Cecilia Lindgren | Academic Influence

Cecilia Lindgren's AcademicInfluence.com Rankings

Cecilia Lindgren

Biology

#9783

World Rank

#13028

Historical Rank

Biotechnology

#253

World Rank

#255

Historical Rank

Molecular Biology

#2338

World Rank

#2374

Historical Rank

Neuroscience

#2397

World Rank

#2462

Historical Rank

biology Degrees

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Biology

Cecilia Lindgren's Degrees

Masters Biology Stockholm University
Bachelors Biotechnology Uppsala University

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Why Is Cecilia Lindgren Influential?

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According to Wikipedia, Cecilia Margareta Lindgren is a Swedish geneticist. She is a Professor of Genomic Endocrinology & Metabolism in the Nuffield Department of Population Health at the University of Oxford, where she is also Group Head at the Wellcome Centre for Human Genetics and a research fellow at St. Anne's College. She became Director of the Big Data Institute at Oxford on 1 April 2021; she had previously been a Senior Group Leader at the Institute. Lindgren is best known for her research on the genetics of obesity and other complex traits.

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Cecilia Lindgren'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)
PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes (2003) (6859)
A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity (2007) (4268)
Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
Discovery and Refinement of Loci Associated with Lipid Levels (2013) (2475)
Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes (2007) (2245)
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)
Hundreds of variants clustered in genomic loci and biological pathways affect human height (2010) (1961)
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) (1882)
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) (1839)
Defining the role of common variation in the genomic and biological architecture of adult human height (2014) (1805)
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) (1801)
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (2009) (1735)
A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease (2015) (1567)
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)
New genetic loci link adipose and insulin biology to body fat distribution (2014) (1227)
Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index (2010) (1179)
The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes (2000) (1150)
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (1028)
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) (933)
The genetic architecture of type 2 diabetes (2016) (927)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) (897)
Genome-wide association analysis identifies 20 loci that influence adult height (2008) (816)
Common variants associated with plasma triglycerides and risk for coronary artery disease (2013) (767)
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. (2000) (763)
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) (758)
Mapping cis- and trans-regulatory effects across multiple tissues in twins (2012) (754)
Variants in MTNR1B influence fasting glucose levels (2009) (742)
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (659)
Cancer etiology. Variation in cancer risk among tissues can be explained by the number of stem cell divisions (2015) (651)
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity (2016) (634)
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (600)
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) (568)
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (2017) (547)
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2015) (532)
Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (516)
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry (2018) (514)
Rare and low-frequency coding variants alter human adult height (2016) (511)
The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits (2012) (506)
Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (465)
The Architecture of Gene Regulatory Variation across Multiple Human Tissues: The MuTHER Study (2011) (460)
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk (2017) (428)
Multi-ethnic genome-wide association study for atrial fibrillation (2018) (425)
A common variant of HMGA2 is associated with adult and childhood height in the general population (2007) (419)
FTO genotype is associated with phenotypic variability of body mass index (2012) (407)
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes (2014) (405)
A genome-wide association meta-analysis identifies new childhood obesity loci (2012) (375)
Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits (2013) (365)
Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci (2015) (349)
Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) (348)
MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction (2005) (346)
Genetics and epigenetics of obesity (2011) (340)
Common Variation in the FTO Gene Alters Diabetes-Related Metabolic Traits to the Extent Expected Given Its Effect on BMI (2008) (317)
Identification of an imprinted master trans-regulator at the KLF14 locus related to multiple metabolic phenotypes (2011) (316)
The impact of low-frequency and rare variants on lipid levels (2015) (300)
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) (294)
Global microRNA expression profiles in insulin target tissues in a spontaneous rat model of type 2 diabetes (2010) (288)
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure (2020) (288)
A brief history of human disease genetics (2020) (288)
Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations (2015) (286)
Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer (2014) (283)
Type 2 diabetes: new genes, new understanding. (2008) (282)
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. (2006) (254)
Integrated Genetic and Epigenetic Analysis Identifies Haplotype-Specific Methylation in the FTO Type 2 Diabetes and Obesity Susceptibility Locus (2010) (254)
A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) (252)
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight (2010) (250)
Genome-wide analysis identifies 12 loci influencing human reproductive behavior (2016) (250)
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals (2018) (249)
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation (2017) (243)
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk (2016) (242)
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria (2018) (241)
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension (2016) (234)
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. (2018) (221)
Genetic evidence of assortative mating in humans (2017) (199)
The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis (2013) (199)
Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes (2009) (199)
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. (2014) (197)
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure underpinning obesity (2017) (193)
The miRNA Profile of Human Pancreatic Islets and Beta-Cells and Relationship to Type 2 Diabetes Pathogenesis (2013) (191)
Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height. (2001) (191)
GWAS identifies 14 loci for device-measured physical activity and sleep duration (2018) (190)
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility (2015) (185)
The Genetics of Obesity (2010) (168)
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals (2020) (161)
Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (153)
Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease (2017) (153)
The Trans-Ancestral Genomic Architecture of Glycemic Traits (2020) (151)
High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes (1999) (150)
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits (2017) (149)
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels (2016) (147)
Smoking is associated with mosaic loss of chromosome Y (2015) (145)
Directional dominance on stature and cognition in diverse human populations (2015) (144)
Interactions between Glutathione S-Transferase P1, Tumor Necrosis Factor, and Traffic-Related Air Pollution for Development of Childhood Allergic Disease (2008) (143)
Type 2 Diabetes Risk Alleles Are Associated With Reduced Size at Birth (2009) (141)
Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study. (2002) (139)
Adiposity-Related Heterogeneity in Patterns of Type 2 Diabetes Susceptibility Observed in Genome-Wide Association Data (2009) (135)
Differential methylation of the TRPA1 promoter in pain sensitivity (2014) (133)
•Australo-Anglo-American Spondylitis Consortium (TASC), et al. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat Genet. 2007 Nov; 39(11):1329-37. * Member of the consortium and T2D analysis subgroup. PMID: 17952073. (2007) (130)
Haplotypes of G protein-coupled receptor 154 are associated with childhood allergy and asthma. (2005) (130)
Mosaic Loss of Chromosome Y in Blood Is Associated with Alzheimer Disease (2016) (127)
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (127)
MicroRNA-125a is over-expressed in insulin target tissues in a spontaneous rat model of Type 2 Diabetes (2009) (127)
Variants in the calpain-10 gene predispose to insulin resistance and elevated free fatty acid levels. (2002) (123)
Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms (2014) (120)
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies (2016) (118)
Large-Scale Zygosity Testing Using Single Nucleotide Polymorphisms (2007) (117)
Association of variants in the fat mass and obesity associated (FTO) gene with polycystic ovary syndrome (2008) (115)
Mendelian Randomization Studies Do Not Support a Causal Role for Reduced Circulating Adiponectin Levels in Insulin Resistance and Type 2 Diabetes (2013) (113)
Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness (2017) (113)
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)
Insights Into the Molecular Mechanism for Type 2 Diabetes Susceptibility at the KCNQ1 Locus From Temporal Changes in Imprinting Status in Human Islets (2013) (106)
Genome Wide Association Identifies Common Variants at the SERPINA6/SERPINA1 Locus Influencing Plasma Cortisol and Corticosteroid Binding Globulin (2014) (106)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2011) (104)
A gene conferring susceptibility to type 2 diabetes in conjunction with obesity is located on chromosome 18p11. (2001) (101)
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation (2016) (100)
Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus (2015) (98)
Mouse-human experimental epigenetic analysis unmasks dietary targets and genetic liability for diabetic phenotypes. (2015) (97)
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function (2017) (96)
Clinical and genetic correlates of growth differentiation factor 15 in the community. (2012) (96)
Meta-analysis of sex-specific genome-wide association studies (2010) (95)
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies (2019) (92)
Genome-wide association study of toxic metals and trace elements reveals novel associations (2015) (90)
Common Variants in Maturity-Onset Diabetes of the Young Genes and Future Risk of Type 2 Diabetes (2008) (89)
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation (2020) (88)
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria (2019) (86)
Causal relationships between obesity and the leading causes of death in women and men (2019) (86)
Meta-Analysis of the INSIG2 Association with Obesity Including 74,345 Individuals: Does Heterogeneity of Estimates Relate to Study Design? (2009) (85)
The Presence of Methylation Quantitative Trait Loci Indicates a Direct Genetic Influence on the Level of DNA Methylation in Adipose Tissue (2013) (85)
Variability of gene expression profiles in human blood and lymphoblastoid cell lines (2010) (85)
Neuropeptide s receptor 1 gene polymorphism is associated with susceptibility to inflammatory bowel disease. (2007) (83)
A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes. (2003) (82)
Genetic loci associated with heart rate variability and their effects on cardiac disease risk (2017) (80)
Genome-wide enrichment analysis between endometriosis and obesity-related traits reveals novel susceptibility loci (2014) (77)
The human GIMAP5 gene has a common polyadenylation polymorphism increasing risk to systemic lupus erythematosus (2007) (77)
Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation (2015) (72)
A genome-wide scan in families with maturity-onset diabetes of the young: evidence for further genetic heterogeneity. (2003) (71)
Liver X receptor gene polymorphisms and adipose tissue expression levels in obesity (2006) (68)
PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION (2018) (67)
Coexpression Network Analysis in Abdominal and Gluteal Adipose Tissue Reveals Regulatory Genetic Loci for Metabolic Syndrome and Related Phenotypes (2012) (67)
Variation in DNA Repair Genes ERCC2, XRCC1, and XRCC3 and Risk of Follicular Lymphoma (2006) (66)
Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants (2015) (66)
Genome-wide association study identifies 48 common genetic variants associated with handedness (2019) (65)
A saturated map of common genetic variants associated with human height (2022) (65)
α2-Heremans–Schmid glycoprotein gene polymorphisms are associated with adipocyte insulin action (2004) (64)
Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci (2016) (63)
A Common Allele in FGF21 Associated with Sugar Intake Is Associated with Body Shape, Lower Total Body-Fat Percentage, and Higher Blood Pressure (2018) (63)
Common variants in HNF-1 α and risk of type 2 diabetes (2006) (62)
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity (2016) (62)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (61)
Mechanisms of Disease: genetic insights into the etiology of type 2 diabetes and obesity (2008) (60)
Corrigendum: Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes (2011) (60)
Large-Scale Genome-Wide Association Studies and Meta-Analyses of Longitudinal Change in Adult Lung Function (2014) (59)
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape (2016) (59)
Phenylketonuria screening registry as a resource for population genetic studies (2005) (58)
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2020) (58)
MicroRNA Expression in Abdominal and Gluteal Adipose Tissue Is Associated with mRNA Expression Levels and Partly Genetically Driven (2011) (58)
Mechanisms of inactivation of MLH1 in hereditary nonpolyposis colorectal carcinoma: a novel approach (2007) (58)
A Powerful Approach to Sub-Phenotype Analysis in Population-Based Genetic Association Studies (2009) (55)
Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (55)
A genome wide scan for early onset primary hypertension in Scandinavians. (2003) (54)
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene. (2015) (53)
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (53)
Sexual dimorphisms in genetic loci linked to body fat distribution (2017) (53)
Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics (2020) (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)
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene. (2016) (52)
New Blood Pressure–Associated Loci Identified in Meta-Analyses of 475 000 Individuals (2017) (50)
Insights into the Genetic Susceptibility to Type 2 Diabetes from Genome-Wide Association Studies of Obesity-Related Traits (2015) (49)
Extent, Causes, and Consequences of Small RNA Expression Variation in Human Adipose Tissue (2012) (49)
Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference (2018) (49)
Evaluation of the genetic overlap between osteoarthritis with body mass index and height using genome-wide association scan data (2012) (48)
The influence of menstrual cycle and endometriosis on endometrial methylome (2016) (48)
Population substructure in Finland and Sweden revealed by the use of spatial coordinates and a small number of unlinked autosomal SNPs (2008) (47)
Population Structure in Contemporary Sweden—A Y‐Chromosomal and Mitochondrial DNA Analysis (2009) (47)
Rheumatoid arthritis association at 6q23. (2007) (46)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (45)
Contribution of 32 GWAS-Identified Common Variants to Severe Obesity in European Adults Referred for Bariatric Surgery (2013) (44)
The Use of Genome-Wide eQTL Associations in Lymphoblastoid Cell Lines to Identify Novel Genetic Pathways Involved in Complex Traits (2011) (44)
Global analysis of uniparental disomy using high density genotyping arrays (2005) (43)
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk (2017) (43)
Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (39)
Expression of Phosphofructokinase in Skeletal Muscle Is Influenced by Genetic Variation and Associated With Insulin Sensitivity (2014) (39)
Interaction between early maternal smoking and variants in TNF and GSTP1 in childhood wheezing (2010) (38)
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction (2019) (38)
Restriction site-specific methylation studies of imprinted genes with quantitative real-time PCR. (2008) (37)
Common variants in HNF-1 alpha and risk of type 2 diabetes. (2006) (37)
Genetic variants mimicking therapeutic inhibition of IL-6 receptor signaling and risk of COVID-19 (2020) (37)
Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2016) (37)
Polymorphisms in the gene encoding the voltage-dependent Ca2+ channel CaV2.3 (CACNA1E) are associated with type 2 diabetes and impaired insulin secretion (2007) (36)
Absence of association between asthma and high serum immunoglobulin E associated GPRA haplotypes and adult atopic dermatitis. (2005) (32)
Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity. (2002) (32)
A Partial Loss-of-Function Variant in AKT2 Is Associated With Reduced Insulin-Mediated Glucose Uptake in Multiple Insulin-Sensitive Tissues: A Genotype-Based Callback Positron Emission Tomography Study (2017) (31)
G protein‐coupled receptor for asthma susceptibility associates with respiratory distress syndrome (2006) (31)
GWAS-identified loci for coronary heart disease are associated with intima-media thickness and plaque presence at the carotid artery bulb. (2015) (31)
Genome-wide DNA methylation study identifies genes associated with the cardiovascular biomarker GDF-15. (2016) (29)
Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes (2018) (29)
Disentangling the genetics of lean mass. (2019) (28)
A quality assessment survey of SNP genotyping laboratories (2006) (27)
Variability of genome-wide DNA methylation and mRNA expression profiles in reproductive and endocrine disease related tissues (2017) (27)
The genetic architecture of sporadic and multiple consecutive miscarriage (2020) (27)
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) (26)
Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (26)
No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis (2016) (25)
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2017) (25)
GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology (2018) (24)
Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy (2020) (22)
Imprinted genes and imprinting control regions show predominant intermediate methylation in adult somatic tissues (2016) (21)
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2017) (20)
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)
Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions (2017) (19)
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology. (2019) (19)
Genome-Wide Association Studies of Estimated Fatty Acid Desaturase Activity in Serum and Adipose Tissue in Elderly Individuals: Associations with Insulin Sensitivity (2018) (19)
Family-based association study of DYX1C1 variants in autism (2005) (19)
A regulatory variant at 3q21.1 confers an increased pleiotropic risk for hyperglycemia and altered bone mineral density (2021) (18)
The Genetics of Type 2 Diabetes (2001) (18)
Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes (2022) (18)
Correction: Corrigendum: Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk (2017) (18)
Identification of MAMDC1 as a Candidate Susceptibility Gene for Systemic Lupus Erythematosus (SLE) (2009) (18)
Meta-analysis fine-mapping is often miscalibrated at single-variant resolution (2022) (17)
Large-scale meta-analysis highlights the hypothalamic–pituitary–gonadal axis in the genetic regulation of menstrual cycle length (2018) (17)
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (17)
Towards Deep Cellular Phenotyping in Placental Histology (2018) (17)
Obesity and risk of female reproductive conditions: A Mendelian randomisation study (2022) (17)
Identification and Functional Characterization of G 6 PC 2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G 6 PC 2-ABCB 11 Locus (2015) (16)
A polygenic and phenotypic risk prediction for Polycystic Ovary Syndrome evaluated by Phenome-wide association studies. (2020) (16)
Association analysis of the LAG3 and CD4 genes in multiple sclerosis in two independent populations (2006) (16)
Genomic evaluation of circulating proteins for drug target characterisation and precision medicine (2020) (15)
Benefits of statistical molecular design, covariance analysis, and reference models in QSAR: a case study on acetylcholinesterase (2014) (15)
Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2011) (15)
Erratum: Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2017) (14)
Genome-Wide Association Studies of Obesity (2014) (14)
Genome-Wide Association Studies of Obesity (2014) (14)
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity (2020) (14)
Assessing association between protein truncating variants and quantitative traits (2013) (14)
Sex Differences in the Risk of Coronary Heart Disease Associated With Type 2 Diabetes: A Mendelian Randomization Analysis (2020) (14)
Genetic analysis of over one million people identifies 535 novel loci for blood pressure (2017) (14)
MicroRNA-196a links human body fat distribution to adipose tissue extracellular matrix composition (2019) (13)
Linking the FTO obesity rs1421085 variant circuitry to cellular, metabolic, and organismal phenotypes in vivo (2021) (12)
Characterization of the annexin I gene and evaluation of its role in type 2 diabetes. (2001) (11)
Genetic and epigenetic studies of adiposity and cardiometabolic disease (2017) (11)
35th Annual meeting of the European Association for the Study of Diabetes. Brussels, Belgium, 28 September-2 October, 1999. Abstracts. (1999) (11)
Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes (2005) (10)
Genome-wide association study of plasma levels of polychlorinated biphenyls disclose an association with the CYP2B6 gene in a population-based sample (2015) (10)
A distribution-centered approach for analyzing human adipocyte size estimates and their association with obesity-related traits and mitochondrial function (2021) (10)
Deep clinical and biological phenotyping of the preterm birth and small for gestational age syndromes: The INTERBIO-21st Newborn Case-Control Study protocol (2018) (10)
Genome-wide association study of adipocyte lipolysis in the GENetics of adipocyte lipolysis (GENiAL) cohort (2020) (10)
Deep clinical and biological phenotyping of the preterm birth and small for gestational age syndromes: The INTERBIO-21 st Newborn Case-Control Study protocol (2018) (10)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (10)
Ovarian Physiology and GWAS: Biobanks, Biology, and Beyond (2016) (10)
Machine Learning based histology phenotyping to investigate the epidemiologic and genetic basis of adipocyte morphology and cardiometabolic traits (2020) (10)
Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation (2019) (9)
Correction: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (9)
Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13 (2008) (9)
Genetic and methylation variation in the CYP2B6 gene is related to circulating p,p′-dde levels in a population-based sample (2017) (9)
Noncovalent Inhibitors of Mosquito Acetylcholinesterase 1 with Resistance-Breaking Potency. (2018) (9)
Genetic variation in the CYP1A1 gene is related to circulating PCB118 levels in a population-based sample. (2014) (9)
Erratum: Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes (Nature Genetics (2011) 43 (561-564)) (2011) (9)
Genetic variation in the CYP2B6 Gene is related to circulating 2,2’,4,4’-tetrabromodiphenyl ether (BDE-47) concentrations: an observational population-based study (2014) (9)
Identification of MAMDC 1 as a candidate susceptibility gene for systemic lupus erythematosus ( SLE ) (9)
Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (8)
Testing the role of predicted gene knockouts in human anthropometric trait variation (2016) (8)
Evidence From Men for Ovary-independent Effects of Genetic Risk Factors for Polycystic Ovary Syndrome (2021) (8)
Corrigendum: Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations (2016) (8)
Robust Linear Models for Cis-eQTL Analysis (2015) (8)
Correction: The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits (2013) (8)
GWAS identifies 10 loci for objectively-measured physical activity and sleep with causal roles in cardiometabolic disease (2018) (8)
Colocalization analysis of polycystic ovary syndrome to identify potential disease-mediating genes and proteins (2021) (7)
Discovering cellular programs of intrinsic and extrinsic drivers of metabolic traits using LipocyteProfiler (2021) (7)
Transcriptome and fatty-acid signatures of adipocyte hypertrophy and its non-invasive MR-based characterization in human adipose tissue (2021) (7)
Identification of novel putative rheumatoid arthritis susceptibility genes via analysis of rare variants (2009) (7)
Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2016) (7)
Genetic IL-6R variants and therapeutic inhibition of IL-6 receptor signalling in COVID-19 – Authors' reply (2020) (7)
Commentary: Mendelian randomization and women's health. (2019) (6)
Lack of association between neuropeptide S receptor 1 gene (NPSR1) and eczema in five European populations. (2008) (6)
Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk (2017) (6)
Index and Predisposes to Childhood and Adult Obesity Gene Is Associated with Body Mass FTO A Common Variant in the (2012) (5)
Adjusting for Confounding in Unsupervised Latent Representations of Images (2018) (5)
Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts (2023) (5)
The genetics of autoimmunity (2004) (5)
Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure (2019) (5)
Erratum: Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene (American Society for Clinical Investigation (2015)125:4 (1739-1751) DOI 10.1172/JCI74692) (2016) (5)
A genome-wide association study of IgM antibody against phosphorylcholine: shared genetics and phenotypic relationship to chronic lymphocytic leukemia (2018) (5)
Obesity--On or Off? (2016) (5)
Making sense of the linear genome, gene function and TADs (2020) (5)
Lifelong genetically lowered sclerostin and risk of cardiovascular disease (2019) (4)
The genetic underpinnings of body fat distribution (2017) (4)
Genome-wide association study identifies 48 common genetic variants associated with handedness (2020) (4)
Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies (2022) (4)
A common allele in FGF21 associated with preference for sugar consumption lowers body fat in the lower body and increases blood pressure (2017) (4)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (4)
Leveraging biobank-scale rare and common variant analyses to identify ASPHD1 as the main driver of reproductive traits in the 16p11.2 locus (2019) (4)
Abstracts from the 50th European Society of Human Genetics Conference: Posters (2018) (4)
Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisation (2017) (4)
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals (2022) (4)
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2018) (4)
Correction: Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria (2019) (4)
Causal analyses, statistical efficiency and phenotypic precision through Recall-by-Genotype study design (2017) (3)
Supplementary Material 5 (2014) (3)
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies (2019) (3)
GWAS meta-analysis highlights the hypothalamic-pituitary-gonadal axis (HPG axis) in the genetic regulation of menstrual cycle length (2018) (3)
Common Genetic Variation in Relation to Brachial Vascular Dimensions and Flow-Mediated Vasodilation (2019) (3)
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (3)
Supplementary Material 7 (2014) (3)
Type 2 Diabetes and Triglyceride Levels Genome-Wide Association Analysis Identifies Loci (3)
Supplementary Material 3 (2015) (3)
Prevalence of Common Gynecological Conditions in the Middle East: Systematic Review and Meta-Analysis (2021) (3)
Using human genetics to guide the repurposing of medicines. (2020) (3)
Supplementary Material 6 (2014) (3)
The genomics of heart failure: design and rationale of the HERMES consortium (2021) (3)
Multi-ethnic genome-wide association study for atrial fibrillation (2018) (3)
Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation (2017) (2)
The genetic architecture of sporadic and recurrent miscarriage (2019) (2)
Independent evidence for the VMP/DCDC2/KAAG1 gene locus on chromosomal region 6p22 as susceptibility factor for dyslexia (2005) (2)
Association of variants within the fat mass and obesity-associated (FTO) gene and polycystic ovary syndrome (2008) (2)
Causal relevance of obesity on the leading causes of death in women and men: A Mendelian randomization study (2019) (2)
Elevated DNA Methylation Gestational Age is associated with the Risk of Later Bipolar Disorder and Anorexia Nervosa in Twins (2020) (2)
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions (2023) (2)
Correction: Obesity and risk of female reproductive conditions: A Mendelian randomisation study (2022) (2)
Genome-wide study identifies association between HLA-B*55:01 and penicillin allergy (2020) (2)
Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume (2013) (2)
Modelling the genetic aetiology of complex disease: human–mouse conservation of noncoding features and disease-associated loci (2022) (2)
•Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease. Nat Genet. 2008 Jun;40(6):710-2. * member of the consortium and analysis subgroup. PMID: 18438406. (2008) (2)
Supplementary Material 4 (2015) (1)
Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (1)
Abstract 048: Association Analyses of up to ~263,000 Individuals Provide New Insights into the Biology and Genetic Architecture of the Extremes of Anthropometric Traits (2012) (1)
Dynamics Determine Signaling in a Multicomponent System Associated with Rheumatoid Arthritis. (2018) (1)
A Genetically Defined Male Counterpart of Polycystic Ovary Syndrome: Evidence for Ovarian-Independent Pathogenesis (2021) (1)
The role of adiposity in cardiometabolic traits (2013) (1)
Loci for insulin processing and secretion provide insight into type 2 diabetes risk. (2023) (1)
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology. (2019) (1)
Trans-ethnic genome-wide association study of kidney function provides novel insight into effector genes and causal effects on kidney-specific disease aetiologies (2018) (1)
Discovery and Refinement Supplementary (2015) (1)
Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function (2022) (1)
Genetic inhibition of interleukin-6 receptor signaling and Covid-19 (2020) (1)
Supplementary Material 15 (2013) (1)
Erratum: Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology (The American Journal of Human Genetics (2019) 105(1) (15–28), (S0002929719301880), (10.1016/j.ajhg.2019.05.002)) (2019) (1)
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (1)
To Stratify Or Not To Stratify: What Can Be Learned From Power Considerations And A Practical Genome-Wide Search On Sex-Difference In The GIANT Consortium (2012) (1)
Supplementary Material 9 (2013) (1)
Meta-analysis of Genetic Associations in up to 339,224 Individuals Identify 66 New Loci for Bmi, Confirming a Neuronal Contribution to Body Weight Regulation and Implicating Several Novel Pathways (2013) (1)
Erratum: Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants (2015) (1)
RNA-Sequencing reveals a downregulation of cholesterol metabolism pathways in granulosa cells from women with PCOS (2017) (1)
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution (2019) (1)
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals (2018) (1)
Publisher Correction: Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations (2020) (1)
A genome scan reveals heterogeneity among European families with maturity onset diabetes of the young (2001) (1)
Tolerance of nonsynonymous variation is closely correlated between human and mouse orthologues (2019) (1)
Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes (2017) (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)
A New Graph Node Classification Benchmark: Learning Structure from Histology Cell Graphs (2022) (1)
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2021) (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)
Hydroxyethylene isosteres introduced in type II collagen fragments substantially alter the structure and dynamics of class II MHC A(q)/glycopeptide complexes. (2015) (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)
Genome-wide physical activity interactions in adiposity (2017) (1)
GWAS identifies 14 loci for device-measured physical activity and sleep duration (2018) (0)
Obesity: is Type II diabetes a foregone conclusion or further dependent on genetic susceptibility? (2011) (0)
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity Authors (2016) (0)
RF10 | PMON217 Replication of PCOS Reproductive and Metabolic Subtypes in Diverse Cohorts – Towards a Rationale Approach to PCOS Classification (2022) (0)
A haplotype association analysis in UK families indicates that variation at the 3 ' end of PDCD1 increases risk of SLE (2005) (0)
Binding Mode of Reversible Inhibitors in Mosquito Acetylcholinesterase 1 Governs their Selective and Resistance-Breaking Potency (2017) (0)
Corrigendum to “Genome-wide association study of adipocyte lipolysis in the GENetics of adipocyte lipolysis (GENiAL) cohort” [Molecular Metabolism 34 (2020) 85–96] (2020) (0)
Assessing the efficacy and safety of angiotensinogen inhibition using human genetics (2020) (0)
A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) (0)
Fine-scale mapping of type 2 diabetes susceptibility loci by imputation and conditional analysis (2010) (0)
Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2019) (0)
Abstract MP067: Six Novel Loci With Evidence For Sexual Dimorphism For Human Anthropometric Traits From Genome-wide Meta Analyses Across 270,722 Individuals (2012) (0)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
Trans-ethnic genome-wide association study provides insight into effector genes and molecular mechanisms for kidney function and highlights a causal effect on kidney-specific disease aetiologies (2018) (0)
Transethnic meta-analysis of exomic variation contributing to central adiposity (2015) (0)
Genetic and epigenetic studies of adiposity and cardiometabolic disease (2017) (0)
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (0)
A brief history of human disease genetics (2020) (0)
Sequencing of 12,940 exomes identifies additional coding variants in G6PC2 which influence fasting glucose levels through effects on protein stability or activity (2015) (0)
Mus musculus acetylcholinesterase in complex with 1-(4-(4-Ethylpiperazin-1-yl)piperidin-1-yl)-2-((4'-methoxy-[1,1'-biphenyl]-4-yl)oxy)ethanone dihydrochloride (15) (2018) (0)
Genome-wide physical activity interactions in adiposity A meta-analysis of 200,452 adults Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (0)
Identification of sex-specific pleiotropic loci underlying endometriosis and obesity-related traits (2013) (0)
Examination of a possible influence of genetic variation at the DYX1C1 locus in the development of dyslexia (2004) (0)
Modification of a Fragment from Type II Collagen Affects the Dynamics of Human Class II MHC Proteins and the Subsequent T-Cell Response, Associated with Rheumatoid Arthritis (2017) (0)
Title : Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (0)
Genome‐Wide Association Studies (GWAS) of Estimated Fatty Acid Desaturase Activity in Serum and Adipose Tissue: Relationships with Insulin Sensitivity (2015) (0)
Novel loci discovery for blood pressure and heart rate using the Exome chip (2016) (0)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
Abstract 4683: Smoking is associated with mosaic loss of chromosome Y (2015) (0)
DESIGN OF BROAD SPECTRUM ANTIDOTES (2018) (0)
Mechanisms of DNA repair have evolved to minimise the probability of nonsense mutations (2021) (0)
Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (0)
Design strategies for new drugs targeting multicomponent systems : focusing on class II MHC proteins and acetylcholinesterase (2017) (0)
Micro-ribonucleic acid expression profiling and expression quantitative trait loci analysis in human gluteal and abdominal adipose tissue (2010) (0)
Genetic variation at RAB3GAP2 and its role in exercise-related adaptation and recovery (2021) (0)
LD relationship for FTO Association SNPs and rs7202116. (2010) (0)
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing (2019) (0)
Insights from the largest genetic study of sporadic and recurrent miscarriage (2019) (0)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (0)
Investigating the Association of Rare Genetic Variants with Blood Pressure traits (2015) (0)
Large-Scale Genome-Wide Association Meta-Analysis using Imputation from 1000 Genomes Project Reference Panel Identifies 29 Novel Lipid Loci and New Variants in Previously known Loci (2013) (0)
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2018) (0)
SESSION 34: ENDOMETRIOSIS/ENDOMETRIUM: MOLECULAR AND CELLULAR INSIGHTS 1 (2012) (0)
Discovery and validation of 107 blood pressure loci from UK Biobank offers novel biological insights into cardiovascular risk (2016) (0)
Genetic characterization of familial hypercholesterolemia in Sweden (2005) (0)
Abstract P360: Meta-Analysis of up to 14,262 Individuals Identifies Loci Associated with Measures of Subcutaneous Fat Volume and Attenuation (2015) (0)
Genome-wide association studies of obesity and related traits (2014) (0)
Epigenome-wide association reveals extensive perturbations in DNA methylation associated with adiposity and its adverse metabolic consequences. Authors (2015) (0)
Search for Type 2 Diabetes Susceptibility Genes Using Multiple Approaches (2002) (0)
Large-scale Genome-wide Association Meta-analysis Using Imputation from 2188-haplotype 1000 Genomes Reference Panel Identifies Novel Susceptibility Loci for Anthropometric and Glycemic Traits (2013) (0)
Identification of additional type 2 diabetes susceptibility loci through large-scale replication using "Metabochip": early result (2010) (0)
Risk genotypes, allele-specific expression and methylation status in human islets at the KCNQ1 type 2 diabetes-susceptibility locus (2010) (0)
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications (2023) (0)
S19PATERNAL ORIGIN DOPA DECARBOXYLASE GENE VARIANTS ARE ASSOCIATED WITH AUTISM SPECTRUM DISORDER (2019) (0)
The influence of menstrual cycle and endometriosis on endometrial methylome (2016) (0)
P–374 Investigating causality of risk factors for miscarriage – a Mendelian randomization analysis (2021) (0)
Biological pathway analysis for type 2 diabetes using genome-wide association data (2007) (0)
Large-scale integration of genetic and 'omics' data to find susceptibility genes for obesity and fat distribution (2019) (0)
Large-scale genome-wide association meta-analysis of the 1000 genomes project imputed data identifies novel susceptibility loci for glycaemic and obesity traits (2013) (0)
Re-evaluation of putative rheumatoid arthritis susceptibility genes in the post-genome wide association study era and hypothesis of a key pathway underlying susceptibility. (2008) (0)
Search for low-frequency variants associated with overall and central adiposity (2009) (0)
The miRNA Expression Profile of Human Islets and Beta-Cells, and Relationship to Type 2 Diabetes Predisposition (2012) (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)
Diabetes and Triglyceride Levels Genome-Wide Association Analysis Identifies Loci for Type 2 (2011) (0)
Epigenetic studies of ovarian cells: understanding the aetiology and management of Polycystic Ovary Syndrome (2018) (0)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (0)
Linkage disequilibrium at PPARG and other genes assessed with dense sets of SNPs. (2001) (0)
Biomarkers of skin ageing using genome wide transcriptomics (2011) (0)
A genome wide scan for linkage in families with early onset maturity-onset diabetes of the young suggests a potential role for genes on chromosomes 2p 3q, 4q and 10q in glucose homeostasis (2007) (0)
Session 06: Endometriosis (2013) (0)
Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference (2018) (0)
Abstracts from the 52nd European Society of Human Genetics (ESHG) Conference: Oral Presentations (2019) (0)
Comprehensive assessment of the role of DNA methylation in obesity and type 2 diabetes (2014) (0)
Large-Scale Integrated Genome-Wide RNA Sequencing, miRNA Array, and Genomic Analyses to Unravel the Functionality of Genome-Wide Association Results in Endometriosis. (2017) (0)
Publisher Correction: Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations (2020) (0)
Variability of Genome-Wide Gene Expression and DNA Methylation Profiles Across Tissue Samples From Women With and Without Endometriosis (2015) (0)
Erratum: A gene conferring susceptibility to type 2 diabetes in conjunction with obesty is located on chromosme 18p11 (Diabetes (2001) 50 (675-680)) (2001) (0)
Genome-wide association study of endometriosis identifies a locus at 7p15.2 with pleiotropic effects (2012) (0)
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene - eScholarship (2015) (0)
Running head: Global analysis of uniparental disomy (2005) (0)
Correction (1960) (0)
Colocalization highlights genes in hypothalamic–pituitary–gonadal axis as potentially mediating polycystic ovary syndrome risk (2020) (0)
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction (2020) (0)
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (0)
Abstract MP84: Trans-ethnic Meta-analysis of Exome Chip Data Reveals Novel Low-frequency Variants Contributing to Central Adiposity (2016) (0)
Results of logistic regression for the 32 genotyped SNPs. (2013) (0)
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure (2020) (0)
Investigation of C5a in multiple sclerosis - two different strategies at the DNA level (2004) (0)
Response to comment on “Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics” (2021) (0)
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2021) (0)
Making sense of the linear genome, gene function and TADs (2022) (0)
Differential microRNA expression in abdominal and gluteal adipose tissue is partly genetically driven (2010) (0)
Genome-wide DNA methylation and mRNA expression profiling in eutopic endometrium, disease tissue and fat: implications for endometriosis research (2016) (0)
Edinburgh Research Explorer Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2018) (0)
A Genome-wide Association Case Study on Obesity (2011) (0)
26 ESTIMATED DNA METHYLATION GESTATIONAL AGE IN NEWBORN MONOZYGOTIC TWINS ASSOCIATE WITH LATER PSYCHIATRIC DISORDERS BETWEEN CON/DISCORDANT PAIRS (2019) (0)
miRNA expression profile in rats correlates with type-2-diabetes phenotype (2008) (0)
Design of Reactive Drugs : Structure and Mechanism of Novel Nerve Agent Antidotes (2017) (0)
Common genetic variants underlie endometriosis and obesity-related traits (2012) (0)
Differences between global miRNA expression profiles in diabetic and normoglycaemic rats (2008) (0)
Genetic effects in replicated miRNA eQTLs in abdominal adipose tissue (see Materials and Methods section for criteria). (2011) (0)
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (0)
The genetic architecture of changes in adiposity during adulthood (2023) (0)
Design and Synthesis of Glycopeptides Targeting the Class II MHC DR4 Protein Associated with Rheumatoid Arthritis. (2012) (0)
Abstract MP83: Exomechip Meta-analysis of 526,508 Individuals From Five Ancestries Identifies Coding Variation in MC4R and KSR2 Associated with Body Mass Index (2016) (0)
Using imputation to investigate association of low-frequency variants with adiposity in the 1966 Northern Finnish birth cohort (2010) (0)
Analysis of asthma and high serum IgE associated haplotypes in atopic dermatitis (AD) (2005) (0)

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