Lista de obras - Verneri Anttila - Dominio Público Uruguay

A high-density association screen of 155 ion transport genes for involvement with common migraine

artículo científico publicado en 2008

A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers

artículo científico publicado en 2012

A visual migraine aura locus maps to 9q21-q22

artículo científico publicado en 2010

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

scientific article published on 03 January 2017

An atlas of genetic correlations across human diseases and traits

artículo científico publicado en 2015

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Analysis of shared heritability in common disorders of the brain

Candidate-gene association study searching for genetic factors involved in migraine chronification

artículo científico publicado en 2014

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

article by Padhraig Gormley et al published 16 May 2018 in Neuron

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

article by Padhraig Gormley et al published September 2018 in Neuron

Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies

artículo científico publicado en 2014

Consistently replicating locus linked to migraine on 10q22-q23

artículo científico publicado en 2008

Correction: Selectivity in Genetic Association with Sub-classified Migraine in Women

artículo científico publicado en 2015

Effect of endocannabinoid degradation on pain: role of FAAH polymorphisms in experimental and postoperative pain in women treated for breast cancer

artículo científico publicado en 2016

Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

artículo científico publicado en 2016

European lactase persistence genotype shows evidence of association with increase in body mass index

artículo científico publicado en 2009

Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging

artículo científico publicado en 2010

Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas

artículo científico publicado en 2016

Gene-based pleiotropy across migraine with aura and migraine without aura patient groups

artículo científico publicado en 2015

Genetic analysis for a shared biological basis between migraine and coronary artery disease

artículo científico publicado en 2015

Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

artículo científico publicado en 2016

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

artículo científico publicado en 2013

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

artículo científico publicado en 2016

Genetics of migraine.

artículo científico publicado en 2018

Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder

artículo científico publicado en 2014

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

scholarly article

Genome-Wide Meta-Analysis of Sciatica in Finnish Population

artículo científico publicado en 2016

Genome-wide association analysis identifies susceptibility loci for migraine without aura

artículo científico publicado en 2012

Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity

artículo científico publicado en 2013

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

artículo científico publicado en 2010

Genome-wide association study reveals three susceptibility loci for common migraine in the general population

artículo científico publicado en 2011

Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts

artículo científico publicado en 2012

Genome-wide meta-analysis identifies new susceptibility loci for migraine

artículo científico publicado en 2013

Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types

article

Heterogeneous Contribution of Microdeletions in the Development of Common Generalized and Focal epilepsies

Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies

artículo científico publicado en 2017

High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms

artículo científico publicado en 2014

IFITM3 restricts the morbidity and mortality associated with influenza

artículo científico publicado en 2012

In silico phenotyping via co-training for improved phenotype prediction from genotype

artículo científico publicado en 2015

Integrating common and rare genetic variation in diverse human populations

artículo científico publicado en 2010

Involvement of astrocyte and oligodendrocyte gene sets in migraine

artículo científico publicado en 2015

LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis

Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria

artículo científico publicado en 2018

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

artículo científico publicado en 2016

Migraine without aura: genome-wide association analysis identifies several novel susceptibility.

artículo científico publicado en 2013

Migraine without aura: genome-wide association analysis identifies several novel susceptibility. ⬇️

artículo científico publicado en 2013

Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene

artículo científico publicado en 2012

Partitioning heritability by functional annotation using genome-wide association summary statistics

artículo científico publicado en 2015

Probing the brain of comorbidity

artículo científico publicado en 2013

Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'.

artículo científico publicado en 2013

SNP Variants in Major Histocompatibility Complex Are Associated with Sarcoidosis Susceptibility-A Joint Analysis in Four European Populations

artículo científico publicado en 2017

Selectivity in genetic association with sub-classified migraine in women

artículo científico publicado en 2014

Serum calcium and risk of migraine: a Mendelian randomization study

artículo científico publicado en 2016

Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants.

artículo científico publicado en 2015

Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants

artículo científico publicado en 2017

Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa

artículo científico publicado en 2017

Statistical power and utility of meta-analysis methods for cross-phenotype genome-wide association studies.

artículo científico publicado en 2018

Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set.

artículo científico publicado en 2015

The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort

artículo científico publicado en 2014

Towards an understanding of genetic predisposition to migraine

artículo científico publicado en 2011

Trait components provide tools to dissect the genetic susceptibility of migraine

artículo científico publicado en 2006

Valsalva Maneuver as Migraine Inducer: A Case Report of a Woman With Patent Foramen Ovale and an Ischemic Stroke

article by Ville Artto et al published January 2009 in Headache

Lista de obras de Verneri Anttila

A high-density association screen of 155 ion transport genes for involvement with common migraine

A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers

A visual migraine aura locus maps to 9q21-q22

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

An atlas of genetic correlations across human diseases and traits

Analysis of shared heritability in common disorders of the brain

Analysis of shared heritability in common disorders of the brain

Candidate-gene association study searching for genetic factors involved in migraine chronification

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies

Consistently replicating locus linked to migraine on 10q22-q23

Correction: Selectivity in Genetic Association with Sub-classified Migraine in Women

Effect of endocannabinoid degradation on pain: role of FAAH polymorphisms in experimental and postoperative pain in women treated for breast cancer

Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

European lactase persistence genotype shows evidence of association with increase in body mass index

Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging

Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas

Gene-based pleiotropy across migraine with aura and migraine without aura patient groups

Genetic analysis for a shared biological basis between migraine and coronary artery disease

Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

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

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

Genetics of migraine.

Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder

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

Genome-Wide Meta-Analysis of Sciatica in Finnish Population

Genome-wide association analysis identifies susceptibility loci for migraine without aura

Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

Genome-wide association study reveals three susceptibility loci for common migraine in the general population

Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts

Genome-wide meta-analysis identifies new susceptibility loci for migraine

Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types

Heterogeneous Contribution of Microdeletions in the Development of Common Generalized and Focal epilepsies

Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies

High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms

IFITM3 restricts the morbidity and mortality associated with influenza

In silico phenotyping via co-training for improved phenotype prediction from genotype

Integrating common and rare genetic variation in diverse human populations

Involvement of astrocyte and oligodendrocyte gene sets in migraine

LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis

Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

Migraine without aura: genome-wide association analysis identifies several novel susceptibility.

Migraine without aura: genome-wide association analysis identifies several novel susceptibility. ⬇️

Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene

Partitioning heritability by functional annotation using genome-wide association summary statistics

Probing the brain of comorbidity

Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'.

SNP Variants in Major Histocompatibility Complex Are Associated with Sarcoidosis Susceptibility-A Joint Analysis in Four European Populations

Selectivity in genetic association with sub-classified migraine in women

Serum calcium and risk of migraine: a Mendelian randomization study

Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants.

Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants

Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa

Statistical power and utility of meta-analysis methods for cross-phenotype genome-wide association studies.

Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set.

The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort

Towards an understanding of genetic predisposition to migraine

Trait components provide tools to dissect the genetic susceptibility of migraine

Valsalva Maneuver as Migraine Inducer: A Case Report of a Woman With Patent Foramen Ovale and an Ischemic Stroke