Polymorphism, Single Nucleotide Concept

subject area of

• CYP7A1, BAAT and UGT1A1 polymorphisms and susceptibility to anti-tuberculosis drug-induced hepatotoxicity  Academic Article
• A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression  Academic Article
• A Candidate-Gene Approach Identifies Novel Associations Between Common Variants in/Near Syndromic Obesity Genes and BMI in Pediatric and Adult European Populations  Academic Article
• A DNA Switch for Detecting Single Nucleotide Polymorphism within a Long DNA Sequence Under Denaturing Conditions  Academic Article
• A DNA Switch for Detecting Single Nucleotide Polymorphism within a Long DNA Sequence Under Denaturing Conditions  Academic Article
• A Discovery Resource of Rare Copy Number Variations in Individuals with Autism Spectrum Disorder  Academic Article
• A Gene Variant in CERS2 Is Associated with Rate of Increase in Albuminuria in Patients with Diabetes from ONTARGET and TRANSCEND  Academic Article
• A Genetic Study of the Ghrelin and Growth Hormone Secretagogue Receptor (GHSR) Genes and Stature  Academic Article
• A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans  Academic Article
• A Genome-Wide Association Study Identifies a Novel Major Locus for Glycemic Control in Type 1 Diabetes, as Measured by Both A1C and Glucose  Academic Article
• A Genome-Wide Association Study Identifies rs2000999 as a Strong Genetic Determinant of Circulating Haptoglobin Levels  Academic Article
• A Genome-Wide Association Study for Coronary Artery Disease Identifies a Novel Susceptibility Locus in the Major Histocompatibility Complex  Academic Article
• A Genome-Wide Association Study for Venous Thromboembolism: The Extended Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium  Academic Article
• A Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms for Acute Kidney Injury  Academic Article
• A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis  Academic Article
• A Multivariate Genome-Wide Association Study of Wing Shape inDrosophila melanogaster  Academic Article
• A Polymorphism Within the G6PC2 Gene Is Associated with Fasting Plasma Glucose Levels  Academic Article
• A Preliminary Study ofDBH(Encoding Dopamine Beta-Hydroxylase) Genetic Variation and Neural Correlates of Emotional and Motivational Processing in Individuals With and Without Pathological Gambling  Academic Article
• A Rare Variant in the Visfatin Gene (NAMPT/PBEF1) Is Associated With Protection From Obesity  Academic Article
• A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia  Academic Article
• A fast algorithm to optimize SNP prioritization for gene-gene and gene-environment interactions  Academic Article
• A functional promoter polymorphism of the δ-globin gene is a specific marker of the Arab-Indian haplotype  Academic Article
• A genetic link between prepregnancy body mass index, postpartum weight retention, and offspring weight in early childhood  Academic Article
• A genome-wide association meta-analysis identifies new childhood obesity loci  Academic Article
• A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease  Academic Article
• A genome-wide association study of sporadic ALS in a homogenous Irish population  Academic Article
• A genome-wide linkage and association scan reveals novel loci for autism  Academic Article
• A genome-wide scan for common alleles affecting risk for autism  Academic Article
• A high-resolution melting approach for analyzing allelic expression dynamics.  Academic Article
• A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders  Academic Article
• A large-scale candidate gene association study of age at menarche and age at natural menopause  Academic Article
• A method to estimate the contribution of regional genetic associations to complex traits from summary association statistics  Academic Article
• A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder  Academic Article
• A novel candidate region for ALS on chromosome 14q11.2  Academic Article
• A novel large deletion and three polymorphisms in the FECH gene associated with erythropoietic protoporphyria  Academic Article
• A pharmacogenetic analysis of the Canadian Cancer Trials Group MY.10 clinical trial of maintenance therapy for multiple myeloma  Academic Article
• A phased SNP-based classification of sickle cell anemia HBB haplotypes  Academic Article
• A phenome-wide association study of a lipoprotein-associated phospholipase A2loss-of-function variant in 90 000 Chinese adults  Academic Article
• A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia  Academic Article
• A preliminary analysis of the DNA and diet of the extinct Beothuk: A systematic approach to ancient human DNA  Academic Article
• A preliminary pharmacogenetic investigation of adverse events from topiramate in heavy drinkers.  Academic Article
• A principal component regression based genome wide analysis approach reveals the presence of a novel QTL on BTA7 for MAP resistance in holstein cattle  Academic Article
• A review of the associations between single nucleotide polymorphisms in taste receptors, eating behaviors, and health  Academic Article
• A robust method to estimate regional polygenic correlation under misspecified linkage disequilibrium structure  Academic Article
• A toolkit for rapid gene mapping in the nematode Caenorhabditis briggsae  Academic Article
• A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity  Academic Article
• A transforming growth factorbeta1 signal peptide variant increases secretion in vitro and is associated with increased incidence of invasive breast cancer.  Academic Article
• A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β0 -thalassaemia homozygotes  Academic Article
• A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk  Academic Article
• ACDC/Adiponectin Polymorphisms Are Associated With Severe Childhood and Adult Obesity  Academic Article
• AGTR1 gene variation: Association with depression and frontotemporal morphology  Academic Article
• APOA5 and APOA1 polymorphisms are associated with triglyceride levels in Mexican children  Academic Article
• APOA5 genetic variants are markers for classic hyperlipoproteinemia phenotypes and hypertriglyceridemia  Academic Article
• Adiponectin, type 2 diabetes and the metabolic syndrome: lessons from human genetic studies  Academic Article
• Advances in Genomic Analysis of Stroke  Academic Article
• An evaluation of logic regression-based biomarker discovery across multiple intergenic regions for predicting host specificity in Escherichia coli  Academic Article
• An initial investigation of associations between dopamine-linked genetic variation and smoking motives in African Americans  Academic Article
• Analysis of Genetic Association of Intestinal Permeability in Healthy First-degree Relatives of Patients with Crohn’s Disease  Academic Article
• Analysis of IFT74as a candidate gene for chromosome 9p-linked ALS-FTD  Academic Article
• Analysis of IL-6, STAT3 and HSPA1L Gene Polymorphisms in Anti-Tuberculosis Drug-Induced Hepatitis in a Nested Case-Control Study  Academic Article
• Analysis of novel risk loci for type 2 diabetes in a general French population: the D.E.S.I.R. study  Academic Article
• Analysis of the SIM1 Contribution to Polygenic Obesity in the French Population  Academic Article
• Analysis of the contribution of FTO, NPC1, ENPP1, NEGR1, GNPDA2 and MC4Rgenes to obesity in Mexican children  Academic Article
• Angiogenin Levels and ANG Genotypes: Dysregulation in Amyotrophic Lateral Sclerosis  Academic Article
• Assessing host-specificity of Escherichia coli using a supervised learning logic-regression-based analysis of single nucleotide polymorphisms in intergenic regions  Academic Article
• Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations  Academic Article
• Assessing the effects of 35 European-derived BMI-associated SNPs in Mexican children  Academic Article
• Association Analysis Indicates That a Variant GATA-Binding Site in the PIK3CB Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and Attenuates Insulin Resistance in Obese Children  Academic Article
• Association Between a Literature-Based Genetic Risk Score and Cardiovascular Events in Women  Academic Article
• Association Studies onGhrelinandGhrelin ReceptorGene Polymorphisms With Obesity  Academic Article
• Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index  Academic Article
• Association analyses of the DAOA/G30 and d-amino-acid oxidase genes in schizophrenia: Further evidence for a role in schizophrenia  Academic Article
• Association between ADIPOQ gene polymorphisms and the risk of new-onset diabetes mellitus after liver transplantation  Academic Article
• Association between C reactive protein and coronary heart disease: mendelian randomisation analysis based on individual participant data  Academic Article
• Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data  Academic Article
• Association between maternal childhood maltreatment and mother-infant attachment disorganization: Moderation by maternal oxytocin receptor gene and cortisol secretion  Academic Article
• Association between phosphodiesterase 4D gene and ischaemic stroke  Academic Article
• Association between the FTO rs9939609 polymorphism and the metabolic syndrome in a non-Caucasian multi-ethnic sample  Academic Article
• Association between tumor necrosis factor-α promoter −308 A/G polymorphism and susceptibility to sepsis and sepsis mortality: A systematic review and meta-analysis  Academic Article
• Association of COX-2 gene haplotypes with prostaglandins production in bronchial asthma  Academic Article
• Association of Granulomatosis With Polyangiitis (Wegener's) WithHLA-DPB1*04andSEMA6AGene Variants: Evidence From Genome-Wide Analysis  Academic Article
• Association of Melanin-Concentrating Hormone Receptor 1 5' Polymorphism With Early-Onset Extreme Obesity  Academic Article
• Association of Variation at the ABO Locus With Circulating Levels of Soluble Intercellular Adhesion Molecule-1, Soluble P-selectin, and Soluble E-selectin  Academic Article
• Association of alpha4beta2 nicotinic receptor and heavy smoking in schizophrenia.  Academic Article
• Association of common variants in the human eyes shut ortholog (EYS) with statin-induced myopathy: Evidence for additional functions of EYS  Academic Article
• Association of polymorphisms in drug transporter genes (SLCO1B1 and SLC10A1) and anti-tuberculosis drug-induced hepatotoxicity in a Chinese cohort  Academic Article
• Association of renin–angiotensin and endothelial nitric oxide synthase gene polymorphisms with blood pressure progression and incident hypertension: prospective cohort study  Academic Article
• Association ofTLR4polymorphisms withMycobacterium aviumsubspeciesparatuberculosisinfection status in Canadian Holsteins  Academic Article
• Association study of brain-derived neurotrophic factor (BDNF) and LIN-7 homolog (LIN-7) genes with adult attention-deficit/hyperactivity disorder  Academic Article
• Association study of tryptophan hydroxylase 2 gene polymorphisms in bipolar disorder patients with panic disorder comorbidity  Academic Article
• Associations between parenting behavior and anxiety in a rodent model and a clinical sample: relationship to peripheral BDNF levels  Academic Article
• Associations of the FTO rs9939609 variant with discrete body fat depots and dietary intake in a multi-ethnic cohort  Academic Article
• BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia  Academic Article
• BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies  Academic Article
• BCL11A represses HBG transcription in K562 cells  Academic Article
• BDNF Val66Metpolymorphism and peripheral protein levels in pediatric bipolar disorder and attention-deficit/hyperactivity disorder  Academic Article
• BDNF-Dependent Effects on Amygdala–Cortical Circuitry and Depression Risk in Children and Youth  Academic Article
• BRCA2 Variants and cardiovascular disease in a multi-ethnic study  Academic Article
• Bardet-Biedl Syndrome Gene Variants Are Associated With Both Childhood and Adult Common Obesity in French Caucasians  Academic Article
• Bayesian methods for meta-analysis of causal relationships estimated using genetic instrumental variables  Academic Article
• Bioinformatic analyses identifies novel protein-coding pharmacogenomic markers associated with paclitaxel sensitivity in NCI60 cancer cell lines  Academic Article
• Biological, clinical and population relevance of 95 loci for blood lipids  Academic Article
• Birth weight interacts with a functional variant of the oxytocin receptor gene (OXTR) to predict executive functioning in children  Academic Article
• Blood CSF1 and CXCL12 as Causal Mediators of Coronary Artery Disease  Academic Article
• Blood HER2 and Uromodulin as Causal Mediators of CKD  Academic Article
• Bovine CLEC7A genetic variants and their association with seropositivity in Johne's disease ELISA  Academic Article
• Bovine IFNGR2, IL12RB1, IL12RB2, and IL23R polymorphisms and MAP infection status  Academic Article
• Bovine PGLYRP1 polymorphisms and their association with resistance to Mycobacterium avium ssp. paratuberculosis  Academic Article
• Brain-derived neurotrophic factor gene val66met polymorphism and executive functioning in patients with bipolar disorder  Academic Article
• Brain-derived neurotrophic factor variants are associated with childhood-onset mood disorder: confirmation in a Hungarian sample  Academic Article
• COL4A2 is associated with lacunar ischemic stroke and deep ICH  Academic Article
• CYP2D6 Genotype as a Marker for Benefit of Adjuvant Tamoxifen in Postmenopausal Women: Lessons Learned  Academic Article
• Caenorhabditis briggsae Recombinant Inbred Line Genotypes Reveal Inter-Strain Incompatibility and the Evolution of Recombination  Academic Article
• Cannabis use and risk of schizophrenia: a Mendelian randomization study  Academic Article
• Causal Effects of Body Mass Index on Cardiometabolic Traits and Events: A Mendelian Randomization Analysis  Academic Article
• Causal Relationship between Adiponectin and Metabolic Traits: A Mendelian Randomization Study in a Multiethnic Population  Academic Article
• Causal Relationship between Obesity and Vitamin D Status: Bi-Directional Mendelian Randomization Analysis of Multiple Cohorts  Academic Article
• Causes and Consequences of Genetic Background Effects Illuminated by Integrative Genomic Analysis  Academic Article
• Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4)  Academic Article
• Cervical artery dissection: Pathology, epidemiology and management  Academic Article
• Characterization of tumor necrosis factor–α block haplotypes associated with susceptibility to chronic venous leg ulcers in Caucasian patients  Academic Article
• Clinical and molecular delineation of the 17q21.31 microdeletion syndrome  Academic Article
• Clinical evaluation of a hemochromatosis next-generation sequencing gene panel  Academic Article
• Clinical, biochemical, and genetic predictors of coronary artery bypass graft failure  Academic Article
• Collagen platelet receptor polymorphisms integrin alpha2beta1 C807T and GPVI Q317L and risk of ischemic stroke  Academic Article
• Combined effects of MC4R and FTO common genetic variants on obesity in European general populations  Academic Article
• Comment On: Valette et al. Melanocortin-4 Receptor Mutations and Polymorphisms Do Not Affect Weight Loss after Bariatric Surgery. PLOS ONE 2012; 7(11):E48221  Academic Article
• Comment on "A Common Genetic Variant Is Associated with Adult and Childhood Obesity"  Academic Article
• Comment on "DNA from Pre-Clovis Human Coprolites in Oregon, North America"  Academic Article
• Common Variants in FTO, MC4R, TMEM18, PRL, AIF1, and PCSK1 Show Evidence of Association With Adult Obesity in the Greek Population  Academic Article
• Common Variation in SIM1 Is Reproducibly Associated With BMI in Pi ma Indians  Academic Article
• Common genetic variation near MC4R is associated with eating behaviour patterns in European populations  Academic Article
• Common nonsynonymous variants in PCSK1 confer risk of obesity  Academic Article
• Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease  Academic Article
• Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus  Academic Article
• Common variants inCACNA1Cand MDD susceptibility: A comprehensive meta-analysis  Academic Article
• Common variants near BDNF and SH2B1 show nominal evidence of association with snacking behavior in European populations  Academic Article
• Common variants near MC4R are associated with fat mass, weight and risk of obesity  Academic Article
• Comparative Genome Analysis Provides Insights into the Evolution and Adaptation of Pseudomonas syringae pv. aesculi on Aesculus hippocastanum  Academic Article
• Comparative genomic and genetic analysis of glioblastoma-derived brain tumor-initiating cells and their parent tumors  Academic Article
• Comprehensive Analysis of Genomic Variation in the LPA Locus and Its Relationship to Plasma Lipoprotein(a) in South Asians, Chinese, and European Caucasians  Academic Article
• Comprehensive identification of pleiotropic loci for body fat distribution using the NHGRI‐EBI Catalog of published genome‐wide association studies  Academic Article
• Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies  Academic Article
• Concept, Design and Implementation of a Cardiovascular Gene-Centric 50 K SNP Array for Large-Scale Genomic Association Studies  Academic Article
• Concordance of two multiple analytical approaches demonstrate that interaction between BMI and ADIPOQ haplotypes is a determinant of LDL cholesterol in a general French population  Academic Article
• Contribution of 24 obesity-associated genetic variants to insulin resistance, pancreatic beta-cell function and type 2 diabetes risk in the French population  Academic Article
• Contribution of BDNF and DRD2 genetic polymorphisms to continued opioid use in patients receiving methadone treatment for opioid use disorder: an observational study  Academic Article
• Contribution of Large Region Joint Associations to Complex Traits Genetics  Academic Article
• Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals  Academic Article
• Correction of Population Stratification in Large Multi-Ethnic Association Studies  Academic Article
• Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection  Academic Article
• Decoding the Genomics of Abdominal Aortic Aneurysm  Academic Article
• Decreased comfort food intake and allostatic load in adolescents carrying the A3669G variant of the glucocorticoid receptor gene  Academic Article
• Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis  Academic Article
• Diagnostic Pitfall in PCR-Based α-Thalassemia Genotyping Resulting from a (G→C) Polymorphism at Nucleotide 71 3′ to the α2-Globin Gene Termination Codon  Academic Article
• Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray  Academic Article
• Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes  Academic Article
• Does genetic heterogeneity account for the divergent risk of type 2 diabetes in South Asian and white European populations?  Academic Article
• Dopamine receptors D1 and D2 are related to observed maternal behavior  Academic Article
• Dose and polymorphic genes xrcc1, xrcc3, gst play a role in the risk of developing erythema in breast cancer patients following single shot partial breast irradiation after conservative surgery  Academic Article
• ENPP1 K121Q polymorphism and obesity, hyperglycaemia and type 2 diabetes in the prospective DESIR Study  Academic Article
• Early Detrimental Metabolic Outcomes of rs17300539-A Allele of ADIPOQ Gene Despite Higher Adiponectinemia  Academic Article
• Effect of PON1 Q192R Genetic Polymorphism on Clopidogrel Efficacy and Cardiovascular Events in the Clopidogrel in the Unstable Angina to Prevent Recurrent Events Trial and the Atrial Fibrillation Clopidogrel Trial With Irbesartan for Prevention of Vascular Events  Academic Article
• Effect of Bile Acid Sequestrants on the Risk of Cardiovascular Events  Academic Article
• Effect of ENPP1/PC-1-K121Q and PPARγ-Pro12Ala polymorphisms on the genetic susceptibility to T2D in the Tunisian population  Academic Article
• Effect of Genetic Variants Associated With Plasma Homocysteine Levels on Stroke Risk  Academic Article
• Effects of Multiple Genetic Loci on Age at Onset in Late-Onset Alzheimer Disease  Academic Article
• Effects of TCF7L2 Polymorphisms on Obesity in European Populations  Academic Article
• Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations  Academic Article
• Evaluating the Association of FAAH Common Gene Variation with Childhood, Adult Severe Obesity and Type 2 Diabetes in the French Population  Academic Article
• Evaluating the transferability of 15 European-derived fasting plasma glucose SNPs in Mexican children and adolescents  Academic Article
• Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALS  Academic Article
• Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index  Academic Article
• Evidence of Naturalized Stress-Tolerant Strains of Escherichia coli in Municipal Wastewater Treatment Plants  Academic Article
• Evidence that Egfr Contributes to Cryptic Genetic Variation for Photoreceptor Determination in Natural Populations of Drosophila melanogaster  Academic Article
• Evidence that Human Chlamydia pneumoniae Was Zoonotically Acquired  Academic Article
• Exome Sequencing as a Diagnostic Tool for Pediatric-Onset Ataxia  Academic Article
• Expression of a Common LQT1 Mutation in Five Apparently Unrelated Families in a Regional Inherited Arrhythmia Clinic  Academic Article
• FUT2 genotype and secretory status are not associated with fecal microbial composition and inferred function in healthy subjects  Academic Article
• Favourable IFNL3 Genotypes Are Associated with Spontaneous Clearance and Are Differentially Distributed in Aboriginals in Canadian HIV-Hepatitis C Co-Infected Individuals  Academic Article
• Fetal hemoglobin in sickle cell anemia: Molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans  Academic Article
• Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans  Academic Article
• Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5′ olfactory receptor gene cluster  Academic Article
• Fine Mapping of the Insulin-Induced Gene 2 Identifies a Variant Associated With LDL Cholesterol and Total Apolipoprotein B Levels  Academic Article
• Fine-mapping of 98 obesity loci in Mexican children  Academic Article
• Forty-Three Loci Associated with Plasma Lipoprotein Size, Concentration, and Cholesterol Content in Genome-Wide Analysis  Academic Article
• GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability  Academic Article
• GWAS-based machine learning approach to predict duloxetine response in major depressive disorder  Academic Article
• Gene × Physical Activity Interactions in Obesity: Combined Analysis of 111,421 Individuals of European Ancestry  Academic Article
• Gene- or region-based analysis of genome-wide association studies  Academic Article
• Gene-Centric Meta-Analysis of Lipid Traits in African, East Asian and Hispanic Populations  Academic Article
• Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci  Academic Article
• Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals  Academic Article
• Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders  Academic Article
• Genetic Analysis of 103 Candidate Genes for Coronary Artery Disease and Associated Phenotypes in a Founder Population Reveals a New Association between Endothelin-1 and High-Density Lipoprotein Cholesterol  Academic Article
• Genetic Control of Vulval Development inCaenorhabditis briggsae  Academic Article
• Genetic Determinants of Dabigatran Plasma Levels and Their Relation to Bleeding  Academic Article
• Genetic Dissection of Diabetes: Facing the Giant  Academic Article
• Genetic Information and the Prediction of Incident Type 2 Diabetes in a High-Risk Multiethnic Population  Academic Article
• Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium  Academic Article
• Genetic Loci Associated With C-Reactive Protein Levels and Risk of Coronary Heart Disease  Academic Article
• Genetic Loci Associated With Plasma Concentration of Low-Density Lipoprotein Cholesterol, High-Density Lipoprotein Cholesterol, Triglycerides, Apolipoprotein A1, and Apolipoprotein B Among 6382 White Women in Genome-Wide Analysis With Replication  Academic Article
• Genetic Predictors of Cardiovascular Mortality During Intensive Glycemic Control in Type 2 Diabetes: Findings From the ACCORD Clinical Trial  Academic Article
• Genetic Risk Evaluation in Wet Age-Related Macular Degeneration Treatment Response  Academic Article
• Genetic Risk Factors for Post-Infectious Irritable Bowel Syndrome Following a Waterborne Outbreak of Gastroenteritis  Academic Article
• Genetic Tools for Coronary Risk Assessment in Type 2 Diabetes: A Cohort Study From the ACCORD Clinical Trial  Academic Article
• Genetic Variants Associated With Myocardial Infarction Risk Factors in Over 8000 Individuals From Five Ethnic Groups  Academic Article
• Genetic Variants and Susceptibility to Neurological Complications Following West Nile Virus Infection  Academic Article
• Genetic Variants in Vitamin D Pathway Genes and Risk of Pancreas Cancer; Results from a Population-Based Case-Control Study in Ontario, Canada  Academic Article
• Genetic analysis of impulsive personality traits: Examination of a priori candidates and genome-wide variation  Academic Article
• Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits  Academic Article
• Genetic and Functional Assessment of the Role of the rs13431652-A and rs573225-A Alleles in the G6PC2 Promoter That Are Strongly Associated With Elevated Fasting Glucose Levels  Academic Article
• Genetic association of rs1344706 in ZNF804A with bipolar disorder and schizophrenia susceptibility in Chinese populations  Academic Article
• Genetic biomarkers associated with changes in quality of life and pain following palliative radiotherapy in patients with bone metastases  Academic Article
• Genetic biomarkers associated with pain flare and dexamethasone response following palliative radiotherapy in patients with painful bone metastases  Academic Article
• Genetic contribution to waist-to-hip ratio in Mexican children and adolescents based on 12 loci validated in European adults  Academic Article
• Genetic determinants of plasma triglycerides  Academic Article
• Genetic determinants of right-ventricular remodeling after tetralogy of Fallot repair  Academic Article
• Genetic determinants of warfarin maintenance dose and time in therapeutic treatment range: a RE-LY genomics substudy  Academic Article
• Genetic influences on ADHD symptom dimensions: Examination of a priori candidates, gene-based tests, genome-wide variation, and SNP heritability  Academic Article
• Genetic influences on delayed reward discounting: A genome-wide prioritized subset approach.  Academic Article
• Genetic meta-analysis of 15,901 African Americans identifies variation inEXOC3L1is associated with HDL concentration  Academic Article
• Genetic predictors of response to treatment with citalopram in depression secondary to traumatic brain injury  Academic Article
• Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs  Academic Article
• Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β0thalassemia  Academic Article
• Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia  Academic Article
• Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedema  Academic Article
• Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes  Academic Article
• Genetic variants of MARCO are associated with susceptibility to pulmonary tuberculosis in a Gambian population  Academic Article
• Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge  Academic Article
• Genetic variation in hyaluronan metabolism loci is associated with plasma plasminogen activator inhibitor-1 concentration  Academic Article
• Genetic variation in oxytocin rs2740210 and early adversity associated with postpartum depression and breastfeeding duration  Academic Article
• Genetically decreased vitamin D and risk of Alzheimer disease  Academic Article
• Genetically determined P2X7 receptor pore formation regulates variability in chronic pain sensitivity  Academic Article
• Genome Wide Association Identifies Common Variants at the SERPINA6/SERPINA1 Locus Influencing Plasma Cortisol and Corticosteroid Binding Globulin  Academic Article
• Genome comparisons reveal a dominant mechanism of chromosome number reduction in grasses and accelerated genome evolution in Triticeae  Academic Article
• Genome sequence of the Brown Norway rat yields insights into mammalian evolution  Academic Article
• Genome-Wide Association Analysis of Soluble ICAM-1 Concentration Reveals Novel Associations at the NFKBIK, PNPLA3, RELA, and SH2B3 Loci  Academic Article
• Genome-Wide Association Studies—Data Generation, Storage, Interpretation, and Bioinformatics  Academic Article
• Genome-Wide Associations and Functional Genomic Studies of Musculoskeletal Adverse Events in Women Receiving Aromatase Inhibitors  Academic Article
• Genome-wide Association Analysis of Blood-Pressure Traits in African-Ancestry Individuals Reveals Common Associated Genes in African and Non-African Populations  Academic Article
• Genome-wide analysis of disease progression in age-related macular degeneration  Academic Article
• Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets  Academic Article
• Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences  Academic Article
• Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk  Academic Article
• Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants  Academic Article
• Genome-wide association scans identified CTNNBL1 as a novel gene for obesity  Academic Article
• Genome-wide association studies identify loci associated with age at menarche and age at natural menopause  Academic Article
• Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis  Academic Article
• Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes  Academic Article
• Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations  Academic Article
• Genome-wide association study of alcohol use disorder identification test (AUDIT) scores in 20 328 research participants of European ancestry  Academic Article
• Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry  Academic Article
• Genome-wide association study of sepsis in extremely premature infants  Academic Article
• Genome-wide meta-analyses identify multiple loci associated with smoking behavior  Academic Article
• Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture  Academic Article
• Genome-wide studies to identify risk factors for kidney disease with a focus on patients with diabetes  Academic Article
• Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders  Academic Article
• Genomic basis of delayed reward discounting  Academic Article
• Genotype-Positive Status in Patients With Hypertrophic Cardiomyopathy Is Associated With Higher Rates of Heart Failure Events  Academic Article
• Genotypic and Phenotypic Analyses of Two “Isogenic” Strains of the Human Fungal Pathogen Cryptococcus neoformans var. neoformans  Academic Article
• Germline variation in inflammation-related pathways and risk of Barrett's oesophagus and oesophageal adenocarcinoma  Academic Article
• Getting Closer to P-Selectin  Academic Article
• Give GWAS a Chance  Academic Article
• Glucocorticoid Receptors, Brain-Derived Neurotrophic Factor, Serotonin and Dopamine Neurotransmission are Associated with Interferon-Induced Depression  Academic Article
• Growth Differentiation Factor 15 as a Novel Biomarker for Metformin  Academic Article
• HS3ST1 genotype regulates antithrombin's inflammomodulatory tone and associates with atherosclerosis  Academic Article
• Helicobacter pylori colonization and obesity – a Mendelian randomization study  Academic Article
• Hierarchical investigation of genetic influences on response inhibition in healthy young adults.  Academic Article
• High resolution mapping in the major histocompatibility complex region identifies multiple independent novel loci for psoriatic arthritis  Academic Article
• Homozygosity for a haplotype in theHBG2-OR51B4region is exclusive to Arab-Indian haplotype sickle cell anemia  Academic Article
• Human milk fatty acid composition is associated with dietary, genetic, sociodemographic, and environmental factors in the CHILD Cohort Study  Academic Article
• Hundreds of variants clustered in genomic loci and biological pathways affect human height  Academic Article
• IFITM3 and Susceptibility to Respiratory Viral Infections in the Community  Academic Article
• IL-10R Polymorphisms Are Associated with Very-early-onset Ulcerative Colitis  Academic Article
• IL28B polymorphism (rs12979860) associated with clearance of HCV infection in Poland: Systematic review of its prevalence in chronic hepatitis C patients and general population frequency  Academic Article
• Identification and functional analysis ofCITED2 mutations in patients with congenital heart defects  Academic Article
• Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody–Associated Vasculitis  Academic Article
• Identification of SNPsin Interferon Gamma, Interleukin-22, and Their Receptors and Associations with Health and Production-Related Traits in Canadian Holstein Bulls  Academic Article
• Identification of a New δ Chain Hemoglobin Variant in a β-Thalassemia Carrier: Hb A2-MUMC [δ13(A10)Ala → Asp]  Academic Article
• Identification of genetic variants associated with susceptibility to West Nile virus neuroinvasive disease  Academic Article
• Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease  Academic Article
• Identification of single nucleotide polymorphisms in the bovine interleukin-12 and interleukin-23 receptor genes and their associations with health and production traits in Holstein cows  Academic Article
• Identifying gene–gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts  Academic Article
• Immunochip Analysis Identifies Multiple Susceptibility Loci for Systemic Sclerosis  Academic Article
• Impact of Common Type 2 Diabetes Risk Polymorphisms in the DESIR Prospective Study  Academic Article
• Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity  Academic Article
• Impact of a Genetic Risk Score on Myocardial Infarction Risk Across Different Ethnic Populations  Academic Article
• Implication of the Pro12Ala polymorphism of the PPAR-gamma 2gene in type 2 diabetes and obesity in the French population  Academic Article
• Imputation of missing genotypes: an empirical evaluation of IMPUTE  Academic Article
• Increased Substitution Rates Surrounding Low-Complexity Regions within Primate Proteins  Academic Article
• Individual common variants exert weak effects on the risk for autism spectrum disorders  Academic Article
• Influence of RGS2 on Sertraline Treatment for Social Anxiety Disorder  Academic Article
• Inhibition of Metabotropic Glutamate Receptor Signaling by the Huntingtin-binding Protein Optineurin  Academic Article
• Initial Evidence that OPRM1 Genotype Moderates Ventral and Dorsal Striatum Functional Connectivity During Alcohol Cues  Academic Article
• Insights into the Development and Evolution of Exaggerated Traits Using De Novo Transcriptomes of Two Species of Horned Scarab Beetles  Academic Article
• Interaction between Oxytocin Genotypes and Early Experience Predicts Quality of Mothering and Postpartum Mood  Academic Article
• Interleukin-4 and interleukin-10 polymorphisms and antituberculosis drug-induced hepatotoxicity in Chinese population  Academic Article
• Investigation of Genetic Variants, Birthweight and Hypothalamic-Pituitary-Adrenal Axis Function Suggests a Genetic Variant in the SERPINA6 Gene Is Associated with Corticosteroid Binding Globulin in the Western Australia Pregnancy Cohort (Raine) Study  Academic Article
• Investigation of the dopamine D5 receptor gene (DRD5) in adult attention deficit hyperactivity disorder  Academic Article
• Is Glutamate Decarboxylase 2 (GAD2) a Genetic Link between Low Birth Weight and Subsequent Development of Obesity in Children?  Academic Article
• Is There a Genetic Predisposition to Anterior Cruciate Ligament Tear? A Systematic Review  Academic Article
• K45R variant of squalene synthase increases total cholesterol levels in two study samples from a French Canadian population  Academic Article
• Kinematic Analysis of Drosophila Larval Locomotion in Response to Intermittent Light Pulses  Academic Article
• Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies  Academic Article
• Lack of Association of CD36 SNPs With Early Onset Obesity: A Meta-Analysis in 9,973 European Subjects  Academic Article
• Lack of Association of Ghrelin Precursor Gene Variants and Percentage Body Fat or Serum Lipid Profiles  Academic Article
• Lack of association between type 2 diabetes and major depression: epidemiologic and genetic evidence in a multiethnic population  Academic Article
• Large meta-analysis of genome-wide association studies identifies five loci for lean body mass  Academic Article
• Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci  Academic Article
• Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci  Academic Article
• Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness  Academic Article
• Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease  Academic Article
• Leveraging cell type specific regulatory regions to detect SNPs associated with tissue factor pathway inhibitor plasma levels  Academic Article
• Linkage analysis for three coagulation factors clustering on chromosome 13q34: factor VII, factor X and protein Z  Academic Article
• Linkage and association analysis in pedigrees from different populations  Academic Article
• Local-Scale Patterns of Genetic Variability, Outcrossing, and Spatial Structure in Natural Stands of Arabidopsis thaliana  Academic Article
• Loci Related to Metabolic-Syndrome Pathways Including LEPR,HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study  Academic Article
• Loci influencing blood pressure identified using a cardiovascular gene-centric array  Academic Article
• Longitudinal Data Analysis in Genome-Wide Association Studies  Academic Article
• Longitudinal relationships between glycemic status and body mass index in a multiethnic study: evidence from observational and genetic epidemiology  Academic Article
• Low prevalence of JAK2 V617F mutation in patients with first unprovoked venous thromboembolism  Academic Article
• MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis  Academic Article
• Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2  Academic Article
• Maternal childhood adversity and child temperament: An association moderated by child 5-HTTLPR genotype  Academic Article
• Mendelian Randomization Studies Do Not Support a Role for Vitamin D in Coronary Artery Disease  Academic Article
• Mendelian randomisation, triglycerides, and CHD  Academic Article
• Mendelian randomization analysis supports the causal role of dysglycaemia and diabetes in the risk of coronary artery disease  Academic Article
• Mendelian randomization of blood lipids for coronary heart disease  Academic Article
• Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution  Academic Article
• Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12  Academic Article
• Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease  Academic Article
• Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height  Academic Article
• Meta-analysis of SNPs involved in variance heterogeneity using Levene’s test for equal variances  Academic Article
• Meta-analysis of genetic association studies under heterogeneity  Academic Article
• Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes  Academic Article
• Methylenetetrahydrofolate Reductase Gene Variant (MTHFR C677T) and Migraine: A Case Control Study and Meta-analysis  Academic Article
• Mineralocorticoid receptor genotype moderates the association between physical neglect and serum BDNF  Academic Article
• Mining the Human Phenome Using Allelic Scores That Index Biological Intermediates  Academic Article
• Moderators of Naltrexone’s Effects on Drinking, Urge, and Alcohol Effects in Non-Treatment-Seeking Heavy Drinkers in the Natural Environment  Academic Article
• Modulation of GLP-1 Levels by a Genetic Variant That Regulates the Cardiovascular Effects of Intensive Glycemic Control in ACCORD  Academic Article
• Molecular breakpoint mapping of 6q11-q14 interstitial deletions in seven patients  Academic Article
• Molecular genetic analysis of severe protein C deficiency.  Academic Article
• Multi-Ethnic Genetic Association Study of Carotid Intima-Media Thickness Using a Targeted Cardiovascular SNP Microarray  Academic Article
• Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes  Academic Article
• Multigene panels in prostate cancer risk assessment.  Academic Article
• Multigene panels in prostate cancer risk assessment: a systematic review  Academic Article
• Multilocus sequence analyses reveal extensive diversity and multiple origins of fluconazole resistance in Candida tropicalis from tropical China  Academic Article
• Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis  Academic Article
• Multiple loci associated with indices of renal function and chronic kidney disease  Academic Article
• Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma  Academic Article
• Multivariate analysis of complex gene expression and clinical phenotypes with genetic marker data  Academic Article
• Mycoplasma genitalium Antibiotic Resistance–Mediating Mutations in Canadian Women With or Without Chlamydia Trachomatis Infection  Academic Article
• NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant inNCF2that results in reduced binding to RAC2  Academic Article
• NCAM1-TTC12-ANKK1-DRD2 variants and smoking motives as intermediate phenotypes for nicotine dependence  Academic Article
• Natural history and genotype-phenotype correlations in 72 individuals with SATB2 -associated syndrome  Academic Article
• New Locus for Skin Intrinsic Fluorescence in Type 1 Diabetes Also Associated With Blood and Skin Glycated Proteins  Academic Article
• New Tools for Investigating the Comparative Biology ofCaenorhabditisbriggsaeandC. elegans  Academic Article
• New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders  Academic Article
• New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk  Academic Article
• No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases  Academic Article
• Non-synonymous polymorphisms in melanocortin-4 receptor protect against obesity: the two facets of a Janus obesity gene  Academic Article
• Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index  Academic Article
• Novel Association of ABO Histo-Blood Group Antigen with Soluble ICAM-1: Results of a Genome-Wide Association Study of 6,578 Women  Academic Article
• Novel Association of HK1 with Glycated Hemoglobin in a Non-Diabetic Population: A Genome-Wide Evaluation of 14,618 Participants in the Women's Genome Health Study  Academic Article
• Novel Associations of CPS1, MUT, NOX4, and DPEP1 With Plasma Homocysteine in a Healthy Population  Academic Article
• Novel Drug Targets for Ischemic Stroke Identified Through Mendelian Randomization Analysis of the Blood Proteome  Academic Article
• Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals  Academic Article
• Novel Loci, Including Those Related to Crohn Disease, Psoriasis, and Inflammation, Identified in a Genome-Wide Association Study of Fibrinogen in 17 686 Women  Academic Article
• Obesity Genes and Risk of Major Depressive Disorder in a Multiethnic Population  Academic Article
• Obesity and Multiple Sclerosis: A Mendelian Randomization Study  Academic Article
• On the Use of Variance per Genotype as a Tool to Identify Quantitative Trait Interaction Effects: A Report from the Women's Genome Health Study  Academic Article
• Oxytocin Receptor Polymorphisms are Differentially Associated with Social Abilities across Neurodevelopmental Disorders  Academic Article
• Paraoxonase promoter and intronic variants modify risk of sporadic amyotrophic lateral sclerosis  Academic Article
• Parental and child genetic contributions to obesity traits in early life based on 83 loci validated in adults: the FAMILY study  Academic Article
• Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study  Academic Article
• Passive Cigarette Smoke Exposure During Various Periods of Life, Genetic Variants, and Breast Cancer Risk Among Never Smokers  Academic Article
• Penetrance of Polygenic Obesity Susceptibility Loci across the Body Mass Index Distribution  Academic Article
• Pharmacogenetic profiling across the irinotecan pathway in Asian patients with cancer  Academic Article
• Phase II trial of vorinostat in advanced melanoma  Academic Article
• Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9  Academic Article
• Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.  Academic Article
• Phylogenetic analysis of emergent Streptococcus pneumoniae serotype 22F causing invasive pneumococcal disease using whole genome sequencing  Academic Article
• Phylogenetic relationship and virulence inference of Streptococcus Anginosus Group: curated annotation and whole-genome comparative analysis support distinct species designation  Academic Article
• Physical activity and genetic predisposition to obesity in a multiethnic longitudinal study  Academic Article
• Physiological and genomic evidence that selection on the transcription factor Epas1 has altered cardiovascular function in high-altitude deer mice  Academic Article
• Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study  Academic Article
• Plasma carboxypeptidase B downregulates inflammatory responses in autoimmune arthritis  Academic Article
• Pleiotropy among Common Genetic Loci Identified for Cardiometabolic Disorders and C-Reactive Protein  Academic Article
• PlexinA polymorphisms mediate the developmental trajectory of human corpus callosum microstructure  Academic Article
• Polygenic Contribution in Individuals With Early-Onset Coronary Artery Disease  Academic Article
• Polymorphic Variation of Genes in the Fibrinolytic System and the Risk of Ovarian Cancer  Academic Article
• Polymorphism in the CETP Gene Region, HDL Cholesterol, and Risk of Future Myocardial Infarction  Academic Article
• Polymorphisms Near TBX5 and GDF7 Are Associated With Increased Risk for Barrett’s Esophagus  Academic Article
• Polymorphisms in the Amino Acid Transporter Solute Carrier Family 6 (Neurotransmitter Transporter) Member 14 Gene Contribute to Polygenic Obesity in French Caucasians  Academic Article
• Polymorphisms in the gene encoding bovine interleukin-10 receptor alpha are associated with Mycobacterium avium ssp. paratuberculosis infection status  Academic Article
• Polymorphisms of 5-HTT LPR and GNβ3 825C>T and Response to Antidepressant Treatment in Functional Dyspepsia: A Study from The Functional Dyspepsia Treatment Trial  Academic Article
• Population-Based Genomewide Genetic Analysis of Common Clinical Chemistry Analytes  Academic Article
• Post Genome-Wide Association Studies of Novel Genes Associated with Type 2 Diabetes Show Gene-Gene Interaction and High Predictive Value  Academic Article
• Prader-Willi syndrome and Tay-Sachs disease in association with mixed maternal uniparental isodisomy and heterodisomy 15 in a girl who also had isochromosome Xq  Academic Article
• Prevalence of Loss-of-Function FTO Mutations in Lean and Obese Individuals  Academic Article
• R125W coding variant in TBC1D1 confers risk for familial obesity and contributes to linkage on chromosome 4p14 in the French population  Academic Article
• RNA-Seq effectively monitors gene expression in Eutrema salsugineum plants growing in an extreme natural habitat and in controlled growth cabinet conditions  Academic Article
• Rank-based genome-wide analysis reveals the association of Ryanodine receptor-2 gene variants with childhood asthma among human populations  Academic Article
• Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions  Academic Article
• Rapid screening of microsatellite markers for polymorphisms using SYBR®Green I and a DNA sequencer  Academic Article
• Rare DNA copy number variants in cardiovascular malformations with extracardiac abnormalities  Academic Article
• Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease  Academic Article
• Rationale and design of GENEiUS: a prospective observational study on the genetic and environmental determinants of body mass index evolution in Canadian undergraduate students  Academic Article
• Reduced hippocampus volume and memory performance in bipolar disorder patients carrying the BDNF val66met met allele  Academic Article
• Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study  Academic Article
• Renin–angiotensin and endothelial nitric oxide synthase gene polymorphisms are not associated with the risk of incident type 2 diabetes mellitus: a prospective cohort study  Academic Article
• Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample  Academic Article
• Resequencing Genomic DNA of Patients With Severe Hypertriglyceridemia (MIM 144650)  Academic Article
• Results of a Pilot Multicenter Genotype-based Randomized Placebo-controlled Trial of Propranolol to Reduce Pain After Major Thermal Burn Injury  Academic Article
• Risk Alleles in/near ADCY5, ADRA2A, CDKAL1, CDKN2A/B, GRB10, and TCF7L2 Elevate Plasma Glucose Levels at Birth and in Early Childhood: Results from the FAMILY Study  Academic Article
• Role of Macrophage Migration Inhibitory Factor in Granulomatosis With Polyangiitis  Conference Paper
• Role of polymorphic bile salt export pump (BSEP, ABCB11) transporters in anti-tuberculosis drug-induced liver injury in a Chinese cohort  Academic Article
• Role of polymorphism of methyltetrahydrofolate-homocysteine methyltransferase (MTR) A2756G and breast cancer risk  Academic Article
• SNPs and coronary heart disease  Academic Article
• SNPs in DNA repair or oxidative stress genes and late subcutaneous fibrosis in patients following single shot partial breast irradiation  Academic Article
• SNPs in the bovine IL-10 receptor are associated with somatic cell score in Canadian dairy bulls  Academic Article
• SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects  Academic Article
• Screening of hypoxia-inducible genes in sporadic ALS  Academic Article
• Second-Pandemic Strain ofVibrio choleraefrom the Philadelphia Cholera Outbreak of 1849  Academic Article
• Secretory granule neuroendocrine protein 1 (SGNE1) genetic variation and glucose intolerance in severe childhood and adult obesity  Academic Article
• Selected polymorphisms in sex hormone-related genes, circulating sex hormones and risk of endometrial cancer  Academic Article
• Sex- and age-interacting eQTLs in human complex diseases  Academic Article
• Should We Have Blind Faith in Bioinformatics Software? Illustrations from the SNAP Web-Based Tool  Academic Article
• Single Nucleotide Polymorphisms Alter the Promoter Activity of Bovine MIF  Academic Article
• Single Nucleotide Polymorphisms in Taste Receptor Genes Are Associated with Snacking Patterns of Preschool-Aged Children in the Guelph Family Health Study: A Pilot Study  Academic Article
• Single nucleotide polymorphism in IL1B is associated with infection risk in paediatric acute myeloid leukaemia  Academic Article
• Single nucleotide polymorphisms in the ectomycorrhizal mushroom Tricholoma matsutake  Academic Article
• Single nucleotide polymorphisms in the neuropeptide Y2 receptor (NPY2R) gene and association with severe obesity in French white subjects  Academic Article
• Smith-Lemli-Opitz syndrome: carrier frequency and spectrum of DHCR7 mutations in Canada  Academic Article
• Stationary phase-induction of G→T mutations in Escherichia coli  Academic Article
• Statistical genetics with application to population-based study design: a primer for clinicians  Academic Article
• Structural Variation of Chromosomes in Autism Spectrum Disorder  Academic Article
• Study of TNFα -308G/A and IL6 -174G/C polymorphisms in type 2 diabetes and obesity risk in the Tunisian population  Academic Article
• Systematic Review and Meta-analysis: Gene Association Studies in Neonatal Sepsis  Academic Article
• TCF7L2 is associated with type 2 diabetes in nonobese individuals from Tunisia  Academic Article
• TCF7L2 rs7903146 variant does not associate with smallness for gestational age in the French population  Academic Article
• TLR5 as an Anti-Inflammatory Target and Modifier Gene in Cystic Fibrosis  Academic Article
• TNF-α −308 G/A polymorphism and responsiveness to TNF-α blockade therapy in moderate to severe rheumatoid arthritis: a systematic review and meta-analysis  Academic Article
• The 9p21.3 locus and cardiovascular risk in familial hypercholesterolemia  Academic Article
• The Effect of Chromosome 9p21 Variants on Cardiovascular Disease May Be Modified by Dietary Intake: Evidence from a Case/Control and a Prospective Study  Academic Article
• The Human Ortholog of Acid-Sensing Ion Channel Gene ASIC1a Is Associated With Panic Disorder and Amygdala Structure and Function  Academic Article
• The Imprinted Gene Neuronatin Is Regulated by Metabolic Status and Associated With Obesity  Academic Article
• The LASSO and Sparse Least Squares Regression Methods for SNP Selection in Predicting Quantitative Traits  Academic Article
• The Q121 Variant of ENPP1 May Protect From Childhood Overweight/obesity in the Italian Population  Academic Article
• The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects  Academic Article
• The association of HBG2 , BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease  Academic Article
• The functional variant rs1048990 in PSMA6 is associated with susceptibility to myocardial infarction in a Chinese population  Academic Article
• The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β0-thalassaemia homozygotes  Academic Article
• The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies  Academic Article
• The genetics of hemoglobin A2regulation in sickle cell anemia  Academic Article
• The genetics of human personality  Academic Article
• The need for inclusion of sex and age of onset variables in genetic association studies of obsessive–compulsive disorder: Overview  Academic Article
• The protective effect of the obesity-associated rs9939609 A variant in fat mass- and obesity-associated gene on depression  Academic Article
• The role of leptin, melanocortin, and neurotrophin system genes on body weight in anorexia nervosa and bulimia nervosa  Academic Article
• The value of studying gene-environment interactions in culturally diverse populations  Academic Article
• Thinking and doing: the effects of dopamine and oxytocin genes and executive function on mothering behaviours  Academic Article
• Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies  Academic Article
• Three New β-Globin Gene Promoter Mutations Identified Through Newborn Screening  Academic Article
• Thrombophilia and location of venous thromboembolism  Academic Article
• Thymic stromal lymphopoietin (TSLP) secretion from human nasal epithelium is a function of TSLP genotype  Academic Article
• Trans-ethnic association study of blood pressure determinants in over 750,000 individuals  Academic Article
• Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders  Academic Article
• Two New Loci for Body-Weight Regulation Identified in a Joint Analysis of Genome-Wide Association Studies for Early-Onset Extreme Obesity in French and German Study Groups  Academic Article
• Type 2 Diabetes Whole-Genome Association Study in Four Populations: The DiaGen Consortium  Academic Article
• Update on bipolar disorder biomarker candidates  Academic Article
• Use of Breed-Specific Single Nucleotide Polymorphisms to Discriminate Between Holstein and Jersey Dairy Cattle Breeds  Academic Article
• Using molecular classification to predict gains in maximal aerobic capacity following endurance exercise training in humans  Academic Article
• Variation at the DPP4 locus influences apolipoprotein B levels in South Asians and exhibits heterogeneity in Europeans related to BMI  Academic Article
• Variation at the NFATC2 Locus Increases the Risk of Thiazolidinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study  Academic Article
• Variation in FTO contributes to childhood obesity and severe adult obesity  Academic Article
• Vascular Endothelial Growth Factor Polymorphisms and Esophageal Cancer Prognosis  Academic Article
• Vitamin D Levels, Vitamin D Receptor Polymorphisms, and Inflammatory Cytokines in Aromatase Inhibitor-Induced Arthralgias: An Analysis of CCTG MA.27  Academic Article
• Vitamin D and Risk of Multiple Sclerosis: A Mendelian Randomization Study  Academic Article
• Vitamin D-Related Genetic Variants, Interactions with Vitamin D Exposure, and Breast Cancer Risk among Caucasian Women in Ontario  Academic Article
• What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations  Academic Article
• Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder  Academic Article
• Whole-Genome SNP Association in the Horse: Identification of a Deletion in Myosin Va Responsible for Lavender Foal Syndrome  Academic Article
• Within-group relatedness is correlated with colony-level social structure and reproductive sharing in a social fish  Academic Article
• Yersinia pestis: New Evidence for an Old Infection  Academic Article
• [Study on polymorphisms of genes with susceptibility to drug induced liver injury in a cohort receiving anti-tuberculosis treatment].  Academic Article
• β+-Thalassemia Trait Due to a Novel Mutation in the β-Globin Gene Promoter: −26 (A>C) [HBB c.−76A>C]  Academic Article