Literature DB >> 12768434

Variants in the ALS2 gene are not associated with sporadic amyotrophic lateral sclerosis.

Ammar Al-Chalabi, Valerie K Hansen, Claire L Simpson, Jing Xi, Betsy A Hosler, John F Powell, Diane McKenna-Yasek, Christopher E Shaw, P Nigel Leigh, Robert H Brown.   

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Year:  2003        PMID： 12768434     DOI： 10.1007/s10048-003-0152-1

Source DB:  PubMed          Journal:  Neurogenetics        ISSN： 1364-6745            Impact factor:   2.660


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  8 in total

1.  Association mapping of disease loci, by use of a pooled DNA genomic screen.

Authors:  L F Barcellos; W Klitz; L L Field; R Tobias; A M Bowcock; R Wilson; M P Nelson; J Nagatomi; G Thomson
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

2.  Monte Carlo tests for associations between disease and alleles at highly polymorphic loci.

Authors:  P C Sham; D Curtis
Journal:  Ann Hum Genet       Date:  1995-01       Impact factor: 1.670

3.  Independence tests for VNTR alleles defined as quantile bins.

Authors:  B S Weir
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

4.  "Sporadic" motoneuron disease due to familial SOD1 mutation with low penetrance.

Authors:  G Suthers; N Laing; S Wilton; S Dorosz; H Waddy
Journal:  Lancet       Date:  1994 Dec 24-31       Impact factor: 79.321

5.  Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation.

Authors:  M Jackson; A Al-Chalabi; Z E Enayat; B Chioza; P N Leigh; K E Morrison
Journal:  Ann Neurol       Date:  1997-11       Impact factor: 10.422

6.  The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.

Authors:  Y Yang; A Hentati; H X Deng; O Dabbagh; T Sasaki; M Hirano; W Y Hung; K Ouahchi; J Yan; A C Azim; N Cole; G Gascon; A Yagmour; M Ben-Hamida; M Pericak-Vance; F Hentati; T Siddique
Journal:  Nat Genet       Date:  2001-10       Impact factor: 38.330

7.  A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.

Authors:  S Hadano; C K Hand; H Osuga; Y Yanagisawa; A Otomo; R S Devon; N Miyamoto; J Showguchi-Miyata; Y Okada; R Singaraja; D A Figlewicz; T Kwiatkowski; B A Hosler; T Sagie; J Skaug; J Nasir; R H Brown; S W Scherer; G A Rouleau; M R Hayden; J E Ikeda
Journal:  Nat Genet       Date:  2001-10       Impact factor: 38.330

8.  Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.

Authors:  D R Rosen; T Siddique; D Patterson; D A Figlewicz; P Sapp; A Hentati; D Donaldson; J Goto; J P O'Regan; H X Deng
Journal:  Nature       Date:  1993-03-04       Impact factor: 49.962
  8 in total
  2 in total

Review 1.  ALS drug development: reflections from the past and a way forward.

Authors:  Swati Aggarwal; Merit Cudkowicz
Journal:  Neurotherapeutics       Date:  2008-10       Impact factor: 7.620

2.  Targeted Genetic Screen in Amyotrophic Lateral Sclerosis Reveals Novel Genetic Variants with Synergistic Effect on Clinical Phenotype.

Authors:  Johnathan Cooper-Knock; Henry Robins; Isabell Niedermoser; Matthew Wyles; Paul R Heath; Adrian Higginbottom; Theresa Walsh; Mbombe Kazoka; Paul G Ince; Guillaume M Hautbergue; Christopher J McDermott; Janine Kirby; Pamela J Shaw
Journal:  Front Mol Neurosci       Date:  2017-11-09       Impact factor: 5.639
  2 in total

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