Latest papers

Genomic analysis of mental illness: a changing landscape.

Heterogeneity of clinical manifestation of hypertrophic cardiomyopathy caused by deletion of lysine 183 in cardiac troponin I gene.

[Desperately seeking heritability].

Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease.

Complete nucleotide sequence and comparative analysis of pPR9, a 41.7-kilobase conjugative staphylococcal multiresistance plasmid conferring high-level mupirocin resistance.

Hb CS-H disease combined with beta-thalassemia--a case report.

Genetic variants and risk of lung cancer in never smokers: a genome-wide association study.

Genetic diversity during the development of Barrett's oesophagus-associated adenocarcinoma: how, when and why?

A two-sex life history model of handicap signaling.

CFTR allelic heterogeneity in Brazil: historical and geographical perspectives and implications for screening and counseling for cystic fibrosis in this country.

Pharmacogenetics of chronic obstructive pulmonary disease: challenges and opportunities.

Males with familial idiopathic scoliosis: a distinct phenotypic subgroup.

Associations between osteoprotegerin polymorphisms and bone mineral density: a meta-analysis.

-765G>C and 8473T>C polymorphisms of COX-2 and cancer risk: a meta-analysis based on 33 case-control studies.

Prevalence and genetic heterogeneity of Borrelia burgdorferi sensu lato in Ixodes ticks in Belgium.

Association between Fc receptor-like 3 C169T polymorphism and risk of systemic lupus erythematosus: a meta-analysis.

MEFV heterogeneity in Turkish Familial Mediterranean Fever patients.

Reinforcement of a minor alternative splicing event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness.

Piebaldism and neurofibromatosis type 1: family report.

No association with the ETM2 locus in Czech patients with familial essential tremor.