Andre F Reis
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Andre F Reis has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- Fernando M. A. Giuffrida
Universidade do Estado da Bahia, Brasil
1 shared publication - Gilberto K Furuzawa
Universidade Federal de São Paulo, Departamento de Medicina, Disciplina de Endocrinologia, R. Pedro de Toledo, 981 12o andar, Vila Clementino, Sao Paulo, SP – Brazil
1 shared publication - Marcos M Oliveira
Universidade Federal de São Paulo, Departamento de Medicina, Disciplina de Endocrinologia, R. Pedro de Toledo, 981 12o andar, Vila Clementino, Sao Paulo, SP – Brazil
1 shared publication - Sergio Atala Dib
Universidade Federal de Sao Paulo, Brasil
1 shared publication - Teresa Kasamatsu
Endocrinology Division, São Paulo Federal University, Rua Botucatu, 740-Vila Clementino, São Paulo, SP CEP 04034-970 Brazil
1 shared publication
Latest Publications
- Open Access
- 1 January 2009
- Published by Springer Nature in Cardiovascular Diabetology
- Vol. 8 (1) , 28
HNF1A gene polymorphisms and cardiovascular risk factors in individuals with late-onset autosomal dominant diabetes: a cross-sectional study
Type 2 diabetes mellitus (T2DM) is a genetically heterogeneous disease, hepatocyte nuclear factor-1 homeobox A (HNF1A) single-nucleotide polymorphisms (SNPs) playing a minor role in its pathogenesis. HNF1A is a frequent cause of monogenic diabetes, albeit with early-onset. Some uncommon subgroups like late-onset autosomal dominant diabetes mellitus (LOADDM) may present peculiar inheritance patterns with a stronger familial component. This study aims to investigate the relationship of HNF1A SNPs with cardiovascular risk factors in this group, as well as to characterize them in contrast with classical T2DM (CT2DM).
- 1 January 2009
- Published by Springer Nature in Cardiovascular Diabetology
- Vol. 8 (1) , 28
Open AccessHNF1A gene polymorphisms and cardiovascular risk factors in individuals with late-onset autosomal dominant diabetes: a cross-sectional study
Type 2 diabetes mellitus (T2DM) is a genetically heterogeneous disease, hepatocyte nuclear factor-1 homeobox A (HNF1A) single-nucleotide polymorphisms (SNPs) playing a minor role in its pathogenesis. HNF1A is a frequent cause of monogenic diabetes, albeit with early-onset. Some uncommon subgroups like late-onset autosomal dominant diabetes mellitus (LOADDM) may present peculiar inheritance patterns with a stronger familial component. This study aims to investigate the relationship of HNF1A SNPs with cardiovascular risk factors in this group, as well as to characterize them in contrast with classical T2DM (CT2DM).