Lista de obras - John P Kemp - Dominio Público Uruguay

A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts

artículo científico publicado en 2016

A Rare Mutation in SMAD9 Associated With High Bone Mass Identifies the SMAD-Dependent BMP Signaling Pathway as a Potential Anabolic Target for Osteoporosis

scientific article published on 14 November 2019

A genome-wide approach to children's aggressive behavior: The EAGLE consortium

artículo científico publicado en 2015

A genome-wide association meta-analysis identifies new childhood obesity loci

artículo científico publicado en 2012

A genome-wide association study of body mass index across early life and childhood

artículo científico publicado en 2015

A novel common variant in DCST2 is associated with length in early life and height in adulthood

artículo científico publicado en 2014

Adult height variants affect birth length and growth rate in children

artículo científico publicado en 2011

An Atlas of Human and Murine Genetic Influences on Osteoporosis

An atlas of genetic influences on osteoporosis in humans and mice

artículo científico publicado en 2018

Associations of vitamin D pathway genes with circulating 25-hydroxyvitamin-D, 1,25-dihydroxyvitamin-D, and prostate cancer: a nested case-control study

artículo científico publicado en 2014

Author Correction: An atlas of genetic influences on osteoporosis in humans and mice

artículo científico publicado en 2019

Birth weight is positively related to bone size in adolescents but inversely related to cortical bone mineral density: findings from a large prospective cohort study

artículo científico publicado en 2014

Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus

artículo científico publicado en 2017

Body stature growth trajectories during childhood and the development of myopia

artículo científico publicado en 2013

Childhood intelligence is heritable, highly polygenic and associated with FNBP1L

artículo científico publicado en 2013

Cis and trans effects of human genomic variants on gene expression.

artículo científico publicado en 2014

Common Genetic Variants Influence Whorls in Fingerprint Patterns

artículo científico publicado en 2015

Common variants at 12q15 and 12q24 are associated with infant head circumference

artículo científico publicado en 2012

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill

artículo científico publicado en 2013

Common variation contributes to the genetic architecture of social communication traits.

artículo científico publicado en 2013

Common variation near ROBO2 is associated with expressive vocabulary in infancy.

artículo científico publicado en 2014

Coordinated genetic scaling of the human eye: shared determination of axial eye length and corneal curvature

artículo científico publicado en 2013

Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study

artículo científico publicado en 2020

Distinct relationships of intramuscular and subcutaneous fat with cortical bone: findings from a cross-sectional study of young adult males and females.

artículo científico publicado en 2013

Does bone resorption stimulate periosteal expansion? A cross-sectional analysis of β-C-telopeptides of type I collagen (CTX), genetic markers of the RANKL pathway, and periosteal circumference as measured by pQCT.

artículo científico publicado en 2014

Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.

artículo científico publicado en 2016

Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference

scholarly article published in Nature Genetics

Erratum: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

article

Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus

artículo científico publicado en 2017

Examination of the relationship between variation at 17q21 and childhood wheeze phenotypes.

artículo científico publicado en 2012

Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants

artículo científico publicado en 2013

Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure

artículo científico publicado en 2013

Genetic influences on trajectories of systolic blood pressure across childhood and adolescence

artículo científico publicado en 2013

Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

scientific article published on 25 November 2020

Genetic variants in adult bone mineral density and fracture risk genes are associated with the rate of bone mineral density acquisition in adolescence

artículo científico publicado en 2015

Genetic variation in prostate-specific antigen-detected prostate cancer and the effect of control selection on genetic association studies

scientific journal article

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

artículo científico publicado en 2018

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 meta-analysis of cortical bone mineral density unravels allelic heterogeneity at the RANKL locus and potential pleiotropic effects on bone

artículo científico publicado en 2010

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

artículo científico publicado en 2014

Genome-wide association study identifies 48 common genetic variants associated with handedness

artículo científico publicado en 2020

Genome-wide association study identifies loci affecting blood copper, selenium and zinc

artículo científico publicado en 2013

Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero.

artículo científico publicado en 2018

Genome-wide association study of blood lead shows multiple associations near ALAD

artículo científico publicado en 2015

Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes

artículo científico publicado en 2018

Genome-wide association study of height-adjusted BMI in childhood identifies functional variant in ADCY3

artículo científico publicado en 2014

Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances

artículo científico publicado en 2013

Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position

artículo científico publicado en 2012

Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk

artículo científico publicado en 2011

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

artículo científico publicado en 2013

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

artículo científico publicado en 2012

Genome-wide population-based association study of extremely overweight young adults--the GOYA study

artículo científico publicado en 2011

Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence

artículo científico publicado en 2014

Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.

artículo científico publicado en 2017

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

artículo científico publicado en 2013

Incorporating Known Genetic Variants Does Not Improve the Accuracy of PSA Testing to Identify High Risk Prostate Cancer on Biopsy

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.

artículo científico publicado en 2016

Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects

artículo científico publicado en 2018

Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium

artículo científico publicado en 2015

Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder

artículo científico publicado en 2015

Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error

artículo científico publicado en 2016

Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization

artículo científico publicado en 2013

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

artículo científico publicado en 2012

Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus

artículo científico publicado en 2012

Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women

artículo científico publicado en 2013

Meta‐Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry

artículo científico publicado en 2019

Mining the human phenome using allelic scores that index biological intermediates

artículo científico publicado en 2013

Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy

artículo científico publicado en 2009

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

artículo científico publicado en 2015

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

artículo científico publicado en 2012

Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error

artículo científico publicado en 2013

Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index

artículo científico publicado en 2014

Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency

artículo científico publicado en 2010

Osteocyte transcriptome mapping identifies a molecular landscape controlling skeletal homeostasis and susceptibility to skeletal disease

artículo científico publicado en 2021

Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment

artículo científico publicado en 2014

Regenerating zebrafish scales express a subset of evolutionary conserved genes involved in human skeletal disease

artículo científico publicado en 2022

Seventy-five genetic loci influencing the human red blood cell

artículo científico publicado en 2012

Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation

artículo científico publicado en 2015

The Effect of Plasma Lipids and Lipid-Lowering Interventions on Bone Mineral Density: A Mendelian Randomization Study

scientific article published on 12 March 2020

The Musculoskeletal Knowledge Portal: Making Omics Data Useful to the Broader Scientific Community

artículo científico publicado en 2020

The case for genome-wide association studies of bone acquisition in paediatric and adolescent populations

artículo científico publicado en 2016

The effects of height and BMI on prostate cancer incidence and mortality: a Mendelian randomization study in 20,848 cases and 20,214 controls from the PRACTICAL consortium

artículo científico publicado en 2015

Using Mendelian randomization to investigate a possible causal relationship between adiposity and increased bone mineral density at different skeletal sites in children

artículo científico publicado en 2016

Using genetic proxies for lifecourse sun exposure to assess the causal relationship of sun exposure with circulating vitamin d and prostate cancer risk

artículo científico publicado en 2013

Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence

scientific article published on 24 February 2014

Variants in the fetal genome near FLT1 are associated with risk of preeclampsia

artículo científico publicado en 2017

WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk

artículo científico publicado en 2012

Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

artículo científico publicado en 2017

Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture

artículo científico publicado en 2015

Lista de obras de John P Kemp

A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts

A Rare Mutation in SMAD9 Associated With High Bone Mass Identifies the SMAD-Dependent BMP Signaling Pathway as a Potential Anabolic Target for Osteoporosis

A genome-wide approach to children's aggressive behavior: The EAGLE consortium

A genome-wide association meta-analysis identifies new childhood obesity loci

A genome-wide association study of body mass index across early life and childhood

A novel common variant in DCST2 is associated with length in early life and height in adulthood

Adult height variants affect birth length and growth rate in children

An Atlas of Human and Murine Genetic Influences on Osteoporosis

An atlas of genetic influences on osteoporosis in humans and mice

Associations of vitamin D pathway genes with circulating 25-hydroxyvitamin-D, 1,25-dihydroxyvitamin-D, and prostate cancer: a nested case-control study

Author Correction: An atlas of genetic influences on osteoporosis in humans and mice

Birth weight is positively related to bone size in adolescents but inversely related to cortical bone mineral density: findings from a large prospective cohort study

Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus

Body stature growth trajectories during childhood and the development of myopia

Childhood intelligence is heritable, highly polygenic and associated with FNBP1L

Cis and trans effects of human genomic variants on gene expression.

Common Genetic Variants Influence Whorls in Fingerprint Patterns

Common variants at 12q15 and 12q24 are associated with infant head circumference

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill

Common variation contributes to the genetic architecture of social communication traits.

Common variation near ROBO2 is associated with expressive vocabulary in infancy.

Coordinated genetic scaling of the human eye: shared determination of axial eye length and corneal curvature

Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study

Distinct relationships of intramuscular and subcutaneous fat with cortical bone: findings from a cross-sectional study of young adult males and females.

Does bone resorption stimulate periosteal expansion? A cross-sectional analysis of β-C-telopeptides of type I collagen (CTX), genetic markers of the RANKL pathway, and periosteal circumference as measured by pQCT.

Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.

Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference

Erratum: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus

Examination of the relationship between variation at 17q21 and childhood wheeze phenotypes.

Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants

Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure

Genetic influences on trajectories of systolic blood pressure across childhood and adolescence

Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

Genetic variants in adult bone mineral density and fracture risk genes are associated with the rate of bone mineral density acquisition in adolescence

Genetic variation in prostate-specific antigen-detected prostate cancer and the effect of control selection on genetic association studies

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

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

Genome-wide association meta-analysis of cortical bone mineral density unravels allelic heterogeneity at the RANKL locus and potential pleiotropic effects on bone

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

Genome-wide association study identifies 48 common genetic variants associated with handedness

Genome-wide association study identifies loci affecting blood copper, selenium and zinc

Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero.

Genome-wide association study of blood lead shows multiple associations near ALAD

Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes

Genome-wide association study of height-adjusted BMI in childhood identifies functional variant in ADCY3

Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances

Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position

Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

Genome-wide population-based association study of extremely overweight young adults--the GOYA study

Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence

Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

Incorporating Known Genetic Variants Does Not Improve the Accuracy of PSA Testing to Identify High Risk Prostate Cancer on Biopsy

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.

Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects

Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium

Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder

Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error

Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus

Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women

Meta‐Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry

Mining the human phenome using allelic scores that index biological intermediates

Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error

Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index

Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency

Osteocyte transcriptome mapping identifies a molecular landscape controlling skeletal homeostasis and susceptibility to skeletal disease

Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment

Regenerating zebrafish scales express a subset of evolutionary conserved genes involved in human skeletal disease

Seventy-five genetic loci influencing the human red blood cell

Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation

The Effect of Plasma Lipids and Lipid-Lowering Interventions on Bone Mineral Density: A Mendelian Randomization Study