Beverly M. Snively, Ph.D.
Professor, Department of Biostatistics
Research Interests
aging, atherosclerosis/thrombosis, genetics/genome, minority health issues, women's health issues
Contact Information
Academic: 336-713-0030 | Department: 336-713-0030
Email: bmellen@wakehealth.edu
Recent Publications
Poehling KA, Edwards KM, Griffin MR, Szilagyi PG, Staat MA, Iwane MK, Snively BM, Suerken CK, Hall CB, Weinberg GA, Chaves SS, Zhu Y, McNeal MM, Bridges CB.
The burden of influenza in young children, 2004-2009. Pediatrics. 2013;131(2):207-216.
Qayyum R, Snively BM, Ziv E, Nalls MA, Liu Y, Tang W, Yanek LR, Lange L, Evans MK, Ganesh S, Austin MA, Lettre G, Becker DM, Zonderman AB, Singleton AB, Harris TB, Mohler ER, Logsdon BA, Kooperberg C, Folsom AR, Wilson JG, Becker LC, Reiner AP.
A meta-analysis and genome-wide association study of platelet count and mean platelet volume in African Americans. PLoS Genet. 2012;8(3):e1002491.
Brashear A, Cook J, Amponsah A, Hill D, Snively B, Light L, Suerken C, McCall WV, Boggs N, Stacy M, Ozelius L, Sweadner K. Psychiatric and neurocognitive morbidity in rapid-onset dystonia Parkinsonism [abstract]. Neurology. 2012;78(Suppl 1):P01.225.
McLaren CE, McLachlan S, Garner CP, Vulpe CD, Gordeuk VR, Eckfeldt JH, Adams PC, Acton RT, Murray JA, Leiendecker-Foster C, Snively BM, Barcellos LF, Cook JD, McLaren GD.
Associations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations. PLoS ONE. 2012;7(6):e38339.
David SP, Hamidovic A, Chen GK, Bergen AW, Wessel J, Kasberger JL, Brown WM, Petruzella S, Thacker EL, Kim Y, Nalls MA, Tranah GJ, Sung YJ, Ambrosone CB, Arnett D, Bandera EV, Becker DM, Becker L, Berndt SI, Bernstein L,.
Genome-wide meta-analyses of smoking behaviors in African Americans. Transl Psychiatry. 2012;2():e119.
Brashear A, Cook JF, Hill DF, Amponsah A, Snively BM, Light L, Boggs N, Suerken CK, Stacy M, Ozelius L, Sweadner KJ, McCall WV.
Psychiatric disorders in rapid-onset dystonia-parkinsonism. Neurology. 2012;79(11):1168-1173.
Brashear A, Mink JW, Hill DF, Boggs N, McCall WV, Stacy MA, Snively B, Light LS, Sweadner KJ, Ozelius LJ, Morrison L.
ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia. Dev Med Child Neurol. 2012;54(11):1065-1067.
McLaren CE, Garner CP, Constantine CC, McLachlan S, Vulpe CD, Snively BM, Gordeuk VR, Nickerson DA, Cook JD, Leiendecker-Foster C, at al.
Genome-wide association study identifies genetic loci associated with iron deficiency. PLoS ONE. 2011;6(3):e17390.
Brashear A, Hill DF, Boggs N, Ozelius L, Sweadner KJ, Light L, Stacy M, Snively BM, McCall WV. Psychosis: part of the rapid-onset dystonia-Parkinsonism (RDP) phenotype? [abstract]. Neurology. 2011;76(9 Suppl 4):A640.
Poehling KA, Szilagyi PG, Staat MA, Snively BM, Payne DC, Bridges CB, Chu SY, Light LS, Prill MM, Finelli L, et al.
Impact of maternal immunization on influenza hospitalizations in infants. Am J Obstet Gynecol. 2011;204(6 Suppl 1):S141-S148.
Reiner AP, Lettre G, Nalls MA, Ganesh SK, Mathias R, Austin MA, Lohman K, Yang L, Liu Y, Snively BM, et al.
Genome-wide association study of white blood cell count in 16,388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT). PLoS Genet. 2011;7(6):e1002108.
McLaren CE, McLachlan S, Garner CP, Vulpe CD, Gordeuk VR, Eckfeldt JH, Adams PC, Acton RT, Murray JA, Leiendecker-Foster C, Snively BM, Barcellos LF, Cook JD, McLaren GD. Associations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations [abstract]. Blood. 2011;118(21):922.
McLaren CE, Barton JC, Eckfledt JH, McLaren GD, Acton RT, Adams PC, Henkin LF, Gordeuk VR, Vulpe CD, Snively BM, et al.
Heritability of serum iron measures in the Hemochromatosis and Iron Overload Screening (HEIRS) family study. Am J Hematol. 2010;85(2):101-105.
Poehling KA, Light LS, Rhodes M, Snively BM, Halasa NB, Mitchel E, Schaffner W, Craig AS, Griffin MR.
Sickle cell trait, hemoglobin C trait, and invasive pneumococcal disease. Epidemiology. 2010;21(3):340-346.
Brashear A, Hill D, Snively BM, Sweadner KJ, Ozelius L. De novo and recurrent mutations in ATP1A3 are common in rapid-onset dystonia-Parkinsonism [abstract]. Neurology. 2010;74(9 Suppl 2):A204.
Brashear A, Hill DF, Snively B, Sweadner KJ, Ozelius L. Now triggers in rapid-onset dystonia-Parkinsonism (RDP) [abstract]. Neurology. 2010;74(9 Suppl 2):A205.
Rodriguez BL, Dabelea D, Liese AD, Fujimoto W, Waitzfelder B, Liu L, Bell R, Talton J, Snively BM, Kershnar A, et al.
Prevalence and correlates of elevated blood pressure in youth with diabetes mellitus: the SEARCH for diabetes in youth study. J Pediatr. 2010;157(2):245-251.
Adams PC, Barton JC, McLaren GD, Acton RT, Speechley M, McLaren CE, Reboussin DM, Leiendecker-Foster C, Harris EL, Snively BM, et al.
Screening for iron overload: lessons from the Hemochromatosis and Iron Overload Screening (HEIRS) Study. Can J Gastroenterol. 2009;23(11):769-772.
Washburn LK, Nixon PA, Snively BM, O'Shea TM. Early weight gain and outcomes at 9 years in very low birth weight children [abstract]. J Dev Orig Health Dis. 2009;1(Suppl 1):S223.
McLaren CE, Garner CP, Constantine CC, Masle S, Vulpe CD, Snively BM, Cook JD, Nickerson DA, Leiendecker-Foster C, Reboussin DM, et al. Genome-wide association study identifies genetic loci associated with iron deficiency [abstract]. Blood. 2009;114(22):1552-1553.
McLaren CE, Gordeuk VR, Chen W-P, Barton JC, Acton RT, Speechley M, Castro O, Adams PC, Snively BM, Reboussin DM, et al.
Bivariate mixture modeling of transferrin saturation and serum ferritin concentration in Asians, African Americans, Hispanics, and whites in the Hemochromatosis and Iron Overload Screening (HEIRS) Study. Transl Res. 2008;151(2):97-109.
Albers JJ, Marcovina SM, Imperatore G, Snively BM, Stafford J, Fujimoto WY, Mayer-Davis EJ, Petitti DB, Pihoker C, Dolan L, et al.
Prevalence and determinants of elevated apolipoprotein B and dense low-density lipoprotein in youths with type 1 and type 2 diabetes. J Clin Endocrinol Metab. 2008;93(3):735-742.
Acton RT, Barton JC, Passmore LV, Adams PC, McLaren GD, Leiendecker-Foster C, Speechley MR, Harris EL, Castro O, Snively BM, et al.
Accuracy of family history of hemochromatosis or iron overload: the Hemochromatosis and Iron Overload Screening Study. Clin Gastroenterol Hepatol. 2008;6(8):934-938.
Maahs DM, Snively BM, Beyer J, Imperatore G, Bell R, Mayer-Davis EJ, Dolan LM, Pettitt DJ, Hirsch I, Rodriguez B, et al.
Weight and elevated albumin to creatinine ratio in youth with diabetes: the SEARCH for Diabetes in Youth study. Pediatr Nephrol. 2008;23(12):2255-2260.
McLaren GD, McLaren CE, Adams PC, Barton JC, Reboussin DM, Gordeuk VR, Acton RT, Harris EL, Speechley MR, Snively BM, et al.
Clinical manifestations of hemochromatosis in HFE C282Y homozygotes identified by screening. Can J Gastroenterol. 2008;22(11):923-930.
McLaren CE, Barton JC, McLaren GD, Acton RT, Adams PC, Henkin LF, Gordeuk VR, Eckfeldt JH, Vulpe CD, Snively BM, et al. Heritability of iron status phenotype in the Hemochromatosis and Iron Overload Screening (HEIRS) Family Study [abstract]. Blood. 2008;112(11):49.
Harris EL, McLaren CE, Reboussin DM, Gordeuk VR, Barton JC, Acton RT, McLaren GD, Vogt TM, Snively BM, Passmore LV, et al.
Serum ferritin and transferrin saturation in Asians and pacific islanders. Arch Intern Med. 2007;167(7):722-726.
Acton RT, Snively BM, Barton JC, McLaren CE, Adams PC, Rich SS, Eckfeldt JH, Press RD, Sholinsky P, Leiendecker-Foster C, et al.
A genome-wide linkage scan for iron phenotype quantitative trait loci: the HEIRS Family Study. Clin Genet. 2007;71(6):518-529.
Rivers CA, Barton JC, Gordeuk VR, Acton RT, Speechley MR, Snively BM, Leiendecker-Foster C, Press RD, Adams PC, Reboussin DM, et al.
Association of ferroportin Q248H polymorphism with elevated levels of serum ferritin in African Americans in the Hemochromatosis and Iron Overload Screening (HEIRS) Study. Blood Cells Mol Dis. 2007;38(3):247-252.
McLaren CE, Harris EL, Reboussin DM, Gordeuk VR, Barton JC, Acton RT, McLaren GD, Vogt TM, Snively BM, Passmore LV, et al. Serum ferritin and transferrin saturation in Asians and Pacific Islanders living in the U.S. and Canada: the Hemochromatosis and Iron Overload Screening (HEIRS) Study. Am J Hematol. 2007;82(6):574.
Dawkins FW, Gordeuk VR, Snively BM, Lovato L, Barton JC, Acton RT, McLaren GD, Leiendecker-Foster C, McLaren CE, Jackson S, et al.
African Americans at risk for increased iron stores or liver disease. Am J Med. 2007;120(8):734.e1-e9.
Gilliam LK, Pihoker C, Ellard S, Snively BM, Dabelea D, Davis C, Dolan L, Imperatore G, Lawrence JM, Mayer-Davis EJ, et al. Unrecognized maturity-onset diabetes of the young (MODY) due to HNF1[alpha] mutations in the SEARCH for Diabetes in Youth Study [abstract]. Diabetes. 2007;56(Suppl 1):A74-A75.
Maahs DM, Snively BM, Bell RA, Dolan L, Hirsch I, Imperatore G, Linder B, Marcovina SM, Mayer-Davis EJ, Pettitt DJ, et al.
Higher prevalence of elevated albumin excretion in youth with type 2 than type 1 diabetes: the SEARCH for Diabetes in Youth Study. Diabetes Care. 2007;30(10):2593-2598.
Wenzel LB, Anderson R, Tucker DC, Palla S, Thomson E, Speechley M, Harrison H, Lewis-Jack O, Fadojutimi-Akinsiku M, Snively BM, et al.
Health-related quality of life in a racially diverse population screened for hemochromatosis: results from the Hemochromatosis and Iron Overload Screening (HEIRS) study. Genet Med. 2007;9(10):705-712.
McLaren GD, McLaren CE, Adams PC, Barton JC, Reboussin DM, Gordeuk VR, Acton RT, Harris EL, Speechley M, Snively BM, et al. Symptoms, signs, and clinical conditions in HFE C282Y homozygotes identified by screening in primary care [abstract]. Am J Hematol. 2007;82(6):553.
Adams PC, Reboussin DM, Barton JC, Gordeuk VR, Leiendecker-Foster C, McLaren CE, Acton RT, Eckfeldt JH, Dawkins FW, Snively BM, et al. Iron removed by quantitative phlebotomy in participants identified from a multi-ethnic, primary care sample [abstract]. Am J Hematol. 2007;82(6):558.
McLaren CE, Gordeuk VR, Chen W-P, Barton JC, Acton RT, Speechley M, Castro O, Adams PC, Snively BM, Harris EL, et al. Subpopulations with iron deficiency, liver disease, or HFE mutations revealed by statistical mixture modeling of transferrin saturation and serum ferritin concentration in Asians, African Americam, Hispanics, and Whites [abstract]. Blood. 2007;110(11 Pt 1):786A.
McLaren CE, Li K-T, McLaren GD, Gordeuk VR, Snively BM, Reboussin DM, Barton JC, Acton RT, Dawkins FW, Harris EL, et al.
Mixture models of serum iron measures in population screening for hemochromatosis and iron overload. Transl Res. 2006;148(4):196-206.
Wadwa RP, Urbina EM, Dabelea D, Daniels SR, Snively BM, Ruggiero AM, Smith CM, Hamman RF, Dolan L. Diabetes type and duration are associated with increased arterial stiffness in the SEARCH for Diabetes in Youth Study [abstract]. Diabetes. 2006;55(Suppl 1):A2.
Bell RA, Stafford JM, Arcury TA, Snively BM, Smith SL, Quandt SA. Depressive symptoms and diabetes self-management among rural older adults [abstract]. Diabetes. 2006;55(Suppl 1):A420.
Urbina EM, Wadwa RP, Dabelea D, Daniels SR, Snively BM, Davis C, Hamman RF, Dolan L. Arterial dysfunction in adolescents with diabetes--the SEARCH for Diabetes in Youth Study [abstract]. ASH 21st Annual Scientific Meeting and Exposition. 2006;():P-36.
Acton RT, Barton JC, Snively BM, McLaren CE, Adams PC, Harris EL, Speechley MR, McLaren GD, Dawkins FW, Balasubramanyam A, et al.
Geographic and racial/ethnic differences in HFE mutation frequencies in the Hemochromatosis and Iron Overload Screening (HEIRS) Study. Ethn Dis. 2006;16(4):815-821.
Marcovina SM, Albers JJ, Snively BM. Lipoprotein abnormalities and glucose control in youth with type 1 and type 2 diabetes [abstract]. Atheroscler Suppl. 2006;7(3):13-14.
McLaren GD, McLaren CE, Adams PC, Barton JC, Reboussin DM, Gordeuk VR, Acton RT, Harris EL, Speechley M, Snively BM, et al. Symptoms and signs of hemochromatosis in HFE C282Y homozygotes identified by screening in primary care [abstract]. Blood. 2006;108(11 Pt 1):444a.
All Publications
For a listing of recent publications, refer to PubMed, a service provided by the National Library of Medicine.
For a list of earlier publications, visit the Carpenter Library Publication Search.