MAX MCGEE PUBLISHED PAPERS
SOUMITRA GHOSH, MD, PhD
Journal Publication/Original Papers:
Glisic-Milosavljevic S, Waukau J, Jailwala P, Jana S, Khoo HJ, Albertz H, Woodliff J, Koppen M, Alemzadeh R, Hagopian W, Ghosh S. At-risk and recent-onset type 1 diabetic subjects have increased apoptosis in the CD4+CD25+high T-cell fraction. PLoS ONE 2:e146, 2007.
Ghosh S, Schork N. Commentary on "Genetics of Type 2 Diabetes: The study of quantitative traits". Commentaries on Perspectives in Diabetes, pp213-214, 2006.
Nolan K, Schiller J, Ghosh S, Magnuson V Identification of a novel HLA-DQB1 allele, DQB1*060403, by sequence-based typing. Tissue Antigens, 68(5):456-457, 2006.
Geoffrey R, Jia S, Kwitek AE, Woodliff J, Ghosh S, Lernmark A, Wang X, Hessner MJ. Evidence of a functional role for mast cells in the development of type 1 diabetes mellitus in the BioBreeding rat. J Immunol 177(10):7275-7286, 2006.
Nittala A, Ghosh S, Stefanovski D, Bergman R, Wang X. Dimensional analysis of MINMOD leads to definition of the disposition index of glucose regulation and improved simulation algorithm. Biomed Eng Online, 5:44, 2006.
Wang X, Jia S, Meyer L, Xiang B, Chen LY, Jiang N, Moreno C, Jacob HJ, Ghosh S, Hessner MJ. Comprehensive quality control utilizing the prehybridization third-dye image leads to accurate gene expression measurements by cDNA microarrays. BMC Bioinformatics, 7(1): 378, 2006.
Wang X, He Z, Ghosh S. Investigation of the age-at-onset heterogeneity in type 1 diabetes through mathematical modeling. Mathematical Biosciences, 203(1):79-99, 2006.
Guo SW, Magnuson VL, Schiller JJ, Wang X, Wu Y, Ghosh S. Meta-Analysis of Vitamin D Receptor Polymorphisms and Type 1 Diabetes: A HuGE Review of Genetic Association Studies. Am J Epidemiology, 164(8):711-724, 2006.
Wu Y, Kajdacsy-Balla A, Strawn E, Basir Z, Halverson G, Jailwala P, Wang Y, Wang X, Ghosh S, Guo SW. Transcriptional Characterizations of differences between Eutopic and Ectopic Endometrium. Endocrinology, Jan;147(1): 232-246, 2006.
Glisic-Milosavljevic S, Waukau J, Jana S, Jailwala P, Rovensky J, Ghosh S. Comparison of apoptosis and mortality measurements in peripheral blood mononuclear cells (PMBCs) using multiple methods. Cell Prolif, 38: 301-311, 2005.
Hessner MJ, Wang X, Meyer L, Geoffrey R, Jia S, Fuller J, Lernmark A, Ghosh, S. Involvement of Eotaxin, Eosinophils, and Pancreatic Predisposition in Development of Type 1 Diabetes Mellitus in the BioBreeding Rat. J Immunol, 173:6993-7002, 2004.
Browning MB, Woodliff JE, Konkol MC, Pati NT, Ghosh S, Truitt RL, Johnson BD. CD150 identifies alloantigen CD4+25+ regulatory T cells. Cellular Immunology 227(2): 129-39, 2004.
Silander K, Scott LJ, Valle TT, Mohlke KL, Stringham HM, Wiles KR, Duren WL, Doheny KF, Pugh EW, Chines P, Narisu N, White PP, Fingerlin TE, Jackson AU, Li C, Ghosh S, Magnuson VL, et al. A Large Set of Finnish Affected Sibling Pair Families with Type 2 Diabetes suggests Susceptibility Loci on Chromosomes 6,11, and 14. Diabetes 53:821-829, 2004.
Pati N, Schowinsky V, Kokanovic O, Magnuson V, Ghosh S. A Comparison between SNaPshot, Pyrosequencing, and Biplex Invader SNP Genotyping Methods: Accuracy, Cost, and Throughput. JBBM 60:1-12, 2004.
Wang X, Jiang N, Feng X, Xie Y, Tonellato P, Ghosh S, Hessner MJ. A novel approach for microarray image processing using third-dye array visualization technology. IEEE trans Nanobioscience 4(2):193, 2003.
Waukau J, Jailwala P, Wang Y, Khoo HJ, Ghosh S, Wang X, Hessner M. The design of a gene chip for functional immunological studies on a high-quality control platform. Annals of NY >Academy of Science. Annals of NY >Academy of Science 1005:284, 2003.
Pati N, Ghosh S, Hessner MJ, Khoo HJ, Wang X. Difference in gene expression profiles between human CD4+CD25+ and CD4+CD25- T cells. Annals of NY >Academy of Science 1005:279, 2003.
Hessner MJ, Wang, X, Khan S, Meyer L, Schlicht M, Tackes J, Datta MW, Jacob HJ, Ghosh S. Use of a three-color cNDA microarray platform to measure and control support-bound probe for improved data quality and reproducibility. Nucleic Acid Research 31(11): e60, 2003 Jun 1.
Wang X, Hessner M, Wu Y, Pati N, Ghosh S. Quantitative quality control in microarray experiments and the application in data filtering, normalization and false positive rate prediction. Bioinformatics 19(11): 1341-1347 2003 July 22.
Hessner M, Wang X, Hulse K, Meyer L, Wu Y, Nye S, Guo SW, Ghosh S. Three color cDNA microarrays: quantitative assessment through the use of fluorescein-labeled probes. Nucleic Acid Research 31(4):1-6, 2003.
Wang Y, Wang X, Guo SW, Ghosh S. Is hybridization truly competitive in two-color cDNA microarray experients? A theoretical modeling and its implications. Biotechniques 32(6):1342-1346, 2002.
Ghosh S, Tuomilehto J, Guo SW. Heterogeneity of type 1 diabetes. International Diabetes Monitor 141(3):18-20, 2002.
Wang X, Ghosh, S, Guo, SW Quantitative quality control in microarray image processing and data acquisition. Nucleic Acid Research Methods 29:15, 2001.
Mohlke KL, Lange EM, Valle T, Ghosh S, Magnuson VL, Silander K, et al. Linkage disequilibrium between microsatellite markers extends beyond 1 cM on chromosome 20 in Finns. Genomic Research 11:1221-1226, 2000.
Watanabe RM, Ghosh S, Langefeld CD, Valle T, Hauser ER, Magnuson VL, et al. The Finland-US investigation of non-insulin dependent diabetes mellitus (FUSION) genetic study: II. An autosomal genome scan for quantitative trait loci. American Journal of Human Genetics 67(5):1186-1200, 2000.
Ghosh S, Watanabe RM, Valle T, Hauser ER, Magnuson VL, Langefeld CD, et al. The Finland-US investigation of non-insulin dependent diabetes mellitus (FUSION) genetic study: I. An autosomal genome scan for genes that predispose to type 2 diabetes. 2000. American Journal of Human Genetics 67(5): 1174-1185, 2000.
Karanjawala Z, Kaariainen H, Ghosh S, Tannenbaum J, Martin C, Ally D, et al. Complete maternal isodisomy for chromosome 8 in an individual with an early- onset ileal carcinoid tumor. American Journal of Medical Genetics 93(3):207-210, 2000.
Brody LC, Baker PJ, Chines PS, Musick A, Molloy AM, Swanson DA, Kirke PN, Ghosh S, Scott JM, Mills JL. Methionine synthase: high resolution mapping of the human gene and evaluation as a candidate locus for neural tube defects. Molecular Genetics and Metabolism 67:324-333, 1999.
Birznieks G, Ghosh S, Watanabe RM, Mitchell BD. The effect of phenotypic variation on detection of linkage in the COGA data. Genetic Epidemiology 17 (Suppl 1):S61-S66, 1999.
Watanabe RM, Ghosh S, Birznieks G, Duren WL, Mitchell BD. Application of a ordered subset analysis approach to the genetics of alcoholism. Genetic Epidemiology 17 (Suppl 1):S385-S390, 1999.
Mitchell BD, Ghosh S, Watanabe R, Slifer SH, Hsueh W-C, Birznieks G. Identifying influential individuals in linkage analysis: application to a quantitative trait locus detected in the COGA data. Genetic Epidemiology 17 (Suppl 1):S259-S264, 1999.
Listwak, S, Barrientos, RM, Koike, G, Ghosh, S, Gomez, M, Misiewicz, B, Sternberg, EM. Identification of a novel inflammation-protective locus in the Fischer rat. Mammalian Genome 10:362-365, 1999.
Watanabe RM, Valle T, Hauser ER, Ghosh S, Eriksson J, Kohtamaki K, Ehnholm C, Tuomilehto J, Collins FS, Bergman RN, and Boehnke M. for the FUSION study investigators. Familiality of quantitative metabolic traits in Finnish families with non-insulin dependent diabetes mellitus. Human Heredity 49:159-168, 1999.
Ghosh S, Watanabe RM, Hauser ER, Valle T, Magnuson VL, Erdos MR, et al. Type 2 Diabetes: Evidence for Linkage on Chromosome 20 in 716 Finnish Affected Sib Pairs. Proceedings of the National >Academy of Sciences 96:2198-2203, 1999.
Ghosh S, Langefeld CD, Ally DS, Watanabe R, Hauser ER, Magnuson VL, et al. Trp64Arg variant of the b3-adrenergic receptor is not associated with type 2 diabetes or obesity in a large Finnish sample. Diabetologia 42:238-244, 1999.
Ghosh S, Hauser ER, Magnuson VL, Valle T, Ally DS, Karanjawala ZK, et al. A large sample of Finnish diabetics reveals no evidence for a NIDDM locus at 2qter. Journal of Clinical Investigation 102 (4): 704-709, 1998.
Valle T, Tuomilehto J, Bergman R, Ghosh S, Hauser ER, Eriksson J, et al. Mapping genes for non-insulin dependent diabetes mellitus: design of the Finland-United States Investigation of NIDDM genetics (FUSION) study. Diabetes Care 21(6):949-958, 1998.
Mitchell BD, Ghosh S, Schneider JL, Birznieks G, Blangero J. Power of variance component linkage analysis to detect epistasis. Genetic Epidemiology 14:1017-1022, 1997.
Perseghin G, Ghosh S, Gerow K, Schulman GI. Metabolic defects in lean, non-diabetic offspring of NIDDM patients: a cross-sectional study. Diabetes 46(6):1001-1010, 1997.
Ghosh S, Karanjawala ZE, Hauser ER, Ally D, Knapp JI, Rayman JB, et al. Methods for precise sizing, automated binning of alleles and reduction of error rates in large-scale genotyping using fluorescently-labeled dinucleotide markers. Genome Research 7(2):165-178, 1997.
Magnuson VL, Ally DS, Nylund SJ, Karanjawala ZE, Rayman JB, Knapp JI, Lowe AL, Ghosh S, Collins FC. Substrate nucleotide-determined non-templated addition of adenine by Taq DNA polymerase: Implications for PCR-based genotyping and cloning. BioTechniques 21:700-709, 1996.
Permutt MA, Ghosh S. Rat model contributes new loci for NIDDM susceptibility in man. Nature Genetics 12:4-6, 1996.
Ghosh S, Collins FC. The geneticist's approach to complex disease. Annual Review of Medicine 47:333-353, 1996.
Ghosh S, Schork NJ. Genetic analysis of type II diabetes: the analysis of quantitative traits. Diabetes 45:1-14, 1996.
Smith JR, Carpten JD, Brownstein MJ, Ghosh S, Magnuson VL, Gilbert DA, et al. Approach to genotyping errors caused by non-templated nucleotide addition by Taq DNA Polymerase. Genome Research 5:312-317, 1995.
Ghosh S. Probability and complex disease genes. Nature Genetics 9:223-224, 1995.
McDonald MT, Papenberg KA, Ghosh S, Glatfelter AA, Bisiecker BB, Helmbold EA, et al. A disease locus for Hereditary Haemorrhagic Telangiectasia maps to 9q33-. Nature Genetics 6:197-203, 1994.
Todd JA, Reed PW, Prins J-B, Bain SC, Palmer SM, Cordell HJ, Ghosh S, et al. Dissection of the pathophysiology of type 1 diabetes by genetic analysis. Journal of Autoimmunity 15 (Suppl):16-17, 1993.
Ghosh S, Palmer SM, Rodrigues N, Cordell HJ, Hearne CM, Cornall RJ, et al. Polygenic control of autoimmune diabetes in nonobese diabetic mice. Nature Genetics 4:404-409, 1993.
Risch N, Ghosh S, Todd JA. Statistical evaluation of multiple-locus linkage data in experimental species and its relevance to human studies: application in NOD mouse and human IDDM, American Journal of Human Genetics. 53:702-714, 1993.
Prins JB, Todd JA, Rodrigues NR, Ghosh S, Hogarth PM, Wicker LS, et al. Linkage on chromosome 3 of autoimmune diabetes and defective Fc receptor for IgG in NOD mice. Science 260: 695-698, 1993.
McAleer MA, Aitman TJ, Cornall RJ, Ghosh S, Hall JS, Hearne CM, et al. Linkage analysis of 84 microsatellite markers in intra- and interspecific backcrosses. Mammalian Genome 3:457-460, 1992.
Hearne CM, Ghosh S, Todd JA. Microsatellites for linkage analysis of genetic traits. TIGS 8:288-294, 1991.
Todd JA, Aitman TJ, Cornall, RJ, Ghosh S, Hall JS, Hearne CM, et al. Genetic analysis of complex multifactorial disease, autoimmune type 1 (insulin-dependent) diabetes. Res. Immun 142:483, 1991.
Hearne CM, McAleer MA, Love JM, Aitman TJ, Cornall RJ, Ghosh S, et al. Additional microsatellite markers for mouse genome mapping. Mammalian Genome 1: 273-282, 1991.
Todd JA, Aitman TJ, Cornall RJ, Ghosh S, Hall JS, Hearne CM, et al. Genetic analysis of autoimmune type I diabetes mellitus in mice. Nature 351:542-547, 1991.
Savill JS, Barrie R, Ghosh S, Muhlemann M, Dawson P, Pusey CD. Fatal Stevens-Johnson syndrome following urography with iopamidol in systemic lupus erythematosus. Postgraduate Medical Journal 64:392-394, 1988.
Book Chapters:
Hessner M, Wang X, Ghosh S. Genetics of type 1 diabetes. Diabetes Mellitus: A fundamental and clinical text. (eds. LeRoith D, Taylor S.I., Olefsky J.M.: Lippincott Williams & Wilkins Publishers), pp. 483-498, 2004.
Nye S, Ghosh S. Genetics of complex diseases. Genetics of Diabetes Mellitus, pp 1-25. Editor William L. Lowe, Jr, MD. Kluwer Academic Publishers. 2001.
Ghosh S. Positional cloning strategies to identify causal genes for type 2 diabetes mellitus. In Diabetes Mellitus: A fundamental and clinical text, (eds. LeRoith D. Taylor S.I., Olefsky J.: Lipincott-Raven Publishers). pp 664-674, 2000.
Ghosh S, Todd JA. Analysis of complex genetic diseases: lessons from type 1 diabetes. In Genome Analysis vol 3, Genes and Phenotypes (eds. Davies K.E. and Tilghman, S.M.: Cold >Spring >Harbor), pp. 79-104, 1991.
RAMIN ALEMZADEH, MD
Journal Publications/Original Papers:
Alemzadeh R, Palma-Sisto, Holzum MK, Parton, E, Kichler J. Continuous Subcutaneous Insulin Infusion Attenuated Glycemic Instability in Preschool Children with type 1 Diabetes Mellitus (DM). Diabet Tech & Therap 2007 (in press).
Glisic-Milosavljevic S, Waukau J, Jailwala P, Jana S, Khoo HJ, Albertz H, Woodlif f J, Koppen M, Alemzadeh R, Hagopian W, Ghosh S. At-risk and recent-onset Type 1 diabetic subjects have increased apoptosis in the CD4+CD25 high T-cell fraction". PLoS ONE 2007; 2:e146.
Hains AA, Berlin KS, Davies WH, Smothers MK, Sato AF, Alemzadeh R. Attributions of Adolescents with Type 1 Diabetes Related to Performing Self-Care around Friends and Peers: The Moderating Role of Friend Support. J Ped Psych . 2006; 10.1093/jpepsy/js1040.
Alemzadeh R, Ellis J, Calhoun M, Kichler J. Predictors of Metabolic Control at One Year in a Population of Pediatric Patients with Type 2 Diabetes (DM): A Retrospective Study . J Pediatric Endocrinology & Metabolism 2006; 19: 1141-1149.
Eversten JM, Alemzadeh R; Increasing Ten-year Burden of Pediatric Type 1 Diabetes Mellitus in Southeastern Wisconsin: Relationship to Body Weight Submitted to Archives of Pediatrics & Adolescent Medicine (January 2007).
Hains AA, Davies WH, Berlin KS, Walos JJ, Jandrisevits MD, Guillen A, Busetto G, Parton EA, Alemzadeh R. Attributions of Adolescents with Type 1 Diabetes in Social Situations. Diabetes Care 2006; 29: 818-822.
Alemzadeh R, Tushaus K. Diazoxide Attenuates Hepatic Lipogenesis in Zucker Diabetic Fatty Rats. Med Science Monitor 2005; 11 (12): BR439-448.
Battaglia MR, Alemzadeh R, Katte H, Hall PL, Perlmuter LC. Brief Report: Disordered Eating and Psychosocial Factors in Female Adolescents with Type 1 Diabetes Mellitus. J Ped Psychology 2006; 31: 552-556. doi:10.1093/jpepsy/jsj047.
Berlin KS, Davies WH, Jastrowski KE, Hains AA, Parton E, Alemzadeh R. Contextual Assessment of Problematic Situations Identified by Adolescents Using Insulin Pumps and Their Parents. Families, Systems, and Health 2006; 24: 33-44.
Alemzadeh R, Palma-Sisto P, Holzum MK, Parton E. Continuous Subcutaneous Insulin Infusion (CSII) and Multiple Dose of Insulin (MDI) Regimen Display Similar Patterns of Blood Glucose Excursions in Pediatric Type 1 Diabetes (DM). Diabetes Technology & Therapeutics 2005; 7 (4): 587-596.
Alemzadeh R, Berhe T, Wyatt DT. Feasibility of Flexible Insulin Therapy with Glargine in Pre-School Children with Type 1 Diabetes Mellitus. Pediatrics 115(5): 1320-1324, 2005.
Alemzadeh R, Tushaus K. Modulation of Adipoinsular Axis in Prediabetic ZDF Rats by Diazoxide. Endocrinology 145: 5476-5484, 2004.
Alemzadeh R, Feehan T. Variable Effects of Beta-Carotene Therapy in a Child with Erythropoietic Protoporphyria. Eur J Ped 163: 547-549, 2004.
Alemzadeh R, Zhang J, Tushaus K, Koontz J. Diazoxide Enhances Adipose Tissue Protein Kinase B Activation and Glucose Transporter-4 Expression in Obese Zucker Rats. Medical Science Monitor 10(3): BR53-60, 2004.
Alemzadeh R, Ellis JN, Holzum MK, Parton EA, Wyatt DT. Beneficial Effects of Continuous Subcutaneous Insulin Infusion (CSII and Flexible Multiple Daily Insulin (FMDI) Regimen Using Insulin Glargine in Type 1 Diabetes Mellitus. Pediatrics 2004; 114: e91-e95. URL: http://www.pediatrics.org/cgi/content/full/114/1/e91.
Alemzadeh R, Fledelius C, Bodvarsdottir T, and Sturis J. Attenuation of Hyperinsulinemia by NN414, a SUR1/Kir6.2 Selective K+ATP Channel Opener, Improves Glucose Tolerance and Lipid Profile in Obese Zucker Rats. Metabolism 53(4): 441-447, 2004.
Alemzadeh R, Loppnow C, Parton E, and Kirby M. Glucose Sensor Evaluation of Glycemic Instability in Pediatric Type 1 Diabetes Mellitus (DM). Diabetes Therapeutics & Technology 5(2); 167-173, 2003.
Alemzadeh R , Sisto P, Parton E, Totka J, Kirby M. Beneficial Effects of Flexible Insulin Therapy in Children and Adolescents with Type 1 Diabetes Mellitus. Acta Diabetologica 40: 137-142, 2003.
Alemzadeh R, Holshouser SJ, Massey P, Koontz J. Chronic Insulin Suppression by Diazoxide Alters the Activities of Key Enzymes Regulating Hepatic Gluconeogenesis in Zucker Rats. European Journal of Endocrinology 146 (6): 871-879, 2002.
Kay JP, Alemzadeh R, Langley G, D'Angelo L, Smith P, Holshouser S. Beneficial Effects of Metformin in Normoglycemic Morbidly Obese Adolescents. Metabolism 50(12): 1457-1461, 2001.
Hensley IE, Lawler JE, Alemzadeh R, and Holshouser SJ. Diazoxide Effects on Hypothalamic and Extra-Hypothalamic NPY Content in Zucker Rats. Peptides 22: 899-908, 2001.
Standrige M, Alemzadeh R, Koontz J, and Moustaid N. Diazoxide Down-Regulates Leptin and Lipid Metabolizing Enzymes in Adipose Tissue of Zucker Rats. FASEB, 14, 445-460, 2000.
Smith DP, Lozzio C, Hennessey M, and Alemzadeh R. Prenatal Diagnosis of Testicular Feminization. Urology 53: 1033-1034, 1999.
Alemzadeh R, Holshouser S. Effect of Diazoxide on Brain Capillary Insulin Receptor Binding and Food Intake in Hyperphagic Zucker Rats. Endocrinology 140: 3197-3202, 1999.
Alemzadeh R, Langley G, Upchurch L, Smith P, and Slonim AE. Beneficial Effect of Diazoxide in Obese Hyperinsulinemic Adults. J Clin Endo Metab 83(6): 1911-1915, 1998.
Alemzadeh R. and Upchurch L. Anabolic Effects of Growth Hormone Treatment in Young Children with Cystic Fibrosis. J Am Coll Nutr 17(5): 419-424, 1998.
Alemzadeh R, Gammeltoft K, Matteson K. Efficacy of Low-Dose Dextromethorphan Treatment in Nonketotic Hyperglycinemia. Pediatrics 97 (6): 924-926, 1996.
Alemzadeh R, Jacobs W, Pitukcheewanont. Antiobesity Effect of Diazoxide in Obese Zucker Rats. Metabolism 45 (3):334-341, 1996.
Pituckeewanont P, Alemzadeh R, Jones BH, Jacobs WR, and Eberle AJ. Does Glycemic Control Affect Growth Velocity in Children with Insulin-dependent Diabetes Mellitus (IDDM)? Acta Diabetolgica 32:148-152, 1995.
Kohn B, Day D, Alemzadeh R, Enerio D, Patel SV, Pelczar and Speiser PW. Splicing Mutation in CYP21 Associated with Delayed Presentation of Salt-Wasting Congenital Adrenal Hyperplasia. Am J Med Genet 57:450-454, 1995.
Alemzadeh R, Slonim AE, Zdanowicz MM, and Maturo J. Modification of Insulin Resistance by Diazoxide in Obese Zucker Rats. Endocrinology 133:705-712, 1993.
Alemzadeh R, Friedman S, Fort P, Recker B, Lifshitz F. Is There "Compensated Hypothyroidism" In Infancy? Pediatrics 90:207-211, 1992.
Alemzadeh R, Goldberg T, Fort P, Recker B, Lifshitz F. Reported Dietary Intakes in Patients with IDDM: Limitations of Dietary Recall. NUTRITION: An International Journal of Applied and Basic Nutritional Science 8:13-19, 1992.
Books, Chapters & Reviews:
Alemzadeh R and Wyatt DT. Diabetes Mellitus. In: Nelson Text Book of Pediatrics, 18th Edition, Eds, Behrman, Kliegman, Jensen; W.B. Saunders, Philadelphia, PA; Chapter 590: 2007 (in press).
Alemzadeh R, Rising R, Lifshitz F. Childhood Obesity; In: Pediatric Endocrinology, 5th edition, Ed, Lifshitz F, Informa Healthcare USA, Inc., New York, Chapter 1:1-36 2007.
Alemzadeh R and Wyatt DT. Diabetes Mellitus. In: Nelson Text Book of Pediatrics, 17th Edition, Eds, Behrman, Kliegman, Jensen; W.B. Saunders, Philadelphia, PA; Chapter 583: 1947-1972, 2003.
Alemzadeh R, Lifshitz F. Childhood Obesity; In: Pediatric Endocrinology, 4th edition, Ed, Lifshitz F, Marcel Dekker, Inc., New York, Chapter 34: 753-774, 2003.
Alemzadeh R, Pugliese M, Lifshitz F. Disorders of Puberty; In: Comprehensive Adolescent Health Care, 2nd edition, Friedman S, Fisher M, & Schonberg Sk, Mosby, St. Louis, MO, Chapter 28: 214-232,1997.
Alemzadeh R, Lifshitz F. Childhood Obesity; In: Pediatric Endocrinology, 3rd edition, Ed, Lifshitz F, Marcel Dekker, Inc., New York, Chapter 52: 753-774, 1995.
Alemzadeh R, Fasano M, Lifshitz F. Childhood Obesity; In: Low-Calorie Foods Handbook, Ed., Altschul AM, Marcel Dekker, Inc., New York, NY, Chapter 3: 37-61, 1993.
Alemzadeh R, Pugliese M, Lifshitz F. Disorders of Puberty; In: Comprehensive Adolescent Health Care, Friedman S, Fisher M, & Schonberg SK, Quality Medical Publishing, Inc., St. Louis, MO, Chapter 26: 187-205, 1992.
Editorials, Letters to Editor, Other
Binion DG, Alemzadeh, R. Selected Summaries (Editorial): Growth of an IBD Controversy: Growth Hormone and Crohn's Disease. Inflammatory Bowel Disease 7(2): 176-178, 2001.
Alemzadeh R. Treatment of Childhood & Adolescent Obesity: A Commentary. Endocrine Practice 4(6): 417-422, November 1998.
Non-referred Journal Publications/Original Papers
Alemzadeh R. Common Pediatric Issue: Type 1 Diabetes Mellitus. Pediatric Rounds (Children's Specialty Group Newsletter): Spring Issue, 2003.
Alemzadeh R. Beneficial Effects of Metformin in Normoglycemic Morbidly Obese Adolescents: An Overview. Compendium Series (Helix Communications): Obesity 3: 15-17, 2002. (Invited Article)
Zimmerman AW, Alemzadeh R, and Eberle AJ. Hormones in Pediatric Epilepsy. Int J Pediatrics 8(2): 272-279, 1993. (Invited Article)
Alemzadeh R. "Missed" Childhood Hypothyroidism: Attenuation of Final Adult Height. >University of Tennessee, Pediatric Update (UT Med Ctr. Publication) 2:1, 1992.
Alemzadeh R. A review article on "Is Nutritional Dwarfing a Consequence of Disturbed Psychosocial Functioning?" (Sandberg et el. 1991; 88:926-933)); >University of Tennessee, Pediatric Update 2: 7, 1992.
MARTIN J. HESSNER, PhD
Journal Publications/Original Papers:
Geoffrey, R., S. Jia, A.E. Kwitek, J., S. Ghosh, Å. Lernmark, X. Wang, M.J. Hessner. 2006. Evidence of a functional role for mast cells in the development of type 1 diabetes mellitus in the BioBreeding rat. The Journal of Immunology 177(10):7275-86.
Wang X., S. Jia, L. Meyer, B. Xiang, L.Y. Chen LY, N. Jiang, C. Moreno, H.J. Jacob, S. Ghosh, M.J. Hessner. 2006. Comprehensive quality control utilizing the prehybridization third-dye image leads to accurate gene expression measurements by cDNA microarrays. BMC Bioinformatics 7:378.
Hessner, M.J., M. Liang, A.E. Kwitek. 2006. The Application of Microarray Analysis to Pediatric Diseases. Pediatric Clinics of North America. 53:579–590.
Hessner, M.J., B. Xiang, S. Jia, R. Geoffrey, S. Holmes, L. Meyer, S. Muheisen, X. Wang. 2006. Three-color cDNA microarrays with prehybridization quality control yield gene expression data comparable to that of commercial platforms. Physiological Genomics 25:166-78
Liang, M., A.W. Cowley Jr., M.J. Hessner, J. Lazar, D.P. Basile, J.L. Pietrusz. 2005. Transcriptome analysis and kidney research: Toward systems biology. Kidney International 67:2114-22.
Yang, J., X. Wang, J. Moibi, M.J. Hessner, S. Greene, J. Wu, R.K. Wong, S. Sukumvanich, B.A. Wolf, Z.Gao 2004. Leucine culture reveals that ATP synthase functions as a fuel sensor in pancreatic β cells. Journal of Biological Chemistry. 279(52):53915-23.
Hessner, M.J., X. Wang, L. Meyer, R. Geoffrey, S. Jia, J. Fuller, A. Lernmark, S. Ghosh. 2004. Involvement of eotaxin, eosinophils, and pancreatic predisposition in development of type 1 diabetes mellitus in the BioBreeding rat. The Journal of Immunology, 173(11):6993-7002.
Schlict, M., B. Matysiak, T. Brodzeller, X. Wen, H. Liu, G. Zhou, R. Dhir, M.J. Hessner, P. Tonellato, M. Suckow, M. Pollard, M.W. Datta. 2004. Cross-species global and subset gene expression profiling identifies genes involved in prostate cancer response to selenium. BMC Genomics. 5(1)58.
Hessner, M.J., L. Meyer, J. Tackes, S. Muheisen, X. Wang. 2004. Immobilized probe and glass surface chemistry as variables in microarray fabrication. BMC Genomics, 5(1):53.
Morrison, J., K. Knoll, M.J. Hessner, M. Liang. 2004. Effect of high glucose on gene expression in mesangial cells: Up-regulation of the thiol pathway is an adaptational response. Physiological Genomics, 17(3):271-82.
Zhou, G., X. We, H. Liu, M. Schlicht, M.J. Hessner, P.J. Tonellato, M.W. Datta. 2004. BEAR GeneInfo: A tool for identifying gene-related biomedical publications through user modifiable queries. BMC Bioinformatics, 5:46.
Patnaik, M., J. Dlott, R. Fontaine, M.J. Hessner, K. Joyner, M.R. Ledford, E. Lau, C. Moehlenkamp, J. Amos-Wilson, B. Zhang, T. Williams. 2004. Detection of genomic polymorphisms associated with venous thrombosis using the InvaderÒ biplex assay. Journal of Molecular Diagnostics, 2:137-144.
Hessner, M.J., V.K. Singh, X. Wang, S. Khan, M.R. Tschannen, T.C. Zahrt. 2004. Utilization of a labeled tracking oligonucleotide for visualization and quality control of spotted 70-mer arrays. Genomics, 5:12.
Wang, X., N. Jiang, X. Feng, Y. Xie, P. Tonellato, S. Ghosh, M.J. Hessner. 2003. A novel approach for microarray image processing using third-dye array visualization technology. IEEE Transactions on Nanobioscience, 2:103-201.
Waukau, J., S. Jailwala, Y. Wang, H-J. Khoo, S. Ghosh, X. Wang, M.J. Hessner. 2003. The design of a gene chip for functional immunological studies on a high-quality control platform. Annals of the New York >Academy of Sciences, 1005: 284-287.
Pati, N., S. Ghosh, M.J. Hessner, H-J Khoo, X. Wang. 2003. Difference in gene expression profiles between human CD4+CD25+ and CD4+CD25- T cells. Annals of the New York >Academy of Sciences, 1005: 279-283.
Wang, X., M.J. Hessner, Y. Wu, N. Pati, S. Ghosh. 2003. Quantitative quality control in microarray experiments and the application in data filtering, normalization, and false-positive rate prediction. Bioinformatics, 19:1341-1347.
Hessner, M.J., X. Wang, S. Khan, L. Meyer, M. Schlicht, J. Tackes, M.W. Datta, H. J. Jacob, S. Ghosh. 2003. Use of a three-color cDNA microarray platform to measure and control support-bound probe for improved data quality and reproducibility. Nucleic Acids Research, 31:e60.
Hessner M.J., X. Wang, K. Hulse, L. Meyer, Y. Wu, S. Nye, S.W. Guo, S Ghosh. 2003. Three color cDNA microarrays: Quantitative assessment through the use of fluorescein-labeled probes. Nucleic Acids Research, 31:e14.
Ekman, G.C., R. Billingsly, M.J. Hessner. 2002. Rh genotyping: Avoiding false-negative and false-positive results among individuals of African ancestry. American Journal of Hematology 69:34-40.
Raife, T.J., S.R. Lentz, B. Atkinson, S.K. Vesely, M.J. Hessner. 2002. Factor V Leiden: a genetic risk factor for thrombotic microangiopathy in patients with normal von Willebrand factor-cleaving protease activity. Blood 99(2):437-42.
Hessner, M.J., K.D. Friedman, K. Voelkerding, S. Huber, D. Ryan, B. Nucci, M. Ledford. 2001. A multisite study for genotyping of the factor II (Prothrombin) G20210A mutation by the Invader assay. Clinical Chemistry 47:2048-2050.
Hessner, M.J., D.M. Dinauer, R. Kwiatkowski, B. Neri, T.J. Raife. 2001. Measurement of vascular disease-associated polymorphisms among age-stratified volunteer blood donors. Clinical Chemistry 47:1879-1884.
Lazzaro B., A. Anderson, A. Kadacszy-Balla, M.J. Hessner. 2001. Antigenic characterization of medullary carcinoma of the breast:HLA-DR expression in lymph node positive cases. Applied Immunohistochemistry and Molecular Morphology 9:234-241.
Hessner, M.J., Luhm, R.A. 2000. The C536T transition in the tissue factor pathway inhibitor (TFPI) gene does not contribute to risk of venous thrombosis among carriers of factor V Leiden. Thrombosis and Haemostasis 84:424-425.
Curtis, B.R., J.T. Edwards, M.J. Hessner, J.P. Klein, R.H. Aster. 2000. Blood group A and B antigens are strongly expressed on platelets of some individuals. Blood 96:1574-1581.
Hessner, M.J., M.A. Budish, K.D. Friedman. 2000. Genotyping of factor V G1691A (Leiden) without the use of PCR by invasive cleavage of oligonucleotide probes. Clinical Chemistry 46:1051-1056.
Ekman, G.C., M.J. Hessner. 2000. Screening of six racial groups for the intron 5 G→A 3' splice acceptor mutation responsible for the Polynesian Kidd (a-b-) phenotype: the null mutation is not always associated with the JKB allele. Transfusion 40:888-889.
Luhm, R.A., D.B. Bellissimo, A.J. Uzgiris, W.R. Drobyski, M.J. Hessner. 2000. Quantitative evaluation of post- bone marrow transplant engraftment status using fluorescently-labeled variable number of tandem repeats (VNTRs). Molecular Diagnosis 5:129-138.
Ledford, M., K.D. Friedman, M.J. Hessner, C. Moehlenkamp, T.M. Williams, R. Larson. 2000. A multi-site study for detection of the factor V (Leiden) mutation from genomic DNA using a homogeneous InvaderTM microtiter plate fluorescence resonance energy transfer (FRET) assay. Journal of Molecular Diagnostics 2:97-104.
Dinauer, D.M., R.A. Luhm, A.J. Uzgiris, D.D. Eckels, M.J. Hessner. 2000. Sequence-based typing of HLA class II DQB1. Tissue Antigens. 55:364-368.
Dinauer, D.M., K.D. Friedman, M.J. Hessner. 1999. Allelic distribution of the glycoprotein Ia (2-Integrin) C807T/G873A dimorphisms among Caucasian venous thrombosis patients and six racial groups. The British Journal of Haematology. 107:563-565.
Hessner, M.J., D.M. Dinauer, R.A. Luhm, J.L. Endres, R.R. Montgomery, K.D. Friedman. 1999. The prothrombin 20210GA genotypes acts as a cooperative risk factor for venous thrombosis among factor V 1691GA (Leiden) carriers. The British Journal of Haematology. 106:237-239.
Drobyski, W.R., M.J. Hessner, J. Klein, C. Kabler-Babbit, D.H. Vesole, C.A. Keever-Taylor. 1999. T-cell depletion plus salvage immunotherapy with donor leukocyte infusions as a strategy to treat chronic phase chronic myelogenous leukemia patients undergoing HLA-identical sibling or partially matched family donor transplants. Blood. 94:434-441.
Hessner, M.J., R.A. Luhm, S.L. Pearson, D.J. Endean, K.D. Friedman, R.R. Montgomery. 1999. Prevalence of prothrombin G20210A, factor V G1691A (Leiden), and methylene tetrahydrofolate reductase C677T in seven different populations by multiplex allele-specific PCR. Thrombosis and Haemostasis. 81:733-738.
Hessner, M.J., R.A. Pircon, S.T. Johnson, R.A. Luhm. 1999. Prenatal genotyping of the Duffy blood group system by allele-specific polymerase chain reaction. Prenatal Diagnosis. 19:41-45.
Hessner, M.J., S. Shivaram, D.M. Dinauer, B.R. Curtis, D.J. Endean, R.H. Aster. 1999. Neutrophil antigen (Fc RIIIB) SH gene frequencies in six racial groups. Blood. 93:1115-1116.
Hessner, M.J., R.A. Pircon, S.T. Johnson, R.A. Luhm. 1998. Prenatal genotyping of Jka and Jkb of the human Kidd blood group system by allele-specific polymerase chain reaction. Prenatal Diagnosis. 12:1225-1231.
Drobyski, W.R., M.J. Hessner. 1998. The use of the polymerase chain reaction to predict for subsequent relapse in unrelated marrow transplantation for chronic myelogenous leukemia. Leukemia and Lymphoma. 31:317-323.
Juckett, M., P. Rowlings, M.J. Hessner, C.A. Taylor, W. Burns, B. Camitta, J.T. Casper, W.R. Drobyski, G. Hanson, M.M. Horowitz, C Lawton, D.A. Margolis, D. Peitryga, D. Vesole. 1998. T-cell depleted allogeneic bone marrow transplant for high risk non-Hodgkin lymphoma: clinical and molecular follow-up. Bone Marrow Transplantation. 21:893-899.
Drobyski, W.R., C. Pelz, C. Kabler-Babbitt, M.J. Hessner, L.A. Baxter-Lowe, C.A. Keever-Taylor. 1998. Successful unrelated marrow transplantation for patients over the age of 40 with chronic myelogenous leukemia. Biology of Blood and Marrow Transplantation. 4:3-12.
Pearson, S.L., M.J. Hessner. 1998. A1,2BO1,2 genotyping by multiplexed allele-specific polymerase chain reaction. The British Journal of Haematology, 100:229-234.
Hessner, M.J. 1997. Clinical application of allele-specific polymerase chain reaction genotyping for identification of fetuses at risk for immune cytopenic disorders. Biotech Lab International, 2:8-11.
Drobyski, W.R., D.J. Endean, J. Klein, M.J. Hessner. 1997. Detection of BCR/ABL transcripts using the polymerase chain reaction is highly predictive for relapse in patients transplanted with unrelated marrow grafts for chronic myelogenous leukemia. The British Journal of Haematology, 98:458-466.
Hessner, M.J., T.A. Agostini, D.B. Bellissimo, D.J. Endean, R.A. Pircon, N.E. Kirschbaum. 1997. The sensitivity of allele-specific PCR can obviate concern of maternal contamination when fetal samples are genotyped for immune cytopenic disorders. The American Journal of Obstetrics and Gynecology, 176:327-333.
Hessner, M.J., B.R. Curtis, D.J. Endean, R.H. Aster. 1996. Determination of neutrophil antigen NA gene frequencies in five different ethnic groups by the polymerase chain reaction with sequence-specific primers (PCR-SSP). Transfusion, 36:895-899.
Hessner, M.J., J.G. McFarland, D.J. Endean. 1996. Genotyping of K1 and K2 of the human Kell blood group system by the polymerase chain reaction with sequence-specific primers (PCR-SSP). Transfusion, 36:495- 499.
Hessner, M.J., D.J. Endean, J.T. Casper, M.M. Horowitz, C.A. Keever-Taylor, M.S. Roth, N. Flomenberg, W.R. Drobyski. 1995. Use of unrelated marrow grafts compensates for loss of graft-versus-leukemia reactivity after T-cell depleted allogeneic BMT for chronic myelogenous leukemia. Blood, 86:3987-3996.
Skogen, B., D.B. Bellissimo, M.J. Hessner, S. Santoso, R.H. Aster, P.J. Newman, J.G. McFarland. 1994. Rapid determination of platelet alloantigen genotypes by polymerase chain reaction using allele-specific primers. Transfusion, 34:955-960.
Hessner, M.J., M.S. Roth, W.R. Drobyski, L.A. Baxter-Lowe. 1994. Development of a sensitive, highly controlled assay for molecular detection of the Philadelphia chromosome in patients with chronic myelogenous leukemia. Genetic Analysis: Techniques and Applications, 11:90-94.
Hessner, M.J., L.A. Baxter-Lowe. 1992. Characterization of novel HLA-DPB1 alleles by oligotyping and nucleotide sequencing. Tissue Antigens, 40:261-263.
Hessner, M.J., P.J. Wejksnora, M.L.P. Collins. 1991. Construction, characterization, and complementation of Rhodospirillum rubrum puf region mutants. Journal of Bacteriology, 173:5712-5722.
BOOK CHAPTERS:
Wang, X., and M.J. Hessner. Quantitative quality control of microarray experiments: toward accurate gene expression measurements. 2006. In Cambridge >University Press: Gene Expression Profiling by Microarrays - Clinical Implications. Wolf-Karsten Hofmann (editor).
Hessner, M.J. and B.R. Curtis. Prenatal genotyping for identification of fetuses at risk for immune cytopenic disorders. 2004. In: Humana Press, Molecular Diagnostics for the Clinical Laboratorian. W.B. Coleman and G.J. Tsongalis (editors).
Broeckel, U. and M.J. Hessner. 2004. Single Nucleotide Polymorphisms: Testing DNA Variation for Disease Association In: Humana Press, Molecular Diagnostics for the Clinical Laboratorian. W.B. Coleman and G.J. Tsongalis (editors).
Hessner, M.J., X. Wang, S. Ghosh. Genetics of Type 1 Diabetes. 2004 In: Lippencott, Williams and Wilkins, Diabetes Mellitus: A Fundamental and Clinical Text. D. LeRoith, S. Taylor, J. Olefsky (editors).
Hessner, M.J. and D.B. Bellissimo. Prenatal Genotyping of the RhD locus by allele-specific polymerase chain reaction for the identification of fetuses at risk for hemolytic disease of the newborn. 2001. In: Humana Press, Methods in Molecular Medicine, Molecular Pathology Protocols. A. Killeen (editor).
XUJING WANG, PhD
Journal publications/Original Papers:
Geoffrey, R., Jia, S., Kwitek, A.E., Woodliff, J., Ghosh, S., Lernmark, A., Wang X., Hessner M.J.,: Evidence of a Functional Role for Mast Cells in the Development of Type 1 Diabetes Mellitus in the BioBreeding Rat. J. Immunol., Nov.; 177:7275-7286, 2006.
Wang, X., He, Z., Ghosh, S.,: Investigation of the age-at-onset heterogeneity in type 1 diabetes through mathematical modeling. Mathematical Biosciences, 203(1):79-99, 2006.
Smith, E.M., Wang, X., Littrell, J., Eckert, J., Cole, R., Kissebah, A.H., Olivier, M., Comparison of linkage disequilibrium patterns between the HapMap CEPH samples and a family-based cohort of Northern-European descent. Genomics, 88(4):407-14, 2006.
Nittala, A., Ghosh, S., Stefanovski, D., Bergman, R., Wang, X.,: Dimensional analysis of MINMOD leads to definition of the disposition index and improved simulation algorithm. Biomedical Engineering Online. 5(44): doi:10.1186/1475-925X-5-44, 2006.
Guo, S.-W., Magnuson, V.L., Schiller, J.J., Wang, X., Wu, Y., Ghosh, S. Meta-Analysis of Vitamin D Receptor Polymorphisms and Type 1 Diabetes: A HuGE Review of Genetic Association Studies. Am J Epidemiol., Oct. 15; 164(8):711-24, 2006.
Wang, X., Jia, S., Xiang, B., Jiang, N., Meyer, L., Chen, Li.-Y., Moreno-Quinn, C. Ghosh, S. Jacob, H.J., Hessner. M.J. Accurate gene expression measurements by cDNA microarrays utilizing TDAV. BMC bioinformatics. 7(1):378, 2006.
Hessner, M.J., Xiang, B., Jia, S., Geoffrey, R., Holmes, S., Meyer, L., Muheisen, S., Wang, X. Three-color cDNA microarrays with prehybridization quality control yield gene expression data comparable to that of commercial platforms. Physiol Genomics. 25(1): 166-78, 2006.
Wu, Y., Kajdacsy-Balla, A., Strawn, E., Basir, Gloria Halverson Z., Jailwala, P., Wang, Y., Wang, X., Ghosh, S., Guo, S.-W. Transcriptional characterizations of differences between eutopic and ectopic endometrium. Endocrinology, 147:232-246, 2006.
Yang, J., Wang, X., Greene, S., Hessner M.J., Wolf, B.A., Gao, Z. Leucine increases pancreatic beta cell sensitivity to glucose via up-regulation of ATP synthase. Journal of Biological Chemistry, 279:53915-53923, 2004.
Hessner, M.J., Wang, X., Meyer, L. Geoffrey, R., Jia, S., Fuller, J., Lernmark, A., Ghosh, S. Microarray analysis reveals involvement of eosinophils, eotaxin, and underlying pancreatic stress in the prediabetic BioBreeding (BB) rat. Journal of Immunology, 173: 6993-7002, 2004.
Olivier, M., Wang, X., Pennacchio, L.A., Cole, R., Gau, B., Kim J., Rubin, E.M. Hyplotype analysis of the apolipoprotein gene cluster on human chromosome 11. Genomics, 83:912-923, 2004.
Hessner, M. J., Meyer, L., Tackes, J., Muheisen, S., Wang, X. Immobilized support-bound probe and glass surface chemistry as variables in microarray fabrication. BMC genomics, 5:53, 2004.
Hessner, M.J., Singh, V.K., Wang, X., Khan, S., Tschannen, M.R., Zahrt, T.C.,Utilization of Labeled Tracking Oligonucleotide for Visualization and Quality Control of Spotted 70-mer Arrays. BMC genomics, 5:12, 2004.
Wang, X., Jiang, N., Feng, X., Xie, Y., Tonellato, P.J., Ghosh, S., Hessner, M.J. A novel approach for high quality microarray processing using third-dye array visualization technology. IEEE trans. Nanobioscience, 4(2):193, 2003.
Tatay, J.W., Feng, X., Sobczak, H., Jiang, N., Chen, C.F., Kirova, R., Struble, C., Jiang, N., Wang, X., Tonellato, P.J. Multiple approach to data mining of proteomic data based on statistical and pattern classification methods. Proteomics, 3(9):1704-1709, 2003.
Waukau, J., Jailwala, P., Wang, Y., Khoo, H., Ghosh, S., Wang, X., Hessner, M.J. The design of a gene chip for functional immunological studies on a high-quality control platform. Annals of the New York >Academy of Sciences. 1005:284, 2003.
Pati, N., Ghosh, S., Hessner, M.J., Khoo H., and Wang, X. Difference in Gene Expression Profiles Between Fresh Human CD4+CD25+ and CD4+CD25- T Cells. Annals of the New York >Academy of Sciences. 1005:279, 2003.
Hessner, M.J., Wang, X., Khan, S., Meyer, L., Schlicht, M., Tackes, J., Datta, M., Jacob, H.J., Ghosh, S. Use of a three-color cDNA microarray platform to measure and control support-bound probe for improved data quality and reproducibility. Nucl. Acids. Res. 31: e60, 2003.
Wang, X., Hessner, M.J., Wu, Y., Pati, N., Ghosh, S. Quantitative quality control in microarray experiment and the application in data filtering, normalization and false positive rate prediction. Bioinformatics, 19:1341-1347, 2003.
Hessner, M.J., Wang, X., Hulse K., Meyer L., Wu, Y., Nye S., Guo S.-W., Ghosh S. Three color cDNA microarrays: quantitative assessment through the use of Fluorescein-Labeled Probes. Nucl. Acids. Res., 31(4): e14, 2003.
Wang, X., Becker, F.F., Gascoyne, P.R.C. Alterations in membrane dielectric responses precede surface expression of PS or DNA-fragmentation in apoptotic HL-60 cells. Biphys. Biochem. Acta. 1564(2):412-420, 2002.
Wang, Y., Wang, X., Ghosh, S., Guo, S.-W. Is hybridization truly competitive in two-color cDNA microarray experiments? A theoretical modeling and its implications. BioTechniques 32:1342-1346, 2002.
Wang, X., Ghosh, S., Guo, S.-W. Quantitative quality control in microarray image processing and data acquisition. Nucl. Acids. Res. 29(15):e75, 2001.
Yang, J., Huang, Y., Wang, X., Becker, F.F., Gascoyne, P.R.C. Dielectric Properties of Human Leukocyte Subpopulations determined by Electrorotation as a Cell Separation Criterion. Biophys. J. 76: 3307-3314, 1999.
Wang, X., Yang, J., Gascoyne, P.R.C. Role of peroxide in AC electrical field exposure effects on Friend murine erythroleukemia cells during dielectrophoretic manipulations. Biochim. Biophys. Acta 1426(1): 53-68, 1999.
Wang, X., Wang, X.-B., Gascoyne, P.R.C. General expressions for dielectrophoretic force and electrorotational torque derived using the Maxwell Stress Tensor method. J. Electrosta. 39:277-295, 1997.
Wang, X.-B., Huang, Y., Wang, X., Becker, F.F., Gascoyne, P.R.C. Dielectrophoretic manipulation of cells with spiral electrodes. Biophys. J. 72:1887-1899, 1997.
Wang, X., Wang, X.-B., Gascoyne, P.R.C., Becker, F.F. A theoretical method of electrical field analysis for dielectrophoretic electrode arrays using Green's theorem. J. Phys. D. 29:1649-1660, 1996.
Jacques, S.L., Wang, X. Path integral description of light transport in tissue. In Proceedings of the Society for Photon-Optical Instrumentation Engineers. 2979:488-499, 1997.
Publications below were in the field of theoretical physics, which has a tradition of listing authors in alphabetical orders based on last names. In terms of contribution, X. Wang deserves first authorship in all highlighted in blue.
Khviengia, Z., Lu, H., Pope, C.N., Sezgin, E. Wang, X., Xu. K. N=1 superstring theory in 2+2 dimensions. Nucl. Phys. B444:468, 1995.
Lu, H., Pope, C.N., Thielemans, K., Wang, X., Xu. K. Quantising higher-spin string theories. Int. J. Mod. Phys. A10:2123-2142, 1995.
Lu, H., Pope, C.N., Wang, X., Zhao, S. A note on W2,s strings. Phys. Lett. 327B:241, 1994.
Lu, H., Pope, C.N., Wang, X., Zhao, S. Critical and non-critical W2,4 strings. Class. Quantum Grav. 11:939, 1994.
Lu, H., Pope, C.N., Wang, X., Xu. K. The complete cohomology of the W3 string. Class. Quantum Grav. 11:967, 1994.
Lu, H., Pope, C.N., Thielemans, K., Wang, X. Higher-spin strings and W minimal models. Class. Quantum Grav. 11:119, 1994.
Lu, H., Pope, C.N., Wang, X. On higher-spin generalisations of string theory. Int. J. Mod. Phys. A9: 527, 1994.
Lu, H., Pope, C.N., Schrans. S., Wang, X. On the spectrum and scattering of W3 strings. Nucl. Phys. B403:351, 1993.
Lu, H., Pope, C.N., Schrans. S., Wang, X. The interacting W3 string. Nucl. Phys. B403:351, 1993.
Pope, C.N., Sezgin, E., Stelle, K.S., Wang, X. Discrete states in the W3 string. Phys. Lett. 299B:247, 1993.
Lu, H., Pope, C.N., Wang, X., Xu. K. Aspects of N=2 super-Wn strings. Int. J. Mod. Phys. A8:351, 1993.
Lu, H., Pope, C.N., Schrans. S., Wang, X. New realisations of W algebras and W strings. Mod. Phys. Lett. A7:1835, 1992.
Lu, H., Pope, C.N., Schrans. S., Wang, X. On sibling and exceptional W strings. Nucl. Phys. B379:47, 1992.
Lu, H., Pope, C.N., Wang, X., Xu. K. N=2 superstrings with (1,2m) spacetime signature. Phys. Lett. 284B:268, 1992.
Lu, H., Pope, C.N., Wang, X., Xu. K. Anomaly freedom and realisations for super-W3 strings. Nucl. Phys. B379:24, 1992.
Shen, X., Wang, X. Bosonisation of the complex-boson realisations of Winf. Phys. Lett. 278B:63, 1992.
Lu, H., Pope, C.N., Shen, X., Wang, X. The complete structure of WNfrom Winf. Phys. Lett. 267B:356, 1991.
Lu, H., Pope, C.N., Romans, L.J., Shen, X., Wang, X. Polyakov construction of the N=2 super-W3 algebra. Phys. Lett. 264B:91, 1991.
BOOK CHAPTER & REVIEWS
Jia, S., Gao, S., Hessner, M.J., Wang, X. Acquisition of accurate gene expression information from microarray measurements. In Current Trends in Genetic Research, World Scientific Publishing. 2006.
Wang, X., Hessner, M.J. Quantitative quality control of microarray experiments: toward accurate gene expression measurements. In Gene expression profiling by microarrays – clinical implications. Cambridge Press, 2006.
Hessner, M.J., Wang, X., Ghosh S. Genetics of Type 1 Diabetes, A chapter for: Diabetes Mellitus: A Fundamental and Clinical Text. Editors: LeRoith D., Taylor S.I. and Olefsky J.M. Lippincott Williams & Wilkins Publishers, 2004.