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1
ALDH1A2 (RALDH2) genetic variation in human congenital heart disease
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ALDH1A2 (RALDH2) genetic variation in human congenital heart disease

Pavan, Marilene ; Ruiz, Viviane F ; Silva, Fábio A ; Sobreira, Tiago J ; Cravo, Roberta M ; Vasconcelos, Michelle ; Marques, Lívia P ; Mesquita, Sonia M F ; Krieger, José E ; Lopes, Antônio A B ; Oliveira, Paulo S ; Pereira, Alexandre C ; Xavier-Neto, José

BMC genetics, 2009-11, Vol.10 (1), p.113-113, Article 113 [Periódico revisado por pares]

England: BioMed Central Ltd

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2
Heritability of physical activity traits in Brazilian families: the Baependi Heart Study
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Heritability of physical activity traits in Brazilian families: the Baependi Heart Study

Horimoto, Andréa R V R ; Giolo, Suely R ; Oliveira, Camila M ; Alvim, Rafael O ; Soler, Júlia P ; de Andrade, Mariza ; Krieger, José E ; Pereira, Alexandre C

BMC genetics, 2011-11, Vol.12 (1), p.155-155, Article 155 [Periódico revisado por pares]

England: BioMed Central Ltd

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3
Evaluating gene by sex and age interactions on cardiovascular risk factors in Brazilian families
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Evaluating gene by sex and age interactions on cardiovascular risk factors in Brazilian families

Giolo, Suely R ; Pereira, Alexandre C ; de Andrade, Mariza ; Krieger, José E ; Soler, Júlia P

BMC genetics, 2010-09, Vol.11 (1), p.132-132, Article 132 [Periódico revisado por pares]

England: BioMed Central Ltd

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4
An empirical evaluation of imputation accuracy for association statistics reveals increased type-I error rates in genome-wide associations
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An empirical evaluation of imputation accuracy for association statistics reveals increased type-I error rates in genome-wide associations

Almeida, Marcio A A ; Oliveira, Paulo S L ; Pereira, Tiago V ; Krieger, José E ; Pereira, Alexandre C

BMC genetics, 2011-01, Vol.12 (1), p.10-10, Article 10 [Periódico revisado por pares]

England: BioMed Central Ltd

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5
Nuclear Factor [kappa]B polymorphism is associated with heart function in patients with heart failure.(Research article)
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Nuclear Factor [kappa]B polymorphism is associated with heart function in patients with heart failure.(Research article)

Santos, Diogo GB ; Resende, Marina F ; Mill, José G ; Mansur, Alfredo J ; Krieger, José E ; Pereira, Alexandre C

BMC genetics, 2010-06, Vol.11 (1), p.89-89 [Periódico revisado por pares]

London: BioMed Central Ltd

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6
Association between UCP2 A55V polymorphism and risk of cardiovascular events in patients with multi-vessel coronary arterial disease
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Association between UCP2 A55V polymorphism and risk of cardiovascular events in patients with multi-vessel coronary arterial disease

Gioli-Pereira, Luciana ; Santos, Paulo Cjl ; Sugaya, Luisa S ; Ferreira, Noely E ; Krieger, José Eduardo ; Pereira, Alexandre C ; Hueb, Whady A

BMC genetics, 2013-03, Vol.14 (1), p.40-40 [Periódico revisado por pares]

England: BioMed Central

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