M. Nauck

Discipline

Anthropologie biologique (3) Psychologie (2) Economies et finances (2)

Type de document

Articles (32) Autres (2)

Co-auteur

Date

Source

Mot-clé

association (25) Social groups (25) Genes (15) Meta-analysis (14) risque (12) Risk (12) Heredity (12) Genealogy (12) roman (12) Phenotype (11) Human beings (11) Family (10) maladie (10) Expression (9) spectacle (8) analyse (8) gène (8) effet (8) maladie (8) Analysis (8) génétique (7) Genetics (7) Obesity (7) Genetics (7) Blood (7) Serum (6) Adulthood (6) Regions (6) région (5) métabolisme (5)

Documents écrit par M. Nauck (32) | parle de M. Nauck (0)

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.
Genome-wide association study of circulating interleukin 6 levels identifies novel loci.
T.S. Ahluwalia et al. (27 avr. 2021)
An individual participant data analysis of prospective cohort studies on the association between subclinical thyroid dysfunction and depressive symptoms.
L. Wildisen et al. (5 nov. 2020)
Associations of autozygosity with a broad range of human phenotypes.
D.W. Clark et al. (31 oct. 2019)
Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances.
P.R. Timmers et al. (15 janv. 2019)
Analysis of shared heritability in common disorders of the brain.
V. Anttila et al. (22 juin 2018)
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
N.R. Wray et al.
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.
E. Wheeler 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.
Rare and low-frequency coding variants alter human adult height.
E. Marouli et al. (9 févr. 2017)
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
C. Pattaro et al. (2016)
Meta-analysis of genome-wide association studies of anxiety disorders.
T. Otowa et al. (2016)
Genome-Wide Association Study with Targeted and Non-targeted NMR Metabolomics Identifies 15 Novel Loci of Urinary Human Metabolic Individuality
J. Raffler et al. (2015)
Modulation of genetic associations with serum urate levels by body-mass-index in humans.
J.E. Huffman et al. (2015)
Defining the role of common variation in the genomic and biological architecture of adult human height.
A.R. Wood et al.
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
A. Köttgen et al. (2013)
Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.
R.G. Walters et al. (2013)
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations.
O'Seaghdha C.M. et al. (2013)

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