Lista de obras - Anna C Need - Dominio Público Uruguay

A comparison of the Cambridge Automated Neuropsychological Test Battery (CANTAB) with "traditional" neuropsychological testing instruments

artículo científico publicado en 2013

A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci.

artículo científico publicado en 2009

A genome-wide genetic signature of Jewish ancestry perfectly separates individuals with and without full Jewish ancestry in a large random sample of European Americans

artículo científico publicado en 2009

A genome-wide investigation of SNPs and CNVs in schizophrenia

artículo científico publicado en 2009

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

artículo científico publicado en 2009

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

scientific article published on 01 May 2019

Brain-derived neurotrophic factor val66met polymorphism and hippocampal activation during episodic encoding and retrieval tasks

artículo científico publicado en 2010

COMT val108/158 met genotype affects neural but not cognitive processing in healthy individuals

artículo científico publicado en 2009

Clinical application of exome sequencing in undiagnosed genetic conditions

artículo científico publicado en 2012

Common genetic variation and performance on standardized cognitive tests

artículo científico publicado en 2010

Common variants conferring risk of schizophrenia

artículo científico publicado en 2009

Control of axonal growth and regeneration of sensory neurons by the p110delta PI 3-kinase

artículo científico publicado en 2007

Copy number variation of KIR genes influences HIV-1 control

artículo científico publicado en 2011

Correction: A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia

Exome sequence analysis of Finnish patients with clozapine-induced agranulocytosis

artículo científico publicado en 2013

Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy

artículo científico publicado en 2012

Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia

artículo científico publicado en 2012

Failure to replicate effect of Kibra on human memory in two large cohorts of European origin

artículo científico publicado en 2008

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

article

Genetic enhancement of cognition in a kindred with cone-rod dystrophy due to RIMS1 mutation

artículo científico publicado en 2007

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

article

Genome-wide scan of copy number variation in late-onset Alzheimer's disease

artículo científico publicado en 2010

Genome-wide tagging for everyone

artículo científico publicado en 2006

Handling and environmental enrichment do not rescue learning and memory impairments in alphaCamKII(T286A) mutant mice

artículo científico publicado en 2003

Large recurrent microdeletions associated with schizophrenia

artículo científico publicado en 2008

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

artículo científico publicado en 2017

Learning and memory impairments in Kv beta 1.1-null mutants are rescued by environmental enrichment or ageing

scientific journal article

Long-range LD can confound genome scans in admixed populations

artículo científico publicado en 2008

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

artículo científico publicado en 2018

Next generation disparities in human genomics: concerns and remedies

artículo científico publicado en 2009

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

Obesity is Associated with Genetic Variants That Alter Dopamine Availability

artículo científico publicado en 2006

Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysis

artículo científico publicado en 2009

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

artículo científico publicado en 2019

Potential genetic causes of heterogeneity of treatment effects

artículo científico publicado en 2007

Priorities and standards in pharmacogenetic research

artículo científico publicado en 2005

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes

artículo científico publicado en 2010

SVA: software for annotating and visualizing sequenced human genomes

artículo científico publicado en 2011

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

artículo científico publicado en 2018

Temporal lobe functional activity and connectivity in young adult APOE varepsilon4 carriers

artículo científico publicado en 2009

The characterization of twenty sequenced human genomes

artículo científico publicado en 2010

The importance of dynamic re-analysis in diagnostic whole exome sequencing

artículo científico publicado en 2016

Using ERDS to infer copy-number variants in high-coverage genomes

artículo científico publicado en 2012

WGAViewer: software for genomic annotation of whole genome association studies

artículo científico publicado en 2008

Lista de obras de Anna C Need

A comparison of the Cambridge Automated Neuropsychological Test Battery (CANTAB) with "traditional" neuropsychological testing instruments

A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci.

A genome-wide genetic signature of Jewish ancestry perfectly separates individuals with and without full Jewish ancestry in a large random sample of European Americans

A genome-wide investigation of SNPs and CNVs in schizophrenia

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

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

Brain-derived neurotrophic factor val66met polymorphism and hippocampal activation during episodic encoding and retrieval tasks

COMT val108/158 met genotype affects neural but not cognitive processing in healthy individuals

Clinical application of exome sequencing in undiagnosed genetic conditions

Common genetic variation and performance on standardized cognitive tests

Common variants conferring risk of schizophrenia

Control of axonal growth and regeneration of sensory neurons by the p110delta PI 3-kinase

Copy number variation of KIR genes influences HIV-1 control

Correction: A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia

Exome sequence analysis of Finnish patients with clozapine-induced agranulocytosis

Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy

Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia

Failure to replicate effect of Kibra on human memory in two large cohorts of European origin

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

Genetic enhancement of cognition in a kindred with cone-rod dystrophy due to RIMS1 mutation

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

Genome-wide scan of copy number variation in late-onset Alzheimer's disease

Genome-wide tagging for everyone

Handling and environmental enrichment do not rescue learning and memory impairments in alphaCamKII(T286A) mutant mice

Large recurrent microdeletions associated with schizophrenia

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

Learning and memory impairments in Kv beta 1.1-null mutants are rescued by environmental enrichment or ageing

Long-range LD can confound genome scans in admixed populations

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

Next generation disparities in human genomics: concerns and remedies

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

Obesity is Associated with Genetic Variants That Alter Dopamine Availability

Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysis

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

Potential genetic causes of heterogeneity of treatment effects

Priorities and standards in pharmacogenetic research

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes

SVA: software for annotating and visualizing sequenced human genomes

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

Temporal lobe functional activity and connectivity in young adult APOE varepsilon4 carriers

The characterization of twenty sequenced human genomes

The importance of dynamic re-analysis in diagnostic whole exome sequencing

Using ERDS to infer copy-number variants in high-coverage genomes

WGAViewer: software for genomic annotation of whole genome association studies