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    Marquitta White, PhD

    TitlePostdoctoral Scholar
    SchoolUCSF School of Medicine
    DepartmentMedicine
    Address1550 4th Street, Bldg 19B
    San Francisco CA 94158
    Phone415-514-9931
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      Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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      1. Neophytou AM, White MJ, Oh SS, Thakur N, Galanter JM, Nishimura KK, Pino-Yanes M, Torgerson DG, Gignoux CR, Eng C, Nguyen EA, Hu D, Mak AC, Kumar R, Seibold MA, Davis A, Farber HJ, Meade K, Avila PC, Serebrisky D, Lenoir MA, Brigino-Buenaventura E, Rodriguez-Cintron W, Bibbins-Domingo K, Thyne SM, Williams LK, Sen S, Gilliland FD, Gauderman WJ, Rodriguez-Santana JR, Lurmann F, Balmes JR, Eisen EA, Burchard EG. Air Pollution and Lung Function in Minority Youth with Asthma in the GALA II (Genes-Environments and Admixture in Latino Americans) and SAGE II (Study of African Americans, Asthma, Genes, and Environments) Studies. Am J Respir Crit Care Med. 2016 Jun 1; 193(11):1271-80. PMID: 26734713.
        View in: PubMed
      2. White MJ, Risse-Adams O, Goddard P, Contreras MG, Adams J, Hu D, Eng C, Oh SS, Davis A, Meade K, Brigino-Buenaventura E, LeNoir MA, Bibbins-Domingo K, Pino-Yanes M, Burchard EG. Novel genetic risk factors for asthma in African American children: Precision Medicine and the SAGE II Study. Immunogenetics. 2016 Jul; 68(6-7):391-400. PMID: 27142222.
        View in: PubMed
      3. Oh SS, White MJ, Gignoux CR, Burchard EG. Making Precision Medicine Socially Precise. Take a Deep Breath. Am J Respir Crit Care Med. 2016 Feb 15; 193(4):348-50. PMID: 26871667.
        View in: PubMed
      4. Oh SS, Galanter J, Thakur N, Pino-Yanes M, Barcelo NE, White MJ, de Bruin DM, Greenblatt RM, Bibbins-Domingo K, Wu AH, Borrell LN, Gunter C, Powe NR, Burchard EG. Diversity in Clinical and Biomedical Research: A Promise Yet to Be Fulfilled. PLoS Med. 2015 Dec; 12(12):e1001918. PMID: 26671224.
        View in: PubMed
      5. White MJ, Kodaman NM, Harder RH, Asselbergs FW, Vaughan DE, Brown NJ, Moore JH, Williams SM. Genetics of Plasminogen Activator Inhibitor-1 (PAI-1) in a Ghanaian Population. PLoS One. 2015; 10(8):e0136379. PMID: 26322636; PMCID: PMC4556460.
      6. White MJ, Eren F, Agirbasli D, Chen J, Hu T, Moore JH, Williams SM, Agirbasli M. A systems genetics approach to dyslipidemia in children and adolescents. OMICS. 2015 Apr; 19(4):248-59. PMID: 25671407.
        View in: PubMed
      7. White MJ, Eren F, Agirbasli D, Williams SM, Agirbasli M. SHBG gene polymorphism (rs1799941) associates with metabolic syndrome in children and adolescents. PLoS One. 2015; 10(2):e0116915. PMID: 25647406; PMCID: PMC4380117.
      8. Ciesielski TH, Pendergrass SA, White MJ, Kodaman N, Sobota RS, Huang M, Bartlett J, Li J, Pan Q, Gui J, Selleck SB, Amos CI, Ritchie MD, Moore JH, Williams SM. Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factors. BioData Min. 2014; 7:10. PMID: 25071867; PMCID: PMC4112852.
      9. Giglia JL, White MJ, Hart AJ, Toro JJ, Freytes CO, Holt CC, Cai Y, Williams SM, Brandt SJ. A single nucleotide polymorphism in SLC7A5 is associated with gastrointestinal toxicity after high-dose melphalan and autologous stem cell transplantation for multiple myeloma. Biol Blood Marrow Transplant. 2014 Jul; 20(7):1014-20. PMID: 24704384; PMCID: PMC4076151.
      10. Darabos C, White MJ, Graham BE, Leung DN, Williams SM, Moore JH. The multiscale backbone of the human phenotype network based on biological pathways. BioData Min. 2014; 7(1):1. PMID: 24460644; PMCID: PMC3924922.
      11. Agirbasli M, Eren F, Agirbasli D, White MJ, Williams SM. Multi-locus candidate gene analyses of lipid levels in a pediatric Turkish cohort: lessons learned on LPL, CETP, LIPC, ABCA1, and SHBG. OMICS. 2013 Dec; 17(12):636-45. PMID: 23988150; PMCID: PMC3837502.
      12. Felder RA, White MJ, Williams SM, Jose PA. Diagnostic tools for hypertension and salt sensitivity testing. Curr Opin Nephrol Hypertens. 2013 Jan; 22(1):65-76. PMID: 23197156; PMCID: PMC3724405.
      13. Sirugo G, Edwards DR, Ryckman KK, Bisseye C, White MJ, Kebbeh B, Morris GA, Adegbola RA, Tacconelli A, Predazzi IM, Novelli G, Vannberg FO, Odunsi K, Page GP, Williams SM. PTX3 genetic variation and dizygotic twinning in the Gambia: could pleiotropy with innate immunity explain common dizygotic twinning in Africa? Ann Hum Genet. 2012 Nov; 76(6):454-63. PMID: 22834944; PMCID: PMC3731069.
      14. Curia MC, De Iure S, De Lellis L, Veschi S, Mammarella S, White MJ, Bartlett J, Di Iorio A, Amatetti C, Lombardo M, Di Gregorio P, Battista P, Mariani-Costantini R, Williams SM, Cama A. Increased variance in germline allele-specific expression of APC associates with colorectal cancer. Gastroenterology. 2012 Jan; 142(1):71-77.e1. PMID: 21995949; PMCID: PMC3246305.
      15. Ryckman KK, Morken NH, White MJ, Velez DR, Menon R, Fortunato SJ, Magnus P, Williams SM, Jacobsson B. Maternal and fetal genetic associations of PTGER3 and PON1 with preterm birth. PLoS One. 2010; 5(2):e9040. PMID: 20140262; PMCID: PMC2815792.
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