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Author Details
Full Name
Loic Yengo
Affiliation
ORCID
Career Start Year
2011
Papers
123
H Index
53
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
38052102
Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity.
Hum Reprod
2024
37292977
Genetics of skeletal proportions in two different populations.
bioRxiv
2023
36138222
Genetic footprints of assortative mating in the Japanese population.
Nat Hum Behav
2023
35987817
Genetic and modifiable risk factors combine multiplicatively in common disease.
Clin Res Cardiol
2023
36422680
Phenotypic and genetic factors associated with donation of DNA and consent to record linkage for prescription history in the Australian Genetics of Depression Study.
Eur Arch Psychiatry Clin Neurosci
2023
37733769
Identification and analysis of individuals who deviate from their genetically-predicted phenotype.
PLoS Genet
2023
37723263
Boosting the power of genome-wide association studies within and across ancestries by using polygenic scores.
Nat Genet
2023
37963177
Cross-ancestry analyses identify new genetic loci associated with 25-hydroxyvitamin D.
PLoS Genet
2023
37693475
Direct and INdirect effects analysis of Genetic lOci (DINGO): A software package to increase the power of locus discovery in GWAS meta-analyses of perinatal phenotypes and traits influenced by indirect genetic effects.
medRxiv
2023
36707517
Estimation and implications of the genetic architecture of fasting and non-fasting blood glucose.
Nat Commun
2023
37069254
Mate choice through a genomic lens.
2023
36634672
15 years of GWAS discovery: Realizing the promise.
2023
36798175
Identification and analysis of individuals who deviate from their genetically-predicted phenotype.
bioRxiv
2023
37228756
Genome-wide CRISPR screening of chondrocyte maturation newly implicates genes in skeletal growth and height-associated GWAS loci.
Cell Genom
2023
35115518
Assortative mating biases marker-based heritability estimators.
Nature Communications
2022
35551307
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Nat Genet
2022
35365697
Author Correction: Assortative mating biases marker-based heritability estimators.
Nature Communications
2022
35322215
Constrained human genes under scrutiny.
Nature
2022
34554790
Discovery and implications of polygenicity of common diseases.
Science
2021
33811805
Estimation of non-additive genetic variance in human complex traits from a large sample of unrelated individuals.
Am J Hum Genet
2021
33961780
Estimation of non-additive genetic variance in human complex traits from a large sample of unrelated individuals.
Am J Hum Genet
2021
33737653
Triangulating evidence from longitudinal and Mendelian randomization studies of metabolomic biomarkers for type 2 diabetes.
Sci Rep
2021
34214457
Genomic partitioning of inbreeding depression in humans.
Am J Hum Genet
2021
33664403
Quantifying genetic heterogeneity between continental populations for human height and body mass index.
Scientific Reports
2021
33608517
Widespread signatures of natural selection across human complex traits and functional genomic categories.
Nat Commun
2021
33558525
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Nat Commun
2021
34315903
Integrative genomic analyses identify susceptibility genes underlying COVID-19 hospitalization.
Nat Commun
2021
33594080
Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals.
Nat Commun
2021
32736793
Risk in Relatives, Heritability, SNP-Based Heritability, and Genetic Correlations in Psychiatric Disorders: A Review.
Biol Psychiatry
2021
32671396
Alzheimer's disease genetic risk and sleep phenotypes in healthy young men: association with more slow waves and daytime sleepiness.
Sleep
2021
33402679
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Nat Commun
2021
34632698
Polygenic burden could explain high rates of affective disorders in a community with restricted founder population.
Am J Med Genet B Neuropsychiatr Genet
2021
32737319
Theoretical and empirical quantification of the accuracy of polygenic scores in ancestry divergent populations.
Nature Communications
2020
31713005
No Evidence for Social Genetic Effects or Genetic Similarity Among Friends Beyond that Due to Population Stratification: A Reappraisal of Domingue et al (2018).
Behavior Genetics
2020
33046911
Pathogenic variants in actionable MODY genes are associated with type 2 diabetes.
Nat Metab
2020
33045005
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits.
PLoS Genet
2020
32925905
Using prior information from humans to prioritize genes and gene-associated variants for complex traits in livestock.
PLoS Genetics
2020
32687259
A unified framework for association and prediction from vertex-wise grey-matter structure.
Hum Brain Mapp
2020
31481654
Extreme inbreeding in a European ancestry sample from the contemporary UK population.
Nat Commun
2019
31636407
Genetic correlates of social stratification in Great Britain.
Nat Hum Behav
2019
31704910
Improved polygenic prediction by Bayesian multiple regression on summary statistics.
Nat Commun
2019
30239722
Meta-analysis of genome-wide association studies for body fat distribution in 694Â 649 individuals of European ancestry.
Hum Mol Genet
2019
31015401
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Nat Commun
2019
31263163
Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals.
Sci Rep
2019
31370963
Assortative Mating in Autism Spectrum Disorder: Toward an Evidence Base From DNA Data, but Not There Yet.
Biol Psychiatry
2019
30988446
Imprint of assortative mating on the human genome.
Nat Hum Behav
2018
30459399
Author Correction: Misestimation of heritability and prediction accuracy of male-pattern baldness.
Nat Commun
2018
30316741
Assortative mating on complex traits revisited: Double first cousins and the X-chromosome.
Theoretical Population Biology
2018
29936532
Association Between Population Density and Genetic Risk for Schizophrenia.
JAMA Psychiatry
2018
29891976
Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood.
Nat Commun
2018
1 - 50 of 123
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