Core Programs

Supporting Publications Data

As a service to interested researchers, the CHG provides supplemental data for selected research publications.

• Ashley_Koch et al. Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease.
  Supporting Data (Excel File)
  
  
• Bartoloni et al. Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31.
  Supporting Data
  
  
• Elliott et al. Genetic Polymorphisms Associated with Priapism in Sickle Cell Disease of Haematology.
  Supporting Data (Excel File)
  
  
• Hauser ER et al. A Genome Wide Scan for Early-Onset Coronary Artery Disease in 438 Families: The GENECARD Study.
  Supporting Data
  
  
• Schmidt et al. Life After the Screen: Making Sense of Many P-Values.
  Supporting Data
  
  
• Shao et al. A Genetic Screen and Follow-up Analysis for Autistic Disorder.
  Supporting Data
  
  
• Speer et al. Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families.
  Supporting Data
  
  
• Speer et al. Clinical and Genetic Investigations of Chiari type I Malformation.
  Supporting Data (PowerPoint Slides)
  
  
• van der Walt et al. Genetic Polymorphisms of the N-acetyltransferase Genes and Risk to Parkinson's Disease.
  Supporting Data

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