Genomewide Linkage Scan for Schizophrenia Susceptibility Loci among Ashkenazi Jewish Families Shows Evidence of Linkage on Chromosome 10q22

This publication has 73 references indexed in Scilit:

• Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia
  American Journal of Human Genetics, 2003
• The Founder Mutation MSH2*1906G→C Is an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Ashkenazi Jewish Population
  American Journal of Human Genetics, 2002
• Genetic linkage and association between chromosome 1q and working memory function in schizophrenia
  American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, 2002
• The Human Genome Browser at UCSC
  Genome Research, 2002
• The Y Chromosome Pool of Jews as Part of the Genetic Landscape of the Middle East
  American Journal of Human Genetics, 2001
• The Risk of Cancer Associated with Specific Mutations ofBRCA1andBRCA2among Ashkenazi Jews
  New England Journal of Medicine, 1997
• Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis
  Molecular Psychiatry, 1997
• Support for a possible schizophrenia vulnerability locus in region 5q22–31 in Irish families
  Molecular Psychiatry, 1997
• Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
  Nature Genetics, 1995
• The common, Near‐Eastern origin of Ashkenazi and Sephardi Jews supported by Y‐chromosome similarity
  Annals of Human Genetics, 1993