User profiles for Mara H. Hutz
 | Mara H. HutzDEPARTAMENTO DE GENETICA, UNIVERSIDADE FEDERAL DO RIO GRANDE DO SUL Verified email at ufrgs.br Cited by 13326 |
[HTML][HTML] The genomic ancestry of individuals from different geographical regions of Brazil is more uniform than expected
…, M Fuchshuber-Moraes, JP Genro, MH Hutz… - PloS one, 2011 - journals.plos.org
Based on pre-DNA racial/color methodology, clinical and pharmacological trials have
traditionally considered the different geographical regions of Brazil as being very heterogeneous. …
traditionally considered the different geographical regions of Brazil as being very heterogeneous. …
Assessing individual interethnic admixture and population substructure using a 48–insertion‐deletion (INSEL) ancestry‐informative marker (AIM) panel
Estimating the proportions of different ancestries in admixed populations is very important in
population genetics studies, and it is particularly important for detecting population …
population genetics studies, and it is particularly important for detecting population …
[PDF][PDF] Y-chromosome evidence for differing ancient demographic histories in the Americas
To scrutinize the male ancestry of extant Native American populations, we examined eight
biallelic and six microsatellite polymorphisms from the nonrecombining portion of the Y …
biallelic and six microsatellite polymorphisms from the nonrecombining portion of the Y …
The role of common variants of ABCB1, CYP3A4, and CYP3A5 genes in lipid‐lowering efficacy and safety of simvastatin treatment
…, MEW Ferreira, RC Pires, MH Hutz - Clinical …, 2005 - Wiley Online Library
Objective Our objective was to investigate the interactions between common polymorphisms
in ABCB1, CYP3A4, and CYP3A5 genes and the lipid‐lowering efficacy and safety of the 3‐…
in ABCB1, CYP3A4, and CYP3A5 genes and the lipid‐lowering efficacy and safety of the 3‐…
MAOA‐uVNTR polymorphism in a Brazilian sample: Further support for the association with impulsive behaviors and alcohol dependence
…, FZC Marques, CED Garcia, MH Hutz… - American Journal of …, 2006 - Wiley Online Library
The enzyme monoamine oxidase A (MAO A) plays an important role in the metabolism of
neurotransmitters. The MAOA gene presents several polymorphisms, including a 30‐bp VNTR …
neurotransmitters. The MAOA gene presents several polymorphisms, including a 30‐bp VNTR …
Historical genetics: spatiotemporal analysis of the formation of the Brazilian population
…, SG Crossetti, ME Ferreira, MH Hutz - American Journal of …, 2003 - Wiley Online Library
A total of 1,037 individuals living in five different sociogeographic regions of Brazil were
studied in relation to 12 short tandem repeat polymorphisms. The objective was to assess the …
studied in relation to 12 short tandem repeat polymorphisms. The objective was to assess the …
Attention-deficit/hyperactivity disorder and the dopaminergic hypotheses
Attention-deficit/hyperactivity disorder (ADHD) is a common psychiatric condition that affects
approximately 5.3% of children worldwide. This disorder is defined by a combination of …
approximately 5.3% of children worldwide. This disorder is defined by a combination of …
Attention‐deficit hyperactivity disorder: A study of association with both the dopamine transporter gene and the dopamine D4 receptor gene
Attention‐deficit hyperactivity disorder (ADHD) is one of the most common psychiatric
disorders of childhood. The role of genetic factors in its etiology is strongly supported by family, …
disorders of childhood. The role of genetic factors in its etiology is strongly supported by family, …
Association of the adrenergic α2A receptor gene with methylphenidate improvement of inattentive symptoms in children and adolescents with attention-deficit …
…, AP Guimarães, T Roman, MH Hutz… - Archives of general …, 2007 - jamanetwork.com
Context Preclinical studies have demonstrated the relevance of adrenergic α2A receptor on
the attentional process and the mechanism of action of methylphenidate hydrochloride. …
the attentional process and the mechanism of action of methylphenidate hydrochloride. …
DRD2 haplotype is associated with dyskinesia induced by levodopa therapy in Parkinson's disease patients
…, SM Callegari-Jacques, CRM Rieder, MH Hutz - …, 2012 - Future Medicine
Aim: Dyskinesia and motor fluctuation are frequent and serious complications of chronic
levodopa therapy in patients with Parkinson’s disease. Since genetic factors could play a role in …
levodopa therapy in patients with Parkinson’s disease. Since genetic factors could play a role in …