2020-12-04T15:54:56+08:002020-03-06|Publish|
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  6. SM Wang, JD Rowley. A Strategy for Gene Identification: Integrated Procedure for Gene Identification. Natl. Acad. Sci. USA 95: 11909-11914, 1998
  7. SM Wang, J Khandekar, K Kaul, D Winchester, R Morimoto. A method for the quantitative analysis of human heat shock gene expression using a multiplex RT-PCR assay. Cell Stress and Chaperones 4: 77-82, 1999
  8. J Chen, JD Rowley, SM Wang. Generation of longer cDNA fragments from serial analysis of gene expression tags for gene identification. Natl. Acad. Sci. USA 97: 349-353, 2000
  9. SM Wang, SC Fears, L Zhang, J-J Chen, JD Rowley. Screening poly dA/dT(-) cDNAs for gene identification. Natl. Acad. Sci. USA 97:4162-4167, 2000. (Commentary by KJ Martin and AB Pardee. Identifying expressed genes. Proc. Natl. Acad. Sci. USA 97: 3789-3791, 2000)
  10. X Yang, AT Ferguson, SJ Nass, P Kim, A Butash, SM Wang, JG Herman, NE Davidson. Transcriptional activation of estrogen receptor in human breast cancer cells by histone deacetylase inhibition. Cancer Res. 60: 6890-6894, 2000
  11. S Lee, J Chen, G Zhou, SM Wang. Generation of high quantity and quality tag/ditag cDNAs for SAGE analysis. BioTechniques 31: 348-354, 2001
  12. S Lee, G Zhou, T Clark, J Chen, JD Rowley, SM Wang. The pattern of gene expression in human CD15+ myeloid progenitor cells. Natl. Acad. Sci. USA 98: 3340-3345, 2001
  13. J Chen, D Rowley, T Clark, S Lee, G Zhou, C Cheers, JD Rowley, SM Wang. Genome-level identification of expressed genes in mouse Gr-1+ myeloid progenitor cells. Genomics 77: 149-162, 2001
  14. G Zhou, J Chen, S Lee, T Clark, JD Rowley, SM Wang. The pattern of gene expression in human CD34+ hematopoietic stem/progenitor cells. Natl. Acad. Sci. USA 98: 13966-13971, 2001
  15. J Chen, S Lee, G Zhou, SM Wang. High-throughput GLGI procedure for converting a large number of serial analysis of gene expression tag sequences into 3’ complementary DNAs. Genes, Chromosomes & Cancer 33: 252-261, 2002
  16. S Lee, T Clark, J Chen, G Zhou, LR Scott, JD Rowley, SM Wang. Correct identification of genes from SAGE tag sequences. Genomics 79: 598-599, 2002
  17. D Nam, S Lee, G Zhou, X Cao, C Wang, J Chen, T Clark, JD Rowley, SM Wang. Oligo dT primer generates a high frequency of truncated cDNAs through internal poly A priming during reverse transcription. Natl. Acad. Sci. USA. 99: 6152-6156, 2002
  18. T Clark, S Lee, LR Scott, SM Wang. Computational analysis of gene identification with SAGE. Journal of Computational Biology  3: 513-526, 2002
  19. M Müschen, S Lee, G Zhou, N Feldhahn, VS Barath, J Chen, C Moers, M Krönke, JD Rowley, SM Wang. Molecular portraits of B cell lineage commitment. Natl. Acad. Sci. USA 99:10014-10019, 2002
  20. J Chen, M Sun, S Lee, G Zhou, JD Rowley, SM Wang. Identifying novel transcripts and novel genes in the human genome by using novel SAGE tags. Natl. Acad. Sci. USA 99: 12257-12262, 2002
  21. SM Wang. The new role of SAGE in gene discovery. Trends in Biotechnology 21: 57-58, 2003
  22. M Sun, G Zhou, S Lee, J Chen, RZ Shi, JD Rowley, SM Wang. SAGE is far more sensitive than EST for detecting low abundant transcripts. BMC Genomics 5: 1-4, 2004
  23. A Silva, J Chen, DM Carraro, SM Wang, AA Camargo. Convert Massive Parallel Signature Sequencing Tags into 3’ cDNA. Nucleic Acid Research 32: e94, 2004
  24. S Lee, J Bao, G Zhou, J Shapino, J Xu, RZ Shi, X Lu, T Clark, D Johnson, YC Kim, C Wing, C Tseng, M Sun, W Lin, J Wang, W Du, CI Wu, X Zhang, SM Wang. Detecting novel low-abundant transcripts in RNA 11: 939-946, 2005
  25. J Bao, S Lee, C Chen, XQ Zhang, Y Zhang, SQ Liu, T Clark, J Wang, ML Cao, HM Yang, SM Wang, J Yu. SAGE (Serial Analysis of Gene Expression) Study of a Hybrid Rice Strain (LYP9) and Its Parental Cultivars. Plant Physiology, 138: 1216-1231, 2005
  26. X Ge, S Yamamoto, S Tsutsumi, Y Midorikawa, S Ihara, SM Wang, H Aburatani. Interpreting expression profiles of cancers by genome-wide survey of breadth of expression in normal tissues. Genomics, 86: 127-141, 2005
  27. S Lee, D Johnson, K Dunbar, H Dong, X Ge, YC Kim, C Wing, N Jayathilaka, N Emmanue, CQ Zhou, HL Gerber, CC Tseng, SM Wang. 2.45 GHz Radiofrequency fields alter gene expression in cultured human cells. FEBS Letters 579:4829-4836, 2005
  28. HS Kang, EM Kim, S Lee, SR Yoon, T Kawamura, YC Lee, S Kim, PK Myung, SM Wang, I Choi. Stage-dependent gene expression profiles during natural killer cell development. Genomics 86: 551-65, 2005
  29. X Ge, YC Jung, Q Wu, WA Kibbe, SM Wang. Annotating non-specific SAGE tags with microarray data, Genomics 87:173-180, 2006
  30. S Lee, J Chen, G Zhou, RZ Shi, G Bouffard, M Kocherginsky, X Ge, M Sun, N Jayathilaka, YC Kim, N Emmanuel, S Bohlander, M Minden, J Kline, O Ozer, R Larson, M LeBeau, E Green,  J Trent, T Karrison, P Liu, SM Wang, JD Rowley. Gene Expression Profiles in Acute Myeloid Leukemia with Common Translocations using SAGE, Natl. Acad. Sci. USA 103: 1030-1035, 2006
  31. SM Wang. Applying the SAGE technique to study the effects of electromagnetic field on biological systems. Proteomics. 6: 4765-4768, 2006 (Invited review)
  32. X Ge, Q Wu, YC Jung, J Chen, SM Wang. A large quantity of novel human antisense transcripts detected by LongSAGE. Bioinformatics. 22: 2475-2479, 2006. (This paper was determined as “the Hot Paper in Computer Science” in 2008 by Essential Science Indicators of Thompson Scientific)
  33. HL Gerber, A Bassi, M Khalid, C Zhou, SM Wang, CC Tseng. Analytical and Experimental Dosimetry of a T-25 Flask in a thermally controlled waveguide. IEEE Transactions on Plasma Science 34: 1449-1454, 2006
  34. X Ge, Q Wu, SM Wang. SAGE detects microRNA precursors. BMC Genomics 7: 285-287, 2006
  35. YC Kim, Y-C Jung, Z Xuan, MQ Zhang, SM Wang. Pan-genome isolation of low abundant transcripts through SAGE tag mis-priming. FEBS Letters 580: 6721–6729, 2006
  36. Q Wu Q, N Tommerup, SM Wang, L Hansen. A novel primate specific gene, CEI, is located in the homeobox gene IRXA2 promoter in Homo sapiens. Gene 371: 167-73, 2006
  37. S Lee, J Hwang, J Ulaszek, YC Kim, H Dong, HS Kim, JW Seok, BK Suh, SJ Yim, D Johnson, NH Choe, KT Chang, ZY Ryoo, CC Tseng, A Wickrema, SM Wang. Stable transcriptional status in the apoptotic erythroid genome. Biochem Biophys Res Commun. 359: 556-562, 2007
  38. SM Wang. Understanding SAGE data. Trends in Genetics 23: 42-50, 2007 (Invited Review)
  39. J Lu, Y Shen, Q Wu, S Kumar, B He, RW Carthew, SM Wang, CI Wu. The birth and death of microRNA genes in Drosophila. Nature Genetics 40: 351-355, 2008.
  40. J Chen, YC. Kim, Y-C Jung, Z Xuan, G Dworkin, Y Zhang, MQ Zhang, SM Wang. Scanning the human genome at kilobase resolution. Genome Research 18: 751-762, 2008
  41. SM Wang. Long-short-long games in transcript identification: the length matters. Current Pharmaceutical Biotechnology, 9: 362-367, 2008 (Invited Review)
  42. Q Wu, YC Kim, J Lu, Z Xuan, J Chen, YL Zheng, T Zhou, MQ Zhang, CI Wu, SM Wang. Poly A- transcripts expressed in HeLa cells. PLoS ONE 3: e2803. doi:10.1371/journal.pone.0002803, 2008
  43. Z Li, RT Luo, S Mi, M Sun, P Chen, J Bao, MB Neilly, N Jayathilaka, DS Johnson, L Wang, C Lavau, Y Zhang, C Tseng, X Zhang, J Wang, J Yu, H Yang, SM Wang, JD Rowley, J Chen, MJ Thirman. Consistent deregulation of gene expression between human and murine MLL rearrangement leukemias. Cancer Res. 69: 1109-1116, 2009
  44. Kim, Q Wu, J Chen, Z Xuan, Y-C Jung, MQ Zhang, JD Rowley, SM Wang. The transcriptome of human CD34+ hematopoietic stem-progenitor cells. Proc. Natl. Acad. Sci. USA 106: 8278-8283, 2009
  45. YC Jung, J Xu, J Chen, YC Kim, DJ Winchester, SM Wang. Simplified DGS procedure for large-scale genome structural study. BioTechniques 47: 969-971, 2009
  46. Lu J, Shen Y, Carthew RW, Wang SM, Wu CI. Reply to “A conservative assessment of microRNA flux in Drosophila. Nature Genetics. 42, 9-10, 2010.
  47. SM Wang, MQ Zhang. The progress and challenge for transcriptome study on human CD34+ hematopoietic stem-progenitor cells. Journal of Cellular Physiology J Cell Physiol. 223:549-552, 2010
  48. X Huang, H Guo, S Tammana, YC Jung, E Mellgren, P Bassi, L Ma, ZJ Tu, SC Ekker, X Wu, SM Wang, XZ Zhou. Gene Transfer Efficiency and Genome-Wide Integration Profiling of Sleeping Beauty, Tol2 and PiggyBac Transposons in Human Primary T Cells. Molecular Therapy. 18(10):1803-13, 2010
  49. Kim, YC Jung, J Chen, AH Alhasan, P kaewsaard, Y Zhang, CI Wu, S Ma, S Rosen, SM Wang, Evidence for widely presence of genomic aberrations in chronic lymphocytic leukemia. BMC Research Notes, 3:341, 2010
  50. J Xu, D Wang, C Zhang, J Song, T Liang, YC Kim, WR Jin, SM Wang, GH Hou. The alternatively expressed genes identified in the CD4+ T cells of skin allograft rejection mice Cell Transplantation 20:333-50, 2011
  51. Wen H, Li Y, Malek SN, Kim YC, Xu J, Chen P, Xiao F, Huang X, Zhou X, Xuan Z, Mankala S, Hou G, Rowley JD, Zhang MQ, Wang SM. New fusion transcripts identified in normal karyotype acute myeloid leukemia. PLoS One 7:e51203, 2012
  52. Gong Q, Tao T, Yang J, Cai J, Yuan Y, Ruan J, Yang J, Lu X, Zhuang S, Wang SM, Wu CI. Identification of medium-sized genomic deletions with low coverage, mate-paired restricted tags. BMC Genomics, 14:51, 2013
  53. Ling M, Ban L, Wen H, Wang SM, Ge SX. Conserved Expression of Natural Antisense Transcripts in Mammals. BMC Genomics, 14:243, 2013
  54. Lynch H, Wen H, Kim YC, Snyder C, Kinarsky Y, Chen PX, Xiao F, Goldgar D, Cowan KH, Wang SM. Can unknown predisposition in familial breast cancer be family-specific? The Breast Journal, 19:520-528, 2013
  55. Xiao F, Kim YC, Wen H, Luo J, Chen P, Cowan K, Wang SM. The genome of polymorphonuclear neutrophils maintains normal coding sequences. PLOSOne 8(11):e78685, 2013
  56. COMPLEXO, Southey MC, Park DJ, Nguyen-Dumont T, Campbell I, Thompson E, Trainer AH, Chenevix-Trench G, Simard J, Dumont M, Soucy P, Thomassen M, Jønson L, Pedersen IS, Hansen TV, Nevanlinna H, Khan S, Sinilnikova O, Mazoyer S, Lesueur F, Damiola F, Schmutzler R, Meindl A, Hahnen E, Dufault MR, Chris Chan T, Kwong A, Barkardóttir R, Radice P, Peterlongo P, Devilee P, Hilbers F, Benitez J, Kvist A, Törngren T, Easton D, Hunter D, Lindstrom S, Kraft P, Zheng W, Gao YT, Long J, Ramus S, Feng BJ, Weitzel JN, Nathanson K, Offit K, Joseph V, Robson M, Schrader K, Wang SM, Kim YC, Lynch H, Snyder C, Tavtigian S, Neuhausen S, Couch FJ, Goldgar DE. COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration. Breast Cancer Res. 15(3):402, 2013
  57. Xiao F, Kim YC, Snyder C, Wen H, Chen PX, Luo J, Becirovic D, Downs B, Cowan KH, Lynch H, Wang SM. Genome instability in blood cells of a BRCA1+ breast cancer family. BMC Cancer 14:342  doi:10.1186/1471-2407-14-342, 2014
  58. Wen H, Kim Y, Snyder C, Xiao F, Fleissner EA, Becirovic D, Luo J, Downs B, Sherman S, Cowan KH, Lynch HT, Wang SM. Family-specific, novel, deleterious germline variants provide a rich source to identify genetic predispositions for BRCAx familial breast cancer. BMC Cancer, 14:470, 2014
  59. Lynch H, Synder C, Wang SM. Considerations for comprehensive assessment of genetic predisposition in familial breast cancer. Breast J. 21(1):67-75, 2015. PMID: 25472498.
  60. Downs B, Wang SM. Epigenetic changes in BRCA1-mutated familial breast cancer. 208(5):237-40, 2015. PMID: 25800897
  61. Downs B, Kim YC, Xiao F, Snyder C, Chen P, Fleissner EA, Becirovic D, Wen H, Sherman S, Cowan KH, Lynch HT, Wang SM. Two PALB2 germline mutations found in both BRCA1+ and BRCAx familial breast cancer. Breast Cancer Res Treat. 151(1):219-24. 2015. PMID: 25833210.
  62. Angulo-Ibáñez M, Rovira-Clavé X, Downs B, Kim YC Wang SM, Tournier C, Reina M, Espel Erk5 contributes to balance cellular nucleotide levels and avoid replicative stress, Cell Cycle, 14(24):3864-76, 2015, PMID: 26697837
  63. Kim KC, Zhao L, Zhang H, Huang Y, Cui J, Xiao F, Downs F, Wang SM. Prevalence and spectrum of BRCA germline variants in mainland Chinese familial breast and ovarian cancer patients. Oncotarget. 7(8):9600-12, 2016. doi: 10.18632/oncotarget.7144, 2016
  64. Cui J, Luo L, KimYC, Synder C, Becirovic D, Downs B, Lynch H, Wang SM. Differences of variable number tandem repeats in XRCC5 promoter are associated with increased or decreased risk of familial breast cancer. Frontiers in Oncology, 6:00092, 2016. doi:10.3389/fonc.2016.00092
  65. Kim YC, Cui J, Luo J, Xiao F, Downs B, Wang SM. Exome-based Variant Detection in Core Promoters. Sci Rep. 6:30716, 2016. PMID: 27464681
  66. Downs B, Xiao F, Kim YC, Chen PX, Huang D, Fleissner EA, Cowan K, Wang SM. Single-base LOH can be used as specific marker to classifyBRCAx familial breast cancer into more homogenous subtypes. The Breast Journal. 23(4):479-481, PMID: 28117528
  67. Kim YC, Soliman AS, Cui J, Ramadan M, Hablas A, Abouelhoda M, Hussien N, Ahmed O, Zekri AN, Seifeldin IA, Wang SM. Unique features of germline variation in five Egyptian Familial Breast Cancer families revealed by exome sequencing. PLOS One. 12(1):e0167581, 2016 PMID:28076423
  68. Wang SM. Pros and cons for population screening BRCA mutation carriers. Clinics in Oncology. 1:1161, 2016
  69. Chen P, Kim YC, Akhtari M, Wang SM. An Example of using Precision Medicine in Cancer Care: Dynamic Change of TET2 Mutation in a Patient with Therapy-related Myelodysplastic Syndrome/ Acute Myeloid Leukemia. Int J Cancer Res Mol Mech. 3(2): doi http://dx.doi.org/10.16966/2381-3318.134, 2017
  70. Liao W, Liu H, Zhang Y, Jung JH, Chen J, Su X, Kim YC, Flores ER, Wang SM, Czarny-Ratajczak M, Li W, Zeng SX, Lu H. Ccdc3: A new p63 target involved in regulation of liver lipid metabolism. Scientific Reports 7(1):9020, 2017
  71. Downs B, Sherman S, Cui J, Kim YC, Snyder C, Christensen M, Luo J, Lynch H, Wang SM. Common genetic variants contribute to incomplete penetrance: evidence from cancer-free BRCA1 mutation carriers. European Journal of Cancer 107:68e78, 2019
  72. Bhaskaran SP, Chandratre K, Gupta H, Zhang L, Wang X, Cui J, Kim YC, Sinha S, Jiang L, Lu B, Wu X, Qin Z, Huang T, Wang SM. Germline variation in BRCA1 and BRCA2 is highly ethnic-specific: evidence from over 30,000 Chinese hereditary breast and ovarian cancer patients. International Journal of Cancer, 107:68e78, 2019
  73. Guo M, Sinha S, Wang SM. Coupled genome-wide DNA methylation and transcription analysis identified rich biomarkers and drug targets in triple negative breast cancer. Cancers.11(11). pii: E1724, 2019
  74. Zhang L, Bhaskaran SP, Huang T, Dong H, Chandratre K, Wu X, Qin Z, Wang X, Cao W, Chen T, Lynch H, Wang SM. Variants of DNA mismatch repair genes derived from 33,998 Chinese cancer and non-cancer individuals reveal their highly ethnic-specific nature. European Journal of Cancer. 125:12-21, 2020
  75. Sinha S, Wang SM. Classification of VUS and unclassified variants in BRCA1 BRCT repeats by molecular dynamics simulation. Computational and Structural Biotechnology Journal 18:723-736, 2020
  76. Dong H, Chandratre K, Qin Y, Zhang J, Tian X, Rong C, Wang N, Guo M, Zhao G, Wang SM. Prevalence of BRCA1/BRCA2 pathogenic mutation in Chinese Han population. Journal of Medical Genetics. Online First:28 May 2020. doi: 1136/jmedgenet-2020-106970. Epub ahead of print.
  77. Qin Z, Kuok CN, Dong H, Jiang L, Zhang L, Guo M, Leong HK, Wang L, Meng G, Wang SM. Can population BRCAscreening be applied in non-Ashkenazi Jewish populations? Experience in Macau population. J Med Genet. 2020 Aug 17:jmedgenet-2020-107181. doi: 10.1136/jmedgenet-2020-107181. Epub ahead of print.
  78. Bhaskaran SP, Huang T, Rajendran BK, Guo M, Luo J, Qin Z, Zhao B, Chian J, Li S, Wang SM. Ethnic-specific BRCA1/2variation within Asia population: evidence from over 78 000 cancer and 40 000 non-cancer cases of Indian, Chinese, Korean and Japanese populations. J Med Genet. 2020 Sep 22:jmedgenet-2020-107299. doi: 10.1136/jmedgenet-2020-107299. Epub ahead of print.
  79. Gupta H, Chandratre K, Sinha S, Huang T, Wu X, Cui J, Zhang MQ, Wang SM. Highly diversified core promoters in the human genome and their effects on gene expression and disease predisposition. MBC Genomics. 2020 (in press)