell LA. Comparative genomic hybridization in a case of melanoma that loses expression of S100, HMB45, Melan A and tyrosinase in metastasis. Int J Clin Exp Pathol. 2014; 7(1):468-73. PMID: 24427375; PMCID: PMC3885509.
    29. Tryggestad JB, Li S, Chernausek SD. Hypogonadotropic hypogonadism presenting with arhinia: a case report. J Med Case Rep. 2013 Feb 22; 7:52. PMID: 23432817; PMCID: PMC3599766.
    30. Kim YM, Lee JY, Xia L, Mulvihill JJ, Li S. Trisomy 8: a common finding in mouse embryonic stem (ES) cell lines. Mol Cytogenet. 2013 Jan 16; 6(1):3. PMID: 23320952; PMCID: PMC3564830.
    31. Ren L, Li Z, Li Y, Zheng B, Li S, Chen X, Liu H. The impact of the condenser on cytogenetic image quality in digital microscope system. Anal Cell Pathol (Amst). 2013; 36(1-2):45-59. PMID: 23676284; PMCID: PMC3748598.
    32. Qiu Y, Chen X, Li Y, Chen WR, Zheng B, Li S, Liu H. Evaluations of auto-focusing methods under a microscopic imaging modality for metaphase chromosome image analysis. Anal Cell Pathol (Amst). 2013; 36(1-2):37-44. PMID: 23629477; PMCID: PMC3748595.
    33. Blackett P, Tryggestad J, Krishnan S, Li S, Xu W, Alaupovic P, Quiroga C, Copeland K. Lipoprotein abnormalities in compound heterozygous lipoprotein lipase deficiency after treatment with a low-fat diet and orlistat. J Clin Lipidol. 2013 Mar-Apr; 7(2):132-9. PMID: 23415432.
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    34. 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.
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    35. Winters KA, Jiang Z, Xu W, Li S, Ammous Z, Jayakar P, Wierenga KJ. Re-assigned diagnosis of D4ST1-deficient Ehlers-Danlos syndrome (adducted thumb-clubfoot syndrome) after initial diagnosis of Marden-Walker syndrome. Am J Med Genet A. 2012 Nov; 158A(11):2935-40. PMID: 22987394.
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    36. Qiu Y, Chen X, Li Y, Zheng B, Li S, Chen WR, Liu H. Impact of the optical depth of field on cytogenetic image quality. J Biomed Opt. 2012 Sep; 17(9):96017-1. PMID: 23085918; PMCID: PMC3444261.
    37. Hassed SJ, Wiley GB, Wang S, Lee JY, Li S, Xu W, Zhao ZJ, Mulvihill JJ, Robertson J, Warner J, Gaffney PM. RBPJ mutations identified in two families affected by Adams-Oliver syndrome. Am J Hum Genet. 2012 Aug 10; 91(2):391-5. PMID: 22883147; PMCID: PMC3415535.
    38. Chen Y, Guo Y, Han J, Ho WT, Li S, Fu X, Zhao ZJ. Generation and characterization of a highly effective protein substrate for analysis of FLT3 activity. J Hematol Oncol. 2012 Jul 16; 5:39. PMID: 22800464; PMCID: PMC3419602.
    39. Fung KM, Chakrabarty JH, Kern WF, Magharyous H, Gehrs BC, Li S. Intravascular large B-cell lymphoma with hemophagocytic syndrome (Asian variant) in a Caucasian patient. Int J Clin Exp Pathol. 2012; 5(5):448-54. PMID: 22808298; PMCID: PMC3396055.
    40. Dillon SP, Kurien BT, Li S, Bruner GR, Kaufman KM, Harley JB, Gaffney PM, Wallace DJ, Weisman MH, Scofield RH. Sex chromosome aneuploidies among men with systemic lupus erythematosus. J Autoimmun. 2012 May; 38(2-3):J129-34. PMID: 22154021; PMCID: PMC3309073.
    41. Zhang R, Kim YM, Yang X, Li Y, Li S, Lee JY. A possible 5'-NRIP1/UHRF1-3' fusion gene detected by array CGH analysis in a Ph+ ALL patient. Cancer Genet. 2011 Dec; 204(12):687-91. PMID: 22285022.
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    42. Yu Z, Bane BL, Lee JY, Pitha JV, Peyton M, Houck J, Li S. Cytogenetic and comparative genomic hybridization studies of an esophageal giant fibrovascular polyp: a case report. Hum Pathol. 2012 Feb; 43(2):293-8. PMID: 21835434.
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    43. Kim YM, Ma Z, Lee S, Lee J, Li S, Yang X. Trisomy chromosome 5 is a recurrent cytogenetic lesion in mammary tumors from parous MMTV-erbB-2 transgenic mice. Oncol Lett. 2011 Nov; 2(6):1077-1081. PMID: 22848270.
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    44. 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.
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    45. 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. Am J Med Genet A. 2011 Jun; 155A(6):1374-8. PMID: 21567906.
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    46. Dillon S, Aggarwal R, Harding JW, Li LJ, Weissman MH, Li S, Cavett JW, Sevier ST, Ojwang JW, D'Souza A, Harley JB, Scofield RH. Klinefelter's syndrome (47,XXY) among men with systemic lupus erythematosus. Acta Paediatr. 2011 Jun; 100(6):819-23. PMID: 21375582.
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    47. Zhao W, Gao R, Lee J, Xing S, Ho WT, Fu X, Li S, Zhao ZJ. Relevance of JAK2V617F positivity to hematological diseases--survey of samples from a clinical genetics laboratory. J Hematol Oncol. 2011 Jan 14; 4:4. PMID: 21235771; PMCID: PMC3032761.
    48. Hu L, Potapova TA, Li S, Rankin S, Gorbsky GJ, Angeletti PC, Ceresa BP. Expression of HPV16 E5 produces enlarged nuclei and polyploidy through endoreplication. Virology. 2010 Sep 30; 405(2):342-51. PMID: 20605566; PMCID: PMC2923234.
    49. Aggarwal R, Namjou B, Li S, D'Souza A, Tsao BP, Bruner BF, James JA, Scofield RH. Male-only systemic lupus. J Rheumatol. 2010 Jul; 37(7):1480-7. PMID: 20472921; PMCID: PMC2978923.
    50. Lee J, Wang J, Torbenson M, Lu Y, Liu QZ, Li S. Loss of SDHB and NF1 genes in a malignant phyllodes tumor of the breast as detected by oligo-array comparative genomic hybridization. Cancer Genet Cytogenet. 2010 Jan 15; 196(2):179-83. PMID: 20082856.
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    51. Wilson PL, Kattman BB, Mulvihill JJ, Li S, Wilkins J, Wagner AF, Goodman JR. Prenatal identification of a novel R937P L1CAM missense mutation. Genet Test Mol Biomarkers. 2009 Aug; 13(4):515-9. PMID: 19594370.
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    52. 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.
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    53. Wang X, Zheng B, Li S, Zhang R, Mulvihill JJ, Chen WR, Liu H. Automated detection and analysis of fluorescent in situ hybridization spots depicted in digital microscopic images of Pap-smear specimens. J Biomed Opt. 2009 Mar-Apr; 14(2):021002. PMID: 19405715.
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    54. Kim YM, Yang S, Xu W, Li S, Yang X. Continuous in vitro exposure to low-dose genistein induces genomic instability in breast epithelial cells. Cancer Genet Cytogenet. 2008 Oct 15; 186(2):78-84. PMID: 18940470; PMCID: PMC2590788.
    55. Wang X, Zheng B, Li S, Mulvihill JJ, Liu H. Development and Assessment of an Integrated Computer-Aided Detection Scheme for Digital Microscopic Images of Metaphase Chromosomes. J Electron Imaging. 2008 Oct 01; 17(4). PMID: 23087585.
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    56. Scofield RH, Bruner GR, Namjou B, Kimberly RP, Ramsey-Goldman R, Petri M, Reveille JD, Alarcón GS, Vilá LM, Reid J, Harris B, Li S, Kelly JA, Harley JB. Klinefelter's syndrome (47,XXY) in male systemic lupus erythematosus patients: support for the notion of a gene-dose effect from the X chromosome. Arthritis Rheum. 2008 Aug; 58(8):2511-7. PMID: 18668569; PMCID: PMC2824898.
    57. 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.
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    58. Wang X, Zheng B, Li S, Mulvihill JJ, Wood MC, Liu H. Automated classification of metaphase chromosomes: optimization of an adaptive computerized scheme. J Biomed Inform. 2009 Feb; 42(1):22-31. PMID: 18585097; PMCID: PMC2673199.
    59. Purandare SM, Mendoza-Londono R, Yatsenko SA, Napierala D, Scott DA, Sibai T, Casas K, Wilson P, Lee J, Muneer R, Leonard JC, Ramji FG, Lachman R, Li S, Stankiewicz P, Lee B, Mulvihill JJ. De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia. Am J Med Genet A. 2008 Feb 15; 146A(4):453-8. PMID: 18203189; PMCID: PMC2663417.
    60. 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.
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    61. Wang X, Zheng B, Li S, Mulvihill JJ, Liu H. A rule-based computer scheme for centromere identification and polarity assignment of metaphase chromosomes. Comput Methods Programs Biomed. 2008 Jan; 89(1):33-42. PMID: 18082909.
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    62. Wang X, Li S, Liu H, Wood M, Chen WR, Zheng B. Automated identification of analyzable metaphase chromosomes depicted on microscopic digital images. J Biomed Inform. 2008 Apr; 41(2):264-71. PMID: 17681496; PMCID: PMC2440955.
    63. Zhang L, Kern WF, Yu Z, Mulvihill JJ, Li S. Cryptic and complex chromosomal rearrangements and the deletion of TP53 gene in a patient with leukemic mantle cell lymphoma. Cancer Genet Cytogenet. 2006 Sep; 169(2):169-73. PMID: 16938577.
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    64. Angelidis P, Kojouri K, Lee J, Kern W, Mulvihill JJ, Li S. Trisomy 1q in a patient with severe aplastic anemia. Cancer Genet Cytogenet. 2006 Aug; 169(1):73-5. PMID: 16875941.
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    65. Wang X, Li S, Liu H, Mulvihill JJ, Chen W, Zheng B. A computer-aided method to expedite the evaluation of prognosis for childhood acute lymphoblastic leukemia. Technol Cancer Res Treat. 2006 Aug; 5(4):429-36. PMID: 16866573.
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    66. Purandare SM, Lee J, Hassed S, Steele MI, Blackett PR, Mulvihill JJ, Li S. Ring chromosome 9 [r(9)(p24q34)]: a report of two cases. Am J Med Genet A. 2005 Oct 15; 138A(3):229-35. PMID: 16158426.
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    67. Blackett PR, Li S, Mulvihill JJ. Ring chromosome 4 in a patient with early onset type 2 diabetes, deafness, and developmental delay. Am J Med Genet A. 2005 Aug 30; 137(2):213-6. PMID: 16082703.
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    68. Lee J, Hopcus-Niccum DJ, Mulvihill JJ, Li S. Cytogenetic and molecular cytogenetic studies of a variant of t(21;22), ins(22;21)(q12;q21q22), with a deletion of the 3' EWSR1 gene in a patient with Ewing sarcoma. Cancer Genet Cytogenet. 2005 Jun; 159(2):177-80. PMID: 15899394.
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    69. Lee J, Kern WF, Cain JB, Mulvihill JJ, Li S. A variant t(8;10;21) in a patient with pathological features mimicking atypical chronic myeloid leukemia. Cancer Genet Cytogenet. 2005 May; 159(1):79-83. PMID: 15860363.
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    70. Lee J, Stanley JR, Vaz SA, Mulvihill JJ, Wilson P, Hopcus-Niccum D, Li S. Down syndrome with pure partial trisomy 21q22 due to a paternal insertion (4;21) uncovered by uncultured amniotic fluid interphase FISH. Am J Med Genet A. 2005 Jan 15; 132A(2):206-8. PMID: 15578618.
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    71. Lee J, Li S, Torbenson M, Liu QZ, Lind S, Mulvihill JJ, Bane B, Wang J. Leiomyosarcoma of the breast: a pathologic and comparative genomic hybridization study of two cases. Cancer Genet Cytogenet. 2004 Feb; 149(1):53-7. PMID: 15104283.
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    72. Zhang L, Parkhurst JB, Kern WF, Scott KV, Niccum D, Mulvihill JJ, Li S. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia. Chin Med J (Engl). 2003 Sep; 116(9):1298-303. PMID: 14527352.
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    73. Wang J, Blakey GL, Zhang L, Bane B, Torbenson M, Li S. Uterine tumor resembling ovarian sex cord tumor: report of a case with t(X;6)(p22.3;q23.1) and t(4;18)(q21.1;q21.3). Diagn Mol Pathol. 2003 Sep; 12(3):174-80. PMID: 12960700.
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    74. Li S, Zhang L, Kern WF, Andrade D, Forsberg JE, Bates FR, Mulvihill JJ. Identification of t(15;17) and a segmental duplication of chromosome 11q23 in a patient with acute myeloblastic leukemia M2. Cancer Genet Cytogenet. 2002 Oct 15; 138(2):149-52. PMID: 12505261.
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    75. Zhang L, Mulvihill JJ, Kern WF, McMinn J, Li S. Duplication 15q as the sole anomaly in an acute promyelocytic leukemia patient without t(15;17). Cancer Genet Cytogenet. 2002 Oct 01; 138(1):17-21. PMID: 12419579.
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    76. Li S, Stanley JR, Draper ML, Mirabile CP, Coleman FH, Mulvihill JJ. Rapid prenatal diagnosis of trisomies 13, 18, 21 and sex chromosome anomalies by fluorescence in situ hybridization: a year's experience. J Okla State Med Assoc. 2002 Apr; 95(4):244-6. PMID: 11957840.
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    77. Zhang L, Mulvihill JJ, Kinasewitz GT, Scott KV, Bates F, Li S. Duplication 15q in a patient with t(8;21) acute myeloblastic leukemia (M2). Cancer Genet Cytogenet. 2002 Mar; 133(2):148-51. PMID: 11943342.
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