Genome-wide scan for Parkinson's disease: the GenePD Study

Neurology. 2001 Sep 25;57(6):1124-6. doi: 10.1212/wnl.57.6.1124.

Abstract

A genome-wide scan for idiopathic PD in a sample of 113 PD-affected sibling pairs is reported. Suggestive evidence for linkage was found for chromosomes 1 (214 cM, lod = 1.20), 9 (136 cM, lod = 1.30), 10 (88 cM, lod = 1.07), and 16 (114 cM, lod = 0.93). The chromosome 9 region overlaps the genes for dopamine beta-hydroxylase and torsion dystonia. Although no strong evidence for linkage was found for any locus, these results may be of value in comparison with similar studies by others.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Chromosomes, Human, Pair 1
  • Chromosomes, Human, Pair 10
  • Chromosomes, Human, Pair 16
  • Chromosomes, Human, Pair 9
  • Dopamine beta-Hydroxylase / genetics
  • Dystonia Musculorum Deformans / genetics
  • Genetic Linkage / genetics
  • Genetic Markers / genetics
  • Genetic Testing*
  • Genome*
  • Humans
  • Male
  • Middle Aged
  • Parkinson Disease / diagnosis
  • Parkinson Disease / genetics*

Substances

  • Genetic Markers
  • Dopamine beta-Hydroxylase