Genetic Predisposition to Disease

subject area of

CYP7A1, BAAT and UGT1A1 polymorphisms and susceptibility to anti-tuberculosis drug-induced hepatotoxicity Academic Article
18-Month Predictors of Later Outcomes in Younger Siblings of Children With Autism Spectrum Disorder: A Baby Siblings Research Consortium Study Academic Article
4-phenylbutyrate and valproate treatment attenuates the progression of atherosclerosis and stabilizes existing plaques Academic Article
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 Academic Article
BRCA1 and BRCA2 Mutation Carriers, Oral Contraceptive Use, and Breast Cancer Before Age 50 Academic Article
CDKN2AMutations in Multiple Primary Melanomas Academic Article
CYP2E1,GSTM1andGSTT1genetic polymorphisms and susceptibility to antituberculosis drug-induced hepatotoxicity: a nested case-control study Academic Article
SCYL1 disease and liver transplantation diagnosed by reanalysis of exome sequencing and deletion/duplication analysis of SCYL1 Academic Article
A 23bp Insertion in the Endothelial Protein C Receptor (EPCR) Gene Impairs EPCR Function Academic Article
A C19MC-LIN28A-MYCN Oncogenic Circuit Driven by Hijacked Super-enhancers Is a Distinct Therapeutic Vulnerability in ETMRs: A Lethal Brain Tumor Academic Article
A Candidate-Gene Approach Identifies Novel Associations Between Common Variants in/Near Syndromic Obesity Genes and BMI in Pediatric and Adult European Populations Academic Article
A FLEXIBLE NONPARAMETRIC APPROACH TO FIND CANDIDATE GENES ASSOCIATED WITH DISEASE IN MICROARRAY EXPERIMENTS Academic Article
A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans Academic Article
A Genome-Wide Association Study for Coronary Artery Disease Identifies a Novel Susceptibility Locus in the Major Histocompatibility Complex Academic Article
A Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms for Acute Kidney Injury Academic Article
A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis Academic Article
A Polymorphism Within the G6PC2 Gene Is Associated with Fasting Plasma Glucose Levels Academic Article
A Prospective Study of Autistic-Like Traits in Unaffected Siblings of Probands With Autism Spectrum Disorder Academic Article
A Rare Variant in the Visfatin Gene (NAMPT/PBEF1 ) Is Associated With Protection From Obesity Academic Article
A biallelic pathogenic variant in the OGDH gene results in a neurological disorder with features of a mitochondrial disease Academic Article
A coding and non-coding transcriptomic perspective on the genomics of human metabolic disease Academic Article
A fatal turkish case of CINCA-NOMID syndrome due to the novel Val-351-Leu CIAS1 gene mutation Academic Article
A genome-wide association meta-analysis identifies new childhood obesity loci Academic Article
A genome-wide association study identifies novel risk loci for type 2 diabetes Academic Article
A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease Academic Article
A genome-wide linkage and association scan reveals novel loci for autism Academic Article
A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees Academic Article
A genome-wide scan for common alleles affecting risk for autism Academic Article
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders Academic Article
A large-scale candidate gene association study of age at menarche and age at natural menopause Academic Article
A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity Academic Article
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder Academic Article
A novel candidate region for ALS on chromosome 14q11.2 Academic Article
A novel large deletion and three polymorphisms in the FECH gene associated with erythropoietic protoporphyria Academic Article
A pharmacogenetic analysis of the Canadian Cancer Trials Group MY.10 clinical trial of maintenance therapy for multiple myeloma Academic Article
A phenome-wide association study of a lipoprotein-associated phospholipase A₂loss-of-function variant in 90 000 Chinese adults Academic Article
A recurrent de novo HSPD1 variant is associated with hypomyelinating leukodystrophy Academic Article
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 Academic Article
A risk-factor model of epistatic interaction, focusing on autism Academic Article
A systematic review of genetic syndromes with obesity Academic Article
A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity Academic Article
A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk Academic Article
ACE and Type 2 Diabetes Risk: A Mendelian Randomization Study Academic Article
APOA5 genetic variants are markers for classic hyperlipoproteinemia phenotypes and hypertriglyceridemia Academic Article
APOL1 Genotype and Renal Function of Black Living Donors Academic Article
Abdominal Aortic Aneurysm Is Associated with a Variant in Low-Density Lipoprotein Receptor-Related Protein 1 Academic Article
Aberrant Epigenetic Regulation: A Central Contributor to Lung Carcinogenesis and a New Therapeutic Target Academic Article
Absence of germline p16INK4a alterations in p53 wild type Li-Fraumeni syndrome families Academic Article
Accuracy of screening women at familial risk of breast cancer without a known gene mutation: Individual patient data meta-analysis Academic Article
Acute disseminated encephalomyelitis: clinical features and HLA-DR linkage Academic Article
Adiponectin, type 2 diabetes and the metabolic syndrome: lessons from human genetic studies Academic Article
Advances in Genomic Analysis of Stroke Academic Article
Advances in the molecular classification of pediatric brain tumors: a guide to the galaxy Academic Article
Age differences in arterial and venous extra-cerebral blood flow in healthy adults: contributions of vascular risk factors and genetic variants Academic Article
Alcohol dehydrogenase 3 genotype modification of the association of alcohol consumption with breast cancer risk. Academic Article
An Increased Burden of Common and Rare Lipid-Associated Risk Alleles Contributes to the Phenotypic Spectrum of Hypertriglyceridemia Academic Article
An atypical pulmonary fibrosis is associated with co-inheritance of mutations in the calcium binding protein genes S100A3 and S100A13 Academic Article
An evaluation of memory and attention in BRCA mutation carriers using an online cognitive assessment tool Academic Article
Analysis of IFT74as a candidate gene for chromosome 9p-linked ALS-FTD Academic Article
Analysis of IL-6, STAT3 and HSPA1L Gene Polymorphisms in Anti-Tuberculosis Drug-Induced Hepatitis in a Nested Case-Control Study Academic Article
Analysis of novel risk loci for type 2 diabetes in a general French population: the D.E.S.I.R. study Academic Article
Analysis of the SIM1 Contribution to Polygenic Obesity in the French Population Academic Article
Analysis of the common genetic component of large-vessel vasculitides through a meta-Immunochip strategy Academic Article
Analysis of the contribution of FTO, NPC1, ENPP1, NEGR1, GNPDA2 and MC4Rgenes to obesity in Mexican children Academic Article
Ancient selection for derived alleles at a GDF5 enhancer influencing human growth and osteoarthritis risk Academic Article
Androgens and Estrogens in the Etiology and Prevention of Breast Cancer Conference Paper
Angiogenin Levels and ANG Genotypes: Dysregulation in Amyotrophic Lateral Sclerosis Academic Article
Anti-Epileptic Drug Target Perturbation and Intracranial Aneurysm Risk: Mendelian Randomization and Colocalization Study Academic Article
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 Academic Article
Applying Aristotle's doctrine of causation to Aboriginal and biomedical understanding of diabetes. Academic Article
Are there epidemiological differences between crohnʼs disease and ulcerative colitis? Academic Article
Asia–Pacific consensus guidelines on gastric cancer prevention Academic Article
Assessing the effects of 35 European-derived BMI-associated SNPs in Mexican children Academic Article
Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study Academic Article
Association Analysis Indicates That a Variant GATA-Binding Site in the PIK3CB Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and Attenuates Insulin Resistance in Obese Children Academic Article
Association Between a Literature-Based Genetic Risk Score and Cardiovascular Events in Women Academic Article
Association BetweenNRASandBRAFMutational Status and Melanoma-Specific Survival Among Patients With Higher-Risk Primary Melanoma Academic Article
Association Studies on Ghrelin and Ghrelin Receptor Gene Polymorphisms With Obesity Academic Article
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index Academic Article
Association analyses of the DAOA/G30 and d-amino-acid oxidase genes in schizophrenia: Further evidence for a role in schizophrenia Academic Article
Association between ADIPOQ gene polymorphisms and the risk of new-onset diabetes mellitus after liver transplantation Academic Article
Association between PPAR-γ2 Pro12Ala genotype and insulin resistance is modified by circulating lipids in Mexican children Academic Article
Association between high expression macrophage migration inhibitory factor (MIF) alleles and West Nile virus encephalitis Academic Article
Association between impulsivity traits and body mass index at the observational and genetic epidemiology level Academic Article
Association between phosphodiesterase 4D gene and ischaemic stroke Academic Article
Association between the -455T>C promoter polymorphism of the APOC3gene and the metabolic syndrome in a multi-ethnic sample Academic Article
Association between the FTO rs9939609 polymorphism and the metabolic syndrome in a non-Caucasian multi-ethnic sample Academic Article
Association between the Lynch syndrome gene MSH2 and breast cancer susceptibility in a Canadian familial cancer registry Academic Article
Association between three functional polymorphisms of the dopamine D2 receptor gene and polydipsia in schizophrenia Academic Article
Association of BRM promoter polymorphisms and esophageal adenocarcinoma outcome Academic Article
Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events Academic Article
Association of Factor V Leiden With Subsequent Atherothrombotic Events Academic Article
Association of Granulomatosis With Polyangiitis (Wegener's) WithHLA-DPB1*04andSEMA6AGene Variants: Evidence From Genome-Wide Analysis Academic Article
Association of Novel Locus With Rheumatic Heart Disease in Black African Individuals Academic Article
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 Academic Article
Association of heart rate and diabetes among 0.5 million adults in the China Kadoorie biobank: Results from observational and Mendelian randomization analyses Academic Article
Association of polymorphisms of the tryptophan hydroxylase 2 gene with risk for bipolar disorder or suicidal behavior Academic Article
Association of renin–angiotensin and endothelial nitric oxide synthase gene polymorphisms with blood pressure progression and incident hypertension: prospective cohort study Academic Article
Association of the H63D polymorphism in the hemochromatosis gene with sporadic ALS Academic Article
Association study of brain-derived neurotrophic factor (BDNF) and LIN-7 homolog (LIN-7) genes with adult attention-deficit/hyperactivity disorder Academic Article
Association study of tryptophan hydroxylase 2 gene polymorphisms in bipolar disorder patients with panic disorder comorbidity Academic Article
Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn’s disease subjects Academic Article
Asthma: epidemiology, etiology and risk factors Academic Article
Autism Spectrum Disorders and Epigenetics Academic Article
BRCA1, BRCA2 and breast cancer: a concise clinical review. Academic Article
BRCA2 Variants and cardiovascular disease in a multi-ethnic study Academic Article
Benefits and limitations of genome-wide association studies Academic Article
Bias in the case-only design applied to studies of gene-environment and gene-gene interaction: a systematic review and meta-analysis Academic Article
Biomarkers in bipolar disorder: A positional paper from the International Society for Bipolar Disorders Biomarkers Task Force Academic Article
Bipolar disorder and 1513A>C P2RX7 polymorphism frequency Academic Article
Breast and ovarian cancer risk perception after prophylactic salpingo-oophorectomy due to an inherited mutation in theBRCA1orBRCA2gene Academic Article
Breast cancer in a BRCA2 mutation carrier with a history of prostate cancer Academic Article
Breast cancer prognostic significance of a single nucleotide polymorphism in the proximal androgen response element of the prostate specific antigen gene promoter Academic Article
Breast cancer risk after age 60 among BRCA1 and BRCA2 mutation carriers Academic Article
Breastfeeding and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers Academic Article
Breastfeeding and the risk of epithelial ovarian cancer among women with a BRCA1 or BRCA2 mutation Academic Article
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 Academic Article
Brief Report: Relationship Between Non-verbal IQ and Gender in Autism Academic Article
CARD15 and IL23R influences Crohnʼs disease susceptibility but not disease phenotype in a Brazilian population Academic Article
Calibrated rare variant genetic risk scores for complex disease prediction using large exome sequence repositories Academic Article
Cancer prevention and screening in a BRCA2-positive male to female transgender patient Academic Article
Causal Association of Haptoglobin With Obesity in Mexican Children: A Mendelian Randomization Study Academic Article
Causal Relationship between Obesity and Vitamin D Status: Bi-Directional Mendelian Randomization Analysis of Multiple Cohorts Academic Article
Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4) Academic Article
Challenges in reproducibility of genetic association studies: lessons learned from the obesity field Academic Article
Changes in PKM2 Associate with Prostate Cancer Progression Academic Article
Characterization of DCTN1 genetic variability in neurodegeneration Academic Article
Characterization of a Mouse Model for Thrombomodulin Deficiency Academic Article
Characterization of a novel SCN5A genetic variant A1294G associated with mixed clinical phenotype Academic Article
Childhood obesity, prevalence and prevention Academic Article
Chromosomal radiosensitivity in breast cancer patients with a known or putative genetic predisposition Academic Article
Chronic Gastrointestinal Consequences of Acute Infectious Diarrhea: Evolving Concepts in Epidemiology and Pathogenesis Academic Article
Clinical evaluation of a hemochromatosis next-generation sequencing gene panel Academic Article
Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study Academic Article
Clinical, environmental, and genetic determinants of multiple sclerosis in children with acute demyelination: a prospective national cohort study Academic Article
Clinically detectable copy number variations in a Canadian catchment population of schizophrenia Academic Article
Co-factors, Microbes, and Immunogenetics in Celiac Disease to Guide Novel Approaches for Diagnosis and Treatment Academic Article
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 Academic Article
Coeliac disease screening in first-degree relatives on the basis of biopsy and genetic risk Academic Article
Colorectal cancer imaging: A challenge for radiologists Academic Article
Colorectal cancer screening for patients with a family history of colorectal cancer or adenomas. Academic Article
Colorectal cancer screening of high-risk individuals. Academic Article
Comment on "A Common Genetic Variant Is Associated with Adult and Childhood Obesity" Academic Article
Comment on "A Common Genetic Variant Is Associated with Adult and Childhood Obesity" Academic Article
Comment on "A Common Genetic Variant Is Associated with Adult and Childhood Obesity" Academic Article
Common Variants in FTO, MC4R, TMEM18, PRL, AIF1 , and PCSK1 Show Evidence of Association With Adult Obesity in the Greek Population Academic Article
Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease,,,, Academic Article
Common nonsynonymous variants in PCSK1 confer risk of obesity Academic Article
Common polymorphisms of cyclooxygenase-2 and prostaglandin E2 receptor and increased risk for acute coronary syndrome in coronary artery disease Academic Article
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease Academic Article
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus Academic Article
Common variants inCACNA1Cand MDD susceptibility: A comprehensive meta-analysis Academic Article
Common variants near BDNF and SH2B1 show nominal evidence of association with snacking behavior in European populations Academic Article
Common variants near MC4R are associated with fat mass, weight and risk of obesity Academic Article
Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons Academic Article
Comprehensive identification of pleiotropic loci for body fat distribution using the NHGRI‐EBI Catalog of published genome‐wide association studies Academic Article
Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements Academic Article
Congenital Thrombophilic States Associated with Venous Thrombosis: A Qualitative Overview and Proposed Classification System Academic Article
Connective Tissue Growth Factor Is Crucial to Inducing a Profibrotic Environment in “Fibrosis-Resistant” Balb/c Mouse Lungs Academic Article
Contending visions in the evolution of genetic medicine: The case of cancer genetic services in Ontario, Canada Academic Article
Contribution of 24 obesity-associated genetic variants to insulin resistance, pancreatic beta-cell function and type 2 diabetes risk in the French population Academic Article
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals Academic Article
Correction of Population Stratification in Large Multi-Ethnic Association Studies Academic Article
Cortical Serotonin Type-2 Receptor Density in Parents of Children with Autism Spectrum Disorders Academic Article
Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection Academic Article
Cytochrome P450 2E1 Gene Polymorphisms/Haplotypes and Anti-Tuberculosis Drug-Induced Hepatitis in a Chinese Cohort Academic Article
Data mining of gene expression changes in Alzheimer brain Academic Article
De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy Academic Article
De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features Academic Article
De novo pathogenic variant in TUBB2A presenting with arthrogryposis multiplex congenita, brain abnormalities, and severe developmental delay Academic Article
Depression, Migraine With Aura and Migraine Without Aura: Their Familiality and Interrelatedness Academic Article
Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing Academic Article
Developmental Trajectories of Infants With Multiplex Family Risk for Autism Academic Article
Developmental delay in P300 production in children at high risk for developing alcohol-related disorders Academic Article
Diabetes and breast cancer among women with BRCA1 and BRCA2 mutations Academic Article
Diagnosis and high incidence of hyperornithinemia-hyperammonemia-homocitrullinemia (HHH) syndrome in northern Saskatchewan Academic Article
Diagnosis and treatment of dementia: 1. Risk assessment and primary prevention of Alzheimer disease Academic Article
Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH Academic Article
Diagnosis of ‘possible’ mitochondrial disease: an existential crisis Academic Article
Diagnostic stability in young children at risk for autism spectrum disorder: a baby siblings research consortium study Academic Article
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals Academic Article
Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome Sequencing Academic Article
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes Academic Article
Does family history predict the age at onset of new breast cancers inBRCA1andBRCA2mutation-positive families? Academic Article
Does genetic heterogeneity account for the divergent risk of type 2 diabetes in South Asian and white European populations? Academic Article
Dose and polymorphic genes xrcc1, xrcc3, gst play a role in the risk of developing erythema in breast cancer patients following single shot partial breast irradiation after conservative surgery Academic Article
Dynamic interaction between fetal adversity and a genetic score reflecting dopamine function on developmental outcomes at 36 months Academic Article
EMSY and CCND1 amplification in familial breast cancer: from the Ontario site of the Breast Cancer Family Registry Academic Article
Early predictors of language skills at 3 years of age vary based on diagnostic outcome: A baby siblings research consortium study Academic Article
Effect Modification by Catalase Genotype Suggests a Role for Oxidative Stress in the Association of Hormone Replacement Therapy with Postmenopausal Breast Cancer Risk Academic Article
Effect of ENPP1/PC-1-K121Q and PPARγ-Pro12Ala polymorphisms on the genetic susceptibility to T2D in the Tunisian population Academic Article
Effect of Genetic Variants Associated With Plasma Homocysteine Levels on Stroke Risk Academic Article
Effects of TCF7L2 Polymorphisms on Obesity in European Populations Academic Article
Effects of Multiple Genetic Loci on Age at Onset in Late-Onset Alzheimer Disease Academic Article
Effects of lifelong testosterone exposure on health and disease using Mendelian randomization Academic Article
Elucidating the role of genomics in neonatal sepsis Academic Article
Ethnic and population differences in the genetic predisposition to human obesity Academic Article
Evaluating the Association of FAAH Common Gene Variation with Childhood, Adult Severe Obesity and Type 2 Diabetes in the French Population Academic Article
Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALS Academic Article
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 Academic Article
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index Academic Article
Evolution of immune genes is associated with the Black Death Academic Article
Excess of Rare Variants in Non–Genome-Wide Association Study Candidate Genes in Patients With Hypertriglyceridemia Academic Article
Exome Sequencing as a Diagnostic Tool for Pediatric‐Onset Ataxia Academic Article
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction Academic Article
Exploring Gene-Environment Relationships in Cardiovascular Disease Academic Article
Exploring design-related bias in clinical studies on receptor genetic polymorphism of hypertension Academic Article
Expression of a Common LQT1 Mutation in Five Apparently Unrelated Families in a Regional Inherited Arrhythmia Clinic Academic Article
Expression profiling of familial breast cancers demonstrates higher expression of FGFR2 in BRCA2-associated tumors Academic Article
Factors That Predict Risk of Thrombosis in Relatives of Patients With Unprovoked Venous Thromboembolism Academic Article
Factors that predict thrombosis in relatives of patients with venous thromboembolism Academic Article
Familial Amyotrophic Lateral Sclerosis Academic Article
Familial and hormonal risk factors for papillary serous uterine cancer. Academic Article
Family history and improving health. Academic Article
Family history and the risk of gastric cancer Academic Article
Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study Academic Article
Fat Infiltration in Muscle: New Evidence for Familial Clustering and Associations With Diabetes Academic Article
Fine-mapping of 98 obesity loci in Mexican children Academic Article
Fine-tuning of Genome-Wide Polygenic Risk Scores and Prediction of Gestational Diabetes in South Asian Women Academic Article
Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants Academic Article
Functional impact of global rare copy number variation in autism spectrum disorders Academic Article
GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability Academic Article
Gain‐of‐function variants in the melanocortin 4 receptor gene confer susceptibility to binge eating disorder in subjects with obesity: a systematic review and meta‐analysis Academic Article
Gender-based differences in oxidative stress parameters do not underlie the differences in mood disorders susceptibility between sexes Academic Article
Gene × Physical Activity Interactions in Obesity: Combined Analysis of 111,421 Individuals of European Ancestry Academic Article
Gene-Centric Meta-Analysis of Lipid Traits in African, East Asian and Hispanic Populations Academic Article
Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders Academic Article
Genes, the environment and personalized medicine Academic Article
Genetic Analysis of 103 Candidate Genes for Coronary Artery Disease and Associated Phenotypes in a Founder Population Reveals a New Association between Endothelin-1 and High-Density Lipoprotein Cholesterol Academic Article
Genetic Determinants of “Cognitive Impairment, No Dementia” Academic Article
Genetic Differential Susceptibility to Socioeconomic Status and Childhood Obesogenic Behavior Academic Article
Genetic Etiology of Isolated Low HDL Syndrome Academic Article
Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium Academic Article
Genetic Loci Associated With Plasma Concentration of Low-Density Lipoprotein Cholesterol, High-Density Lipoprotein Cholesterol, Triglycerides, Apolipoprotein A1, and Apolipoprotein B Among 6382 White Women in Genome-Wide Analysis With Replication Academic Article
Genetic Predictors of Cardiovascular Mortality During Intensive Glycemic Control in Type 2 Diabetes: Findings From the ACCORD Clinical Trial Academic Article
Genetic Risk Evaluation in Wet Age-Related Macular Degeneration Treatment Response Academic Article
Genetic Risk Factors Are Not Associated with Wet Age-Related Macular Degeneration Treatment Response to Ranibizumab Academic Article
Genetic Risk Factors for Post-Infectious Irritable Bowel Syndrome Following a Waterborne Outbreak of Gastroenteritis Academic Article
Genetic Susceptibility for Atrial Fibrillation in Patients Undergoing Atrial Fibrillation Ablation Academic Article
Genetic Susceptibility to West Nile Virus and Dengue Academic Article
Genetic Tools for Coronary Risk Assessment in Type 2 Diabetes: A Cohort Study From the ACCORD Clinical Trial Academic Article
Genetic Variants and Susceptibility to Neurological Complications Following West Nile Virus Infection Academic Article
Genetic Variants in Vitamin D Pathway Genes and Risk of Pancreas Cancer; Results from a Population-Based Case-Control Study in Ontario, Canada Academic Article
Genetic Variation in the Ontario Neurodegenerative Disease Research Initiative Academic Article
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits Academic Article
Genetic and phenotypic determinants of blood pressure and other cardiovascular risk factors (GAPP) Academic Article
Genetic considerations in recurrent congenital diaphragmatic hernia in two siblings Academic Article
Genetic influences on ADHD symptom dimensions: Examination of a priori candidates, gene-based tests, genome-wide variation, and SNP heritability Academic Article
Genetic interaction between α4 and β2 subunits of high affinity nicotinic receptor: analysis in schizophrenia Academic Article
Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration Academic Article
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs Academic Article
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies Academic Article
Genetic risk for dengue hemorrhagic fever and dengue fever in multiple ancestries Academic Article
Genetic susceptibility loci of idiopathic interstitial pneumonia do not represent risk for systemic sclerosis: a case control study in Caucasian patients Academic Article
Genetic susceptibility to beryllium: a case–referent study of men and women of working age with sarcoidosis or other chronic lung disease Academic Article
Genetic testing for atherosclerosis risk: Inevitability or pipe dream? Academic Article
Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes Academic Article
Genetic variants of MARCO are associated with susceptibility to pulmonary tuberculosis in a Gambian population Academic Article
Genetics in obstetricians? offices: a survey study*1 Academic Article
Genetics of Coagulation: What the Cardiologist Needs to Know Academic Article
Genitourinary Cancer Predisposition Syndromes Academic Article
Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24 Academic Article
Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias Academic Article
Genome-Wide Association Studies of Hypertension: Have They Been Fruitful? Academic Article
Genome-Wide Association Studies—Data Generation, Storage, Interpretation, and Bioinformatics Academic Article
Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke Academic Article
Genome-wide Association Analysis of Blood-Pressure Traits in African-Ancestry Individuals Reveals Common Associated Genes in African and Non-African Populations Academic Article
Genome-wide Linkage Analysis for Severe Obesity in French Caucasians Finds Significant Susceptibility Locus on Chromosome 19q Academic Article
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets Academic Article
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences Academic Article
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk Academic Article
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Academic Article
Genome-wide association scans identified CTNNBL1 as a novel gene for obesity Academic Article
Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations Academic Article
Genome-wide association study of alcohol use disorder identification test (AUDIT) scores in 20 328 research participants of European ancestry Academic Article
Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status Academic Article
Genome-wide detection of tandem DNA repeats that are expanded in autism Academic Article
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture Academic Article
Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke Academic Article
Genome‐Wide Association Study Identifies First Locus Associated with Susceptibility to Cerebral Venous Thrombosis Academic Article
Genomic architecture of autism from comprehensive whole-genome sequence annotation Academic Article
Genotype and phenotype in 12 additional individuals with SATB2 -associated syndrome Academic Article
Germline HOXB13 p.Gly84Glu mutation and risk of colorectal cancer Academic Article
Germline variation in inflammation-related pathways and risk of Barrett's oesophagus and oesophageal adenocarcinoma Academic Article
Germline variation in the insulin-like growth factor pathway and risk of Barrett’s esophagus and esophageal adenocarcinoma Academic Article
Give GWAS a Chance Academic Article
Glucocorticoid Receptors, Brain-Derived Neurotrophic Factor, Serotonin and Dopamine Neurotransmission are Associated with Interferon-Induced Depression Academic Article
Gross motor problems and psychiatric disorders in children Academic Article
HDL Cholesterol, LDL Cholesterol, and Triglycerides as Risk Factors for CKD: A Mendelian Randomization Study Academic Article
HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome Academic Article
Hereditary risk factors for the development of gastric cancer in younger patients Academic Article
High Urinary Calcium Excretion and Genetic Susceptibility to Hypertension and Kidney Stone Disease Conference Paper
High resolution mapping in the major histocompatibility complex region identifies multiple independent novel loci for psoriatic arthritis Academic Article
Homocysteine and stroke Academic Article
Hormone Replacement Therapy After Oophorectomy and Breast Cancer Risk Among BRCA1 Mutation Carriers Academic Article
How Effective Are Antioxidant Supplements in Obesity and Diabetes? Academic Article
Hundreds of variants clustered in genomic loci and biological pathways affect human height Academic Article
IFITM3 and Susceptibility to Respiratory Viral Infections in the Community Academic Article
IL-10R Polymorphisms Are Associated with Very-early-onset Ulcerative Colitis Academic Article
Identification of Circulating Proteins Associated With Blood Pressure Using Mendelian Randomization Academic Article
Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody–Associated Vasculitis Academic Article
Identification of Multiple Genetic Susceptibility Loci in Takayasu Arteritis Academic Article
Identification of Susceptibility Loci inIL6,RPS9/LILRB3, and an Intergenic Locus on Chromosome 21q22 in Takayasu Arteritis in a Genome-Wide Association Study Academic Article
Identification of amino acid variation in the prion protein associated with classical scrapie in Canadian dairy goats Academic Article
Identification of genetic effects underlying type 2 diabetes in South Asian and European populations Academic Article
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease Academic Article
Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study Academic Article
Identifying genetic and environmental risk factors for chronic orofacial pain syndromes: human models. Academic Article
Immunochip Analysis Identifies Multiple Susceptibility Loci for Systemic Sclerosis Academic Article
Impact of Inherited Thrombophilia on Venous Thromboembolism in Children Academic Article
Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity Academic Article
Impact of a Genetic Risk Score on Myocardial Infarction Risk Across Different Ethnic Populations Academic Article
Implication of the Pro12Ala polymorphism of the PPAR-gamma 2gene in type 2 diabetes and obesity in the French population Academic Article
Increased Extra-axial Cerebrospinal Fluid in High-Risk Infants Who Later Develop Autism Academic Article
Increased Hepatic PDGF-AA Signaling Mediates Liver Insulin Resistance in Obesity-Associated Type 2 Diabetes Academic Article
Increased intestinal permeability precedes the onset of Crohn's disease in a subject with familial risk Academic Article
Increased prevalence of pathogenic bacteria in the gut microbiota of infants at risk of developing celiac disease: The PROFICEL study Academic Article
Individual common variants exert weak effects on the risk for autism spectrum disorders Academic Article
Influence of Milk-Feeding Type and Genetic Risk of Developing Coeliac Disease on Intestinal Microbiota of Infants: The PROFICEL Study Academic Article
Influence of Parental Concordance for Psychiatric Disorders on Psychopathology in Offspring Academic Article
Influence of depression on genetic predisposition to type 2 diabetes in a multiethnic longitudinal study Academic Article
Influence of early environmental factors on lymphocyte subsets and gut microbiota in infants at risk of celiac disease; the PROFICEL study. Academic Article
Influence of thrombophilia on risk of recurrent venous thromboembolism while on warfarin: results from a randomized trial Academic Article
Informative phenotypes for genetic studies of psychiatric disorders Academic Article
Inherited Thrombophilia and the Risk of Arterial Ischemic Stroke: A Systematic Review and Meta‐Analysis Academic Article
Interaction between GPR120 p.R270H loss-of-function variant and dietary fat intake on incident type 2 diabetes risk in the D.E.S.I.R. study Academic Article
Investigation on ERCC5 genetic polymorphisms and the development of gastric cancer in a Chinese population Academic Article
Is There a Genetic Predisposition to Anterior Cruciate Ligament Tear? A Systematic Review Academic Article
Is serotonin transporter polymorphism (5-HTTLPR) allele status a predictor for obsessive-compulsive disorder? A meta-analysis Academic Article
Krüppel-like factor 1: hematologic phenotypes associated withKLF1gene mutations Academic Article
Lack of Association ofCD36SNPs With Early Onset Obesity: A Meta-Analysis in 9,973 European Subjects Academic Article
Lack of association between type 2 diabetes and major depression: epidemiologic and genetic evidence in a multiethnic population Academic Article
Language delay aggregates in toddler siblings of children with autism spectrum disorder Academic Article
Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci Academic Article
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation Academic Article
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease Academic Article
Lifestyle Interaction With Fat Mass and Obesity-Associated (FTO) Genotype and Risk of Obesity in Apparently Healthy U.S. Women Academic Article
Lifestyle factors and fetal and childhood origins of type 2 diabetes: a prospective study of Chinese and European adults Academic Article
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 Academic Article
LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemias Academic Article
Loci influencing blood pressure identified using a cardiovascular gene-centric array Academic Article
Longitudinal Decline in Lung Volume in a Population of Children with Sickle Cell Disease Academic Article
Longitudinal relationships between glycemic status and body mass index in a multiethnic study: evidence from observational and genetic epidemiology Academic Article
Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations Academic Article
Loss‐of‐function mutations in the melanocortin‐3 receptor gene confer risk for human obesity: A systematic review and meta‐analysis Academic Article
Low copy number of the salivary amylase gene predisposes to obesity Academic Article
Lung Development and Susceptibility to Chronic Obstructive Pulmonary Disease Academic Article
MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation Academic Article
Magnetic Resonance Imaging Improves Breast Screening Sensitivity in BRCA Mutation Carriers Age ≥ 50 Years: Evidence From an Individual Patient Data Meta-Analysis Academic Article
Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2 Academic Article
Management of the BRCA Mutation Carrier or High-Risk Patient Academic Article
Manifestations of Von Hippel Lindau syndrome: a retrospective national review Academic Article
Mapping autism risk loci using genetic linkage and chromosomal rearrangements Academic Article
Maternal Obesity and Developmental Programming of Metabolic Disorders in Offspring: Evidence from Animal Models Academic Article
Maternal childhood adversity and child temperament: An association moderated by child 5-HTTLPR genotype Academic Article
Mendelian Genes and Risk of Intracerebral Hemorrhage and Small-Vessel Ischemic Stroke in Sporadic Cases Academic Article
Mendelian Randomization Studies Do Not Support a Role for Vitamin D in Coronary Artery Disease Academic Article
Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels Academic Article
Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12 Academic Article
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease Academic Article
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia Academic Article
Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes Academic Article
Methylenetetrahydrofolate Reductase Gene Variant (MTHFR C677T) and Migraine: A Case Control Study and Meta-analysis Academic Article
Methylenetetrahydrofolate Reductase Polymorphisms and Homocysteine-Lowering Effect of Vitamin Therapy in Singaporean Stroke Patients Academic Article
Mining the Human Phenome Using Allelic Scores That Index Biological Intermediates Academic Article
Modeling Complex Disease with Demographic and Environmental Covariates and a Candidate Gene Marker Academic Article
Modelling the Community as a Determinant of Health Academic Article
Modulation of GLP-1 Levels by a Genetic Variant That Regulates the Cardiovascular Effects of Intensive Glycemic Control in ACCORD Academic Article
Modulatory effect of the SLC9A3 gene on susceptibility to infections and pulmonary function in children with cystic fibrosis Academic Article
Molecular Genetic Analysis of the Idd4 Locus Implicates the IFN Response in Type 1 Diabetes Susceptibility in Nonobese Diabetic Mice Academic Article
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression Academic Article
Mothers and daughters from breast cancer families: a qualitative study of their perceptions of risks and benefits associated with minor's participation in genetic susceptibility research. Academic Article
Mouse models of cystathionine β‐synthase deficiency reveal significant threshold effects of hyperhomocysteinemia Academic Article
Moyamoya Disease Susceptibility Variant RNF213 p.R4810K Increases the Risk of Ischemic Stroke Attributable to Large-Artery Atherosclerosis Academic Article
Multi-Ethnic Genetic Association Study of Carotid Intima-Media Thickness Using a Targeted Cardiovascular SNP Microarray Academic Article
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction Academic Article
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation Academic Article
Multi-ethnic genome-wide association study for atrial fibrillation Academic Article
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes Academic Article
Multigene panels in prostate cancer risk assessment. Academic Article
Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis Academic Article
Multivariate Meta-Analysis of Genetic Association Studies: A Simulation Study Academic Article
Mutations That Alter the Carboxy-Terminal-Propeptide Cleavage Site of the Chains of Type I Procollagen Are Associated With a Unique Osteogenesis Imperfecta Phenotype Academic Article
Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation Academic Article
NAT2 genetic polymorphisms and anti-tuberculosis drug-induced hepatotoxicity in Chinese community population Academic Article
Natural history and genotype‐phenotype correlations in 72 individuals with SATB2 ‐associated syndrome Academic Article
Neuronal Correlates of Brain-derived Neurotrophic Factor Val66Met Polymorphism and Morphometric Abnormalities in Bipolar Disorder Academic Article
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders Academic Article
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk Academic Article
Next-Generation Sequencing to Diagnose Muscular Dystrophy, Rhabdomyolysis, and HyperCKemia Academic Article
No Association between the 20210 G/A Prothrombin Gene Mutation and Premature Coronary Artery Disease Academic Article
North American Thrombosis Forum, AF Action Initiative Consensus Document Academic Article
Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index Academic Article
Novel Drug Targets for Ischemic Stroke Identified Through Mendelian Randomization Analysis of the Blood Proteome Academic Article
Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals Academic Article
Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity Academic Article
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits Academic Article
Novel players in coeliac disease pathogenesis: role of the gut microbiota Academic Article
Nutrition and the early origins of adult disease Academic Article
Obesity Genes and Risk of Major Depressive Disorder in a Multiethnic Population Academic Article
Obesity genetics: insights from the Pakistani population Academic Article
Obsessive-compulsive disorder (OCD): is this disorder under-recognized? Academic Article
On the origin of obesity: identifying the biological, environmental and cultural drivers of genetic risk among human populations Academic Article
Oxytocin Receptor Polymorphisms are Differentially Associated with Social Abilities across Neurodevelopmental Disorders Academic Article
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study Academic Article
PDZK1 in leukocytes protects against cellular apoptosis and necrotic core development in atherosclerotic plaques in high fat diet fed ldl receptor deficient mice Academic Article
Pan-urologic cancer genomic subtypes that transcend tissue of origin Academic Article
Paraoxonase promoter and intronic variants modify risk of sporadic amyotrophic lateral sclerosis Academic Article
Parental and child genetic contributions to obesity traits in early life based on 83 loci validated in adults: the FAMILY study Academic Article
Parents’ Understanding of Genetics and Heritability Academic Article
Parkinson-susceptibility gene DJ-1/PARK7 protects the murine heart from oxidative damage in vivo Academic Article
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome Academic Article
PedSplit: pedigree management for stratified analysis Academic Article
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 Conference Paper
Penetrance of Polygenic Obesity Susceptibility Loci across the Body Mass Index Distribution Academic Article
Per3 length polymorphism in patients with type 2 diabetes mellitus Academic Article
Perceptions About Genetic Testing for the Susceptibility to Alcohol Dependence and Other Multifactorial Diseases Academic Article
Performance characteristics of a brief Family History Questionnaire to screen for Lynch syndrome in women with newly diagnosed endometrial cancer Academic Article
Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition Syndromes Academic Article
Pharmacogenetics in Cardiovascular Disease: The Challenge of Moving From Promise to Realization Academic Article
Phenotypic Analysis of Arrhythmogenic Cardiomyopathy in the Hutterite Population: Role of Electrocardiogram in Identifying High‐Risk Desmocollin‐2 Carriers Academic Article
Physical activity and genetic predisposition to obesity in a multiethnic longitudinal study Academic Article
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study Academic Article
Polygenic Risk Score for Alzheimer's Disease in Caribbean Hispanics Academic Article
Polygenic determinants of severe hypertriglyceridemia Academic Article
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders Academic Article
Polymorphism in the CETP Gene Region, HDL Cholesterol, and Risk of Future Myocardial Infarction Academic Article
Polymorphisms Near TBX5 and GDF7 Are Associated With Increased Risk for Barrett’s Esophagus Academic Article
Population-Based Study to Determine the Health System Costs of Using the 21-Gene Assay Academic Article
Predicting novel disease mutations in the cardiac sodium channel Academic Article
Predictive genetic testing for coronary artery disease Academic Article
Predictive genetic tests and health system costs. Academic Article
Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders Academic Article
Pregnancy and Birth Complications in Autism and Liability to the Broader Autism Phenotype Academic Article
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 Academic Article
Presence of Alanine-to-Valine Substitutions in Myofibrillogenesis Regulator 1 in Paroxysmal Nonkinesigenic Dyskinesia Academic Article
Prevalence of common MEFV mutations and carrier frequencies in a large cohort of Iranian populations Academic Article
Primary mediastinal paraganglioma associated with a familial variant in the succinate dehydrogenase B subunit gene Academic Article
Prospective study of high-risk, BRCA1/2-mutation negative women: the ‘negative study’ Academic Article
Protein Z Levels, Protein Z G79A Polymorphism, and Prothrombotic Conditions Academic Article
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways Academic Article
Psychopathology and Achievement in Children at High Risk for Developing Alcoholism Academic Article
Quality of life and psychosexual adjustment after prophylactic oophorectomy for a family history of ovarian cancer. Academic Article
Quebec Platelet Disorder: Update on Pathogenesis, Diagnosis, and Treatment Academic Article
R125W coding variant in TBC1D1 confers risk for familial obesity and contributes to linkage on chromosome 4p14 in the French population Academic Article
RAD51 polymorphisms and breast cancer risk Academic Article
Rank-based genome-wide analysis reveals the association of Ryanodine receptor-2 gene variants with childhood asthma among human populations Academic Article
Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions Academic Article
Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD Academic Article
Rare DNA copy number variants in cardiovascular malformations with extracardiac abnormalities Academic Article
Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes Academic Article
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease Academic Article
Re: Magnetic Resonance Imaging and Mammography in Women With a Hereditary Risk of Breast Cancer Academic Article
Recent insights into neuromuscular junction biology in Duchenne muscular dystrophy: Impacts, challenges, and opportunities Academic Article
Recent progress in genetics, epigenetics and metagenomics unveils the pathophysiology of human obesity Academic Article
Recognizing BRCA gene mutation risk subsequent to breast cancer diagnosis in southwestern Ontario. Academic Article
Recommendations for national and local regulatory authorities concerning research in genetic markers of disease Academic Article
Reduced expression of hemopoietic cytokine receptors on cord blood progenitor cells in neonates at risk for atopy. Academic Article
Relationship Between Genetic Risk and Age of Diagnosis in Systemic Lupus Erythematosus Academic Article
Repetitive Behavior in 12-Month-Olds Later Classified With Autism Spectrum Disorder Academic Article
Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample Academic Article
Responses to panic induction procedures in subjects with multiple chemical sensitivity/idiopathic environmental intolerance: understanding the relationship with panic disorder. Academic Article
Restricted and Repetitive Behavior and Brain Functional Connectivity in Infants at Risk for Developing Autism Spectrum Disorder Academic Article
Revisiting the evolutionary origins of obesity: lazy versus peppy-thrifty genotype hypothesis Academic Article
Risk Alleles in/near ADCY5, ADRA2A, CDKAL1, CDKN2A/B, GRB10, and TCF7L2 Elevate Plasma Glucose Levels at Birth and in Early Childhood: Results from the FAMILY Study Academic Article
Risk factors for ovarian cancer and early-onset breast cancer in Mongolia. Academic Article
Role of Macrophage Migration Inhibitory Factor in Granulomatosis With Polyangiitis Conference Paper
Role of genetics in the prediction of statin-associated muscle symptoms and optimization of statin use and adherence Academic Article
Role of polymorphic bile salt export pump (BSEP, ABCB11) transporters in anti-tuberculosis drug-induced liver injury in a Chinese cohort Academic Article
Role of polymorphism of methyltetrahydrofolate-homocysteine methyltransferase (MTR) A2756G and breast cancer risk Academic Article
Ruling in and ruling out: Implications of molecular genetic diagnoses for disease classification Academic Article
SAMHD1 Mutations Are Also Responsible for Aicardi–Goutières in the Cree Population Academic Article
SNPs and coronary heart disease Academic Article
ST3GAL3 Mutations Impair the Development of Higher Cognitive Functions Academic Article
Screening of hypoxia-inducible genes in sporadic ALS Academic Article
Second Primary Malignancy Risk in Thyroid Cancer Survivors: A Systematic Review and Meta-Analysis Academic Article
Segregating patterns of copy number variations in extended autism spectrum disorder ( ASD ) pedigrees Academic Article
Selecting a BRCA risk assessment model for use in a familial cancer clinic Academic Article
Sentinel Symptoms in Patients with Unexplained Cardiac Arrest: From the Cardiac Arrest Survivors with Preserved Ejection Fraction Registry (CASPER) Academic Article
Sex differences in repetitive stereotyped behaviors in autism: Implications for genetic liability Academic Article
Sex-Specific Effect of Insulin-Dependent Diabetes 4 on Regulation of Diabetes Pathogenesis in the Nonobese Diabetic Mouse Academic Article
Sex/Gender Modifies the Association Between the MC4R p.Ile269Asn Mutation and Type 2 Diabetes in the Mexican Population Academic Article
Simoctocog Alfa (Nuwiq) in Previously Untreated Patients with Severe Haemophilia A: Final Results of the NuProtect Study Academic Article
Single nucleotide polymorphism in IL1B is associated with infection risk in paediatric acute myeloid leukaemia Academic Article
Single nucleotide polymorphisms in the matrix metalloproteinase gene family and the frequency and duration of gastroesophageal reflux disease influence the risk of esophageal adenocarcinoma Academic Article
Small rodent models of atherosclerosis Academic Article
Sodium Intake and Cardiovascular Health Academic Article
Spontaneous Degeneration of Supraventricular Tachycardia to Ventricular Fibrillation Academic Article
Strain-Related Difference in Susceptibility to Anaphylactic Shock Correlates with Measures of Spontaneous Activity Academic Article
StrandAdvantage test for early-line and advanced-stage treatment decisions in solid tumors Academic Article
Stroke genetics informs drug discovery and risk prediction across ancestries Academic Article
Study of TNFα -308G/A and IL6 -174G/C polymorphisms in type 2 diabetes and obesity risk in the Tunisian population Academic Article
Susceptibility to chronic pain following nerve injury is genetically affected by CACNG2 Academic Article
Synaptic, transcriptional and chromatin genes disrupted in autism Academic Article
Systematic Review and Meta-analysis: Gene Association Studies in Neonatal Sepsis Academic Article
Targeted Gene Sequencing Identifies Variants in the Protein C and Endothelial Protein C Receptor Genes in Patients With Unprovoked Venous Thromboembolism Academic Article
Telomere Length, Oxidative Stress, Inflammation and BDNF Levels in Siblings of Patients with Bipolar Disorder: Implications for Accelerated Cellular Aging Academic Article
Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care Academic Article
The 9p21.3 locus and cardiovascular risk in familial hypercholesterolemia Academic Article
The Brain-Derived Neurotrophic Factor Val66Met Polymorphism, Hippocampal Volume, and Cognitive Function in Geriatric Depression Academic Article
The Complex Genetic Basis of Plasma Triglycerides Academic Article
The Effect of Prothrombotic Blood Abnormalities on Risk of Deep Vein Thrombosis in Users of Hormone Replacement Therapy Academic Article
The Emergence of Network Inefficiencies in Infants With Autism Spectrum Disorder Academic Article
The Familial Aggregation of the Lesser Variant in Biological and Nonbiological Relatives of PDD Probands: a Family History Study Academic Article
The Familial Predisposition toward Tearing the Anterior Cruciate Ligament Academic Article
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 Academic Article
The Genetic Factors of the Airway Epithelium Associated with the Pathology of Asthma Academic Article
The Genetic Link Between Diabetes and Atherosclerosis Academic Article
The Idd4 Locus Displays Sex-Specific Epistatic Effects on Type 1 Diabetes Susceptibility in Nonobese Diabetic Mice Academic Article
The MC4R p.Ile269Asn mutation confers a high risk for type 2 diabetes in the Mexican population via obesity dependent and independent effects Academic Article
The Melanocortin 4 Receptor p.Ile269Asn Mutation Is Associated with Childhood and Adult Obesity in Mexicans Academic Article
The Psychodynamic Psychotherapist's Guide to the Interaction among Sex, Genes, and Environmental Adversity in the Etiology of Depression for Women Academic Article
The Role of Endogenous Hormones in the Etiology and Prevention of Breast Cancer: The Epidemiological Evidence Conference Paper
The T-786→C Mutation in Endothelial Nitric Oxide Synthase Is Associated With Hypertension Academic Article
The association between HLA-DQB1 polymorphism and antituberculosis drug-induced liver injury: a Case-Control Study Academic Article
The association between glutathione S-transferase M1 genotype and polycyclic aromatic hydrocarbon-DNA adducts in breast tissue. Academic Article
The association of HTR2A polymorphisms with obsessive-compulsive disorder and its subtypes: A meta-analysis Academic Article
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 Academic Article
The complex genetics of amyotrophic lateral sclerosis Academic Article
The double-edged sword of gut bacteria in celiac disease and implications for therapeutic potential Academic Article
The functional variant rs1048990 in PSMA6 is associated with susceptibility to myocardial infarction in a Chinese population Academic Article
The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies Academic Article
The impact of prophylactic salpingo-oophorectomy on menopausal symptoms and sexual function in women who carry a BRCA mutation Academic Article
The impact of prophylactic salpingo-oophorectomy on quality of life and psychological distress in women with a BRCA mutation Academic Article
The importance of gene–environment interactions in human obesity Academic Article
The incidence of leukaemia in women with BRCA1 and BRCA2 mutations: an International Prospective Cohort Study Academic Article
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 Academic Article
The long-term functional consequences of acute infectious diarrhea Academic Article
The need for inclusion of sex and age of onset variables in genetic association studies of obsessive–compulsive disorder: Overview Academic Article
The phenotypic manifestations of rare genic CNVs in autism spectrum disorder Academic Article
The potential to predict the course of childhood asthma Academic Article
The protective effect of the obesity-associated rs9939609 A variant in fat mass- and obesity-associated gene on depression Academic Article
The risks of cancer in older women with BRCA pathogenic variants: How far have we come? Academic Article
The search for autism disease genes Academic Article
Thiopurine S-methyltransferase testing for averting drug toxicity: a meta-analysis of diagnostic test accuracy Academic Article
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies Academic Article
Thrombocytopenic Platelet Disorders Academic Article
Thrombophilia and location of venous thromboembolism Academic Article
Thrombus stability explains the factor V Leiden paradox: a mouse model Academic Article
Towards the genetic basis of cerebral venous thrombosis—the BEAST Consortium: a study protocol: Table 1 Academic Article
Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders Academic Article
Transcription Factor TCF7L2 Genetic Study in the French Population Academic Article
Translating genomic analyses into improved management of coronary artery disease Academic Article
Treatment of infertility does not increase the risk of ovarian cancer among women with a BRCA1 or BRCA2 mutation Academic Article
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia Academic Article
Tumor Necrosis Factor Alpha Gene Polymorphism Associated with Increased Susceptibility to Venous Leg Ulceration Academic Article
Two BRM promoter insertion polymorphisms increase the risk of early‐stage upper aerodigestive tract cancers Academic Article
Two New Loci for Body-Weight Regulation Identified in a Joint Analysis of Genome-Wide Association Studies for Early-Onset Extreme Obesity in French and German Study Groups Academic Article
Type 2 Diabetes Whole-Genome Association Study in Four Populations: The DiaGen Consortium Academic Article
Understanding the Role of DISC1 in Psychiatric Disease and during Normal Development Academic Article
Upcoming biomarkers for the diagnosis of Kawasaki disease: A review Academic Article
Update on bipolar disorder biomarker candidates Academic Article
Use of latent class models to accommodate inter-laboratory variation in assessing genetic polymorphisms associated with disease risk Academic Article
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes Academic Article
Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes Academic Article
Variants of the SFTPA1 and SFTPA2 genes and susceptibility to tuberculosis in Ethiopia Academic Article
Variation in FTO contributes to childhood obesity and severe adult obesity Academic Article
Vitamin D Levels, Vitamin D Receptor Polymorphisms, and Inflammatory Cytokines in Aromatase Inhibitor-Induced Arthralgias: An Analysis of CCTG MA.27 Academic Article
Weight Gain and the Risk of Ovarian Cancer in BRCA1 and BRCA2 Mutation Carriers Conference Paper
What have we learned from basic science studies on idiopathic pulmonary fibrosis? Academic Article
White Matter Microstructure and Atypical Visual Orienting in 7-Month-Olds at Risk for Autism Academic Article
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder Academic Article
Whole-exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study Academic Article
Whole-genome sequencing of quartet families with autism spectrum disorder Academic Article
Why don't pigs get diabetes? Explanations for variations in diabetes susceptibility in human populations living in a diabetogenic environment Academic Article
[Study on polymorphisms of genes with susceptibility to drug induced liver injury in a cohort receiving anti-tuberculosis treatment]. Academic Article
c.1058C>T variant in theSERPINC1gene is pathogenic for antithrombin deficiency Academic Article
eQTL Set–Based Association Analysis Identifies Novel Susceptibility Loci for Barrett Esophagus and Esophageal Adenocarcinoma Academic Article
“Benign” early repolarization versus malignant early abnormalities: Clinical-electrocardiographic distinction and genetic basis Academic Article
“If He Has it, We Know What to Do”: Parent Perspectives on Familial Risk for Autism Spectrum Disorder Academic Article

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