M.A. Nalls

Discipline

Anthropologie biologique (8)

Type de document

Articles (24)

Co-auteur

Date

Source

Mot-clé

association (21) Social groups (21) Genes (17) Human beings (17) Heredity (14) Genealogy (14) Family (13) effet (11) Meta-analysis (11) biologie (9) Evidence (9) Biology (9) spectacle (8) risque (8) Phenotype (8) Risk (8) roman (8) lipide (7) adulte (7) Obesity (7) Sizes (7) adulte (7) génétique (6) gène (6) règlement (6) Variation (6) Genetics (6) Genetics (6) Regulation (6) corps (6)

Documents écrit par M.A. Nalls (24) | parle de M.A. Nalls (0)

Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.
S. Kanoni et al. (27 déc. 2022)
Stroke genetics informs drug discovery and risk prediction across ancestries.
A. Mishra et al.
A saturated map of common genetic variants associated with human height.
L. Yengo et al.
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.
S. Ramdas et al. (4 août 2022)
The power of genetic diversity in genome-wide association studies of lipids.
S.E. Graham 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.
Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.
R. Noordam et al. (12 nov. 2019)
Associations of autozygosity with a broad range of human phenotypes.
D.W. Clark et al. (31 oct. 2019)
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.
T.O. Kilpeläinen et al. (22 janv. 2019)
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.
M.F. Feitosa et al. (2018)
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
V. Turcot 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.
Rare and low-frequency coding variants alter human adult height.
E. Marouli et al. (9 févr. 2017)
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk.
Y. Lu et al. (2016)
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels.
T.O. Kilpeläinen et al. (2016)
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
M.C. Cornelis et al.
Genetic studies of body mass index yield new insights for obesity biology
A.E. Locke et al. (2015)
New genetic loci link adipose and insulin biology to body fat distribution.
D. Shungin et al. (2015)
Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adults.
E. Zimmermann 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)
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
G.B. Ehret et al. (2011)
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study.
E.R. Fox et al. (2011)
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.
C.E. Elks et al. (2010)