1 - 25 of 50 results for author:"Raby B.A." in Literature citations
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| Different polymorphisms of the mineralocorticoid receptor gene are associated with either glucocorticoid or mineralocorticoid levels in hypertension. Sun B., Chamarthi B., Williams J.S., Krug A.W., Lasky-Su J., Raby B.A., Hopkins P.N., Jeunemaitre X., Ferri C., Williams G.H. J. Clin. Endocrinol. Metab. 97:E1825-9(2012) · Mapped (6) |
| Lysine-specific demethylase 1: an epigenetic regulator of salt-sensitive hypertension. Williams J.S., Chamarthi B., Goodarzi M.O., Pojoga L.H., Sun B., Garza A.E., Raby B.A., Adler G.K., Hopkins P.N., Brown N.J. et al. Am. J. Hypertens. 25:812-817(2012) · Mapped (3) |
| Replication and meta-analysis of the gene-environment interaction between body mass index and the interleukin-6 promoter polymorphism with higher insulin resistance. Underwood P.C., Chamarthi B., Williams J.S., Sun B., Vaidya A., Raby B.A., Lasky-Su J., Hopkins P.N., Adler G.K., Williams G.H. Metab. Clin. Exp. 61:667-671(2012) · Mapped (5) |
| Gene-by-environment effect of house dust mite on purinergic receptor P2Y12 (P2RY12) and lung function in children with asthma. Bunyavanich S., Boyce J.A., Raby B.A., Weiss S.T. Clin. Exp. Allergy 42:229-237(2012) · Mapped (5) |
| Variants of the caveolin-1 gene: a translational investigation linking insulin resistance and hypertension. Pojoga L.H., Underwood P.C., Goodarzi M.O., Williams J.S., Adler G.K., Jeunemaitre X., Hopkins P.N., Raby B.A., Lasky-Su J., Sun B. et al. J. Clin. Endocrinol. Metab. 96:E1288-92(2011) · Mapped (6) |
| Renin gene polymorphism: its relationship to hypertension, renin levels and vascular responses. Sun B., Williams J.S., Pojoga L., Chamarthi B., Lasky-Su J., Raby B.A., Hopkins P.N., Jeunemaitre X., Brown N.J., Ferri C. et al. J Renin Angiotensin Aldosterone Syst 12:564-571(2011) · Mapped (3) |
| Association of SERPINE2 with asthma. Himes B.E., Klanderman B., Ziniti J., Senter-Sylvia J., Soto-Quiros M.E., Avila L., Celedon J.C., Lange C., Mariani T.J., Lasky-Su J. et al. Chest 140:667-674(2011) · Mapped (2) |
| Comprehensive genetic assessment of a functional TLR9 promoter polymorphism: no replicable association with asthma or asthma-related phenotypes. Lange N.E., Zhou X., Lasky-Su J., Himes B.E., Lazarus R., Soto-Quiros M., Avila L., Celedon J.C., Hawrylowicz C.M., Raby B.A. et al. BMC Med. Genet. 12:26-26(2011) · Mapped (1) |
| The relationship between peroxisome proliferator-activated receptor-gamma and renin: a human genetics study. Underwood P.C., Sun B., Williams J.S., Pojoga L.H., Chamarthi B., Lasky-Su J., Raby B.A., Hopkins P.N., Jeunemaitre X., Brown N.J. et al. J. Clin. Endocrinol. Metab. 95:E75-9(2010) · Mapped (9) |
| TSLP polymorphisms are associated with asthma in a sex-specific fashion. Hunninghake G.M., Soto-Quiros M.E., Avila L., Kim H.P., Lasky-Su J., Rafaels N., Ruczinski I., Beaty T.H., Mathias R.A., Barnes K.C. et al. Allergy 65:1566-1575(2010) · Mapped (3) |
| Genetic influences on asthma susceptibility in the developing lung. Carpe N., Mandeville I., Ribeiro L., Ponton A., Martin J.G., Kho A.T., Chu J.H., Tantisira K., Weiss S.T., Raby B.A. et al. Am. J. Respir. Cell Mol. Biol. 43:720-730(2010) · Mapped (3) |
| Stronger evidence for replication of NPPA using genome-wide genotyping data. Rogers A.J., Raby B.A., Lima J., Lasky-Su J.A., Murphy A., Lazarus R., Klanderman B., Sylvia J.S., Ziniti J.P., Lange C. et al. Am. J. Respir. Crit. Care Med. 181:96-96(2010) · Mapped (1) |
| MMP12, lung function, and COPD in high-risk populations. Hunninghake G.M., Cho M.H., Tesfaigzi Y., Soto-Quiros M.E., Avila L., Lasky-Su J., Stidley C., Melen E., Soderhall C., Hallberg J. et al. N. Engl. J. Med. 361:2599-2608(2009) · Mapped (3) |
| A genome-wide association study on African-ancestry populations for asthma. Mathias R.A., Grant A.V., Rafaels N., Hand T., Gao L., Vergara C., Tsai Y.J., Yang M., Campbell M., Foster C. et al. J. Allergy Clin. Immunol. 125:336-346.e4(2010) · Mapped (26) |
| The interaction of glutathione S-transferase M1-null variants with tobacco smoke exposure and the development of childhood asthma. Rogers A.J., Brasch-Andersen C., Ionita-Laza I., Murphy A., Sharma S., Klanderman B.J., Raby B.A. Clin. Exp. Allergy 39:1721-1729(2009) · Mapped (2) |
| Asthma and genes encoding components of the vitamin D pathway. Bosse Y., Lemire M., Poon A.H., Daley D., He J.Q., Sandford A., White J.H., James A.L., Musk A.W., Palmer L.J. et al. Respir. Res. 10:98-98(2009) · Mapped (34) |
| Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease. Verlaan D.J., Berlivet S., Hunninghake G.M., Madore A.M., Lariviere M., Moussette S., Grundberg E., Kwan T., Ouimet M., Ge B. et al. Am. J. Hum. Genet. 85:377-393(2009) · Mapped (8) |
| Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children. Hancock D.B., Romieu I., Shi M., Sienra-Monge J.J., Wu H., Chiu G.Y., Li H., del Rio-Navarro B.E., Willis-Owen S.A., Willis-Owens S.A. et al. PLoS Genet. 5:e1000623-e1000623(2009) · Mapped (5) |
| Importin-13 genetic variation is associated with improved airway responsiveness in childhood asthma. Raby B.A., Van Steen K., Lasky-Su J., Tantisira K., Kaplan F., Weiss S.T. Respir. Res. 10:67-67(2009) · Mapped (4) |
| Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. Himes B.E., Hunninghake G.M., Baurley J.W., Rafaels N.M., Sleiman P., Strachan D.P., Wilk J.B., Willis-Owen S.A., Klanderman B., Lasky-Su J. et al. Am. J. Hum. Genet. 84:581-593(2009) · Mapped (4) |
| Assessing the reproducibility of asthma candidate gene associations, using genome-wide data. Rogers A.J., Raby B.A., Lasky-Su J.A., Murphy A., Lazarus R., Klanderman B.J., Sylvia J.S., Ziniti J.P., Lange C., Celedon J.C. et al. Am. J. Respir. Crit. Care Med. 179:1084-1090(2009) · Mapped (152) |
| Association of VEGF polymorphisms with childhood asthma, lung function and airway responsiveness. Sharma S., Murphy A.J., Soto-Quiros M.E., Avila L., Klanderman B.J., Sylvia J.S., Celedon J.C., Raby B.A., Weiss S.T. Eur. Respir. J. 33:1287-1294(2009) · Mapped (7) |
| Folliculin mutations are not associated with severe COPD. Cho M.H., Klanderman B.J., Litonjua A.A., Sparrow D., Silverman E.K., Raby B.A. BMC Med. Genet. 9:120-120(2008) · Mapped (2) |
| Variants in TGFB1, dust mite exposure, and disease severity in children with asthma. Sharma S., Raby B.A., Hunninghake G.M., Soto-Quiros M., Avila L., Murphy A.J., Lasky-Su J., Klanderman B.J., Sylvia J.S., Weiss S.T. et al. Am. J. Respir. Crit. Care Med. 179:356-362(2009) · Mapped (11) |
| Analysis of exonic elastin variants in severe, early-onset chronic obstructive pulmonary disease. Cho M.H., Ciulla D.M., Klanderman B.J., Hersh C.P., Litonjua A.A., Sparrow D., Raby B.A., Silverman E.K. Am. J. Respir. Cell Mol. Biol. 40:751-755(2009) · Mapped (14) |