Polymorphism, Single Nucleotide

subject area of

CYP7A1, BAAT and UGT1A1 polymorphisms and susceptibility to anti-tuberculosis drug-induced hepatotoxicity Journal Articles
BDNF Val66Met polymorphism and peripheral protein levels in pediatric bipolar disorder and attention‐deficit/hyperactivity disorder Journal Articles
COL4A2 is associated with lacunar ischemic stroke and deep ICH Journal Articles
DCC gene network in the prefrontal cortex is associated with total brain volume in childhood Journal Articles
PPARA Polymorphism Influences the Cardiovascular Benefit of Fenofibrate in Type 2 Diabetes: Findings From ACCORD-Lipid Journal Articles
p53 Arg72Pro and MDM2 T309G Polymorphisms, Histology, and Esophageal Cancer Prognosis Journal Articles
ABCB1 Gene Variants and Antidepressant Treatment Outcomes: A Systematic Review and Meta‐Analysis Including Results from the CAN‐BIND‐1 Study Journal Articles
A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression Journal Articles
A DNA Switch for Detecting Single Nucleotide Polymorphism within a Long DNA Sequence Under Denaturing Conditions Journal Articles
A DNA Switch for Detecting Single Nucleotide Polymorphism within a Long DNA Sequence Under Denaturing Conditions Journal Articles
A Discovery Resource of Rare Copy Number Variations in Individuals with Autism Spectrum Disorder Journal Articles
A Gene Variant in CERS2 Is Associated with Rate of Increase in Albuminuria in Patients with Diabetes from ONTARGET and TRANSCEND Journal Articles
A Genome-Wide Association Study Identifies a Novel Major Locus for Glycemic Control in Type 1 Diabetes, as Measured by Both A1C and Glucose Journal Articles
A Genome-Wide Association Study for Coronary Artery Disease Identifies a Novel Susceptibility Locus in the Major Histocompatibility Complex Journal Articles
A Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms for Acute Kidney Injury Journal Articles
A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis Journal Articles
A Genome‐Wide Association Study for Venous Thromboembolism: The Extended Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Journal Articles
A High-Resolution Melting Approach for Analyzing Allelic Expression Dynamics Journal Articles
A Multivariate Genome-Wide Association Study of Wing Shape in Drosophila melanogaster Journal Articles
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 Journal Articles
A candidate transacting modulator of fetal hemoglobin gene expression in the Arab—Indian haplotype of sickle cell anemia Journal Articles
A common TLR1 polymorphism is associated with higher parasitaemia in a Southeast Asian population with Plasmodium falciparum malaria Journal Articles
A fast algorithm to optimize SNP prioritization for gene-gene and gene-environment interactions Journal Articles
A functional promoter polymorphism of the δ‐globin gene is a specific marker of the Arab‐Indian haplotype Journal Articles
A genetic link between prepregnancy body mass index, postpartum weight retention, and offspring weight in early childhood Journal Articles
A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease Journal Articles
A genome-wide association study of sporadic ALS in a homogenous Irish population Journal Articles
A genome-wide linkage and association scan reveals novel loci for autism Journal Articles
A genome-wide scan for common alleles affecting risk for autism Journal Articles
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders Journal Articles
A large-scale candidate gene association study of age at menarche and age at natural menopause Journal Articles
A large-scale genome-wide association study meta-analysis of cannabis use disorder Journal Articles
A method to estimate the contribution of regional genetic associations to complex traits from summary association statistics Journal Articles
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder Journal Articles
A novel candidate region for ALS on chromosome 14q11.2 Journal Articles
A novel large deletion and three polymorphisms in the FECH gene associated with erythropoietic protoporphyria Journal Articles
A pharmacogenetic analysis of the Canadian Cancer Trials Group MY.10 clinical trial of maintenance therapy for multiple myeloma Journal Articles
A phased SNP-based classification of sickle cell anemia HBB haplotypes Journal Articles
A phenome-wide association study of a lipoprotein-associated phospholipase A₂loss-of-function variant in 90 000 Chinese adults Journal Articles
A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia Journal Articles
A preliminary analysis of the DNA and diet of the extinct Beothuk: A systematic approach to ancient human DNA Journal Articles
A preliminary pharmacogenetic investigation of adverse events from topiramate in heavy drinkers. Journal Articles
A review of the associations between single nucleotide polymorphisms in taste receptors, eating behaviors, and health Journal Articles
A robust method to estimate regional polygenic correlation under misspecified linkage disequilibrium structure Journal Articles
A systematic review of GWAS identified SNPs associated with outcomes of medications for opioid use disorder Journal Articles
A thymic stromal lymphopoietin polymorphism may provide protection from asthma by altering gene expression Journal Articles
A toolkit for rapid gene mapping in the nematode Caenorhabditis briggsae Journal Articles
A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity Journal Articles
A transforming growth factorbeta1 signal peptide variant increases secretion in vitro and is associated with increased incidence of invasive breast cancer. Journal Articles
A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β⁰‐thalassaemia homozygotes Journal Articles
ACE and Type 2 Diabetes Risk: A Mendelian Randomization Study Journal Articles
AGTR1 gene variation: Association with depression and frontotemporal morphology Journal Articles
APOA5 genetic variants are markers for classic hyperlipoproteinemia phenotypes and hypertriglyceridemia Journal Articles
Abdominal Aortic Aneurysm Is Associated with a Variant in Low-Density Lipoprotein Receptor-Related Protein 1 Journal Articles
Advances in Genomic Analysis of Stroke Journal Articles
An evaluation of logic regression-based biomarker discovery across multiple intergenic regions for predicting host specificity in Escherichia coli Journal Articles
An initial investigation of associations between dopamine-linked genetic variation and smoking motives in African Americans Journal Articles
An intron variant of the GLI family zinc finger 3 (GLI3) gene differentiates resistance training‐induced muscle fiber hypertrophy in younger men Journal Articles
Analysis of Genetic Association of Intestinal Permeability in Healthy First-degree Relatives of Patients with Crohn’s Disease Journal Articles
Analysis of IFT74as a candidate gene for chromosome 9p-linked ALS-FTD Journal Articles
Analysis of IL-6, STAT3 and HSPA1L Gene Polymorphisms in Anti-Tuberculosis Drug-Induced Hepatitis in a Nested Case-Control Study Journal Articles
Angiogenin Levels and ANG Genotypes: Dysregulation in Amyotrophic Lateral Sclerosis Journal Articles
Anti-Epileptic Drug Target Perturbation and Intracranial Aneurysm Risk: Mendelian Randomization and Colocalization Study Journal Articles
Assessing host-specificity of Escherichia coli using a supervised learning logic-regression-based analysis of single nucleotide polymorphisms in intergenic regions Journal Articles
Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations Journal Articles
Association Between a Literature-Based Genetic Risk Score and Cardiovascular Events in Women Journal Articles
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index Journal Articles
Association analyses of the DAOA/G30 and d-amino-acid oxidase genes in schizophrenia: Further evidence for a role in schizophrenia Journal Articles
Association between ADIPOQ gene polymorphisms and the risk of new-onset diabetes mellitus after liver transplantation Journal Articles
Association between C reactive protein and coronary heart disease: mendelian randomisation analysis based on individual participant data Journal Articles
Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data Journal Articles
Association between impulsivity traits and body mass index at the observational and genetic epidemiology level Journal Articles
Association between maternal childhood maltreatment and mother-infant attachment disorganization: Moderation by maternal oxytocin receptor gene and cortisol secretion Journal Articles
Association between phosphodiesterase 4D gene and ischaemic stroke Journal Articles
Association between the FTO rs9939609 polymorphism and the metabolic syndrome in a non-Caucasian multi-ethnic sample Journal Articles
Association between tumor necrosis factor-α promoter −308 A/G polymorphism and susceptibility to sepsis and sepsis mortality: A systematic review and meta-analysis Journal Articles
Association of COX-2 gene haplotypes with prostaglandins production in bronchial asthma Journal Articles
Association of Factor V Leiden With Subsequent Atherothrombotic Events Journal Articles
Association of Granulomatosis With Polyangiitis (Wegener's) With HLA–DPB1*04 and SEMA6A Gene Variants: Evidence From Genome‐Wide Analysis Journal Articles
Association of Variation at the ABO Locus With Circulating Levels of Soluble Intercellular Adhesion Molecule-1, Soluble P-selectin, and Soluble E-selectin Journal Articles
Association of alpha4beta2 nicotinic receptor and heavy smoking in schizophrenia. Journal Articles
Association of common variants in the human eyes shut ortholog (EYS) with statin‐induced myopathy: Evidence for additional functions of EYS Journal Articles
Association of heart rate and diabetes among 0.5 million adults in the China Kadoorie biobank: Results from observational and Mendelian randomization analyses Journal Articles
Association of polymorphisms in drug transporter genes (SLCO1B1 and SLC10A1) and anti-tuberculosis drug-induced hepatotoxicity in a Chinese cohort Journal Articles
Association of renin–angiotensin and endothelial nitric oxide synthase gene polymorphisms with blood pressure progression and incident hypertension: prospective cohort study Journal Articles
Association study of brain‐derived neurotrophic factor (BDNF) and LIN‐7 homolog (LIN‐7) genes with adult attention‐deficit/hyperactivity disorder Journal Articles
Association study of tryptophan hydroxylase 2 gene polymorphisms in bipolar disorder patients with panic disorder comorbidity Journal Articles
Associations between parenting behavior and anxiety in a rodent model and a clinical sample: relationship to peripheral BDNF levels Journal Articles
Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn’s disease subjects Journal Articles
Associations of the FTO rs9939609 variant with discrete body fat depots and dietary intake in a multi-ethnic cohort Journal Articles
BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia Journal Articles
BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies Journal Articles
BCL11A represses HBG transcription in K562 cells Journal Articles
BDNF-Dependent Effects on Amygdala–Cortical Circuitry and Depression Risk in Children and Youth Journal Articles
BRCA2 Variants and cardiovascular disease in a multi-ethnic study Journal Articles
Bayesian methods for meta‐analysis of causal relationships estimated using genetic instrumental variables Journal Articles
Bioinformatic analyses identifies novel protein-coding pharmacogenomic markers associated with paclitaxel sensitivity in NCI60 cancer cell lines Journal Articles
Biological, clinical and population relevance of 95 loci for blood lipids Journal Articles
Bipolar disorder and 1513A>C P2RX7 polymorphism frequency Journal Articles
Birth weight interacts with a functional variant of the oxytocin receptor gene (OXTR) to predict executive functioning in children Journal Articles
Blood CSF1 and CXCL12 as Causal Mediators of Coronary Artery Disease Journal Articles
Blood HER2 and Uromodulin as Causal Mediators of CKD Journal Articles
Brain-derived neurotrophic factor gene val66met polymorphism and executive functioning in patients with bipolar disorder Journal Articles
Brain-derived neurotrophic factor variants are associated with childhood-onset mood disorder: confirmation in a Hungarian sample Journal Articles
CADM2 is implicated in impulsive personality and numerous other traits by genome- and phenome-wide association studies in humans and mice Journal Articles
CYP2D6 Genotype as a Marker for Benefit of Adjuvant Tamoxifen in Postmenopausal Women: Lessons Learned Journal Articles
Caenorhabditis briggsae Recombinant Inbred Line Genotypes Reveal Inter-Strain Incompatibility and the Evolution of Recombination Journal Articles
Cancer Antigen 15-3/Mucin 1 Levels in CCTG MA.32: A Breast Cancer Randomized Trial of Metformin vs Placebo Journal Articles
Cannabis use and risk of schizophrenia: a Mendelian randomization study Journal Articles
Causal Effects of Body Mass Index on Cardiometabolic Traits and Events: A Mendelian Randomization Analysis Journal Articles
Causal Relationship between Adiponectin and Metabolic Traits: A Mendelian Randomization Study in a Multiethnic Population Journal Articles
Causes and Consequences of Genetic Background Effects Illuminated by Integrative Genomic Analysis Journal Articles
Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4) Journal Articles
Cervical artery dissection: Pathology, epidemiology and management Journal Articles
Characterization of tumor necrosis factor–α block haplotypes associated with susceptibility to chronic venous leg ulcers in Caucasian patients Journal Articles
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome Journal Articles
Clinical evaluation of a hemochromatosis next‐generation sequencing gene panel Journal Articles
Collagen platelet receptor polymorphisms integrin α2β1 C807T and GPVI Q317L and risk of ischemic stroke Journal Articles
Comment on “DNA from Pre-Clovis Human Coprolites in Oregon, North America” Journal Articles
Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries Journal Articles
Common coding variant in SERPINA1 increases the risk for large artery stroke Journal Articles
Common genetic variation near MC4R is associated with eating behaviour patterns in European populations Journal Articles
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease Journal Articles
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus Journal Articles
Comparative Genome Analysis Provides Insights into the Evolution and Adaptation of Pseudomonas syringae pv. aesculi on Aesculus hippocastanum Journal Articles
Comparative genomic and genetic analysis of glioblastoma-derived brain tumor-initiating cells and their parent tumors Journal Articles
Comparison of biochemical and genotypic speciation methods for vancomycin-resistant enterococci isolated from urban wastewater treatment plants Journal Articles
Comprehensive Analysis of Genomic Variation in the LPA Locus and Its Relationship to Plasma Lipoprotein(a) in South Asians, Chinese, and European Caucasians Journal Articles
Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies Journal Articles
Concept, Design and Implementation of a Cardiovascular Gene-Centric 50 K SNP Array for Large-Scale Genomic Association Studies Journal Articles
Contribution of BDNF and DRD2 genetic polymorphisms to continued opioid use in patients receiving methadone treatment for opioid use disorder: an observational study Journal Articles
Contribution of Large Region Joint Associations to Complex Traits Genetics Journal Articles
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 Journal Articles
Correction of Population Stratification in Large Multi-Ethnic Association Studies Journal Articles
Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection Journal Articles
Cytochrome P450 2E1 Gene Polymorphisms/Haplotypes and Anti-Tuberculosis Drug-Induced Hepatitis in a Chinese Cohort Journal Articles
DNA Damage Repair in Huntington’s Disease and Other Neurodegenerative Diseases Journal Articles
Decreased comfort food intake and allostatic load in adolescents carrying the A3669G variant of the glucocorticoid receptor gene Journal Articles
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis Journal Articles
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 Journal Articles
Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray Journal Articles
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals Journal Articles
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes Journal Articles
Does genetic heterogeneity account for the divergent risk of type 2 diabetes in South Asian and white European populations? Journal Articles
Dopamine receptors D1 and D2 are related to observed maternal behavior Journal Articles
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 Journal Articles
Early evolutionary loss of the lipid A modifying enzyme PagP resulting in innate immune evasion inYersinia pestis Journal Articles
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 Journal Articles
Effect of Bile Acid Sequestrants on the Risk of Cardiovascular Events Journal Articles
Effect of Genetic Variants Associated With Plasma Homocysteine Levels on Stroke Risk Journal Articles
Effects of Multiple Genetic Loci on Age at Onset in Late-Onset Alzheimer Disease Journal Articles
Elevated Lipoprotein(a) and Risk of Atrial Fibrillation Journal Articles
Enzymatic Litmus Test for Selective Colorimetric Detection of C–C Single Nucleotide Polymorphisms Journal Articles
Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALS Journal Articles
Evidence of Naturalized Stress-Tolerant Strains of Escherichia coli in Municipal Wastewater Treatment Plants Journal Articles
Evidence that Egfr Contributes to Cryptic Genetic Variation for Photoreceptor Determination in Natural Populations of Drosophila melanogaster Journal Articles
Exome Sequencing as a Diagnostic Tool for Pediatric‐Onset Ataxia Journal Articles
Expression of a Common LQT1 Mutation in Five Apparently Unrelated Families in a Regional Inherited Arrhythmia Clinic Journal Articles
FUT2 genotype and secretory status are not associated with fecal microbial composition and inferred function in healthy subjects Journal Articles
Favourable IFNL3 Genotypes Are Associated with Spontaneous Clearance and Are Differentially Distributed in Aboriginals in Canadian HIV-Hepatitis C Co-Infected Individuals Journal Articles
Fetal hemoglobin in sickle cell anemia: Molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans Journal Articles
Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans Journal Articles
Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5′ olfactory receptor gene cluster Journal Articles
Fibroblast Growth Factor-23 and Risk of Cardiovascular Diseases Journal Articles
Fine Mapping of the Insulin-Induced Gene 2 Identifies a Variant Associated With LDL Cholesterol and Total Apolipoprotein B Levels Journal Articles
Forty-Three Loci Associated with Plasma Lipoprotein Size, Concentration, and Cholesterol Content in Genome-Wide Analysis Journal Articles
GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability Journal Articles
GWAS-based machine learning approach to predict duloxetine response in major depressive disorder Journal Articles
Gene × Physical Activity Interactions in Obesity: Combined Analysis of 111,421 Individuals of European Ancestry Journal Articles
Gene-Centric Meta-Analysis of Lipid Traits in African, East Asian and Hispanic Populations Journal Articles
Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci Journal Articles
Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals Journal Articles
Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders Journal Articles
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 Journal Articles
Genetic Control of Vulval Development inCaenorhabditis briggsae Journal Articles
Genetic Determinants of Dabigatran Plasma Levels and Their Relation to Bleeding Journal Articles
Genetic Determinants of “Cognitive Impairment, No Dementia” Journal Articles
Genetic Dissection of Diabetes: Facing the Giant Journal Articles
Genetic Information and the Prediction of Incident Type 2 Diabetes in a High-Risk Multiethnic Population Journal Articles
Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium Journal Articles
Genetic Loci Associated With C-Reactive Protein Levels and Risk of Coronary Heart Disease Journal Articles
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 Journal Articles
Genetic Predictors of Cardiovascular Mortality During Intensive Glycemic Control in Type 2 Diabetes: Findings From the ACCORD Clinical Trial Journal Articles
Genetic Risk Evaluation in Wet Age-Related Macular Degeneration Treatment Response Journal Articles
Genetic Risk Factors for Post-Infectious Irritable Bowel Syndrome Following a Waterborne Outbreak of Gastroenteritis Journal Articles
Genetic Susceptibility for Atrial Fibrillation in Patients Undergoing Atrial Fibrillation Ablation Journal Articles
Genetic Tools for Coronary Risk Assessment in Type 2 Diabetes: A Cohort Study From the ACCORD Clinical Trial Journal Articles
Genetic Variants Associated With Myocardial Infarction Risk Factors in Over 8000 Individuals From Five Ethnic Groups Journal Articles
Genetic Variants and Susceptibility to Neurological Complications Following West Nile Virus Infection Journal Articles
Genetic Variants in Vitamin D Pathway Genes and Risk of Pancreas Cancer; Results from a Population-Based Case-Control Study in Ontario, Canada Journal Articles
Genetic Variations of TAP1 Gene Exon 3 Affects Gene Expression and Escherichia coli F18 Resistance in Piglets Journal Articles
Genetic analysis of impulsive personality traits: Examination of a priori candidates and genome-wide variation Journal Articles
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits Journal Articles
Genetic biomarkers associated with changes in quality of life and pain following palliative radiotherapy in patients with bone metastases Journal Articles
Genetic biomarkers associated with pain flare and dexamethasone response following palliative radiotherapy in patients with painful bone metastases Journal Articles
Genetic determinants of plasma triglycerides Journal Articles
Genetic determinants of right-ventricular remodeling after tetralogy of Fallot repair Journal Articles
Genetic determinants of warfarin maintenance dose and time in therapeutic treatment range: a RE-LY genomics substudy Journal Articles
Genetic influences on ADHD symptom dimensions: Examination of a priori candidates, gene‐based tests, genome‐wide variation, and SNP heritability Journal Articles
Genetic influences on delayed reward discounting: A genome-wide prioritized subset approach. Journal Articles
Genetic loci associated with delayed clearance of Plasmodium falciparum following artemisinin treatment in Southeast Asia Journal Articles
Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration Journal Articles
Genetic predictors of response to treatment with citalopram in depression secondary to traumatic brain injury Journal Articles
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs Journal Articles
Genetic studies of fetal hemoglobin in the Arab‐Indian haplotype sickle cell‐β⁰ thalassemia Journal Articles
Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedema Journal Articles
Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes Journal Articles
Genetic variants of MARCO are associated with susceptibility to pulmonary tuberculosis in a Gambian population Journal Articles
Genetic variation in hyaluronan metabolism loci is associated with plasma plasminogen activator inhibitor-1 concentration Journal Articles
Genetic variation in oxytocin rs2740210 and early adversity associated with postpartum depression and breastfeeding duration Journal Articles
Genetically decreased vitamin D and risk of Alzheimer disease Journal Articles
Genetically determined P2X7 receptor pore formation regulates variability in chronic pain sensitivity Journal Articles
Genetically proxied therapeutic inhibition of antihypertensive drug targets and risk of common cancers: A mendelian randomization analysis Journal Articles
Gene‐ or region‐based analysis of genome‐wide association studies Journal Articles
Genome Wide Association Identifies Common Variants at the SERPINA6/SERPINA1 Locus Influencing Plasma Cortisol and Corticosteroid Binding Globulin Journal Articles
Genome sequence of the Brown Norway rat yields insights into mammalian evolution Journal Articles
Genome-Wide Association Analysis of Soluble ICAM-1 Concentration Reveals Novel Associations at the NFKBIK, PNPLA3, RELA, and SH2B3 Loci Journal Articles
Genome-Wide Association Studies—Data Generation, Storage, Interpretation, and Bioinformatics Journal Articles
Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke Journal Articles
Genome-Wide Associations and Functional Genomic Studies of Musculoskeletal Adverse Events in Women Receiving Aromatase Inhibitors Journal Articles
Genome-wide Association Analysis of Blood-Pressure Traits in African-Ancestry Individuals Reveals Common Associated Genes in African and Non-African Populations Journal Articles
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets Journal Articles
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences Journal Articles
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk Journal Articles
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Journal Articles
Genome-wide association studies identify loci associated with age at menarche and age at natural menopause Journal Articles
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis Journal Articles
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 Journal Articles
Genome-wide association study identifies 48 common genetic variants associated with handedness Journal Articles
Genome-wide association study identifies a novel maternal gene × stress interaction associated with spontaneous preterm birth Journal Articles
Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry Journal Articles
Genome-wide association study of sepsis in extremely premature infants Journal Articles
Genome-wide meta-analyses identify multiple loci associated with smoking behavior Journal Articles
Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke Journal Articles
Genome-wide studies to identify risk factors for kidney disease with a focus on patients with diabetes Journal Articles
Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders Journal Articles
Genome‐wide association study of alcohol use disorder identification test (AUDIT) scores in 20 328 research participants of European ancestry Journal Articles
Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases Journal Articles
Genomic basis of delayed reward discounting Journal Articles
Genotype-Positive Status in Patients With Hypertrophic Cardiomyopathy Is Associated With Higher Rates of Heart Failure Events Journal Articles
Genotypic and Phenotypic Analyses of Two “Isogenic” Strains of the Human Fungal Pathogen Cryptococcus neoformans var. neoformans Journal Articles
Germline variation in inflammation-related pathways and risk of Barrett's oesophagus and oesophageal adenocarcinoma Journal Articles
Germline variation in the insulin-like growth factor pathway and risk of Barrett’s esophagus and esophageal adenocarcinoma Journal Articles
Getting Closer to P-Selectin Journal Articles
Global DNA methylation and one-carbon metabolism gene polymorphisms and the risk of breast cancer in the Sister Study Journal Articles
Glucocorticoid Receptors, Brain-Derived Neurotrophic Factor, Serotonin and Dopamine Neurotransmission are Associated with Interferon-Induced Depression Journal Articles
Gluten-induced RNA methylation changes regulate intestinal inflammation via allele-specific XPO1 translation in epithelial cells Journal Articles
Growth Differentiation Factor 15 as a Novel Biomarker for Metformin Journal Articles
HS3ST1 genotype regulates antithrombin's inflammomodulatory tone and associates with atherosclerosis Journal Articles
Hierarchical investigation of genetic influences on response inhibition in healthy young adults. Journal Articles
High resolution mapping in the major histocompatibility complex region identifies multiple independent novel loci for psoriatic arthritis Journal Articles
Homozygosity for a haplotype in the HBG2‐OR51B4 region is exclusive to Arab‐Indian haplotype sickle cell anemia Journal Articles
Host Genetic Determinants Associated With Helicobacter pylori Eradication Treatment Failure: A Systematic Review and Meta-analysis Journal Articles
Human milk fatty acid composition is associated with dietary, genetic, sociodemographic, and environmental factors in the CHILD Cohort Study Journal Articles
Hundreds of variants clustered in genomic loci and biological pathways affect human height Journal Articles
IFITM3 and Susceptibility to Respiratory Viral Infections in the Community Journal Articles
IL-10R Polymorphisms Are Associated with Very-early-onset Ulcerative Colitis Journal Articles
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 Journal Articles
Identification and functional analysis ofCITED2 mutations in patients with congenital heart defects Journal Articles
Identification of Circulating Proteins Associated With Blood Pressure Using Mendelian Randomization Journal Articles
Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody–Associated Vasculitis Journal Articles
Identification of a New δ Chain Hemoglobin Variant in a β-Thalassemia Carrier: Hb A₂-MUMC [δ13(A10)Ala → Asp] Journal Articles
Identification of genetic effects underlying type 2 diabetes in South Asian and European populations Journal Articles
Identification of genetic variants associated with susceptibility to West Nile virus neuroinvasive disease Journal Articles
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease Journal Articles
Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study Journal Articles
Identifying gene–gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts Journal Articles
Immunochip Analysis Identifies Multiple Susceptibility Loci for Systemic Sclerosis Journal Articles
Impact of ACE2 gene polymorphism on antihypertensive efficacy of ACE inhibitors Journal Articles
Impact of a Genetic Risk Score on Myocardial Infarction Risk Across Different Ethnic Populations Journal Articles
Implications of OPRM1 and CYP2B6 variants on treatment outcomes in methadone-maintained patients in Ontario: Exploring sex differences Journal Articles
Imputation of missing genotypes: an empirical evaluation of IMPUTE Journal Articles
Increased Substitution Rates Surrounding Low-Complexity Regions within Primate Proteins Journal Articles
Individual common variants exert weak effects on the risk for autism spectrum disorders Journal Articles
Influence of RGS2 on Sertraline Treatment for Social Anxiety Disorder Journal Articles
Inhibition of Metabotropic Glutamate Receptor Signaling by the Huntingtin-binding Protein Optineurin Journal Articles
Initial Evidence that OPRM1 Genotype Moderates Ventral and Dorsal Striatum Functional Connectivity During Alcohol Cues Journal Articles
Insights into the Development and Evolution of Exaggerated Traits Using De Novo Transcriptomes of Two Species of Horned Scarab Beetles Journal Articles
Integrated genome-wide methylation and expression analyses reveal functional predictors of response to antidepressants Journal Articles
Interaction between Oxytocin Genotypes and Early Experience Predicts Quality of Mothering and Postpartum Mood Journal Articles
Interleukin-4 and interleukin-10 polymorphisms and antituberculosis drug-induced hepatotoxicity in Chinese population Journal Articles
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 Journal Articles
Investigation of the dopamine D5 receptor gene (DRD5) in adult attention deficit hyperactivity disorder Journal Articles
Investigation on ERCC5 genetic polymorphisms and the development of gastric cancer in a Chinese population Journal Articles
Is There a Genetic Predisposition to Anterior Cruciate Ligament Tear? A Systematic Review Journal Articles
Isolation, Sequence, Infectivity, and Replication Kinetics of Severe Acute Respiratory Syndrome Coronavirus 2 Journal Articles
K45R variant of squalene synthase increases total cholesterol levels in two study samples from a French Canadian population Journal Articles
Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies Journal Articles
Lack of Association of Ghrelin Precursor Gene Variants and Percentage Body Fat or Serum Lipid Profiles Journal Articles
Lack of association between type 2 diabetes and major depression: epidemiologic and genetic evidence in a multiethnic population Journal Articles
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass Journal Articles
Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci Journal Articles
Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci Journal Articles
Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness Journal Articles
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease Journal Articles
Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility Journal Articles
Leveraging cell type specific regulatory regions to detect SNPs associated with tissue factor pathway inhibitor plasma levels Journal Articles
Linkage analysis for three coagulation factors clustering on chromosome 13q34: factor VII, factor X and protein Z Journal Articles
Linkage and association analysis in pedigrees from different populations Journal Articles
Lipoprotein(a): An independent, genetic, and causal factor for cardiovascular disease and acute myocardial infarction Journal Articles
Loci Related to Metabolic-Syndrome Pathways Including LEPR,HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study Journal Articles
Loci influencing blood pressure identified using a cardiovascular gene-centric array Journal Articles
Longitudinal Data Analysis in Genome‐Wide Association Studies Journal Articles
Longitudinal relationships between glycemic status and body mass index in a multiethnic study: evidence from observational and genetic epidemiology Journal Articles
Low prevalence of JAK2 V617F mutation in patients with first unprovoked venous thromboembolism Journal Articles
MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis Journal Articles
Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2 Journal Articles
Maternal childhood adversity and child temperament: An association moderated by child 5‐HTTLPR genotype Journal Articles
Mendelian Randomization Studies Do Not Support a Role for Vitamin D in Coronary Artery Disease Journal Articles
Mendelian randomisation, triglycerides, and CHD Journal Articles
Mendelian randomization analysis supports the causal role of dysglycaemia and diabetes in the risk of coronary artery disease Journal Articles
Mendelian randomization of blood lipids for coronary heart disease Journal Articles
Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin Journal Articles
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways Journal Articles
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution Journal Articles
Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12 Journal Articles
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease Journal Articles
Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height Journal Articles
Meta-analysis of SNPs involved in variance heterogeneity using Levene’s test for equal variances Journal Articles
Meta-analysis of genetic association studies under heterogeneity Journal Articles
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 Journal Articles
Methylenetetrahydrofolate Reductase Gene Variant (MTHFR C677T) and Migraine: A Case Control Study and Meta-analysis Journal Articles
Mineralocorticoid receptor genotype moderates the association between physical neglect and serum BDNF Journal Articles
Moderating effect of PLIN4 genetic variant on impulsivity traits in 5-year-old-children born small for gestational age Journal Articles
Moderators of Naltrexone’s Effects on Drinking, Urge, and Alcohol Effects in Non‐Treatment‐Seeking Heavy Drinkers in the Natural Environment Journal Articles
Modulation of GLP-1 Levels by a Genetic Variant That Regulates the Cardiovascular Effects of Intensive Glycemic Control in ACCORD Journal Articles
Molecular breakpoint mapping of 6q11‐q14 interstitial deletions in seven patients Journal Articles
Molecular genetic analysis of severe protein C deficiency. Journal Articles
Multi-Ethnic Genetic Association Study of Carotid Intima-Media Thickness Using a Targeted Cardiovascular SNP Microarray Journal Articles
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation Journal Articles
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes Journal Articles
Multigene panels in prostate cancer risk assessment. Journal Articles
Multigene panels in prostate cancer risk assessment: a systematic review Journal Articles
Multilocus sequence analyses reveal extensive diversity and multiple origins of fluconazole resistance in Candida tropicalis from tropical China Journal Articles
Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis Journal Articles
Multiple loci associated with indices of renal function and chronic kidney disease Journal Articles
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma Journal Articles
Multivariate analysis of complex gene expression and clinical phenotypes with genetic marker data Journal Articles
Mycoplasma genitalium Antibiotic Resistance–Mediating Mutations in Canadian Women With or Without Chlamydia Trachomatis Infection Journal Articles
NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant inNCF2that results in reduced binding to RAC2 Journal Articles
NCAM1-TTC12-ANKK1-DRD2 variants and smoking motives as intermediate phenotypes for nicotine dependence Journal Articles
Natural history and genotype‐phenotype correlations in 72 individuals with SATB2‐associated syndrome Journal Articles
New Locus for Skin Intrinsic Fluorescence in Type 1 Diabetes Also Associated With Blood and Skin Glycated Proteins Journal Articles
New Tools for Investigating the Comparative Biology of Caenorhabditis briggsae and C. elegans Journal Articles
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders Journal Articles
Novel Association of ABO Histo-Blood Group Antigen with Soluble ICAM-1: Results of a Genome-Wide Association Study of 6,578 Women Journal Articles
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 Journal Articles
Novel Associations of CPS1, MUT, NOX4, and DPEP1 With Plasma Homocysteine in a Healthy Population Journal Articles
Novel Drug Targets for Ischemic Stroke Identified Through Mendelian Randomization Analysis of the Blood Proteome Journal Articles
Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals Journal Articles
Novel Loci, Including Those Related to Crohn Disease, Psoriasis, and Inflammation, Identified in a Genome-Wide Association Study of Fibrinogen in 17 686 Women Journal Articles
Obesity Genes and Risk of Major Depressive Disorder in a Multiethnic Population Journal Articles
Obesity and Multiple Sclerosis: A Mendelian Randomization Study Journal Articles
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 Journal Articles
Oxytocin Receptor Polymorphisms are Differentially Associated with Social Abilities across Neurodevelopmental Disorders Journal Articles
Paraoxonase promoter and intronic variants modify risk of sporadic amyotrophic lateral sclerosis Journal Articles
Parental and child genetic contributions to obesity traits in early life based on 83 loci validated in adults: the FAMILY study Journal Articles
Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study Journal Articles
Passive Cigarette Smoke Exposure During Various Periods of Life, Genetic Variants, and Breast Cancer Risk Among Never Smokers Journal Articles
Penetrance of Polygenic Obesity Susceptibility Loci across the Body Mass Index Distribution Journal Articles
Phase II trial of vorinostat in advanced melanoma Journal Articles
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 Journal Articles
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative. Journal Articles
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiative Journal Articles
Phylogenetic analysis of emergent Streptococcus pneumoniae serotype 22F causing invasive pneumococcal disease using whole genome sequencing Journal Articles
Phylogenetic relationship and virulence inference of Streptococcus Anginosus Group: curated annotation and whole-genome comparative analysis support distinct species designation Journal Articles
Physical activity and genetic predisposition to obesity in a multiethnic longitudinal study Journal Articles
Physiological and genomic evidence that selection on the transcription factor Epas1 has altered cardiovascular function in high-altitude deer mice Journal Articles
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study Journal Articles
Pleiotropy among Common Genetic Loci Identified for Cardiometabolic Disorders and C-Reactive Protein Journal Articles
PlexinA polymorphisms mediate the developmental trajectory of human corpus callosum microstructure Journal Articles
Polygenic Contribution in Individuals With Early-Onset Coronary Artery Disease Journal Articles
Polymorphism in the CETP Gene Region, HDL Cholesterol, and Risk of Future Myocardial Infarction Journal Articles
Polymorphisms Near TBX5 and GDF7 Are Associated With Increased Risk for Barrett’s Esophagus Journal Articles
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 Journal Articles
Population-Based Genomewide Genetic Analysis of Common Clinical Chemistry Analytes Journal Articles
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 Journal Articles
Prefrontal Cortex Dopamine Transporter Gene Network Moderates the Effect of Perinatal Hypoxic-Ischemic Conditions on Cognitive Flexibility and Brain Gray Matter Density in Children Journal Articles
RNA-Seq effectively monitors gene expression in Eutrema salsugineum plants growing in an extreme natural habitat and in controlled growth cabinet conditions Journal Articles
Rank-based genome-wide analysis reveals the association of Ryanodine receptor-2 gene variants with childhood asthma among human populations Journal Articles
Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions Journal Articles
Rapid detection of single nucleotide polymorphisms associated with spinal muscular atrophy by use of a reusable fibre-optic biosensor Journal Articles
Rapid screening of microsatellite markers for polymorphisms using SYBR^® Green I and a DNA sequencer Journal Articles
Rare DNA copy number variants in cardiovascular malformations with extracardiac abnormalities Journal Articles
Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes Journal Articles
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease Journal Articles
Rationale and design of GENEiUS: a prospective observational study on the genetic and environmental determinants of body mass index evolution in Canadian undergraduate students Journal Articles
Real-Time RT-PCR Allelic Discrimination Assay for Detection of N501Y Mutation in the Spike Protein of SARS-CoV-2 Associated with B.1.1.7 Variant of Concern Journal Articles
Recent developments in the genetic history of East Asia and Oceania Journal Articles
Reduced hippocampus volume and memory performance in bipolar disorder patients carrying the BDNF val66met met allele Journal Articles
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 Journal Articles
Relationship Between Genetic Risk and Age of Diagnosis in Systemic Lupus Erythematosus Journal Articles
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 Journal Articles
Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample Journal Articles
Resequencing Genomic DNA of Patients With Severe Hypertriglyceridemia (MIM 144650) Journal Articles
Results of a Pilot Multicenter Genotype-based Randomized Placebo-controlled Trial of Propranolol to Reduce Pain After Major Thermal Burn Injury Journal Articles
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 Journal Articles
Role of Macrophage Migration Inhibitory Factor in Granulomatosis With Polyangiitis Conferences
Role of polymorphic bile salt export pump (BSEP, ABCB11) transporters in anti-tuberculosis drug-induced liver injury in a Chinese cohort Journal Articles
Role of polymorphism of methyltetrahydrofolate-homocysteine methyltransferase (MTR) A2756G and breast cancer risk Journal Articles
SNP Panel and Genomic Sex Identification in Atlantic Halibut (Hippoglossus hippoglossus) Journal Articles
SNPs and coronary heart disease Journal Articles
SNPs in DNA repair or oxidative stress genes and late subcutaneous fibrosis in patients following single shot partial breast irradiation Journal Articles
SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects Journal Articles
Screening of hypoxia-inducible genes in sporadic ALS Journal Articles
Second-Pandemic Strain ofVibrio choleraefrom the Philadelphia Cholera Outbreak of 1849 Journal Articles
Selected polymorphisms in sex hormone-related genes, circulating sex hormones and risk of endometrial cancer Journal Articles
Serum magnesium and calcium levels in relation to ischemic stroke Journal Articles
Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes: Evidence from genome‐wide association studies Journal Articles
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 Journal Articles
Single nucleotide polymorphism in IL1B is associated with infection risk in paediatric acute myeloid leukaemia Journal Articles
Single nucleotide polymorphisms in the ectomycorrhizal mushroom Tricholoma matsutake Journal Articles
Single nucleotide polymorphisms in the matrix metalloproteinase gene family and the frequency and duration of gastroesophageal reflux disease influence the risk of esophageal adenocarcinoma Journal Articles
Smith-Lemli-Opitz syndrome: carrier frequency and spectrum of DHCR7 mutations in Canada Journal Articles
Stationary phase-induction of G→T mutations in Escherichia coli Journal Articles
Statistical genetics with application to population-based study design: a primer for clinicians Journal Articles
StrandAdvantage test for early‐line and advanced‐stage treatment decisions in solid tumors Journal Articles
Structural Variation of Chromosomes in Autism Spectrum Disorder Journal Articles
Systematic Review and Meta-analysis: Gene Association Studies in Neonatal Sepsis Journal Articles
TLR5 as an Anti-Inflammatory Target and Modifier Gene in Cystic Fibrosis Journal Articles
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 Journal Articles
The 9p21.3 locus and cardiovascular risk in familial hypercholesterolemia Journal Articles
The Effect of Chromosome 9p21 Variants on Cardiovascular Disease May Be Modified by Dietary Intake: Evidence from a Case/Control and a Prospective Study Journal Articles
The Genetic Factors of the Airway Epithelium Associated with the Pathology of Asthma Journal Articles
The Human Ortholog of Acid-Sensing Ion Channel Gene ASIC1a Is Associated With Panic Disorder and Amygdala Structure and Function Journal Articles
The LASSO and Sparse Least Squares Regression Methods for SNP Selection in Predicting Quantitative Traits Journal Articles
The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease Journal Articles
The functional variant rs1048990 in PSMA6 is associated with susceptibility to myocardial infarction in a Chinese population Journal Articles
The genetic basis of asymptomatic codon 8 frame‐shift (HBB:c25_26delAA) β⁰‐thalassaemia homozygotes Journal Articles
The genetics of hemoglobin A₂ regulation in sickle cell anemia Journal Articles
The genetics of human personality Journal Articles
The need for inclusion of sex and age of onset variables in genetic association studies of obsessive–compulsive disorder: Overview Journal Articles
The protective effect of the obesity-associated rs9939609 A variant in fat mass- and obesity-associated gene on depression Journal Articles
The value of studying gene-environment interactions in culturally diverse populations Journal Articles
Thinking and doing: the effects of dopamine and oxytocin genes and executive function on mothering behaviours Journal Articles
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies Journal Articles
Three New β-Globin Gene Promoter Mutations Identified Through Newborn Screening Journal Articles
Thrombophilia and location of venous thromboembolism Journal Articles
Thymic stromal lymphopoietin (TSLP) secretion from human nasal epithelium is a function of TSLP genotype Journal Articles
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals Journal Articles
Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders Journal Articles
Update on bipolar disorder biomarker candidates Journal Articles
Using molecular classification to predict gains in maximal aerobic capacity following endurance exercise training in humans Journal Articles
Variation at the NFATC2 Locus Increases the Risk of Thiazolidinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study Journal Articles
Variation at the DPP4 locus influences apolipoprotein B levels in South Asians and exhibits heterogeneity in Europeans related to BMI Journal Articles
Vascular Endothelial Growth Factor Polymorphisms and Esophageal Cancer Prognosis Journal Articles
Vitamin D Levels, Vitamin D Receptor Polymorphisms, and Inflammatory Cytokines in Aromatase Inhibitor-Induced Arthralgias: An Analysis of CCTG MA.27 Journal Articles
Vitamin D and Risk of Multiple Sclerosis: A Mendelian Randomization Study Journal Articles
Vitamin D levels and risk of type 1 diabetes: A Mendelian randomization study Journal Articles
Vitamin D-Related Genetic Variants, Interactions with Vitamin D Exposure, and Breast Cancer Risk among Caucasian Women in Ontario Journal Articles
What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations Journal Articles
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder Journal Articles
Whole-Genome SNP Association in the Horse: Identification of a Deletion in Myosin Va Responsible for Lavender Foal Syndrome Journal Articles
Within‐group relatedness is correlated with colony‐level social structure and reproductive sharing in a social fish Journal Articles
Yersinia pestis: New Evidence for an Old Infection Journal Articles
[Study on polymorphisms of genes with susceptibility to drug induced liver injury in a cohort receiving anti-tuberculosis treatment]. Journal Articles
β⁺-Thalassemia Trait Due to a Novel Mutation in the β-Globin Gene Promoter: −26 (A>C) [HBB c.−76A>C] Journal Articles

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