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Volumn 10, Issue 10, 2014, Pages 549-550

Common genetic variants and the heritability of ALS

Author keywords

[No Author keywords available]

Indexed keywords

AMYOTROPHIC LATERAL SCLEROSIS; DISEASE ASSOCIATION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; HERITABILITY; HUMAN; PRIORITY JOURNAL; SHORT SURVEY; SINGLE NUCLEOTIDE POLYMORPHISM; FEMALE; GENETICS; GENOME-WIDE ASSOCIATION STUDY; MALE;

EID: 84926528112     PISSN: 17594758     EISSN: 17594766     Source Type: Journal    
DOI: 10.1038/nrneurol.2014.166     Document Type: Short Survey
Times cited : (12)

References (10)
  • 1
    • 84907562357 scopus 로고    scopus 로고
    • Genome-wide analysis of the heritability of amyotrophic lateral sclerosis
    • Keller, M. F. et al. Genome-wide analysis of the heritability of amyotrophic lateral sclerosis. JAMA Neurol. http://dx.doi.org/10.1001/jamaneurol.2014.1184.
    • JAMA Neurol.
    • Keller, M.F.1
  • 3
    • 81555223367 scopus 로고    scopus 로고
    • The risk to relatives of patients with sporadic amyotrophic lateral sclerosis
    • Hanby, M. F. et al. The risk to relatives of patients with sporadic amyotrophic lateral sclerosis. Brain 134, 3454-3457 (2011).
    • (2011) Brain , vol.134 , pp. 3454-3457
    • Hanby, M.F.1
  • 4
    • 78649632679 scopus 로고    scopus 로고
    • An estimate of amyotrophic lateral sclerosis heritability using twin data
    • Al-Chalabi, A. et al. An estimate of amyotrophic lateral sclerosis heritability using twin data. J. Neurol. Neurosurg. Psychiatry 81, 1324-1326 (2010).
    • (2010) J. Neurol. Neurosurg. Psychiatry , vol.81 , pp. 1324-1326
    • Al-Chalabi, A.1
  • 5
    • 81555218171 scopus 로고    scopus 로고
    • The heritability of amyotrophic lateral sclerosis in a clinically ascertained United States research registry
    • Wingo, T. S., Cutler, D. J., Yarab, N., Kelly, C. M. & Glass, J. D. The heritability of amyotrophic lateral sclerosis in a clinically ascertained United States research registry. PLoS ONE 6, e27985 (2011).
    • (2011) PLoS ONE , vol.6 , pp. e27985
    • Wingo, T.S.1    Cutler, D.J.2    Yarab, N.3    Kelly, C.M.4    Glass, J.D.5
  • 6
    • 84897859556 scopus 로고    scopus 로고
    • A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
    • Fogh, I. et al. A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. Hum. Mol. Genet. 23, 2220-2231 (2014).
    • (2014) Hum. Mol. Genet. , vol.23 , pp. 2220-2231
    • Fogh, I.1
  • 7
    • 0029010496 scopus 로고
    • Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase
    • Andersen, P. M. et al. Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase. Nat. Genet. 10, 61-66 (1995).
    • (1995) Nat. Genet. , vol.10 , pp. 61-66
    • Andersen, P.M.1
  • 8
    • 84865071988 scopus 로고    scopus 로고
    • Evidence for an oligogenic basis of amyotrophic lateral sclerosis
    • van Blitterswijk, M. et al. Evidence for an oligogenic basis of amyotrophic lateral sclerosis. Hum. Mol. Genet. 21, 3776-3784 (2012).
    • (2012) Hum. Mol. Genet. , vol.21 , pp. 3776-3784
    • Van Blitterswijk, M.1
  • 9
    • 80051586618 scopus 로고    scopus 로고
    • Modelling the effects of penetrance and family size on rates of sporadic and familial disease
    • Al-Chalabi, A. & Lewis, C. M. Modelling the effects of penetrance and family size on rates of sporadic and familial disease. Hum. Hered. 71, 281-288 (2011).
    • (2011) Hum. Hered. , vol.71 , pp. 281-288
    • Al-Chalabi, A.1    Lewis, C.M.2
  • 10
    • 79955777846 scopus 로고    scopus 로고
    • Proposed criteria for familial amyotrophic lateral sclerosis
    • Byrne, S. et al. Proposed criteria for familial amyotrophic lateral sclerosis. Amyotroph. Lateral Scler. 12, 157-159 (2011).
    • (2011) Amyotroph. Lateral Scler. , vol.12 , pp. 157-159
    • Byrne, S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.