A. Teumer

Discipline

Anthropologie biologique (19) Psychologie (2) Economies et finances (2)

Type de document

Articles (65) Autres (3)

Co-auteur

Date

Source

Mot-clé

association (51) Social groups (51) Human beings (35) Genes (31) Meta-analysis (30) Heredity (27) Genealogy (27) Family (23) roman (22) effet (21) Phenotype (20) risque (19) Risk (19) Evidence (18) maladie (18) maladie (17) Obesity (16) gène (15) spectacle (14) adulte (14) adulte (14) analyse (13) Expression (13) Body mass index (13) Analysis (13) Blood (12) Regions (12) corps (12) Women (11) Women (11)

Documents écrit par A. Teumer (65) | parle de A. Teumer (0)

A saturated map of common genetic variants associated with human height.
L. Yengo et al.
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention.
Z. Wang et al.
Limited evidence for blood eQTLs in human sexual dimorphism.
E. Porcu et al. (11 août 2022)
Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus.
A. Tin et al. (9 déc. 2021)
Meta-analyses identify DNA methylation associated with kidney function and damage.
P. Schlosser et al. (9 déc. 2021)
Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome.
E. Porcu et al. (24 sept. 2021)
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression.
U. Võsa et al.
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.
L. de Las Fuentes et al.
Genome-wide association study of circulating interleukin 6 levels identifies novel loci.
T.S. Ahluwalia et al. (27 avr. 2021)
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans.
I.E. Sønderby et al. (22 mars 2021)
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.
I.E. Sønderby et al.
Associations of autozygosity with a broad range of human phenotypes.
D.W. Clark et al. (31 oct. 2019)
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.
A.E. Justice et al.
Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances.
P.R. Timmers et al. (15 janv. 2019)
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation.
A. Teumer et al. (26 oct. 2018)
Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels.
A. Tin et al. (12 oct. 2018)
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
N.R. Wray et al.
Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in Men.
H. Chen et al.
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
V. Turcot et al.
Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
M. Graff et al.
Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
M. Gorski et al. (26 mai 2017)
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
M. Gorski et al. (28 avr. 2017)
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
A.E. Justice et al. (26 avr. 2017)
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
M. Graff et al.
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium.
R.A. Power et al. (15 févr. 2017)

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