PUBLISHED ARTICLES

SCIENTIFIC ARTICLES MEDICAL WRITING PUBLICATIONS

• Zneimer, S. M. (2020). Validation of Fluorescence In Situ Hybridization (FISH) for Clinical Testing. Current Protocols in Human Genetics, e96. doi: 10.1002/cphg.96.
  
• Bik, E, Zneimer, S. et. al., (2019) A novel sequencing-based vaginal health assay combining self-sampling, HPV detection and genotyping, STI detection, and vaginal microbiome analysis.  PLOS ONE  PONE-D-18-10359R2. May 2019.
  
• Gupta S, Zneimer S, et al. (2018) Self-sampling for HPV testing: Increased cervical cancer screening participation and incorporation in international screening programs. Front. Public Health doi: 10.3389/fpubh.2018.00077. March 2018.
• Samango-Sprouse, C., Zneimer, S.M., et al., (2016) Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population. PLOS ONE DOI:10.1371/journal.pone. 0161045 August 11, 2016.
• Liu, S.V., Zneimer, S., Tahbaz A, Douer D. (2011) Therapy Related AML Following Treatment with Trabectedin for Ewing’s Sarcoma.  Acta Hematologica, 126:76-78.
• Cutter, D., & Zneimer, S. M. (2009). Early Acquisition of American Sign Language: An Innovative Approach for Treating Attention-Deficit/Hyperactivity Disorder. Sign Language Journal, 1(1), Retrieved January 8, 2009, from Lifeprint.
• Zneimer, S.M.  (2002) The Human Genome Project: Exploring its progress and successes and the ethical, legal, and social implication.  Clin Leadership and Management Review 16:151-161.
• Zneimer, S.M., P. Cotter, S.D. Stewart (2000).
• Telomere-telomere fusion of chromosomes 7 and 22 with an interstitial deletion of chromosome 7p11.2-p15.1: phenotypic consequences and possible mechanisms.  Clin Genet 58:129-133.
• Zneimer, S.M., B. Zeil, R. Bachman (1998) Partial Trisomy of chromosome 6q, an interstitial duplication of the long arm.  AJMG 80:133-135.
• Zneimer, S.M., J.B. Ravnan, L.S. Jenkins (1997) Assessment of cytogenetic results of 1339 cancer bone marrow chromosome studies.  AJHG 61:A2144.
• Zneimer, S.M. and J.B. Ravnan (1996) Fluorescent in situ hybridization-FISHing for answers.  The Screen, Kaiser Permanente Genetics/Perinatal Newsletter vol. 2, issue 7.
• Ravnan, J.B, LS. Jenkins and S.M. Zneimer (1996) Mosaicism for multiple structural abnormalities in chorionic villus samples confirmed in the fetus.  AJHG 59:A130.
• Cowles, T.A., S.M. Zneimer and F.B. Elder (1996) A prospective cytogenetic study in third trimester placentas of fetuses with unexplained intrauterine growth restriction.  J. Maternal-Fetal Investigation 6:207-209.
• Zneimer, S.M., N.R. Schneider and C.S. Richards (1993) In situ hybridization shows direct evidence of skewed X inactivation in one of monozygotic twin females manifesting Duchenne muscular dystrophy.  AJMG 45:601-605.
• Zneimer, S.M., K.S. Lau, R.L. Eddy, T.B. Shows, D.T. Chuang and R.P. Cox  (1991)  Regional Assignment of two genes of the human branched-chain a-keto acid dehydrogenase complex: the E1B gene (BCKDHB) to chromosome 6p21-22 and the E2 gene (DBT) to 1p31.  Genomics 10:740-747.
• Wilson, G.N., J.P. Stout, N.R. Schneider, S.M. Zneimer, and L.C. Gilstrap (1991)  Balanced translocation 12/13 and situs abnormalities: homology of early pattern formation in man and lower organisms?  Am J Med Genet 38:601-607.
• Fleishman, R.A., D.L. Saltman, V. Stastney and S. Zneimer (1991) Deletion of the c-kit proto-oncogene in the human developmental defect piebald trait.  PNAS 23:10885.
• Zneimer, S.M., D. Crawford, N.R. Schneider and B. Beutler (1990) Mapping of the human ribonuclease inhibitor gene (RNH) to chromosome 11p15 by in situ hybridization.  Genomics 8:175-178.
• Zneimer, S.M. and J.E. Womack (1989) Regional localization of the fibronectin and gamma crystallin genes to bovine chromosome 8.  Genomics 5:215-220.
• Womack, J.E., D.W. Threadgill, Y.D. Moll,   L.K. Faber, M.L. Foreman, A.B. Dietz, T.C. Dobin, L.C. Skow, S.M. Zneimer, D.S. Gallagher and D.S. Rogers  (1989)  Syntenic mapping of 37 loci in cattle.  Cytogenet Cell Genet.
• Zneimer, S.M. and J.E. Womack (1988) Regional localization of the fibronectin and gamma crystallin genes to mouse chromosome 1 by in situ hybridization.  Cytogenet Cell Genet 48:238-241.
• Zneimer, S.M., A.T. Kumamoto and K. Benirschke  (1979)  Banding patterns of the chromosomes of two langur species, Pygathrix nemeus and Presbytis entellus; a comparative study.  Chrom Info Serv 26:19-22.

• Book entitled: Hot Topics in Medicine, Genetics and Biology, Kindle Direct Publishing, 2019
• Book entitled: Cytogenetic Laboratory Management: Chromosomal, FISH and Microarray-Based Best Practices and Procedures.  Wiley Publishers, 2016.
• Book entitled: Cytogenetic Abnormalities: Chromosomal, FISH and Microarray-Based Clinical Reporting.  Wiley Publishers, 2014.
• Essays for Genetics and Inherited Disorders, Salem Press.  Titles of essays include: Genomics and The Human Genome Project, 2011.
• Essays for Magill’s Medical Guide, Sixth Edition, Salem Press.  Title of essay: Biological Therapy, 2011.
• Essays for Salem Sciences: Applied Sciences.  Title of essay: Stem Cell Research and Therapies, 2011.
• Essays for Salem Sciences: Infectious Diseases and Conditions.  Title of essays: Prion diseases, Diagnosis, Treatment and Immune Response, 2010.
• Essays for Salem Press. Title of essay: Proteomics and Protein Engineering, 2010.