JOHN WILLIAM BELMONT

Summary

Affiliation: Baylor College of Medicine
Country: USA

Publications

  1. pmc Integrative genomic analysis of the human immune response to influenza vaccination
    Luis M Franco
    Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, United States Department of Medicine, Baylor College of Medicine, Houston, United States
    elife 2:e00299. 2013
  2. pmc SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing
    Muhammad Tariq
    Division of Molecular Cardiovascular Biology, Cincinnati Children s Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA
    Genome Biol 12:R91. 2011
  3. pmc Assessing the utility of whole-genome amplified serum DNA for array-based high throughput genotyping
    KRISTINE L BUCASAS
    Department of Immunology, Baylor College of Medicine, Houston, TX 77030, USA
    BMC Genet 10:85. 2009
  4. doi request reprint Genetic disorders with both hearing loss and cardiovascular abnormalities
    John W Belmont
    Department of Molecular and Human Genetics, and Pediatrics, Baylor College of Medicine, Houston, Tex, USA
    Adv Otorhinolaryngol 70:66-74. 2011

Research Grants

Collaborators

  • KRISTINE L BUCASAS
  • Luis M Franco
  • Muhammad Tariq
  • Janet M Wells
  • Molly S Bray
  • Alexander Renwick
  • Robert B Couch
  • Xueqing Wang
  • Gladys E Zapata
  • Nancy Arden
  • Peng Yu
  • Chad A Shaw
  • Diane Nino
  • John M Quarles
  • Seema Lalani
  • Stephanie M Ware
  • Teresa Smolarek
  • Robert D Fleischmann
  • Scott N Peterson
  • Sonal Pradhan
  • Gagan A Pandya

Detail Information

Publications4

  1. pmc Integrative genomic analysis of the human immune response to influenza vaccination
    Luis M Franco
    Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, United States Department of Medicine, Baylor College of Medicine, Houston, United States
    elife 2:e00299. 2013
    ..More broadly, we demonstrate that an integrative study design is an efficient alternative to existing methods for the identification of genes involved in complex traits. DOI:http://dx.doi.org/10.7554/eLife.00299.001. ..
  2. pmc SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing
    Muhammad Tariq
    Division of Molecular Cardiovascular Biology, Cincinnati Children s Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA
    Genome Biol 12:R91. 2011
    ..In this study, high-resolution SNP genotyping and exon-targeted array comparative genomic hybridization platforms were coupled to whole-exome sequencing to identify a novel disease candidate gene...
  3. pmc Assessing the utility of whole-genome amplified serum DNA for array-based high throughput genotyping
    KRISTINE L BUCASAS
    Department of Immunology, Baylor College of Medicine, Houston, TX 77030, USA
    BMC Genet 10:85. 2009
    ..This study provides a realistic and high-precision assessment of WGA DNA genotyping performance from 20-year old archived serum samples using the Affymetrix Genome-Wide Human SNP Array 6.0 (SNP6.0) platform...
  4. doi request reprint Genetic disorders with both hearing loss and cardiovascular abnormalities
    John W Belmont
    Department of Molecular and Human Genetics, and Pediatrics, Baylor College of Medicine, Houston, Tex, USA
    Adv Otorhinolaryngol 70:66-74. 2011
    ....

Research Grants2

  1. MOLECULAR GENETICS OF MAMMALIAN BARREN (BRRN 1)
    John Belmont; Fiscal Year: 2001
    ..Elucidation of these events has broader implications for understanding chromosome non-disjunction and other human disorders associated with chromosome instability. ..
  2. GENETIC STUDIES OF COMMON CONGENITAL HEART DEFECTS
    John Belmont; Fiscal Year: 2004
    ..The proposed studies will provide a base on which to advance genetic analyses of a substantial group of congenital heart defects with the aim of reducing their occurrence and providing new treatment opportunities. ..