Lista de obras - Jakob Grove - Dominio Público Uruguay

30. COMT Val158Met and MTHFR C677T Moderate Risk of Schizophrenia in Response to Childhood Trauma.

artículo científico publicado en 2017

A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex

artículo científico publicado en 2022

A polygenic resilience score moderates the genetic risk for schizophrenia

artículo científico publicado en 2019

A review of software for microarray genotyping

artículo científico publicado en 2011

ASD and ADHD have a similar burden of rare protein-truncating variants

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

scientific article published on 03 January 2017

AUTOMORPHISM FIXED POINTS IN THE MODULI SPACE OF SEMI-STABLE BUNDLES

Amniotic fluid MMP-9 and neurotrophins in autism spectrum disorders: an exploratory study.

artículo científico publicado en 2012

Amniotic fluid chemokines and autism spectrum disorders: an exploratory study utilizing a Danish Historic Birth Cohort

artículo científico publicado en 2011

Amniotic fluid inflammatory cytokines: potential markers of immunologic dysfunction in autism spectrum disorders

artículo científico publicado en 2011

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder

artículo científico publicado en 2014

Analyzing the Role of MicroRNAs in Schizophrenia in the Context of Common Genetic Risk Variants.

artículo científico publicado en 2016

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

artículo científico

Asphyxia-Related Risk Factors and Their Timing in Spastic Cerebral Palsy

scholarly article by L F. Nielsen et al published February 2009 in Obstetrical and Gynecological Survey

Asphyxia-related risk factors and their timing in spastic cerebral palsy

artículo científico publicado en 2008

Association of Childhood Exposure to Nitrogen Dioxide and Polygenic Risk Score for Schizophrenia With the Risk of Developing Schizophrenia

scientific article published on 01 November 2019

Association of GRIN1 and GRIN2A-D with schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk

artículo científico publicado en 2011

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

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

artículo científico publicado en 2019

Autism spectrum disorders and maternal serum α-fetoprotein levels during pregnancy

artículo científico publicado en 2011

Brain proteome changes in female Brd1 mice unmask dendritic spine pathology and show enrichment for schizophrenia risk

scientific article published on 24 December 2018

CACNA1C hypermethylation is associated with bipolar disorder.

artículo científico publicado en 2016

COMT Val158Met and MTHFR C677T moderate risk of schizophrenia in response to childhood adversity.

artículo científico publicado en 2017

CONSTRUCTING TQFTS FROM MODULAR FUNCTORS

article published in 2001

Cerebral palsy among children born after in vitro fertilization: the role of preterm delivery--a population-based, cohort study

artículo científico publicado en 2006

Combination of vaginal pH with vaginal sialidase and prolidase activities for prediction of low birth weight and preterm birth

artículo científico publicado en 2005

Common risk variants identified in autism spectrum disorder

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.

artículo científico publicado en 2018

Congenital cerebral palsy, child sex and parent cardiovascular risk

artículo científico publicado en 2013

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

Estimating the functional impact of INDELs in transcription factor binding sites: a genome-wide landscape

article

Examining Sex-Differentiated Genetic Effects Across Neuropsychiatric and Behavioral Traits

artículo científico publicado en 2021

GWAS, cytomegalovirus infection, and schizophrenia.

artículo científico publicado en 2014

Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study

scientific article published on 22 May 2019

Genetic architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis

artículo científico publicado en 2022

Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls

scientific article published on 17 September 2018

Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM

scientific article published on 18 October 2018

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

artículo científico publicado en 2016

Genetic risk scores for major psychiatric disorders and the risk of postpartum psychiatric disorders

scientific article published on 11 November 2019

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 analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa.

artículo científico publicado en 2018

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

artículo científico publicado en 2018

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

artículo científico publicado en 2019

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.

artículo científico publicado en 2019

Genome-wide association study implicates CHRNA2 in cannabis use disorder

artículo científico publicado en 2019

Genome-wide association study implicatesCHRNA2in cannabis use disorder

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 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

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

Identification of the BRD1 interaction network and its impact on mental disorder risk

scientific journal article

Infections during pregnancy and after birth, and the risk of autism spectrum disorders: a register-based study utilizing a Danish historic birth cohort.

artículo científico publicado en 2012

Interrelationship of cytokines, hypothalamic-pituitary-adrenal axis hormones, and psychosocial variables in the prediction of preterm birth

artículo científico publicado en 2010

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

artículo científico publicado en 2015

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

artículo científico publicado en 2012

LandScape: a simple method to aggregate p-values and other stochastic variables without a priori grouping

artículo científico publicado en 2016

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

scientific article published on 23 January 2020

Lifestyle during pregnancy: neurodevelopmental effects at 5 years of age. The design and implementation of a prospective follow-up study

artículo científico publicado en 2010

Low to Moderate Average Alcohol Consumption and Binge Drinking in Early Pregnancy: Effects on Choice Reaction Time and Information Processing Time in Five-Year-Old Children

artículo científico publicado en 2015

Maternal caffeine intake during pregnancy is associated with birth weight but not with gestational length: results from a large prospective observational cohort study

artículo científico publicado en 2013

Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age at onset of schizophrenia: no consistent evidence for an association in the Nordic population

artículo científico publicado en 2012

Multiplicity and early gestational age contribute to an increased risk of cerebral palsy from assisted conception: a population-based cohort study

artículo científico publicado en 2010

Neonatal chemokine levels and risk of autism spectrum disorders: findings from a Danish historic birth cohort follow-up study

artículo científico publicado en 2012

Neonatal levels of cytokines and risk of autism spectrum disorders: an exploratory register-based historic birth cohort study utilizing the Danish Newborn Screening Biobank

artículo científico publicado en 2012

Neonatal levels of neurotrophic factors and risk of autism spectrum disorders

artículo científico publicado en 2012

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

article

Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios ⬇️

artículo científico publicado en 2015

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

article

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.

artículo científico publicado en 2017

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

Preterm delivery predicted by soluble CD163 and CRP in women with symptoms of preterm delivery

artículo científico publicado en 2005

Psychiatric comorbidities in autism spectrum disorders: findings from a Danish Historic Birth Cohort

artículo científico publicado en 2011

Publisher Correction: A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex

artículo científico publicado en 2022

Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

artículo científico publicado en 2019

Risk of autism spectrum disorders in children born after assisted conception: a population-based follow-up study

artículo científico publicado en 2010

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

artículo científico publicado en 2011

Schizophrenia risk variants affecting microRNA function and site-specific regulation of NT5C2 by miR-206.

artículo científico publicado en 2016

Sequencing and de novo assembly of 150 genomes from Denmark as a population reference

artículo científico publicado en 2017

Serum macrophage migration inhibitory factor in the prediction of preterm delivery

artículo científico publicado en 2008

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

artículo científico publicado en 2022

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

artículo científico publicado en 2020

Shared polygenetic variation between ASD and ADHD exerts opposite association patterns with educational attainment

Social and non-social autism symptoms and trait domains are genetically dissociable

scientific article published on 03 September 2019

The Anorexia Nervosa Genetics Initiative: Overview and Methods

article

The anorexia nervosa genetics initiative (ANGI): Overview and methods

article

The effects of low to moderate alcohol consumption and binge drinking in early pregnancy on selective and sustained attention in 5-year-old children

artículo científico publicado en 2012

The effects of low to moderate prenatal alcohol exposure in early pregnancy on IQ in 5-year-old children

artículo científico publicado en 2012

The iPSYCH2012 case-cohort sample: New directions for unravelling genetic and environmental architectures of severe mental disorders

The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders.

artículo científico publicado en 2017

The importance of data structure in statistical analysis of dendritic spine morphology.

artículo científico publicado en 2017

Validation of self-reported data on assisted conception in The Danish National Birth Cohort

artículo científico publicado en 2009

Validity of childhood autism in the Danish Psychiatric Central Register: findings from a cohort sample born 1990-1999.

artículo científico publicado en 2009

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

Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder

artículo científico publicado en 2017

‘Vanishing embryo syndrome’ in IVF/ICSI

artículo científico publicado en 2005

Lista de obras de Jakob Grove

30. COMT Val158Met and MTHFR C677T Moderate Risk of Schizophrenia in Response to Childhood Trauma.

A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex

A polygenic resilience score moderates the genetic risk for schizophrenia

A review of software for microarray genotyping

ASD and ADHD have a similar burden of rare protein-truncating variants

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

AUTOMORPHISM FIXED POINTS IN THE MODULI SPACE OF SEMI-STABLE BUNDLES

Amniotic fluid MMP-9 and neurotrophins in autism spectrum disorders: an exploratory study.

Amniotic fluid chemokines and autism spectrum disorders: an exploratory study utilizing a Danish Historic Birth Cohort

Amniotic fluid inflammatory cytokines: potential markers of immunologic dysfunction in autism spectrum disorders

Analysis of shared heritability in common disorders of the brain

Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder

Analyzing the Role of MicroRNAs in Schizophrenia in the Context of Common Genetic Risk Variants.

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

Asphyxia-Related Risk Factors and Their Timing in Spastic Cerebral Palsy

Asphyxia-related risk factors and their timing in spastic cerebral palsy

Association of Childhood Exposure to Nitrogen Dioxide and Polygenic Risk Score for Schizophrenia With the Risk of Developing Schizophrenia

Association of GRIN1 and GRIN2A-D with schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk

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

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

Autism spectrum disorders and maternal serum α-fetoprotein levels during pregnancy

Brain proteome changes in female Brd1 mice unmask dendritic spine pathology and show enrichment for schizophrenia risk

CACNA1C hypermethylation is associated with bipolar disorder.

COMT Val158Met and MTHFR C677T moderate risk of schizophrenia in response to childhood adversity.

CONSTRUCTING TQFTS FROM MODULAR FUNCTORS

Cerebral palsy among children born after in vitro fertilization: the role of preterm delivery--a population-based, cohort study

Combination of vaginal pH with vaginal sialidase and prolidase activities for prediction of low birth weight and preterm birth

Common risk variants identified in autism spectrum disorder

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.

Congenital cerebral palsy, child sex and parent cardiovascular risk

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

Estimating the functional impact of INDELs in transcription factor binding sites: a genome-wide landscape

Examining Sex-Differentiated Genetic Effects Across Neuropsychiatric and Behavioral Traits

GWAS, cytomegalovirus infection, and schizophrenia.

Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study

Genetic architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis

Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls

Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM

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

Genetic risk scores for major psychiatric disorders and the risk of postpartum psychiatric disorders

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

Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa.

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

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

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.

Genome-wide association study implicates CHRNA2 in cannabis use disorder

Genome-wide association study implicatesCHRNA2in cannabis use disorder

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

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

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

Identification of the BRD1 interaction network and its impact on mental disorder risk

Infections during pregnancy and after birth, and the risk of autism spectrum disorders: a register-based study utilizing a Danish historic birth cohort.

Interrelationship of cytokines, hypothalamic-pituitary-adrenal axis hormones, and psychosocial variables in the prediction of preterm birth

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

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

LandScape: a simple method to aggregate p-values and other stochastic variables without a priori grouping

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

Lifestyle during pregnancy: neurodevelopmental effects at 5 years of age. The design and implementation of a prospective follow-up study

Low to Moderate Average Alcohol Consumption and Binge Drinking in Early Pregnancy: Effects on Choice Reaction Time and Information Processing Time in Five-Year-Old Children

Maternal caffeine intake during pregnancy is associated with birth weight but not with gestational length: results from a large prospective observational cohort study

Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age at onset of schizophrenia: no consistent evidence for an association in the Nordic population

Multiplicity and early gestational age contribute to an increased risk of cerebral palsy from assisted conception: a population-based cohort study

Neonatal chemokine levels and risk of autism spectrum disorders: findings from a Danish historic birth cohort follow-up study

Neonatal levels of cytokines and risk of autism spectrum disorders: an exploratory register-based historic birth cohort study utilizing the Danish Newborn Screening Biobank

Neonatal levels of neurotrophic factors and risk of autism spectrum disorders

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios ⬇️

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.

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

Preterm delivery predicted by soluble CD163 and CRP in women with symptoms of preterm delivery

Psychiatric comorbidities in autism spectrum disorders: findings from a Danish Historic Birth Cohort