Lista de obras - Stephanie Le Hellard - Dominio Público Uruguay

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

artículo científico publicado en 2021

A 6.9-Mb high-resolution BAC/PAC contig of human 4p15.3-p16.1, a candidate region for bipolar affective disorder.

artículo científico publicado en 2001

A genetic association study of CSMD1 and CSMD2 with cognitive function

artículo científico publicado en 2016

A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder

artículo científico publicado en 2013

A genome-wide association study of anorexia nervosa

artículo científico publicado en 2014

A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE).

artículo científico publicado en 2008

A possible genetic association with chronic fatigue in primary Sjögren's syndrome: a candidate gene study

artículo científico publicado en 2013

Association analysis of the chromosome 4p15–p16 candidate region for bipolar disorder and schizophrenia

article

Association between genetic variants in the tumour necrosis factor/lymphotoxin α/lymphotoxin β locus and primary Sjogren's syndrome in Scandinavian samples

artículo científico publicado en 2012

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

artículo científico publicado en 2019

Association of MCTP2 gene variants with schizophrenia in three independent samples of Scandinavian origin (SCOPE).

artículo científico publicado en 2009

Association study of energy homeostasis genes and antipsychotic-induced weight gain in patients with schizophrenia

Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

scientific article published on 01 May 2019

Candidate psychiatric illness genes identified in patients with pericentric inversions of chromosome 18

artículo científico publicado en 2005

Common brain disorders are associated with heritable patterns of apparent aging of the brain

scientific article published on 24 September 2019

Common genetic variants influence human subcortical brain structures

artículo científico publicado en 2015

Common variants in the ARC gene are not associated with cognitive abilities

artículo científico publicado en 2015

Conservation of Distinct Genetically-Mediated Human Cortical Pattern

artículo científico publicado en 2016

Convergence of linkage, association and GWAS findings for a candidate region for bipolar disorder and schizophrenia on chromosome 4p

scientific article published on 30 March 2010

Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

artículo científico publicado en 2020

DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder

artículo científico publicado en 2012

Differences in white blood cell proportions between schizophrenia cases and controls are influenced by medication and variations in time of day

artículo científico publicado en 2023

F5. Brain Disorders are Associated With Increased Brain Age

GWAS meta-analysis (N=279,930) identifies new genes and functional links to intelligence

article

GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.

artículo científico publicado en 2017

GWAS-based pathway analysis differentiates between fluid and crystallized intelligence.

artículo científico publicado en 2014

Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders

artículo científico publicado en 2012

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

scholarly article published 28 August 2017

Genetic architecture of cognitive traits

artículo científico

Genetic architecture of subcortical brain structures in 38,851 individuals

scientific article published on 21 October 2019

Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).

artículo científico publicado en 2015

Genetic control of variability in subcortical and intracranial volumes

artículo científico publicado en 2020

Genetic evidence for a role of the SREBP transcription system and lipid biosynthesis in schizophrenia and antipsychotic treatment

artículo científico publicado en 2016

Genetics of brain age suggest an overlap with common brain disorders

article

Genetics of structural connectivity and information processing in the brain

artículo científico publicado en 2016

Genome-Wide Association Study Reveals First Locus for Anorexia Nervosa and Metabolic Correlations

scholarly article

Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence

article

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

artículo científico publicado en 2019

Haplotype Analysis and a Novel Allele-Sharing Method Refines a Chromosome 4p Locus Linked to Bipolar Affective Disorder

article

How mutations in the nAChRs can cause ADNFLE epilepsy

artículo científico publicado en 2002

Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins.

artículo científico publicado en 2014

Identification of Gene Loci That Overlap Between Schizophrenia and Educational Attainment

artículo científico publicado en 2016

Identification of common variants associated with human hippocampal and intracranial volumes

artículo científico publicado en 2012

Identification of pleiotropy at the gene level between psychiatric disorders and related traits

artículo científico publicado en 2021

Imaging and cognitive genetics: the Norwegian Cognitive NeuroGenetics sample

artículo científico publicado en 2012

Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment

artículo científico publicado en 2015

Ion channel variation causes epilepsies ⬇️

artículo científico publicado el 1 de octubre de 2001

Lack of Association Between Juvenile Myoclonic Epilepsy and HLA-DR13

artículo científico publicado en 1999

Lack of association of the rs1344706 ZNF804A variant with cognitive functions and DTI indices of white matter microstructure in two independent healthy populations

artículo científico publicado en 2014

Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets

artículo científico publicado en 2017

Large-scale genomics unveil polygenic architecture of human cortical surface area

artículo científico publicado en 2015

Linkage-disequilibrium-based binning affects the interpretation of GWASs

artículo científico publicado en 2012

Lipogenic effects of psychotropic drugs: focus on the SREBP system

artículo científico publicado en 2011

Multi-Trait Analysis of GWAS and Biological Insights Into Cognition: A Response to Hill (2018)

artículo científico publicado en 2018

Nationwide Genomic Study in Denmark Reveals Remarkable Population Homogeneity

artículo científico publicado en 2016

Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)

No association of primary Sjögren's syndrome with Fcγ receptor gene variants

artículo científico publicado en 2013

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

Personality traits and hardiness as risk- and protective factors for mental distress during the COVID-19 pandemic: a Norwegian two-wave study

artículo científico publicado en 2022

Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways

artículo científico publicado en 2019

Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples

artículo científico publicado en 2008

Publisher Correction: Common brain disorders are associated with heritable patterns of apparent aging of the brain

scientific article published on 01 February 2020

Recently evolved human-specific methylated regions are enriched in schizophrenia signals.

artículo científico publicado en 2018

SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis.

artículo científico publicado en 2002

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

artículo científico publicado en 2017

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

artículo científico publicado en 2020

Simple method to analyze SNP-based association studies using DNA pools

scientific article published on 01 May 2003

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

artículo científico publicado en 2018

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

artículo científico publicado en 2014

The Imaging and Cognition Genetics Conference 2011, ICG 2011: A Meeting of Minds.

artículo científico publicado en 2012

The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia

artículo científico publicado en 2011

The genetic architecture of human brainstem structures and their involvement in common brain disorders

artículo científico publicado en 2020

The genetic architecture of the human cerebral cortex

artículo científico publicado en 2020

Variants in doublecortin- and calmodulin kinase like 1, a gene up-regulated by BDNF, are associated with memory and general cognitive abilities

scientific article published on 21 October 2009

Lista de obras de Stephanie Le Hellard

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

A 6.9-Mb high-resolution BAC/PAC contig of human 4p15.3-p16.1, a candidate region for bipolar affective disorder.

A genetic association study of CSMD1 and CSMD2 with cognitive function

A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder

A genome-wide association study of anorexia nervosa

A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE).

A possible genetic association with chronic fatigue in primary Sjögren's syndrome: a candidate gene study

Association analysis of the chromosome 4p15–p16 candidate region for bipolar disorder and schizophrenia

Association between genetic variants in the tumour necrosis factor/lymphotoxin α/lymphotoxin β locus and primary Sjogren's syndrome in Scandinavian samples

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

Association of MCTP2 gene variants with schizophrenia in three independent samples of Scandinavian origin (SCOPE).

Association study of energy homeostasis genes and antipsychotic-induced weight gain in patients with schizophrenia

Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

Candidate psychiatric illness genes identified in patients with pericentric inversions of chromosome 18

Common brain disorders are associated with heritable patterns of apparent aging of the brain

Common genetic variants influence human subcortical brain structures

Common variants in the ARC gene are not associated with cognitive abilities

Conservation of Distinct Genetically-Mediated Human Cortical Pattern

Convergence of linkage, association and GWAS findings for a candidate region for bipolar disorder and schizophrenia on chromosome 4p

Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder

Differences in white blood cell proportions between schizophrenia cases and controls are influenced by medication and variations in time of day

F5. Brain Disorders are Associated With Increased Brain Age

GWAS meta-analysis (N=279,930) identifies new genes and functional links to intelligence

GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.

GWAS-based pathway analysis differentiates between fluid and crystallized intelligence.

Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders

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

Genetic architecture of cognitive traits

Genetic architecture of subcortical brain structures in 38,851 individuals

Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).

Genetic control of variability in subcortical and intracranial volumes

Genetic control of variability in subcortical and intracranial volumes

Genetic evidence for a role of the SREBP transcription system and lipid biosynthesis in schizophrenia and antipsychotic treatment

Genetics of brain age suggest an overlap with common brain disorders

Genetics of structural connectivity and information processing in the brain

Genome-Wide Association Study Reveals First Locus for Anorexia Nervosa and Metabolic Correlations

Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence

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

Haplotype Analysis and a Novel Allele-Sharing Method Refines a Chromosome 4p Locus Linked to Bipolar Affective Disorder

How mutations in the nAChRs can cause ADNFLE epilepsy

Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins.

Identification of Gene Loci That Overlap Between Schizophrenia and Educational Attainment

Identification of common variants associated with human hippocampal and intracranial volumes

Identification of pleiotropy at the gene level between psychiatric disorders and related traits

Imaging and cognitive genetics: the Norwegian Cognitive NeuroGenetics sample

Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment

Ion channel variation causes epilepsies ⬇️

Lack of Association Between Juvenile Myoclonic Epilepsy and HLA-DR13

Lack of association of the rs1344706 ZNF804A variant with cognitive functions and DTI indices of white matter microstructure in two independent healthy populations

Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets

Large-scale genomics unveil polygenic architecture of human cortical surface area

Linkage-disequilibrium-based binning affects the interpretation of GWASs

Lipogenic effects of psychotropic drugs: focus on the SREBP system

Multi-Trait Analysis of GWAS and Biological Insights Into Cognition: A Response to Hill (2018)

Nationwide Genomic Study in Denmark Reveals Remarkable Population Homogeneity

Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)

No association of primary Sjögren's syndrome with Fcγ receptor gene variants

Novel genetic loci associated with hippocampal volume

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

Personality traits and hardiness as risk- and protective factors for mental distress during the COVID-19 pandemic: a Norwegian two-wave study

Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways

Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples

Publisher Correction: Common brain disorders are associated with heritable patterns of apparent aging of the brain

Recently evolved human-specific methylated regions are enriched in schizophrenia signals.

SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis.

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

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

Simple method to analyze SNP-based association studies using DNA pools

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

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

The Imaging and Cognition Genetics Conference 2011, ICG 2011: A Meeting of Minds.

The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia

The genetic architecture of human brainstem structures and their involvement in common brain disorders

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

Variants in doublecortin- and calmodulin kinase like 1, a gene up-regulated by BDNF, are associated with memory and general cognitive abilities