Gaofeng Wang

Summary

Affiliation: University of Miami
Country: USA

Publications

  1. ncbi Localization of age-related macular degeneration-associated ARMS2 in cytosol, not mitochondria
    Gaofeng Wang
    Miami Institute for Human Genomics, University of Miami, Miami, Florida 33136, USA
    Invest Ophthalmol Vis Sci 50:3084-90. 2009
  2. ncbi Analysis of the indel at the ARMS2 3'UTR in age-related macular degeneration
    Gaofeng Wang
    Dr John T Macdonald Foundation Department of Human Genetics, John P Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL 33136, USA
    Hum Genet 127:595-602. 2010
  3. ncbi Inverse association of female hormone replacement therapy with age-related macular degeneration and interactions with ARMS2 polymorphisms
    Digna R Velez Edwards
    Dr John T Macdonald Foundation Department of Human Genetics and John P Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, Florida, USA
    Invest Ophthalmol Vis Sci 51:1873-9. 2010
  4. ncbi Analysis of single nucleotide polymorphisms in the NOS2A gene and interaction with smoking in age-related macular degeneration
    Juan A Ayala-Haedo
    John P Hussman Institute for Human Genomics and the Dr John T Macdonald Foundation Department of Human Genetics, University of Miami Miller School of Medicine, Miami, FL 33136, USA
    Ann Hum Genet 74:195-201. 2010
  5. ncbi Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease
    Todd L Edwards
    John P Hussman Institute for Human Genomics, University of Miami, FL 33136, USA
    Ann Hum Genet 74:97-109. 2010
  6. ncbi Copy number variations are a rare cause of non-CMT1A Charcot-Marie-Tooth disease
    Jia Huang
    Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, FL 33136, USA
    J Neurol 257:735-41. 2010

Collaborators

Detail Information

Publications6

  1. ncbi Localization of age-related macular degeneration-associated ARMS2 in cytosol, not mitochondria
    Gaofeng Wang
    Miami Institute for Human Genomics, University of Miami, Miami, Florida 33136, USA
    Invest Ophthalmol Vis Sci 50:3084-90. 2009
    ....
  2. ncbi Analysis of the indel at the ARMS2 3'UTR in age-related macular degeneration
    Gaofeng Wang
    Dr John T Macdonald Foundation Department of Human Genetics, John P Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL 33136, USA
    Hum Genet 127:595-602. 2010
    ..Conclusively, the indel at 3'UTR of ARMS2 actually contains two side-by-side indels. The indels are associated with risk of AMD, but not correlated with ARMS2 mRNA level...
  3. ncbi Inverse association of female hormone replacement therapy with age-related macular degeneration and interactions with ARMS2 polymorphisms
    Digna R Velez Edwards
    Dr John T Macdonald Foundation Department of Human Genetics and John P Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, Florida, USA
    Invest Ophthalmol Vis Sci 51:1873-9. 2010
    ..These results highlight the genetic and environmental complexity of the etiologic architecture of AMD; however, further replication is necessary to validate them...
  4. ncbi Analysis of single nucleotide polymorphisms in the NOS2A gene and interaction with smoking in age-related macular degeneration
    Juan A Ayala-Haedo
    John P Hussman Institute for Human Genomics and the Dr John T Macdonald Foundation Department of Human Genetics, University of Miami Miller School of Medicine, Miami, FL 33136, USA
    Ann Hum Genet 74:195-201. 2010
    ..Our data suggests that SNPs in the NOS2A gene are associated with increased risk for AMD and might modulate the effect of smoking on AMD...
  5. ncbi Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease
    Todd L Edwards
    John P Hussman Institute for Human Genomics, University of Miami, FL 33136, USA
    Ann Hum Genet 74:97-109. 2010
    ..79] T vs. C allele, PAR%= 8%) were genome-wide significant. No other SNPs were genome-wide significant in this analysis. This study confirms that SNCA and the MAPT region are major genes whose common variants are influencing risk of PD...
  6. ncbi Copy number variations are a rare cause of non-CMT1A Charcot-Marie-Tooth disease
    Jia Huang
    Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, FL 33136, USA
    J Neurol 257:735-41. 2010
    ..Their potential relevance as disease modifiers remains to be evaluated. The present study design cannot rule out that specific CMT forms exist where CNVs play a larger role...