Lista de obras - G. Bragi Walters - Dominio Público Uruguay

15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia

artículo científico publicado en 2017

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

artículo científico publicado en 2021

A genome-wide association search for type 2 diabetes genes in African Americans

artículo científico publicado en 2012

A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome

artículo científico publicado en 2022

A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration

article by Hannes Helgason et al published 15 September 2013 in Nature Genetics

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

artículo científico publicado en 2011

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

artículo científico publicado en 2009

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

artículo científico publicado en 2010

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

artículo científico publicado en 2019

Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder ⬇️

scientific article published on 17 October 2019

Brain age prediction using deep learning uncovers associated sequence variants

scientific article published on 27 November 2019

CNVs conferring risk of autism or schizophrenia affect cognition in controls

artículo científico publicado en 2013

Common genetic variants associated with open-angle glaucoma

artículo científico publicado en 2011

Common risk variants identified in autism spectrum disorder

Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma

artículo científico publicado en 2007

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

artículo científico publicado en 2010

Composition of the founding population of Iceland: biological distance and morphological variation in early historic Atlantic Europe.

artículo científico publicado en 2004

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

artículo científico publicado en 2020

Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution.

artículo científico publicado en 2009

Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

scholarly article published in Nature Genetics

Discovery of common variants associated with low TSH levels and thyroid cancer risk

scientific journal article

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

artículo científico publicado en 2018

Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

artículo científico publicado en 2011

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

Genetic evidence of assortative mating in humans

scholarly article

Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution

artículo científico publicado en 2009

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

scientific journal article

Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium

artículo científico publicado en 2016

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.

artículo científico publicado en 2012

Germline variants at SOHLH2 influence multiple myeloma risk

artículo científico publicado en 2021

Hundreds of variants clustered in genomic loci and biological pathways affect human height

artículo científico publicado en 2010

Identification of common genetic risk variants for autism spectrum disorder

artículo científico publicado en 2019

Identification of genetic overlap and novel risk loci for attention-deficit/hyperactivity disorder and bipolar disorder

scientific article published on 02 December 2019

Identification of low-frequency variants associated with gout and serum uric acid levels

artículo científico publicado en 2011

Male-pattern baldness susceptibility locus at 20p11.

artículo científico publicado en 2008

Many sequence variants affecting diversity of adult human height

artículo científico publicado en 2008

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

artículo científico publicado en 2010

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

artículo científico publicado en 2012

Polygenic risk scores for schizophrenia and bipolar disorder predict creativity

artículo científico publicado en 2015

Rare and Common Variants Conferring Risk of Tooth Agenesis.

artículo científico publicado en 2018

Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study

Reproductive fitness and genetic risk of psychiatric disorders in the general population

artículo científico publicado en 2017

Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation

artículo científico publicado en 2017

Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption

artículo científico publicado en 2011

Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density

scientific journal article

The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts

artículo científico publicado en 2007

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

article

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

artículo científico publicado en 2010

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

artículo científico publicado en 2006

Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample

artículo científico publicado en 2022

Lista de obras de G. Bragi Walters

15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia

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

A genome-wide association search for type 2 diabetes genes in African Americans

A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome

A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

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

Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder ⬇️

Brain age prediction using deep learning uncovers associated sequence variants

CNVs conferring risk of autism or schizophrenia affect cognition in controls

Common genetic variants associated with open-angle glaucoma

Common risk variants identified in autism spectrum disorder

Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

Composition of the founding population of Iceland: biological distance and morphological variation in early historic Atlantic Europe.

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

Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution.

Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

Discovery of common variants associated with low TSH levels and thyroid cancer risk

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

Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Genetic evidence of assortative mating in humans

Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.

Germline variants at SOHLH2 influence multiple myeloma risk

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Identification of common genetic risk variants for autism spectrum disorder

Identification of genetic overlap and novel risk loci for attention-deficit/hyperactivity disorder and bipolar disorder

Identification of low-frequency variants associated with gout and serum uric acid levels

Male-pattern baldness susceptibility locus at 20p11.

Many sequence variants affecting diversity of adult human height

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

Polygenic risk scores for schizophrenia and bipolar disorder predict creativity

Rare and Common Variants Conferring Risk of Tooth Agenesis.

Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study

Reproductive fitness and genetic risk of psychiatric disorders in the general population

Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation

Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption

Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density

The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample