Alleles Concept

subject area of

• Genetic knockdown of a single organic anion transporter alters the expression of functionally related genes in Malpighian tubules ofDrosophila melanogaster  Journal Articles
• Per3 length polymorphism in patients with type 2 diabetes mellitus  Journal Articles
• Salmonella Vitkin Outbreak Associated with Bearded Dragons, Canada and United States, 2020–2022  Journal Articles
• sli-3 Negatively Regulates the LET-23/Epidermal Growth Factor Receptor-Mediated Vulval Induction Pathway in Caenorhabditis elegans  Journal Articles
• TSPEAR variants are primarily associated with ectodermal dysplasia and tooth agenesis but not hearing loss: A novel cohort study  Journal Articles
• A CGG-Repeat Expansion Mutation inZNF713Causes FRA7A: Association with Autistic Spectrum Disorder in two Families  Journal Articles
• A Genome-Wide Association Study for Coronary Artery Disease Identifies a Novel Susceptibility Locus in the Major Histocompatibility Complex  Journal Articles
• A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis  Journal Articles
• A High-Resolution Melting Approach for Analyzing Allelic Expression Dynamics  Journal Articles
• A Reanalysis of Protein Polymorphism in Drosophila Melanogaster, D. Simulans, D. Sechellia and D. Mauritiana: Effects of Population Size and Selection  Journal Articles
• A Variable-Number-of-Tandem-Repeats Polymorphism in the Dopamine D4 Receptor Gene Affects Social Adaptation of Alcohol Use  Journal Articles
• A comprehensive study of genic variation in natural populations of Drosophila melanogaster. VI. Patterns and processes of genic divergence between D. melanogaster and its sibling species, Drosophila simulans.  Journal Articles
• A genome-wide association study of sporadic ALS in a homogenous Irish population  Journal Articles
• A genome-wide scan for common alleles affecting risk for autism  Journal Articles
• A mixability theory for the role of sex in evolution  Journal Articles
• A molecular genetic study of factor XI deficiency  Journal Articles
• A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genes  Journal Articles
• A novel candidate region for ALS on chromosome 14q11.2  Journal Articles
• A novel multisystem disease associated with recessive mutations in the tyrosyl‐tRNA synthetase (YARS) gene  Journal Articles
• A putative Lipid Transfer Protein involved in systemic resistance signaling in Arabidopsis  Journal Articles
• A recurrent de novo HSPD1 variant is associated with hypomyelinating leukodystrophy  Journal Articles
• A sampling theory of selectively neutral alleles in a subdivided population.  Journal Articles
• Accelerated decline in lung function in cigarette smokers is associated with TP53/MDM2 polymorphisms  Journal Articles
• Activation of the Hedgehog Signaling Pathway in the Developing Lens Stimulates EctopicFoxE3Expression and Disruption in Fiber Cell Differentiation  Journal Articles
• Adrenergic alpha 2C receptor genomic organization: Association study in adult ADHD  Journal Articles
• Allele frequency data for VNTR locus D17S79: Identification of an internalHaeIII polymorphism in the black population  Journal Articles
• Allelic Stability of VNTR Locus 3’αHVR: Linkage Disequilibrium with the Common α-Thalassaemia-1-Deletion of South-East Asia (--SEA/)  Journal Articles
• Allelic and phenotypic spectrum of plasma triglycerides  Journal Articles
• Allelic variants of the amylose extender mutation of maize demonstrate phenotypic variation in starch structure resulting from modified protein-protein interactions  Journal Articles
• An Engineered Allele of afsQ1 Facilitates the Discovery and Investigation of Cryptic Natural Products  Journal Articles
• An Increased Burden of Common and Rare Lipid-Associated Risk Alleles Contributes to the Phenotypic Spectrum of Hypertriglyceridemia  Journal Articles
• Ancient selection for derived alleles at a GDF5 enhancer influencing human growth and osteoarthritis risk  Journal Articles
• Angiogenin Levels and ANG Genotypes: Dysregulation in Amyotrophic Lateral Sclerosis  Journal Articles
• Antithrombin III‐Amiens: A new family with an Arg⁴⁷ → cys inherited variant of antithrombin iii with impaired heparin cofactor activity  Journal Articles
• Antithrombin-III-Hamilton, Ala 382 to Thr: an antithrombin-III variant that acts as a substrate but not an inhibitor of alpha-thrombin and factor Xa  Journal Articles
• Antithrombin-III-Hamilton: a gene with a point mutation (guanine to adenine) in codon 382 causing impaired serine protease reactivity  Journal Articles
• Apolipoprotein E e4 allele affects risk of hyperhomocysteinemia in the elderly  Journal Articles
• Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations  Journal Articles
• Assessing non-Mendelian inheritance in inherited axonopathies  Journal Articles
• Assigning a probability for paternity in apparent cases of mutation.  Journal Articles
• Association Between a Literature-Based Genetic Risk Score and Cardiovascular Events in Women  Journal Articles
• Association between HLA Class I and Class II Alleles and the Outcome of West Nile Virus Infection: An Exploratory Study  Journal Articles
• Association between high expression macrophage migration inhibitory factor (MIF) alleles and West Nile virus encephalitis  Journal Articles
• Association between maternal childhood maltreatment and mother-infant attachment disorganization: Moderation by maternal oxytocin receptor gene and cortisol secretion  Journal Articles
• Association between the seven-repeat allele of the dopamine-4 receptor gene (DRD4) and spontaneous food intake in pre-school children  Journal Articles
• Association of BRM promoter polymorphisms and esophageal adenocarcinoma outcome  Journal Articles
• Association of Granulomatosis With Polyangiitis (Wegener's) With HLA–DPB1*04 and SEMA6A Gene Variants: Evidence From Genome‐Wide Analysis  Journal Articles
• Association of autism severity with a monoamine oxidase A functional polymorphism  Journal Articles
• Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3  Journal Articles
• Association study between fibronectin and coronary heart disease  Journal Articles
• Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn’s disease subjects  Journal Articles
• Associations of the FTO rs9939609 variant with discrete body fat depots and dietary intake in a multi-ethnic cohort  Journal Articles
• Atypical clinical course in juvenile metachromatic leukodystrophy involving novel arylsulfatase A gene mutations  Journal Articles
• Autism and the X chromosome: No linkage to microsatellite loci detected using the affected sibling pair method  Journal Articles
• BRCA2 Variants and cardiovascular disease in a multi-ethnic study  Journal Articles
• Betaine aldehyde dehydrogenase polymorphism in spinach: Genetic and biochemical characterization  Journal Articles
• Bi-allelic Loss of Human APC2, Encoding Adenomatous Polyposis Coli Protein 2, Leads to Lissencephaly, Subcortical Heterotopia, and Global Developmental Delay  Journal Articles
• Biotinidase deficiency: Spectrum of molecular, enzymatic and clinical information from newborn screening Ontario, Canada (2007–2014)  Journal Articles
• Birth weight interacts with a functional variant of the oxytocin receptor gene (OXTR) to predict executive functioning in children  Journal Articles
• Bovine IFNGR2, IL12RB1, IL12RB2, and IL23R polymorphisms and MAP infection status  Journal Articles
• Breast cancer prognostic significance of a single nucleotide polymorphism in the proximal androgen response element of the prostate specific antigen gene promoter  Journal Articles
• CARD15 and IL23R influences Crohnʼs disease susceptibility but not disease phenotype in a Brazilian population  Journal Articles
• CORRIGENDUM  Journal Articles
• Caenorhabditis elegans SMA-10/LRIG Is a Conserved Transmembrane Protein that Enhances Bone Morphogenetic Protein Signaling  Journal Articles
• Carrier frequency of the RSH/Smith‐Lemli‐Opitz IVS8‐1G>C mutation in African Americans  Journal Articles
• Carving out turf in a biodiversity hotspot: multiple, previously unrecognized shrew species co‐occur onJavaIsland,Indonesia  Journal Articles
• Case Report: Eosinophilic Esophagitis in a Patient With a Novel STAT1 Gain-of-Function Pathogenic Variant  Journal Articles
• Characterization of Class I– and Class II–Like Major Histocompatibility Complex Loci in Pedigrees of North Atlantic Right Whales  Journal Articles
• Characterization of Three Novel δ Chain Hemoglobin Variants and Two δ-Thalassemia Alleles  Journal Articles
• Characterization of tumor necrosis factor–α block haplotypes associated with susceptibility to chronic venous leg ulcers in Caucasian patients  Journal Articles
• Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesis  Journal Articles
• Clinical Next-Generation Sequencing Pipeline Outperforms a Combined Approach Using Sanger Sequencing and Multiplex Ligation-Dependent Probe Amplification in Targeted Gene Panel Analysis  Journal Articles
• Clinical evaluation of a hemochromatosis next‐generation sequencing gene panel  Journal Articles
• Codon Usage and Selection on Proteins  Journal Articles
• Combining direct and indirect genetic methods to estimate dispersal for informing wildlife disease management decisions  Journal Articles
• Common Low-Density Lipoprotein Receptor p.G116S Variant Has a Large Effect on Plasma Low-Density Lipoprotein Cholesterol in Circumpolar Inuit Populations  Journal Articles
• Comorbidities and complications in adults with pyruvate kinase deficiency  Journal Articles
• Comparative analysis of Shwachman-Diamond syndrome to other inherited bone marrow failure syndromes and genotype-phenotype correlation  Journal Articles
• Compensatory neutral mutations and the evolution of RNA.  Journal Articles
• Complications in the genotypic molecular diagnosis of pseudo arylsulfatase A deficiency  Journal Articles
• Contemporary Gene Flow is a Major Force Shaping the Aspergillus fumigatus Population in Auckland, New Zealand  Journal Articles
• Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals  Journal Articles
• Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection  Journal Articles
• DHCR7 nonsense mutations and characterisation of mRNA nonsense mediated decay in Smith-Lemli-Opitz syndrome  Journal Articles
• DIVERSIFICATION OF SULAWESI MACAQUE MONKEYS: DECOUPLED EVOLUTION OF MITOCHONDRIAL AND AUTOSOMAL DNA  Journal Articles
• DNA Marker Studies Show That Machado Joseph Disease is Not an Allele of The Huntingdon Disease Locus  Journal Articles
• Decreased comfort food intake and allostatic load in adolescents carrying the A3669G variant of the glucocorticoid receptor gene  Journal Articles
• Delayed prezygotic isolating mechanisms: evolution with a twist  Journal Articles
• Demographic expansion and genetic load of the halophyte model plant Eutrema salsugineum  Journal Articles
• Determination of lipoprotein(a) kringle repeat number from genomic DNA: copy number variation genotyping using qPCR  Journal Articles
• Determining the cause of patchwork HBA1 and HBA2 genes: recurrent gene conversion or crossing over fixation events.  Journal Articles
• Diagnosis of arylsulfatase A deficiency  Journal Articles
• Differences in gluten metabolism among healthy volunteers, coeliac disease patients and first-degree relatives  Journal Articles
• Differential permeability of rivers to raccoon gene flow corresponds to rabies incidence in Ontario, Canada  Journal Articles
• Dinucleotide repeat polymorphism at the D21S65 locus  Journal Articles
• Distinct Mechanisms of Action of theLozengeLocus inDrosophilaEye and Antennal Development are Suggested by the Analysis of Dominant Enhancers  Journal Articles
• Divergence, hybridization, and recombination in the mitochondrial genome of the human pathogenic yeast Cryptococcus gattii  Journal Articles
• Diversity, functional classification and genotyping of SHV β-lactamases in Klebsiella pneumoniae.  Journal Articles
• Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis?  Journal Articles
• Drosophila RhoGAP68F is a putative GTPase activating protein for RhoA participating in gastrulation  Journal Articles
• Effects of Nicotine Deprivation and Replacement on BOLD-fMRI Response to Smoking Cues as a Function of DRD4 VNTR Genotype  Journal Articles
• Effects of Source of DNA on Genotyping Success Rates and Allele Percentages in the Preschoolers with Attention-Deficit/Hyperactivity Disorder Treatment Study (PATS)  Journal Articles
• Environmental and allele‐specific influences on T cell receptor gene rearrangement: skewed α, δ and γ gene rearrangement patterns in chimeric mice  Journal Articles
• Establishment of real time allele specific locked nucleic acid quantitative PCR for detection of HBV YIDD (ATT) mutation and evaluation of its application.  Journal Articles
• Evaluating the effects of historic bottleneck events: an assessment of microsatellite variability in the endangered, North Atlantic right whale  Journal Articles
• Evidence for a gene–gene interaction in predicting children's behavior problems: Association of serotonin transporter short and dopamine receptor D4 long genotypes with internalizing and externalizing behaviors in typically developing 7-year-olds  Journal Articles
• Evidence for genetic incompatibilities associated with post-zygotic reproductive isolation in the human fungal pathogenCryptococcus neoformans  Journal Articles
• Evidence that Egfr Contributes to Cryptic Genetic Variation for Photoreceptor Determination in Natural Populations of Drosophila melanogaster  Journal Articles
• Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA  Journal Articles
• Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction  Journal Articles
• Exon-skipping in BCR/ABL is induced by ABL exon 2  Journal Articles
• Fetal growth interacts with multilocus genetic score reflecting dopamine signaling capacity to predict spontaneous sugar intake in children  Journal Articles
• Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype  Journal Articles
• Fetal hemoglobin in sickle cell anemia: Molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans  Journal Articles
• Fine-Scale Patterns of Population Stratification Confound Rare Variant Association Tests  Journal Articles
• Fixed-bin analysis for statistical evaluation of continuous distributions of allelic data from VNTR loci, for use in forensic comparisons.  Journal Articles
• Founder effect for the T93MDHCR7mutation in Smith‐Lemli‐Opitz syndrome  Journal Articles
• Fumarase deficiency: a rare disorder on the crossroads of clinical and metabolic genetics, neurology and cancer  Journal Articles
• GENETIC HETEROGENEITY WITHIN ELECTROPHORETIC "ALLELES" OF XANTHINE DEHYDROGENASE IN DROSOPHILA PSEUDOOBSCURA  Journal Articles
• GENIC VARIATION IN ABUNDANT SOLUBLE PROTEINS OF DROSOPHILA MELANOGASTER AND DROSOPHILA PSEUDOOBSCURA  Journal Articles
• Gene duplication and divergence produce divergent MHC genotypes without disassortative mating  Journal Articles
• Gene × Physical Activity Interactions in Obesity: Combined Analysis of 111,421 Individuals of European Ancestry  Journal Articles
• Gene-Centric Meta-Analysis of Lipid Traits in African, East Asian and Hispanic Populations  Journal Articles
• Genetic Differential Susceptibility to Socioeconomic Status and Childhood Obesogenic Behavior  Journal Articles
• Genetic Diversity and Dispersal of Aspergillus fumigatus in Arctic Soils  Journal Articles
• Genetic Diversity of Populations of Monilinia fructicola (Fungi, Ascomycota, Helotiales) from China  Journal Articles
• Genetic Susceptibility to West Nile Virus and Dengue  Journal Articles
• Genetic Variants Associated With Myocardial Infarction Risk Factors in Over 8000 Individuals From Five Ethnic Groups  Journal Articles
• Genetic Variants and Susceptibility to Neurological Complications Following West Nile Virus Infection  Journal Articles
• Genetic Variations of TAP1 Gene Exon 3 Affects Gene Expression and Escherichia coli F18 Resistance in Piglets  Journal Articles
• Genetic analysis of inherited bone marrow failure syndromes from one prospective, comprehensive and population-based cohort and identification of novel mutations  Journal Articles
• Genetic variation of the St. Lawrence beluga whale population assessed by DNA fingerprinting  Journal Articles
• Genetically determined low maternal serum dopamine ?-hydroxylase levels and the etiology of autism spectrum disorders  Journal Articles
• Genetics of microenvironmental canalization in Arabidopsis thaliana  Journal Articles
• Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets  Journal Articles
• Genome-wide meta-analyses identify multiple loci associated with smoking behavior  Journal Articles
• Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders  Journal Articles
• Geographic Distribution of Mating Type Alleles of Cryptococcus neoformans in Four Areas of the United States  Journal Articles
• Gigantic splenomegaly in a 27‐year‐old male of South‐East Asian descent with concurrent diagnosis of myeloproliferative neoplasm and hemoglobin H disease  Journal Articles
• Gova/b alloantigen system on human platelets  Journal Articles
• HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome  Journal Articles
• Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family  Journal Articles
• How well do you know your mutation? Complex effects of genetic background on expressivity, complementation, and ordering of allelic effects  Journal Articles
• Human XPF controls TRF2 and telomere length maintenance through distinctive mechanisms  Journal Articles
• Human milk fatty acid composition is associated with dietary, genetic, sociodemographic, and environmental factors in the CHILD Cohort Study  Journal Articles
• Huntingtin is a scaffolding protein in the ATM oxidative DNA damage response complex  Journal Articles
• IL28B polymorphism (rs12979860) associated with clearance of HCV infection in Poland: Systematic review of its prevalence in chronic hepatitis C patients and general population frequency  Journal Articles
• Identification of complex DNA polymorphisms based on variable number of tandem repeats (VNTR) and restriction site polymorphism  Journal Articles
• Identification of restriction-fragment-length polymorphisms in genomic DNA of the lesser snow goose (Anser caerulescens caerulescens).  Journal Articles
• Identification of two novel β°-thalassemia mutations in a filipino family: Frameshift codon 67 (− TG) and a β-globin gene deletion  Journal Articles
• IgA and IgG antineutrophil cytoplasmic antibody engagement of Fc receptor genetic variants influences granulomatosis with polyangiitis  Journal Articles
• Immunochip Analysis Identifies Multiple Susceptibility Loci for Systemic Sclerosis  Journal Articles
• Implications of OPRM1 and CYP2B6 variants on treatment outcomes in methadone-maintained patients in Ontario: Exploring sex differences  Journal Articles
• Increased FGF8 signaling promotes chondrogenic rather than osteogenic development in the embryonic skull  Journal Articles
• Increased pyruvate orthophosphate dikinase activity results in an alternative gluconeogenic pathway in Rhizobium (Sinorhizobium) meliloti  Journal Articles
• Individual common variants exert weak effects on the risk for autism spectrum disorders  Journal Articles
• Induction of antimicrobial activities in heterologous streptomycetes using alleles of the Streptomyces coelicolor gene absA1  Journal Articles
• Investigation of Intercellular Salicylic Acid Accumulation during Compatible and Incompatible Arabidopsis-Pseudomonas syringae Interactions Using a Fast Neutron-Generated Mutant Allele of EDS5 Identified by Genetic Mapping and Whole-Genome Sequencing  Journal Articles
• Investigation of the dopamine D5 receptor gene (DRD5) in adult attention deficit hyperactivity disorder  Journal Articles
• Investigation on ERCC5 genetic polymorphisms and the development of gastric cancer in a Chinese population  Journal Articles
• Is serotonin transporter polymorphism (5-HTTLPR) allele status a predictor for obsessive-compulsive disorder? A meta-analysis  Journal Articles
• Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease  Journal Articles
• Large-scale functional screen identifies genetic variants with splicing effects in modern and archaic humans  Journal Articles
• Late‐onset metachromatic leukodystrophy clinically presenting as isolated peripheral neuropathy: Compound heterozygosity for the IVS2+1G→a mutation and a newly identified missense mutation (Thr408Ile) in a Spanish family  Journal Articles
• Linking Gene, Brain, and Behavior  Journal Articles
• Localization of dystrophin isoform Dp71 to the inner limiting membrane of the retina suggests a unique functional contribution of Dp71 in the retina  Journal Articles
• Loss-of-Function KCNE2 Variants  Journal Articles
• Low genic variation in male-reproductive-tract proteins of Drosophila melanogaster and D. simulans.  Journal Articles
• Lunatic Fringe-mediated Notch signaling is required for lung alveogenesis  Journal Articles
• MHC Class I-Mediated Antigen Presentation and Induction of CD8+ Cytotoxic T-Cell Responses in Autoimmune Diabetes-Prone NOD Mice  Journal Articles
• MOLECULAR AND PHARMACOLOGICAL CHARACTERISATION OF THE MSH-R ALLELES IN SWISS CATTLE BREEDS  Conferences
• 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  Journal Articles
• Mesectodermal cell fate analysis in Drosophila midline mutants  Journal Articles
• Mesenteric-portal Vein Thrombosis in a Patient with Hyperhomocysteinemia and Heterozygous for 20210A Prothrombin Allele  Journal Articles
• Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes  Journal Articles
• Metabolic Myopathies Discovered During Investigations of Statin Myopathy  Journal Articles
• Metachromatic leukodystrophy: Multiple nonfunctional and pseudodeficiency alleles in a pedigree: Problems with diagnosis and counseling  Journal Articles
• Mild β⁺-Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A)  Journal Articles
• Mitochondrial recombination in natural populations of the button mushroom Agaricus bisporus  Journal Articles
• Modeling Complex Disease with Demographic and Environmental Covariates and a Candidate Gene Marker  Journal Articles
• Moderating effect of PLIN4 genetic variant on impulsivity traits in 5-year-old-children born small for gestational age  Journal Articles
• Molecular Analysis of Phyllodes Tumors Reveals Distinct Changes in the Epithelial and Stromal Components  Journal Articles
• Molecular basis of inherited human antithrombin deficiency  Journal Articles
• Mutant Alleles at the Locus elav in Drosophila melanogaster lead to Nervous System Defects. A Developmental-Genetic Analysis  Journal Articles
• Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly  Journal Articles
• Mutations in TBCK, Encoding TBC1-Domain-Containing Kinase, Lead to a Recognizable Syndrome of Intellectual Disability and Hypotonia  Journal Articles
• Mutations in the Chromatin Regulator Gene BRPF1 Cause Syndromic Intellectual Disability and Deficient Histone Acetylation  Journal Articles
• Mutations in the Chromosomal Passenger Complex and the Condensin Complex Differentially Affect Synaptonemal Complex Disassembly and Metaphase I Configuration in Drosophila Female Meiosis  Journal Articles
• Mutations in the genestand still disrupt germ cell differentiation inDrosophila ovaries  Journal Articles
• Mutual regulation of the Drosophila disconnected (disco) and Distal-less (Dll) genes contributes to proximal-distal patterning of antenna and leg  Journal Articles
• Negative regulation of sigma 54-dependent dctA expression by the transcriptional activator DctD  Journal Articles
• New Locus for Skin Intrinsic Fluorescence in Type 1 Diabetes Also Associated With Blood and Skin Glycated Proteins  Journal Articles
• Oncogenic events regulate tissue factor expression in colorectal cancer cells: implications for tumor progression and angiogenesis  Journal Articles
• Oxytocin Receptor Polymorphisms are Differentially Associated with Social Abilities across Neurodevelopmental Disorders  Journal Articles
• Parental and child genetic contributions to obesity traits in early life based on 83 loci validated in adults: the FAMILY study  Journal Articles
• Patients with thalassemia in the United States  Journal Articles
• Patterns of allele distribution in a hybrid population of the Cryptococcus neoformans species complex  Journal Articles
• Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expression  Journal Articles
• Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.  Journal Articles
• PhoPQ regulates acidic glycerophospholipid content of the Salmonella Typhimurium outer membrane  Journal Articles
• Physical activity and genetic predisposition to obesity in a multiethnic longitudinal study  Journal Articles
• Plasminogen Alleles Influence Susceptibility to Invasive Aspergillosis  Journal Articles
• Polygenic Contribution in Individuals With Early-Onset Coronary Artery Disease  Journal Articles
• Polymorphism in the CETP Gene Region, HDL Cholesterol, and Risk of Future Myocardial Infarction  Journal Articles
• Population Genetic Structure of Aldabra Giant Tortoises  Journal Articles
• Prediction of the excessive perioperative bleeding in patients undergoing coronary artery bypass grafting: Role of aspirin and platelet glycoprotein IIIa polymorphism  Journal Articles
• Prenatal maternal depression and child serotonin transporter linked polymorphic region (5-HTTLPR) and dopamine receptor D4 (DRD4) genotype predict negative emotionality from 3 to 36 months  Journal Articles
• Prevalence of meconium ileus marks the severity of mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene  Journal Articles
• Prostate Cancer Transcriptomic Regulation by the Interplay of Germline Risk Alleles, Somatic Mutations, and 3D Genomic Architecture  Journal Articles
• Protein Z Levels, Protein Z G79A Polymorphism, and Prothrombotic Conditions  Journal Articles
• Pseudomonas aeruginosa type IV minor pilins and PilY1 regulate virulence by modulating FimS-AlgR activity  Journal Articles
• Quebec platelet disorder is linked to the urokinase plasminogen activator gene (PLAU) and increases expression of the linked allele in megakaryocytes  Journal Articles
• Rank-based genome-wide analysis reveals the association of Ryanodine receptor-2 gene variants with childhood asthma among human populations  Journal Articles
• Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes  Journal Articles
• Real-Time RT-PCR Allelic Discrimination Assay for Detection of N501Y Mutation in the Spike Protein of SARS-CoV-2 Associated with B.1.1.7 Variant of Concern  Journal Articles
• Reconstructing the Prior Probabilities of Allelic Phylogenies  Journal Articles
• Reduced hippocampus volume and memory performance in bipolar disorder patients carrying the BDNF val66met met allele  Journal Articles
• Repellent Signaling by Slit Requires the Leucine-Rich Repeats  Journal Articles
• Replication of an Egfr-Wing Shape Association in a Wild-Caught Cohort of Drosophila melanogaster  Journal Articles
• Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample  Journal Articles
• 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  Journal Articles
• Risk Alleles in/near ADCY5, ADRA2A, CDKAL1, CDKN2A/B, GRB10, and TCF7L2 Elevate Plasma Glucose Levels at Birth and in Early Childhood: Results from the FAMILY Study  Journal Articles
• Role of Macrophage Migration Inhibitory Factor in Granulomatosis With Polyangiitis  Conferences
• SLOS carrier frequency in Poland as determined by screening for Trp151X and Val326Leu DHCR7 mutations  Journal Articles
• Second site mutations specifically suppress the Fix- phenotype of Rhizobium meliloti ndvF mutations on alfalfa: identification of a conditional ndvF-dependent mucoid colony phenotype.  Journal Articles
• Secretory Phospholipase A2-IIA and Cardiovascular Disease  Journal Articles
• Sequence variation at the major histocompatibility complex DRB loci in beluga ( Delphinapterus leucas ) and narwhal ( Monodon monoceros )  Journal Articles
• Sequence variation at the major histocompatibility complex locus DQ beta in beluga whales (Delphinapterus leucas)  Journal Articles
• Sex-Specific Effect of Insulin-Dependent Diabetes 4 on Regulation of Diabetes Pathogenesis in the Nonobese Diabetic Mouse  Journal Articles
• Significant differences in type IV pilin allele distribution among Pseudomonas aeruginosa isolates from cystic fibrosis (CF) versus non-CF patients  Conferences
• Single nucleotide polymorphisms in the matrix metalloproteinase gene family and the frequency and duration of gastroesophageal reflux disease influence the risk of esophageal adenocarcinoma  Journal Articles
• Single-Tube Multiplex-PCR Screen for Anti-3.7 and Anti-4.2 α-Globin Gene Triplications  Journal Articles
• Sizing bands on autoradiograms: A study of precision for scoring DNA fingerprints  Journal Articles
• Somatic cell hybridization studies on the genetic regulation and allelic mutations in metachromatic leukodystrophy  Journal Articles
• Spatial heterogeneity in resources alters selective dynamics in Drosophila melanogaster  Journal Articles
• Spectrum of β-Thalassemia Mutations in Egypt  Journal Articles
• Stabilizing selection on microsatellite allele length at arginine vasopressin 1a receptor and oxytocin receptor loci  Journal Articles
• Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis  Journal Articles
• Study of alleles of the second complement component (C2) on Canadian HLA haplotypes  Journal Articles
• Symbiotic nitrogen fixation by a nifA deletion mutant of Rhizobium meliloti: the role of an unusual ntrC allele  Journal Articles
• TATA-binding protein activates transcription when upstream of a GCN4-binding site in a novel yeast promoter.  Journal Articles
• THE EFFECT OF COMBINING ALLELES INTO ELECTROPHORETIC CLASSES ON DETECTING LINKAGE DISEQUILIBRIUM  Journal Articles
• THE Hb S/β⁺-Thalassemia Phenotype Demonstrates that the IVS-I (−2) (A>C) Mutation is a Mild β-Thalassemia Allele  Journal Articles
• THE SAMPLING DISTRIBUTION OF LINKAGE DISEQUILIBRIUM  Journal Articles
• TLR5 as an Anti-Inflammatory Target and Modifier Gene in Cystic Fibrosis  Journal Articles
• The BDNF Val66Met polymorphism and health‐related quality of life in youth with obesity  Journal Articles
• The Brain-Derived Neurotrophic Factor Val66Met Polymorphism, Hippocampal Volume, and Cognitive Function in Geriatric Depression  Journal Articles
• The E2F cell cycle regulator is required for Drosophila nurse cell DNA replication and apoptosis  Journal Articles
• The Effect of Chromosome 9p21 Variants on Cardiovascular Disease May Be Modified by Dietary Intake: Evidence from a Case/Control and a Prospective Study  Journal Articles
• The Effect of Vitamin E Supplementation on Cardiovascular Risk in Diabetic Individuals With Different Haptoglobin Phenotypes  Journal Articles
• The Fat-Mass and Obesity-Associated (FTO) gene, physical activity, and risk of incident cardiovascular events in white women  Journal Articles
• The Risk of Recurrent Venous Thromboembolism in Carriers and Non-carriers of the G1691A Allele in the Coagulation Factor V Gene and the G20210A Allele in the Prothrombin Gene  Journal Articles
• The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease  Journal Articles
• The distribution of nucleotide site differences between two finite sequences  Journal Articles
• The environmental and genetic regulation of obake expressivity: morphogenetic fields as evolvable systems  Journal Articles
• The interplay of birth weight, dopamine receptor D4 gene (DRD4), and early maternal care in the prediction of disorganized attachment at 36 months of age  Journal Articles
• The prospects for polymorphisms shared between species  Journal Articles
• The risk of recurrent venous thromboembolism in carriers and non-carriers of the G1691A allele in the coagulation factor V gene and the G20210A allele in the prothrombin gene. DURAC Trial Study Group. Duration of Anticoagulation.  Journal Articles
• The risks of breast and ovarian cancer associated with the Ashkenazi Jewish founder allele BRCA2 6174delT  Journal Articles
• The sampling theory of neutral alleles and an urn model in population genetics  Journal Articles
• The tissue polarity gene nemo carries out multiple roles in patterning during Drosophila development  Journal Articles
• The variance of linkage disequilibrium between three loci in a finite population  Journal Articles
• Thymic stromal lymphopoietin (TSLP) secretion from human nasal epithelium is a function of TSLP genotype  Journal Articles
• Towards a genetic architecture of cryptic genetic variation and genetic assimilation: The contribution of K. G. Bateman  Journal Articles
• Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders  Journal Articles
• Treatment of a Lysosomal Storage Disease, Mucopolysaccharidosis VII, with Microencapsulated Recombinant Cells  Journal Articles
• Trinucleotide repeat polymorphism within the human antithrombin gene (AT3): allele frequency data for three population groups  Journal Articles
• Tryptophan hydroxylase polymorphisms in suicide victims  Journal Articles
• Utilising red cell antigen genotyping and serological phenotyping in sickle cell disease patients to risk‐stratify patients for alloimmunisation risk  Journal Articles
• Virulence of a Porphyromonas gingivalis W83 mutant defective in the prtH gene  Journal Articles
• slit: an extracellular protein necessary for development of midline glia and commissural axon pathways contains both EGF and LRR domains.  Journal Articles
• α₁-Antitrypsin Deficiency Alleles in Cystic Fibrosis Lung Disease  Journal Articles
• α⁺-Thalassemia Trait Caused by a Frameshift Mutation in Exon 2 of the α2-Globin Gene [HBA2 c.244delT]  Journal Articles
• β-Thalassemia intermedia in a lebanese child due to homozygosity for the -88 (C→T) Mutation  Journal Articles