Lista de obras -

Candidate genes for anorexia nervosa in the 1p33-36 linkage region: serotonin 1D and delta opioid receptor loci exhibit significant association to anorexia nervosa.

artículo científico publicado en 2003

Case control and family-based studies of tryptophan hydroxylase gene A218C polymorphism and suicidality in adolescents.

artículo científico publicado en 2001

Cohort profile: Epidemiology and Genetics of Obsessive-compulsive disorder and chronic tic disorders in Sweden (EGOS)

scientific article published on 06 January 2020

De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

artículo científico publicado en 2018

De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

artículo científico publicado en 2018

Diagnostic validity of early-onset obsessive-compulsive disorder in the Danish Psychiatric Central Register: findings from a cohort sample

artículo científico publicado en 2017

Dr Nurnberger and Colleagues Reply

scientific article published on 09 April 2019

Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype

scientific article published on 03 August 2020

Evidence for a susceptibility gene for anorexia nervosa on chromosome 1.

artículo científico publicado en 2002

Familial clustering of tic disorders and obsessive-compulsive disorder

artículo científico publicado en 2015

Gender differences in substance use disorders

artículo científico publicado en 1993

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

artículo científico publicado en 2013

Genetics of obsessive-compulsive disorder and related disorders

artículo científico publicado en 2014

Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative.

artículo científico publicado en 2003

Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden

artículo científico publicado en 2017

Identification of five mouse mu-opioid receptor (MOR) gene (Oprm1) splice variants containing a newly identified alternatively spliced exon.

artículo científico publicado en 2007

Identification of rare de novo epigenetic variations in congenital disorders.

artículo científico publicado en 2018

Identification of three mouse mu-opioid receptor (MOR) gene (Oprm1) splice variants containing a newly identified alternatively spliced exon.

artículo científico publicado en 2006

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

artículo científico publicado en 2015

Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach.

artículo científico publicado en 2017

Maternal Effects as Causes of Risk for Obsessive-Compulsive Disorder

scientific article published on 22 January 2020

Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.

artículo científico publicado en 2014

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

artículo científico publicado en 2011

Normalization of Augmented TRH Stimulation Test in Response to ECT.

artículo científico publicado en 1991

Obsessive-Compulsive Disorder

artículo científico publicado en 2014

Parental Age and Differential Estimates of Risk for Neuropsychiatric Disorders: Findings From the Danish Birth Cohort

scientific article published on 27 February 2019

Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder

artículo científico publicado en 2016

Prenatal Maternal Smoking and Increased Risk for Tourette Syndrome and Chronic Tic Disorders.

artículo científico publicado en 2016

Rare structural variation of synapse and neurotransmission genes in autism ⬇️

artículo científico publicado el 1 de marzo de 2011

SLITRK1 binds 14-3-3 and regulates neurite outgrowth in a phosphorylation-dependent manner

scientific journal article

Symptoms of obsessive-compulsive disorder ⬇️

artículo científico publicado el 1 de julio de 1997

The genetics of autism spectrum disorders.

artículo científico publicado en 2006

The increasing prevalence of reported diagnoses of childhood psychiatric disorders: a descriptive multinational comparison

artículo científico publicado en 2014

Transcriptional profiling of C57 and DBA strains of mice in the absence and presence of morphine.

artículo científico publicado en 2007

What Should a Psychiatrist Know About Genetics? Review and Recommendations From the Residency Education Committee of the International Society of Psychiatric Genetics

artículo científico publicado en 2018

Lista de obras de

Candidate genes for anorexia nervosa in the 1p33-36 linkage region: serotonin 1D and delta opioid receptor loci exhibit significant association to anorexia nervosa.

Case control and family-based studies of tryptophan hydroxylase gene A218C polymorphism and suicidality in adolescents.

Cohort profile: Epidemiology and Genetics of Obsessive-compulsive disorder and chronic tic disorders in Sweden (EGOS)

De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

Diagnostic validity of early-onset obsessive-compulsive disorder in the Danish Psychiatric Central Register: findings from a cohort sample

Dr Nurnberger and Colleagues Reply

Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype

Evidence for a susceptibility gene for anorexia nervosa on chromosome 1.

Familial clustering of tic disorders and obsessive-compulsive disorder

Gender differences in substance use disorders

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

Genetics of obsessive-compulsive disorder and related disorders

Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative.

Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden

Identification of five mouse mu-opioid receptor (MOR) gene (Oprm1) splice variants containing a newly identified alternatively spliced exon.

Identification of rare de novo epigenetic variations in congenital disorders.

Identification of three mouse mu-opioid receptor (MOR) gene (Oprm1) splice variants containing a newly identified alternatively spliced exon.

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach.

Maternal Effects as Causes of Risk for Obsessive-Compulsive Disorder

Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Normalization of Augmented TRH Stimulation Test in Response to ECT.

Obsessive-Compulsive Disorder

Parental Age and Differential Estimates of Risk for Neuropsychiatric Disorders: Findings From the Danish Birth Cohort

Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder

Prenatal Maternal Smoking and Increased Risk for Tourette Syndrome and Chronic Tic Disorders.

Rare structural variation of synapse and neurotransmission genes in autism ⬇️

SLITRK1 binds 14-3-3 and regulates neurite outgrowth in a phosphorylation-dependent manner

Symptoms of obsessive-compulsive disorder ⬇️

The genetics of autism spectrum disorders.

The increasing prevalence of reported diagnoses of childhood psychiatric disorders: a descriptive multinational comparison

Transcriptional profiling of C57 and DBA strains of mice in the absence and presence of morphine.

What Should a Psychiatrist Know About Genetics? Review and Recommendations From the Residency Education Committee of the International Society of Psychiatric Genetics