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New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes
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Quantifying heterogeneity in a meta‐analysis
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Type 2 diabetes risk alleles near ADCY5, CDKAL1 and HHEX-IDE are associated with reduced birthweight
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Low birth weight and blood pressure
inferredcites →https://doi.org/10.1016/s0140-6736(98)07546-1openalex-snapshot
The fetal insulin hypothesis: an alternative explanation of the association of low bir thweight with diabetes and vascular disease
inferredcites →https://doi.org/10.1038/79216openalex-snapshot
The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
inferredcites →https://doi.org/10.1038/953openalex-snapshot
Mutations in the glucokinase gene of the fetus result in reduced birth weight
inferredcites →https://doi.org/10.1038/ejhg.2011.39openalex-snapshot
Genomic inflation factors under polygenic inheritance
inferredcites →https://doi.org/10.1038/nature05616openalex-snapshot
A genome-wide association study identifies novel risk loci for type 2 diabetes
inferredcites →https://doi.org/10.1038/nature08625openalex-snapshot
Parental origin of sequence variants associated with complex diseases
inferredcites →https://doi.org/10.1038/nature09270openalex-snapshot
Biological, clinical and population relevance of 95 loci for blood lipids
inferredcites →https://doi.org/10.1038/nature09410openalex-snapshot
Hundreds of variants clustered in genomic loci and biological pathways affect human height
inferredcites →https://doi.org/10.1038/nature10405openalex-snapshot
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
inferredcites →https://doi.org/10.1038/ng.120openalex-snapshot
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
inferredcites →https://doi.org/10.1038/ng.121openalex-snapshot
Genome-wide association analysis identifies 20 loci that influence adult height
inferredcites →https://doi.org/10.1038/ng.2238openalex-snapshot
Common variants at 12q15 and 12q24 are associated with infant head circumference
inferredcites →https://doi.org/10.1038/ng.2245openalex-snapshot
Common variants at 6q22 and 17q21 are associated with intracranial volume
inferredcites →https://doi.org/10.1038/ng.290openalex-snapshot
Variants in MTNR1B influence fasting glucose levels
inferredcites →https://doi.org/10.1038/ng.443openalex-snapshot
Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia
inferredcites →https://doi.org/10.1038/ng.520openalex-snapshot
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
inferredcites →https://doi.org/10.1038/ng.521openalex-snapshot
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge
inferredcites →https://doi.org/10.1038/ng.567openalex-snapshot
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight
inferredcites →https://doi.org/10.1038/ng.609openalex-snapshot
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
inferredcites →https://doi.org/10.1038/ng.660openalex-snapshot
A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B
inferredcites →https://doi.org/10.1038/ng.686openalex-snapshot
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
inferredcites →https://doi.org/10.1038/ng.921openalex-snapshot
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci
inferredcites →https://doi.org/10.1038/ng0612-732copenalex-snapshot
Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume
inferredcites →https://doi.org/10.1038/ng1732openalex-snapshot
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes
inferredcites →https://doi.org/10.1038/ng2043openalex-snapshot
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes
inferredcites →https://doi.org/10.1038/ng2062openalex-snapshot
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes
inferredcites →https://doi.org/10.1038/ng2067openalex-snapshot
Common variants in WFS1 confer risk of type 2 diabetes
inferredcites →https://doi.org/10.1038/ng2088openalex-snapshot
A new multipoint method for genome-wide association studies by imputation of genotypes
inferredcites →https://doi.org/10.1056/nejmoa0707943openalex-snapshot
Hyperglycemia and Adverse Pregnancy Outcomes
inferredcites →https://doi.org/10.1086/518517openalex-snapshot
Type 2 Diabetes TCF7L2 Risk Genotypes Alter Birth Weight: A Study of 24,053 Individuals
inferredcites →https://doi.org/10.1086/519795openalex-snapshot
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
inferredcites →https://doi.org/10.1093/ajcn/71.5.1344sopenalex-snapshot
Fetal nutrition and adult disease
inferredcites →https://doi.org/10.1093/aje/kwm042openalex-snapshot
Birth Weight and Systolic Blood Pressure in Adolescence and Adulthood: Meta-Regression Analysis of Sex- and Age-specific Results from 20 Nordic Studies
inferredcites →https://doi.org/10.1093/bioinformatics/btm108openalex-snapshot
GenABEL: an R library for genome-wide association analysis
inferredcites →https://doi.org/10.1093/bioinformatics/btp420openalex-snapshot
A System for Information Management in BioMedical Studies—SIMBioMS
inferredcites →https://doi.org/10.1093/bioinformatics/btq340openalex-snapshot
METAL: fast and efficient meta-analysis of genomewide association scans
inferredcites →https://doi.org/10.1097/01.aoa.0000344706.95925.dcopenalex-snapshot
Hyperglycemia and Adverse Pregnancy Outcomes
inferredcites →https://doi.org/10.1111/j.0006-341x.1999.00997.xopenalex-snapshot
Genomic Control for Association Studies
inferredcites →https://doi.org/10.1111/j.1651-2227.1991.tb11945.xopenalex-snapshot
An Update of the Swedish Reference Standards for Weight, Length and Head Circumference at Birth for Given Gestational Age (1977‐1981)
inferredcites →https://doi.org/10.1126/science.1142358openalex-snapshot
Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels
inferredcites →https://doi.org/10.1126/science.1142364openalex-snapshot
Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes
inferredcites →https://doi.org/10.1126/science.1142382openalex-snapshot
A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants
inferredcites →https://doi.org/10.1159/000353879openalex-snapshot
Genetics of Food Intake Self-Regulation in Childhood: Literature Review and Research Opportunities
inferredcites →https://doi.org/10.1159/000368657openalex-snapshot
Identification of Candidate Gene Variants in Korean MODY Families by Whole-Exome Sequencing
inferredcites →https://doi.org/10.1161/hypertensionaha.110.158667openalex-snapshot
Association of Hypertension Drug Target Genes With Blood Pressure and Hypertension in 86 588 Individuals
inferredcites →https://doi.org/10.1186/1471-2105-11-134openalex-snapshot
ProbABEL package for genome-wide association analysis of imputed data
inferredcites →https://doi.org/10.1186/1471-2105-11-288openalex-snapshot
GWAMA: software for genome-wide association meta-analysis
inferredcites →https://doi.org/10.1371/journal.pgen.1000409openalex-snapshot
Genetic Determinants of Height Growth Assessed Longitudinally from Infancy to Adulthood in the Northern Finland Birth Cohort 1966
inferredcites →https://doi.org/10.2337/db08-1739openalex-snapshot
Type 2 Diabetes Risk Alleles Are Associated With Reduced Size at Birth
inferredcites →https://doi.org/10.2337/db09-0506openalex-snapshot
Examination of Type 2 Diabetes Loci Implicates CDKAL1 as a Birth Weight Gene
inferredcites →https://doi.org/10.2337/db10-0177openalex-snapshot
Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study: Common Genetic Variants in GCK and TCF7L2 Are Associated With Fasting and Postchallenge Glucose Levels in Pregnancy and With the New Consensus Definition of Gestational Diabetes Mellitus From the International Association of Diabetes and…
inferredcites →https://doi.org/10.2337/db11-0415openalex-snapshot
Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes
inferredcites →https://doi.org/10.2337/diabetes.54.2.576openalex-snapshot
Genetic Regulation of Birth Weight and Fasting Glucose by a Common Polymorphism in the Islet Cell Promoter of the Glucokinase Gene
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Association of Birth Weight With Type 2 Diabetes and Glycemic Traits
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Genetics of Birth Weight
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Fetal nutrition and disease in later life
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Are genes destiny? Exploring the role of intrauterine environment in moderating genetic influences on body mass
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A genetic stochastic process model for genome‐wide joint analysis of biomarker dynamics and disease susceptibility with longitudinal data
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The obesity associated FTO gene variant and the risk of adverse pregnancy outcomes: Evidence from the SCOPE study
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Genetic determinants of adiponectin regulation revealed by pregnancy
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Detecting pleiotropy in Mendelian randomisation studies with summary data and a continuous outcome
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A Bayesian approach to Mendelian randomisation with dependent instruments
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Genetic Variants of Adrenoceptors
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Genetics of Type 2 Diabetes
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Nutrigenetics of Type 2 Diabetes
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Genetics of Type 2 Diabetes
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Genetics of Cardiovascular Risk in Obesity
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Genetics of Type 2 Diabetes
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Genetics of Type 2 Diabetes
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Genetics of Cardiovascular Risk in Obesity
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The Role of the GWAS Identified FTO Locus in Regulating Body Size and Composition
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Post-Transcriptional Modifications of RNA: Impact on RNA Function and Human Health
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Biomarkers of Abnormal Birth Weight in Pregnancy
inferred← citeshttps://doi.org/10.1007/978-981-13-2194-8_4openalex-snapshot
Developmental Origins of Health and Disease (DOHaD) Cohorts and Interventions: Status and Perspective
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Gene–Environment Interactions to Detect Adverse Health Effects on the Next Generation
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Identification of PDXDC1 as a novel pleiotropic susceptibility locus shared between lumbar spine bone mineral density and birth weight
inferred← citeshttps://doi.org/10.1007/s00125-015-3516-9openalex-snapshot
Genetic and phenotypic correlations between surrogate measures of insulin release obtained from OGTT data
inferred← citeshttps://doi.org/10.1007/s00125-016-4019-zopenalex-snapshot
Low birthweight and risk of type 2 diabetes: a Mendelian randomisation study
inferred← citeshttps://doi.org/10.1007/s00125-016-4057-6openalex-snapshot
Can genetic evidence help us to understand the fetal origins of type 2 diabetes?
inferred← citeshttps://doi.org/10.1007/s00125-018-4783-zopenalex-snapshot
A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria
inferred← citeshttps://doi.org/10.1007/s00125-020-05331-0openalex-snapshot
Hyperglycemia and Adverse Pregnancy Outcome Follow-Up Study: newborn anthropometrics and childhood glucose metabolism
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Higher maternal adiposity reduces offspring birthweight if associated with a metabolically favourable profile
inferred← citeshttps://doi.org/10.1007/s00125-024-06101-yopenalex-snapshot
Low birthweight and overweight during childhood and young adulthood and the risk of type 2 diabetes in men: a population-based cohort study
inferred← citeshttps://doi.org/10.1007/s00125-025-06420-8openalex-snapshot
The genetics of low and high birthweight and their relationship with cardiometabolic disease
inferred← citeshttps://doi.org/10.1007/s00125-026-06669-7openalex-snapshot
Maternal and fetal genetic predispositions to insulin deficiency and resistance affect fetal growth through distinct pathways
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Exploring evidence of positive selection signatures in cattle breeds selected for different traits
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Genetic variants in the glucocorticoid pathway genes and birth weight
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Admixture mapping and fine-mapping of birth weight loci in the Black Women’s Health Study
inferred← citeshttps://doi.org/10.1007/s00439-021-02265-4openalex-snapshot
Admixture mapping identifies African and Amerindigenous local ancestry loci associated with fetal growth
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Die Rolle der HMGA-Proteine („high mobility group AT-hook“) bei Proliferation und Differenzierung mesenchymaler Zellen und Gewebe
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Passive rGE or Developmental Gene-Environment Cascade? An Investigation of the Role of Xenobiotic Metabolism Genes in the Association Between Smoke Exposure During Pregnancy and Child Birth Weight
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The Prenatal Environment in Twin Studies: A Review on Chorionicity
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The Generation R Study: Biobank update 2015
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The Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) consortia: design, results and future prospects
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Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood
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MIR146A and ADIPOQ genetic variants are associated with birth weight in relation to gestational age: a cohort study
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Genetic diversity and population structure of Tibetan sheep breeds determined by whole genome resequencing
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Insights into the Genetic Susceptibility to Type 2 Diabetes from Genome-Wide Association Studies of Glycaemic Traits
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How Can Genetic Studies Help Us to Understand Links Between Birth Weight and Type 2 Diabetes?
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Familial Aggregation and Childhood Blood Pressure
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Association of diabetes-related variants in ADCY5 and CDKAL1 with neonatal insulin, C-peptide, and birth weight
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Assessing the effect of modifiable risk factors on hepatocellular carcinoma: evidence from a bidirectional Mendelian randomization analysis
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Long-Term Health Effects and Underlying Biological Mechanisms of Developmental Exposure to Arsenic
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Glucocorticoids and Programming of the Fetal Brain
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Diet, maternal nutrition, and long-term health consequences
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Food glycemic index changes in overweight/obese pregnant women enrolled in a lifestyle program: a randomized controlled trial
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Impact of Polygenic Risk for Schizophrenia on Cortical Structure in UK Biobank
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Assessing the genetic correlations between early growth parameters and bone mineral density: A polygenic risk score analysis
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Lower birth weight is associated with alterations in dietary intake in adolescents independent of genetic factors: A twin study
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Obesity and FTO: Changing Focus at a Complex Locus
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The Association between Height and Hypertension in Indonesia
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12q14 microdeletion syndrome: A family with short stature and Silver-Russell syndrome (SRS)-like phenotype and review of the literature
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Polymorphic variants of bovine ADCY5 gene identified in GWAS analysis were significantly associated with ovarian morphological related traits
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Examining How Our Shared Evolutionary History Shapes Future Disease Outcomes
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Season of birth is associated with birth weight, pubertal timing, adult body size and educational attainment: a UK Biobank study
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Incidence of atrial fibrillation in relation to birth weight and preterm birth
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Single Nucleotide Polymorphism Heritability of Behavior Problems in Childhood: Genome-Wide Complex Trait Analysis
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Genomic analyses reveal distinct genetic architectures and selective pressures in Chinese donkeys
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Large-scale low-coverage whole-genome sequencing reveals the genetic architecture of wool and growth traits in fine-wool sheep
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Developmental origins of health and disease theory in cardiology
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The Role of miRNAs in Regulating Gene Expression Networks
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Birth weight and its association with blood pressure and nutritional status in adolescents
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Birth weight and its association with blood pressure and nutritional status in adolescents
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The role of the FTO (Fat Mass and Obesity Related) locus in regulating body size and composition
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Could consanguineous marriage provide a cultural alleviation for the obstetric dilemma?
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Quantitative magnetic resonance imaging traits as endophenotypes for genetic mapping in epilepsy
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Relation of FTO gene variants to fetal growth trajectories: Findings from the Southampton Women's survey
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An Anas pangenome graph reveals the role of structural variations in duck domestication
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DDT exposure during pregnancy and DNA methylation alterations in female offspring in the Child Health and Development Study
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Health inequities start early in life, even before birth: Why race-specific fetal and neonatal growth references disadvantage Black infants
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Trans-ancestry genome-wide association study of childhood body mass index identifies novel loci and age-specific effects
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Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing
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Gene expression profiling of archived dried blood spot samples from the Danish Neonatal Screening Biobank
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Evaluation of whole genome amplified DNA to decrease material expenditure and increase quality
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Association between type 2 diabetes and prenatal exposure to the Ukraine famine of 1932–33: a retrospective cohort study
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Divergent associations of height with cardiometabolic disease and cancer: epidemiology, pathophysiology, and global implications
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Longitudinal follow-up of the relationship between dietary intake and growth and development in the Lifeways cross-generation cohort study 2001–2013
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Polygenic prediction of the phenome, across ancestry, in emerging adulthood
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The ‘Developmental Origins’ Hypothesis: relevance to the obstetrician and gynecologist
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The role of genetics in fetal programming of adult cardiometabolic disease
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Variants Close to NTRK2 Gene Are Associated With Birth Weight in Female Twins
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DNA Methylation Changes in theIGF1RGene in Birth Weight Discordant Adult Monozygotic Twins
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Isomerization Kinetics of AT Hook Decapeptide Solution Structures
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Practical Strategies and Concepts in GPCR Allosteric Modulator Discovery: Recent Advances with Metabotropic Glutamate Receptors
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Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer
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Longitudinal weight differences, gene expression and blood biomarkers in BMI-discordant identical twins
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Maternal and fetal genetic contribution to gestational weight gain
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A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP
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Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
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Genome-wide associations for birth weight and correlations with adult disease
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Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels
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New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
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Height-reducing variants and selection for short stature in Sardinia
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An atlas of genetic correlations across human diseases and traits
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Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits
inferred← citeshttps://doi.org/10.1038/nn.4398openalex-snapshot
Novel genetic loci underlying human intracranial volume identified through genome-wide association
inferred← citeshttps://doi.org/10.1038/nrendo.2012.248openalex-snapshot
Genetic links between birth weight and adult-onset disease
inferred← citeshttps://doi.org/10.1038/nrendo.2013.227openalex-snapshot
The bigger picture of FTO—the first GWAS-identified obesity gene
inferred← citeshttps://doi.org/10.1038/nrendo.2014.11openalex-snapshot
Susceptibility to type 2 diabetes mellitus—from genes to prevention
inferred← citeshttps://doi.org/10.1038/nrendo.2015.167openalex-snapshot
Molecular insights into the aetiology of female reproductive ageing
inferred← citeshttps://doi.org/10.1038/nutd.2014.35openalex-snapshot
The chromosome 3q25 locus associated with fetal adiposity is not associated with childhood adiposity
inferred← citeshttps://doi.org/10.1038/s10038-022-01010-7openalex-snapshot
Admixture mapping of anthropometric traits in the Black Women’s Health Study: evidence of a shared African ancestry component with birth weight and type 2 diabetes
inferred← citeshttps://doi.org/10.1038/s41467-022-30007-1openalex-snapshot
Placental multi-omics integration identifies candidate functional genes for birthweight
inferred← citeshttps://doi.org/10.1038/s41467-024-53495-9openalex-snapshot
DINGO: increasing the power of locus discovery in maternal and fetal genome-wide association studies of perinatal traits
inferred← citeshttps://doi.org/10.1038/s41467-025-67449-2openalex-snapshot
Partitioned polygenic scores show mechanistic heterogeneity in type 2 diabetes and hypertension comorbidity
inferred← citeshttps://doi.org/10.1038/s41588-018-0225-6openalex-snapshot
Identifying loci affecting trait variability and detecting interactions in genome-wide association studies
inferred← citeshttps://doi.org/10.1038/s41588-019-0403-1openalex-snapshot
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
inferred← citeshttps://doi.org/10.1038/s41598-017-06469-5openalex-snapshot
CDK5 Regulatory Subunit-Associated Protein 1-like 1 Negatively Regulates Adipocyte Differentiation through Activation of Wnt Signaling Pathway
inferred← citeshttps://doi.org/10.1038/s41598-018-25706-zopenalex-snapshot
Genetic and Environmental Influences on Fetal Growth Vary during Sensitive Periods in Pregnancy
inferred← citeshttps://doi.org/10.1038/s41598-018-26752-3openalex-snapshot
Birth weight variants are associated with variable fetal intrauterine growth from 20 weeks of gestation
inferred← citeshttps://doi.org/10.1038/s41598-019-40834-wopenalex-snapshot
Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine
inferred← citeshttps://doi.org/10.1038/s41598-020-80084-9openalex-snapshot
Pleiotropic genetic influence on birth weight and childhood obesity
inferred← citeshttps://doi.org/10.1038/s41598-021-84491-4openalex-snapshot
Polymorphic variants in Sweet and Umami taste receptor genes and birthweight
inferred← citeshttps://doi.org/10.1038/s41598-022-26572-6openalex-snapshot
Genetically-predicted placental gene expression is associated with birthweight and adult body mass index
inferred← citeshttps://doi.org/10.1038/s41598-023-46910-6openalex-snapshot
The influence of insulin-related genetic variants on fetal growth, fetal blood flow, and placental weight in a prospective pregnancy cohort
inferred← citeshttps://doi.org/10.1038/s43587-024-00733-wopenalex-snapshot
Genetics of female and male reproductive traits and their relationship with health, longevity and consequences for offspring
inferred← citeshttps://doi.org/10.1038/srep38420openalex-snapshot
Birth weight and risk of ischemic heart disease: A Mendelian randomization study
inferred← citeshttps://doi.org/10.1038/srep42048openalex-snapshot
Searching for new loci and candidate genes for economically important traits through gene-based association analysis of Simmental cattle
inferred← citeshttps://doi.org/10.1038/tp.2016.32openalex-snapshot
The effects of maternal anxiety during pregnancy on IGF2/H19 methylation in cord blood
inferred← citeshttps://doi.org/10.1071/rd23174openalex-snapshot
Expression of transforming growth factor β signalling molecules and their correlations with genes in loci linked to polycystic ovary syndrome in human foetal and adult tissues
inferred← citeshttps://doi.org/10.1073/pnas.2023860118openalex-snapshot
Morphological integration of the human brain across adolescence and adulthood
inferred← citeshttps://doi.org/10.1080/01443615.2022.2125300openalex-snapshot
The effects of intrauterine growth on physical and intellectual development of one-year-old infants: a study on monochorionic twins with selective intrauterine growth restriction
inferred← citeshttps://doi.org/10.1080/07853890.2016.1193786openalex-snapshot
Developmental Origins of Health and Disease – from a small body size at birth to epigenetics
inferred← citeshttps://doi.org/10.1080/14767058.2021.1989404openalex-snapshot
Placental cadmium, placental genetic variations, and birth size
inferred← citeshttps://doi.org/10.1080/14767058.2022.2053843openalex-snapshot
Is birthweight influenced equally by maternal and paternal anthropometry?
inferred← citeshttps://doi.org/10.1080/15592294.2018.1435243openalex-snapshot
Breast cancer family history and allele-specific DNA methylation in the legacy girls study
inferred← citeshttps://doi.org/10.1093/advances/nmx012openalex-snapshot
ω-3 Fatty Acids, Impaired Fetal Growth, and Cardiovascular Risk: Nutrition as Precision Medicine
inferred← citeshttps://doi.org/10.1093/aje/kwx034openalex-snapshot
The Effect of Birth Weight on Academic Performance: Instrumental Variable Analysis
inferred← citeshttps://doi.org/10.1093/aje/kwx340openalex-snapshot
Intergenerational Transmission of Birth Weight Across 3 Generations
inferred← citeshttps://doi.org/10.1093/bib/bbac039openalex-snapshot
PGS-server: accuracy, robustness and transferability of polygenic score methods for biobank scale studies
inferred← citeshttps://doi.org/10.1093/bioinformatics/btw577openalex-snapshot
Gene- and pathway-based association tests for multiple traits with GWAS summary statistics
inferred← citeshttps://doi.org/10.1093/bioinformatics/btw613openalex-snapshot
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis
inferred← citeshttps://doi.org/10.1093/emph/eoae002openalex-snapshot
Reconsidering the developmental origins of adult disease paradigm
inferred← citeshttps://doi.org/10.1093/eurjpc/zwad296openalex-snapshot
Genetically predicted gestational age and birth weight are associated with cardiac and pulmonary vascular remodelling in adulthood
inferred← citeshttps://doi.org/10.1093/hmg/ddaa074openalex-snapshot
Relationship between birth weight and chronic kidney disease: evidence from systematics review and two-sample Mendelian randomization analysis
inferred← citeshttps://doi.org/10.1093/hmg/ddab121openalex-snapshot
Genetic meta-analysis of twin birth weight shows high genetic correlation with singleton birth weight
inferred← citeshttps://doi.org/10.1093/hmg/ddt168openalex-snapshot
The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study
inferred← citeshttps://doi.org/10.1093/hmg/ddt231openalex-snapshot
Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances
inferred← citeshttps://doi.org/10.1093/hmg/ddu510openalex-snapshot
A novel common variant in DCST2 is associated with length in early life and height in adulthood
inferred← citeshttps://doi.org/10.1093/hmg/ddx429openalex-snapshot
Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics
inferred← citeshttps://doi.org/10.1093/humrep/deae008openalex-snapshot
The epidemiology of pregnancy loss: global burden, variable risk factors, and predictions
inferred← citeshttps://doi.org/10.1093/humrep/deae019openalex-snapshot
Fetal genetically determined birth weight plays a causal role in earlier puberty timing: evidence from human genetic studies
inferred← citeshttps://doi.org/10.1093/ije/dyad142openalex-snapshot
Partitioning genetic effects on birthweight at classical human leukocyte antigen loci into maternal and fetal components, using structural equation modelling
inferred← citeshttps://doi.org/10.1093/ije/dyt220openalex-snapshot
Parental diabetes and birthweight in 236 030 individuals in the UK Biobank Study
inferred← citeshttps://doi.org/10.1093/ije/dyw127openalex-snapshot
Commentary: Two-sample Mendelian randomization: opportunities and challenges
inferred← citeshttps://doi.org/10.1093/ije/dyw129openalex-snapshot
Mendelian randomization study of adiposity-related traits and risk of breast, ovarian, prostate, lung and colorectal cancer
inferred← citeshttps://doi.org/10.1093/ije/dyw196openalex-snapshot
Genome-wide DNA methylation study in human placenta identifies novel loci associated with maternal smoking during pregnancy
inferred← citeshttps://doi.org/10.1093/ije/dyw255openalex-snapshot
Metabolic signatures of birthweight in 18 288 adolescents and adults
inferred← citeshttps://doi.org/10.1093/ije/dyx190openalex-snapshot
Cohort Profile: Pregnancy And Childhood Epigenetics (PACE) Consortium
inferred← citeshttps://doi.org/10.1093/jamia/ocx026openalex-snapshot
The landscape of genetic susceptibility correlations among diseases and traits
inferred← citeshttps://doi.org/10.1093/med/9780198757672.003.0031openalex-snapshot
Molecular exercise physiology
inferred← citeshttps://doi.org/10.1093/nar/gkac115openalex-snapshot
AT-hook peptides bind the major and minor groove of AT-rich DNA duplexes
inferred← citeshttps://doi.org/10.1093/nar/gkv069openalex-snapshot
A rapid and sensitive high-throughput screening method to identify compounds targeting protein–nucleic acids interactions
inferred← citeshttps://doi.org/10.1093/ndt/gfv274openalex-snapshot
Smaller kidney size at birth in South Asians: findings from the Born in Bradford birth cohort study
inferred← citeshttps://doi.org/10.1093/nsr/nwz108openalex-snapshot
Prioritizing natural-selection signals from the deep-sequencing genomic data suggests multi-variant adaptation in Tibetan highlanders
inferred← citeshttps://doi.org/10.1097/cm9.0000000000003043openalex-snapshot
Birth weight, ideal cardiovascular health metrics in adulthood, and incident cardiovascular disease
inferred← citeshttps://doi.org/10.1097/hjh.0000000000001051openalex-snapshot
Paternal programming of offspring cardiometabolic diseases in later life
inferred← citeshttps://doi.org/10.1097/jbr.0000000000000056openalex-snapshot
Genetic hypothesis for the developmental origins of health and disease theory
inferred← citeshttps://doi.org/10.1097/mco.0000000000000757openalex-snapshot
Genetic architecture of type 2 diabetes and its shared genetic component with low birth weight in African Americans
inferred← citeshttps://doi.org/10.1097/psy.0000000000001022openalex-snapshot
Cardiometabolic Disorders in the Offspring of Parents With Severe Mental Illness
inferred← citeshttps://doi.org/10.1098/rstb.2014.0067openalex-snapshot
Between Scylla and Charybdis: renegotiating resolution of the ‘obstetric dilemma’ in response to ecological change
inferred← citeshttps://doi.org/10.1101/049247openalex-snapshot
Metabolic signatures of birth weight in 18 288 adolescents and adults
inferred← citeshttps://doi.org/10.1101/167551openalex-snapshot
Polygenic Adaptation has Impacted Multiple Anthropometric Traits
inferred← citeshttps://doi.org/10.1101/2020.06.09.141903openalex-snapshot
Whole Genome Sequencing of 5 Tibetan Sheep Breeds Identifies Selective Signatures to Adaptability at Different High-Altitude Areas in Qinghai-Tibetan Plateau
inferred← citeshttps://doi.org/10.1101/2020.10.30.20222844openalex-snapshot
The Interplay between Maternal Smoking and Genes in Offspring Birth Weight
inferred← citeshttps://doi.org/10.1101/2022.08.23.505053openalex-snapshot
Partitioning genetic effects on birth weight at classical human leukocyte antigen loci into indirect maternal and direct fetal components using structural equation modelling
inferred← citeshttps://doi.org/10.1101/2025.03.02.25323190openalex-snapshot
Mechanistic Heterogeneity in Type 2 Diabetes and Hypertension Comorbidity Revealed with Partitioned Polygenic Scores
inferred← citeshttps://doi.org/10.1101/203257openalex-snapshot
Polygenic risk scores applied to a single cohort reveal pleiotropy among hundreds of human phenotypes
inferred← citeshttps://doi.org/10.1111/1753-0407.12510openalex-snapshot
Increased identification of novel variants in type 2 diabetes, birth weight and their pleiotropic loci
inferred← citeshttps://doi.org/10.1111/adb.12317openalex-snapshot
Genome‐wide association study of body mass index in subjects with alcohol dependence
inferred← citeshttps://doi.org/10.1111/age.13382openalex-snapshot
Genome‐wide association study of growth traits and validation of key mutations (MSTN c. C861T ) associated with the muscle mass of meat pigeons
inferred← citeshttps://doi.org/10.1111/andr.12388openalex-snapshot
Mendelian randomisation analysis provides no evidence for a relationship between adult height and testicular cancer risk
inferred← citeshttps://doi.org/10.1111/aogs.12494openalex-snapshot
Genetic, nongenetic and epigenetic risk determinants in developmental programming of type 2 diabetes
inferred← citeshttps://doi.org/10.1111/apha.12196openalex-snapshot
Programming effects of FTO in the development of obesity
inferred← citeshttps://doi.org/10.1111/biom.12619openalex-snapshot
Integrative Genetic Risk Prediction Using Non-Parametric Empirical Bayes Classification
inferred← citeshttps://doi.org/10.1111/dme.12630openalex-snapshot
Non‐linear relationship between birthweight and cardiometabolic risk factors in Chinese adolescents and adults
inferred← citeshttps://doi.org/10.1111/dom.13405openalex-snapshot
tRNA modifications and islet function
inferred← citeshttps://doi.org/10.1111/eva.13284openalex-snapshot
Whole‐genome sequencing reveals the artificial selection and local environmental adaptability of pigeons (Columba livia)
inferred← citeshttps://doi.org/10.1111/ijpo.12175openalex-snapshot
The contribution of recently identified adult BMI risk loci to paediatric obesity in a Singaporean Chinese childhood dataset
inferred← citeshttps://doi.org/10.1111/ijpo.12205openalex-snapshot
Parental and child genetic contributions to obesity traits in early life based on 83 loci validated in adults: the FAMILY study
inferred← citeshttps://doi.org/10.1111/ijpo.12214openalex-snapshot
IRX3 is a genetic modifier for birth weight, adolescent obesity and transaminase metabolism
inferred← citeshttps://doi.org/10.1111/ijpo.12227openalex-snapshot
Associations between birthweight and overweight and obesity in school‐age children
inferred← citeshttps://doi.org/10.1111/jdi.12067openalex-snapshot
Insights into the genetic basis of type 2 diabetes
inferred← citeshttps://doi.org/10.1111/mcn.12672openalex-snapshot
Associations of maternal and fetal vitamin D status with childhood body composition and cardiovascular risk factors
inferred← citeshttps://doi.org/10.1111/obr.13033openalex-snapshot
Body Composition Measurements from Birth through 5 Years: Challenges, Gaps, and Existing & Emerging Technologies—A National Institutes of Health workshop
inferred← citeshttps://doi.org/10.1111/pai.12579openalex-snapshot
Role of environmental exposures and filaggrin mutations on associations of ethnic origin with risk of childhood eczema. The Generation R Study
inferred← citeshttps://doi.org/10.1124/pr.113.008219openalex-snapshot
Polymorphic Variants of Adrenoceptors: Pharmacology, Physiology, and Role in Disease
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