SGI Publications

Peer-Reviewed Articles

2007

Davis, A.H.T., Wang, J., Tsang, T.C., Harris, D.T. (2008). Direct sequencing is more accurate and feasible in detecting single nucleotide polymorphisms than RFLP: Using human vascular endothelial growth factor gene as a model. Biological Research in Nursing, In Press.

Edwards, Q., Maradiegue, A., Seibert, D., MacDonald, D., Jasperson, K., Lowstutter, K. & Weitzel, J. (2008). When to suspect and an inherited predisposition to breast cancer. Advance for Nurse Practitioners. In Press.

Seibert, D., Edwards, Q.T., Maradiegue, A. (2007). Integrating genetics into advanced practice nursing curriculum: strategies for success. Community Genet, 10(1):45-51.

Hershberger, P., Klock, S.C. & Barnes, R.B. (2007). Disclosure decisions among pregnant women who received donor oocytes: a phenomenological study. Fertil Steril, 87(2):288-96.

Hutson, S.P. & Alter, B.P. (2007). Experiences of siblings of patients with Fanconi anemia. Pediatr Blood Cancer, 48(1):72-9.

Cabral, W.A., Makareeva, E., Letocha, A.D., Scribanu, N., Fertala, A., Steplewski, A., Keene, D.R., Persikov, A.V., Leikin, S. & Marini, J.C. (2007). Y-position cysteine substitution in type I collagen (alpha1(I) R888C/p.R1066C) is associated with osteogenesis imperfecta/Ehlers-Danlos syndrome phenotype. Hum Mutat. Jan 5; [E-pub ahead of print].

Dillard, J.P., Shen, L., Tluczek, A., Modaff, P. & Farrell, P.J. (2007). The effect of disruptions during counseling on recall of genetic risk information: The case of cystic fibrosis. Genet Couns. Feb 3; [E-pub ahead of print)].

2006

Kerr, M.E., Kamboh, M.I., Kong, Y., Alexander, S. & Yonas, H. (2006). Apolipoprotein E genotype and CBF in traumatic brain injured patients. Adv Exp Med Biol, 578:291-6.

Anderson, G. & Metcalfe, A. (2006). Calling for international collaborative research in nursing, genetics and genomics: A discussion paper. Int J Nurs Stud. [E-pub ahead of print].

Hern, M.J., Beery, T.A. & Barry, D.G. (2006). Experiences of college-ages youths in families with a recessive genetic condition. J Fam Nurs, 12(2):119-42.

Cashion, A., Sabek, O., Driscoll, C., Gaber, L., Kotb, M., & Gaber, O. (2006). Correlation of genetic markers of rejection with biopsy findings following human pancreas transplant. Clin Transplant, 20(1):106-12.

Cheek D.J., Smith, H.M. & Good, J. (2006). New respect for the humble endothelium. Nursing, 36(3):44-7.

Edkins, R., Cheek, D. (2006). Pharmacogenetics. In M. runge & C Patterson (Eds.), Principles of molecular medicine (2^nd ed.). Totowa, N.J.: Humana Press.

Day, S. & Chismark, E. (2006). The cognitive and academic impact of sickle cell disease. J Sch Nurs, 22(6):330-5.

Morris, A.P. Tawil, A., Berkova, Z., Wible, L., Smith, C.W. & Cunningham, S.A. (2006). Junctional Adhesion Molecules (JAMs) are differentially expressed in fibroblasts and co-localize with ZO-1 to adherens-like junctions. Cell Commun Adhes, 13(4):233-47.

Avila, J.R., Jezewski, P.A., Vieira, A.R., Orioli, I.M., Castilla, E.E., Christensen, K., Daack-Hirsch, S., Romitti, P.A., Murray, J.C. (2006). PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations. Am J Med Genet, 140(23):2562-70.

Edwards, Q.T., Maradiegue, A., Seibert, D., Macri, C. & Sitzer, L. (2006). Faculty members' perceptions of medical genetics and its integration into nurse practitioner curricula. J Nurs Educ, 45(3):124-30.

Sharma, S.M., Hu, R., Bronisz, A., Meadows, N., Lusby, T., Fletcher, B., Hume, D.A., Cassady, A.I. & Ostrowski, M.C. (2006). Genetics and genomics of osteoclast differentiation: integrating cell signaling pathways and gene networks. Crit Rev Eukaryot Gene Expr, 16(3):253-77.

Frazier, L., Calvin, A.O., Mudd, G.T. & Cohen, M.Z. (2006). Understanding of genetics among older adults. J Nurs Scholarsh, 38(2):126-32.

Skirton, H., Frazier, L.Q., Calvin, A.O. & Cohen, M.Z. (2006). A legacy for the children – attitudes of older adults in the United Kingdom to genetic testing. J Clin Nurs, 15(5):565-73.

Giarratano, G. (2006). Genetic influences on preterm birth. Am J Matern Child Nurs, 31(3):169-75.

Hardie, T.L., Moss, H.B. & Lynch, K.G. (2006). Genetic correlations between smoking initiation and smoking behaviors in a twin sample. Addict Behav, 31(11):2030-7.

Schutte, D.L. & Holston, E.C. (2006). Chronic dementing conditions, genomics, and new opportunities for nursing interventions. J Nurs Scholarsh, 38(4):328-34.

Jacob, E., Miaskowski, C., Savedra, M., Beyer, J.E., Treadwell, M., Styles, L. (2006). Changes in sleep, food intake, and activity levels during acute painful episodes in children with sickle cell disease. Journal of Pediatric Nursing, 21(1):23-34.

Johnson, R.L., Williams, S.M. & Spruill, I.J. (2006). Genomics, nutrition, obesity, and diabetes. J Nurs Scholarsh, 38(1):11-8.

Park, N.J. & Kang, D.H. (2006). Breast cancer risk and immune responses in healthy women. Oncol Nurs Forum, 33(6):1151-9.

Lewis, J.A. (2006). Genetics: another nursing specialty. Am J Matern Child Nurs, 31(3):142.

Lewis, J.A., Calzone, K.M. & Jenkins, J. (2006). Essential nursing competencies and curricula guidelines for genetics and genomics. Am J Matern Child Nurs, 31(3):146-53.

Maradiegue, A. & Edwards, Q.T. (2006). An overview of ethnicity and assessment of family history in primary care settings. J Am Acad Nurse Pract, 18(10):447-56.

Reyes-Gibby, C.C., Shete, S., Rakvag, T., Bhat, S.V., Skorpen, F., Bruera, E., Kaasa, S. & Klepstad, P. (2006). Exploring joint effects of genes and the clinical efficacy of morphine for cancer pain: OPRM1 and COMT gene. Pain, Dec 5; [E-pub ahead of print].

Tluczek, A., Koscik, R.L., Modaff, P., Pfeil, D., Rock, M.J., Farrell, P.M., Lifchez, C., Freeman, M.E., Gershan, W., Zaleski, C. & Sullivan, B.J. (2006). Newborn screening for cystic fibrosis: parents’ preferences regarding counseling at the time of the infants’ sweat test. Genet Couns, 15(4):277-91.

Twomey, J.G. (2006). Issues in genetic testing of children. Am J Matern Child Nurs, 31(3):156-63.

2005

Beery, T. T. (2005). The genetics of cardiac arrhythmias. Biolological Research for Nursing, 6 (4), 249-261.

Constantin, C.M. (2005). Genetics in Clinical Practice: a Team Approach. Journal of Midwifery and Womens Health, 50(3), 252-253.

Constantin, C.M., Faucett, A., Lubin, I.M. (2005). A primer on genetic testing.
Journal of Midwifery and Womens Health, 50(3), 197-204.

Mansilla, M. A., Kimani, J., Mitchell, L.E., Christensen, K., Boomsma, D.I., Daack-Hirsch, S., et al. (2005). Discordant MZ twins with cleft lip and palate: a model for identifying genes in complex traits. Twin Research and Human Genetics, 8 (1), 39-46.

Scott NM, Weinberg SM, Neiswanger, K., Daack-Hirsch, S., O'Brien, S., Murray, J.C., Marazita, M.L. (2005). Dermatoglyphic pattern types in subjects with nonsyndromic cleft lip with or without cleft palate (CL/P) and their unaffected relatives in the Philippines. Cleft Palate Craniofacial Journal, 42(4), 362-366.

Scott, N.M., Weinberg, S.M., Neiswanger, K., Brandon, C.A., Daack-Hirsch, S., Murray, J.C., Liu, Y.E., & Marazita, M.L. (2005). Dermatoglyphic fingerprint heterogeneity among individuals with nonsyndromic cleft lip with or without cleft palate and their unaffected relatives in China and the Philippines. Human Biology. 77(2), 257-266.

Vieira, A.R., Avila, J.R., Daack-Hirsch, S., Dragan, E., Felix, T.M., Rahimov, F., Harrington, J., Schultz, R.R., Watanabe, Y., Johnson, M., Fang, J. & O'brien, S.E., Orioli IM, Castilla EE, Fitzpatrick DR, Jiang R, Marazita ML, Murray JC. (2005). Medical sequencing of candidate genes for nonsyndromic cleft lip and palate. PLoS Genetics, 1(6), e64.

Graham, J. M., Jr., Gomez, M., Halberg, A., Earl, D. L., Kreutzman, J. T., Cui, J., et al. (2005). Management of deformational plagiocephaly: repositioning versus orthotic therapy. Journal of Pediatrics, 146 (2), 258-262.

Frazier, L., Johnson, R.L., & Sparks, E. (2005). Genomics and cardiovascular disease. Journal of Nursing Scholarship, 37(4):315-321.

Giger, J.N., Strickland, O.L., Weaver, M., Taylor, H., & Acton, R.T. (2005). Genetic predictors of coronary heart disease risk factors in premenopausal African-American women. Ethnicity and Disease, 15(2):221-232.

Holston, E.C. (2005). Stigmatization in Alzheimer's disease research on African American elders. Issues in Mental Health Nursing, 26(10):1103-1127.

Jacob, E., Beyer, J. E., Miaskowski, C., Savedra, M., Treadwell, M., & Styles, L. (2005). Are there phases to the vaso-occlusive painful episode in sickle cell disease? Journal of Pain and Symptom Management, 29 (4), 392-400.

Jacob, E., Miaskowski, C., Savedra, M., Beyer, J. E., Treadwell, M., & Styles, L. (2005). Trends in complete blood count values during acute painful episodes in children with sickle cell disease. Journal of Pediatric Oncology Nursing, 22 (3), 152-159.

Jamerson, P. A. (2005). The association between acute fatty liver of pregnancy and fatty acid oxidation disorders. Journal of Obstetric Gynecologic and Neonatal Nursing 34 (1), 87-92.

Keltner, N.L. (2005). Genomic influences on schizophrenia-related neurotransmitter systems. Journal of Nursing Scholarship, 37(4):322-328.

Letocha, A. D., Cintas, H. L., Troendle, J. F., Reynolds, J. C., Cann, C. E., Chernoff, E. J., et al. (2005). Controlled trial of pamidronate in children with types III and IV osteogenesis imperfecta confirms vertebral gains but not short-term functional improvement. Journal of Bone and Mineral Research, 20 (6), 977-986.

Cabral, W. A., Makareeva, E., Colige, A., Letocha, A.D., Ty, J.M., Yeowell, H.N., et al. (2005). Mutations near amino end of alpha1(I) collagen cause combined osteogenesis imperfecta/Ehlers-Danlos syndrome by interference with N-propeptide processing. Journal of Biological Chemistry, 280 (19), 19259-19269.

Maradiegue, A., Edwards, Q.T., Seibert, D., Macri, C., & Sitzer, L. (2005). Knowledge, perceptions, and attitudes of advanced practice nursing students regarding medical genetics. Journal of the American Academy Nurse Practitioners. (11):472-479.

McLemore, M. R., & Aouizerat, B. (2005). Introducing the MUC16 gene: implications for prevention and early detection in epithelial ovarian cancer. Biological Research for Nursing, 6 (4), 262-267.

Axilbund, J.E., Hamby, L.A., Thompson, D.B., Olsen, S.J., & Griffin, C.A. (2005). Assessment of the use and feasibility of video to supplement the genetic counseling process: a cancer genetic counseling perspective. Journal of Genetic Counseling, 14(3), 235-243.

McLean, D. C., Jr., Spruill, I ., Argyropoulos, G., Page, G.P., Shiver, M.D., & Garvey, W. T. (2005). Mitochondrial DNA (mtDNA) haplotypes reveal maternal population genetic affinities of Sea Island Gullah-speaking African Americans. American Journal Physical Anthropology, 127 (4), 427-438.

Tluczek, A., Koscik, R L., Farrell, P.M., & Rock, M. J. (2005). Psychosocial risk associated with newborn screening for cystic fibrosis: parents' experience while awaiting the sweat-test appointment. Pediatric, 115 (6), 1692-1703.

Dillard, J.P. & Tluczek, A.(2005). Information flow after a positive newborn screening for cystic fibrosis. Journal of Pediatrics,147(3 Suppl):S94-97.

Kimmel, R.J., Kovacs, I.,Vrabel, C., Wood, B., Schalling, M., Kelsoe, J.R. (2005).Cosegregation of bipolar disorder and autosomal-dominant medullary cystic kidney disease in a large family. American Journal of Psychiatry, 162(10), 1972-1974.

Whitt, K.J. (2005). Experiences from the National Institute of Nursing Research: Summer Genetics Institute 2004. Policy Politics and Nursing Practice, (1), 15-16.

Farina, L. & Winkelman, C. (2005). A review of the role of proinflammatory cytokines in labor and noninfectious preterm labor. Biological Research for Nursing, 6 (3), 230-238.

Wung, S.F. & Merkle, C.J. (2005). BRCA1 genetic mutation and its link to ovarian cancer: implications for advanced practice nurses. Journal of the American Academy of Nurse Practitioners, 17(12):518-526.

2004

Beery, T. A. & Hern, M. J. (2004). Genetic practice, education, and research: an overview for advanced practice nurses. Clinical Nurse Specialist, 18 (3), 126-32; quiz 133-134.

Beery, T. A. & Shooner, K. A. (2004). Family history: the first genetic screen. Nurse Practitioner, 29 (11), 14-25.

Cashion, A. K., Driscoll, C. J., & Sabek. O. (2004). Emerging genetic technologies in clinical and research settings. Biological Research for Nursing, 5 (3), 159-167.

Manthei, E. R., Siminerio, L.M., Conley, Y., Charron-Prochownik, D., Feathers, A.S., Charles, B., et al. (2004). Genetics and type 1 diabetes: online resources for diabetes educators. Diabetes Educator, 30 (6), 961-971.

Marazita, M. L., Murray, J.C., Lidral, A.C., Arcos-Burgos, M., Cooper, M.E., Goldstein, T., Maher, B.S., Daack-Hirsch, S., et al. (2004). Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. American Journal of Human Genetics, 75 (2), 161-173.

Munger, R. G., Sauberlich, H. E., Vorvoran, C., Nepomucceno, B., Daack-Hirsch, S. & Solon, F.S. et al. (2004). Maternal vitamin B-6 and folate status and risk of oral cleft birth defects in the Philippines. Birth Defects Research Part A Clinical and Molecular Teratology, 70 (7), 464-471.

Schultz, R. E.,Cooper, M.E., Daack-Hirsch, S., Shi, M., Nepomuccena, B., Graf, K.A., et al. (2004). Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families. American Journal of Medical Genetics Part A, 125 (1), 17-22.

Zucchero, T.M., Cooper, M.E., Maher, B.S., Daack-Hirsch, S., Nepomuceno, B., Ribeiro, L., et. al. (2004). Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. New England Journal of Medicine, 351(8):769-780.

Dudley-Brown, S. (2004). The genetic family history assessment in gastroenterology nursing practice. Gastroenterology Nursing, 27 (3), 107-110.

Dudley-Brown, S. (2004). A shot of good cholesterol: synthetic HDL, a new intervention for atherosclerosis. Journal of Cardiovascular Nursing, 19 (6), 421-424.

Edwards, Q. T., Seibert, D., Macri, C., Covington, C., & Tilghman, J. (2004). Assessing ethnicity in preconception counseling: genetics--what nurse practitioners need to know. Journal of American Academy of Nurse Practitioners, 16 (11), 472-480.

Frazier, L., Meininger, J., Halsey, Lea D., & Boerwinkle, E. (2004). Genetic discoveries and nursing implications for complex disease prevention and management. Journal of Professional Nursing, 20 (4), 222-229.

Frazier,L., Turner, S.T., Schwartz ,G.L., Chapman ,A.B., & Boerwinkle, E. (2004). Multilocus effects of the renin-angiotensin-aldosterone system genes on blood pressure response to a thiazide diuretic. Pharmacogenomics Journal. 4(1), 17-23.

Giger, J. N. (2004). Understanding genetics: the relationship of disease and genetic predisposition in African-Americans. Journal of the National Black Nurses Association, 15(2), vii-viii.

Holston, E. C. & Schutte, D. L. (2004). The clinical utility of genetic information in the care of persons with Alzheimer's disease. Medsurg Nursing, 13 (6), 415-419.

Hutson, S. P. & Loud, J. T. (2004). Cancer genetics resources: an organizational guide for nurses and patients. Seminars in Oncology Nursing, 20 (3) 213-215.

Loud, J. T. & Hutson, S. P. (2004). The art and science of cancer nursing in the genomic era. Seminars in Oncology Nursing, 20 (3), 143-144.

Jacob, E. (2004). Neuropathic pain in children with cancer. Journal of Pediatric Oncology Nursing, 21 (6), 350-357.

Keltner, N. L. (2004). Summer Genetics Institute. Perspectives in Psychiatric Care 40 (4), 133-134.

Olsen, S., Dudley-Brown, S., & McMullen, P. (2004). Case for blending pedigrees, genograms and ecomaps: nursing's contribution to the 'big picture'. Nursing and Health Sciences, 6 (4), 295-308.

Ramirez, C. T. & McKelvey, K.D. (2004). Genetics of Cardiovascular Diseases: an Overview. Proceedings of the International Society of Nurse Geneticists Meeting.

Roscigno, C. I. (2004). Neuronal pathway finding: from neurons to initial neural networks. Journal of Neuroscience Nursing, 36 (5), 263-272.

Spruill, I. (2004). Project Sugar: a recruitment model for successful African-American participation in health research. Journal of the National Black Nurses Association, 15 (2), 48-53.

Horner, S. D., Abel, E., Taylor, K., & Sands, D. (2004). Using theory to guide the diffusion of genetics content in nursing curricula. Nursing Outlook 52 (2), 80-84.

Markowitz, J. A., Tinkle, M.B., & Fischbeck, K. H. (2004). Spinal muscular atrophy in the neonate. Journal of Obstetric, Gynecologic and Neonatal Nursing, 33 (1), 12-20.

Twomey, J. G. (2004). Genetic testing of children: confluence or collision between parents and professionals? AACN Clinical Issues, 13 (4), 557-566.

Winkelman, C. (2004). Genomics. What every critical care nurse needs to know about the genetic contribution to critical illness. Critical Care Nurse., 24(3), 34-45.

Wung SF, Aouizerat BE. (2004). Newly mapped gene for thoracic aortic aneurysm and dissection. Journal of Cardiovascular Nursing, 19(6), 409-16.

2003

Beery, T., Dyment, M., Schooner, K., Knilans, T., & Benson, W. (2003). A candidate locus approach identifies a long QT syndrome gene mutation. Biological Research in Nursing, 5 (2), 97-104.

Beery, T.A. (2003). Sex differences in infection and sepsis. Critical Care Nursing Clinics North American, 15 (1), 55-62.

Cashion, A.K., & Driscoll, C.J. (2003). Genetics and kidney dysfunction. Nephrology Nursing Journal, 31 (1), 14-18, 29 .

Velasquez-Mieyer, P.A., Cowan, P.A., Umpierrez, G.E., Lustig, R.H., Cashion, A.K., & Burghen, G.A. (2003). Racial differences in glucagon-like peptide-1 (GLP-1) concentrations and insulin dynamics during oral glucose tolerance test in obese subjects. International Journal of Obesity Related Metabolic Disorders, 27 (11), 1359-1364.

Cheek, D.J., & Cesan, A. (2003). Genetic predictors of cardiovascular disease: the use of chip technology. Journal of Cardiovascular Nursing, 18 (1), 505-506.

Jezewski, PA., Vieira, AR., Nishimura, C., Ludwig, B., Johnson, M., O'Brien, SE., Daack-Hirsch, S., et al. (2003). Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate. Journal of Medical Genetics, 40 (6), 399-407.

Schweitzer, D.N., Yano, S., Earl, D.L., & Graham, J.M Jr. (2003). Johnson-McMillin syndrome, a neuroectodermal syndrome with conductive hearing loss and microtia: report of a new case. American Journal of Medical Genetics. 120A (3), 400-405.

Frazier, L. (2003). Novel predictors of acute coronary syndrome outcomes. Biological Research for Nursing, 5 (1), 30-36.

Tsujino, K., Tsukahara, M., Frazier, L., Lino H., & Murakami, K. (2003). Genetic content in Japanese language nursing textbooks. Research and Theory in Nursing Practice, 17 (4), 353-362.

Giger, J.N. (2003). Human genetics: can we reallyeliminatehealth disparities.
Journal of the National Black Nurses Association,14 (1), vii-viii.

Bolton, L.B., Giger, J.N., & Georges, A. (2003). Eliminating structural and racial barriers: a plausible solution to eliminating health disparities. Journal of National Black Nurses Association, 14 (1), 57-65.

Hutson, S.P. (2003). Attitudes and psychological impact of genetic testing, genetic counseling, and breast cancer risk assessment among women at increased risk. Oncology Nursing Forum, 30 (2), 241-246.

Kang, D. (2003). Psychoneuroimmunology in nursing research: a biobehavioral model. Research in Nursing and Health, 26, 421-423.

Lewis, J.A. (2003). Genetic testing: a personal story of one nurse's involvement in health policy. Newborn and Infant Nursing Reviews, 3 (1), 11-12.

Olsen, S.J., Feetham, S.L., Jenkins, J., Lewis, J., Nissly, T.L., Sigmon, H.D., et al.. (2003). Creating a vision for leadership in genetics. Medsurg Nursing, 12 (3), 177-183.

Phillips M. (2003). Genetics of hearing loss. Medsurg Nursing. 12 (6), 386-390, 411.

Garvey, T., McLean, D., & Spruill, I. (2003). The search for obesity genes in isolated populations: Gullah-speaking African Americans and the role of uncoupling protein 3 as a thrifty gene. Progress in Obesity Research, (9), 373-379.

McLean, D., Spruill, I., Gevano, S., Morrison, E. Y., Bernard, O.S.., Argyropoulos, G., et al. (2003). Three novel mtDNA site polymorphisms allow exploration of population affinities of African Americans. Human Biology, 75 (2), 147-161.

Wung, S.F., & Aouizerat, B.E. (2003). Gender and ethnic differences in a case-control study of dyslipidemia: using apolipoprotein A-V gene as an exemplar in cardiovascular genetics. Research and Theory for Nursing Practice: An International Journal, 17 (4), 281-299; discussion 335-338.

Codori, A.M., Zawacki, K.L., Petersen, G.M., Miglioretti, D.L., Bacon, J.A., Trimbath, J.D., et al. (2003). Genetic testing for hereditary colorectal cancer in children: long-term psychological effects. American Journal of Medical Genetics, 116A (2), 117-128.

2002

Cashion, A. (2002). Genetics in transplantation. Medsurg Nursing, 11 (2), 91-94.

Frazier, L. & Ostwald, S. K. (2002). Genetics and gerontological nursing: a need to stimulate research. Annual Review of Nursing Research, 20, 323-337.

Hardie, T.L. (2002). The genetics of substance abuse. AACN Clinical Issues, 13 (4), 511-522.

Kang, D.H. (2002). Oxidate stress, DNA damage, and breast cancer. AACN Clinical Issues, 13 (4), 540-549.

Long, J., Covington, C., Delaney-Black, V., & Nordstrom B. (2002). Allelic variation and environmental lead exposure in urban children. AACN Clinical Issues, 13 (4), 550-556.

Marlowe, A., Pepin, M.G., & Byers, P.H. (2002). Testing for osteogenesis imperfecta in cases of suspected non-accidental injury. Journal of Medical Genetics, 39, 382-386.

Olsen, S. (2002). Cancer genetics: information sources for patients and families. Cancer Practice, 10 (6), 323-326.

Sparks, E.A., & Frazier, L.Q. (2002). Heritable cardiovascular disease in women. Journal of Obstetric, Gynecologic and Neonatal Nursing, 31 (2), 217-228.

Arad, M., Benson, W., Perez-Atayde, A.R., McKenna, W.J., Sparks, E.A., Kanter, R.J., et al. (2002). Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy. Journal of Clinical Investigation, 109 (3), 357-362.

Raman, S.V., Sparks, E.A., Boudooulas, H., & Wooley, CF. (2002). Tricuspid valve Disease: Tricuspid valve complex perspective. Current Problems in Cardiology, 27 (3), 97-144.

Tinkle, M.B. (2002). Cystic fibrosis carrier screening. Are nurses ready to be on the front line? AWHONN Lifelines, 6 (2), 134-139.

Tinkle, M.B., & Castora F. (2002). Mitochondrial disorders, a clinician's primer. Medsurg Nursing, 11 (1), 25-29.

Tinkle, M.B., & Cheek, D.J. (2002). Human genomics: challenges and opportunities. Journal of Obstetric, Gynecologic and Neonatal Nursing, 31 (2), 178-187.

Twomey, J. G. (2002). Considerations for policies regarding genetic testing of children. Policy, politics & nursing practice, 3 (2), 140-148.

Twomey, J. G. (2002). How wise is it to screen all newborns for cystic fibrosis? Newborn and Infant Nursing Reviews, 2 (4), 214-220.

Wung, S.F. (2002). Genetic advances in coronary artery disease. Medsurg Nursing, (6), 296-300.

Zawacki, K.L. (2002). Hereditary cancer syndromes of the gastrointestinal system. AACN Clinical Issues, 13 (4), 523-539.

Zawacki, K.L., & Phillips, M. (2002). Cancer genetics and women's health. Journal of Obstetric, Gynecologic and Neonatal Nursing, 31 (2), 208-216.

2000/2001

Buxton, I.L., Kaiser, R.A., Oxhorn, B.C., & Cheek, D.J. (2001). Evidence supporting the nucleotide axis hypothesis, ATP release and metabolism by coronary endothelium. American Journal of Physiology, Heart and Circulatory Physiology, 281, 1657-1666.

Persing BF, Cheek DJ. (2000). Pharmacogenomics. Nursing Clinics of North America, 35(4), 975-80.

Kang, D.H. (2001). Molecular and genetic epidemiology. Experimental Molecular Medicine, 33 (1 Suppl), 73-82. Korean.

Chapters in Books, Newsletters, Testimony

Bove, C, & Twomey, J. (2004). Advocacy for patients considering genetic testing. In Nursing Ethics Continuing Education Series, Sara Fry, (Ed.). New England Research Institute , https://www.nursingethicsce.com/courselisting.asp

Lewis, J. A. (2004). Testimony of Virginia nurse to Secretary's Advisory Committee on genetics, health & society. Virginia Nurses Today , 11.

Lewis, S. M. and D. Kang. (2004). Genetics and altered immune responses. In S.M. Lewis, M.M. Heitkemper & S.R. Dirksen (Eds.) Medical surgical nursing . Assessment and management of clinical problems. St. Louis, MO: Mosby.

Roscigno, C. I. (2004). Genetics for the neuroscience nurse part I: transmission of single gene disorders. Neurotransmitter: The Official Newsletter of the Northwest Chapter of AANN , 5-15.

Roscigno, C. I. (2004). Genetics for the neuroscience nurse part II: Genetic association studies: the biologic processes neuroscience nurses need to know. Neurotransmitter: The Official Newsletter of the Northwest Chapter of AANN ,: 4-11