David Evans

Q: What Schools Are Affiliated With David Evans

David Evans is affiliated with the following schools: University of Sheffield, University of Queensland, University of Bristol, University of Melbourne, University of Edinburgh, University of Manchester

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David Evans

Mathematics

#4877

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#6893

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Statistics

#713

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#800

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mathematics Degrees

David Evans

Biology

#10645

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#13989

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Genetics

#1131

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#1230

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biology Degrees

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Mathematics
Biology

David Evans 's Degrees

Bachelors Genetics University of Melbourne

Why Is David Evans Influential?

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According to Wikipedia, David M. Evans is Professor of Statistical Genetics and Head of Genomic Medicine at the Diamantina Institute at the University of Queensland. He received his Ph.D. from the University of Queensland in 2003, after which he completed a four-year postdoc at the University of Oxford's Wellcome Trust Centre for Human Genetics. During his postdoc, he conducted research for the International HapMap Project and the Wellcome Trust Case Control Consortium. In 2007, he became a senior lecturer at the University of Bristol, where he conducted research on genome-wide association studies based on the Avon Longitudinal Study of Parents and Children. He became a professor at the University of Queensland in 2013. He is known for researching the genetics of complex traits in humans, such as osteoporosis, asthma, and binge eating. He was an ISI Highly Cited Researcher in 2015 and 2016.

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David Evans '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

A second generation human haplotype map of over 3.1 million SNPs (2007) (4567)
The MR-Base platform supports systematic causal inference across the human phenome (2018) (2168)
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (2009) (1735)
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)
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture (2012) (1045)
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 (2010) (947)
The UK10K project identifies rare variants in health and disease (2015) (926)
Genome-wide association analysis identifies 20 loci that influence adult height (2008) (816)
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility (2011) (807)
GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (2013) (803)
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 (2016) (775)
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) (758)
Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci (2013) (689)
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) (568)
Genome-wide association study identifies five loci associated with lung function (2010) (560)
Collider scope: when selection bias can substantially influence observed associations (2017) (529)
Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (465)
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)
Systematic identification of genetic influences on methylation across the human life course (2016) (427)
New gene functions in megakaryopoiesis and platelet formation (2011) (423)
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)
An atlas of genetic influences on osteoporosis in humans and mice (2018) (409)
Genome-wide association and large scale follow-up identifies 16 new loci influencing lung function (2011) (401)
Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture (2015) (399)
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (2013) (379)
Blaming the consumer – once again: the social and material contexts of everyday food waste practices in some English households (2011) (378)
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)
Seventy-five genetic loci influencing the human red blood cell (2012) (357)
Multi-ethnic genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis (2015) (356)
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population (2015) (343)
Recent Developments in Mendelian Randomization Studies (2017) (341)
Genome-wide meta-analysis identifies new susceptibility loci for migraine (2013) (336)
META-ANALYSIS OF GENOME-WIDE ASSOCIATION STUDIES IDENTIFIES THREE NEW RISK LOCI FOR ATOPIC DERMATITIS (2011) (325)
Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis (2017) (323)
Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk. (2009) (308)
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)
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) (296)
A Comprehensive Evaluation of Potential Lung Function Associated Genes in the SpiroMeta General Population Sample (2011) (281)
Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder. (2015) (281)
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors (2018) (269)
Genome-Wide Association Study Using Extreme Truncate Selection Identifies Novel Genes Affecting Bone Mineral Density and Fracture Risk (2011) (262)
WNT16 Influences Bone Mineral Density, Cortical Bone Thickness, Bone Strength, and Osteoporotic Fracture Risk (2012) (257)
Data Resource Profile: Accessible Resource for Integrated Epigenomic Studies (ARIES). (2015) (251)
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight (2010) (250)
Childhood intelligence is heritable, highly polygenic and associated with FNBP1L (2014) (247)
Two-Stage Two-Locus Models in Genome-Wide Association (2006) (244)
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk (2016) (242)
Mendelian Randomization: New Applications in the Coming Age of Hypothesis-Free Causality. (2015) (235)
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)
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets (2017) (217)
Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1 (2015) (214)
Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight. (2016) (214)
Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position. (2012) (204)
Review: Consumption-stage food waste reduction interventions – What works and how to design better interventions (2019) (201)
Genetic evidence of assortative mating in humans (2017) (199)
Genetic and environmental causes of variation in basal levels of blood cells (1999) (196)
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype. (2014) (193)
MR-Base: a platform for systematic causal inference across the phenome using billions of genetic associations (2016) (190)
Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity. (2013) (176)
Constructing and mobilizing ‘the consumer’: Responsibility, consumption and the politics of sustainability (2017) (172)
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. (2018) (171)
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)
Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps. (2004) (164)
Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium (2015) (164)
Genetics (AAGC) (2015). Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis. (2015) (157)
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)
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. (2013) (143)
Investigating the genetic association between ERAP1 and ankylosing spondylitis (2009) (142)
Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill (2013) (141)
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)
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)
Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses (2020) (128)
Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses (2020) (128)
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 (2018) (126)
Common variants at 12q15 and 12q24 are associated with infant head circumference (2012) (121)
A comparison of linkage disequilibrium patterns and estimated population recombination rates across multiple populations. (2005) (120)
A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q. (2004) (119)
A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts. (2016) (118)
Cis and Trans Effects of Human Genomic Variants on Gene Expression (2014) (118)
A genome-wide association study of body mass index across early life and childhood (2015) (115)
Consuming conventions: Sustainable consumption, ecological citizenship and the worlds of worth (2011) (115)
Harmonization of Neuroticism and Extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of Item Response Theory (2014) (113)
Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness (2017) (113)
A novel common variant in DCST2 is associated with length in early life and height in adulthood (2014) (112)
ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties (2017) (112)
Genetic Dissection of Acute Anterior Uveitis Reveals Similarities and Differences in Associations Observed With Ankylosing Spondylitis (2015) (112)
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation (2015) (110)
Genome-wide screening for DNA variants associated with reading and language traits (2014) (108)
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 association study identifies loci affecting blood copper, selenium and zinc. (2013) (106)
The validity of twin studies (2000) (105)
Genetic Determinants of Trabecular and Cortical Volumetric Bone Mineral Densities and Bone Microstructure (2013) (104)
Association of Genetic Loci With Glucose Levels in Childhood and Adolescence (2011) (103)
Effects of BMI, Fat Mass, and Lean Mass on Asthma in Childhood: A Mendelian Randomization Study (2014) (101)
Sustainable Consumption, Behaviour Change Policies and Theories of Practice (2012) (100)
Association of IL23R and ERAP1 genes with ankylosing spondylitis in a Portuguese population. (2009) (100)
What is consumption, where has it been going, and does it still matter? (2019) (98)
Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error (2016) (98)
A variant in LIN28B is associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure. (2010) (97)
A genome-wide association study for reading and language abilities in two population cohorts (2013) (96)
Identification of atopic dermatitis subgroups in children from 2 longitudinal birth cohorts (2017) (95)
Using Mendelian randomization to determine causal effects of maternal pregnancy (intrauterine) exposures on offspring outcomes: Sources of bias and methods for assessing them (2017) (91)
Sequence variants in three loci influence monocyte counts and erythrocyte volume. (2009) (87)
ERAP2 is associated with ankylosing spondylitis in HLA-B27-positive and HLA-B27-negative patients (2015) (86)
Shared Genetic Influences Between Attention-Deficit/Hyperactivity Disorder (ADHD) Traits in Children and Clinical ADHD (2015) (86)
Within family Mendelian randomization studies. (2019) (85)
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)
Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. (2010) (83)
International Review of Behaviour Change Initiatives (2011) (82)
A Population-Based Study of Genetic Variation and Psychotic Experiences in Adolescents (2013) (82)
Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium (2016) (80)
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)
Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances (2013) (79)
Do the genetic or environmental determinants of anxiety and depression change with age? A longitudinal study of Australian twins. (2004) (79)
Polygenic Scores Predict Alcohol Problems in an Independent Sample and Show Moderation by the Environment (2014) (78)
Mining the Human Phenome Using Allelic Scores That Index Biological Intermediates (2013) (77)
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (2017) (77)
Association of Forced Vital Capacity with the Developmental Gene NCOR2 (2016) (76)
Resolving the Effects of Maternal and Offspring Genotype on Dyadic Outcomes in Genome Wide Complex Trait Analysis (“M-GCTA”) (2014) (75)
Common variation near ROBO2 is associated with expressive vocabulary in infancy (2014) (74)
Within-family studies for Mendelian randomization: avoiding dynastic, assortative mating, and population stratification biases (2019) (74)
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability (2018) (74)
Genome-wide association study of height-adjusted BMI in childhood identifies functional variant in ADCY3 (2014) (73)
Circulating Selenium and Prostate Cancer Risk: A Mendelian Randomization Analysis (2017) (72)
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)
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus (2017) (70)
Applying polygenic risk scores to postpartum depression (2014) (70)
Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index (2014) (69)
Genetic Variants in the Vitamin D Receptor Are Associated with Advanced Prostate Cancer at Diagnosis: Findings from the Prostate Testing for Cancer and Treatment Study and a Systematic Review (2009) (69)
Examination of the relationship between variation at 17q21 and childhood wheeze phenotypes. (2013) (69)
Genome-wide association study identifies 48 common genetic variants associated with handedness (2019) (65)
Using structural equation modelling to jointly estimate maternal and fetal effects on birthweight in the UK Biobank (2017) (63)
Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence (2014) (63)
Postnatal Growth and DNA Methylation Are Associated With Differential Gene Expression of the TACSTD2 Gene and Childhood Fat Mass (2012) (62)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (61)
Joint developmental trajectories of internalizing and externalizing disorders between childhood and adolescence (2016) (61)
Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects (2022) (59)
Within-sibship GWAS improve estimates of direct genetic effects (2021) (58)
Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy (2010) (58)
The power of multivariate quantitative-trait loci linkage analysis is influenced by the correlation between variables. (2002) (58)
Genome-wide Scan of IQ Finds Significant Linkage to a Quantitative Trait Locus on 2q (2006) (56)
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (2013) (55)
Using Mendelian randomization to investigate a possible causal relationship between adiposity and increased bone mineral density at different skeletal sites in children (2016) (54)
Genome-wide prediction of childhood asthma and related phenotypes in a longitudinal birth cohort. (2012) (53)
Elucidating the role of maternal environmental exposures on offspring health and disease using two-sample Mendelian randomization (2019) (53)
Assumption-free estimation of the genetic contribution to refractive error across childhood (2015) (53)
Rethinking material cultures of sustainability: commodity consumption, cultural biographies and following the thing (2018) (52)
Prospects and pitfalls in whole genome association studies (2005) (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)
Genome-Wide Association Study to Identify Common Variants Associated with Brachial Circumference: A Meta-Analysis of 14 Cohorts (2012) (50)
Adult height variants affect birth length and growth rate in children (2011) (49)
Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference (2018) (49)
Identification of Novel Loci Associated With Hip Shape: A Meta‐Analysis of Genomewide Association Studies (2018) (46)
Association analysis of 31 common polymorphisms with type 2 diabetes and its related traits in Indian sib pairs (2011) (46)
Genetic Variation Associated with Differential Educational Attainment in Adults Has Anticipated Associations with School Performance in Children (2014) (45)
Dnmt3a-mutated clonal hematopoiesis promotes osteoporosis (2021) (45)
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)
Dirtying Linen: Re‐evaluating the sustainability of domestic laundry (2016) (44)
Are obesity risk genes associated with binge eating in adolescence? (2015) (43)
Epigenome‐wide Association of DNA Methylation in Whole Blood With Bone Mineral Density (2017) (42)
3D Models of the NCI60 Cell Lines for Screening Oncology Compounds (2017) (42)
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero (2018) (42)
Collider Scope: How selection bias can induce spurious associations (2016) (41)
Common variation contributes to the genetic architecture of social communication traits (2013) (41)
Effects of Memory Load and Distraction on Performance and Event-Related Slow Potentials in a Visuospatial Working Memory Task (1997) (41)
Associations of vitamin D pathway genes with circulating 25-hydroxyvitamin-D, 1,25-dihydroxyvitamin-D, and prostate cancer: a nested case–control study (2014) (40)
OPG and RANK Polymorphisms Are Both Associated with Cortical Bone Mineral Density: Findings from a Metaanalysis of the Avon Longitudinal Study of Parents and Children and Gothenburg Osteoporosis and Obesity Determinants Cohorts (2010) (40)
Genome-wide association: a promising start to a long race. (2006) (38)
Osteocyte transcriptome mapping identifies a molecular landscape controlling skeletal homeostasis and susceptibility to skeletal disease (2020) (38)
Genome-Wide Association Study Identifies Four Loci Associated with Eruption of Permanent Teeth (2011) (38)
Who’s responsible for food waste? Consumers, retailers and the food waste discourse coalition in the United Kingdom (2018) (38)
A genome-wide scan for Eysenckian personality dimensions in adolescent twin sibships: psychoticism, extraversion, neuroticism, and lie. (2008) (37)
Power calculations in genetic studies. (2012) (37)
Using a two-sample Mendelian randomization design to investigate a possible causal effect of maternal lipid concentrations on offspring birth weight (2019) (37)
Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study (2020) (36)
Urban food sharing: Emerging geographies of production, consumption and exchange (2019) (34)
Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants. (2014) (34)
Genetic variants in adult bone mineral density and fracture risk genes are associated with the rate of bone mineral density acquisition in adolescence (2015) (33)
Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants. (2005) (33)
Major quantitative trait locus for eosinophil count is located on chromosome 2q. (2004) (33)
Challenges and opportunities for re-framing resource use policy with practice theories: The change points approach (2020) (32)
The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis (2015) (32)
Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes (2018) (32)
A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways. (2016) (32)
Coordinated genetic scaling of the human eye: shared determination of axial eye length and corneal curvature. (2013) (31)
A genome-wide association study to identify genetic determinants of atopy in subjects from the United Kingdom. (2011) (30)
Genotype prediction using a dense map of SNPs (2004) (30)
Genetic Variation in Prostate-Specific Antigen–Detected Prostate Cancer and the Effect of Control Selection on Genetic Association Studies (2014) (30)
Heritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE Consortium. (2016) (29)
Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP 1 (2015) (29)
Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease (2016) (29)
The Effect of Plasma Lipids and Lipid‐Lowering Interventions on Bone Mineral Density: A Mendelian Randomization Study (2020) (29)
Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort (2020) (29)
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium (2014) (28)
Integrative pathway genomics of lung function and airflow obstruction. (2015) (28)
Maternal and fetal genetic contribution to gestational weight gain (2017) (28)
Genetic Influences on Trajectories of Systolic Blood Pressure Across Childhood and Adolescence (2013) (26)
A major quantitative trait locus for CD4–CD8 ratio is located on chromosome 11 (2004) (26)
Is there a higher genetic load of susceptibility loci in familial ankylosing spondylitis? (2012) (26)
Calculating Power to Detect Maternal and Offspring Genetic Effects in Genetic Association Studies (2019) (26)
Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2) (2014) (25)
A genetic two-factor model of the covariation among a subset of Multidimensional Aptitude Battery and Wechsler Adult Intelligence Scale—Revised subtests (2003) (25)
Developmental Changes Within the Genetic Architecture of Social Communication Behavior: A Multivariate Study of Genetic Variance in Unrelated Individuals (2017) (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)
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)
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color (2021) (24)
To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies? (2008) (23)
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)
Common variants at 12q15 and 12q24 are associated with infant head circumference (2013) (22)
Resolving the Effects of Maternal and Offspring Genotype on Dyadic Outcomes in Genome Wide Complex Trait Analysis (“M-GCTA”) (2014) (22)
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2018) (22)
Multivariate QTL linkage analysis suggests a QTL for platelet count on chromosome 19q (2004) (22)
RSPO3 impacts body fat distribution and regulates adipose cell biology in vitro (2020) (21)
Estimating indirect parental genetic effects on offspring phenotypes using virtual parental genotypes derived from sibling and half sibling pairs (2020) (21)
Copy number variants and therapeutic response to antidepressant medication in major depressive disorder (2014) (21)
Measurability, austerity and edibility: Introducing waste into food regime theory (2017) (21)
A Simulation Study Concerning the Effect of Varying the Residual Phenotypic Correlation on the Power of Bivariate Quantitative Trait Loci Linkage Analysis (2004) (21)
Novel directions in antipsychotic target identification using gene arrays. (2002) (21)
Association Study of 25 Type 2 Diabetes Related Loci with Measures of Obesity in Indian Sib Pairs (2013) (20)
Genome-wide Association Study for Radiographic Vertebral Fractures: A Potential Role for the 16q24 BMD Locus versus Lessons Learned from Challenging Phenotype Definition. (2014) (20)
Understanding plastic packaging: The co-evolution of materials and society (2020) (20)
Genomic influences on alcohol problems in a population-based sample of young adults. (2015) (19)
Are serum concentrations of vitamin B-12 causally related to cardiometabolic risk factors and disease? A Mendelian randomization study. (2018) (19)
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error (2020) (18)
After Practice? Material Semiotic Approaches to Consumption and Economy (2020) (18)
Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence (2014) (18)
Consumption policies within different theoretical frameworks (2017) (18)
Use of Mendelian Randomization to Examine Causal Inference in Osteoporosis (2019) (18)
Introducing M-GCTA a Software Package to Estimate Maternal (or Paternal) Genetic Effects on Offspring Phenotypes (2019) (18)
Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans (2018) (18)
Molecular and Population Analysis of Natural Selection on the Human Haptoglobin Duplication (2012) (17)
Exploring the genetic relationship between hearing impairment and Alzheimer's disease (2020) (17)
Genetic and Environmental Influences on Acne in Adolescent Twins (2001) (17)
Limb development genes underlie variation in human fingerprint patterns (2022) (17)
Genome-wide association study of circulating interleukin 6 levels identifies novel loci (2021) (16)
Direct and Indirect Effects of Maternal, Paternal, and Offspring Genotypes: Trio-GCTA (2020) (16)
Market coordination and the making of conventions: qualities, consumption and sustainability in the agro-food industry (2019) (16)
Environmental leapfrogging and everyday climate cultures: sustainable water consumption in the Global South (2018) (16)
Association and interaction analyses of eight genes under asthma linkage peaks (2009) (15)
Genome-wide association study for radiographic vertebral fractures: a potential role for the 16q24 BMD locus. (2014) (14)
Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study (2010) (14)
Letter to the EditorCommon Genetic Variants Influence Whorls in Fingerprint Patterns (2016) (14)
Ten simple rules for conducting a mendelian randomization study (2021) (14)
A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Paediatric Cohorts (2016) (13)
Genomewide scans of red cell indices suggest linkage on chromosome 6q23 (2006) (13)
Incorporating Known Genetic Variants Does Not Improve the Accuracy of PSA Testing to Identify High Risk Prostate Cancer on Biopsy (2015) (13)
A Note on the Power to Detect Transmission Distortion in Parent-Child Trios via the Transmission Disequilibrium Test (2006) (13)
Maternal and paternal effects on offspring internalizing problems: Results from genetic and family‐based analyses (2020) (13)
Genome-Wide Association Study of Height-Adjusted BMI in Childhood Identifies Functional Variant in ADCY 3 (2014) (13)
Integrating Family-Based and Mendelian Randomization Designs. (2020) (12)
Assessing the Role of DNA Methylation-Derived Neutrophil-to-Lymphocyte Ratio in Rheumatoid Arthritis (2018) (11)
A cautionary note on using Mendelian randomization to examine the Barker hypothesis and Developmental Origins of Health and Disease (DOHaD) (2020) (11)
The case for genome-wide association studies of bone acquisition in paediatric and adolescent populations. (2016) (11)
Genetic variant influence on whorls in fingerprint patterns (2015) (11)
Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort. (2018) (11)
Metabolomics analysis in adults with high bone mass identifies a relationship between bone resorption and circulating citrate which replicates in the general population (2019) (11)
Exploring the role of genetic confounding in the association between maternal and offspring body mass index: evidence from three birth cohorts (2019) (11)
Estimating direct and indirect genetic effects on offspring phenotypes using genome-wide summary results data (2020) (10)
Machine Learning to Predict Osteoporotic Fracture Risk from Genotypes (2018) (10)
Leveraging therapeutic potential of multi-targeted siRNA inhibitors. (2009) (10)
A haplotype map of the human genome The International HapMap Consortium (2005) (10)
Partitioning Phenotypic Variance Due to Parent-of-Origin Effects Using Genomic Relatedness Matrices (2017) (10)
The effect of plasma lipids and lipid lowering interventions on bone mineral density: a Mendelian randomization study (2018) (9)
An Atlas of Human and Murine Genetic Influences on Osteoporosis (2018) (9)
Direct and Indirect Effects of Maternal, Paternal, and Offspring Genotypes: Trio-GCTA (2021) (9)
MHC-Dependent Mate Selection within 872 Spousal Pairs of European Ancestry from the Health and Retirement Study (2018) (9)
Single Nucleotide Polymorphisms Associated with Reading Ability Show Connection to Socio-Economic Outcomes (2017) (9)
Il-23r is a major determinant of ankylosing spondylitis risk - The tasc study (2007) (8)
A Note on Including Phenotypic Information from Monozygotic Twins in Variance Components Qtl Linkage Analysis (2003) (8)
The Association between Primary Tooth Emergence and Anthropometric Measures in Young Adults: Findings from a Large Prospective Cohort Study (2014) (7)
Genomewide association study in Ankylosing spondylitis identifies major Non-MHC genetic determinants of disease susceptibility (2008) (7)
How selection bias can induce spurious associations (2016) (7)
The relationship between adrenocortical candidate gene expression and clinical response to hydrocortisone in patients with septic shock (2021) (7)
Exploring the causal effect of maternal pregnancy adiposity on offspring adiposity: Mendelian randomisation using polygenic risk scores (2022) (7)
Developmental Genetics of Red Cell Indices During Puberty: A Longitudinal Twin Study (2001) (7)
LD hub and MR-base: online platforms for preforming LD score regression and Mendelian randomization analysis using GWAS summary data (2016) (7)
Plasma Cortisol, Aldosterone, and Ascorbic Acid Concentrations in Patients with Septic Shock do not Predict Treatment Effect of Hydrocortisone on Mortality: A Nested Cohort Study. (2020) (7)
HAPRAP: a haplotype-based iterative method for statistical fine mapping using GWAS summary statistics (2016) (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)
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)
Exposure time versus cytotoxicity for anticancer agents (2019) (6)
Genetic Simplex Modeling of Eysenck's Dimensions of Personality in a Sample of Young Australian Twins (2004) (6)
Association analyses of 47,500 individuals identifies six fracture loci and 82 BMD loci clustering in biological pathways that regulate osteoblast and osteoclast activity (2011) (5)
Higher maternal adiposity reduces offspring birthweight if associated with a metabolically favourable profile (2021) (5)
Imprinted loci may be more widespread in humans than previously appreciated and enable limited assignment of parental allelic transmissions in unrelated individuals (2017) (5)
Investigating a Potential Causal Relationship Between Maternal Blood Pressure During Pregnancy and Future Offspring Cardiometabolic Health (2021) (5)
Genome Wide Association Metanalysis Of Skull Bone Mineral Density Identifies Loci Relevant For Osteoporosis And Craniosynostosis (2021) (5)
The Augmented Classical Twin Design: Incorporating Genome‐Wide Identity by Descent Sharing Into Twin Studies in Order to Model Violations of the Equal Environments Assumption (2021) (5)
DNA methylation in peripheral tissues and left-handedness (2021) (5)
Septic Shock: A Genomewide Association Study and Polygenic Risk Score Analysis (2020) (5)
A Metabolic Screen in Adolescents Reveals an Association Between Circulating Citrate and Cortical Bone Mineral Density (2019) (5)
Effect on tumor growth by TGF-β1/COX-2 siRNA combination product (STP705) in a human cholangiocarcinoma (HuCCT-1) xenograft tumor model in nude mice. (2019) (5)
Genome Wide Association Study Identifies Two Novel Loci Associated with Female Stress and Urgency Urinary Incontinence. (2021) (5)
Sustainable Communities: Neo-Tribalism between Modern Lifestyles and Social Change (2010) (5)
Genome-wide association study identifies 48 common genetic variants associated with handedness (2020) (4)
The ontological politics of freshness: Qualities of food and sustainability governance (2021) (4)
Modeling Parent-Specific Genetic Nurture in Families with Missing Parental Genotypes: Application to Birthweight and BMI (2020) (4)
The Genetic Basis of Spondyloarthritis: SPARTAN/IGAS 2009 (2010) (4)
A novel siRNA–gemcitabine construct as a potential therapeutic for treatment of pancreatic cancer (2020) (4)
Elucidating the genetics of craniofacial shape (2018) (4)
Detailing patient specific modeling to aid clinical decision-making (2012) (4)
Correction: Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy (2010) (4)
Pulmonary Delivery of Small Interfering RNA for Novel Therapeutics (2009) (3)
Haplotype-based heritability estimations reveal gestational duration as a maternal trait and fetal size measurements at birth as fetal traits in human pregnancy (2020) (3)
Household Recycling and Consumption Work: Social and Moral Economies, by Kathryn Wheeler and Miriam Glucksmann (2017) (3)
Causal analyses, statistical efficiency and phenotypic precision through Recall-by-Genotype study design (2017) (3)
Variants associated with HHIP expression have sex-differential effects on lung function. (2020) (3)
Oral Abstracts 7: RA ClinicalO37. Long-Term Outcomes of Early RA Patients Initiated with Adalimumab Plus Methotrexate Compared with Methotrexate Alone Following a Targeted Treatment Approach (2013) (3)
Causal effects of maternal circulating amino acids on offspring birthweight: a Mendelian randomisation study (2022) (3)
Genome-wide association study of primary tooth eruption (2012) (3)
Genetic variants in the DNA repair genes (2008) (3)
Gene-Gene Interaction and Epistasis (2011) (3)
Maternal genome-wide association study identifies a fasting glucose variant associated with offspring birth weight (2015) (3)
Publisher Correction: Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability (2019) (2)
Investigating the causal effect of maternal vitamin B12 and folate levels on offspring birthweight (2020) (2)
Why consumption, why society, why now? Consumption studies and societal challenges (2022) (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)
Systematic identification of genetic influences on methylation across the human life course (2016) (2)
Genotype by sex interactions in ankylosing spondylitis (2023) (2)
Exploring the causal effect of maternal pregnancy adiposity on offspring adiposity: Mendelian randomization using polygenic risk scores (2021) (2)
15580 Effect of TGF-β1/COX-2 small interfering RNA combination product (STP705) on cell viability and tumor growth in a human squamous carcinoma xenograft tumor model in nude mice (2020) (2)
A Genomewide Association Study of Anterior Uveiti (2012) (2)
What is a Fresh Fish?: Knowledge and Lived Experience in the UK and Portugal (2020) (2)
Phenotypic dissection of bone mineral density facilitates the identification of skeletal site specificity on the genetic regulation of bone (2013) (2)
The Boulder Workshop Question Box (2020) (2)
Back to school to protect against coronary heart disease? (2017) (2)
Abstract 5508: Bromodomain and hegdehog pathway targets in small cell lung cancer (2014) (2)
Complex Tumor Spheroids, a Tissue-Mimicking Tumor Model, for Drug Discovery and Precision Medicine (2021) (2)
Using Genomic Structural Equation Modeling to Partition the Genetic Covariance Between Birthweight and Cardiometabolic Risk Factors into Maternal and Offspring Components in the Norwegian HUNT Study (2022) (2)
Authors’ response to Hartwig and Davies (2016) (2)
Vitamin D-Binding Protein Deficiency and Homozygous Deletion of the GC Gene. (2019) (2)
Supermarkets, ‘the Consumer’ and Responsibilities for Sustainable Food (2018) (2)
Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (2019) (2)
Associations of BMI, fat mass and lean mass with childhood asthma: Mendelian randomization study (2013) (1)
Diagnostic capacity of genetic tests in Ankylosing spondylitis can exceed MRI scanning (2008) (1)
Mendelian randomization analysis of factors related to ovulation and reproductive function and endometrial cancer risk (2022) (1)
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2019) (1)
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus (2017) (1)
Educational attainment, health outcomes and mortality: a within-sibship Mendelian randomization study (2022) (1)
Author Correction: An atlas of genetic influences on osteoporosis in humans and mice (2019) (1)
Mapping complex disease genes using linkage disequilibrium and genome-wide association scans (2011) (1)
Introduction to the Special Issue on Statistical Genetic Methods for Human Complex Traits (2021) (1)
Identification and Validation of Targets for Osteoporosis: Evidence from Whole exome Sequencing in 42,263 individuals, CRISPR-Cas9 and murine models (2019) (1)
RSPO3 impacts body fat distribution and regulates adipose cell biology in vitro (2020) (1)
Variants associated with HHIP expression have sex-differential effects on lung function (2021) (1)
The importance of RANKL in volumetric bone mineral density: Findings from a genome-wide association meta-analysis (2010) (1)
Novel variants for cartilage thickness and hip osteoarthritis: revealing genes implicated in cartilage and bone development (2014) (1)
Proxy gene-by-environment Mendelian randomization for assessing causal effects of maternal exposures on offspring outcomes. (2020) (1)
From Waste to Resource Productivity (2017) (1)
Fresh is Best? New Perspectives on Sustainable Food Systems (2019) (1)
3D Cell Culture Models (2017) (1)
Antibody response to common human viruses is shaped by genetic factors. (2019) (1)
Do maternal intrauterine environmental influences that lower offspring birthweight causally increase offspring cardiometabolic risk factors in later life? A Mendelian randomization study of 45,849 genotyped parent offspring pairs in the HUNT study (2020) (1)
Genome-wide association and large scale follow-up identifies 16 novel loci for lung function (2011) (1)
Epigenome-wide association study of left-handedness for different tissues and ages (2021) (1)
Shedding light on the genetics of fetal growth (2021) (1)
Mendelian randomization study of maternal coffee consumption and its influence on birthweight, stillbirth, miscarriage, gestational age and pre-term birth (2022) (1)
Dense genotyping of candidate genes identifies 16 new susceptibility loci in ankylosing spondylitis (2012) (1)
15 EFFECTS OF ASSORTATIVE MATING ON ESTIMATES OF SNP HERITABILITY (2019) (1)
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error (2020) (1)
Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics (2017) (1)
Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes (2017) (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)
The association of endoplasmic reticulum aminopeptidase 2 (ERAP2) with ankylosing spondylitis (AS) was recently described in the large International Genetics of AS Consortium (2015) (0)
Birth weight and cardiometabolic risk factors: a discordant twin study in the UK Biobank (2022) (0)
Correction to: The Augmented Classical Twin Design: Incorporating Genome-Wide Identity by Descent Sharing Into Twin Studies in Order to Model Violations of the Equal Environments Assumption (2021) (0)
Title : Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (0)
Universitet Low-frequency variation in TP 53 has large effects on head circumference and intracranial (2019) (0)
Using structural equation modelling to jointly estimate maternal and fetal effects on birthweight in the UK Biobank. International Journal of Epidemiology (2018) (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)
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error (2018) (0)
Full title: Exploring the causal effect of maternal pregnancy adiposity on offspring 1 adiposity: Mendelian randomization using polygenic risk scores 2 Short title: Exploring the causal effect of maternal pregnancy adiposity on offspring (2021) (0)
Using Mendelian randomization to estimate the causal effect of maternal (intrauterine) exposures on late onset offspring outcomes (2019) (0)
Introduction Power Calculations in Genetic Studies (2012) (0)
Investigating a possible causal relationship between maternal serum urate concentrations and offspring birthweight: a Mendelian randomization study (2022) (0)
Do the Genetic or Environmental Determinants of Anxiety and Depression Change with Age? A Longitudinal Study of Australian Twins (2004) (0)
Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity (2016) (0)
M20 TRAIT-SPECIFIC PATTERNS OF COMMON GENETIC FACTORS INFLUENCE SOCIAL-COMMUNICATION DIFFICULTIES AND ADHD SYMPTOMS DURING CHILD AND ADOLESCENT DEVELOPMENT (2017) (0)
Using adopted individuals to partition maternal genetic effects into prenatal and postnatal effects on offspring phenotypes (2021) (0)
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium (2014) (0)
longitudinal analysis of atopic dermatitis in Alspac shows that known genetic variants are associated with early-onset or persistent atopic dermatitis, but not late-onset disease : 5 (2013) (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)
Genetic studies of birth weight give biological insights into links with adult disease (2016) (0)
It’s in the Bloody Genes! (2020) (0)
UK 10 K Consortium (2019) (0)
A Genome Scan for Eye Color in 502 Twin Families: Most Variation is due to a QTL on Chromosome 15q (2004) (0)
Geneti c and envi r onmental causes of var i ati on i n basal l evel s of bl ood cel l s (2007) (0)
Functional characterization of GWAS loci associated with fracture risk (2013) (0)
A large-Scale Deep-Coverage Whole Genome Sequencing to Identify Less Common and Rare Variants Associated with BMD and Fractures: The NHLBI Trans-Omics for Precision Medicine (TOPMED) Study (2019) (0)
Genome-wide association study identifies klotho and other novel loci as contributors to BMD variation in postmenopausal women (2008) (0)
Whole-genome sequencing identifies non-coding variants near EN 1 with large effects on bone mineral density (2014) (0)
An atlas of genetic influences on osteoporosis in humans and mice (2018) (0)
The relationship between lower back pain, inflammatory markers and genetic variants robustly associated with risk of Ankylosing Spondylitis in a population-based cohort (2015) (0)
Novel BMD loci identified by whole genome sequencing and CRISPR editing in zebrafish: The NHLBI Trans-Omics for Precision Medicine (TOPMED) study (2021) (0)
Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence (2016) (0)
association studies cancer and the effect of control selection on genetic Genetic variation in protein specific antigen detected prostate (2014) (0)
The genetic basis of cross-phenotype correlation with bone fracture risk: the GEFOS consortium (2013) (0)
Genome-wide association study identifies five novel genetic determinants of dental maturation (2017) (0)
Cathepsins B and S Are Novel Biomarkers for Bone Mineral Density: A Mendelian Randomization Study (2017) (0)
Author Correction: An atlas of genetic influences on osteoporosis in humans and mice (2019) (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)
Meta-Analysis of Genome-Wide Scans for Total Body Bmd Reveals An Interaction with Weight Bearing At the Wnt16 Locus (2012) (0)
Genome-wide association study of extreme high bone mass identifies NPR3 as a novel BMD-associated gene and highlights the contribution of common genetic variation to extreme BMD phenotypes (2017) (0)
A Genome-Wide Association Meta-Analysis and a Mouse Gene Deletion Model Identify Wnt16 as a Potential Regulator of Cortical Bone Thickness (2012) (0)
Genomic Prediction of Osteoporosis Using 426,000 Individuals from UK Biobank (2018) (0)
Abstract 605: Building better cell models for screening oncology compounds (2016) (0)
Abstract 5450: Screening more than 60 human SCLC lines with approved and investigational agents indicates complex patterns of response: Identification of HSP90 and HDACs as potential targets (2014) (0)
Abstract 3072: A clinical pharmacodynamic biomarker assay that distinguishes potentially repairable, cytotoxic drug-induced DNA double strand breaks (DSBs) from DSBs associated with apoptotic cell death (2017) (0)
Abstract 5178: Determinants of response to temozolomide in an exceptionally sensitive patient derived model (2016) (0)
Abstract A150: Complex 3D cultures for combination compound screens reveal new insights (2018) (0)
Insulin and Body Mass Index Decrease Serum Soluble Leptin Receptor Levels in Humans (2022) (0)
Abstract C106: Screening small cell lung cancer lines against approved oncology drugs and investigational agents elucidates patterns of sensitivity. (2013) (0)
Abstract 5406: Osteosarcoma cell lines response to approved and investigational anticancer agents and statins along with gene and microRNA expression (2015) (0)
Abstract 606: Similar 3D pharmacodynamic (3D-PD) responses of human tumor spheroids and xenografts to topoisomerase 1 inhibitor-induced DNA damage (2016) (0)
Abstract 348: Comparison of the response of the NCI60 NSCLC panel with the response of patient-derived NSCLC lines to approved and investigational agents (2017) (0)
Investigation into the genetic architecture of Giant Cell Arteritis through a genome-wide association study. (2016) (0)
A phase 1 Genome-wide association study in Ostoeporosis (2007) (0)
A Phase 1 Genomewide Association Study in Osteoporosis (2007) (0)
The Genetic Basis of Spondyloarthritis: SPARTAN/IGAS 2009 (2011) (0)
A genomewide association study of anterior uveitis (2012) (0)
The Identification of New Genetic Associations for Acute Anterior Uveitis in a Genomewide Scan Comparison of Ankylosing Spondylitis Cases With vs. Without Uveitis (2010) (0)
ANKYLOSING SPONDYLITIS IS STRONGLY ASSOCIATED WITH VARIANTS IN THE CMG2 GENE (2013) (0)
Antxr2 Is Associated with Ankylosing Spondylitis (2014) (0)
Ankylosing spondylitis is associated with single nucleotide polymorphisms in loci implicating four aminopeptidases (2012) (0)
Longitudinal Expression Profiling of T Lymphocytes in Patients with Active to Quiescent Giant Cell Arteritis (2016) (0)
586Effects of maternal circulating amino acids on offspring birthweight: a Mendelian randomisation analysis (2021) (0)
Publisher Correction: Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability (2019) (0)
Faster, Cheaper, Better – Can Utilities Keep Up? New EM&V and Program Approaches for Smart Connected Devices (2014) (0)
Rare variant analyses across multiethnic cohorts identify novel genes for refractive error (2021) (0)
Do environmental effects indexed by parental genetic variation influence common psychiatric symptoms in childhood? (2023) (0)
Single Nucleotide Polymorphisms Associated with Reading Ability Show Connection to Socio-Economic Outcomes (2017) (0)
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability (2018) (0)
Genes Within The Context of Development: Changes In Genetic Trait Architectures During Childhood and Adolescence (2019) (0)
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors (2019) (0)
Using adopted individuals to partition indirect maternal genetic effects into prenatal and postnatal effects on offspring phenotypes (2022) (0)
Partitioning genetic effects on birth weight at classical human leukocyte antigen loci into indirect maternal and direct fetal components using structural equation modelling (2022) (0)
Where is ‘the consumer’ (and consumption) in sustainable practices research? (2016) (0)
Money, Debt and Finance: Reclaiming the Conditions of Possibility in Consumption Research (2023) (0)
Rapid but complete? Qualitative Essentials (2012) (0)
Follow the thing: an approach to everyday climate cultures: Invited Presentation (2016) (0)
University of Dundee Identification of atopic dermatitis subgroups in children from two longitudinal birth cohorts (2017) (0)
Gifts, commodities, and consumption in the sharing economy: Masterclass (2016) (0)
New insights into the genetic etiology of 57 essential and non-essential trace elements in humans (2023) (0)
Modelling changes in genetic variances during development - The re-birth of twin modelling strategies in the GWAS era (2017) (0)
Exiting the field: writing materials, writing culture: Masterclass (2015) (0)
Division of Labour (2011) (0)
M. Gitik Blowing up power of a singular cardinalYwider gaps 1 D. Pitteloud Algebraic properties of rings of generalized power series 39 (2002) (0)
Edinburgh Research Explorer IMI - Myopia Genetics Report (2019) (0)
Production and consumption in agri‐food transformations: Rethinking integrative perspectives (2023) (0)
Re-use and Recycling (2011) (0)
Blaming the Consumer—Once Again: The Social and Material Contexts of Everyday Food Waste Practices in Some English Households (2021) (0)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (0)
SNPs associated with HHIP expression have differential effects on lung function in males and females (2019) (0)
Edinburgh Research Explorer Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index (2017) (0)
Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity (2016) (0)
Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence (2016) (0)
Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference (2018) (0)
HLA-B27 and not variation in MICA is responsible for genotype by sex interaction in risk of Ankylosing Spondylitis (2021) (0)
Can Mendelian randomization inform drug development research for neurobehavioural conditions? A study of Alzheimer's disease (2016) (0)
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals (2018) (0)
OP-IJEJ190097 233..245 (2020) (0)
Partitioning Phenotypic Variance Due to Parent-of-Origin Effects Using Genomic Relatedness Matrices (2017) (0)
Parental body mass index and offspring childhood body size and eating behaviour: causal inference via parental comparisons and extended children of twins structural equation modelling (2023) (0)
Associations of vitamin D pathway genes with circulating 25-hydroxyvitamin-D, 1,25-dihydroxyvitamin-D, and prostate cancer: a nested case–control study (2014) (0)
Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for Forced Vital Capacity. BMC Genetics (2016) (0)
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (2018) (0)
Harmonization of Neuroticism and Extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of Item Response Theory (2014) (0)
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder (2018) (0)
Life-course GWAS approach for total body BMD unveils 16 new BMD loci with some exerting age-specific effects (2016) (0)
Calculating Power to Detect Maternal and Offspring Genetic Effects in Genetic Association Studies (2019) (0)
Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (2019) (0)
Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence (2014) (0)
Meta-analysis of genome-wide association studies on atopic dermatitis identifies three novel risk loci (2012) (0)
Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium (2015) (0)
Introducing M-GCTA a Software Package to Estimate Maternal (or Paternal) Genetic Effects on Offspring Phenotypes (2019) (0)
University of Groningen Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index Hoggart, (2014) (0)
A genome-wide association meta-analysis and mouse gene deletion identify WNT16 as a regulator of cortical bone thickness (2012) (0)

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