Lista de obras -

A cross-over medication trial for patients with autosomal-dominant hypertension with brachydactyly

An integrated genome research network for studying the genetics of alcohol addiction

artículo científico publicado en 2010

Familial aggregation of pure tone hearing thresholds in an aging European population

artículo científico publicado en 2013

Feasible and Successful: Genome-Wide Interaction Analysis Involving All 1.9 × 1011 Pair-Wise Interaction Tests

article

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

artículo científico publicado en 2013

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia

artículo científico publicado en 2005

Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait

artículo científico publicado en 2008

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

artículo científico publicado en 2012

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

artículo científico publicado en 2011

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

artículo científico publicado en 2009

Genome-wide association study of alcohol dependence

scientific journal article

Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study

artículo científico publicado en 2014

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

artículo científico publicado en 2010

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

scientific journal article

Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.

artículo científico publicado en 2005

Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation.

artículo científico publicado en 2017

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

artículo científico publicado en 2009

No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach.

artículo científico publicado en 2003

Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter study

artículo científico publicado en 2008

PDE3A mutations cause autosomal dominant hypertension with brachydactyly

artículo científico publicado en 2015

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

artículo científico publicado en 2006

Schizophrenia risk polymorphisms in the TCF4 gene interact with smoking in the modulation of auditory sensory gating

artículo científico publicado en 2012

Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypes

artículo científico publicado en 2008

Susceptibility variants for male-pattern baldness on chromosome 20p11.

artículo científico publicado en 2008

The contribution of GJB2 (Connexin 26) 35delG to age-related hearing impairment and noise-induced hearing loss

artículo científico publicado en 2007

The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q.

artículo científico publicado en 2007

The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment

artículo científico publicado en 2007

The opioid peptides enkephalin and beta-endorphin in alcohol dependence

artículo científico publicado en 2008

VEGF Gene Haplotypes Are Associated With Sarcoidosis

article

Lista de obras de

A cross-over medication trial for patients with autosomal-dominant hypertension with brachydactyly

An integrated genome research network for studying the genetics of alcohol addiction

Familial aggregation of pure tone hearing thresholds in an aging European population

Feasible and Successful: Genome-Wide Interaction Analysis Involving All 1.9 × 1011 Pair-Wise Interaction Tests

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

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia

Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

Genome-wide association study of alcohol dependence

Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study

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

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.

Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation.

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach.

Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter study

PDE3A mutations cause autosomal dominant hypertension with brachydactyly

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

Schizophrenia risk polymorphisms in the TCF4 gene interact with smoking in the modulation of auditory sensory gating

Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypes

Susceptibility variants for male-pattern baldness on chromosome 20p11.

The contribution of GJB2 (Connexin 26) 35delG to age-related hearing impairment and noise-induced hearing loss

The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q.

The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment

The opioid peptides enkephalin and beta-endorphin in alcohol dependence

VEGF Gene Haplotypes Are Associated With Sarcoidosis