Literature DB >> 8541850

Familial non-specific dementia maps to chromosome 3.

J Brown1, A Ashworth, S Gydesen, A Sorensen, M Rossor, J Hardy, J Collinge.   

Abstract

A significant minority of degenerative dementias lack distinctive inclusion bodies, plagues or tangles on pathological examination. Half of these cases have a positive family history of dementia. We have studied the largest published family with such a dementia and mapped the disease locus to a 12 cM region of chromosome 3 spanning the centromere. Haplotype analysis demonstrates a common region shared between all affected individuals between the markers D3S1284 and D3S1603. Like a number of other late onset neurodegenerative diseases, the disease presents at an earlier age when paternally inherited.

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Year:  1995        PMID: 8541850     DOI: 10.1093/hmg/4.9.1625

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  22 in total

Review 1.  Frontotemporal dementia.

Authors:  Erik D Roberson
Journal:  Curr Neurol Neurosci Rep       Date:  2006-11       Impact factor: 5.081

2.  Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17.

Authors:  J R Murrell; D Koller; T Foroud; M Goedert; M G Spillantini; H J Edenberg; M R Farlow; B Ghetti
Journal:  Am J Hum Genet       Date:  1997-11       Impact factor: 11.025

3.  Linkage of frontotemporal dementia to chromosome 17: clinical and neuropathological characterization of phenotype.

Authors:  L H Yamaoka; K A Welsh-Bohmer; C M Hulette; P C Gaskell; M Murray; J L Rimmler; B R Helms; M Guerra; A D Roses; D E Schmechel; M A Pericak-Vance
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

4.  Clinical rationale of genetic testing in dementia.

Authors:  G B Frisoni; M Trabucchi
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-03       Impact factor: 10.154

5.  Assignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13.

Authors:  P Pekkarinen; I Hovatta; P Hakola; O Järvi; M Kestilä; U Lenkkeri; R Adolfsson; G Holmgren; P O Nylander; L Tranebjaerg; J D Terwilliger; J Lönnqvist; L Peltonen
Journal:  Am J Hum Genet       Date:  1998-02       Impact factor: 11.025

6.  Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.

Authors:  M J Kovach; B Waggoner; S M Leal; D Gelber; R Khardori; M A Levenstien; C A Shanks; G Gregg; M T Al-Lozi; T Miller; W Rakowicz; G Lopate; J Florence; G Glosser; Z Simmons; J C Morris; M P Whyte; A Pestronk; V E Kimonis
Journal:  Mol Genet Metab       Date:  2001-12       Impact factor: 4.797

7.  Mendelian and Sporadic FTD: Disease Risk and Avenues from Genetics to Disease Pathways Through In Silico Modelling.

Authors:  Claudia Manzoni; Raffaele Ferrari
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

Review 8.  The genetics of frontotemporal lobar degeneration.

Authors:  Rosa Rademakers; Mike Hutton
Journal:  Curr Neurol Neurosci Rep       Date:  2007-09       Impact factor: 5.081

9.  Genetics and genetic counseling: recommendations for Alzheimer's disease, frontotemporal dementia, and Creutzfeldt-Jakob disease.

Authors:  Jennifer Williamson; Susan LaRusse
Journal:  Curr Neurol Neurosci Rep       Date:  2004-09       Impact factor: 5.081

10.  [Frontotemporal dementia. Results from "Frontotemporal Demential and Pick's Disease Conference"].

Authors:  J Diehl; I R Mackenzie; H Förstl; A Kurz
Journal:  Nervenarzt       Date:  2003-05-10       Impact factor: 1.214

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