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Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation
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Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation

Wood, Andrew R ; Perry, John R B ; Tanaka, Toshiko ; Hernandez, Dena G ; Zheng, Hou-Feng ; Melzer, David ; Gibbs, J Raphael ; Nalls, Michael A ; Weedon, Michael N ; Spector, Tim D ; Richards, J Brent ; Bandinelli, Stefania ; Ferrucci, Luigi ; Singleton, Andrew B ; Frayling, Timothy M Arking, Dan E.

PloS one, 2013-05, Vol.8 (5), p.e64343-e64343 [Periódico revisado por pares]

United States: Public Library of Science

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2
Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients
Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients
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Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients

Guven, Gamze ; Lohmann, Ebba ; Bras, Jose ; Gibbs, J Raphael ; Gurvit, Hakan ; Bilgic, Basar ; Hanagasi, Hasmet ; Rizzu, Patrizia ; Heutink, Peter ; Emre, Murat ; Erginel-Unaltuna, Nihan ; Just, Walter ; Hardy, John ; Singleton, Andrew ; Guerreiro, Rita Dermaut, Bart

PloS one, 2016-09, Vol.11 (9), p.e0162592-e0162592 [Periódico revisado por pares]

United States: Public Library of Science

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3
Genetic variability in CLU and its association with Alzheimer's disease
Genetic variability in CLU and its association with Alzheimer's disease
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Genetic variability in CLU and its association with Alzheimer's disease

Guerreiro, Rita J ; Beck, John ; Gibbs, J Raphael ; Santana, Isabel ; Rossor, Martin N ; Schott, Jonathan M ; Nalls, Michael A ; Ribeiro, Helena ; Santiago, Beatriz ; Fox, Nick C ; Oliveira, Catarina ; Collinge, John ; Mead, Simon ; Singleton, Andrew ; Hardy, John Weedon, Michael Nicholas

PloS one, 2010-03, Vol.5 (3), p.e9510-e9510 [Periódico revisado por pares]

United States: Public Library of Science

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4
Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected by HapMap Based Imputation. e64343
Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected by HapMap Based Imputation. e64343
Material Type:
Artigo 		Adicionar ao Meu Espaço

Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected by HapMap Based Imputation. e64343

Wood, Andrew R ; Perry, John RB ; Tanaka, Toshiko ; Hernandez, Dena G ; Zheng, Hou-Feng ; Melzer, David ; Gibbs, J Raphael ; Nalls, Michael A ; Weedon, Michael N ; Spector, Tim D

PloS one, 2013-05, Vol.8 (5) [Periódico revisado por pares]

Texto completo disponível

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