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A Candidate Gene Association Study Identifies DAPL1 as a Female-Specific Susceptibility Locus for Age-Related Macular Degeneration (AMD).

artículo científico publicado en 2015

A genomewide association study points to multiple loci that predict antidepressant drug treatment outcome in depression

artículo científico publicado en 2009

A mega-analysis of genome-wide association studies for major depressive disorder

artículo científico publicado en 2012

A novel deletion in progranulin gene is associated with FTDP-17 and CBS.

artículo científico publicado en 2006

Estimating the age of the most common Italian GRN mutation: walking back to Canossa times

artículo científico publicado en 2013

Genetic markers within glutamate receptors associated with antidepressant treatment-emergent suicidal ideation

artículo científico publicado en 2008

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression

artículo científico publicado en 2010

Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci

artículo científico publicado en 2014

Ghrelin receptor gene: identification of several sequence variants in extremely obese children and adolescents, healthy normal-weight and underweight students, and children with short normal stature

artículo científico publicado en 2004

Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

artículo científico publicado en 2012

Linkage disequilibrium patterns and tagSNP transferability among European populations

artículo científico publicado en 2005

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error

artículo científico publicado en 2013

Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error

artículo científico publicado en 2013

Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation

artículo científico publicado en 2016

Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment

artículo científico publicado en 2004

Polymorphisms in the drug transporter gene ABCB1 predict antidepressant treatment response in depression

artículo científico publicado en 2008

Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from Germany

artículo científico publicado en 2006

Resistance to antidepressant treatment is associated with polymorphisms in the leptin gene, decreased leptin mRNA expression, and decreased leptin serum levels

artículo científico publicado en 2012

SNP-based analysis of genetic substructure in the German population.

artículo científico publicado en 2006

Sequence diversity of KIAA0027/MLC1: are megalencephalic leukoencephalopathy and schizophrenia allelic disorders?

artículo científico publicado en 2003

Spondylo-ocular syndrome: a new entity with crystalline lens malformation, cataract, retinal detachment, osteoporosis, and platyspondyly

artículo científico publicado en 2003

The neuronal transporter gene SLC6A15 confers risk to major depression

artículo científico publicado en 2011

Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome

artículo científico publicado en 2008

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