Genotype Concept

subject area of

• 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
• A Discovery Resource of Rare Copy Number Variations in Individuals with Autism Spectrum Disorder  Academic Article
• A Genetic Study of the Ghrelin and Growth Hormone Secretagogue Receptor (GHSR) Genes and Stature  Academic Article
• A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans  Academic Article
• A Genome-Wide Association Study Identifies rs2000999 as a Strong Genetic Determinant of Circulating Haptoglobin Levels  Academic Article
• A Genome-Wide Association Study for Coronary Artery Disease Identifies a Novel Susceptibility Locus in the Major Histocompatibility Complex  Academic Article
• A Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms for Acute Kidney Injury  Academic Article
• A Large Pseudoautosomal Region on the Sex Chromosomes of the Frog Silurana tropicalis  Academic Article
• A Large-Scale Genetic Analysis Reveals a Strong Contribution of the HLA Class II Region to Giant Cell Arteritis Susceptibility  Academic Article
• A Mild Phenotype of Severe β+ Thalassemia in a 16-Month-Old Boy  Academic Article
• A New Mutation in the Thyroid Hormone Receptor (TR) β Gene (V458A) in a Family with Resistance to Thyroid Hormone (RTH)  Academic Article
• A Novel Sickling Hemoglobinopathy  Academic Article
• A Novel Type 2A von Willebrand Factor Mutation (V1499E) Associated With Variable Clinical Expression  Academic Article
• A Population Genetics Model for Multiple Quantitative Traits Exhibiting Pleiotropy and Epistasis  Academic Article
• A Rare Variant in the Visfatin Gene (NAMPT/PBEF1 ) Is Associated With Protection From Obesity  Academic Article
• A genome-wide scan for common alleles affecting risk for autism  Academic Article
• A genotype-directed comparative effectiveness trial of Bucindolol and metoprolol succinate for prevention of symptomatic atrial fibrillation/atrial flutter in patients with heart failure: Rationale and design of the GENETIC-AF trial  Academic Article
• A genotype-to-phenotype map of in vitro selected RNA-cleaving DNAzymes: implications for accessing the target phenotype  Academic Article
• A large-scale candidate gene association study of age at menarche and age at natural menopause  Academic Article
• A method to estimate the contribution of regional genetic associations to complex traits from summary association statistics  Academic Article
• A molecular genetic study of factor XI deficiency.  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 multisystem disease associated with recessive mutations in the tyrosyl-tRNA synthetase (YARS) gene  Academic Article
• A novel mutation in the PYGM gene in a family with pseudo-dominant transmission of McArdle disease  Academic Article
• A phenome-wide association study of a lipoprotein-associated phospholipase A2loss-of-function variant in 90 000 Chinese adults  Academic Article
• A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia  Academic Article
• A randomised, double blind comparison of tecarfarin, a novel vitamin K antagonist, with warfarin  Academic Article
• A randomized study of alpha-interferon plus ribavirin for 6 months or 12 months for the treatment of chronic hepatitis C in patients with bleeding disorders  Academic Article
• A role for corticotropin releasing factor (CRF) in ethanol consumption, sensitivity, and reward as revealed by CRF-deficient mice  Academic Article
• A standardised method for interpreting the association between mutations and phenotypic drug resistance inMycobacterium tuberculosis  Academic Article
• AGTR1 gene variation: Association with depression and frontotemporal morphology  Academic Article
• APOA5 and APOA1 polymorphisms are associated with triglyceride levels in Mexican children  Academic Article
• APOL1 Genotype and Renal Function of Black Living Donors  Academic Article
• Absence of germline and somatic p53 alterations in children with sporadic brain tumors.  Academic Article
• Accuracy and Biological Variation of Human Serum Paraoxonase 1 Activity and Polymorphism (Q192R) by Kinetic Enzyme Assay  Academic Article
• Accuracy of p53 Codon 72 Polymorphism Status Determined by Multiple Laboratory Methods: A Latent Class Model Analysis  Academic Article
• Active metabolite concentration of clopidogrel in patients taking different doses of aspirin: results of the interaction trial  Academic Article
• Adenoviral Transfer of Murine Oncostatin M Elicits Periosteal Bone Apposition in Knee Joints of Mice, Despite Synovial Inflammation and Up-Regulated Expression of Interleukin-6 and Receptor Activator of Nuclear Factor-κB Ligand  Academic Article
• Admixture mapping of male nuptial colour and body shape in a recently formed hybrid population of threespine stickleback  Academic Article
• Adrenergic alpha 2C receptor genomic organization: Association study in adult ADHD  Academic Article
• Advances in Genomic Analysis of Stroke  Academic Article
• Adverse effects of β-agonists  Academic Article
• Alcohol dehydrogenase 3 genotype modification of the association of alcohol consumption with breast cancer risk.  Academic Article
• An image database of Drosophila melanogaster wings for phenomic and biometric analysis  Academic Article
• An initial investigation of associations between dopamine-linked genetic variation and smoking motives in African Americans  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 the contribution of FTO, NPC1, ENPP1, NEGR1, GNPDA2 and MC4Rgenes to obesity in Mexican children  Academic Article
• Analytical strategies to include the X‐chromosome in variance heterogeneity analyses: Evidence for trait‐specific polygenic variance structure  Academic Article
• Angiogenin Levels and ANG Genotypes: Dysregulation in Amyotrophic Lateral Sclerosis  Academic Article
• Angiotensin converting enzyme genotypes and disease  Academic Article
• Apnea and Oxygen Desaturations in Children Treated with Opioids after Adenotonsillectomy for Obstructive Sleep Apnea Syndrome  Academic Article
• Apolipoprotein E e4 allele affects risk of hyperhomocysteinemia in the elderly  Academic Article
• Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations  Academic Article
• Assessing the effects of 35 European-derived BMI-associated SNPs in Mexican children  Academic Article
• Assessing the time dependence of prognostic values of cytology and human papillomavirus testing in cervical cancer screening  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 PPAR-γ2 Pro12Ala genotype and insulin resistance is modified by circulating lipids in Mexican children  Academic Article
• Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data  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 maternal childhood maltreatment and mother-infant attachment disorganization: Moderation by maternal oxytocin receptor gene and cortisol secretion  Academic Article
• Association between the seven-repeat allele of the dopamine-4 receptor gene (DRD4) and spontaneous food intake in pre-school children  Academic Article
• Association between three functional polymorphisms of the dopamine D2 receptor gene and polydipsia in schizophrenia  Academic Article
• Association between tumor necrosis factor-α promoter −308 A/G polymorphism and susceptibility to sepsis and sepsis mortality: A systematic review and meta-analysis  Academic Article
• Association of BRM promoter polymorphisms and esophageal adenocarcinoma outcome  Academic Article
• Association of Granulomatosis With Polyangiitis (Wegener's) WithHLA-DPB1*04andSEMA6AGene Variants: Evidence From Genome-Wide Analysis  Academic Article
• Association of Melanin-Concentrating Hormone Receptor 1 5' Polymorphism With Early-Onset Extreme Obesity  Academic Article
• Association of autism severity with a monoamine oxidase A functional polymorphism  Academic Article
• Association of common variants in the human eyes shut ortholog (EYS) with statin-induced myopathy: Evidence for additional functions of EYS  Academic Article
• Association of polymorphisms of the tryptophan hydroxylase 2 gene with risk for bipolar disorder or suicidal behavior  Academic Article
• Association of the CPT1B Gene with Skeletal Muscle Fat Infiltration in Afro-Caribbean Men  Academic Article
• Association study between fibronectin and coronary heart disease  Academic Article
• Association study of the estrogen receptor gene ESR1 with postpartum depression—a pilot study  Academic Article
• Associations between Dopamine D4 Receptor Gene Variation with Both Infidelity and Sexual Promiscuity  Academic Article
• Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn’s disease subjects  Academic Article
• Associations of plasma homocysteine and the methylenetetrahydrofolate reductase C677T polymorphism with carotid intima media thickness among South Asian, Chinese and European Canadians  Academic Article
• Associations of the FTO rs9939609 variant with discrete body fat depots and dietary intake in a multi-ethnic cohort  Academic Article
• BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia  Academic Article
• BRCA2 Variants and cardiovascular disease in a multi-ethnic study  Academic Article
• Behavioral abnormalities in synapsin II knockout mice implicate a causal factor in schizophrenia  Academic Article
• Benefits and limitations of genome-wide association studies  Academic Article
• Beyond the Brain  Academic Article
• Bioinformatics of antimicrobial resistance in the age of molecular epidemiology  Academic Article
• Biological and clinicopathological features associated with hepatitis C virus type 5 infections  Academic Article
• Biological, clinical and population relevance of 95 loci for blood lipids  Academic Article
• Bivariate Analysis of Age-Related Macular Degeneration Progression Using Genetic Risk Scores  Academic Article
• Boron levels in man: Preliminary evidence of genetic regulation and some implications for human biology  Academic Article
• Brain-derived neurotrophic factor gene val66met polymorphism and executive functioning in patients with bipolar disorder  Academic Article
• Brain-derived neurotrophic factor val66met polymorphism affects prefrontal energy metabolism in bipolar disorder  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
• Brief Report  Academic Article
• Brown Norway Chromosome 13 Confers Protection From High Salt to Consomic Dahl S Rat  Academic Article
• Bucindolol for the Maintenance of Sinus Rhythm in a Genotype-Defined HF Population  Academic Article
• CFTR2: How will it help care?  Academic Article
• CYP2E1,GSTM1andGSTT1genetic polymorphisms and susceptibility to antituberculosis drug-induced hepatotoxicity: a nested case-control study  Academic Article
• Caenorhabditis briggsae Recombinant Inbred Line Genotypes Reveal Inter-Strain Incompatibility and the Evolution of Recombination  Academic Article
• Can activated recombinant factor VII be used to postpone the exposure of infants to factor VIII until after 2 years of age?  Academic Article
• Carboxypeptidase B2 and N play different roles in regulation of activated complements C3a and C5a in mice  Academic Article
• Carrier frequency of the RSH/Smith-Lemli-Opitz IVS8-1G>C mutation in African Americans  Academic Article
• Causal Relationship between Adiponectin and Metabolic Traits: A Mendelian Randomization Study in a Multiethnic Population  Academic Article
• Central aromatization of testosterone in testicular feminized mice  Academic Article
• Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4)  Academic Article
• Cerebral amyloid angiopathy with and without hemorrhage: Evidence for different disease phenotypes  Academic Article
• Changes in 2-Hydroxyestrone and 16 -Hydroxyestrone Metabolism with Flaxseed Consumption: Modification by COMT and CYP1B1 Genotype  Academic Article
• Changes in the Epidemiology of Thalassemia in North America: A New Minority Disease  Academic Article
• Characterization of Androgenetic/Biparental Mosaic/Chimeric Conceptions, Including Those With a Molar Component  Academic Article
• Characterization of DCTN1 genetic variability in neurodegeneration  Academic Article
• Characterization of Escherichia coli urinary tract infection isolates in remote northern Saskatchewan communities: the Northern Antibiotic Resistance Partnership  Academic Article
• Characterization of Streptococcus milleri Group Isolates from Expectorated Sputum of Adult Patients with Cystic Fibrosis  Academic Article
• Characterization of human disease phenotypes associated with mutations inTREX1,RNASEH2A,RNASEH2B,RNASEH2C,SAMHD1,ADAR, andIFIH1  Academic Article
• Characterization of long RNA-cleaving deoxyribozymes with short catalytic cores: the effect of excess sequence elements on the outcome of in vitro selection  Academic Article
• Chronic hepatitis C treatment outcomes in low- and middle-income countries: a systematic review and meta-analysis  Academic Article
• Chronic venous abnormalities in symptomatic and asymptomatic protein C deficiency  Academic Article
• Clinical Next-Generation Sequencing Pipeline Outperforms a Combined Approach Using Sanger Sequencing and Multiplex Ligation-Dependent Probe Amplification in Targeted Gene Panel Analysis  Academic Article
• Clinical and analytical considerations in the utilization of cholinesterase measurements  Academic Article
• Clinical evaluation of a hemochromatosis next-generation sequencing gene panel  Academic Article
• Clinical features of facioscapulohumeral muscular dystrophy 2  Academic Article
• Clinical implications and characterization of Group A Streptoccoccus infections in adults with cystic fibrosis  Academic Article
• Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study  Academic Article
• Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study  Academic Article
• Clonal Expansion of the Pseudogymnoascus destructans Genotype in North America Is Accompanied by Significant Variation in Phenotypic Expression  Academic Article
• Clonal Genotype of Geomyces destructans among Bats with White Nose Syndrome, New York, USA  Academic Article
• Clonal and Spontaneous Origins of Fluconazole Resistance in Candida albicans  Academic Article
• Clustering the autisms using glutamate synapse protein interaction networks from cortical and hippocampal tissue of seven mouse models  Academic Article
• Co-Infection by Hepatitis C Virus in HIV-Infected Patients in Southern Brazil: Genotype Distribution and Clinical Correlates  Academic Article
• Co-circulation of multiple genotypes of human rhinovirus during a large outbreak of respiratory illness in a veterans’ long-term care home  Academic Article
• Coinheritance of α-thalassemia-1 and hemoglobin E/β0-thalassemia: Practical implications for neonatal screening and genetic counseling  Academic Article
• Collaborative Effort for a Centralized Worldwide Tuberculosis Relational Sequencing Data Platform: Figure 1.  Academic Article
• Collagen platelet receptor polymorphisms integrin alpha2beta1 C807T and GPVI Q317L and risk of ischemic stroke  Academic Article
• Combined effects of MC4R and FTO common genetic variants on obesity in European general populations  Academic Article
• Combining direct and indirect genetic methods to estimate dispersal for informing wildlife disease management decisions  Academic Article
• Common Reservoirs forPenicillium marneffeiInfection in Humans and Rodents, China  Academic Article
• Common Variants in FTO, MC4R, TMEM18, PRL, AIF1 , and PCSK1 Show Evidence of Association With Adult Obesity in the Greek Population  Academic Article
• Common Variation in SIM1 Is Reproducibly Associated With BMI in Pi ma Indians  Academic Article
• Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease  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
• Comparative Gene Genealogies Indicate that Two Clonal Lineages of Cryptococcus gattii in British Columbia Resemble Strains from Other Geographical Areas  Academic Article
• Comparative evaluation of AMPLICOR HPV PCR and Linear Array assays on SurePath liquid-based Pap samples for the detection of high-risk HPV genotypes  Academic Article
• Comparing Genetic Ancestry and Self-Described Race in African Americans Born in the United States and in Africa  Academic Article
• Comparing the American and European diagnostic guidelines for cystic fibrosis: same disease, different language?  Academic Article
• Comparison of in-house and commercial 16S rRNA sequencing with high-performance liquid chromatography and genotype AS and CM for identification of nontuberculous mycobacteria  Academic Article
• Comparison of responses evoked by mild indirect cooling and by sound in the forearm vasculature in patients with homozygous sickle cell disease and in normal subjects  Academic Article
• Complex two-gene modulation of lung disease severity in children with cystic fibrosis  Academic Article
• Complications in the genotypic molecular diagnosis of pseudo arylsulfatase A deficiency  Academic Article
• Compound Heterozygosity For Triplicated α-Globin Gene and (- -SEA ) α-Globin Gene Deletion: Implication For Thalassaemia Screening  Academic Article
• Compound Heterozygosity for two Genotypes of α-Thalassemia-2 : Hematological, Biosynthetic and DNA Studies  Academic Article
• Comprehensive Analysis of Genomic Variation in the LPA Locus and Its Relationship to Plasma Lipoprotein(a) in South Asians, Chinese, and European Caucasians  Academic Article
• Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies  Academic Article
• Concept, Design and Implementation of a Cardiovascular Gene-Centric 50 K SNP Array for Large-Scale Genomic Association Studies  Academic Article
• Concordance of two multiple analytical approaches demonstrate that interaction between BMI and ADIPOQ haplotypes is a determinant of LDL cholesterol in a general French population  Academic Article
• Contribution of 24 obesity-associated genetic variants to insulin resistance, pancreatic beta-cell function and type 2 diabetes risk in the French population  Academic Article
• Contribution of BDNF and DRD2 genetic polymorphisms to continued opioid use in patients receiving methadone treatment for opioid use disorder: an observational study  Academic Article
• Contribution of rare coding mutations in CD36 to type 2 diabetes and cardio-metabolic complications  Academic Article
• Correction of Population Stratification in Large Multi-Ethnic Association Studies  Academic Article
• Correlation between Azole Susceptibilities, Genotypes, and ERG11 Mutations in Candida albicans Isolates Associated with Vulvovaginal Candidiasis in China  Academic Article
• Correlation of MRI-Based Bone Marrow Burden Score with Genotype and Spleen Status in Gaucher's Disease  Academic Article
• Cryptococcosis in patients with diabetes mellitus II in mainland China: 1993-2015  Academic Article
• Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection  Academic Article
• D-2-hydroxyglutarate produced by mutant IDH1 perturbs collagen maturation and basement membrane function  Academic Article
• DHCR7 genotypes of cousins with Smith-Lemli-Opitz syndrome  Academic Article
• DHCR7 mutations and genotype-phenotype correlation in 37 Polish patients with Smith-Lemli-Opitz syndrome  Academic Article
• DHCR7 nonsense mutations and characterisation of mRNA nonsense mediated decay in Smith-Lemli-Opitz syndrome  Academic Article
• DRD2 and SLC6A3 moderate impact of maternal depressive symptoms on infant cortisol  Academic Article
• DRD2/ANKK1 TaqI A genotype moderates the relationship between alexithymia and the relative value of alcohol among male college binge drinkers  Academic Article
• De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy  Academic Article
• Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene  Academic Article
• Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly  Academic Article
• Demonstration of a splenic cytotoxic effector cell in mice of genotype SCID/SCID.BG/BG  Academic Article
• Detection of Clinically Relevant Genotypes of Vancomycin-Resistant Enterococci in Nosocomial Surveillance Specimens by PCR  Academic Article
• Detection of Human Papillomavirus Type 16 in Plasma Cells  Academic Article
• Determination of lipoprotein(a) kringle repeat number from genomic DNA: copy number variation genotyping using qPCR  Academic Article
• Diagnosis of arylsulfatase A deficiency  Academic Article
• Diagnostic Pitfall in PCR-Based α-Thalassemia Genotyping Resulting from a (G→C) Polymorphism at Nucleotide 71 3′ to the α2-Globin Gene Termination Codon  Academic Article
• Diesel exhaust augments allergen-induced lower airway inflammation in allergic individuals: a controlled human exposure study  Academic Article
• Discussion of "Repetitive Deoxyribonucleic Acid (DNA) and Human Genome Variation--A Concise Review Relevant to Forensic Biology".  Academic Article
• Distribution and Characteristics of Listeria monocytogenes Isolates from Surface Waters of the South Nation River Watershed, Ontario, Canada  Academic Article
• Distribution and Diversity of Escherichia coli Populations in the South Nation River Drainage Basin, Eastern Ontario, Canada  Academic Article
• Distribution of human papillomavirus genotypes in cervical intraepithelial neoplasia and invasive cervical cancer in Canada  Academic Article
• Diverse Evolutionary Trajectories Characterize a Community of RNA-Cleaving Deoxyribozymes: A Case Study into the Population Dynamics of In Vitro Selection  Academic Article
• Diversity and origins of Indian multi-triazole resistant strains ofAspergillus fumigatus  Academic Article
• Diversity and relationships among strains of culturable yeasts in agricultural soils in Cameroon  Academic Article
• Diversity of Rotavirus Strains Circulating in Botswana before and after introduction of the Monovalent Rotavirus Vaccine  Academic Article
• Diversity of commensal yeasts within and among healthy hosts  Academic Article
• Do plasma biomarkers of coagulation and fibrinolysis differ between patients who have experienced an acute myocardial infarction versus stable exertional angina?  Academic Article
• Does Integration of Various Ion Channel Measurements Improve Diagnostic Performance in Cystic Fibrosis?  Academic Article
• Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis?  Academic Article
• Does your gene need a background check? How genetic background impacts the analysis of mutations, genes, and evolution  Academic Article
• Dopamine Receptor Gene D4 Polymorphisms and Early Sexual Onset: Gender and Environmental Moderation in a Sample of African-American Youth  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 and Heterogeneous Mutations to Fluconazole Resistance in Cryptococcus neoformans  Academic Article
• Dynamic interaction between fetal adversity and a genetic score reflecting dopamine function on developmental outcomes at 36 months  Academic Article
• Dysregulation of Peripheral Cytokine Production in Irritable Bowel Syndrome  Academic Article
• Early Detrimental Metabolic Outcomes of rs17300539-A Allele of ADIPOQ Gene Despite Higher Adiponectinemia  Academic Article
• Ecological and physical barriers shape genetic structure of the Alpine porcini (Boletus reticuloceps)  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 GST variants on lung function following diesel exhaust and allergen co-exposure in a controlled human crossover study  Academic Article
• Effect of apolipoprotein E and butyrylcholinesterase genotypes on cognitive response to cholinesterase inhibitor treatment at different stages of Alzheimer's disease  Academic Article
• Effect of wzx (rfbX) Mutations on A-Band and B-Band Lipopolysaccharide Biosynthesis in Pseudomonas aeruginosa O5  Academic Article
• Effectiveness of Monovalent Rotavirus Vaccine After Programmatic Implementation in Botswana: A Multisite Prospective Case-Control Study  Academic Article
• Effects of Dystrophin Isoforms on Signal Transduction through Neural Retina: Genotype–Phenotype Analysis of Duchenne Muscular Dystrophy Mouse Mutants  Academic Article
• Effects of Genotype and Sleep on Temperament  Academic Article
• Effects of Multiple Genetic Loci on Age at Onset in Late-Onset Alzheimer Disease  Academic Article
• Effects of Nicotine Deprivation and Replacement on BOLD-fMRI Response to Smoking Cues as a Function of DRD4 VNTR Genotype  Academic Article
• Effects of Source of DNA on Genotyping Success Rates and Allele Percentages in the Preschoolers with Attention-Deficit/Hyperactivity Disorder Treatment Study (PATS)  Academic Article
• Effects ofCYP2C19Genotype on Outcomes of Clopidogrel Treatment  Academic Article
• Efficacy and safety of a two‐drug direct‐acting antiviral agent regimen ruzasvir 180 mg and uprifosbuvir 450 mg for 12 weeks in adults with chronic hepatitis C virus genotype 1, 2, 3, 4, 5 or 6  Academic Article
• Eighteenth century Yersinia pestis genomes reveal the long-term persistence of an historical plague focus  Academic Article
• Electrical properties of muscle fibre membranes in man.  Academic Article
• Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations  Academic Article
• Endothelin A receptor is necessary for O2 constriction but not closure of ductus arteriosus  Academic Article
• Enhanced Detection and Typing of Human Papillomavirus (HPV) DNA in Anogenital Samples with PGMY Primers and the Linear Array HPV Genotyping Test  Academic Article
• Environment factors can influence mitochondrial inheritance in the fungus Cryptococcus neoformans  Academic Article
• Epidemiologic Approaches to Evaluating the Potential for Human Papillomavirus Type Replacement Postvaccination  Academic Article
• Epidemiologic Evaluation of Human Papillomavirus Type Competition and the Potential for Type Replacement Post-Vaccination  Academic Article
• Epidemiology of Clonal Pseudomonas aeruginosa Infection in a Canadian Cystic Fibrosis Population  Academic Article
• Epidermal Growth Factor Receptor and Transforming Growth Factor-β Signaling Contributes to Variation for Wing Shape inDrosophila melanogaster  Academic Article
• Eradication of an epidemic methicillin-resistant Staphylococcus aureus (MRSA) from a geriatric university hospital: evidence from a 10-year follow-up  Academic Article
• Ethnicity Does Not Affect the Homocysteine-Lowering Effect of B-Vitamin Therapy in Singaporean Stroke Patients  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 A2BP1 as an Obesity Gene  Academic Article
• Evaluation of Genes Encoding for the Transient Outward Current (Ito) Identifies the KCND2 Gene as a Cause of J-Wave Syndrome Associated With Sudden Cardiac Death  Academic Article
• Evaluation of the Disease Liability of CFTR Variants  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 a link between local and seasonal cycles in gene frequencies and latitudinal gene clines in a cyclic parthenogen  Academic Article
• Evidence for genetic incompatibilities associated with post-zygotic reproductive isolation in the human fungal pathogen Cryptococcus neoformans  Academic Article
• Evidence of Naturalized Stress-Tolerant Strains of Escherichia coli in Municipal Wastewater Treatment Plants  Academic Article
• Evidence of unique genetic diversity inAspergillus fumigatusisolates from Cameroon  Academic Article
• Exercise-induced mitochondrial p53 repairs mtDNA mutations in mutator mice  Academic Article
• Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect  Academic Article
• FUT2 genotype and secretory status are not associated with fecal microbial composition and inferred function in healthy subjects  Academic Article
• Factor V Leiden and prothrombin gene G20210A mutations in Italian patients with Behçet's disease and deep vein thrombosis  Academic Article
• Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene  Academic Article
• Factors Contributing to the Lack of Human Immunodeficiency Virus Type 1 (HIV‐1) Transmission in HIV‐1–Discordant Partners  Academic Article
• Factors independently associated with cardiac troponin I levels in young and healthy adults from the general population  Academic Article
• Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletion  Academic Article
• Fantastic yeasts and where to find them: the discovery of a predominantly clonal Cryptococcus deneoformans population in Saudi Arabian soils  Academic Article
• Favourable IFNL3 Genotypes Are Associated with Spontaneous Clearance and Are Differentially Distributed in Aboriginals in Canadian HIV-Hepatitis C Co-Infected Individuals  Academic Article
• Fetal erythropoiesis in steel mutant mice  Academic Article
• Field measurements of genotype by environment interaction for fitness caused by spontaneous mutations inArabidopsis thaliana  Academic Article
• Fine Mapping of the Insulin-Induced Gene 2 Identifies a Variant Associated With LDL Cholesterol and Total Apolipoprotein B Levels  Academic Article
• Fine-scale genetic analyses reveal unexpected spatial-temporal heterogeneity in two natural populations of the commercial mushroom Agaricus bisporus  Academic Article
• Fitness consequences of plants growing with siblings: reconciling kin selection, niche partitioning and competitive ability  Academic Article
• Fitness distribution and transgressive segregation across 40 environments in a hybrid progeny population of the human-pathogenic yeast Cryptococcus neoformans  Academic Article
• Foetal Erythropoiesis in Steel Mutant Mice.  Academic Article
• Folate levels in pregnant women who smoke: An important gene/environment interaction  Academic Article
• Founder effect for the T93MDHCR7 mutation in Smith-Lemli-Opitz syndrome  Academic Article
• Functional effects and gender association of COX-2 gene polymorphism G-765C in bronchial asthma  Academic Article
• Fundamentals of Fungal Molecular Population Genetic Analyses  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
• Gene duplication and divergence produce divergent MHC genotypes without disassortative mating  Academic Article
• Gene- or region-based analysis of genome-wide association studies  Academic Article
• Gene-Centric Meta-Analysis of Lipid Traits in African, East Asian and Hispanic Populations  Academic Article
• Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci  Academic Article
• General transduction in Rhizobium meliloti.  Academic Article
• Genetic Analyses of a Hybrid Cross Between Serotypes A and D Strains of the Human Pathogenic FungusCryptococcus neoformans  Academic Article
• Genetic Analyses of the Internal Transcribed Spacer Sequences Suggest Introgression and Duplication in the Medicinal Mushroom Agaricus subrufescens  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 Differential Susceptibility to Socioeconomic Status and Childhood Obesogenic Behavior  Academic Article
• Genetic Dissection of Behavior: Modulation of Locomotion by Light in theDrosophila melanogasterLarva Requires Genetically Distinct Visual System Functions  Academic Article
• Genetic Diversity of Populations ofMonilinia fructicola(Fungi, Ascomycota, Helotiales) from China  Academic Article
• Genetic Factors and Genotype-Environment Interactions Contribute to Variation in Melanin Production in the Fungal Pathogen Cryptococcus neoformans  Academic Article
• Genetic Information and the Prediction of Incident Type 2 Diabetes in a High-Risk Multiethnic Population  Academic Article
• Genetic Loci Associated With C-Reactive Protein Levels and Risk of Coronary Heart Disease  Academic Article
• Genetic Modifiers of Lung Disease in Cystic Fibrosis  Academic Article
• Genetic Polymorphisms of Glutathione S-Transferases and the Risk of Adult Brain Tumors: A Meta-analysis  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 Variants Associated With Myocardial Infarction Risk Factors in Over 8000 Individuals From Five Ethnic Groups  Academic Article
• Genetic Variants and Susceptibility to Neurological Complications Following West Nile Virus Infection  Academic Article
• Genetic Variation in the Ontario Neurodegenerative Disease Research Initiative  Academic Article
• Genetic and epidemiological analysis of norovirus from children with gastroenteritis in Botswana, 2013–2015  Academic Article
• Genetic association of the GDNF alpha-receptor genes with schizophrenia and clozapine response  Academic Article
• Genetic contribution to waist-to-hip ratio in Mexican children and adolescents based on 12 loci validated in European adults  Academic Article
• Genetic deficiency of the tumor suppressor protein p53 influences erythrocyte survival  Academic Article
• Genetic determinants of right-ventricular remodeling after tetralogy of Fallot repair  Academic Article
• Genetic determinants of warfarin maintenance dose and time in therapeutic treatment range: a RE-LY genomics substudy  Academic Article
• Genetic differentiation, recombination and clonal expansion in environmental populations of Cryptococcus gattii in India  Academic Article
• Genetic predictors of response to treatment with citalopram in depression secondary to traumatic brain injury  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 variant in HK1 is associated with a proanemic state and A1C but not other glycemic control-related traits.  Academic Article
• Genetic variation in hyaluronan metabolism loci is associated with plasma plasminogen activator inhibitor-1 concentration  Academic Article
• Genetically determined P2X7 receptor pore formation regulates variability in chronic pain sensitivity  Academic Article
• Genetics of microenvironmental canalization in Arabidopsis thaliana  Academic Article
• Genome duplication events have led to a diversification in the CPT I gene family in fish  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 Analysis of Soluble ICAM-1 Concentration Reveals Novel Associations at the NFKBIK, PNPLA3, RELA, and SH2B3 Loci  Academic Article
• Genome-Wide Associations and Functional Genomic Studies of Musculoskeletal Adverse Events in Women Receiving Aromatase Inhibitors  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 studies of placebo and duloxetine response in major depressive disorder  Academic Article
• Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry  Academic Article
• Genome-wide association study of emotional empathy in children  Academic Article
• Genome-wide association study of sepsis in extremely premature infants  Academic Article
• Genome-wide meta-analyses identify multiple loci associated with smoking behavior  Academic Article
• Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture  Academic Article
• Genomic and transcriptomic analyses of the tangerine pathotype of Alternaria alternata in response to oxidative stress  Academic Article
• Genomic approaches to bleeding disorders  Conference Paper
• Genotype and phenotype in 12 additional individuals with SATB2 -associated syndrome  Academic Article
• Genotype-Environment Interactions of Spontaneous Mutations for Vegetative Fitness in the Human Pathogenic FungusCryptococcus neoformans  Academic Article
• Genotype-Positive Status in Patients With Hypertrophic Cardiomyopathy Is Associated With Higher Rates of Heart Failure Events  Academic Article
• Genotype-by-environment interactions for cuticular hydrocarbon expression inDrosophila simulans  Academic Article
• Genotype-guided versus standard vitamin K antagonist dosing algorithms in patients initiating anticoagulation  Academic Article
• Genotypes of chronic progressive external ophthalmoplegia in a large adult-onset cohort  Academic Article
• Genotypes, phenotypes and whole genome sequence: Approaches from theMy Life Our Futurehaemophilia project  Academic Article
• Genotypic and Phenotypic Analyses of Two “Isogenic” Strains of the Human Fungal Pathogen Cryptococcus neoformans var. neoformans  Academic Article
• Genotypic diversity and antifungal susceptibility ofCryptococcus neoformansisolates from paediatric patients in China  Academic Article
• Germline HOXB13 p.Gly84Glu mutation and risk of colorectal cancer  Academic Article
• Glial cell line-derived neurotrophic factor (GDNF) is required for differentiation of pontine noradrenergic neurons and patterning of central respiratory output  Academic Article
• Global molecular diversity of RSV – the “INFORM RSV” study  Academic Article
• Glucose-6-phosphate dehydrogenase deficiency genotypes and allele frequencies in the Kavango and Zambezi regions of northern Namibia  Academic Article
• Glycoproteins E and I facilitate neuron-to-neuron spread of herpes simplex virus.  Academic Article
• HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome  Academic Article
• HS3ST1 genotype regulates antithrombin's inflammomodulatory tone and associates with atherosclerosis  Academic Article
• HYBRIDIZATION AND POPULATION GENETICS OF TWO MACAQUE SPECIES IN SULAWESI, INDONESIA  Academic Article
• Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese family  Academic Article
• Hb Castilla [β32(B14)Leu → Arg] Caused by a De Novo Mutation  Academic Article
• Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family  Academic Article
• Hemagglutinin sequence clusters and the antigenic evolution of influenza A virus  Academic Article
• Hemoglobin E/beta Thalassemia: The Canadian Experience  Academic Article
• Hemoglobin H (Hb H) disease in Canada: Molecular diagnosis and review of 116 cases  Academic Article
• Hemoglobin H identification by high-performance liquid chromatography in confirmed hemoglobin H disease  Academic Article
• Hemopoietic stem cells in murine embryonic yolk sac and peripheral blood.  Academic Article
• Hepatitis C genotypes in Australian haemophilia patients  Academic Article
• Heterogeneity in phenotypic and genotypic characteristics among strains of Hafnia alvei.  Academic Article
• Heterozygous Mutations Causing Partial Prohormone Convertase 1 Deficiency Contribute to Human Obesity  Academic Article
• Hierarchical investigation of genetic influences on response inhibition in healthy young adults.  Academic Article
• High Coffee Intake, but Not Caffeine, is Associated with Reduced Estrogen Receptor Negative and Postmenopausal Breast Cancer Risk with No Effect Modification by CYP1A2 Genotype  Academic Article
• Homocysteine and Coronary Heart Disease: Meta-analysis of MTHFR Case-Control Studies, Avoiding Publication Bias  Academic Article
• How to Use an Article About Genetic Association  Academic Article
• How well do you know your mutation? Complex effects of genetic background on expressivity, complementation, and ordering of allelic effects  Academic Article
• Human embryonic zeta-globin chains in fetal and newborn blood.  Academic Article
• Human milk fatty acid composition is associated with dietary, genetic, sociodemographic, and environmental factors in the CHILD Cohort Study  Academic Article
• IL28B polymorphism (rs12979860) associated with clearance of HCV infection in Poland: Systematic review of its prevalence in chronic hepatitis C patients and general population frequency  Academic Article
• IQ and the Genetics of Autism  Academic Article
• Identification of QTLs Associated with Virulence Related Traits and Drug Resistance in Cryptococcus neoformans  Academic Article
• Identification of a New δ Chain Hemoglobin Variant in a β-Thalassemia Carrier: Hb A2-MUMC [δ13(A10)Ala → Asp]  Academic Article
• Identification of a Novel Hepatitis C Virus Genotype From Punjab, India: Expanding Classification of Hepatitis C Virus Into 8 Genotypes  Academic Article
• Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome  Academic Article
• Identification of numerous hepatitis C virus genotypes in Montreal, Canada.  Academic Article
• Identification of the origin of faecal contamination in estuarine oysters using Bacteroidales and F-specific RNA bacteriophage markers  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
• Immunocytological test to detect adult carriers of (--SEA/) deletional α-thalassaemia  Academic Article
• Impact of Common Type 2 Diabetes Risk Polymorphisms in the DESIR Prospective Study  Academic Article
• Impact of hemochromatosis gene mutations on cardiac status in doxorubicin-treated survivors of childhood high-risk leukemia  Academic Article
• Imputation of missing genotypes: an empirical evaluation of IMPUTE  Academic Article
• In vitro antifungal susceptibility profiles and genotypes of 308 clinical and environmental isolates of Cryptococcus neoformans var. grubii and Cryptococcus gattii serotype B from north-western India  Academic Article
• Incidence and Treatment Outcomes of PharyngealNeisseria gonorrhoeaeandChlamydia trachomatisInfections in Men Who Have Sex with Men: A 13‐Year Retrospective Cohort Study  Academic Article
• Individual common variants exert weak effects on the risk for autism spectrum disorders  Academic Article
• Infliximab-Induced Psoriasis and Psoriasiform Skin Lesions in Pediatric Crohn Disease and a Potential Association With IL-23 Receptor Polymorphisms  Academic Article
• Influence of maternal educational level on the association between the rs3809508 neuromedin B gene polymorphism and the risk of obesity in the HELENA study  Academic Article
• Initial Evidence that OPRM1 Genotype Moderates Ventral and Dorsal Striatum Functional Connectivity During Alcohol Cues  Academic Article
• Interaction between Oxytocin Genotypes and Early Experience Predicts Quality of Mothering and Postpartum Mood  Academic Article
• Interaction between serotonin transporter gene variants and life events predicts response to antidepressants in the GENDEP project  Academic Article
• Interleukin-4 and interleukin-10 polymorphisms and antituberculosis drug-induced hepatotoxicity in Chinese population  Academic Article
• Interspecific hybrids and chimeras in mice  Academic Article
• Investigation of dopamine system genes in obsessive-compulsive disorder  Academic Article
• Isolation of Candida dubliniensis in an Aboriginal Community in Ontario, Canada  Academic Article
• Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation  Academic Article
• Isolation, Sequence, Infectivity, and Replication Kinetics of Severe Acute Respiratory Syndrome Coronavirus 2  Academic Article
• K45R variant of squalene synthase increases total cholesterol levels in two study samples from a French Canadian population  Academic Article
• Kin recognition, not competitive interactions, predicts root allocation in young Cakile edentula seedling pairs  Academic Article
• Krüppel-like factor 1: hematologic phenotypes associated withKLF1gene mutations  Academic Article
• LPS-Induced Occult Loss in Mice Requires FGL2  Academic Article
• Lack of Association of CD36 SNPs With Early Onset Obesity: A Meta-Analysis in 9,973 European Subjects  Academic Article
• Lack of Association of Ghrelin Precursor Gene Variants and Percentage Body Fat or Serum Lipid Profiles  Academic Article
• Lack of Genetic Differentiation between Two Geographically Diverse Samples of Candida albicans Isolated from Patients Infected with Human Immunodeficiency Virus  Academic Article
• Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci  Academic Article
• Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci  Academic Article
• Ledipasvir-Sofosbuvir Plus Ribavirin in Treatment-Naive Patients With Hepatitis C Virus Genotype 3 Infection: An Open-Label Study  Academic Article
• Lens-Specific Expression of TGF-β Induces Anterior Subcapsular Cataract Formation in the Absence of Smad3  Academic Article
• Lifestyle Interaction With Fat Mass and Obesity-Associated (FTO) Genotype and Risk of Obesity in Apparently Healthy U.S. Women  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
• Local Frequency Dependence and Global Coexistence  Academic Article
• Local-Scale Patterns of Genetic Variability, Outcrossing, and Spatial Structure in Natural Stands of Arabidopsis thaliana  Academic Article
• Loci influencing blood pressure identified using a cardiovascular gene-centric array  Academic Article
• Long-distance dispersal and recombination in environmental populations of Cryptococcus neoformans var. grubii from India  Academic Article
• Longitudinal Data Analysis in Genome-Wide Association Studies  Academic Article
• Longitudinal Decline in Lung Volume in a Population of Children with Sickle Cell Disease  Academic Article
• Longitudinal relationship between physical activity and lung health in patients with cystic fibrosis  Academic Article
• Loss-of-Function KCNE2 Variants  Academic Article
• Lung Cancer in Humans Is Not Associated with Lifetime Total Alcohol Consumption or with Genetic Variation in Alcohol Dehydrogenase 3 (ADH3)  Conference Paper
• Lys 42/43/44 and Arg 12 of thrombin-activable fibrinolysis inhibitor comprise a thrombomodulin exosite essential for its antifibrinolytic potential  Academic Article
• MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis  Academic Article
• MTNR1B G24E Variant Associates With BMI and Fasting Plasma Glucose in the General Population in Studies of 22,142 Europeans  Academic Article
• Maternal DRD2, SLC6A3, and OXTR genotypes as potential moderators of the relation between maternal history of care and maternal cortisol secretion in the context of mother-infant separation  Academic Article
• Maternal Uniparental Isodisomy of Human Chromosome 14 Associated with a Paternal t(13q14q) and Precocious Puberty  Academic Article
• Mechanisms of innate immune activation by gluten peptide p31-43 in mice  Academic Article
• Mendelian randomisation, triglycerides, and CHD  Academic Article
• Mendelian randomization of blood lipids for coronary heart disease  Academic Article
• Menin Is a Regulator of the Stress Response in Drosophila melanogaster  Academic Article
• Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12  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
• Metachromatic leukodystrophy: Multiple nonfunctional and pseudodeficiency alleles in a pedigree: Problems with diagnosis and counseling  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
• Mild β+-Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A)  Academic Article
• Mineralocorticoid receptor genotype moderates the association between physical neglect and serum BDNF  Academic Article
• Mining the Human Phenome Using Allelic Scores That Index Biological Intermediates  Academic Article
• Mitochondrial inheritance in haploid × non-haploid crosses in Cryptococcus neoformans  Academic Article
• Modulation of GLP-1 Levels by a Genetic Variant That Regulates the Cardiovascular Effects of Intensive Glycemic Control in ACCORD  Academic Article
• Molecular Epidemiology of Candidemia: Evidence of Clusters of Smoldering Nosocomial Infections  Academic Article
• Molecular analysis and genotype-phenotype correlation of Diamond-Blackfan anemia  Academic Article
• Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression  Academic Article
• Multilocus Sequence Typing Reveals both Shared and Unique Genotypes of Cryptococcus neoformans in Jiangxi Province, China  Academic Article
• Multilocus sequence analyses reveal extensive diversity and multiple origins of fluconazole resistance in Candida tropicalis from tropical China  Academic Article
• Multiple Minisequencing Screen for Seven Southeast Asian Nondeletional α-Thalassemia Mutations  Academic Article
• Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis  Academic Article
• Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy  Academic Article
• Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly  Academic Article
• Natural history and genotype-phenotype correlations in 72 individuals with SATB2 -associated syndrome  Academic Article
• Network meta-analysis of direct-acting antivirals in combination with peginterferon–ribavirin for previously untreated patients with hepatitis C genotype 1 infection  Academic Article
• Neuronal Correlates of Brain-derived Neurotrophic Factor Val66Met Polymorphism and Morphometric Abnormalities in Bipolar Disorder  Academic Article
• New Locus for Skin Intrinsic Fluorescence in Type 1 Diabetes Also Associated With Blood and Skin Glycated Proteins  Academic Article
• No Association between the 20210 G/A Prothrombin Gene Mutation and Premature Coronary Artery Disease  Academic Article
• Non-synonymous polymorphisms in melanocortin-4 receptor protect against obesity: the two facets of a Janus obesity gene  Academic Article
• Nonisotopic Detection of Human Papillomavirus DNA in Clinical Specimens Using a Consensus PCR and a Generic Probe Mix in an Enzyme-Linked Immunosorbent Assay Format  Academic Article
• Normal Hb A2β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) inCiswith the Hb A2’δ-Globin Gene Missense Mutation (HBD: c.49G>C)  Academic Article
• Normal IQ is possible in Smith-Lemli-Opitz syndrome  Academic Article
• Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index  Academic Article
• Novel DNA Sequences from Natural Strains of the Nitrogen-Fixing Symbiotic Bacterium Sinorhizobium meliloti  Academic Article
• Novel Microsphere-Based Method for Detection and Typing of 46 Mucosal Human Papillomavirus Types  Academic Article
• Novel disease-causing mutations in the dihydropyrimidine dehydrogenase gene interpreted by analysis of the three-dimensional protein structure  Academic Article
• On the Accessibility of Adaptive Phenotypes of a Bacterial Metabolic Network  Academic Article
• On the Use of Variance per Genotype as a Tool to Identify Quantitative Trait Interaction Effects: A Report from the Women's Genome Health Study  Academic Article
• Ondansetron Reduces Naturalistic Drinking in Nontreatment-Seeking Alcohol-Dependent Individuals with the LL 5′-HTTLPR Genotype: A Laboratory Study  Academic Article
• Ondansetron and sertraline may interact with 5-HTTLPR and DRD4 polymorphisms to reduce drinking in non-treatment seeking alcohol-dependent women: Exploratory findings  Academic Article
• Optimal Manual Exchange Transfusion Protocol for Sickle Cell Disease: A Retrospective Comparison of Two Comprehensive Care Centers in the United Kingdom and Canada  Academic Article
• Optimization and validation of rep-PCR genotypic libraries for microbial source tracking of environmental Escherichia coli isolates  Academic Article
• Oral-facial-digital syndrome VII is oral-facial-digital syndrome I: A clarification  Academic Article
• Outcomes of Chronic Hepatitis C Therapy in Patients Treated in Community Versus Academic Centres in Canada: Final Results of APPROACH (A Prospective Study of Peginterferon alfa-2a and Ribavirin at Academic and Community Centres in Canada)  Academic Article
• Oxytocin Receptor Polymorphisms are Differentially Associated with Social Abilities across Neurodevelopmental Disorders  Academic Article
• P2Y12 receptor inhibitor resistance and coronary artery disease  Academic Article
• PCR–restriction fragment length polymorphism (RFLP) analyses reveal both extensive clonality and local genetic differences inCandidaalbicans  Academic Article
• PLASTICITY, CANALIZATION, AND DEVELOPMENTAL STABILITY OF THEDROSOPHILAWING: JOINT EFFECTS OF MUTATIONS AND DEVELOPMENTAL TEMPERATURE  Academic Article
• POP-Brazil study protocol: a nationwide cross-sectional evaluation of the prevalence and genotype distribution of human papillomavirus (HPV) in Brazil  Academic Article
• PPARA Polymorphism Influences the Cardiovascular Benefit of Fenofibrate in Type 2 Diabetes: Findings From ACCORD-Lipid  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
• Passive Cigarette Smoke Exposure During Various Periods of Life, Genetic Variants, and Breast Cancer Risk Among Never Smokers  Academic Article
• Pathbase: a database of mutant mouse pathology  Academic Article
• Pathbase: a new reference resource and database for laboratory mouse pathology  Academic Article
• Patients with thalassemia in the United States  Academic Article
• Patterns of allele distribution in a hybrid population of the Cryptococcus neoformans species complex  Academic Article
• Pharmacogenetic profiling across the irinotecan pathway in Asian patients with cancer  Academic Article
• Pharmacogenetic-Based Efavirenz Dose Modification: Suggestions for an African Population and the Different CYP2B6 Genotypes  Academic Article
• PhenCode: connecting ENCODE data with mutations and phenotype  Academic Article
• Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.  Academic Article
• Phylogeography and evolution of a fungal-insect association on the Tibetan Plateau  Academic Article
• Physical Exercise Moderates the Relationship of Apolipoprotein E (APOE) Genotype and Dementia Risk: A Population-Based Study  Academic Article
• Physical activity and genetic predisposition to obesity in a multiethnic longitudinal study  Academic Article
• Plasma Concentrations and Genetic Variation of Matrix Metalloproteinase 9 and Prognosis of Patients With Cardiovascular Disease  Academic Article
• Plasma carboxypeptidase B downregulates inflammatory responses in autoimmune arthritis  Academic Article
• Plasticity in male mating behavior modulates female life history in fruit flies  Academic Article
• Platelet glycoprotein Ibα Kozak polymorphism is associated with an increased risk of ischemic stroke  Academic Article
• PlexinA polymorphisms mediate the developmental trajectory of human corpus callosum microstructure  Academic Article
• Polygenic Contribution in Individuals With Early-Onset Coronary Artery Disease  Academic Article
• Polygenic determinants of severe hypertriglyceridemia  Academic Article
• Polymorphic Variation of Genes in the Fibrinolytic System and the Risk of Ovarian Cancer  Academic Article
• Polymorphism in the CETP Gene Region, HDL Cholesterol, and Risk of Future Myocardial Infarction  Academic Article
• Polymorphism of the beta2-adrenoceptor and the response to long-term beta2-agonist therapy in asthma.  Academic Article
• Polymorphisms in the Amino Acid Transporter Solute Carrier Family 6 (Neurotransmitter Transporter) Member 14 Gene Contribute to Polygenic Obesity in French Caucasians  Academic Article
• Polymorphisms of 5-HTT LPR and GNβ3 825C>T and Response to Antidepressant Treatment in Functional Dyspepsia: A Study from The Functional Dyspepsia Treatment Trial  Academic Article
• Population Genetic Analyses of the Fungal Pathogen Colletotrichum fructicola on Tea-Oil Trees in China  Academic Article
• Positional effect of cis/trans alpha globin gene deletions on the formation of “H” bodies  Academic Article
• Predictive power of individual genetic and environmental factor scores  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
• Prenatal sonographic diagnosis of hypochondroplasia in a high‐risk fetus  Academic Article
• Prevalence and Genotypes of α- and β-Thalassemia Carriers in Hong Kong — Implications for Population Screening  Academic Article
• Prevalence and predictors of human papillomavirus infection in women in Ontario, Canada. Survey of HPV in Ontario Women (SHOW) Group.  Academic Article
• Prevalence of G6PD deficiency and associated haematological parameters in children from Botswana  Academic Article
• Prevalence of infection with carcinogenic human papillomavirus among older women.  Academic Article
• Prevalence of insulin resistance in chronic hepatitis C genotype 1 and 3 patients  Academic Article
• Prevalence of meconium ileus marks the severity of mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene  Academic Article
• Prevalence of specific and phylogenetically closely related genotypes in the population of Candida albicans associated with genital candidiasis in China  Academic Article
• Prevalent nosocomial clusters among causative agents for candidemia in Hamilton, Canada  Academic Article
• Probability genotype imputation method and integrated weighted lasso for QTL identification  Academic Article
• Prolonged shedding of rhinovirus and re-infection in adults with respiratory tract illness  Academic Article
• Prospective Evaluation of the 21-Gene Recurrence Score Assay for Breast Cancer Decision-Making in Ontario  Academic Article
• Protein Z Gene Polymorphisms, Protein Z Concentrations, and Ischemic Stroke  Academic Article
• Putting the Genome in Context: Gene-Environment Interactions in Type 2 Diabetes  Academic Article
• Quantitative genetics of larval life-history traits in Rana temporaria in different environmental conditions  Academic Article
• Quantitative variation of biofilms among strains in natural populations of Candida albicans  Academic Article
• RAD51 polymorphisms and breast cancer risk  Academic Article
• ROLE OF THE NEURAL TUBE IN THE PATHOGENESIS OF HEREDITARY MUSCULAR DYSTROPHY IN THE CHICKEN: STUDIES WITH TRANSPLANTATION CHIMERAS  Academic Article
• Radiation-induced apoptosis in mouse lymphocytes is modified by a complex dietary supplement: the effect of genotype and gender  Academic Article
• Randomized Trial of Benznidazole for Chronic Chagas’ Cardiomyopathy  Academic Article
• Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions  Academic Article
• Rare ATGL haplotypes are associated with increased plasma triglyceride concentrations in the Greenland Inuit  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
• Rarity of the Alzheimer Disease–ProtectiveAPPA673T Variant in the United States  Academic Article
• Real-world effectiveness of peginterferon α-2b plus ribavirin in a Canadian cohort of treatment-naïve chronic hepatitis C patients with genotypes 2 or 3: results of the PoWer and RediPEN studies  Academic Article
• Recombination and genetic differentiation among natural populations of the ectomycorrhizal mushroom Tricholoma matsutake from southwestern China  Academic Article
• Recombination, mutation, or constitutive expression at a Gm locus and familial hypergammaglobulinemia.  Academic Article
• Red cell N5-methyltetrahydrofolate concentrations and C677T methylenetetrahydrofolate reductase genotype in patients with stroke  Academic Article
• Redefining Disease? The Nosologic Implications of Molecular Genetic Knowledge  Academic Article
• Reduced hippocampus volume and memory performance in bipolar disorder patients carrying the BDNF val66met met allele  Academic Article
• Reemergence of Lower-Airway Microbiota in Lung Transplant Patients with Cystic Fibrosis  Academic Article
• Regulation of basal gastric acid secretion by the glycogen synthase kinase GSK3  Academic Article
• Relation of Factor V Leiden Genotype to Risk for Acute Deep Venous Thrombosis after Joint Replacement Surgery  Academic Article
• Renal venous thrombosis in a newborn with prothrombotic risk factors  Academic Article
• Renin–angiotensin and endothelial nitric oxide synthase gene polymorphisms are not associated with the risk of incident type 2 diabetes mellitus: a prospective cohort study  Academic Article
• Replication of anEgfr-Wing Shape Association in a Wild-Caught Cohort ofDrosophila melanogaster  Academic Article
• Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample  Academic Article
• Respiratory sinus arrhythmia in the fourth decade of life depends on birth weight and the DRD4 gene: Implications for understanding the development of emotion regulation  Academic Article
• Responder Interferon λ Genotypes Are Associated With Higher Risk of Liver Fibrosis in HIV–Hepatitis C Virus Coinfection  Conference Paper
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• Results of a Pilot Multicenter Genotype-based Randomized Placebo-controlled Trial of Propranolol to Reduce Pain After Major Thermal Burn Injury  Academic Article
• Retreatment with Pegylated Interferon Alpha-2a and Ribavirin in Patients with Chronic Hepatitis C Who Have Relapsed or Not Responded to a First Course of Pegylated Interferon-Based Therapy  Academic Article
• Review of aspirin and clopidogrel resistance in peripheral arterial disease  Academic Article
• Revisiting the evolutionary origins of obesity: lazy versus peppy-thrifty genotype hypothesis  Academic Article
• RhD status of a fetus at risk for haemolytic disease with a discrepant maternal DNA-based RhD genotype  Academic Article
• Robust demarcation of fourteen different species groups within the genus Streptococcus based on genome-based phylogenies and molecular signatures  Academic Article
• Robustness of the BMP morphogen gradient in Drosophila embryonic patterning  Academic Article
• Role of Cystic Fibrosis Transmembrane Conductance Regulator in Patients With Chronic Sinopulmonary Disease  Academic Article
• Role of Macrophage Migration Inhibitory Factor in Granulomatosis With Polyangiitis  Conference Paper
• Role of polymorphic bile salt export pump (BSEP, ABCB11) transporters in anti-tuberculosis drug-induced liver injury in a Chinese cohort  Academic Article
• Role of polymorphism of methyltetrahydrofolate-homocysteine methyltransferase (MTR) A2756G and breast cancer risk  Academic Article
• Role ofKRASandEGFRAs Biomarkers of Response to Erlotinib in National Cancer Institute of Canada Clinical Trials Group Study BR.21  Academic Article
• SELECTION ON LEAF ECOPHYSIOLOGICAL TRAITS IN A DESERT HYBRID HELIANTHUS SPECIES AND EARLY-GENERATION HYBRIDS  Academic Article
• Screening of hypoxia-inducible genes in sporadic ALS  Academic Article
• Secretory granule neuroendocrine protein 1 (SGNE1) genetic variation and glucose intolerance in severe childhood and adult obesity  Academic Article
• Sensitive and Efficient Detection of RB1 Gene Mutations Enhances Care for Families with Retinoblastoma  Academic Article
• Sensitivity of APTIMA HPV E6/E7 mRNA test in comparison with hybrid capture 2 HPV DNA test for detection of high risk oncogenic human papillomavirus in 396 biopsy confirmed cervical cancers  Academic Article
• Sensitivity to suppression of cytotoxic T cell generation by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) is dependent on the Ah genotype of the murine host  Academic Article
• Serotonin transporter allelic variation in mothers predicts maternal sensitivity, behavior and attitudes toward 6-month-old infants  Academic Article
• Sex- and age-interacting eQTLs in human complex diseases  Academic Article
• Should We Have Blind Faith in Bioinformatics Software? Illustrations from the SNAP Web-Based Tool  Academic Article
• Single-Tube Multiplex-PCR Screen for Anti-3.7 and Anti-4.2 α-Globin Gene Triplications  Academic Article
• Size and location of the transforming region in human adenovirus type 5 DNA  Academic Article
• Sizing bands on autoradiograms: A study of precision for scoring DNA fingerprints  Academic Article
• Smith-Lemli-Opitz (RHS) syndrome: holoprosencephaly and homozygous IVS8-1G?C genotype  Academic Article
• Spatiotemporal Analysis of Cryptosporidium Species/Genotypes and Relationships with Other Zoonotic Pathogens in Surface Water from Mixed-Use Watersheds  Academic Article
• Spectrum of β-Thalassemia Mutations in Egypt  Academic Article
• Statistical genetics with application to population-based study design: a primer for clinicians  Academic Article
• Strength training: importance of genetic factors  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
• Succinylcholine sensitivity in a nova scotia family  Academic Article
• Sudanese (δβ)0-Thalassemia: Identification and Characterization of a Novel 9.6 kb Deletion  Academic Article
• Susceptibility to chronic pain following nerve injury is genetically affected by CACNG2  Academic Article
• Synaesthesia: A Case Study of Discordant Monozygotic Twins  Academic Article
• TCF7L2 is associated with type 2 diabetes in nonobese individuals from Tunisia  Academic Article
• TCF7L2 is reproducibly associated with type 2 diabetes in various ethnic groups: a global meta-analysis  Academic Article
• TCF7L2 rs7903146 variant does not associate with smallness for gestational age in the French population  Academic Article
• TERT promoter mutations are highly recurrent in SHH subgroup medulloblastoma  Academic Article
• THE EFFECT OF TEMPERATURE ON FLUORIDE-RESISTANT SERUM CHOLINESTERASE  Academic Article
• Tentative classification of neuropsychiatric disturbances in Parader-Willi syndrome  Academic Article
• The Association Between HLA Genetic Susceptibility Markers and Sonographic Enthesitis in Psoriatic Arthritis  Conference Paper
• The Association of HLA-class I Genes and the Extent of Atherosclerotic Plaques in Patients with Psoriatic Disease  Academic Article
• The Complex Genetic Basis of Plasma Triglycerides  Academic Article
• The Conditional Nature of Genetic Interactions: The Consequences of Wild-Type Backgrounds on Mutational Interactions in a Genome-Wide Modifier Screen  Academic Article
• The Diagnosis and Prognosis of Autosomal Dominant Polycystic Kidney Disease  Academic Article
• The Effect of Chromosome 9p21 Variants on Cardiovascular Disease May Be Modified by Dietary Intake: Evidence from a Case/Control and a Prospective Study  Academic Article
• The Effects of Weak Genetic Perturbations on the Transcriptome of the Wing Imaginal Disc and Its Association With Wing Shape inDrosophila melanogaster  Academic Article
• The Fat-Mass and Obesity-Associated (FTO) gene, physical activity, and risk of incident cardiovascular events in white women  Academic Article
• The GABA A-Receptor γ2 (GABRG2) Gene in obsessive-compulsive disorder  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 Imprinted Gene Neuronatin Is Regulated by Metabolic Status and Associated With Obesity  Academic Article
• The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype  Academic Article
• The Ocular Manifestations of Jacobsen Syndrome: A Report of Four Cases and a Review of the Literature  Academic Article
• The Position of the Polycystic Kidney Disease 1 (PKD1) Gene Mutation Correlates with the Severity of Renal Disease  Academic Article
• The Q121 Variant of ENPP1 May Protect From Childhood Overweight/obesity in the Italian Population  Academic Article
• The Relationship between Genotype and Exercise Tolerance in Children with Cystic Fibrosis  Academic Article
• The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families  Academic Article
• The Smith-Lemli-Opitz syndrome: a novel metabolic way of understanding developmental biology, embryogenesis, and dysmorphology  Academic Article
• The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects  Academic Article
• The T-786→C Mutation in Endothelial Nitric Oxide Synthase Is Associated With Hypertension  Academic Article
• The advantage of recombination when selection is acting at many genetic Loci  Academic Article
• The association between glutathione S-transferase M1 genotype and polycyclic aromatic hydrocarbon-DNA adducts in breast tissue.  Academic Article
• The detection of Cryptosporidium and the resolution of mixtures of species and genotypes from water  Academic Article
• The diagnosis of inborn errors of metabolism by examination of the genotype  Academic Article
• The dopamine D4 receptor gene, birth weight, maternal depression, maternal attention, and the prediction of disorganized attachment at 36 months of age: A prospective gene × environment analysis  Academic Article
• The dopamine D4Receptor (DRD4) gene exon III polymorphism, problematic alcohol use and novelty seeking: direct and mediated genetic effects  Academic Article
• The effect of alpha-hemoglobin gene deletions on the red blood cells' mean cell volume and hemoglobin levels.  Academic Article
• The effect of iron status on vascular health  Academic Article
• The effects of environmental and genetic factors on the germination of basidiospores in the Cryptococcus gattii species complex  Academic Article
• The environmental and genetic regulation of obake expressivity: morphogenetic fields as evolvable systems  Academic Article
• The generation of a simian adenoviral vectored HCV vaccine encoding genetically conserved gene segments to target multiple HCV genotypes  Academic Article
• The genetics of hemoglobin A2regulation in sickle cell anemia  Academic Article
• The importance of individuals: intraspecific diversity of mycorrhizal plants and fungi in ecosystems  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 methylenetetrahydrofolate reductase C677T mutation induces cell-specific changes in genomic DNA methylation and uracil misincorporation: A possible molecular basis for the site-specific cancer risk modification  Academic Article
• The motor phenotype of Parkinson's disease in relation to age at onset.  Academic Article
• The nature of the hodgkin cell  Academic Article
• The pharmacogenetics of carboxylesterases: CES1 and CES2 genetic variants and their clinical effect  Academic Article
• The prenatal identification of fetal compatibility in neonatal alloimmune thrombocytopenia using amniotic fluid and variable number of tandem repeat (VNTR) analysis  Academic Article
• The protective effect of the obesity-associated rs9939609 A variant in fat mass- and obesity-associated gene on depression  Academic Article
• The relationship between CYP2C19 polymorphisms and ischaemic and bleeding outcomes in stable outpatients: the CHARISMA genetics study  Academic Article
• The serotonin transporter polymorphisms and major depression following traumatic brain injury  Academic Article
• TheINSVNTR Locus Does Not Associate with Smallness for Gestational Age (SGA) but Interacts with SGA to Increase Insulin Resistance in Young Adults  Academic Article
• Three New α-Thalassemia Point Mutations Ascertained Through Newborn Screening  Academic Article
• Tissue Factor and Thrombosis Models  Academic Article
• Towards a more accurate quantitative assessment of seasonal Cryptosporidium infection risks in surface waters using species and genotype information  Academic Article
• Tracking Host Sources of Cryptosporidium spp. in Raw Water for Improved Health Risk Assessment  Academic Article
• Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders  Academic Article
• Treatment Outcomes of Treatment-Naïve Hepatitis C Patients Co-Infected with HIV: A Systematic Review and Meta-Analysis of Observational Cohorts  Academic Article
• Treatment responses in Asians and Caucasians with chronic hepatitis C infection  Academic Article
• Twenty-Five-Year Outbreak of Pseudomonas aeruginosa Infecting Individuals with Cystic Fibrosis: Identification of the Prairie Epidemic Strain  Academic Article
• Type and intensity of FVIII exposure on inhibitor development in PUPs with haemophilia A  Academic Article
• Type of CFTR Mutation Determines Risk of Pancreatitis in Patients With Cystic Fibrosis  Academic Article
• UK consensus guidelines for the use of the protease inhibitors boceprevir and telaprevir in genotype 1 chronic hepatitis C infected patients  Academic Article
• Understanding naltrexone mechanism of action and pharmacogenetics in Asian Americans via behavioral economics: A preliminary study.  Academic Article
• Understanding the population structure of North American patients with cystic fibrosis  Academic Article
• Undetected factor VIII in a patient with type 3 von Willebrands disease mistaken as severe haemophilia A  Academic Article
• Uniparental Mitochondrial Transmission in Sexual Crosses in Cryptococcus neoformans  Academic Article
• Universal Newborn Screening for Hb H Disease in California  Academic Article
• Use of genetic data to guide therapy in arterial disease  Academic Article
• Use of latent class models to accommodate inter-laboratory variation in assessing genetic polymorphisms associated with disease risk  Academic Article
• Utility of Treadmill Testing in Identification and Genotype Prediction in Long-QT Syndrome  Academic Article
• Vascular Endothelial Growth Factor Polymorphisms and Esophageal Cancer Prognosis  Academic Article
• Vitamin D and cause-specific vascular disease and mortality: a Mendelian randomisation study involving 99,012 Chinese and 106,911 European adults  Academic Article
• Weight Loss–Associated Induction of Peroxisome Proliferator–Activated Receptor-α and Peroxisome Proliferator–Activated Receptor-γ Correlate With Reduced Atherosclerosis and Improved Cardiovascular Function in Obese Insulin-Resistant Mice  Academic Article
• White matter integrity in major depressive disorder: Implications of childhood trauma, 5-HTTLPR and BDNF polymorphisms  Academic Article
• Whole-Genome SNP Association in the Horse: Identification of a Deletion in Myosin Va Responsible for Lavender Foal Syndrome  Academic Article
• Why is ALS so Difficult to Treat?  Academic Article
• X-Linked Deafness-2 (DFNX2) Phenotype Associated With a Paracentric Inversion Upstream of POU3F4  Academic Article
• Yersinia pestis genotyping.  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
• α+-Thalassemia Due to a Frameshift Mutation of theα2-Globin Gene [codons 55/56 (+T) orHBA2: c.168dup]  Academic Article
• α+-Thalassemia Trait Caused by a Frameshift Mutation in Exon 2 of the α2-Globin Gene [HBA2 c.244delT]  Academic Article
• α-Thalassemia: Hb H Disease and Hb Barts Hydrops Fetalis  Academic Article
• α1-Antitrypsin Deficiency Alleles in Cystic Fibrosis Lung Disease  Academic Article
• β-thalassemia intermedia caused by compound heterozygosity for Hb Malay (β codon 19 AAC→AGC; Asn→Ser) and codons 41/42 (-CTTT) β0-thalassemia mutation  Academic Article
• β-thalassemia intermedia due to compound heterozygosity for two β-globin gene promoter mutations, including a novel TATA box deletion  Academic Article