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Lista de obras de Bertram Müller-Myhsok

"DNA Methylation signatures in panic disorder".

artículo científico publicado en 2017

A Gene Locus Responsible for the Familial Hair Shaft Abnormality Pili Annulati Maps to Chromosome 12q24.32–24.33

article

A beginners guide to SNP calling from high-throughput DNA-sequencing data

artículo científico publicado en 2012

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A different view on fine-scale population structure in Western African populations

scientific article published on 19 October 2019

A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder

artículo científico publicado en 2015

A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.

artículo científico publicado en 2014

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

artículo científico publicado en 2009

A hypomorphic vasopressin allele prevents anxiety-related behavior

artículo científico publicado en 2009

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

artículo científico publicado en 2007

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

artículo científico publicado en 2012

A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.

artículo científico publicado en 2012

A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany

artículo científico publicado en 2009

ABCB1 gene variants and antidepressant treatment outcome: A meta-analysis

artículo científico publicado en 2015

ANK3 and CACNA1C--missing genetic link for bipolar disorder and major depressive disorder in two German case-control samples

artículo científico

An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype

artículo científico publicado en 2016

An examination of single nucleotide polymorphism selection prioritization strategies for tests of gene-gene interaction

artículo científico publicado en 2011

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder

artículo científico publicado en 2006

Analyzing pathways from childhood maltreatment to internalizing symptoms and disorders in children and adolescents (AMIS): a study protocol

artículo científico publicado en 2015

Apolipoprotein B-100 gene mutations and cholesterol control in German patients

artículo científico publicado en 2003

Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample

artículo científico publicado en 2012

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

scholarly article by Miruna C. Barbu et al published July 2018 in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging

Association of a Rare Variant with Mismatch Negativity in a Region Between KIAA0319 and DCDC2 in Dyslexia

scientific article published on 21 November 2010

Association of a brain methylation site with clinical outcomes in depression does not replicate across populations

artículo científico publicado en 2015

Association of a specific haplotype across the genes MMP1 and MMP3 with radiographic joint destruction in rheumatoid arthritis

artículo científico publicado en 2004

Association of genetic variants in the neurotrophic receptor-encoding gene NTRK2 and a lifetime history of suicide attempts in depressed patients

artículo científico publicado en 2010

Association of polymorphisms in P2RX7 and CaMKKb with anxiety disorders

artículo científico publicado en 2007

Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome

artículo científico publicado en 2014

CEACAM6 gene variants in inflammatory bowel disease

artículo científico publicado en 2011

CLOCK gene variants associate with sleep duration in two independent populations

artículo científico publicado en 2010

Can previous preterm birth classification influence treatment of short cervix in a subsequent pregnancy? Comparison of vaginal progesterone and Arabin pessary

Characterizing the genetic basis of innate immune response in TLR4-activated human monocytes

artículo científico publicado en 2014

Childhood maltreatment is associated with distinct genomic and epigenetic profiles in posttraumatic stress disorder

artículo científico publicado en 2013

Children with ADHD symptoms have a higher risk for reading, spelling and math difficulties in the GINIplus and LISAplus cohort studies

artículo científico publicado en 2013

Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression

artículo científico publicado en 2019

Clinically apparent and occult metastasized seminoma: almost indistinguishable on the transcriptional level

artículo científico publicado en 2014

Cognitive mechanisms underlying reading and spelling development in five European orthographies

article

Combined effects of exonic polymorphisms in CRHR1 and AVPR1B genes in a case/control study for panic disorder

artículo científico publicado en 2008

Commentary: The importance of exploring dose-dependent, subtype-specific, and age-related effects of maltreatment on the HPA axis and the mediating link to psychopathology. A response to Fisher (2017).

artículo científico publicado en 2017

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

article by Padhraig Gormley et al published September 2018 in Neuron

Common genetic variants influence human subcortical brain structures

artículo científico publicado en 2015

Common variants at ten loci modulate the QT interval duration in the QTSCD Study

artículo científico publicado en 2009

Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families

article

Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies

artículo científico publicado en 2014

Connecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 Mice

artículo científico publicado en 2015

Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis

artículo científico publicado en 2015

Correction: Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1

Creating sparser prediction models of treatment outcome in depression: a proof-of-concept study using simultaneous feature selection and hyperparameter tuning

artículo científico publicado en 2022

Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations

artículo científico publicado en 2016

DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning

artículo científico publicado en 2020

Determination of the real effect of genes identified in GWAS: the example of IL2RA in multiple sclerosis

artículo científico publicado en 2011

Developmental dyslexia--recurrence risk estimates from a german bi-center study using the single proband sib pair design

artículo científico publicado en 2005

Dexamethasone stimulated gene expression in peripheral blood is a sensitive marker for glucocorticoid receptor resistance in depressed patients

artículo científico publicado en 2012

Dilution of candidates: the case of iron-related genes in restless legs syndrome

artículo científico publicado en 2012

Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

artículo científico publicado en 2022

Dissecting the genetic heterogeneity of depression through age at onset

artículo científico publicado en 2012

EPIBLASTER-fast exhaustive two-locus epistasis detection strategy using graphical processing units

artículo científico publicado en 2010

Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene

artículo científico publicado en 2002

Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials

artículo científico publicado en 2018

Efficient branch-and-bound techniques for two-locus association mapping.

artículo científico publicado en 2011

Epidemiology of amebiasis in a region of high incidence of amebic liver abscess in central Vietnam.

artículo científico publicado en 2002

Epigenetic upregulation of FKBP5 by aging and stress contributes to NF-κB-driven inflammation and cardiovascular risk.

artículo científico publicado en 2019

Epistasis between Toll-like receptor-9 polymorphisms and variants in NOD2 and IL23R modulates susceptibility to Crohn's disease

artículo científico publicado en 2009

Epistasis detection on quantitative phenotypes by exhaustive enumeration using GPUs ⬇️

artículo científico publicado en 2011

Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome

artículo científico publicado en 2005

Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

artículo científico publicado en 2016

Erratum: Dexamethasone Stimulated Gene Expression in Peripheral Blood is a Sensitive Marker for Glucocorticoid Receptor Resistance in Depressed Patients

article

Evaluation of Nyholt's procedure for multiple testing correction

scientific article published on 23 August 2005

Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study

artículo científico publicado en 2009

Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset

artículo científico publicado en 2010

Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis

scientific journal article

Evidence for associations between MDGA2 polymorphisms and harm avoidance: replication and extension of a genome-wide association finding.

artículo científico publicado en 2011

Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome

artículo científico publicado en 2006

Evidence for the late MMN as a neurophysiological endophenotype for dyslexia

artículo científico publicado en 2012

Further evidence for DYX1C1 as a susceptibility factor for dyslexia

artículo científico publicado en 2009

Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21.

artículo científico publicado en 2008

GLIDE: GPU-based linear regression for detection of epistasis

artículo científico publicado en 2012

GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.

artículo científico publicado en 2019

Gender-specific association of galanin polymorphisms with HPA-axis dysregulation, symptom severity, and antidepressant treatment response

artículo científico publicado en 2010

Gene expression patterns associated with posttraumatic stress disorder following exposure to the World Trade Center attacks

artículo científico publicado en 2009

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

artículo científico publicado en 2017

Gene-based pleiotropy across migraine with aura and migraine without aura patient groups

artículo científico publicado en 2015

Genes from Chagas susceptibility loci that are differentially expressed in T. cruzi-resistant mice are candidates accounting for impaired immunity

artículo científico publicado en 2006

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

scholarly article published 28 August 2017

Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis

artículo científico

Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders

artículo científico publicado en 2015

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort

artículo científico publicado en 2013

Genetic markers for PTSD risk and resilience among survivors of the World Trade Center attacks

artículo científico publicado en 2011

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

Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study

artículo científico publicado en 2014

Genetic variants in RBFOX3 are associated with sleep latency

artículo científico publicado en 2016

Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with an increased risk of ischemic stroke in white Europeans

artículo científico publicado en 2008

Genetic variation in the Major Histocompatibility Complex and association with depression

Genetic variation in the lymphotoxin-alpha pathway and the risk of ischemic stroke in European populations

artículo científico publicado en 2009

Genetics of restless legs syndrome: A burning urge to move

artículo científico publicado en 2008

Genome Wide Association Scan identifies new variants associated with a cognitive predictor of dyslexia

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

artículo científico publicado en 2016

Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder

artículo científico publicado en 2016

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

artículo científico publicado en 2018

Genome-wide association analysis identifies susceptibility loci for migraine without aura

artículo científico publicado en 2012

Genome-wide association analysis identifies three new breast cancer susceptibility loci

artículo científico publicado en 2012

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

artículo científico publicado en 2013

Genome-wide association study identifies 30 loci associated with bipolar disorder.

artículo científico publicado en 2019

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

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 novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1

scientific journal article

Genome-wide association study of PR interval

artículo científico publicado en 2010

Genome-wide association study of antidepressant treatment-emergent suicidal ideation

artículo científico publicado en 2011

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

artículo científico publicado en 2010

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression

scientific article published on 11 November 2019

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

artículo científico publicado en 2007

Genome-wide association study reveals two new risk loci for bipolar disorder

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 genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL.

artículo científico publicado en 2014

Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families with unknown genetic defects

artículo científico publicado en 2012

Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus

artículo científico publicado en 2017

Genome-wide meta-analysis identifies new susceptibility loci for migraine

artículo científico publicado en 2013

Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster

artículo científico publicado en 2011

Genomewide association scan of suicidal thoughts and behaviour in major depression

artículo científico publicado en 2011

Genomewide linkage analysis identifies polymorphism in the human interferon-gamma receptor affecting Helicobacter pylori infection

artículo científico publicado en 2003

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

artículo científico publicado en 2017

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

artículo científico publicado en 2010

HTR2A gene variation is involved in antidepressant treatment response

artículo científico publicado en 2010

Hair cortisol in maltreated children and adolescents: Importance of developmental period and maltreatment characteristics

scholarly article by Tobias Stalder et al published September 2016 in Psychoneuroendocrinology

Heritability of MRI lesion volume in CADASIL: evidence for genetic modifiers

artículo científico publicado en 2006

Identification and characterization of HPA-axis reactivity endophenotypes in a cohort of female PTSD patients

artículo científico publicado en 2015

Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

artículo científico publicado en 2014

Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1.

artículo científico publicado en 2016

Identification of common variants associated with human hippocampal and intracranial volumes

artículo científico publicado en 2012

Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis

artículo científico publicado en 2017

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

artículo científico publicado en 2017

Imaging genetics of FOXP2 in dyslexia

artículo científico publicado en 2011

Integrating gene expression and epidemiological data for the discovery of genetic interactions associated with cancer risk

artículo científico publicado en 2013

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

artículo científico publicado en 2022

Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals

artículo científico publicado en 2017

Investigating the genetic variation underlying episodicity in major depressive disorder: suggestive evidence for a bipolar contribution

artículo científico publicado en 2013

Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample

artículo científico publicado en 2008

Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample

artículo científico publicado en 2008

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

artículo científico publicado en 2013

Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients

artículo científico publicado en 2010

Lysyl oxidase-like 1 gene polymorphisms in German patients with normal tension glaucoma, pigmentary glaucoma and exfoliation glaucoma

artículo científico publicado en 2010

MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease

artículo científico publicado en 2011

Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21

article

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

artículo científico publicado en 2022

Meta analysis of whole-genome linkage scans with data uncertainty: an application to Parkinson's disease

artículo científico publicado en 2007

Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility

artículo científico publicado en 2012

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

artículo científico publicado en 2016

MicroRNA related polymorphisms and breast cancer risk

artículo científico publicado en 2014

Mitochondrial haplogroup U is associated with a reduced risk to develop exfoliation glaucoma in the German population

artículo científico publicado en 2010

Mouse to human comparative genetics reveals a novel immunoglobulin E-controlling locus on Hsa8q12

artículo científico publicado en 2008

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

artículo científico publicado en 2004

Mutations in the pantothenate kinase gene PANK2 are not associated with Parkinson disease

artículo científico publicado en 2005

Neurobiology of Self-Regulation: Longitudinal Influence of FKBP5 and Intimate Partner Violence on Emotional and Cognitive Development in Childhood

scientific article published on 05 April 2019

Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels

artículo científico publicado en 2010

Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017

Novel genetic loci underlying human intracranial volume identified through genome-wide association

artículo científico publicado en 2016

Novel genetic risk markers for ulcerative colitis in the IL2/IL21 region are in epistasis with IL23R and suggest a common genetic background for ulcerative colitis and celiac disease

artículo científico publicado en 2009

Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation

artículo científico publicado en 2016

P2RX7, a gene coding for a purinergic ligand-gated ion channel, is associated with major depressive disorder

artículo científico publicado en 2006

PARK11 is not linked with Parkinson's disease in European families

article

PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites

artículo científico publicado en 2012

PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome

artículo científico publicado en 2008

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

artículo científico publicado en 2004

Polymorphisms in GRIK4, HTR2A, and FKBP5 show interactive effects in predicting remission to antidepressant treatment

artículo científico publicado en 2009

Polymorphisms in the FKBP5 gene region modulate recovery from psychosocial stress in healthy controls

artículo científico publicado en 2008

Polymorphisms in the GAD2 gene-region are associated with susceptibility for unipolar depression and with a risk factor for anxiety disorders

artículo científico publicado en 2009

Polymorphisms in the angiotensin-converting enzyme gene region predict coping styles in healthy adults and depressed patients

artículo científico

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

artículo científico publicado en 2008

Polymorphisms in the galanin gene are associated with symptom-severity in female patients suffering from panic disorder

artículo científico publicado en 2007

Polymorphisms in the serotonin receptor gene HTR2A are associated with quantitative traits in panic disorder

artículo científico publicado en 2007

Polymorphisms within the metabotropic glutamate receptor 1 gene are associated with depression phenotypes

artículo científico publicado en 2011

Possible associations of NTRK2 polymorphisms with antidepressant treatment outcome: findings from an extended tag SNP approach

artículo científico publicado en 2013

Predictors of developmental dyslexia in European orthographies with varying complexity

artículo científico

Rare variants in PLXNA4 and Parkinson's disease

artículo científico publicado en 2013

Rare variants in TMEM132D in a case-control sample for panic disorder

artículo científico publicado en 2012

Reduced hair cortisol after maltreatment mediates externalizing symptoms in middle childhood and adolescence

artículo científico publicado en 2017

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

Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon

scientific journal article

Role of the NFKB1 -94ins/delATTG promoter polymorphism in IBD and potential interactions with polymorphisms in the CARD15/NOD2, IKBL, and IL-1RN genes

artículo científico publicado en 2006

Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

artículo científico publicado en 2022

Shared genetic etiology between alcohol dependence and major depressive disorder.

artículo científico publicado en 2018

SimPed: a simulation program to generate haplotype and genotype data for pedigree structures

artículo científico publicado en 2005

Small RNAs in the peripheral blood discriminate metastasized from non-metastasized seminoma

artículo científico publicado en 2014

Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array

artículo científico publicado en 2015

Sunlight exposure exerts immunomodulatory effects to reduce multiple sclerosis severity

artículo científico publicado en 2021

Supportive evidence for FOXP1, BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma

artículo científico publicado en 2015

Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome

artículo científico publicado en 2014

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

artículo científico publicado en 2014

The NOD2 Single Nucleotide Polymorphisms rs2066843 and rs2076756 Are Novel and Common Crohn's Disease Susceptibility Gene Variants ⬇️

artículo científico publicado el 30 de diciembre de 2010

The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval

artículo científico publicado en 2003

The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language

artículo científico publicado en 2012

The challenges of genome-wide interaction studies: lessons to learn from the analysis of HDL blood levels

artículo científico publicado en 2014

The endocrine stress response is linked to one specific locus on chromosome 3 in a mouse model based on extremes in trait anxiety

artículo científico publicado en 2012

The genetic architecture of the human cerebral cortex

The neuronal transporter gene SLC6A15 confers risk to major depression

artículo científico publicado en 2011

The usefulness of single nucleotide polymorphisms (SNPs) for genetic epidemiological investigation of complex psychiatric diseases

artículo científico publicado en 2005

Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

scholarly article published 10 March 2018

Tyrosine kinase 2 variant influences T lymphocyte polarization and multiple sclerosis susceptibility

artículo científico

Using affected sib-pairs to uncover rare disease variants

artículo científico publicado en 2012

Using polymorphisms in FKBP5 to define biologically distinct subtypes of posttraumatic stress disorder: evidence from endocrine and gene expression studies

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

Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia.

artículo científico publicado en 2010

XRCC5 as a risk gene for alcohol dependence: evidence from a genome-wide gene-set-based analysis and follow-up studies in Drosophila and humans

artículo científico publicado en 2014

rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants

artículo científico publicado en 2007

rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population

artículo científico publicado en 2009

vipR: variant identification in pooled DNA using R ⬇️

artículo científico publicado el 1 de julio de 2011

αCaMKII autophosphorylation controls the establishment of alcohol drinking behavior

artículo científico publicado en 2013

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