JOHN WILLIAM BELMONT

Summary

Affiliation: Baylor College of Medicine
Country: USA

Publications

  1. ncbi 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
  2. ncbi 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
  3. ncbi 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

  1. Novel Genomic Disorders Causing Cardiovascular Malformations
    JOHN WILLIAM BELMONT; Fiscal Year: 2010
  2. GENETIC STUDIES OF COMMON CONGENITAL HEART DEFECTS
    John Belmont; Fiscal Year: 2004
  3. MOLECULAR GENETICS OF MAMMALIAN BARREN (BRRN 1)
    John Belmont; Fiscal Year: 2001
  4. Genome Wide Association Study for Hypoplastic Left Heart and Related Defects
    JOHN WILLIAM BELMONT; Fiscal Year: 2010

Collaborators

  • Muhammad Tariq
  • KRISTINE L BUCASAS
  • Teresa Smolarek
  • Seema Lalani
  • Stephanie M Ware
  • Gagan A Pandya
  • Robert D Fleischmann
  • Scott N Peterson
  • Sonal Pradhan

Detail Information

Publications3

  1. ncbi 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...
  2. ncbi 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...
  3. ncbi 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 Grants13

  1. Novel Genomic Disorders Causing Cardiovascular Malformations
    JOHN WILLIAM BELMONT; Fiscal Year: 2010
    ..Improved ability to screen for chromosomal imbalances and mutations in relevant genes will aid in diagnosis and early intervention for CVM. ..
  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. ..
  3. 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. ..
  4. Genome Wide Association Study for Hypoplastic Left Heart and Related Defects
    JOHN WILLIAM BELMONT; Fiscal Year: 2010
    ..Identification of genes involved in congenital LVOTO defects should provide both new mechanistic insights and improve diagnostic testing in individual patients and families. ..