Genetic Predisposition to Disease

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CYP7A1, BAAT and UGT1A1 polymorphisms and susceptibility to anti-tuberculosis drug-induced hepatotoxicity Journal Articles
4-phenylbutyrate and valproate treatment attenuates the progression of atherosclerosis and stabilizes existing plaques Journal Articles
50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosis Journal Articles
BRCA1 and BRCA2 Mutation Carriers, Oral Contraceptive Use, and Breast Cancer Before Age 50 Journal Articles
CDKN2AMutations in Multiple Primary Melanomas Journal Articles
CYP2E1,GSTM1andGSTT1genetic polymorphisms and susceptibility to antituberculosis drug-induced hepatotoxicity: a nested case-control study Journal Articles
Per3 length polymorphism in patients with type 2 diabetes mellitus Journal Articles
SCYL1 disease and liver transplantation diagnosed by reanalysis of exome sequencing and deletion/duplication analysis of SCYL1 Journal Articles
A 23bp Insertion in the Endothelial Protein C Receptor (EPCR) Gene Impairs EPCR Function Journal Articles
A C19MC-LIN28A-MYCN Oncogenic Circuit Driven by Hijacked Super-enhancers Is a Distinct Therapeutic Vulnerability in ETMRs: A Lethal Brain Tumor Journal Articles
A FLEXIBLE NONPARAMETRIC APPROACH TO FIND CANDIDATE GENES ASSOCIATED WITH DISEASE IN MICROARRAY EXPERIMENTS 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 Prospective Study of Autistic-Like Traits in Unaffected Siblings of Probands With Autism Spectrum Disorder Journal Articles
A biallelic pathogenic variant in the OGDH gene results in a neurological disorder with features of a mitochondrial disease Journal Articles
A coding and non-coding transcriptomic perspective on the genomics of human metabolic disease Journal Articles
A common TLR1 polymorphism is associated with higher parasitaemia in a Southeast Asian population with Plasmodium falciparum malaria Journal Articles
A fatal turkish case of CINCA-NOMID syndrome due to the novel Val-351-Leu CIAS1 gene mutation 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 linkage and association scan reveals novel loci for autism Journal Articles
A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees 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 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 phenome-wide association study of a lipoprotein-associated phospholipase A₂loss-of-function variant in 90 000 Chinese adults Journal Articles
A polygenic two-hit hypothesis for prostate cancer Journal Articles
A principal component regression based genome wide analysis approach reveals the presence of a novel QTL on BTA7 for MAP resistance in holstein cattle Journal Articles
A recurrent de novo HSPD1 variant is associated with hypomyelinating leukodystrophy Journal Articles
A retrospective population-based cohort study to evaluate the impact of an older sibling with undescended testis and hypospadias on the known maternal and fetal risk factors for undescended testis and hypospadias in Ontario, Canada, 1997–2007 Journal Articles
A risk‐factor model of epistatic interaction, focusing on autism Journal Articles
A systematic review of genetic syndromes with obesity Journal Articles
A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity Journal Articles
ACE and Type 2 Diabetes Risk: A Mendelian Randomization Study Journal Articles
APOA5 genetic variants are markers for classic hyperlipoproteinemia phenotypes and hypertriglyceridemia Journal Articles
APOL1 Genotype and Renal Function of Black Living Donors Journal Articles
Abdominal Aortic Aneurysm Is Associated with a Variant in Low-Density Lipoprotein Receptor-Related Protein 1 Journal Articles
Aberrant Epigenetic Regulation: A Central Contributor to Lung Carcinogenesis and a New Therapeutic Target Journal Articles
Acute disseminated encephalomyelitis: clinical features and HLA‐DR linkage Journal Articles
Advances in Genomic Analysis of Stroke Journal Articles
Advances in the molecular classification of pediatric brain tumors: a guide to the galaxy Journal Articles
Age differences in arterial and venous extra-cerebral blood flow in healthy adults: contributions of vascular risk factors and genetic variants Journal Articles
Alcohol dehydrogenase 3 genotype modification of the association of alcohol consumption with breast cancer risk. Journal Articles
An Increased Burden of Common and Rare Lipid-Associated Risk Alleles Contributes to the Phenotypic Spectrum of Hypertriglyceridemia Journal Articles
An atypical pulmonary fibrosis is associated with co-inheritance of mutations in the calcium binding protein genes S100A3 and S100A13 Journal Articles
An evaluation of memory and attention in BRCA mutation carriers using an online cognitive assessment tool Journal Articles
An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructure 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
Analysis of the common genetic component of large-vessel vasculitides through a meta-Immunochip strategy Journal Articles
Ancient selection for derived alleles at a GDF5 enhancer influencing human growth and osteoarthritis risk Journal Articles
Androgens and Estrogens in the Etiology and Prevention of Breast Cancer Conferences
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
Anti-Microbial Antibody Response is Associated With Future Onset of Crohn’s Disease Independent of Biomarkers of Altered Gut Barrier Function, Subclinical Inflammation, and Genetic Risk Journal Articles
Application of Breast Cancer Risk Prediction Models in Clinical Practice Journal Articles
Applying Aristotle's doctrine of causation to Aboriginal and biomedical understanding of diabetes. Journal Articles
Are there epidemiological differences between crohnʼs disease and ulcerative colitis? Journal Articles
Asia–Pacific consensus guidelines on gastric cancer prevention Journal Articles
Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study Journal Articles
Association Between a Literature-Based Genetic Risk Score and Cardiovascular Events in Women Journal Articles
Association BetweenNRASandBRAFMutational Status and Melanoma-Specific Survival Among Patients With Higher-Risk Primary Melanoma 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 high expression macrophage migration inhibitory factor (MIF) alleles and West Nile virus encephalitis Journal Articles
Association between impulsivity traits and body mass index at the observational and genetic epidemiology level Journal Articles
Association between phosphodiesterase 4D gene and ischaemic stroke Journal Articles
Association between the -455T>C promoter polymorphism of the APOC3gene and the metabolic syndrome in a multi-ethnic sample Journal Articles
Association between the FTO rs9939609 polymorphism and the metabolic syndrome in a non-Caucasian multi-ethnic sample Journal Articles
Association between the Lynch syndrome gene MSH2 and breast cancer susceptibility in a Canadian familial cancer registry Journal Articles
Association between three functional polymorphisms of the dopamine D2 receptor gene and polydipsia in schizophrenia Journal Articles
Association of TLR4 polymorphisms with Mycobacterium avium subspecies paratuberculosis infection status in Canadian Holsteins Journal Articles
Association of Apolipoprotein E With Intracerebral Hemorrhage Risk by Race/Ethnicity Journal Articles
Association of BRM promoter polymorphisms and esophageal adenocarcinoma outcome Journal Articles
Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events 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 Novel Locus With Rheumatic Heart Disease in Black African Individuals Journal Articles
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3 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 of the tryptophan hydroxylase 2 gene with risk for bipolar disorder or suicidal behavior 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 of the H63D polymorphism in the hemochromatosis gene with sporadic ALS 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 of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn’s disease subjects Journal Articles
Asthma: epidemiology, etiology and risk factors Journal Articles
Autism Spectrum Disorders and Epigenetics Journal Articles
BRCA1, BRCA2 and breast cancer: a concise clinical review. Journal Articles
BRCA2 Variants and cardiovascular disease in a multi-ethnic study Journal Articles
Benefits and limitations of genome-wide association studies Journal Articles
Bias in the case-only design applied to studies of gene-environment and gene-gene interaction: a systematic review and meta-analysis Journal Articles
Biomarkers in bipolar disorder: A positional paper from the International Society for Bipolar Disorders Biomarkers Task Force Journal Articles
Bipolar disorder and 1513A>C P2RX7 polymorphism frequency Journal Articles
Bovine CLEC7A genetic variants and their association with seropositivity in Johne's disease ELISA Journal Articles
Bovine IFNGR2, IL12RB1, IL12RB2, and IL23R polymorphisms and MAP infection status Journal Articles
Breast and ovarian cancer risk perception after prophylactic salpingo‐oophorectomy due to an inherited mutation in the BRCA1 or BRCA2 gene Journal Articles
Breast cancer in a BRCA2 mutation carrier with a history of prostate cancer Journal Articles
Breast cancer prognostic significance of a single nucleotide polymorphism in the proximal androgen response element of the prostate specific antigen gene promoter Journal Articles
Breast cancer risk after age 60 among BRCA1 and BRCA2 mutation carriers Journal Articles
Breastfeeding and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers Journal Articles
Breastfeeding and the risk of epithelial ovarian cancer among women with a BRCA1 or BRCA2 mutation Journal Articles
Brief Report: Evaluation of the Short Quantitative Checklist for Autism in Toddlers (Q-CHAT-10) as a Brief Screen for Autism Spectrum Disorder in a High-Risk Sibling Cohort Journal Articles
Brief Report: Relationship Between Non-verbal IQ and Gender in Autism Journal Articles
CARD15 and IL23R influences Crohnʼs disease susceptibility but not disease phenotype in a Brazilian population Journal Articles
CRISPRi screens reveal a DNA methylation-mediated 3D genome dependent causal mechanism in prostate cancer Journal Articles
Calibrated rare variant genetic risk scores for complex disease prediction using large exome sequence repositories Journal Articles
Cancer prevention and screening in a BRCA2-positive male to female transgender patient Journal Articles
Carrier Screening for Genetic Disorders in Individuals of Ashkenazi Jewish Descent Journal Articles
Case Report: Eosinophilic Esophagitis in a Patient With a Novel STAT1 Gain-of-Function Pathogenic Variant Journal Articles
Caspase-12 Dampens the Immune Response to Malaria Independently of the Inflammasome by Targeting NF-κB Signaling Journal Articles
Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4) Journal Articles
Changes in PKM2 Associate with Prostate Cancer Progression Journal Articles
Characterization of a Mouse Model for Thrombomodulin Deficiency Journal Articles
Characterization of a novel SCN5A genetic variant A1294G associated with mixed clinical phenotype Journal Articles
Childhood obesity, prevalence and prevention Journal Articles
Chromosomal radiosensitivity in breast cancer patients with a known or putative genetic predisposition Journal Articles
Chronic Gastrointestinal Consequences of Acute Infectious Diarrhea: Evolving Concepts in Epidemiology and Pathogenesis Journal Articles
Clinical evaluation of a hemochromatosis next‐generation sequencing gene panel Journal Articles
Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study Journal Articles
Clinical, environmental, and genetic determinants of multiple sclerosis in children with acute demyelination: a prospective national cohort study Journal Articles
Clinically detectable copy number variations in a Canadian catchment population of schizophrenia Journal Articles
Co-factors, Microbes, and Immunogenetics in Celiac Disease to Guide Novel Approaches for Diagnosis and Treatment Journal Articles
Codon 24 (TAT>TAG) and Codon 32 (ATG>AGG) (Hb Rotterdam): Two Novel α2 Gene Mutations Associated with Mild α-Thalassemia Found in the Same Family After Newborn Screening Journal Articles
Coeliac disease screening in first-degree relatives on the basis of biopsy and genetic risk Journal Articles
Colorectal cancer imaging: A challenge for radiologists Journal Articles
Colorectal cancer screening for patients with a family history of colorectal cancer or adenomas. Journal Articles
Colorectal cancer screening of high-risk individuals. Journal Articles
Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease Journal Articles
Common polymorphisms of cyclooxygenase-2 and prostaglandin E2 receptor and increased risk for acute coronary syndrome in coronary artery disease 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
Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons Journal Articles
Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements Journal Articles
Congenital Thrombophilic States Associated with Venous Thrombosis: A Qualitative Overview and Proposed Classification System Journal Articles
Connective Tissue Growth Factor Is Crucial to Inducing a Profibrotic Environment in “Fibrosis-Resistant” Balb/c Mouse Lungs Journal Articles
Contending visions in the evolution of genetic medicine: The case of cancer genetic services in Ontario, Canada Journal Articles
Contralateral Breast Cancer in BRCA1 and BRCA2 Mutation Carriers 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
Cortical Serotonin Type-2 Receptor Density in Parents of Children with Autism Spectrum Disorders Journal Articles
Current State and Future of Polygenic Risk Scores in Cardiometabolic Disease: A Scoping Review 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
Data mining of gene expression changes in Alzheimer brain Journal Articles
De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy Journal Articles
De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features Journal Articles
De novo pathogenic variant in TUBB2A presenting with arthrogryposis multiplex congenita, brain abnormalities, and severe developmental delay Journal Articles
Depression, Migraine With Aura and Migraine Without Aura: Their Familiality and Interrelatedness Journal Articles
Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing Journal Articles
Developmental delay in P300 production in children at high risk for developing alcohol-related disorders Journal Articles
Diabetes and breast cancer among women with BRCA1 and BRCA2 mutations Journal Articles
Diagnosis and high incidence of hyperornithinemia‐hyperammonemia‐homocitrullinemia (HHH) syndrome in northern Saskatchewan Journal Articles
Diagnosis and treatment of dementia: 1. Risk assessment and primary prevention of Alzheimer disease Journal Articles
Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH Journal Articles
Diagnosis of ‘possible’ mitochondrial disease: an existential crisis Journal Articles
Direct-to-consumer genetic testing: letting the genie out of the bottle? 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 family history predict the age at onset of new breast cancers in BRCA1 and BRCA2 mutation‐positive families? Journal Articles
Does genetic heterogeneity account for the divergent risk of type 2 diabetes in South Asian and white European populations? 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
Dynamic interaction between fetal adversity and a genetic score reflecting dopamine function on developmental outcomes at 36 months Journal Articles
EMSY and CCND1 amplification in familial breast cancer: from the Ontario site of the Breast Cancer Family Registry Journal Articles
Effect Modification by Catalase Genotype Suggests a Role for Oxidative Stress in the Association of Hormone Replacement Therapy with Postmenopausal Breast Cancer Risk 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
Effects of lifelong testosterone exposure on health and disease using Mendelian randomization Journal Articles
Elucidating the role of genomics in neonatal sepsis Journal Articles
Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALS Journal Articles
Evidence for a gene–gene interaction in predicting children's behavior problems: Association of serotonin transporter short and dopamine receptor D4 long genotypes with internalizing and externalizing behaviors in typically developing 7-year-olds Journal Articles
Evolution of immune genes is associated with the Black Death Journal Articles
Excess of Rare Variants in Non–Genome-Wide Association Study Candidate Genes in Patients With Hypertriglyceridemia Journal Articles
Exercise Not Asthma Journal Articles
Exome Sequencing as a Diagnostic Tool for Pediatric‐Onset Ataxia Journal Articles
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction Journal Articles
Exploring Gene-Environment Relationships in Cardiovascular Disease Journal Articles
Exploring design-related bias in clinical studies on receptor genetic polymorphism of hypertension Journal Articles
Expression of a Common LQT1 Mutation in Five Apparently Unrelated Families in a Regional Inherited Arrhythmia Clinic Journal Articles
Expression profiling of familial breast cancers demonstrates higher expression of FGFR2 in BRCA2-associated tumors Journal Articles
Factors That Predict Risk of Thrombosis in Relatives of Patients With Unprovoked Venous Thromboembolism Journal Articles
Factors that predict thrombosis in relatives of patients with venous thromboembolism Journal Articles
Familial and hormonal risk factors for papillary serous uterine cancer. Journal Articles
Family history and improving health. Journal Articles
Family history and the risk of gastric cancer Journal Articles
Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study Journal Articles
Fat Infiltration in Muscle: New Evidence for Familial Clustering and Associations With Diabetes Journal Articles
Fine-mapping of retinal vascular complexity loci identifies Notch regulation as a shared mechanism with myocardial infarction outcomes Journal Articles
Fine-tuning of Genome-Wide Polygenic Risk Scores and Prediction of Gestational Diabetes in South Asian Women Journal Articles
Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants Journal Articles
Functional impact of global rare copy number variation in autism spectrum disorders 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
Gender-based differences in oxidative stress parameters do not underlie the differences in mood disorders susceptibility between sexes 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-Gene Interaction Between Factor- XI and ABO Genes in Cerebral Venous Thrombosis Journal Articles
Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders Journal Articles
Genes, the environment and personalized medicine 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 Determinants of Vascular Dementia Journal Articles
Genetic Determinants of “Cognitive Impairment, No Dementia” Journal Articles
Genetic Differential Susceptibility to Socioeconomic Status and Childhood Obesogenic Behavior Journal Articles
Genetic Etiology of Isolated Low HDL Syndrome 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 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 Are Not Associated with Wet Age-Related Macular Degeneration Treatment Response to Ranibizumab 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 Susceptibility to West Nile Virus and Dengue Journal Articles
Genetic Tools for Coronary Risk Assessment in Type 2 Diabetes: A Cohort Study From the ACCORD Clinical Trial 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 Variation in the Ontario Neurodegenerative Disease Research Initiative Journal Articles
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits Journal Articles
Genetic and phenotypic determinants of blood pressure and other cardiovascular risk factors (GAPP) Journal Articles
Genetic basis of cannabis use: a systematic review Journal Articles
Genetic considerations in recurrent congenital diaphragmatic hernia in two siblings Journal Articles
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology 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 interaction between α4 and β2 subunits of high affinity nicotinic receptor: analysis in schizophrenia Journal Articles
Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration Journal Articles
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs Journal Articles
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies Journal Articles
Genetic risk for dengue hemorrhagic fever and dengue fever in multiple ancestries Journal Articles
Genetic susceptibility loci of idiopathic interstitial pneumonia do not represent risk for systemic sclerosis: a case control study in Caucasian patients Journal Articles
Genetic susceptibility to beryllium: a case–referent study of men and women of working age with sarcoidosis or other chronic lung disease Journal Articles
Genetic testing for atherosclerosis risk: Inevitability or pipe dream? 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
Genetics and Genomics of Pulmonary Fibrosis: Charting the Molecular Landscape and Shaping Precision Medicine Journal Articles
Genetics in obstetricians? offices: a survey study*1 Journal Articles
Genetics of Coagulation: What the Cardiologist Needs to Know Journal Articles
Genetics of cannabis use in opioid use disorder: A genome-wide association and polygenic risk score study Journal Articles
Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24 Journal Articles
Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias Journal Articles
Genome-Wide Association Studies of Hypertension: Have They Been Fruitful? 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 Association Analysis of Blood-Pressure Traits in African-Ancestry Individuals Reveals Common Associated Genes in African and Non-African Populations Journal Articles
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits 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 and transcriptome studies identify target genes and risk loci for breast cancer Journal Articles
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Journal Articles
Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status Journal Articles
Genome-wide detection of tandem DNA repeats that are expanded in autism Journal Articles
Genome-wide germline correlates of the epigenetic landscape of prostate cancer Journal Articles
Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke Journal Articles
Genome‐Wide Association Study Identifies First Locus Associated with Susceptibility to Cerebral Venous Thrombosis 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 architecture of autism from comprehensive whole-genome sequence annotation Journal Articles
Genotype and phenotype in 12 additional individuals with SATB2‐associated syndrome Journal Articles
Germline HOXB13 p.Gly84Glu mutation and risk of colorectal cancer 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
Glucocorticoid Receptors, Brain-Derived Neurotrophic Factor, Serotonin and Dopamine Neurotransmission are Associated with Interferon-Induced Depression Journal Articles
Guidelines for best practices in monitoring established coeliac disease in adult patients Journal Articles
HDL Cholesterol, LDL Cholesterol, and Triglycerides as Risk Factors for CKD: A Mendelian Randomization Study Journal Articles
HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome Journal Articles
Hereditary risk factors for the development of gastric cancer in younger patients Journal Articles
High Urinary Calcium Excretion and Genetic Susceptibility to Hypertension and Kidney Stone Disease Conferences
High resolution mapping in the major histocompatibility complex region identifies multiple independent novel loci for psoriatic arthritis Journal Articles
Homocysteine and stroke Journal Articles
Hormone Replacement Therapy After Oophorectomy and Breast Cancer Risk Among BRCA1 Mutation Carriers Journal Articles
How Effective Are Antioxidant Supplements in Obesity and Diabetes? Journal Articles
How interested is the public in genetic testing for colon cancer susceptibility? Report of a cross-sectional population survey. Journal Articles
Hundreds of variants clustered in genomic loci and biological pathways affect human height Journal Articles
IL-10R Polymorphisms Are Associated with Very-early-onset Ulcerative Colitis 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 Multiple Genetic Susceptibility Loci in Takayasu Arteritis Journal Articles
Identification of Susceptibility Loci in IL6, RPS9/LILRB3, and an Intergenic Locus on Chromosome 21q22 in Takayasu Arteritis in a Genome‐Wide Association Study Journal Articles
Identification of amino acid variation in the prion protein associated with classical scrapie in Canadian dairy goats Journal Articles
Identification of genetic effects underlying type 2 diabetes in South Asian and European populations Journal Articles
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease Journal Articles
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 Journal Articles
Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study Journal Articles
Identifying genetic and environmental risk factors for chronic orofacial pain syndromes: human models. Journal Articles
Immunochip Analysis Identifies Multiple Susceptibility Loci for Systemic Sclerosis Journal Articles
Impact of Inherited Thrombophilia on Venous Thromboembolism in Children Journal Articles
Impact of a Genetic Risk Score on Myocardial Infarction Risk Across Different Ethnic Populations Journal Articles
Impaired parasympathetic function increases susceptibility to inflammatory bowel disease in a mouse model of depression Journal Articles
Incidence of endometrial cancer in BRCA mutation carriers. Journal Articles
Increased Hepatic PDGF-AA Signaling Mediates Liver Insulin Resistance in Obesity-Associated Type 2 Diabetes Journal Articles
Increased intestinal permeability precedes the onset of Crohn's disease in a subject with familial risk Journal Articles
Increased prevalence of pathogenic bacteria in the gut microbiota of infants at risk of developing celiac disease: The PROFICEL study Journal Articles
Increased rectal mucosal expression of interleukin 1beta in recently acquired post-infectious irritable bowel syndrome Journal Articles
Individual common variants exert weak effects on the risk for autism spectrum disorders Journal Articles
Influence of Milk-Feeding Type and Genetic Risk of Developing Coeliac Disease on Intestinal Microbiota of Infants: The PROFICEL Study Journal Articles
Influence of Parental Concordance for Psychiatric Disorders on Psychopathology in Offspring Journal Articles
Influence of depression on genetic predisposition to type 2 diabetes in a multiethnic longitudinal study Journal Articles
Influence of early environmental factors on lymphocyte subsets and gut microbiota in infants at risk of celiac disease; the PROFICEL study. Journal Articles
Influence of thrombophilia on risk of recurrent venous thromboembolism while on warfarin: results from a randomized trial Journal Articles
Informative phenotypes for genetic studies of psychiatric disorders Journal Articles
Inherited Thrombophilia and the Risk of Arterial Ischemic Stroke: A Systematic Review and Meta‐Analysis 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
Is serotonin transporter polymorphism (5-HTTLPR) allele status a predictor for obsessive-compulsive disorder? A meta-analysis Journal Articles
Krüppel‐like factor 1: hematologic phenotypes associated with KLF1 gene mutations Journal Articles
Lack of association between type 2 diabetes and major depression: epidemiologic and genetic evidence in a multiethnic population Journal Articles
Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci Journal Articles
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation 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
Lifestyle Interaction With Fat Mass and Obesity-Associated (FTO) Genotype and Risk of Obesity in Apparently Healthy U.S. Women Journal Articles
Lifestyle factors and fetal and childhood origins of type 2 diabetes: a prospective study of Chinese and European adults Journal Articles
Limited Protective Effect of the CCR5Δ32/CCR5Δ32 Genotype on Human Immunodeficiency Virus Infection Incidence in a Cohort of Patients with Hemophilia and Selection for Genotypic X4 Virus Journal Articles
LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemias Journal Articles
Loci influencing blood pressure identified using a cardiovascular gene-centric array Journal Articles
Longitudinal Decline in Lung Volume in a Population of Children with Sickle Cell Disease Journal Articles
Longitudinal relationships between glycemic status and body mass index in a multiethnic study: evidence from observational and genetic epidemiology Journal Articles
Low copy number of the salivary amylase gene predisposes to obesity Journal Articles
Lung Development and Susceptibility to Chronic Obstructive Pulmonary Disease Journal Articles
MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation 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
Management of the BRCA Mutation Carrier or High-Risk Patient Journal Articles
Manifestations of Von Hippel Lindau syndrome: a retrospective national review Journal Articles
Mapping autism risk loci using genetic linkage and chromosomal rearrangements Journal Articles
Maternal Obesity and Developmental Programming of Metabolic Disorders in Offspring: Evidence from Animal Models Journal Articles
Maternal childhood adversity and child temperament: An association moderated by child 5‐HTTLPR genotype Journal Articles
Mendelian Genes and Risk of Intracerebral Hemorrhage and Small-Vessel Ischemic Stroke in Sporadic Cases Journal Articles
Mendelian Randomization Studies Do Not Support a Role for Vitamin D in Coronary Artery Disease Journal Articles
Meta-Analyses of Genome-Wide Association Studies for Postpartum Depression Journal Articles
Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels 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 GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia 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
Methylenetetrahydrofolate Reductase Polymorphisms and Homocysteine-Lowering Effect of Vitamin Therapy in Singaporean Stroke Patients Journal Articles
Modeling Complex Disease with Demographic and Environmental Covariates and a Candidate Gene Marker Journal Articles
Modelling the Community as a Determinant of Health Journal Articles
Moderating effect of PLIN4 genetic variant on impulsivity traits in 5-year-old-children born small for gestational age Journal Articles
Modulation of GLP-1 Levels by a Genetic Variant That Regulates the Cardiovascular Effects of Intensive Glycemic Control in ACCORD Journal Articles
Modulatory effect of the SLC9A3 gene on susceptibility to infections and pulmonary function in children with cystic fibrosis Journal Articles
Molecular Genetic Analysis of the Idd4 Locus Implicates the IFN Response in Type 1 Diabetes Susceptibility in Nonobese Diabetic Mice Journal Articles
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression Journal Articles
Mouse models of cystathionine β‐synthase deficiency reveal significant threshold effects of hyperhomocysteinemia Journal Articles
Moyamoya Disease Susceptibility Variant RNF213 p.R4810K Increases the Risk of Ischemic Stroke Attributable to Large-Artery Atherosclerosis Journal Articles
Multi-Ethnic Genetic Association Study of Carotid Intima-Media Thickness Using a Targeted Cardiovascular SNP Microarray Journal Articles
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction Journal Articles
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation Journal Articles
Multi-ethnic genome-wide association study for atrial fibrillation 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
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset Journal Articles
Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis Journal Articles
Multivariate Meta-Analysis of Genetic Association Studies: A Simulation Study Journal Articles
Mutations That Alter the Carboxy-Terminal-Propeptide Cleavage Site of the Chains of Type I Procollagen Are Associated With a Unique Osteogenesis Imperfecta Phenotype Journal Articles
Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation Journal Articles
NAT2 genetic polymorphisms and anti-tuberculosis drug-induced hepatotoxicity in Chinese community population Journal Articles
Natural history and genotype‐phenotype correlations in 72 individuals with SATB2‐associated syndrome Journal Articles
Neuronal Correlates of Brain-derived Neurotrophic Factor Val66Met Polymorphism and Morphometric Abnormalities in Bipolar Disorder Journal Articles
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders Journal Articles
Next-Generation Sequencing to Diagnose Muscular Dystrophy, Rhabdomyolysis, and HyperCKemia Journal Articles
No Association between the 20210 G/A Prothrombin Gene Mutation and Premature Coronary Artery Disease Journal Articles
Non-Host Factors Influencing Onset and Severity of Celiac Disease Journal Articles
North American Thrombosis Forum, AF Action Initiative Consensus Document 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 players in coeliac disease pathogenesis: role of the gut microbiota Journal Articles
Nutrition and the early origins of adult disease Journal Articles
Obesity Genes and Risk of Major Depressive Disorder in a Multiethnic Population Journal Articles
Obesity genetics: insights from the Pakistani population Journal Articles
Obsessive-compulsive disorder (OCD): is this disorder under-recognized? Journal Articles
On the origin of obesity: identifying the biological, environmental and cultural drivers of genetic risk among human populations Journal Articles
Oophorectomy and risk of contralateral breast cancer among BRCA1 and BRCA2 mutation carriers Journal Articles
Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2 Journal Articles
Oxytocin Receptor Polymorphisms are Differentially Associated with Social Abilities across Neurodevelopmental Disorders Journal Articles
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study Journal Articles
PDZK1 in leukocytes protects against cellular apoptosis and necrotic core development in atherosclerotic plaques in high fat diet fed ldl receptor deficient mice Journal Articles
Pan-urologic cancer genomic subtypes that transcend tissue of origin 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
Parents’ Understanding of Genetics and Heritability Journal Articles
Parkinson-susceptibility gene DJ-1/PARK7 protects the murine heart from oxidative damage in vivo Journal Articles
Pathogenic Germline Variants in 10,389 Adult Cancers Journal Articles
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome Journal Articles
PedSplit: pedigree management for stratified analysis Journal Articles
Pediatric patients with pheochromocytoma and paraganglioma should have routine preoperative genetic testing for common susceptibility genes in addition to imaging to detect extra-adrenal and metastatic tumors Conferences
Penetrance of Polygenic Obesity Susceptibility Loci across the Body Mass Index Distribution Journal Articles
Perceived family history risk and symptomatic diagnosis of prostate cancer Journal Articles
Perceptions About Genetic Testing for the Susceptibility to Alcohol Dependence and Other Multifactorial Diseases Journal Articles
Performance characteristics of a brief Family History Questionnaire to screen for Lynch syndrome in women with newly diagnosed endometrial cancer Journal Articles
Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition Syndromes Journal Articles
Pharmacogenetics in Cardiovascular Disease: The Challenge of Moving From Promise to Realization Journal Articles
Phenotype Driven Analysis of Whole Genome Sequencing Identifies Deep Intronic Variants that Cause Retinal Dystrophies by Aberrant Exonization Journal Articles
Phenotypic Analysis of Arrhythmogenic Cardiomyopathy in the Hutterite Population: Role of Electrocardiogram in Identifying High‐Risk Desmocollin‐2 Carriers Journal Articles
Physical activity and genetic predisposition to obesity in a multiethnic longitudinal study Journal Articles
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study Journal Articles
Plasminogen Alleles Influence Susceptibility to Invasive Aspergillosis Journal Articles
Polygenic Risk Score for Alzheimer's Disease in Caribbean Hispanics Journal Articles
Polygenic contributions to performance on the Balloon Analogue Risk Task Journal Articles
Polygenic determinants of severe hypertriglyceridemia Journal Articles
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders 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 in the gene encoding bovine interleukin-10 receptor alpha are associated with Mycobacterium avium ssp. paratuberculosis infection status Journal Articles
Population genetics of chronic kidney disease: The evolving story of APOL1 Journal Articles
Population-Based Study to Determine the Health System Costs of Using the 21-Gene Assay Journal Articles
Predicting novel disease mutations in the cardiac sodium channel Journal Articles
Predictive genetic testing for coronary artery disease Journal Articles
Predictive genetic tests and health system costs. Journal Articles
Pregnancy and Birth Complications in Autism and Liability to the Broader Autism Phenotype Journal Articles
Prenatal maternal depression and child serotonin transporter linked polymorphic region (5-HTTLPR) and dopamine receptor D4 (DRD4) genotype predict negative emotionality from 3 to 36 months Journal Articles
Presence of Alanine-to-Valine Substitutions in Myofibrillogenesis Regulator 1 in Paroxysmal Nonkinesigenic Dyskinesia Journal Articles
Primary mediastinal paraganglioma associated with a familial variant in the succinate dehydrogenase B subunit gene Journal Articles
Prospective study of high-risk, BRCA1/2-mutation negative women: the ‘negative study’ Journal Articles
Protein Z Levels, Protein Z G79A Polymorphism, and Prothrombotic Conditions Journal Articles
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways Journal Articles
Psychopathology and Achievement in Children at High Risk for Developing Alcoholism Journal Articles
Quality of life and psychosexual adjustment after prophylactic oophorectomy for a family history of ovarian cancer. Journal Articles
Quebec Platelet Disorder: Update on Pathogenesis, Diagnosis, and Treatment 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 progression of prostate cancer in men with a BRCA2 mutation Journal Articles
Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD 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
Re: Magnetic Resonance Imaging and Mammography in Women With a Hereditary Risk of Breast Cancer Journal Articles
Recent insights into neuromuscular junction biology in Duchenne muscular dystrophy: Impacts, challenges, and opportunities Journal Articles
Recent progress in genetics, epigenetics and metagenomics unveils the pathophysiology of human obesity Journal Articles
Recognizing BRCA gene mutation risk subsequent to breast cancer diagnosis in southwestern Ontario. Journal Articles
Recommendations for national and local regulatory authorities concerning research in genetic markers of disease Journal Articles
Reduced expression of hemopoietic cytokine receptors on cord blood progenitor cells in neonates at risk for atopy. Journal Articles
Reduced expression of hemopoietic cytokine receptors on cord blood progenitor cells in neonates at risk for atopy☆☆☆★ Journal Articles
Relationship Between Genetic Risk and Age of Diagnosis in Systemic Lupus Erythematosus Journal Articles
Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample Journal Articles
Responses to panic induction procedures in subjects with multiple chemical sensitivity/idiopathic environmental intolerance: understanding the relationship with panic disorder. Journal Articles
Revisiting the evolutionary origins of obesity: lazy versus peppy‐thrifty genotype hypothesis 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
Risk factors for ovarian cancer and early-onset breast cancer in Mongolia. Journal Articles
Risk loci involved in giant cell arteritis susceptibility: a genome-wide association study Journal Articles
Role of Macrophage Migration Inhibitory Factor in Granulomatosis With Polyangiitis Conferences
Role of genetics in the prediction of statin-associated muscle symptoms and optimization of statin use and adherence Journal Articles
Role of polymorphic bile salt export pump (BSEP, ABCB11) transporters in anti-tuberculosis drug-induced liver injury in a Chinese cohort Journal Articles
Ruling in and ruling out: Implications of molecular genetic diagnoses for disease classification Journal Articles
SAMHD1 Mutations Are Also Responsible for Aicardi–Goutières in the Cree Population Journal Articles
Screening of hypoxia-inducible genes in sporadic ALS Journal Articles
Second Primary Malignancy Risk in Thyroid Cancer Survivors: A Systematic Review and Meta-Analysis Journal Articles
Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees Journal Articles
Selecting a BRCA risk assessment model for use in a familial cancer clinic Journal Articles
Sentinel Symptoms in Patients with Unexplained Cardiac Arrest: From the Cardiac Arrest Survivors with Preserved Ejection Fraction Registry (CASPER) Journal Articles
Sex differences in repetitive stereotyped behaviors in autism: Implications for genetic liability Journal Articles
Sex-Specific Effect of Insulin-Dependent Diabetes 4 on Regulation of Diabetes Pathogenesis in the Nonobese Diabetic Mouse Journal Articles
Simoctocog Alfa (Nuwiq) in Previously Untreated Patients with Severe Haemophilia A: Final Results of the NuProtect Study Journal Articles
Single Nucleotide Polymorphisms Alter the Promoter Activity of Bovine MIF Journal Articles
Single nucleotide polymorphism in IL1B is associated with infection risk in paediatric acute myeloid leukaemia 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
Small rodent models of atherosclerosis Journal Articles
Sodium Intake and Cardiovascular Health Journal Articles
Spontaneous Degeneration of Supraventricular Tachycardia to Ventricular Fibrillation Journal Articles
Strain-Related Difference in Susceptibility to Anaphylactic Shock Correlates with Measures of Spontaneous Activity Journal Articles
Strain-specific differences in cell proliferation and differentiation in the dentate gyrus of C57BL/6N and C3H/HeN mice fed a high fat diet Journal Articles
StrandAdvantage test for early‐line and advanced‐stage treatment decisions in solid tumors Journal Articles
Stroke genetics informs drug discovery and risk prediction across ancestries Journal Articles
Susceptibility to chronic pain following nerve injury is genetically affected by CACNG2 Journal Articles
Synaptic, transcriptional and chromatin genes disrupted in autism Journal Articles
Systematic Review and Meta-analysis: Gene Association Studies in Neonatal Sepsis Journal Articles
Systematic Review: Using Magnetic Resonance Imaging to Screen Women at High Risk for Breast Cancer Journal Articles
Tamoxifen and contralateral breast cancer in BRCA1 and BRCA2 carriers: An update Journal Articles
Targeted Gene Sequencing Identifies Variants in the Protein C and Endothelial Protein C Receptor Genes in Patients With Unprovoked Venous Thromboembolism Journal Articles
Telomere Length, Oxidative Stress, Inflammation and BDNF Levels in Siblings of Patients with Bipolar Disorder: Implications for Accelerated Cellular Aging Journal Articles
Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care Journal Articles
The 9p21.3 locus and cardiovascular risk in familial hypercholesterolemia Journal Articles
The Brain-Derived Neurotrophic Factor Val66Met Polymorphism, Hippocampal Volume, and Cognitive Function in Geriatric Depression Journal Articles
The Complex Genetic Basis of Plasma Triglycerides Journal Articles
The Effect of Prothrombotic Blood Abnormalities on Risk of Deep Vein Thrombosis in Users of Hormone Replacement Therapy Journal Articles
The Familial Aggregation of the Lesser Variant in Biological and Nonbiological Relatives of PDD Probands: a Family History Study Journal Articles
The Familial Predisposition toward Tearing the Anterior Cruciate Ligament Journal Articles
The Generation R study: a candidate gene study and genome-wide association study (GWAS) on health-related quality of life (HRQOL) of mothers and young children Journal Articles
The Genetic Factors of the Airway Epithelium Associated with the Pathology of Asthma Journal Articles
The Genetic Link Between Diabetes and Atherosclerosis Journal Articles
The Idd4 Locus Displays Sex-Specific Epistatic Effects on Type 1 Diabetes Susceptibility in Nonobese Diabetic Mice Journal Articles
The Psychodynamic Psychotherapist's Guide to the Interaction among Sex, Genes, and Environmental Adversity in the Etiology of Depression for Women Journal Articles
The Role of Endogenous Hormones in the Etiology and Prevention of Breast Cancer: The Epidemiological Evidence Conferences
The T-786→C Mutation in Endothelial Nitric Oxide Synthase Is Associated With Hypertension Journal Articles
The association between HLA-DQB1 polymorphism and antituberculosis drug-induced liver injury: a Case-Control Study Journal Articles
The association between glutathione S-transferase M1 genotype and polycyclic aromatic hydrocarbon-DNA adducts in breast tissue. Journal Articles
The association of HTR2A polymorphisms with obsessive-compulsive disorder and its subtypes: A meta-analysis Journal Articles
The association of attempted suicide with genetic variants in the SLC6A4 and TPH genes depends on the definition of suicidal behavior: a systematic review and meta-analysis Journal Articles
The complex genetics of amyotrophic lateral sclerosis Journal Articles
The double-edged sword of gut bacteria in celiac disease and implications for therapeutic potential Journal Articles
The functional variant rs1048990 in PSMA6 is associated with susceptibility to myocardial infarction in a Chinese population Journal Articles
The impact of prophylactic salpingo-oophorectomy on menopausal symptoms and sexual function in women who carry a BRCA mutation Journal Articles
The impact of prophylactic salpingo‐oophorectomy on quality of life and psychological distress in women with a BRCA mutation Journal Articles
The incidence of leukaemia in women with BRCA1 and BRCA2 mutations: an International Prospective Cohort Study Journal Articles
The interplay of birth weight, dopamine receptor D4 gene (DRD4), and early maternal care in the prediction of disorganized attachment at 36 months of age Journal Articles
The long-term functional consequences of acute infectious diarrhea 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 phenotypic manifestations of rare genic CNVs in autism spectrum disorder Journal Articles
The potential to predict the course of childhood asthma Journal Articles
The protective effect of the obesity-associated rs9939609 A variant in fat mass- and obesity-associated gene on depression Journal Articles
The risks of cancer in older women with BRCA pathogenic variants: How far have we come? Journal Articles
The search for autism disease genes Journal Articles
Thiopurine S-methyltransferase testing for averting drug toxicity: a meta-analysis of diagnostic test accuracy Journal Articles
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies Journal Articles
Thrombocytopenic Platelet Disorders Journal Articles
Thrombophilia and location of venous thromboembolism Journal Articles
Thrombus stability explains the factor V Leiden paradox: a mouse model Journal Articles
Towards the genetic basis of cerebral venous thrombosis—the BEAST Consortium: a study protocol Journal Articles
Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders Journal Articles
Translating Genomic Analyses into Improved Management of Coronary Artery Disease Journal Articles
Treatment of infertility does not increase the risk of ovarian cancer among women with a BRCA1 or BRCA2 mutation Journal Articles
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia Journal Articles
Tryptophan hydroxylase polymorphisms in suicide victims Journal Articles
Tumor Necrosis Factor Alpha Gene Polymorphism Associated with Increased Susceptibility to Venous Leg Ulceration Journal Articles
Two BRM promoter insertion polymorphisms increase the risk of early‐stage upper aerodigestive tract cancers Journal Articles
Understanding the Role of DISC1 in Psychiatric Disease and during Normal Development Journal Articles
Upcoming biomarkers for the diagnosis of Kawasaki disease: A review Journal Articles
Update of the spectrum of GJB2 mutations in 107 patients with nonsyndromic hearing loss in the Fujian population of China. Journal Articles
Update on bipolar disorder biomarker candidates Journal Articles
Use of latent class models to accommodate inter-laboratory variation in assessing genetic polymorphisms associated with disease risk Journal Articles
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes Journal Articles
Variability of polygenic prediction for body mass index in Africa Journal Articles
Variants of the SFTPA1 and SFTPA2 genes and susceptibility to tuberculosis in Ethiopia Journal Articles
Weight Gain and the Risk of Ovarian Cancer in BRCA1 and BRCA2 Mutation Carriers Conferences
What Causes Premature Coronary Artery Disease? Journal Articles
What have we learned from basic science studies on idiopathic pulmonary fibrosis? Journal Articles
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder Journal Articles
Whole-genome sequencing of quartet families with autism spectrum disorder Journal Articles
Whole‐exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study Journal Articles
Why don't pigs get diabetes? Explanations for variations in diabetes susceptibility in human populations living in a diabetogenic environment Journal Articles
[Study on polymorphisms of genes with susceptibility to drug induced liver injury in a cohort receiving anti-tuberculosis treatment]. Journal Articles
c.1058C>T variant in the SERPINC1 gene is pathogenic for antithrombin deficiency Journal Articles
eQTL Set–Based Association Analysis Identifies Novel Susceptibility Loci for Barrett Esophagus and Esophageal Adenocarcinoma Journal Articles
“Benign” early repolarization versus malignant early abnormalities: Clinical-electrocardiographic distinction and genetic basis Journal Articles

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