Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study
Open Access
- 31 October 2010
- journal article
- research article
- Published by Elsevier BV in The Lancet Neurology
- Vol. 9 (10), 986-994
- https://doi.org/10.1016/s1474-4422(10)70197-6
Abstract
No abstract availableFunding Information
- Motor Neurone Disease Association (3/3, 070122/A/02/Z)
- Wellcome Trust
- Motor Neurone Disease Association (10/57)
- Medical Research Council (G0000934)
- The Wellcome Trust (068545/Z/02)
- the Medical Research Council (G0701420)
- the National Institute on Aging (Z01-AG000949-02)
- the Fondazione Vialli e Mauro per la SLA (3/2008)
- the Federazione Italiana Giuoco Calcio (2/2008)
This publication has 36 references indexed in Scilit:
- Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association studyThe Lancet Neurology, 2010
- Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS familyJournal of Neurology, Neurosurgery & Psychiatry, 2010
- FuncBase : a resource for quantitative gene function annotationBioinformatics, 2010
- Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusionsNature Genetics, 2010
- Reduced expression of the Kinesin-Associated Protein 3 ( KIFAP3 ) gene increases survival in sporadic amyotrophic lateral sclerosisProceedings of the National Academy of Sciences of the United States of America, 2009
- A second generation human haplotype map of over 3.1 million SNPsNature, 2007
- PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage AnalysesAmerican Journal of Human Genetics, 2007
- A new multipoint method for genome-wide association studies by imputation of genotypesNature Genetics, 2007
- Principal components analysis corrects for stratification in genome-wide association studiesNature Genetics, 2006
- The International HapMap ProjectNature, 2003