M. Hutz

Clinical Features and Molecular Analysis of the a Thalsemia/Mental Retardation Syndromes. 1. Cases Due to Deletions Involving Chromosome Band 16pl3.3

D. Weatherall, D. Higgs, P. Harris, 2006 .

Clinical Features andMolecular Analysis ofthea Thalsemia/Mental Retardation Syndromes. 1.CasesDueto Deletions Involving ChromosomeBand16pl3.3

J. Lamb, J. Tolmie, D. Weatherall, 1990 .

Association analysis of genes involved in the leptin-signaling pathway with obesity in Brazil

M. Hutz, VS Mattevi, VM Zembrzuski, 2002, International Journal of Obesity.

Application of an African Ancestry Index as a Genomic Control Approach in a Brazilian Population

S. Callegari-Jacques, M. Hutz, V. Zembrzuski, 2006, Annals of human genetics.

The influence of the S19W SNP of the APOA5 gene on triglyceride levels in southern Brazil: interactions with the APOE gene, sex and menopause status.

J. Lucatelli, A. Barros, J. Schuch, 2011, Nutrition, metabolism, and cardiovascular diseases : NMCD.

Association between −250G/A polymorphism of the hepatic lipase gene promoter and coronary artery disease and HDL‐C levels in a Southern Brazilian population

M. Hutz, A. Zago, M. Arsand, 2004, Clinical genetics.

Association study of GIT1 gene with attention‐deficit hyperactivity disorder in Brazilian children and adolescents

L A Rohde, L. Rohde, C. Zeni, 2012, Genes, brain, and behavior.

Adrenergic α2A receptor gene and response to methylphenidate in attention-deficit/hyperactivity disorder-predominantly inattentive type

L. Rohde, M. Hutz, S. Faraone, 2008, Journal of Neural Transmission.

Interaction between SREBP‐1a and APOB polymorphisms influences total and low‐density lipoprotein cholesterol levels in patients with coronary artery disease

M. Hutz, S. Callegari-Jacques, A. Zago, 2003, Clinical genetics.