Yao-Shan Fan, M.D., Ph.D.

  1. Chapman JR, Alvarez JP, White K, Sanchez S, Khanlari M, Algashaamy K, Cassidy D, Peng JH, Fan YS, Alencar A, Alderuccio JP, Lossos IS, Vega F. Unusual Variants of Follicular Lymphoma: Case-based Review. Am J Surg Pathol. 2020 Mar; 44 (3):329-339
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  2. Cassidy DP, Chapman JR, Lopez R, White K, Fan YS, Casas C, Severson EA, Vega F. Comparison Between Integrated Genomic DNA/RNA Profiling and Fluorescence In Situ Hybridization in the Detection of MYC, BCL-2, and BCL-6 Gene Rearrangements in Large B-Cell Lymphomas. Am J Clin Pathol. 2020 Feb 8; 153 (3):353-359
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  3. Nimer SD, Chapman J, Reidy L, Alencar A, Wu Y, Williams S, Pagan L, Gjolaj L, MacIntyre J, Triana M, Vance B, Andrews D, Fan YS, Zhou Y, Martinez O, Garcia-Buitrago M, Cray C, Tekin M, McCauley JL, Ruiz P, Pagan P, Lamar W, Alencar M, Bilbao D, Prieto S, Polania M, Suarez M, Lujardo M, Campos G, Morris M, Shukla B, Caban-Martinez A, Kobetz E, Parekh DJ, Jorda M. A How-to Guide to Building a Robust SARS-CoV-2 Testing Program at a University-Based Health System. Acad Pathol. 2020 Jan-Dec; 7:2374289520958200 Epub 2020 Sept 30
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  4. Riggs ER, Nelson T, Merz A, Ackley T, Bunke B, Collins CD, Collinson MN, Fan YS, Goodenberger ML, Golden DM, Haglund-Hazy L, Krgovic D, Lamb AN, Lewis Z, Li G, Liu Y, Meck J, Neufeld-Kaiser W, Runke CK, Sanmann JN, Stavropoulos DJ, Strong E, Su M, Tayeh MK, Kokalj Vokac N, Thorland EC, Andersen E, Martin CL. Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar. Hum Mutat. 2018 Nov; 39(11):1650-1659.
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  5. Su M, Benke PJ, Bademci G, Cengiz FB, Ouyang X, Peng J, Casas CE, Tekin M, Fan YS. Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomalies. Mol Cytogenet. 2018; 11:43 Epub 2018 Aug 01
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  6. Watts JM, Perez A, Pereira L, Fan YS, Brown G, Vega F, Petrie K, Swords RT, Zelent A. A Case of AML Characterized by a Novel t(4;15)(q31;q22) Translocation That Confers a Growth-Stimulatory Response to Retinoid-Based Therapy. Int J Mol Sci. 2017 Jul 11; 18 (7) Epub 2017 July 11
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  7. Yan D, Xiang G, Chai X, Qing J, Shang H, Zou B, Mittal R, Shen J, Smith RJ, Fan YS, Blanton SH, Tekin M, Morton C, Xing W, Cheng J, Liu XZ. Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach. PLoS One. 2017; 12 (3):e0169219 Epub 2017 Mar 08
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  8. Campuzano-Zuluaga G, Ortiz D, Peng JH, Francis Ikpatt O, Fan YS, Barredo JC, Vega F, Chapman JR. Primary Mediastinal Large B-Cell Lymphoma With Translocations Involving BCL6 and MYC (Double-Hit Lymphoma). Am J Clin Pathol. 2016 May; 145 (5):710-6 Epub 2016 Mar 27
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  9. Fan YS, Casas CE, Peng J, Watkins M, Fan L, Chapman J, Ikpatt OF, Gomez C, Zhao W, Reis IM. HER2 FISH classification of equivocal HER2 IHC breast cancers with use of the 2013 ASCO/CAP practice guideline. Breast Cancer Res Treat. 2016 Feb; 155 (3):457-62 Epub 2016 Feb 19
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  10. Ikpatt OF, Reavill D, Chatfield J, Clubb S, Rosenblatt JD, Fonte G, Fan YS, Cray C. Diagnosis and treatment of diffuse large B-cell lymphoma in an orangutan (Pongo pygmaeus). J Zoo Wildl Med. 2014 Dec; 45 (4):935-40
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  11. Blieden C, Fan YS, Chapman JR, Vega F. De novo acute myeloid leukemia with monocytoid blasts and erythrophagocytosis. Clin Case Rep. 2014 Dec; 2 (6):333-5 Epub 2014 Sept 15
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  12. Ribeiro A, Peng J, Casas C, Fan YS. Endoscopic ultrasound guided fine needle aspiration with fluorescence in situ hybridization analysis in 104 patients with pancreatic mass. J Gastroenterol Hepatol. 2014 Aug; 29 (8):1654-8
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  13. A Ribeiro, J Peng, C Casas, YS Fan. EUS FNA with FISH analysis in 104 patients with pancreatic mass. Gastroenterol Hepatol. 2014; 29:1654-1658.
  14. Li D, Bodamer OA, Fan YS. A 420 Kb Deletion within the Minimum Critical Region of the 15q24 Microdeletion Syndrome in a Female Infant. N Am J Med Sci. 2014; 7:171-175.
  15. Pinto A, Nose V, Rojas C, Fan YS, Gomez-Fernandez C. Searching for mammary analogue [corrected] secretory carcinoma of salivary gland among its mimics. Mod Pathol. 2014 Jan; 27 (1):30-7 Epub 2013 June 28
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  16. Fan YS, Ouyang X, Peng J, Sacharow S, Tekin M, Barbouth D, Bodamer O, Yusupov R, Navarrete C, Heller AH, Pena SDj. Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarray. Mol Cytogenet. 2013 Sep 20; 6 (1):38 Epub 2013 Sept 20
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  17. Zhu D, Ikpatt OF, Dubovy SR, Lossos C, Natkunam Y, Chapman-Fredricks JR, Fan YS, Lossos IS. Molecular and genomic aberrations in Chlamydophila psittaci negative ocular adnexal marginal zone lymphomas. Am J Hematol. 2013 Sep; 88 (9):730-5 Epub 2013 July 23
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  18. Ozcakar ZB, Foster J 2nd, Diaz-Horta O, Kasapcopur O, Fan YS, Yalcinkaya F, Tekin M. DNASE1L3 mutations in hypocomplementemic urticarial vasculitis syndrome. Arthritis Rheum. 2013 Aug; 65 (8):2183-9
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  19. Fan YS. Companion diagnostic testing for targeted cancer therapies: an overview. Genet Test Mol Biomarkers. 2013 Jul; 17 (7):515-23 Epub 2013 Apr 10
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  20. Chapman-Fredricks J, Younes SF, Fan YS, Sandoval-Sus JD, Natkunam Y, Lossos IS. Usefulness of HGAL and LMO2 immunohistochemistry in the identification of follicular lymphomas of the non-gastric gastrointestinal tract. Appl Immunohistochem Mol Morphol. 2013 May; 21 (3):200-4
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  21. Strehle EM, Yu L, Rosenfeld JA, Donkervoort S, Zhou Y, Chen TJ, Martinez JE, Fan YS, Barbouth D, Zhu H, Vaglio A, Smith R, Stevens CA, Curry CJ, Ladda RL, Fan ZJ, Fox JE, Martin JA, Abdel-Hamid HZ, McCracken EA, McGillivray BC, Masser-Frye D, Huang T. Genotype-phenotype analysis of 4q deletion syndrome: proposal of a critical region. Am J Med Genet A. 2012 Sep; 158A (9):2139-51 Epub 2012 July 27
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  22. Li D, Tekin M, Buch M, Fan YS. Co-existence of other copy number variations with 22q11.2 deletion or duplication: a modifier for variable phenotypes of the syndrome? Mol Cytogenet. 2012 Apr 9; 5 (1):18 Epub 2012 Apr 09
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  23. Sacharow S, Li D, Fan YS, Tekin M. Familial 16q24.3 microdeletion involving ANKRD11 causes a KBG-like syndrome. Am J Med Genet A. 2012 Mar; 158A (3):547-52 Epub 2012 Feb 03
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  24. Kubiliun N, Ribeiro A, Fan YS, Rocha-Lima CM, Sleeman D, Merchan J, Barkin J, Levi J. EUS-FNA with rescue fluorescence in situ hybridization for the diagnosis of pancreatic carcinoma in patients with inconclusive on-site cytopathology results. Gastrointest Endosc. 2011 Sep; 74 (3):541-7 Epub 2011 July 12
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  25. Liewluck T, Sacharow SJ, Fan Y, Lopez-Alberola R. A novel sporadic 614-Kb duplication of the 22q11.2 chromosome in a child with amyoplasia. J Child Neurol. 2011 Aug; 26 (8):1005-8 Epub 2011 May 13
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  26. Xiang B, Zhu H, Shen Y, Miller DT, Lu K, Hu X, Andersson HC, Narumanchi TM, Wang Y, Martinez JE, Wu BL, Li P, Li MM, Chen TJ, Fan YS. Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical cases. J Mol Diagn. 2010 Mar; 12 (2):204-12 Epub 2010 Jan 21
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  27. Vincek V, Xu S, Fan YS. Comparative genome hybridization analysis of laser-capture microdissected in situ melanoma. J Cutan Pathol. 2010 Jan; 37 (1):3-7 Epub 2009 June 11
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  28. Xu J, Fan YS, Siu VM. A child with features of Goldenhar syndrome and a novel 1.12 Mb deletion in 22q11.2 by cytogenetics and oligonucleotide array CGH: is this a candidate region for the syndrome? Am J Med Genet A. 2008 Jul 15; 146A (14):1886-9
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  29. Zhang ZF, Ruivenkamp C, Staaf J, Zhu H, Barbaro M, Petillo D, Khoo SK, Borg A, Fan YS, Schoumans J. Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platforms. Eur J Hum Genet. 2008 Jul; 16 (7):786-92 Epub 2008 Feb 20
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  30. Xu S, Han JC, Morales A, Menzie CM, Williams K, Fan YS. Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism. Cytogenet Genome Res. 2008; 122 (2):181-7 Epub 2008 Dec 18
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  31. Fan YS, Jayakar P, Zhu H, Barbouth D, Sacharow S, Morales A, Carver V, Benke P, Mundy P, Elsas LJ. Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization. Hum Mutat. 2007 Nov; 28 (11):1124-32
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  32. Quadrelli A, Vaglio A, Quadrelli R, Mechoso B, Fan YS, Huang T. High-density array comparative genomic hybridization analysis and follow-up of a child with a de novo complex chromosome rearrangement detected prenatally. Prenat Diagn. 2007 Oct; 27 (10):982-3
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  33. Quadrelli R, Strehle EM, Vaglio A, Larrandaburu M, Mechoso B, Quadrelli A, Fan YS, Huang T. A girl with del(4)(q33) and occipital encephalocele: clinical description and molecular genetic characterization of a rare patient. Genet Test. 2007 Spring; 11 (1):4-10
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  34. Yu S, Barbouth D, Benke PJ, Warburton PE, Fan YS. Characterization of a neocentric supernumerary marker chromosome originating from the Xp distal region by FISH, CENP-C staining, and array CGH. Cytogenet Genome Res. 2007; 116 (1-2):141-5
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  35. Uddin RK, Zhang Y, Siu VM, Fan YS, O'Reilly RL, Rao J, Singh SM. 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 Med Genet. 2006 Mar 2; 7:18 Epub 2006 Mar 02
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  36. Fan YS, Rizkalla K. Comprehensive cytogenetic analysis including multicolor spectral karyotyping and interphase fluorescence in situ hybridization in lymphoma diagnosis. a summary of 154 cases. Cancer Genet Cytogenet. 2003 May; 143 (1):73-9
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  37. Takhar J, Malla AK, Siu V, MacPherson C, Fan YS, Townsend L. An interstitial deletion of the long arm of chromosome 21 in a case of a first episode of psychosis. Acta Psychiatr Scand. 2002 Jul; 106 (1):71-4; discussion 74-5
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  38. Fan YS, Zhang Y, Speevak M, Farrell S, Jung JH, Siu VM. Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probes. Genet Med. 2001 Nov-Dec; 3 (6):416-21
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  39. Fan YS, Siu VM, Jung JH, Farrell SA, Cote GB. Direct duplication of 8p21.3-->p23.1: a cytogenetic anomaly associated with developmental delay without consistent clinical features. Am J Med Genet. 2001 Oct 15; 103 (3):231-4
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  40. Li S, Fan YS, Chow LH, Van Den Diepstraten C, van Der Veer E, Sims SM, Pickering JG. Innate diversity of adult human arterial smooth muscle cells: cloning of distinct subtypes from the internal thoracic artery. Circ Res. 2001 Sep 14; 89 (6):517-25
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  41. Fan YS, Siu VM. Molecular cytogenetic characterization of a derivative chromosome 8 with an inverted duplication of 8p21.3-->p23.3 and a rearranged duplication of 8q24.13-->qter. Am J Med Genet. 2001 Aug 15; 102 (3):266-71
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  42. Steele MM, Al-Adeimi M, Siu VM, Fan YS. Brief report: A case of autism with interstitial deletion of chromosome 13. J Autism Dev Disord. 2001 Apr; 31 (2):231-4
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  43. Fan, YS. CCMG Guidelines: Chromosome analysis of clinical specimens. CCMG Newsletter. 2001.
  44. Drs Dallaire, Fan YS. CCMG Guidelines: Retention of cytogenetic records. CCMG Newsletter. 2001.
  45. Fan YS, Rizkalla K, William BF, Engel CJ. Jumping translocations of 11q in acute myeloid leukemia and 1q in follicular lymphoma. Cancer Genet Cytogenet. 2000 Apr 1; 118 (1):35-41
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  46. Fan YS, Siu VM, Jung JH, Xu J. Sensitivity of multiple color spectral karyotyping in detecting small interchromosomal rearrangements. Genet Test. 2000; 4 (1):9-14
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  47. Fan YS, Rizkalla K, Barr RM. A new complex variant Philadelphia chromosome, t(1;9;22)ins(17;22), characterized by fluorescence in situ hybridization in an adult ALL. Leuk Res. 1999 Nov; 23 (11):1001-6
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  48. Fan YS, Rizkalla K, Engel J. Interstitial deletion of 8(q13q22) in diffuse large B-cell gastric lymphoma. Cancer Genet Cytogenet. 1999 Nov; 115 (1):28-31
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  49. Fan YS, Jung J, Hamilton B. Small terminal deletion of 1p and duplication of 1q: cytogenetics, FISH studies, and clinical observations at newborn and at age 16 years. Am J Med Genet. 1999 Sep 10; 86 (2):118-23
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  50. Winsor EJ, Tomkins DJ, Kalousek D, Farrell S, Wyatt P, Fan YS, Carter R, Wang H, Dallaire L, Eydoux P, Welch JP, Dawson A, Lin JC, Singer J, Johnson J, Wilson RD. Cytogenetic aspects of the Canadian early and mid-trimester amniotic fluid trial (CEMAT). Prenat Diagn. 1999 Jul; 19 (7):620-7
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  51. Randomised trial to assess safety and fetal outcome of early and midtrimester amniocentesis. The Canadian Early and Mid-trimester Amniocentesis Trial (CEMAT) Group. Lancet. 1998 Jan 24; 351 (9098):242-7
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  52. Cote G, Dallaire L, Fan YS, Horsman D, Kalousek P, Tomkins D, Roland B. CCMG Guidelines; Clinical Indications for Cytogenetic Investigation CCMG Newsletter. 1997; 3:2-3.
  53. Cote G, Dallaire L, Fan YS, Horsman D, Kalousek P, Tomkins D, Roland B. CCMG Position Statement on the Clinical Application of Fluorescence In Situ Hybridization CCMG Newsletter. 1997; 3:4-5.
  54. Cote G, Dallaire L, Fan YS, Horsman D, Kalousek P, Tomkins D, Roland B. CCMG Guidelines: Chromosome Analysis Clinical Specimens CCMG Newsletter. 1997; 3:6-9.
  55. Sung LA, Fan Y, Lin CC. Gene assignment, expression, and homology of human tropomodulin. Genomics. 1996 May 15; 34 (1):92-6
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  56. Li YS, Fan YS, Armstrong RF. Endoreduplication and telomeric association in a choroid plexus carcinoma. Cancer Genet Cytogenet. 1996 Mar; 87 (1):7-10
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  57. Li YS, Ramsay DA, Fan YS, Armstrong RF, Del Maestro RF. Cytogenetic evidence that a tumor suppressor gene in the long arm of chromosome 1 contributes to glioma growth. Cancer Genet Cytogenet. 1995 Oct 1; 84 (1):46-50
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  58. Farrell SA, Fan YS. Balanced nonacrocentric whole-arm reciprocal translocations: a de novo case and literature review. Am J Med Genet. 1995 Feb 13; 55 (4):423-6
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  59. Farrell SA, Sue-Chue-Lam A, Miskin M, Fan YS. Fetal nuchal oedema and antenatal diagnosis of trisomy 10. Prenat Diagn. 1994 Jun; 14 (6):463-7
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  60. Fowler ML, Fan YS, Mueller OT, Henry WM, Shows TB. Correction of mucolipidosis III in vitro by gene transfer. Genomics. 1993 Nov; 18 (2):236-43
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  61. Lin CC, Sasi R, Lee C, Fan YS, Court D. Isolation and identification of a novel tandemly repeated DNA sequence in the centromeric region of human chromosome 8. Chromosoma. 1993 May; 102 (5):333-9
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  62. Fan YS, Sasi R, Lee C, Winter JS, Waterman MR, Lin CC. Localization of the human CYP17 gene (cytochrome P450(17 alpha)) to 10q24.3 by fluorescence in situ hybridization and simultaneous chromosome banding. Genomics. 1992 Dec; 14 (4):1110-1
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  63. Fan YS, Sasi R, Lee C, Court D, Lin CC. Mapping of 50 cosmid clones isolated from a flow-sorted human X chromosome library by fluorescence in situ hybridization. Genomics. 1992 Oct; 14 (2):542-5
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  64. Sung LA, Chien S, Fan YS, Lin CC, Lambert K, Zhu L, Lam JS, Chang LS. Human erythrocyte protein 4.2: isoform expression, differential splicing, and chromosomal assignment. Blood. 1992 May 15; 79 (10):2763-70
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  65. Mitchell A, Bale AE, Lee BJ, Hatfield D, Harley H, Rundle SA, Fan YS, Fukushima Y, Shows TB, McBride OW. Regional localization of the selenocysteine tRNA gene (TRSP) on human chromosome 19. Cytogenet Cell Genet. 1992; 61 (2):117-20
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  66. Fan YS, Li P, Qi SY. Sister chromatid exchanges, chromosomal aberrations and satellite associations in women taking oral contraceptive methylnorethindroni compostas for long term Reproduction & Contraception. 1982; 2(3):45-48.
  67. Fan YS, Yang HM, Lin CC. Assignment of the human muscle adenine nucleotide translocator gene (ANT1) to 4q35 by fluorescence in situ hybridization. Cytogenet Cell Genet. 1992; 60 (1):29-30
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  68. Lin CC, Sasi R, Fan YS, Chen ZQ. New evidence for tandem chromosome fusions in the karyotypic evolution of Asian muntjacs. Chromosoma. 1991 Oct; 101 (1):19-24
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  69. Sasi R, Fan YS, Lin CC. Prenatal sexing and detection of ZFY gene sequences in sex chromosome disorders by polymerase chain reaction. J Clin Lab Anal. 1991; 5 (3):193-6
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  70. Kayano T, Burant CF, Fukumoto H, Gould GW, Fan YS, Eddy RL, Byers MG, Shows TB, Seino S, Bell GI. Human facilitative glucose transporters. Isolation, functional characterization, and gene localization of cDNAs encoding an isoform (GLUT5) expressed in small intestine, kidney, muscle, and adipose tissue and an unusual glucose transporter pseudogene-like sequence (GLUT6). J Biol Chem. 1990 Aug 5; 265 (22):13276-82
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  71. Fan YS, Davis LM, Shows TB. Mapping small DNA sequences by fluorescence in situ hybridization directly on banded metaphase chromosomes. Proc Natl Acad Sci U S A. 1990 Aug; 87 (16):6223-7
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  72. Huhtala P, Eddy RL, Fan YS, Byers MG, Shows TB, Tryggvason K. Completion of the primary structure of the human type IV collagenase preproenzyme and assignment of the gene (CLG4) to the q21 region of chromosome 16. Genomics. 1990 Mar; 6 (3):554-9
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  73. Nishi M, Sanke T, Seino S, Eddy RL, Fan YS, Byers MG, Shows TB, Bell GI, Steiner DF. Human islet amyloid polypeptide gene: complete nucleotide sequence, chromosomal localization, and evolutionary history. Mol Endocrinol. 1989 Nov; 3 (11):1775-81
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  74. Bell GI, Murray JC, Nakamura Y, Kayano T, Eddy RL, Fan YS, Byers MG, Shows TB. Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13. Diabetes. 1989 Aug; 38 (8):1072-5
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  75. Yano H, Seino Y, Fujita J, Yamada Y, Inagaki N, Takeda J, Bell GI, Eddy RL, Fan YS, Byers MG. Exon-intron organization, expression, and chromosomal localization of the human motilin gene. FEBS Lett. 1989 Jun 5; 249 (2):248-52
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  76. Fan YS, Eddy RL, Byers MG, Haley LL, Henry WM, Nowak NJ, Shows TB. The human mineralocorticoid receptor gene (MLR) is located on chromosome 4 at q31.2. Cytogenet Cell Genet. 1989; 52 (1-2):83-4
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  77. Kayano T, Fukumoto H, Eddy RL, Fan YS, Byers MG, Shows TB, Bell GI. Evidence for a family of human glucose transporter-like proteins. Sequence and gene localization of a protein expressed in fetal skeletal muscle and other tissues. J Biol Chem. 1988 Oct 25; 263 (30):15245-8
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  78. Fan YS, Rowe JM, Dal Cin PD, Sandberg AA. A translocation t(9;11)(p11;q23) in T-cell acute lymphoblastic leukemia (FAB-l2). Cancer Genet Cytogenet. 1988 Apr; 31 (2):263-9
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  79. Wang TY, Raza A, Fan YS, Sait SN, Kirschner J, Sandberg AA. Complex cytogenetic changes in Ph-negative chronic myelogenous leukemia. Cancer Genet Cytogenet. 1988 Apr; 31 (2):241-5
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  80. Bristol A, Hall SM, Kriz RW, Stahl ML, Fan YS, Byers MG, Eddy RL, Shows TB, Knopf JL. Phospholipase C-148: chromosomal location and deletion mapping of functional domains. Cold Spring Harb Symp Quant Biol. 1988; 53 Pt 2:915-20
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  81. Fan YS, Baer MR, Sait SN, Dal Cin P, Prentice TC, Preisler HD, Sandberg AA. An acquired Robertsonian translocation dic(14;14)(p11;p11) in a patient with a myelodysplastic syndrome following treatment of multiple myeloma. Cancer Genet Cytogenet. 1988 Jan; 30 (1):133-7
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  82. Fan YS, Raza A, Schumer J, Sait SN, Block AW, Snyderman M, Sandberg AA. Translocation t(6;9)(p22.3;q34) in myelodysplastic syndrome--refractory anemia with excess blasts. Cancer Genet Cytogenet. 1987 Nov; 29 (1):135-8
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  83. Fan YS, Li P. Cytogenetic studies of four human lung adenocarcinoma cell lines. Cancer Genet Cytogenet. 1987 Jun; 26 (2):317-25
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  84. Fan YS, Li P, Wang XY, Xing CH, Wang YL. Chromosomal analysis of a human lung adenocarcinoma cell line, AGZY83-A. Chin Med J (Engl). 1987 Mar; 100 (3):198-203
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  85. Fan YS, Li P, Suen YN, Wang H, Yao DP, Lai BT. A high resolution study of chromosomes in a human lung adenocarcinoma cell line LTEP-a1 Acta Genetica Sinica. 1986; 13:227-231.
  86. Chen LN, Li P, Fan YS, Wang ZZ, Li HS. The chromosomal aberration in the patients with hyperthyroidism before and after the treatment with 131-I J Harbin Med University. 1985; 19(4):8-10.
  87. Fan YS, Li P, Suen YN, Wang YL, Wang XY, Xing CH, Xing ZH, Li JD. The preliminary report of cytogenetic studies on human lung adenocarcinoma cell line AGZY83-a J Harbin Med University. 1985; 19(1):4-6.
  88. Chen LN, Li P, Fan YS, Suen YN, Wang ZZ. Cytogenetic study on 46,XX true hermaphroditism J Harbin Med University. 1984; 18(1):13-15.
  89. Fan YS, Li P, Chen LN, Suen GZ. Sister chromatid exchanges induced by thiotepa in xeroderma pigmentosum lymphocytes Natl Med J China. 1984; 64(7):346-347.
  90. Chen LN, Fan YS, Li P, Huang TH, Suen EZ. Study of sister chromatid exchanges in peripheral lymphocytes from patients with acute lymphocytic leukemia Chinese J Hematol. 1983; 4(4):221-222.
  91. Fan YS. Down Syndrome and associations of acrocentric chromosomes J Harbin Med University. 1983; 17(4):89-92.
  92. Fan YS, Chen LN, Li P, Wu CY, Lou HM. Studies of silver-stained nucleolar organizer regions in twins Hereditas. 1983; 5(5):31-33.
  93. Huang TH, Fan YS, Qi SY, Li P. Studies of silver-stained nucleolar organizer regions in women taking oral contraceptive tablet norethindrone compositae over a long period Reproduction & Contraception. 1983; 3(1):48-52.
  94. Huang TH, Fan YS, Miao YS, Li QC, Li P. The effect of gossypol acetate on the function of RNA gene and acrocentric chromosome association in human cells Natl Med J China. 1983; 63:97-100.
  95. Chen LN, Fan YS, Li P, Huang TH, Miao YS, Li CC. Effect of long-term taking gossypol acetate on SCE frequency in man Hereditas. 1983; 5(3):35-36.
  96. Qi SY, Fan YS, Guo JD, Li P. Sister chromatid exchanges in women taking oral contraceptive tablet norethindrone compostas for a long term Reproduction & Contraception. 1982; 2(4):42-43.
  97. Fan YS. Chromosomal studies of retinoblastoma J Harbin Med University. 1981; 15:5-11.
  98. Fan YS. High resolution chromosome analysis and its use in clinical medicine Medicine in Foreign Countries, Med Genet. 1981; 4(3):114-122.
  99. Hu WM, Yie YY, SD Liu, Zhao BW, Zhang GY, Fan YS. A new subtype of hereditary sensory neuropathy J Harbin Med University. 1981; 15:57-61.
  100. Fan YS. Chromosomal disease and maternal age Med References Heilongjiang. 1979; 5:46-50.