Odity Mukherjee

Summary

Affiliation: Washington University School of Medicine
Country: USA

Publications

  1. ncbi Haplotype-based association analysis of the MAPT locus in late onset Alzheimer's disease
    Odity Mukherjee
    Department of Psychiatry, Washington University School of Medicine, St Louis, MO, USA
    BMC Genet 8:3. 2007
  2. ncbi Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia
    Odity Mukherjee
    Department of Psychiatry, Washington University School of Medicine, St Louis, Missouri 63110, USA
    Hum Mutat 29:512-21. 2008
  3. ncbi Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation
    Maria I Behrens
    Alzheimer s Disease Research Center, Department of Pathology and Immunology, Washington University School of Medicine, 660 South Euclid Avenue, St Louis, MO 63110, USA
    Alzheimer Dis Assoc Disord 21:1-7. 2007
  4. ncbi HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin
    Odity Mukherjee
    Washington University Alzheimer s Disease Research Center, Washington University School of Medicine, St Louis, MO 63110, USA
    Ann Neurol 60:314-22. 2006

Detail Information

Publications4

  1. ncbi Haplotype-based association analysis of the MAPT locus in late onset Alzheimer's disease
    Odity Mukherjee
    Department of Psychiatry, Washington University School of Medicine, St Louis, MO, USA
    BMC Genet 8:3. 2007
    ..A recent study showed a significant haplotype association (H1c) with AD. The current study is an attempt to replicate this association in an independently ascertained cohort...
  2. ncbi Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia
    Odity Mukherjee
    Department of Psychiatry, Washington University School of Medicine, St Louis, Missouri 63110, USA
    Hum Mutat 29:512-21. 2008
    ....
  3. ncbi Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation
    Maria I Behrens
    Alzheimer s Disease Research Center, Department of Pathology and Immunology, Washington University School of Medicine, 660 South Euclid Avenue, St Louis, MO 63110, USA
    Alzheimer Dis Assoc Disord 21:1-7. 2007
    ..5913 A>G (IVS6-2 A>G) segregating with FTLD-U in this kindred. In conclusion, HDDD1 is an FTLD-U caused by a PGRN mutation and is neuropathologically heterogeneous with Alzheimer disease as a common comorbidity...
  4. ncbi HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin
    Odity Mukherjee
    Washington University Alzheimer s Disease Research Center, Washington University School of Medicine, St Louis, MO 63110, USA
    Ann Neurol 60:314-22. 2006
    ....