Connection

JOHN BELMONT to Case-Control Studies

This is a "connection" page, showing publications JOHN BELMONT has written about Case-Control Studies.
Connection Strength

0.255
  1. Global gene expression profiling in infants with acute respiratory syncytial virus broncholitis demonstrates systemic activation of interferon signaling networks. Pediatr Infect Dis J. 2013 Feb; 32(2):e68-76.
    View in: PubMed
    Score: 0.064
  2. Edematous severe acute malnutrition is characterized by hypomethylation of DNA. Nat Commun. 2019 12 19; 10(1):5791.
    View in: PubMed
    Score: 0.026
  3. A genome-wide association study of LCH identifies a variant in SMAD6 associated with susceptibility. Blood. 2017 11 16; 130(20):2229-2232.
    View in: PubMed
    Score: 0.022
  4. Water Load Test in Children with Chronic Abdominal Pain or Obesity Compared with Nonobese Controls. South Med J. 2017 03; 110(3):168-171.
    View in: PubMed
    Score: 0.021
  5. Laterality defects in the national birth defects prevention study (1998-2007): birth prevalence and descriptive epidemiology. Am J Med Genet A. 2014 Oct; 164A(10):2581-91.
    View in: PubMed
    Score: 0.018
  6. Association between thyroxine levels at birth and choanal atresia or stenosis among infants in Texas, 2004-2007. Birth Defects Res A Clin Mol Teratol. 2012 Nov; 94(11):951-4.
    View in: PubMed
    Score: 0.016
  7. The association between neonatal thyroxine and craniosynostosis, Texas, 2004-2007. Birth Defects Res A Clin Mol Teratol. 2012 Dec; 94(12):1004-9.
    View in: PubMed
    Score: 0.016
  8. Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1. Nat Genet. 2011 Sep 11; 43(10):996-1000.
    View in: PubMed
    Score: 0.014
  9. Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections. PLoS Genet. 2011 Jun; 7(6):e1002118.
    View in: PubMed
    Score: 0.014
  10. NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling. Hum Mol Genet. 2008 Sep 15; 17(18):2886-93.
    View in: PubMed
    Score: 0.012
  11. Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly. Am J Hum Genet. 2008 Jul; 83(1):18-29.
    View in: PubMed
    Score: 0.012
  12. Amerindian ancestry in Argentina is associated with increased risk for systemic lupus erythematosus. Genes Immun. 2008 Jun; 9(4):389-93.
    View in: PubMed
    Score: 0.011
  13. Heritability of plasma amino acid levels in different nutritional states. Mol Genet Metab. 2007 Feb; 90(2):217-20.
    View in: PubMed
    Score: 0.010
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.