Lista de obras - Mads Vilhelm Hollegaard - Dominio Público Uruguay

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

A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations

artículo científico publicado en 2014

A population-based association study of glutamate decarboxylase 1 as a candidate gene for autism

artículo científico publicado en 2009

ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties

scientific article published on 03 January 2017

Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing

artículo científico

CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastoma

artículo científico publicado en 2015

Common risk variants identified in autism spectrum disorder

Common variant at 16p11.2 conferring risk of psychosis.

artículo científico publicado en 2012

Common variants associated with general and MMR vaccine-related febrile seizures

artículo científico publicado en 2014

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

artículo científico publicado en 2011

Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis

artículo científico publicado en 2012

Cytokine gene polymorphism in human disease: on-line databases, Supplement 3.

artículo científico publicado en 2006

DNA Methylation at the Neonatal State and at the Time of Diagnosis: Preliminary Support for an Association with the Estrogen Receptor 1, Gamma-Aminobutyric Acid B Receptor 1, and Myelin Oligodendrocyte Glycoprotein in Female Adolescent Patients with

artículo científico publicado en 2016

DNA methylome profiling using neonatal dried blood spot samples: a proof-of-principle study

artículo científico

Detection of increased gene copy number in DNA from dried blood spot samples allows efficient screening for Klinefelter syndrome

article

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

scholarly article published 3 June 2017

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

artículo científico publicado en 2018

Elevated polygenic burden for autism is associated with differential DNA methylation at birth

artículo científico publicado en 2018

Evaluation of whole genome amplified DNA to decrease material expenditure and increase quality

artículo científico publicado en 2017

Extreme Neonatal Hyperbilirubinemia and a Specific Genotype: A Population-Based Case-Control Study

artículo científico publicado en 2014

Gene expression profiling of archived dried blood spot samples from the Danish Neonatal Screening Biobank

artículo científico

Genetic Variation in NFKBIE Is Associated With Increased Risk of Pneumococcal Meningitis in Children

artículo científico publicado en 2015

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

artículo científico publicado en 2016

Genome-wide association analyses identify variants in developmental genes associated with hypospadias

artículo científico publicado en 2014

Genome-wide associations for birth weight and correlations with adult disease

artículo científico publicado en 2016

Genome-wide scans using archived neonatal dried blood spot samples.

artículo científico publicado en 2009

Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci

artículo científico publicado en 2013

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genotyping whole-genome-amplified DNA from 3- to 25-year-old neonatal dried blood spot samples with reference to fresh genomic DNA.

artículo científico publicado en 2009

High loading of polygenic risk in cases with chronic schizophrenia

artículo científico publicado en 2015

High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA.

artículo científico publicado en 2016

High-throughput genotyping on archived dried blood spot samples

artículo científico

Identification of common genetic risk variants for autism spectrum disorder

artículo científico publicado en 2019

Investigating interactions between early life stress and two single nucleotide polymorphisms in HSD11B2 on the risk of schizophrenia

artículo científico publicado en 2015

Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia

artículo científico publicado en 2014

Joint analysis of SNPs and proteins identifies regulatory IL18 gene variations decreasing the chance of spastic cerebral palsy

artículo científico publicado en 2012

Mannose-Binding Lectin Gene, MBL2, Polymorphisms Do Not Increase Susceptibility to Invasive Meningococcal Disease in a Population of Danish Children

artículo científico publicado en 2015

Mannose-binding lectin gene, MBL2, polymorphisms are not associated with susceptibility to invasive pneumococcal disease in children

artículo científico publicado en 2014

Modelling the contribution of family history and variation in single nucleotide polymorphisms to risk of schizophrenia: a Danish national birth cohort-based study

artículo científico publicado en 2011

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

artículo científico publicado en 2012

Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia: A Danish Population-Based Study and Meta-analysis.

artículo científico publicado en 2015

Polymorphisms in the promoter region of relaxin-2 and preterm birth: involvement of relaxin in the etiology of preterm birth

Polymorphisms in the tumor necrosis factor alpha and interleukin 1-beta promoters with possible gene regulatory functions increase the risk of preterm birth

article

RNA sequencing of archived neonatal dried blood spots

artículo científico publicado en 2016

Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder

artículo científico publicado en 2012

Risk of schizophrenia in relation to parental origin and genome-wide divergence

artículo científico publicado en 2011

Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source

artículo científico publicado en 2011

Synopsis of preterm birth genetic association studies: the preterm birth genetics knowledge base (PTBGene).

artículo científico publicado en 2010

The Prevalence of Mutations inKCNQ1, KCNH2,andSCN5Ain an Unselected National Cohort of Young Sudden Unexplained Death Cases

article by BO GREGERS WINKEL et al published 6 August 2012 in Journal of Cardiovascular Electrophysiology

The role of the sodium current complex in a nonreferred nationwide cohort of sudden infant death syndrome

UGT1A1*28 Genotypes and Respiratory Disease in Very Preterm Infants: A Cohort Study

artículo científico publicado en 2015

UGT1A1*28 polymorphism and acute lymphoblastic leukemia in children: a Danish case-control study

artículo científico publicado en 2014

Variable DNA methylation in neonates mediates the association between prenatal smoking and birth weight

Whole Genome Amplification and Genetic Analysis after Extraction of Proteins from Dried Blood Spots

artículo científico publicado en 2007

Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis

artículo científico publicado en 2011

Lista de obras de Mads Vilhelm Hollegaard

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

A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations

A population-based association study of glutamate decarboxylase 1 as a candidate gene for autism

ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties

Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing

CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastoma

Common risk variants identified in autism spectrum disorder

Common variant at 16p11.2 conferring risk of psychosis.

Common variants associated with general and MMR vaccine-related febrile seizures

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis

Cytokine gene polymorphism in human disease: on-line databases, Supplement 3.

DNA Methylation at the Neonatal State and at the Time of Diagnosis: Preliminary Support for an Association with the Estrogen Receptor 1, Gamma-Aminobutyric Acid B Receptor 1, and Myelin Oligodendrocyte Glycoprotein in Female Adolescent Patients with

DNA methylome profiling using neonatal dried blood spot samples: a proof-of-principle study

Detection of increased gene copy number in DNA from dried blood spot samples allows efficient screening for Klinefelter syndrome

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

Elevated polygenic burden for autism is associated with differential DNA methylation at birth

Evaluation of whole genome amplified DNA to decrease material expenditure and increase quality

Extreme Neonatal Hyperbilirubinemia and a Specific Genotype: A Population-Based Case-Control Study

Gene expression profiling of archived dried blood spot samples from the Danish Neonatal Screening Biobank

Genetic Variation in NFKBIE Is Associated With Increased Risk of Pneumococcal Meningitis in Children

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

Genome-wide association analyses identify variants in developmental genes associated with hypospadias

Genome-wide associations for birth weight and correlations with adult disease

Genome-wide scans using archived neonatal dried blood spot samples.

Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Genotyping whole-genome-amplified DNA from 3- to 25-year-old neonatal dried blood spot samples with reference to fresh genomic DNA.

High loading of polygenic risk in cases with chronic schizophrenia

High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA.

High-throughput genotyping on archived dried blood spot samples

Identification of common genetic risk variants for autism spectrum disorder

Investigating interactions between early life stress and two single nucleotide polymorphisms in HSD11B2 on the risk of schizophrenia

Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia

Joint analysis of SNPs and proteins identifies regulatory IL18 gene variations decreasing the chance of spastic cerebral palsy

Mannose-Binding Lectin Gene, MBL2, Polymorphisms Do Not Increase Susceptibility to Invasive Meningococcal Disease in a Population of Danish Children

Mannose-binding lectin gene, MBL2, polymorphisms are not associated with susceptibility to invasive pneumococcal disease in children

Modelling the contribution of family history and variation in single nucleotide polymorphisms to risk of schizophrenia: a Danish national birth cohort-based study

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia: A Danish Population-Based Study and Meta-analysis.

Polymorphisms in the promoter region of relaxin-2 and preterm birth: involvement of relaxin in the etiology of preterm birth

Polymorphisms in the tumor necrosis factor alpha and interleukin 1-beta promoters with possible gene regulatory functions increase the risk of preterm birth

RNA sequencing of archived neonatal dried blood spots

Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder

Risk of schizophrenia in relation to parental origin and genome-wide divergence

Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source

Synopsis of preterm birth genetic association studies: the preterm birth genetics knowledge base (PTBGene).

The Prevalence of Mutations inKCNQ1, KCNH2,andSCN5Ain an Unselected National Cohort of Young Sudden Unexplained Death Cases

The role of the sodium current complex in a nonreferred nationwide cohort of sudden infant death syndrome

UGT1A1*28 Genotypes and Respiratory Disease in Very Preterm Infants: A Cohort Study

UGT1A1*28 polymorphism and acute lymphoblastic leukemia in children: a Danish case-control study

Variable DNA methylation in neonates mediates the association between prenatal smoking and birth weight

Whole Genome Amplification and Genetic Analysis after Extraction of Proteins from Dried Blood Spots

Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis