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Cell‐Free DNA: An Upcoming Biomarker in Transplantation

American journal of transplantation, 2015-10, Vol.15 (10), p.2541-2551

2015

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Progranulin locus deletion in frontotemporal dementia

Human mutation, 2008, Vol.29 (1), p.53-58

2008

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Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder

Molecular psychiatry, 2001-09, Vol.6 (5), p.579-585

2001

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A major SNP haplotype of the arginine vasopressin 1B receptor protects against recurrent major depression

Molecular psychiatry, 2004-03, Vol.9 (3), p.287-292

2004

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Meta-analyses of genetic studies on major depressive disorder

Molecular psychiatry, 2008-08, Vol.13 (8), p.772-785

2008

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MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene sets

Molecular psychiatry, 2015-04, Vol.20 (4), p.472-481

2015

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Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations

Neurology, 2010-09, Vol.75 (13), p.1159-1165

2010

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HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study

Molecular psychiatry, 2007-09, Vol.12 (9), p.797-798

2007

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Gene expression analysis of estrogenic compounds in the liver of common carp (Cyprinus carpio) using a custom cDNA microarray

Journal of biochemical and molecular toxicology, 2007-01, Vol.21 (5), p.299-311

2007

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Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families

Molecular psychiatry, 2008-04, Vol.13 (4), p.442-450

2008

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Mutations in SACS cause atypical and late-onset forms of ARSACS

Neurology, 2010-09, Vol.75 (13), p.1181-1188

2010

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Mood stabilizing drugs regulate transcription of immune, neuronal and metabolic pathway genes in Drosophila

Psychopharmacology, 2016-05, Vol.233 (9), p.1751-1762

2016

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Caspase deficiency alters the murine gut microbiome

Cell death & disease, 2011-10, Vol.2 (10), p.e220-e220

2011

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Association between COMT (Val Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study

Molecular psychiatry, 2005-06, Vol.10 (6), p.598-605

2005

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The serotonin transporter promoter repeat length polymorphism, seasonal affective disorder and seasonality

Psychological medicine, 2003-07, Vol.33 (5), p.785-792

2003

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Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9q

Neurology, 2007-06, Vol.68 (23), p.1995-2002

2007

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Evaluation of a multiplex-PCR detection in combination with an isolation method for STEC O26, O103, O111, O145 and sorbitol fermenting O157 in food

Food microbiology, 2012-02, Vol.29 (1), p.49-55

2012

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Comprehensive Profiling of the Androgen Receptor in Liquid Biopsies from Castration-resistant Prostate Cancer Reveals Novel Intra-AR Structural Variation and Splice Variant Expression Patterns

European urology, 2017-08, Vol.72 (2), p.192-200

2017

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Novel locus on chromosome 12q22–q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizures

Journal of medical genetics, 2004-09, Vol.41 (9), p.710-714

2004

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De novo KCNQ2 mutations in patients with benign neonatal seizures

Neurology, 2004-12, Vol.63 (11), p.2155-2158

2004

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A novel susceptibility locus at 2p24 for generalised epilepsy with febrile seizures plus

Journal of medical genetics, 2005-12, Vol.42 (12), p.947-952

2005

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P.1.a.004 Associations between AVPR1b and NR3C1 gene variants and HPA axis responses to psychosocial stress

European neuropsychopharmacology, 2010, Vol.20, p.S214-S215

2010

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SNPbox: web-based high-throughput primer design from gene to genome

Nucleic acids research, 2004-07, Vol.32 (Web Server issue), p.W170-W172

2004

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S63-04 Stress responsivity in childhood and adulthood: Role of the glucocorticoid receptor gene

European psychiatry, 2009, Vol.24, p.S304-S304

2009

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APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.2977-2983

2006

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Cell‐Free DNA: An Upcoming Biomarker in Transplantation

Progranulin locus deletion in frontotemporal dementia

Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder

A major SNP haplotype of the arginine vasopressin 1B receptor protects against recurrent major depression

Meta-analyses of genetic studies on major depressive disorder

MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene sets

Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations

HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study

Gene expression analysis of estrogenic compounds in the liver of common carp (Cyprinus carpio) using a custom cDNA microarray

Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families

Mutations in SACS cause atypical and late-onset forms of ARSACS

Mood stabilizing drugs regulate transcription of immune, neuronal and metabolic pathway genes in Drosophila

Caspase deficiency alters the murine gut microbiome

Association between COMT (Val Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study

The serotonin transporter promoter repeat length polymorphism, seasonal affective disorder and seasonality

Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9q

Evaluation of a multiplex-PCR detection in combination with an isolation method for STEC O26, O103, O111, O145 and sorbitol fermenting O157 in food

Comprehensive Profiling of the Androgen Receptor in Liquid Biopsies from Castration-resistant Prostate Cancer Reveals Novel Intra-AR Structural Variation and Splice Variant Expression Patterns

Novel locus on chromosome 12q22–q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizures

De novo KCNQ2 mutations in patients with benign neonatal seizures

A novel susceptibility locus at 2p24 for generalised epilepsy with febrile seizures plus

P.1.a.004 Associations between AVPR1b and NR3C1 gene variants and HPA axis responses to psychosocial stress

SNPbox: web-based high-throughput primer design from gene to genome

S63-04 Stress responsivity in childhood and adulthood: Role of the glucocorticoid receptor gene

APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

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