Association Between Genetics of Diabetes, Coronary Artery Disease, and Macrovascular Complications: Exploring a Common Ground Hypothesis

Por Sousa, André G., Selvatici, Lívia, Krieger, José E., Pereira, Alexandre C.
Publicado em 2011

Molecular Diagnostic and Pathogenesis of Hereditary Hemochromatosis

Por Santos, Paulo C. J. L., Krieger, Jose E., Pereira, Alexandre C.
Publicado em 2012

Global individual ancestry using principal components for family data

Por de Andrade, Mariza, Ray, Debashree, Pereira, Alexandre C., Soler, Júlia P.
Publicado no Hum Hered (2015)

Genetic mapping of a new heart rate QTL on chromosome 8 of spontaneously hypertensive rats

Por Silva, Gustavo JJ, Pereira, Alexandre C, Krieger, Eduardo M, Krieger, José E
Publicado em 2007

Gene by environment QTL mapping through multiple trait analyses in blood pressure salt-sensitivity: identification of a novel QTL in rat chromosome 5

Por Soler, Júlia M Pavan, Pereira, Alexandre C, Tôrres, César H, Krieger, José E
Publicado em 2006

Association of alpha1a-adrenergic receptor polymorphism and blood pressure phenotypes in the Brazilian population

Por Freitas, Silvia R, Pereira, Alexandre C, Floriano, Marcilene S, Mill, José G, Krieger, José E
Publicado em 2008

LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography

Por Santos, Paulo CJL, Bueno, Carolina T, Lemos, Pedro A, Krieger, José E, Pereira, Alexandre C
Publicado em 2014

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

Por Pereira Alexandre C, Krieger José E, Pereira Tiago V, Oliveira Paulo SL, Almeida Marcio AA
Publicado em 2011-01-01

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

Por Giolo, Suely R, Pereira, Alexandre C, de Andrade, Mariza, Krieger, José E, Soler, Júlia P
Publicado em 2010

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

Por Almeida, Marcio AA, Oliveira, Paulo SL, Pereira, Tiago V, Krieger, José E, Pereira, Alexandre C
Publicado em 2011

A negative screen for mutations in calstabin 1 and 2 genes in patients with dilated cardiomyopathy

Por Biagi, Diogo G, Mill, José G, Mansur, Alfredo J, Krieger, José E, Pereira, Alexandre C
Publicado em 2012

Heritability of cardiovascular risk factors in a Brazilian population: Baependi Heart Study

Por de Oliveira, Camila M, Pereira, Alexandre C, de Andrade, Mariza, Soler, Júlia M, Krieger, José E
Publicado em 2008

Genetic Variants of Diabetes Risk and Incident Cardiovascular Events in Chronic Coronary Artery Disease

Por Sousa, André Gustavo P., Lopes, Neuza H., Hueb, Whady A., Krieger, José Eduardo, Pereira, Alexandre C.
Publicado em 2011

Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease

Por Smemo, Scott, Campos, Luciene C., Moskowitz, Ivan P., Krieger, José E., Pereira, Alexandre C., Nobrega, Marcelo A.
Publicado em 2012

Nuclear Factor (NF) κB polymorphism is associated with heart function in patients with heart failure

Por Santos, Diogo GB, Resende, Marina F, Mill, José G, Mansur, Alfredo J, Krieger, José E, Pereira, Alexandre C
Publicado em 2010

Assessment of the Relationship between Self-Declared Ethnicity, Mitochondrial Haplogroups and Genomic Ancestry in Brazilian Individuals

Por Cardena, Mari M. S. G., Ribeiro-dos-Santos, Ândrea, Santos, Sidney, Mansur, Alfredo J., Pereira, Alexandre C., Fridman, Cintia
Publicado em 2013

DiGeorge Syndrome: a not so rare disease

Por Fomin, Angela BF, Pastorino, Antonio Carlos, Kim, Chong Ae, Pereira, Alexandre C, Carneiro‐Sampaio, Magda, Abe Jacob, Cristina Miuki
Publicado em 2010

Influence of the C242T Polymorphism of the p22-phox Gene (CYBA) on the Interaction between Urinary Sodium Excretion and Blood Pressure in an Urban Brazilian Population

Por Schreiber, Roberto, Bellinazzi, Vera Regina, Sposito, Andrei C., Mill, José G., Krieger, José E., Pereira, Alexandre C., Nadruz, Wilson
Publicado em 2013

No evidence for an association between the -36A>C phospholamban gene polymorphism and a worse prognosis in heart failure

Por Santos, Diogo GB, Medeiros, Alessandra, Brum, Patrícia C, Mill, José G, Mansur, Alfredo J, Krieger, José E, Pereira, Alexandre C
Publicado em 2009

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

Por Gioli-Pereira, Luciana, Santos, Paulo CJL, Sugaya, Luisa S, Ferreira, Noely E, Krieger, José Eduardo, Pereira, Alexandre C, Hueb, Whady A
Publicado em 2013