Pages that link to "Q37634241"
Jump to navigation
Jump to search
The following pages link to Loic Yengo (Q37634241):
Displaying 50 items.
- Genetic studies of body mass index yield new insights for obesity biology (Q22305005) (← links)
- Genome-wide association analyses identify 18 new loci associated with serum urate concentrations (Q24620065) (← links)
- Genomic insights into the origin of farming in the ancient Near East (Q27480271) (← links)
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (Q28272915) (← links)
- Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human (Q28591078) (← links)
- Directional dominance on stature and cognition in diverse human populations (Q28646221) (← links)
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (Q29417007) (← links)
- Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases (Q29417103) (← links)
- The genetic architecture of type 2 diabetes (Q29583824) (← links)
- KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference (Q30275308) (← links)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (Q30277642) (← links)
- Genome-wide analysis identifies 12 loci influencing human reproductive behavior (Q30313778) (← links)
- Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. (Q30352681) (← links)
- Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults (Q33610252) (← links)
- Low-dose exposure to bisphenols A, F and S of human primary adipocyte impacts coding and non-coding RNA profiles (Q33811808) (← links)
- Defining the role of common variation in the genomic and biological architecture of adult human height (Q34441746) (← links)
- Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci (Q34501150) (← links)
- Detection of human adaptation during the past 2000 years (Q34542582) (← links)
- Analysis of the contribution of FTO, NPC1, ENPP1, NEGR1, GNPDA2 and MC4R genes to obesity in Mexican children. (Q34572543) (← links)
- The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (Q34673513) (← links)
- Parental history of type 2 diabetes, TCF7L2 variant and lower insulin secretion are associated with incident hypertension. Data from the DESIR and RISC cohorts (Q34940230) (← links)
- GUESS-ing polygenic associations with multiple phenotypes using a GPU-based evolutionary stochastic search algorithm (Q34945566) (← links)
- New genetic loci link adipose and insulin biology to body fat distribution (Q35114362) (← links)
- Disruption of a novel Kruppel-like transcription factor p300-regulated pathway for insulin biosynthesis revealed by studies of the c.-331 INS mutation found in neonatal diabetes mellitus. (Q35150213) (← links)
- Post-Bariatric Surgery Changes in Quinolinic and Xanthurenic Acid Concentrations Are Associated with Glucose Homeostasis (Q36057967) (← links)
- Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (Q36207326) (← links)
- Relationship between salivary/pancreatic amylase and body mass index: a systems biology approach (Q36287821) (← links)
- Epigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control study (Q36496178) (← links)
- Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes. (Q36508365) (← links)
- New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk (Q36541220) (← links)
- Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index (Q36861322) (← links)
- Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders (Q36968428) (← links)
- Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes (Q37173576) (← links)
- Impact of statistical models on the prediction of type 2 diabetes using non-targeted metabolomics profiling (Q37279013) (← links)
- The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals (Q37297746) (← links)
- Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms (Q37336104) (← links)
- Early metabolic markers identify potential targets for the prevention of type 2 diabetes (Q38673034) (← links)
- An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (Q38752732) (← links)
- KAT2B Is Required for Pancreatic Beta Cell Adaptation to Metabolic Stress by Controlling the Unfolded Protein Response (Q38775183) (← links)
- European genetic variants associated with type 2 diabetes in North African Arabs (Q38934939) (← links)
- (Q39195846) (redirect page) (← links)
- 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. (Q40045602) (← links)
- Beneficial effect of a high number of copies of salivary amylase AMY1 gene on obesity risk in Mexican children. (Q40234695) (← links)
- Associations Between Type 2 Diabetes-Related Genetic Scores and Metabolic Traits, in Obese and Normal-Weight Youths. (Q40492812) (← links)
- Heterozygous mutations causing partial prohormone convertase 1 deficiency contribute to human obesity (Q40666599) (← links)
- Low-frequency variants in HMGA1 are not associated with type 2 diabetes risk (Q40666739) (← links)
- The loss-of-function PCSK9 p.R46L genetic variant does not alter glucose homeostasis (Q40863199) (← links)
- Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults (Q42348998) (← links)
- Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (Q42502463) (← links)
- Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family (Q43984990) (← links)