Search Results - "Langefeld, C.D."

Refine Results
  1. 1

    The APOL1 Gene and Allograft Survival after Kidney Transplantation by Reeves‐Daniel, A. M., DePalma, J. A., Bleyer, A. J., Rocco, M. V., Murea, M., Adams, P. L., Langefeld, C. D., Bowden, D. W., Hicks, P. J., Stratta, R. J., Lin, J.‐J., Kiger, D. F., Gautreaux, M. D., Divers, J., Freedman, B. I.

    Published in American journal of transplantation (01-05-2011)
    “…Coding variants in the apolipoprotein L1 gene (APOL1) are strongly associated with nephropathy in African Americans (AAs). The effect of transplanting kidneys…”
    Get full text
    Journal Article
  2. 2
  3. 3
  4. 4
  5. 5

    GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region by Armstrong, D L, Zidovetzki, R, Alarcón-Riquelme, M E, Tsao, B P, Criswell, L A, Kimberly, R P, Harley, J B, Sivils, K L, Vyse, T J, Gaffney, P M, Langefeld, C D, Jacob, C O

    Published in Genes and immunity (01-09-2014)
    “…In a genome-wide association study (GWAS) of individuals of European ancestry afflicted with systemic lupus erythematosus (SLE) the extensive utilization of…”
    Get full text
    Journal Article
  6. 6

    Salivary dysbiosis and the clinical spectrum in anti-Ro positive mothers of children with neonatal lupus by Clancy, R.M., Marion, M.C., Ainsworth, H.C., Blaser, M.J., Chang, M., Howard, T.D., Izmirly, P.M., Lacher, C., Masson, M., Robins, K., Buyon, J.P., Langefeld, C.D.

    Published in Journal of autoimmunity (01-02-2020)
    “…Mothers giving birth to children with manifestations of neonatal lupus (NL) represent a unique population at risk for the development of clinically evident…”
    Get full text
    Journal Article
  7. 7

    MHC associations with clinical and autoantibody manifestations in European SLE by Morris, D L, Fernando, M M A, Taylor, K E, Chung, S A, Nititham, J, Alarcón-Riquelme, M E, Barcellos, L F, Behrens, T W, Cotsapas, C, Gaffney, P M, Graham, R R, Pons-Estel, B A, Gregersen, P K, Harley, J B, Hauser, S L, Hom, G, Langefeld, C D, Noble, J A, Rioux, J D, Seldin, M F, Vyse, T J, Criswell, L A

    Published in Genes and immunity (01-06-2014)
    “…Systemic lupus erythematosus (SLE) is a clinically heterogeneous disease affecting multiple organ systems and characterized by autoantibody formation to…”
    Get full text
    Journal Article
  8. 8
  9. 9

    Adiponectin as a novel determinant of bone mineral density and visceral fat by Lenchik, L, Register, T.C, Hsu, F-C, Lohman, K, Nicklas, B.J, Freedman, B.I, Langefeld, C.D, Carr, J.J, Bowden, D.W

    Published in Bone (New York, N.Y.) (01-10-2003)
    “…Growing evidence suggests that positive associations between fat mass (FM) and bone mineral density (BMD) are mediated by not only biomechanical but also…”
    Get full text
    Journal Article
  10. 10

    Implication of European-derived adiposity loci in African Americans by Hester, J M, Wing, M R, Li, J, Palmer, N D, Xu, J, Hicks, P J, Roh, B H, Norris, J M, Wagenknecht, L E, Langefeld, C D, Freedman, B I, Bowden, D W, Ng, M C Y

    Published in International Journal of Obesity (01-03-2012)
    “…Objective: Recent genome-wide association studies (GWAS) have identified multiple novel loci associated with adiposity in European-derived study populations…”
    Get full text
    Journal Article
  11. 11
  12. 12

    Variants in Intron 13 of the ELMO1 Gene are Associated with Diabetic Nephropathy in African Americans by Leak, T. S., Perlegas, P. S., Smith, S. G., Keene, K. L., Hicks, P. J., Langefeld, C. D., Mychaleckyj, J. C., Rich, S. S., Kirk, J. K., Freedman, B. I., Bowden, D. W., Sale, M. M.

    Published in Annals of human genetics (01-03-2009)
    “…Summary Variants in the engulfment and cell motility 1 (ELMO1) gene are associated with nephropathy due to type 2 diabetes mellitus (T2DM) in a Japanese…”
    Get full text
    Journal Article
  13. 13

    Analysis of FTO gene variants with obesity and glucose homeostasis measures in the multiethnic Insulin Resistance Atherosclerosis Study cohort by WIng, M.R, Ziegler, J.M, Langefeld, C.D, Roh, B.H, Palmer, N.D, Mayer-Davis, E.J, Rewers, M.J, Haffner, S.M, Wagenknecht, L.E, Bowden, D.W

    Published in International Journal of Obesity (01-09-2011)
    “…Objective: Previous studies have replicated the association of variants within FTO (fat mass- and obesity-associated) intron 1 with obesity and adiposity…”
    Get full text
    Journal Article
  14. 14
  15. 15
  16. 16

    Heterogeneity in gene loci associated with type 2 diabetes on human chromosome 20q13.1 by Bento, J.L., Palmer, N.D., Zhong, M., Roh, B., Lewis, J.P., Wing, M.R., Pandya, H., Freedman, B.I., Langefeld, C.D., Rich, S.S., Bowden, D.W., Mychaleckyj, J.C.

    Published in Genomics (San Diego, Calif.) (01-10-2008)
    “…Human chromosome 20q12-q13.1 has been linked to type 2 diabetes mellitus (T2DM) in multiple studies. We screened a 5.795-Mb region for diabetes-related…”
    Get full text
    Journal Article
  17. 17

    Evaluation of C1q genomic region in minority racial groups of lupus by Namjou, B, Gray-McGuire, C, Sestak, A L, Gilkeson, G S, Jacob, C O, Merrill, J T, James, J A, Wakeland, E K, Li, Q-Z, Langefeld, C D, Divers, J, Ziegler, J, Moser, K L, Kelly, J A, Kaufman, K M, Harley, J B

    Published in Genes and immunity (01-07-2009)
    “…Complement cascade plasma proteins play a complex role in the etiopathogenesis of systemic lupus erythematosus (SLE). Hereditary C1q deficiency has been…”
    Get full text
    Journal Article
  18. 18
  19. 19
  20. 20