Nicholas J. Timpson

Nicholas J. Timpson's AcademicInfluence.com Rankings

Nicholas J. Timpson

Medical

#2372

World Rank

#2793

Historical Rank

Epidemiology

#422

World Rank

#442

Historical Rank

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Medical

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Nicholas J. Timpson's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (2007) (9208)
A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity (2007) (4268)
Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes (2007) (2245)
Mendelian randomization: Using genes as instruments for making causal inferences in epidemiology (2008) (2175)
The MR-Base platform supports systematic causal inference across the human phenome (2018) (2168)
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (2010) (2087)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (2010) (2011)
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) (1882)
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (2009) (1735)
Newly identified loci that influence lipid concentrations and risk of coronary artery disease (2008) (1626)
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (2007) (1421)
Common variants near MC4R are associated with fat mass, weight and risk of obesity (2008) (1307)
Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index (2010) (1179)
Genome-wide association study identifies 74 loci associated with educational attainment (2016) (1114)
The UK10K project identifies rare variants in health and disease (2015) (926)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) (897)
The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis (2012) (864)
GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (2013) (803)
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) (758)
Using published data in Mendelian randomization: a blueprint for efficient identification of causal risk factors (2015) (615)
Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses (2016) (563)
HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials (2015) (559)
Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (516)
Parent-of-origin specific allelic associations among 106 genomic loci for age at menarche (2014) (511)
Physical Activity Attenuates the Influence of FTO Variants on Obesity Risk: A Meta-Analysis of 218,166 Adults and 19,268 Children (2011) (508)
Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals (2012) (459)
Using multiple genetic variants as instrumental variables for modifiable risk factors (2012) (451)
Clustered Environments and Randomized Genes: A Fundamental Distinction between Conventional and Genetic Epidemiology (2007) (424)
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (421)
A common variant of HMGA2 is associated with adult and childhood height in the general population (2007) (419)
Common variants in the GDF5-UQCC region are associated with variation in human height (2008) (400)
Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture (2015) (399)
Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood (2019) (391)
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (2013) (379)
A genome-wide association meta-analysis identifies new childhood obesity loci (2012) (375)
Genome-wide associations for birth weight and correlations with adult disease (2016) (371)
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk (2017) (359)
C-reactive protein and its role in metabolic syndrome: mendelian randomisation study (2005) (341)
Prenatal exposure to maternal smoking and offspring DNA methylation across the lifecourse: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC) (2014) (325)
META-ANALYSIS OF GENOME-WIDE ASSOCIATION STUDIES IDENTIFIES THREE NEW RISK LOCI FOR ATOPIC DERMATITIS (2011) (325)
Common Variation in the FTO Gene Alters Diabetes-Related Metabolic Traits to the Extent Expected Given Its Effect on BMI (2008) (317)
The Avon Longitudinal Study of Parents and Children (ALSPAC): an update on the enrolled sample of index children in 2019 (2019) (304)
Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study (2017) (302)
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism (2012) (300)
Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders (2013) (299)
Genetic architecture: the shape of the genetic contribution to human traits and disease (2017) (298)
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) (296)
Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder. (2015) (281)
Genetic Associations with Subjective Well-Being Also Implicate Depression and Neuroticism (2015) (276)
The Effect of Elevated Body Mass Index on Ischemic Heart Disease Risk: Causal Estimates from a Mendelian Randomisation Approach (2012) (273)
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors (2018) (269)
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (2014) (262)
The fat mass- and obesity-associated locus and dietary intake in children. (2008) (262)
WNT16 Influences Bone Mineral Density, Cortical Bone Thickness, Bone Strength, and Osteoporotic Fracture Risk (2012) (257)
Association of plasma uric acid with ischaemic heart disease and blood pressure: mendelian randomisation analysis of two large cohorts (2013) (257)
Mental health before and during the COVID-19 pandemic in two longitudinal UK population cohorts (2020) (256)
A road map for efficient and reliable human genome epidemiology (2006) (252)
Genome-wide analysis identifies 12 loci influencing human reproductive behavior (2016) (250)
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight (2010) (250)
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals (2018) (249)
Childhood intelligence is heritable, highly polygenic and associated with FNBP1L (2014) (247)
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index. (2016) (245)
C-reactive protein levels and body mass index: Elucidating direction of causation through reciprocal Mendelian randomization (2010) (241)
Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization (2013) (236)
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci (2013) (228)
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. (2018) (221)
Association Between Genetic Variants on Chromosome 15q25 Locus and Objective Measures of Tobacco Exposure (2012) (215)
Association of C-Reactive Protein With Blood Pressure and Hypertension: Life Course Confounding and Mendelian Randomization Tests of Causality (2005) (210)
Apparent latent structure within the UK Biobank sample has implications for epidemiological analysis (2019) (207)
Large-scale association analyses identify host factors influencing human gut microbiome composition (2020) (206)
Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position. (2012) (204)
Strengthening the Reporting of Observational Studies in Epidemiology Using Mendelian Randomization: The STROBE-MR Statement. (2021) (204)
Genetic evidence of assortative mating in humans (2017) (199)
Does Greater Adiposity Increase Blood Pressure and Hypertension Risk?: Mendelian Randomization Using the FTO/MC4R Genotype (2009) (197)
MR-Base: a platform for systematic causal inference across the phenome using billions of genetic associations (2016) (190)
Association between Common Variation at the FTO Locus and Changes in Body Mass Index from Infancy to Late Childhood: The Complex Nature of Genetic Association through Growth and Development (2011) (187)
Exploring the Developmental Overnutrition Hypothesis Using Parental–Offspring Associations and FTO as an Instrumental Variable (2008) (183)
Genetic Markers of Adult Obesity Risk Are Associated with Greater Early Infancy Weight Gain and Growth (2010) (182)
Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity. (2013) (176)
Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels. (2008) (170)
Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers (2015) (168)
Obesity and Multiple Sclerosis: A Mendelian Randomization Study (2016) (168)
Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals. (2010) (168)
A genome‐wide approach to children's aggressive behavior: The EAGLE consortium (2016) (165)
A Genome-Wide Association Study Reveals Variants in ARL15 that Influence Adiponectin Levels (2009) (164)
Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium (2015) (164)
Assessing Causality in the Association between Child Adiposity and Physical Activity Levels: A Mendelian Randomization Analysis (2014) (162)
Genetic Determinants of Height Growth Assessed Longitudinally from Infancy to Adulthood in the Northern Finland Birth Cohort 1966 (2009) (156)
Early Cannabis Use, Polygenic Risk Score for Schizophrenia and Brain Maturation in Adolescence. (2015) (151)
The Trans-Ancestral Genomic Architecture of Glycemic Traits (2020) (151)
Inflammation, Insulin Resistance, and Diabetes—Mendelian Randomization Using CRP Haplotypes Points Upstream (2008) (148)
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels (2016) (147)
Meta-Analysis of Genome-Wide Scans for Total Body BMD in Children and Adults Reveals Allelic Heterogeneity and Age-Specific Effects at the WNT16 Locus (2012) (147)
The thermolabile variant of MTHFR is associated with depression in the British Women's Heart and Health Study and a meta-analysis (2006) (145)
Directional dominance on stature and cognition in diverse human populations (2015) (144)
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. (2013) (143)
Type 2 Diabetes Risk Alleles Are Associated With Reduced Size at Birth (2009) (141)
Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill (2013) (141)
Strengthening the reporting of observational studies in epidemiology using mendelian randomisation (STROBE-MR): explanation and elaboration (2021) (139)
Mendelian randomization: where are we now and where are we going? (2015) (137)
Genome-Wide Population-Based Association Study of Extremely Overweight Young Adults – The GOYA Study (2011) (137)
Common variants in the region around Osterix are associated with bone mineral density and growth in childhood (2009) (135)
Adiposity-Related Heterogeneity in Patterns of Type 2 Diabetes Susceptibility Observed in Genome-Wide Association Data (2009) (135)
Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. (2011) (133)
BMI as a Modifiable Risk Factor for Type 2 Diabetes: Refining and Understanding Causal Estimates Using Mendelian Randomization (2016) (133)
Worldwide population differentiation at disease-associated SNPs (2008) (132)
Functional Gene Group Analysis Reveals a Role of Synaptic Heterotrimeric G Proteins in Cognitive Ability (2010) (132)
Phenotypic Dissection of Bone Mineral Density Reveals Skeletal Site Specificity and Facilitates the Identification of Novel Loci in the Genetic Regulation of Bone Mass Attainment (2014) (131)
Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport (2016) (131)
The power of genetic diversity in genome-wide association studies of lipids (2021) (129)
A common haplotype of the glucokinase gene alters fasting glucose and birth weight: association in six studies and population-genetics analyses. (2006) (128)
Copy number variations and cognitive phenotypes in unselected populations. (2015) (122)
Common variants at 12q15 and 12q24 are associated with infant head circumference (2012) (121)
A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts. (2016) (118)
Remnant Cholesterol, Low-Density Lipoprotein Cholesterol, and Blood Pressure as Mediators From Obesity to Ischemic Heart Disease (2015) (116)
Melanesian Blond Hair Is Caused by an Amino Acid Change in TYRP1 (2012) (116)
A genome-wide association study of body mass index across early life and childhood (2015) (115)
Severe Obesity in Young Women and Reproductive Health: The Danish National Birth Cohort (2009) (115)
GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals (2019) (114)
The Emergence of Networks in Human Genome Epidemiology: Challenges and Opportunities (2007) (112)
A novel common variant in DCST2 is associated with length in early life and height in adulthood (2014) (112)
The Association of C-Reactive Protein and CRP Genotype with Coronary Heart Disease: Findings from Five Studies with 4,610 Cases amongst 18,637 Participants (2008) (110)
Dietary Energy Density Affects Fat Mass in Early Adolescence and Is Not Modified by FTO Variants (2009) (110)
Common variants at 6q22 and 17q21 are associated with intracranial volume (2012) (110)
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits (2017) (110)
AHRR (cg05575921) hypomethylation marks smoking behaviour, morbidity and mortality (2017) (107)
Genome-wide association study identifies loci affecting blood copper, selenium and zinc. (2013) (106)
Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis (2015) (106)
Genome Wide Association Identifies Common Variants at the SERPINA6/SERPINA1 Locus Influencing Plasma Cortisol and Corticosteroid Binding Globulin (2014) (106)
Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data (2019) (104)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2011) (104)
Genetic association study of BDNF in depression: Finding from two cohort studies and a meta‐analysis (2008) (104)
Association of Genetic Loci With Glucose Levels in Childhood and Adolescence (2011) (103)
Genome-wide associations of human gut microbiome variation and implications for causal inference analyses (2020) (103)
Obesity and cancer: Mendelian randomization approach utilizing the FTO genotype. (2009) (103)
How Does Body Fat Influence Bone Mass in Childhood? A Mendelian Randomization Approach (2009) (100)
Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error (2016) (98)
Genetic variation at the SLC23A1 locus is associated with circulating concentrations of L-ascorbic acid (vitamin C): evidence from 5 independent studies with >15,000 participants. (2010) (98)
A variant in LIN28B is associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure. (2010) (97)
TAS2R38 (phenylthiocarbamide) haplotypes, coronary heart disease traits, and eating behavior in the British Women's Heart and Health Study. (2005) (96)
STROBE-MR: Guidelines for strengthening the reporting of Mendelian randomization studies (2019) (96)
Strengthening causal inference in cardiovascular epidemiology through Mendelian randomization (2008) (94)
Height-reducing variants and selection for short stature in Sardinia (2015) (94)
Association of the DRD2 gene Taq1A polymorphism and smoking behavior: a meta-analysis and new data. (2009) (91)
Genome-wide Association Study for Vitamin D Levels Reveals 69 Independent Loci. (2020) (89)
Whole-genome sequence-based analysis of thyroid function (2015) (89)
The association of the PON1 Q192R polymorphism with coronary heart disease: findings from the British Women's Heart and Health cohort study and a meta-analysis (2004) (87)
Shared Genetic Influences Between Attention-Deficit/Hyperactivity Disorder (ADHD) Traits in Children and Clinical ADHD (2015) (86)
Meta‐analysis of genome‐wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women (2013) (84)
Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy (2010) (84)
Two British women studies replicated the association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) and BMI (2009) (84)
Long COVID burden and risk factors in 10 UK longitudinal studies and electronic health records (2022) (83)
A Population-Based Study of Genetic Variation and Psychotic Experiences in Adolescents (2013) (82)
Dietary Intake, FTO Genetic Variants, and Adiposity: A Combined Analysis of Over 16,000 Children and Adolescents (2015) (81)
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals (2022) (80)
Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium (2016) (80)
Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium (2016) (80)
Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances (2013) (79)
MR-PheWAS: hypothesis prioritization among potential causal effects of body mass index on many outcomes, using Mendelian randomization (2015) (77)
Mining the Human Phenome Using Allelic Scores That Index Biological Intermediates (2013) (77)
Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits. (2019) (77)
Mental health during the COVID-19 pandemic in two longitudinal UK population cohorts (2020) (77)
Avoiding milk is associated with a reduced risk of insulin resistance and the metabolic syndrome: findings from the British Women's Heart and Health Study (2005) (76)
Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty. (2014) (75)
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps (2016) (75)
Common variation near ROBO2 is associated with expressive vocabulary in infancy (2014) (74)
Genome-wide association study of height-adjusted BMI in childhood identifies functional variant in ADCY3 (2014) (73)
Meta-analysis of human genome-microbiome association studies: the MiBioGen consortium initiative (2018) (73)
Meta-analysis of human genome-microbiome association studies: the MiBioGen consortium initiative (2018) (73)
Assessing the utility of intermediate phenotypes for genetic mapping of psychiatric disease (2014) (73)
Genome-Wide Association Meta-Analysis of Cortical Bone Mineral Density Unravels Allelic Heterogeneity at the RANKL Locus and Potential Pleiotropic Effects on Bone (2010) (71)
Associations of Body Mass and Fat Indexes With Cardiometabolic Traits (2018) (71)
Examination of the relationship between variation at 17q21 and childhood wheeze phenotypes. (2013) (69)
Association Between C-Reactive Protein Genotype, Circulating Levels, and Aortic Pulse Wave Velocity (2009) (69)
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans (2014) (69)
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans (2014) (69)
Lactase persistence-related genetic variant: population substructure and health outcomes (2009) (68)
Genetic and Environmental Risk Factors Associated With Trajectories of Depression Symptoms From Adolescence to Young Adulthood (2019) (68)
Associations of autozygosity with a broad range of human phenotypes (2019) (68)
GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI (2019) (67)
Using Genetic Variation to Explore the Causal Effect of Maternal Pregnancy Adiposity on Future Offspring Adiposity: A Mendelian Randomisation Study (2017) (67)
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis. (2017) (66)
Lifetime body mass index and later atherosclerosis risk in young adults: examining causal links using Mendelian randomization in the Cardiovascular Risk in Young Finns study (2008) (66)
Genome-wide association study identifies 48 common genetic variants associated with handedness (2019) (65)
Using genetic loci to understand the relationship between adiposity and psychological distress: a Mendelian Randomization study in the Copenhagen General Population Study of 53 221 adults (2011) (65)
A saturated map of common genetic variants associated with human height (2022) (65)
Potentiation of the anti-tumour effect of melphalan by the vasoactive agent, hydralazine. (1988) (65)
European lactase persistence genotype shows evidence of association with increase in body mass index (2009) (65)
Association between polygenic risk scores for attention-deficit hyperactivity disorder and educational and cognitive outcomes in the general population (2016) (64)
Prenatal alcohol exposure and offspring mental health: A systematic review (2019) (64)
Influence of puberty timing on adiposity and cardiometabolic traits: A Mendelian randomisation study (2018) (64)
Identifying Critical Points of Trajectories of Depressive Symptoms from Childhood to Young Adulthood (2018) (64)
The Causal Effect of Vitamin D Binding Protein (DBP) Levels on Calcemic and Cardiometabolic Diseases: A Mendelian Randomization Study (2014) (63)
Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence (2014) (63)
Is population structure in the genetic biobank era irrelevant, a challenge, or an opportunity? (2019) (62)
Mendelian Randomization Analysis Identifies CpG Sites as Putative Mediators for Genetic Influences on Cardiovascular Disease Risk (2017) (61)
Common variants at 6q22 and 17q21 are associated with intracranial volume (2012) (61)
Association of a Body Mass Index Genetic Risk Score with Growth throughout Childhood and Adolescence (2013) (60)
BMI and Mortality in UK Biobank: Revised Estimates Using Mendelian Randomization (2018) (59)
Genetic Relationship between Schizophrenia and Nicotine Dependence (2016) (58)
Genetic Relationship between Schizophrenia and Nicotine Dependence (2016) (58)
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2020) (58)
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (2013) (55)
A Powerful Approach to Sub-Phenotype Analysis in Population-Based Genetic Association Studies (2009) (55)
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits (2020) (55)
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (53)
Genome-wide prediction of childhood asthma and related phenotypes in a longitudinal birth cohort. (2012) (53)
Assessing the Causal Role of Body Mass Index on Cardiovascular Health in Young Adults (2017) (53)
Assumption-free estimation of the genetic contribution to refractive error across childhood (2015) (53)
Adiponectin and its association with bone mass accrual in childhood (2010) (52)
A common variant in the FTO gene region is associated with BMI in the general population and predisposes to adult and childhood obesity (2007) (52)
The CHRNA5–A3–B4 Gene Cluster and Smoking: From Discovery to Therapeutics (2016) (52)
Associations of FTO and MC4R Variants with Obesity Traits in Indians and the Role of Rural/Urban Environment as a Possible Effect Modifier (2011) (52)
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis. (2018) (52)
The influence of obesity-related factors in the etiology of renal cell carcinoma—A mendelian randomization study (2019) (51)
A Trans-ancestral Meta-Analysis of Genome-Wide Association Studies Reveals Loci Associated with Childhood Obesity. (2019) (51)
Risk factors for long COVID: analyses of 10 longitudinal studies and electronic health records in the UK (2021) (51)
Does High C-reactive Protein Concentration Increase Atherosclerosis? The Whitehall II Study (2008) (51)
C-Reactive Protein and Cardiovascular Disease Risk: Still an Unknown Quantity? (2006) (50)
Worldwide patterns of haplotype diversity at 9p21.3, a locus associated with type 2 diabetes and coronary heart disease (2009) (50)
Genome-Wide Association Study to Identify Common Variants Associated with Brachial Circumference: A Meta-Analysis of 14 Cohorts (2012) (50)
Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference (2018) (49)
Adiposity, metabolites, and colorectal cancer risk: Mendelian randomization study (2020) (49)
Adult height variants affect birth length and growth rate in children (2011) (49)
Mosaic structural variation in children with developmental disorders (2015) (48)
Refining associations between TAS2R38 diplotypes and the 6-n-propylthiouracil (PROP) taste test: findings from the Avon Longitudinal Study of Parents and Children (2007) (48)
Systematic Mendelian randomization framework elucidates hundreds of CpG sites which may mediate the influence of genetic variants on disease (2018) (47)
Shared genetic variants suggest common pathways in allergy and autoimmune diseases (2017) (47)
Evaluation of the causal effects between subjective wellbeing and cardiometabolic health: mendelian randomisation study (2018) (47)
Comment on Papers by Evans et al. and Mekel-Bobrov et al. on Evidence for Positive Selection of MCPH1 and ASPM (2007) (46)
Association analysis of 31 common polymorphisms with type 2 diabetes and its related traits in Indian sib pairs (2011) (46)
The Avon Longitudinal Study of Parents and Children - A resource for COVID-19 research: Questionnaire data capture April-May 2020. (2020) (46)
Genetic Variation Associated with Differential Educational Attainment in Adults Has Anticipated Associations with School Performance in Children (2014) (45)
Collaborative pooled analysis of data on C-reactive protein gene variants and coronary disease: judging causality by Mendelian randomisation (2008) (45)
Managing clinically significant findings in research: the UK10K example (2014) (45)
Cigarette smoke but not electronic cigarette aerosol activates a stress response in human coronary artery endothelial cells in culture (2016) (44)
A genome-wide association study for corneal curvature identifies the platelet-derived growth factor receptor alpha gene as a quantitative trait locus for eye size in white Europeans (2013) (44)
Morning plasma cortisol as a cardiovascular risk factor: findings from prospective cohort and Mendelian randomization studies (2019) (44)
Using genetics to test the causal relationship of total adiposity and periodontitis: Mendelian randomization analyses in the Gene-Lifestyle Interactions and Dental Endpoints (GLIDE) Consortium. (2015) (44)
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (43)
A meta-analysis of the associations between common variation in the PDE8B gene and thyroid hormone parameters, including assessment of longitudinal stability of associations over time and effect of thyroid hormone replacement (2011) (43)
Genome‐Wide Association Scan Allowing for Epistasis in Type 2 Diabetes (2011) (42)
Tooth loss is a complex measure of oral disease: Determinants and methodological considerations (2018) (41)
Common variation contributes to the genetic architecture of social communication traits (2013) (41)
Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2 (2016) (41)
Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci (2019) (41)
The Dementias Platform UK (DPUK) Data Portal (2019) (40)
Paradoxical Relationship Between Body Mass Index and Thyroid Hormone Levels: A Study Using Mendelian Randomization. (2016) (39)
Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (39)
Genome-Wide Association Study Identifies Four Loci Associated with Eruption of Permanent Teeth (2011) (38)
Loss of function mutations in the melanocortin 4 receptor in a UK birth cohort (2021) (37)
KCTD8 gene and brain growth in adverse intrauterine environment: a genome-wide association study. (2012) (37)
The association of the PON1 Q192R polymorphism with complications and outcomes of pregnancy: findings from the British Women's Heart and Health cohort study. (2006) (37)
International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents (2016) (36)
GARFIELD - GWAS Analysis of Regulatory or Functional Information Enrichment with LD correction (2016) (36)
Age- and puberty-dependent association between IQ score in early childhood and depressive symptoms in adolescence (2010) (36)
Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants. (2014) (34)
Lack of association between DRD2 and OPRM1 genotypes and adiposity (2013) (34)
Common Variation in the WNK1 Gene and Blood Pressure in Childhood: The Avon Longitudinal Study of Parents and Children (2008) (33)
Association between fat mass through adolescence and arterial stiffness: a population-based study from The Avon Longitudinal Study of Parents and Children (2019) (33)
A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways. (2016) (32)
Validation of Dual Energy X-Ray Absorptiometry Measures of Abdominal Fat by Comparison with Magnetic Resonance Imaging in an Indian Population (2012) (32)
The association of oestrogen receptor alpha-haplotypes with cardiovascular risk factors in the British Women's Heart and Health Study. (2006) (31)
Alcohol dehydrogenase type 1C (ADH1C) variants, alcohol consumption traits, HDL-cholesterol and risk of coronary heart disease in women and men: British Women's Heart and Health Study and Caerphilly cohorts. (2008) (31)
Coordinated genetic scaling of the human eye: shared determination of axial eye length and corneal curvature. (2013) (31)
Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis (2019) (31)
Common genetic variants and health outcomes appear geographically structured in the UK Biobank sample: Old concerns returning and their implications (2018) (31)
Associations of device-measured physical activity across adolescence with metabolic traits: Prospective cohort study (2018) (31)
Determinants of Intima-Media Thickness in the Young (2019) (30)
Ten years on: Is dental general anaesthesia in childhood a risk factor for caries and anxiety? (2017) (30)
Consortium-based genome-wide meta-analysis for childhood dental caries traits (2018) (30)
Vitamin B-12 Status during Pregnancy and Child’s IQ at Age 8: A Mendelian Randomization Study in the Avon Longitudinal Study of Parents and Children (2012) (30)
Mendelian Randomization: Application to Cardiovascular Disease (2012) (30)
The CRP genotype, serum levels and lung function in men: the Caerphilly Prospective Study. (2011) (30)
Vitamin D levels and risk of type 1 diabetes: A Mendelian randomization study (2021) (30)
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour (2021) (29)
Association of Common Genetic Variants with Lipid Traits in the Indian Population (2014) (29)
Heritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE Consortium. (2016) (29)
Re-Examining the Association between Vitamin D and Childhood Caries (2015) (28)
Longitudinal evidence for persistent anxiety in young adults through COVID-19 restrictions (2020) (28)
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium (2014) (28)
MC3R links nutritional state to childhood growth and the timing of puberty (2021) (28)
Genetic Influences on Trajectories of Systolic Blood Pressure Across Childhood and Adolescence (2013) (26)
Metabolic Characterization of a Rare Genetic Variation Within APOC3 and Its Lipoprotein Lipase–Independent Effects (2016) (26)
Carcinogenicity of radon/radon decay product inhalation in rats – effect of dose, dose rate and unattached fraction (2005) (25)
Genome-wide association study of blood lead shows multiple associations near ALAD. (2015) (25)
The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects (2010) (25)
Emotional symptoms in children: The effect of maternal depression, life events, and COMT genotype (2009) (24)
Does Bone Resorption Stimulate Periosteal Expansion? A Cross‐Sectional Analysis of β‐C‐telopeptides of Type I Collagen (CTX), Genetic Markers of the RANKL Pathway, and Periosteal Circumference as Measured by pQCT (2014) (24)
A recall-by-genotype study of CHRNA5-A3-B4 genotype, cotinine and smoking topography: study protocol (2014) (24)
Using Genetic Proxies for Lifecourse Sun Exposure to Assess the Causal Relationship of Sun Exposure with Circulating Vitamin D and Prostate Cancer Risk (2013) (23)
The Avon Longitudinal Study of Parents and Children - A resource for COVID-19 research: Questionnaire data capture May-July 2020 (2020) (23)
Data Resource Profile: The ALSPAC birth cohort as a platform to study the relationship of environment and health and social factors (2019) (22)
Variation in the SERPINA6/SERPINA1 locus alters morning plasma cortisol, hepatic corticosteroid binding globulin expression, gene expression in peripheral tissues, and risk of cardiovascular disease (2021) (22)
Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (2016) (22)
Common variants at 12q15 and 12q24 are associated with infant head circumference (2013) (22)
Narrow-sense heritability estimation of complex traits using identity-by-descent information (2017) (22)
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2018) (22)
Can Lactase Persistence Genotype Be Used to Reassess the Relationship between Renal Cell Carcinoma and Milk Drinking? Potentials and Problems in the Application of Mendelian Randomization (2010) (21)
Exploring possible epigenetic mediation of early-life environmental exposures on adiposity and obesity development. (2015) (21)
Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116)) (2010) (20)
Association Study of 25 Type 2 Diabetes Related Loci with Measures of Obesity in Indian Sib Pairs (2013) (20)
The association of the paraoxonase (PON1) Q192R polymorphism with depression in older women: findings from the British Women’s Heart and Health Study (2006) (20)
Does a short breastfeeding period protect from FTO-induced adiposity in children? (2011) (19)
Heritability of Caries Scores, Trajectories, and Disease Subtypes (2020) (19)
Polygenic risk for depression, anxiety and neuroticism are associated with the severity and rate of change in depressive symptoms across adolescence. (2021) (19)
Common Variation in the WNK 1 Gene and Blood Pressure in Childhood The Avon Longitudinal Study of Parents and Children (2008) (18)
Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence (2014) (18)
Bias from questionnaire invitation and response in COVID-19 research: an example using ALSPAC (2021) (18)
The Avon Longitudinal Study of Parents and Children - A resource for COVID-19 research: Generation 2 questionnaire data capture May-July 2020. (2020) (18)
Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan (2020) (18)
Body mass index: Has epidemiology started to break down causal contributions to health and disease? (2016) (18)
Early Metabolic Features of Genetic Liability to Type 2 Diabetes: Cohort Study With Repeated Metabolomics Across Early Life (2019) (18)
Assessment of reproducibility and biological variability of fasting and postprandial plasma metabolite concentrations using 1H NMR spectroscopy (2019) (18)
Maturation in Serum Thyroid Function Parameters Over Childhood and Puberty: Results of a Longitudinal Study (2017) (18)
Assessment and visualization of phenome-wide causal relationships using genetic data: an application to dental caries and periodontitis (2019) (17)
The role of common genetic variation in educational attainment and income: evidence from the National Child Development Study (2015) (17)
Association of Prenatal Alcohol Exposure and Offspring Depression: A Negative Control Analysis of Maternal and Partner Consumption (2020) (16)
Genome-wide association study of circulating interleukin 6 levels identifies novel loci (2021) (16)
Investigating the impact of cigarette smoking behaviours on DNA methylation patterns in adolescence (2018) (16)
Cholesterol auxotrophy as a targetable vulnerability in clear cell renal cell carcinoma. (2021) (16)
The Avon Longitudinal Study of Parents and Children - A resource for COVID-19 research: Questionnaire data capture April-May 2020 (2020) (15)
Screening for familial hypercholesterolaemia in childhood: Avon Longitudinal Study of Parents and Children (ALSPAC) (2017) (15)
Variation in the SLC23A1 gene does not influence cardiometabolic outcomes to the extent expected given its association with l-ascorbic acid1234 (2014) (15)
An interactive genome browser of association results from the UK10K cohorts project (2015) (14)
Investigating the role of insulin in increased adiposity: Bi-directional Mendelian randomization study (2017) (14)
FUT2 secretor genotype and susceptibility to infections and chronic conditions in the ALSPAC cohort (2018) (14)
AHRR ( cg 05575921 ) hypomethylation marks smoking behaviour , morbidity and mortality (2017) (14)
The Avon Longitudinal Study of Parents and Children - A resource for COVID-19 research: Home-based antibody testing results, October 2020. An emphasis on self-screening at a population level (2021) (14)
Assessing the causal association between 25‐hydroxyvitamin D and the risk of oral and oropharyngeal cancer using Mendelian randomization (2018) (14)
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention (2022) (14)
Association of Maternal Smoking With Child Cotinine Levels (2013) (14)
Copy Number Variations and Cognitive Phenotypes in Unselected Populations (2015) (14)
Letter to the EditorCommon Genetic Variants Influence Whorls in Fingerprint Patterns (2016) (14)
A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Paediatric Cohorts (2016) (13)
Genome-Wide Association Study of Height-Adjusted BMI in Childhood Identifies Functional Variant in ADCY 3 (2014) (13)
FUT2 secretor genotype and susceptibility to infections and chronic conditions in the ALSPAC cohort. (2018) (12)
Genetics of human gut microbiome composition (2020) (12)
1B-5 Exploring the developmental overnutrition hypothesis using parental offspring associations and the FTO gene as an instrumental variable for maternal adiposity. The Avon Longitudinal Study of Parents And Children (ALSPAC) (2007) (12)
The Role of Inflammatory Cytokines as Intermediates in the Pathway from Increased Adiposity to Disease (2021) (12)
A pathway-centric approach to rare variant association analysis (2016) (12)
The ethics conundrum in Recall by Genotype (RbG) research: Perspectives from birth cohort participants (2017) (12)
The Avon Longitudinal Study of Parents and Children - A resource for COVID-19 research: Questionnaire data capture May-July 2020. (2020) (12)
Prospective associations between problematic eating attitudes in midchildhood and the future onset of adolescent obesity and high blood pressure123 (2016) (11)
Incorporating Non-Coding Annotations into Rare Variant Analysis (2016) (11)
Effects of adiposity on the human plasma proteome: observational and Mendelian randomisation estimates (2020) (11)
Genetic variant influence on whorls in fingerprint patterns (2015) (11)
Coronary artery disease, genetic risk and the metabolome in young individuals. (2018) (10)
Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism (2021) (10)
Glycoprotein Acetyls: A Novel Inflammatory Biomarker of Early Cardiovascular Risk in the Young (2022) (10)
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche DTU Orbit (05/11/2017) (2014) (10)
Testing the principles of Mendelian randomization: Opportunities and complications on a genomewide scale (2017) (9)
An assessment of the portability of ancestry informative markers between human populations (2009) (9)
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus (2020) (9)
Common maternal and fetal genetic variants show expected polygenic effects on risk of small- or large-for-gestational-age (SGA or LGA), except in the smallest 3% of babies (2020) (9)
Effect of low thyroid hormone bioavailability on childhood cognitive development: data from the Avon Longitudinal Study of Parents and Children birth cohort (2014) (9)
Collapsed methylation quantitative trait loci analysis for low frequency and rare variants (2016) (9)
Genetics, sleep and memory: a recall-by-genotype study of ZNF804A variants and sleep neurophysiology (2015) (9)
Genome-wide association study identifies SNPs in the MHC class II loci that are associated with self-reported history of whooping cough (2015) (9)
Current opportunities to catalyze research in nutrition and cancer prevention – an interdisciplinary perspective (2019) (9)
Is the adiposity‐associated FTO gene variant related to all‐cause mortality independent of adiposity? Meta‐analysis of data from 169,551 Caucasian adults (2015) (9)
Intelligence in offspring born to women exposed to intimate partner violence: a population-based cohort study (2019) (9)
Blood pressure and mortality: using offspring blood pressure as an instrument for own blood pressure in the HUNT study (2015) (9)
Coronary artery disease, genetic risk and the metabolome in young individuals (2019) (8)
The blood metabolome of incident kidney cancer: A case–control study nested within the MetKid consortium (2021) (8)
The association of the PON 1 Q 192 R polymorphism with coronary heart disease : findings from the British Women ' s Heart and Health cohort study and a meta-analysis (2015) (8)
The Avon Longitudinal Study of Parents and Children - A resource for COVID-19 research: Questionnaire data capture November 2020 - March 2021. (2021) (8)
Evaluation of seven common lipid associated loci in a large Indian sib pair study (2012) (8)
Letter regarding article, "Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis". (2019) (8)
Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits (2022) (7)
A Polygenic Risk Score to Predict Future Adult Short Stature Among Children (2021) (7)
Causal epigenome-wide association study identifies CpG sites that influence cardiovascular disease risk (2017) (7)
Genotype-Based Recall Studies in Complex Cardiometabolic Traits (2018) (7)
Polymorphisms in the CRP gene and cardiovascular events. (2007) (7)
Fraction of exhaled nitric oxide values in childhood are associated with 17 q 11 . 2q 12 and 17 q 12-q 21 variants (7)
Systematic Mendelian randomization framework elucidates hundreds of genetic loci which may influence disease through changes in DNA methylation levels (2017) (6)
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids (2021) (6)
Characterization of alcohol polygenic risk scores in the context of mental health outcomes: Within-individual and intergenerational analyses in the Avon Longitudinal Study of Parents and Children (2021) (6)
KCTD 8 Gene and Brain Growth in Adverse Intrauterine Environment : A Genome-wide Association Study (2012) (6)
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (6)
Recent Findings on the Genetics of Obesity: Is there Public Health Relevance? (2012) (6)
Letter by Timpson et al regarding article, "Contribution of clinical correlates and 13 C-reactive protein gene polymorphisms to interindividual variability in serum C-reactive protein level". (2006) (6)
Dominant role of abdominal adiposity in circulating lipoprotein, lipid, and metabolite levels in UK Biobank: Mendelian randomization study (2021) (6)
Psychological distress, depression, anxiety, and life satisfaction following COVID-19 infection: evidence from 11 UK longitudinal population studies (2022) (6)
Pleiotropic associations of heterozygosity for the SERPINA1 Z allele in the UK Biobank (2021) (6)
Genome-Wide Association Study Identifies Genetic Associations with Perceived Age (2020) (6)
The UK Biobank: A Shining Example of Genome-Wide Association Study Science with the Power to Detect the Murky Complications of Real-World Epidemiology. (2022) (6)
Investigation of the Interplay between Circulating Lipids and IGF-I and Relevance to Breast Cancer Risk: An Observational and Mendelian Randomization Study (2021) (6)
A Protein Domain and Family Based Approach to Rare Variant Association Analysis (2016) (6)
The Avon Longitudinal Study of Parents and Children - A resource for COVID-19 research: Generation 2 questionnaire data capture May-July 2020 (2021) (6)
Trajectories of child emotional and behavioural difficulties before and during the COVID-19 pandemic in a longitudinal UK cohort (2020) (5)
Index and Predisposes to Childhood and Adult Obesity Gene Is Associated with Body Mass FTO A Common Variant in the (2012) (5)
GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome (2021) (5)
Expanded genomic analyses for male voice-breaking highlights a shared phenotypic and genetic basis between puberty timing and hair colour (2018) (5)
Body mass index and mortality in UK Biobank: revised estimates using Mendelian randomization (2018) (5)
Reassessing the Association between Circulating Vitamin D and IGFBP-3: Observational and Mendelian Randomization Estimates from Independent Sources (2018) (5)
The Avon Longitudinal Study of Parents and Children - a resource for COVID-19 research: approaches to the identification of cases November 2020 (2021) (5)
The Avon Longitudinal Study of Parents and Children - A resource for COVID-19 research: Antibody testing results, April – June 2021 (2021) (4)
Enhanced Protection Against Diarrhea Among Breastfed Infants of Nonsecretor Mothers. (2020) (4)
Effects of general and central adiposity on circulating lipoprotein, lipid, and metabolite levels in UK Biobank: A multivariable Mendelian randomization study (2022) (4)
Erratum: Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (Proc Natl Acad Sci USA (2014) 111 (13790-13794) DOI: 10.1073/pnas.1404623111) (2015) (4)
Commentary: One size fits all: are there standard rules for the use of genetic instruments in Mendelian randomization? (2016) (4)
Using Y-Chromosomal Haplogroups in Genetic Association Studies and Suggested Implications (2018) (4)
Correction: Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy (2010) (4)
Genome-wide association study identifies 48 common genetic variants associated with handedness (2020) (4)
Direct evidence to support the fetal insulin hypothesis as the type 2 diabetes risk alleles at the CDKALI and HHEX-IDE gene loci reduce birth weight (2008) (4)
Variation in ERAP2 has opposing effects on severe respiratory infection and autoimmune disease (2022) (4)
Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: Findings from a Mendelian randomisation study (2022) (4)
Correction to: Is population structure in the genetic biobank era irrelevant, a challenge, or an opportunity? (2019) (4)
Genetic architecture of early childhood growth phenotypes gives insights into their link with later obesity (2017) (4)
Estimating the causal effect of BMI on mortality risk in people with heart disease, diabetes and cancer using Mendelian randomization. (2021) (4)
Heritable contributions versus genetic architecture (2018) (3)
19 Testing causality in the association of plasma cortisol with risk of coronary heart disease: a mendelian randomisation study (2015) (3)
Type 2 Diabetes and Triglyceride Levels Genome-Wide Association Analysis Identifies Loci (3)
The range of peripapillary retinal nerve fibre layer and optic disc parameters, in children aged up to but not including 18 years of age who were born prematurely: protocol for a systematic review (2016) (3)
Higher body mass index raises immature platelet count: potential contribution to obesity-related thrombosis (2022) (3)
Comments on ‘Mendelian randomization: Using genes as instruments for making causal inference in epidemiology’: Authors' response (2008) (3)
LongITools: Dynamic longitudinal exposome trajectories in cardiovascular and metabolic noncommunicable diseases (2021) (3)
Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity (2022) (3)
Erratum to: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps : (Nature Genetics, (2016), 48, 11, (1303-1312), 10.1038/ng.3668) (2018) (3)
Correction: Vitamin D levels and risk of type 1 diabetes: A Mendelian randomization study (2021) (3)
Gene discovery for oral ulceration: a UK Biobank Study (2017) (3)
Examining the causal association between 25-hydroxyvitamin D and caries in children and adults: a two-sample Mendelian randomization approach (2021) (3)
The Avon Longitudinal Study of Parents and Children - A resource for COVID-19 research: Questionnaire data capture November 2020 – March 2021 (2021) (3)
The Avon Longitudinal Study of Parents and children ALSPAC G0 Partners: A cohort profile (2023) (3)
Erratum: Obesity BMI and Mortality in UK Biobank: Revised Estimates Using Mendelian Randomization (2019) (3)
Common variation at 16p11.2 is associated with glycosuria in pregnancy: findings from a genome-wide association study in European women (2020) (3)
Causal analyses, statistical efficiency and phenotypic precision through Recall-by-Genotype study design (2017) (3)
Longitudinal serological measures of common infection in the Avon Longitudinal Study of Parents and Children cohort (2018) (2)
Ethnicity, heart failure, atrial fibrillation and diabetes: collider bias (2019) (2)
Elevated glycoprotein acetyl levels in adolescence and early adulthood predict adverse cardiometabolic profiles and risk of metabolic syndrome in up to 10 year follow-up (2020) (2)
Epigenetic Regulation of F2RL3 Associates With Myocardial Infarction and Platelet Function (2022) (2)
A framework for research into continental ancestry groups of the UK Biobank (2021) (2)
Evaluating the association of TRPA1 gene polymorphisms with pain sensitivity: a protocol for an adaptive recall by genotype study (2022) (2)
The ‘ALSPAC in London’ dataset: adiposity, cardiometabolic risk profiles, and the emerging arterial phenotype in young adulthood (2018) (2)
Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity, pleiotropy and age-specific effects at the WNT16 locus (2012) (2)
Phenotypic dissection of bone mineral density facilitates the identification of skeletal site specificity on the genetic regulation of bone (2013) (2)
Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility (2016) (2)
Physical Inactivity and Sleep Inefficiency Accentuate the Genetic Risk of Obesity (2018) (2)
HMOX1 genetic polymorphisms and outcomes in infectious disease: A systematic review (2021) (2)
Bias from questionnaire invitation and response in COVID-19 research: an example using ALSPAC. (2021) (2)
GWAS of stool frequency reveals genes, pathways, and cell types relevant to human gastrointestinal motility and irritable bowel syndrome (2020) (2)
Chlamydia trachomatis in the age of the genome: application of molecular genotyping to improve our understanding of the immunopathogenesis of Chlamydia genital tract disease. (2011) (2)
The effect of genetic variation in PDE8B and DIO1 on thyroid hormone levels (2010) (2)
Body muscle gain and markers of cardiovascular disease susceptibility in young adulthood: A cohort study (2021) (2)
Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume (2013) (2)
Large-scale genome-wide association study of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits (2021) (2)
Evaluation of isotype specific salivary antibody assays for detecting previous SARS-CoV-2 infection in children and adults (2022) (2)
Antibody levels following vaccination against SARS-CoV-2: associations with post-vaccination infection and risk factors in two UK longitudinal studies (2022) (2)
University of Groningen Physical Activity Attenuates the Influence of FTO Variants on Obesity Risk (2011) (2)
Impact of voluntary risk-mitigation behaviour on transmission of the Omicron SARS-CoV-2 variant in England (2022) (2)
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk (2023) (2)
Collection of DNA samples and genetic data at scale in the UK Millennium Cohort Study (2020) (2)
ASSOCIATION BETWEEN FTO POLYMORPHISM, ADIPOSITY PEAK AND ADIPOSITY REBOUND IN THE NORTHERN FINLAND BIRTH COHORT 1966 (2009) (2)
Epigenetic regulation of PAR4-related platelet activation: mechanistic links between environmental exposure and cardiovascular disease (2018) (2)
Pleiotropic effects of heterozygosity for the SERPINA1 Z allele in the UK Biobank (2020) (2)
Limits of lockdown: characterising essential contacts during strict physical distancing (2021) (2)
The range of peripapillary retinal nerve fibre layer and optic disc parameters in children aged up to but not including 18 years of age, as measured by optical coherence tomography: protocol for a systematic review (2016) (2)
Prospective associations between problematic eating attitudes in midchildhood and the future onset of adolescent obesity and high blood pressure (2017) (2)
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (2)
Metabolic characterisation of disturbances in the APOC3/triglyceride-rich lipoprotein pathway through sample-based recall by genotype (2020) (2)
Impact of voluntary risk-mitigation behaviour on the magnitude of a COVID-19 Omicron variant wave in England (2)
Testing causality in the association of plasma cortisol with risk of coronary heart disease: a Mendelian randomisation study (2015) (2)
Characterising patterns of COVID-19 and long COVID symptoms: evidence from nine UK longitudinal studies (2022) (2)
Schizophrenia-associated variation at ZNF804A correlates with altered experience-dependent dynamics of sleep slow waves and spindles in healthy young adults (2020) (2)
Physical activity and sedentary behavior; mechanistic insights and role in disease prevention (2021) (1)
Genetics of early-life head circumference and genetic correlations with neurological, psychiatric and cognitive outcomes (2022) (1)
Development and evaluation of low-volume tests to detect and characterise antibodies to SARS-CoV-2 (2022) (1)
The effect of genetically proxied IL-6 signalling on severe malaria: A Mendelian randomisation analysis (2022) (1)
Body muscle gain and markers of cardiovascular disease susceptibility in young adulthood: prospective cohort study (2020) (1)
Phenotypic associations with the HMOX1 GT(n) promoter repeat in European populations (2022) (1)
Testing the causal effects between subjective wellbeing and physical health using Mendelian randomisation (2018) (1)
Separating the effects of early and later life adiposity on colorectal cancer risk: a Mendelian randomization study (2022) (1)
Prevalence and expressivity of loss of function mutations in the Melanocortin 4 Receptor (MC4R) in a UK birth cohort (2020) (1)
P11 The association of alcohol PRS on mental health phenotypes: a PheWAS in the avon longitudinal study of parents and children (ALSPAC) (2019) (1)
Association of Early Childhood Caries with Bitter Taste Receptors: A Meta-Analysis of Genome-Wide Association Studies and Transcriptome-Wide Association Study (2022) (1)
Shared Genetic Effects Between Clinical ADHD and Smoking, Alcohol and Breastfeeding in Mothers from the General Population (2015) (1)
Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps (2018) (1)
Loci for insulin processing and secretion provide insight into type 2 diabetes risk. (2023) (1)
Piloting the objective measurement of eating weight and speed at a population scale: a nested study within the Avon Longitudinal Study of Parents and Children (2021) (1)
Genome-wide association (GWA) analysis in 4000 members of a Finnish birth cohort identifies common variants associated with fasting insulin levels and related metabolic traits (2008) (1)
Piloting the objective measurement of eating behaviour at a population scale: a nested study within the Avon Longitudinal Study of Parents and Children. (2020) (1)
Erratum: Whole-genome sequence-based analysis of thyroid function (2015) (1)
Bivariate genetic association analysis of pediatric total-body DXA parameters identifies two novel genetic variants that jointly influence bone mineral content and bone area (2014) (1)
Participant acceptability of digital footprint data collection strategies: an exemplar approach to participant engagement and involvement in the ALSPAC birth cohort study. (2022) (1)
Stratified analysis of the Wellcome Trust Case Control Consortium scan for type 2 diabetes reveals susceptibility loci that may affect age of diagnosis (2008) (1)
Participant acceptability of digital footprint data collection strategies: an exemplar approach to participant engagement and involvement in the ALSPAC birth cohort study (2022) (1)
Using inactivating mutations to provide insight into drug action (2015) (1)
Exploring the variance in complex traits captured by DNA methylation assays (2020) (1)
Using Y chromosomal haplogroups in genetic association studies and suggested implications (2016) (1)
Evaluation of seven common lipid associated loci in a large Indian sib pair study (2012) (1)
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2021) (1)
Development and evaluation of low-volume tests to detect and characterize antibodies to SARS-CoV-2 (2022) (1)
Exploration of the role of CHRNA5-A3-B4 genotype in smoking behaviours (2019) (1)
First-generation scan of genome-wide association data allowing for epistasis prioritises multiple interacting candidate loci in T2D (2008) (1)
Intrauterine alcohol exposure and offspring mental health: A systematic review (2018) (1)
metaboprep: an R package for pre-analysis data description and processing (2021) (1)
Low Frequency Coding Variation in CYP2R1 has Large Effects on Vitamin D Level and Risk of Multiple Sclerosis (2017) (1)
Variation in the SLC 23 A 1 genedoesnot influencecardiometabolicoutcomes to the extent expected given its association with L-ascorbic acid 1 – 4 (2014) (1)
Abstract 17003: Increased Body Mass Index and Increased Risk of Ischemic Heart Disease: Using Genomewide Association Results to Estimate Causal Effects With Mendelian Randomization (2010) (1)
An observational and Mendelian randomisation study on iron status and sepsis (2023) (1)
Erratum: Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height ((The American Journal of Human Genetics (2010) 88 (6-18)) (2012) (1)
Polygenic Risk for Depression is Associated with the Severity and Rate of Change in Depressive Symptoms Across Adolescence (2020) (1)
Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes (2017) (1)
Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans (2015) (1)
Systematic review and meta-analyses: What has the application of Mendelian randomization told us about the causal effect of adiposity on health outcomes? (2022) (1)
Mapping complex disease genes using linkage disequilibrium and genome-wide association scans (2011) (1)
Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study (2023) (1)
Novel Genetic Determinants of Dental Maturation in Children (2022) (1)
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2019) (1)
The Genetic Sphygmomanometer: an argument for routine genome-wide genotyping in the population and a new view on its use to inform clinical practice (2018) (1)
A multivariant recall‐by‐genotype study of the metabolomic signature of BMI (2022) (1)
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals (2018) (1)
The association of alcohol polygenic risk scores with mental health outcomes: A multi-generational analysis in the Avon Longitudinal Study of Parents and Children (2020) (1)
metaboprep: an R package for preanalysis data description and processing (2022) (1)
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (1)
Bioinformatics and Functional Genomics. Pevsner J. Chichester: John Wiley & Sons Inc, 2003, pp. 753, £58.50 ISBN: 0-471-21004-8. (2004) (1)
Common variation in the FTO (fused toes) gene is strongly associated with adiposity measures in the northern finnish birth cohort of 1966 (2007) (1)
Epidemiology and Prevention. John Yarnell (ed). (2008) (0)
Higher body mass index raises immature platelet count: evidence from Mendelian randomization analyses (2021) (0)
204Effects of adiposity on the human proteome: Mendelian randomization study using individual-level data (2021) (0)
Results : A novel SNP , downstream from the FAM 120 AOS gene on chromosome 9 , was detected in the meta-analysis of ALSPAC and Raine (2015) (0)
Materials for the crowdsourced data analysis (2019) (0)
GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals (2019) (0)
Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan (2020) (0)
Publisher Correction: Identification of 371 genetic variants for age at first sex and birth linked to externalising behavior (2021) (0)
Inflammation proteomics datasets in the ALSPAC cohort [version 1; peer review: awaiting peer review] (2022) (0)
(2016). The range of peripapillary retinal nerve fibre layer and optic disc parameters, in children aged up to but not including 18 years of age who were born prematurely: protocol for a systematic review. (2016) (0)
The objective measurement of feeding behaviour and associations with obesity, genetic variation and health (2014) (0)
Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps (2018) (0)
A framework for research into continental ancestry groups of the UK Biobank (2022) (0)
Abstract 18433: Remnant Cholesterol, Low-Density Lipoprotein Cholesterol, and Blood Pressure as Mediators from Obesity to Ischemic Heart Disease (2014) (0)
Abstract 10469: Cardiometabolic Risk Factors as Causal Mediators of the Relationship Between High Body Mass Index and Chronic Kidney Disease: A Two-Step Mendelian Randomization Study and Mediation Analyses (2021) (0)
Low frequency genetic variation in the TP53 locus has large effects on head circumference and intracranial volume (2018) (0)
Using inactivating mutations to provide insight into drug action (2015) (0)
In: Book of abstracts of the European Society of Cardiology Conference, Munich, Germany (2004) (0)
P697Assessing the causal role of adiposity on early markers of cardiovascular disease: increases in blood pressure, but not metabolic risk factors, are related to arterial stiffness in young adults (2017) (0)
Association of C-reactive protein with blood pressure - Response (2005) (0)
The effect of IL-6 signalling on severe malaria: A Mendelian randomisation analysis. (2023) (0)
Universitet Dietary intake , FTO genetic variants and adiposity (2015) (0)
Evaluation and deployment of isotype-specific salivary antibody assays for detecting previous SARS-CoV-2 infection in children and adults (2023) (0)
Genetics of early-life head circumference and genetic correlations with neurological, psychiatric and cognitive outcomes (2022) (0)
Coronary artery disease , genetic risk and the metabolome in young individuals [ version 2 ; peer review : 2 approved ] (2020) (0)
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium (2014) (0)
association of Maternal s moking With Child Cotinine l evels (2013) (0)
Protocol and synthesis (2019) (0)
A genome-wide association screen of quantitative reading and language traits in >22,000 people in the GenLang consortium (2019) (0)
Application of Mendelian randomization to explore the causal role of the human gut microbiome in colorectal cancer (2023) (0)
Altered IL-6 signalling and risk of tuberculosis disease: a meta-analysis and Mendelian randomisation study (2023) (0)
A multi-variant recall-by-genotype study of the metabolomic signature of body mass index (2021) (0)
The Avon Longitudinal Study of Parents and Children - A resource for COVID-19 research: Antibody testing results, April - June 2021. (2022) (0)
A comparison of the genes and genesets identified by GWAS and EWAS of fifteen complex traits (2022) (0)
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals (2018) (0)
Genome-Wide Association Study Identiﬁes Genetic Associations with Perceived Age (LD) score regression analysis (2020) (0)
Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence (2016) (0)
Genetics of Birth Weight (2013) (0)
Maturation in serum thyroid function parameters over childhood results of a longitudinal study. (2017) (0)
Variation in the SERPINA6SERPINA1 locusalters morning plasma cortisol, hepatic corticosteroid binding globulin expression, gene expressionin peripheral tissues, and risk of cardiovascular disease (2021) (0)
Genetic studies of birth weight give biological insights into links with adult disease (2016) (0)
Erratum (2004) (0)
Genome-wide associations of human gut microbiome variation and implications for causal inference analyses (2020) (0)
Erratum: Adiponectin and its association with bone mass accrual in childhood (2012) (0)
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors (2019) (0)
Correction to: Metabolic characterisation of disturbances in the APOC3/triglyceride‑rich lipoprotein pathway through sample‑based recall by genotype (2021) (0)
Biological pathway analysis for type 2 diabetes using genome-wide association data (2007) (0)
Title : Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (0)
Coronary artery disease, genetic risk and the metabolome in young individuals [version 1; peer review: 2 approved] (2020) (0)
Shared genetic origins of allergy and autoimmune diseases (2015) (0)
Genome-wide association study identifies five novel genetic determinants of dental maturation (2017) (0)
Prevalence of Prop Tasters among Children in the ALSPAC Study, Bristol, England and Associations with Genetic Profile and Nutritional Intake (2008) (0)
Childhood Phenotypes Related to Adult Obesity: The Application of Genetic Risk Variants (2009) (0)
Characterisation of the metabolic impact of rare genetic variation within APOC3: Proton NMR based analysis of rare variant gene effects (2015) (0)
Consortium genome-wide meta-analysis for childhood dental caries traits (2017) (0)
Genetic Relationship between Schizophrenia and Nicotine Dependence (2016) (0)
Additional file 2: of The range of peripapillary retinal nerve fibre layer and optic disc parameters in children aged up to but not including 18Â years of age, as measured by optical coherence tomography: protocol for a systematic review (2016) (0)
MAPS: Mapping the Analytical PathS of a Crowdsourced Data Analysis (2018) (0)
1 Assessing the causal role of body mass index on cardiovascular health in young adults : 1 Mendelian randomization and recall-by-genotype analyses 2 (2017) (0)
TITLE: A multi-variant recall-by-genotype study of the metabolomic signature of body mass index (2021) (0)
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder (2018) (0)
Voluntary risk mitigation behaviour can reduce impact of SARS-CoV-2: a real-time modelling study of the January 2022 Omicron wave in England (2023) (0)
Diabetes and Triglyceride Levels Genome-Wide Association Analysis Identifies Loci for Type 2 (2011) (0)
Metabolic characterisation of disturbances in the APOC3/triglyceride-rich lipoprotein pathway through sample-based recall by genotype (2020) (0)
Correction to: Is population structure in the genetic biobank era irrelevant, a challenge, or an opportunity? (2019) (0)
Association of intrauterine alcohol exposure and offspring depression: A negative control analysis of maternal and partner consumption (2018) (0)
Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci (2019) (0)
SEnsitivity and specificity of biochemical screening for familial hypercholesterolaemia in childhood: avon longitudinal study of parents and children (ALSPAC). (2017) (0)
Universitet AHRR ( cg 05575921 ) hypomethylation marks smoking behaviour , morbidity and mortality (2017) (0)
Piloting the objective measurement of eating weight and speed at a population scale: a nested study within the Avon Longitudinal Study of Parents and Children. (2020) (0)
Whole-genome sequencing and deep imputation identifies non-coding variants near Engrailed-1 with large effects on bone mineral density and fracture (2015) (0)
Variants in the DGKB Gene Influence Fasting Glucose Levels in Populations of European and East Asian Descent (2009) (0)
Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference (2018) (0)
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error (2018) (0)
Loughborough University Institutional Repository Associations of device-measured physical activity across adolescence with metabolic traits : prospective cohort study (2019) (0)
Diving deep—multipronged investigations into RIPK1 as a risk factor for obesity (2020) (0)
HMOX1 STR polymorphism and malaria: an analysis of a large clinical dataset (2022) (0)
Large scale genome-wide association study for birth weight identifies 13 novel loci and reveals genetic links with a variety of adult metabolic and anthropometric traits (2015) (0)
Systematic review and meta-analyses: What has the application of Mendelian randomization told us about the causal effect of adiposity on health outcomes? [version 1; peer review: awaiting peer review] (2022) (0)
Genetic epidemiology - principles relevant to epigenetics (2012) (0)
Characterising the index mothers in the Avon Longitudinal Study of Parents and Children (ALSPAC) who are also UKBioBank participants (2022) (0)
Is vitamin D a modifiable risk factor for dental caries? (2020) (0)
Collection of genetic data at scale for a nationally representative population: the UK Millennium Cohort Study. (2021) (0)
(2020). Association of prenatal alcohol exposure and offspring depression: A negative control analysis of maternal and partner consumption. Alcoholism: Clinical and Experimental Research. (2020) (0)
551 EFFECT OF BODY MASS INDEX ON ISCHAEMIC HEART DISEASE RISK: OBSERVATIONAL AND CAUSAL ESTIMATES ON 76000 INDIVIDUALS (2011) (0)
P90 Indexing Left Ventricular Mass to Body Size: Which Method is the Most Appropriate in Early Adulthood? (2020) (0)
Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence (2016) (0)
Hypothesis-free analysis of deep vein thrombosis aetiology: a Mendelian randomization study (2018) (0)
Whole-genome sequencing identifies non-coding variants near EN 1 with large effects on bone mineral density (2014) (0)
Estimating the effect of lipids on IGF axis and subsequent breast cancer risk (2020) (0)
Meta-Analysis of Genome-Wide Scans for Total Body Bmd Reveals An Interaction with Weight Bearing At the Wnt16 Locus (2012) (0)
Correction: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (2016) (0)
A phenome-wide approach to identify causal risk factors for deep vein thrombosis (2022) (0)
Whole-genome sequence-based analysis of thyroid function (vol 6, 5681, 2015) (2015) (0)
Statistical Methods in Genetic Epidemiology. Duncan Thomas, Oxford University Press, 2004, £42.50, ISBN 0-19-515939-X. (2006) (0)
Large-scale replication typing of modest signals from genome-wide association studies identifies additional type 2 diabetes susceptibility variants in the IGF2BP2 and VEGFA genes (2007) (0)
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2021) (0)
Age 23 years + oral health questionnaire in Avon Longitudinal Study of Parents and Children. (2018) (0)
Estimating the effect of lipids on IGF axis and subsequent breast risk (2020) (0)
Is population structure in the genetic biobank era irrelevant, a challenge, or an opportunity? (2019) (0)
Polygenic Risk Scores for Clinical ADHD are Associated with Impaired Educational Achievement and Lower IQ in Children and Adults from the General Population (2015) (0)
Propagation of Embothrium coccineum, Carpenteria californica, and Fremontodendron 'California Glory' (1987) (0)
Cytokines GWAS results (2020) (0)
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error (2014) (0)
Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence (2014) (0)
Identifying Critical Points of Trajectories of Depressive Symptoms from Childhood to Young Adulthood (2019) (0)
FGFP 16S mGWAS results/mGWAS/targeted_meta/method_em/popgen (2020) (0)
Genome-wide Scan of Dental Fear and Anxiety Nominates Novel Genes (2022) (0)
Is obesity causally linked to CVD (2014) (0)
Low frequency genetic variation in TP53 is associated with final head circumference (2017) (0)
A genome-wide association meta-analysis and mouse gene deletion identify WNT16 as a regulator of cortical bone thickness (2012) (0)
Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium (2015) (0)
Common maternal and fetal genetic variants show expected polygenic effects on the probability of being born small- or large-for-gestational-age (SGA or LGA), except in the smallest 3% of babies (2020) (0)
Enhanced Protection Against Diarrhea Among Breastfed (2021) (0)
Timpson, N. J. (2014). Assessing Causality in the Association between Child Adiposity and Physical Activity Levels: A Mendelian Randomization (2014) (0)
Genetic Links between Social-Communication Traits, ADHD Traits and Clinical ADHD During Development (2015) (0)
Mis-matches between adiposity and glycaemic traits: A replicated genome-wide association study for metabolic disparity (2014) (0)
Asthma and the genes : from GWAS to next generation transcriptome analyses 1862 Meta-analysis of genome-wide association studies of single nucleotide polymorphisms in selected genes of the WNT signaling pathway (2012) (0)
Characterisation of COVID-19 long-term immunity (2020) (0)
s moking With Child Cotinine l evels (2013) (0)
Longitudinal serological measures of common infection in the Avon Longitudinal Study of Parents and Children cohort. (2018) (0)
C-reactive protein and its role in metabolic syndrome: mendelian randomisation study Detailed statistical methods (2005) (0)
Evaluating the association of TRPA1 gene polymorphisms with pain sensitivity: a protocol for an adaptive recall by genotype study (2022) (0)
Analysis of common and less frequent genetic variation for head circumference: Next-generation genetic association studies within the UK10K COHORTS project (2015) (0)
The causal effect of adiposity on vascular dysfunction in healthy adolescents (2015) (0)
Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data (2019) (0)
Iron status and risk of sepsis: a Mendelian randomisation analysis. (2022) (0)
Genome-wide association data highlight an aetiological role for disturbances in cyclin-dependent kinase pathways in type 2 diabetes (2007) (0)
Prenatal urban environment and blood pressure trajectories from childhood to early adulthood (2023) (0)
The Thr92Ala substitution in deiodonase-2 is associated with increased odds of a sub-optimal IQ score in children with low-normal thyroid function (2014) (0)
Mental health outcomes following COVID-19 infection: Evidence from 11 UK longitudinal population studies (2022) (0)
COL6A3-derived endotrophin mediates the effect of obesity on coronary artery disease: an integrative proteogenomics analysis (2023) (0)
DNA co-methylation has a stable structure and is related to specific aspects of genome regulation (2022) (0)
Developmental Changes in Genetic Relationships Between Traits and Disease: Analyses of Genetic Overlaps Between Social-communication Difficulties, Autism Spectrum Disorders and Schizophrenia (2015) (0)
Tracking population mental health before and across stages of the COVID-19 pandemic in young adults (2022) (0)
Identifying metabolic features of colorectal cancer liability using Mendelian randomization (2023) (0)
High-resolution African HLA resource uncovers HLA-DRB1 expression effects underlying vaccine response (2022) (0)
Exploring the causal role of the human gut microbiome in colorectal cancer: Application of Mendelian randomization (2022) (0)
Apparent latent structure within the UK Biobank sample has implications for epidemiological analysis (2019) (0)
The metabolomic signature of weight loss in the Diabetes Remission Clinical Trial (DiRECT) (2022) (0)
Circulating white blood cell traits and colorectal cancer risk: A Mendelian randomization study (2023) (0)
P2-303 Development of predictive equations for DXA measures of adiposity in an Indian population (2011) (0)
The association of C-reactive protein and CRP genotype with coronary heart disease: findings from five studies with 4610 cases amongst 18637 participants (2015) (0)
Edinburgh Research Explorer Variation in the SERPINA6SERPINA1 locusalters morning plasma cortisol, hepatic corticosteroid binding globulin expression, gene expressionin peripheral tissues, and risk of cardiovascular disease (2021) (0)
The Architecture Of Association: Detailed Examination Of The Relationship Between Variation At 17q21 And Childhood Wheeze Phenotypes (2012) (0)
OR09-04 Common Genetic Variants Associated with SERPINA6 Expression in Liver Influence Cortisol-Responsive Transcriptional Networks in Human Adipose Tissue (2020) (0)
Meta-analysis of human genome-microbiome association studies: the MiBioGen consortium initiative (2018) (0)
Meta-analysis of human genome-microbiome association studies: the MiBioGen consortium initiative (2018) (0)
Polymorphic variability in steroidogenic factor-1 (SF-1, NR5A1, Ad4BP) related to growth and blood pressure in children (2009) (0)

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