Literature DB >> 19319700

ParkScreen: a low-cost rapid linkage marker panel for Parkinson's disease.

Alessandro De Grandi1, Claudia Béu Volpato, Elisa Bedin, Cristian Pattaro, Fabio Marroni, Irene Pichler, Andrew Antony Hicks, Giorgio Casari, Peter Paul Pramstaller.   

Abstract

A genetic marker screening panel, ParkScreen, optimized for simultaneous marker amplification, was constructed to test or exclude linkage in families with parkinsonism or Parkinson's disease, using only a few affected individuals per family. ParkScreen functionality was proven by detection of linkage to PARK2 in a family with known Parkin mutations, exclusion of linkage to several of the known loci, and detection of suggestive linkage to PARK8, PARK3, and PARK11 in some families. In a novel approach, we also tested the ability of ParkScreen to screen patients originating from isolated populations. Using apparently sporadic patients from geographically isolated Alpine villages, suggestive linkage to PARK11 was found in one village. ParkScreen is a useful and inexpensive tool that allows the rapid screening of patients in families suitable for clinical follow-up and further characterization in order to identify specific mutations or novel genes.

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Year:  2009        PMID: 19319700     DOI: 10.1007/s12031-009-9193-8

Source DB:  PubMed          Journal:  J Mol Neurosci        ISSN: 0895-8696            Impact factor:   3.444


  12 in total

1.  Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene.

Authors:  Peter P Pramstaller; Bernhard Kis; Cordula Eskelson; Katja Hedrich; Monika Scherer; Eberhard Schwinger; Xandra O Breakefield; Patricia L Kramer; Laurie J Ozelius; Christine Klein
Journal:  Mov Disord       Date:  2002-03       Impact factor: 10.338

2.  Mega2: data-handling for facilitating genetic linkage and association analyses.

Authors:  Nandita Mukhopadhyay; Lee Almasy; Mark Schroeder; William P Mulvihill; Daniel E Weeks
Journal:  Bioinformatics       Date:  2005-03-03       Impact factor: 6.937

3.  Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27.

Authors:  H Matsumine; M Saito; S Shimoda-Matsubayashi; H Tanaka; A Ishikawa; Y Nakagawa-Hattori; M Yokochi; T Kobayashi; S Igarashi; H Takano; K Sanpei; R Koike; H Mori; T Kondo; Y Mizutani; A A Schäffer; Y Yamamura; S Nakamura; S Kuzuhara; S Tsuji; Y Mizuno
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

4.  Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease.

Authors:  Corinne Lautier; Stefano Goldwurm; Alexandra Dürr; Barbara Giovannone; William G Tsiaras; Gianni Pezzoli; Alexis Brice; Robert J Smith
Journal:  Am J Hum Genet       Date:  2008-03-20       Impact factor: 11.025

5.  Linkage analysis in families with recurrent neuroblastoma.

Authors:  Patrizia Perri; Luca Longo; Carmel McConville; Roberto Cusano; Sally A Rees; Marco Seri; Massimo Conte; Giovanni Romeo; Marcella Devoto; Gian Paolo Tonini
Journal:  Ann N Y Acad Sci       Date:  2002-06       Impact factor: 5.691

6.  Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations.

Authors:  Nathan Pankratz; William C Nichols; Sean K Uniacke; Cheryl Halter; Alice Rudolph; Cliff Shults; P Michael Conneally; Tatiana Foroud
Journal:  Am J Hum Genet       Date:  2002-06-07       Impact factor: 11.025

Review 7.  Parkinson's disease: piecing together a genetic jigsaw.

Authors:  M C J Dekker; V Bonifati; C M van Duijn
Journal:  Brain       Date:  2003-05-21       Impact factor: 13.501

8.  Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease.

Authors:  Karsten M Strauss; L Miguel Martins; Helene Plun-Favreau; Frank P Marx; Sabine Kautzmann; Daniela Berg; Thomas Gasser; Zbginiew Wszolek; Thomas Müller; Antje Bornemann; Hartwig Wolburg; Julian Downward; Olaf Riess; Jörg B Schulz; Rejko Krüger
Journal:  Hum Mol Genet       Date:  2005-06-16       Impact factor: 6.150

9.  Hereditary early-onset Parkinson's disease caused by mutations in PINK1.

Authors:  Enza Maria Valente; Patrick M Abou-Sleiman; Viviana Caputo; Miratul M K Muqit; Kirsten Harvey; Suzana Gispert; Zeeshan Ali; Domenico Del Turco; Anna Rita Bentivoglio; Daniel G Healy; Alberto Albanese; Robert Nussbaum; Rafael González-Maldonado; Thomas Deller; Sergio Salvi; Pietro Cortelli; William P Gilks; David S Latchman; Robert J Harvey; Bruno Dallapiccola; Georg Auburger; Nicholas W Wood
Journal:  Science       Date:  2004-04-15       Impact factor: 47.728

10.  A linkage study of candidate loci in familial Parkinson's Disease.

Authors:  Karin Wirdefeldt; Catherine E Burgess; Lisa Westerberg; Haydeh Payami; Martin Schalling
Journal:  BMC Neurol       Date:  2003-07-26       Impact factor: 2.474

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