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Genetic knockdown of a single organic anion transporter alters the expression of functionally related genes in Malpighian tubules ofDrosophila melanogaster Journal Articles
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Per3 length polymorphism in patients with type 2 diabetes mellitus Journal Articles
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Salmonella Vitkin Outbreak Associated with Bearded Dragons, Canada and United States, 2020–2022 Journal Articles
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sli-3 Negatively Regulates the LET-23/Epidermal Growth Factor Receptor-Mediated Vulval Induction Pathway in Caenorhabditis elegans Journal Articles
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TSPEAR variants are primarily associated with ectodermal dysplasia and tooth agenesis but not hearing loss: A novel cohort study Journal Articles
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A CGG-Repeat Expansion Mutation inZNF713Causes FRA7A: Association with Autistic Spectrum Disorder in two Families Journal Articles
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A Genome-Wide Association Study for Coronary Artery Disease Identifies a Novel Susceptibility Locus in the Major Histocompatibility Complex Journal Articles
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A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis Journal Articles
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A High-Resolution Melting Approach for Analyzing Allelic Expression Dynamics Journal Articles
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A Reanalysis of Protein Polymorphism in Drosophila Melanogaster, D. Simulans, D. Sechellia and D. Mauritiana: Effects of Population Size and Selection Journal Articles
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A Variable-Number-of-Tandem-Repeats Polymorphism in the Dopamine D4 Receptor Gene Affects Social Adaptation of Alcohol Use Journal Articles
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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
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A genome-wide association study of sporadic ALS in a homogenous Irish population Journal Articles
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A genome-wide scan for common alleles affecting risk for autism Journal Articles
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A mixability theory for the role of sex in evolution Journal Articles
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A molecular genetic study of factor XI deficiency Journal Articles
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A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genes Journal Articles
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A novel candidate region for ALS on chromosome 14q11.2 Journal Articles
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A novel multisystem disease associated with recessive mutations in the tyrosyl‐tRNA synthetase (YARS) gene Journal Articles
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A putative Lipid Transfer Protein involved in systemic resistance signaling in Arabidopsis Journal Articles
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A recurrent de novo HSPD1 variant is associated with hypomyelinating leukodystrophy Journal Articles
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A sampling theory of selectively neutral alleles in a subdivided population. Journal Articles
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Accelerated decline in lung function in cigarette smokers is associated with TP53/MDM2 polymorphisms Journal Articles
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Activation of the Hedgehog Signaling Pathway in the Developing Lens Stimulates EctopicFoxE3Expression and Disruption in Fiber Cell Differentiation Journal Articles
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Adrenergic alpha 2C receptor genomic organization: Association study in adult ADHD Journal Articles
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Allele frequency data for VNTR locus D17S79: Identification of an internalHaeIII polymorphism in the black population Journal Articles
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Allelic Stability of VNTR Locus 3’αHVR: Linkage Disequilibrium with the Common α-Thalassaemia-1-Deletion of South-East Asia (--SEA/) Journal Articles
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Allelic and phenotypic spectrum of plasma triglycerides Journal Articles
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Allelic variants of the amylose extender mutation of maize demonstrate phenotypic variation in starch structure resulting from modified protein-protein interactions Journal Articles
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An Engineered Allele of afsQ1 Facilitates the Discovery and Investigation of Cryptic Natural Products Journal Articles
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An Increased Burden of Common and Rare Lipid-Associated Risk Alleles Contributes to the Phenotypic Spectrum of Hypertriglyceridemia Journal Articles
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Ancient selection for derived alleles at a GDF5 enhancer influencing human growth and osteoarthritis risk Journal Articles
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Angiogenin Levels and ANG Genotypes: Dysregulation in Amyotrophic Lateral Sclerosis Journal Articles
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Antithrombin III‐Amiens: A new family with an Arg47 → cys inherited variant of antithrombin iii with impaired heparin cofactor activity Journal Articles
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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
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Antithrombin-III-Hamilton: a gene with a point mutation (guanine to adenine) in codon 382 causing impaired serine protease reactivity Journal Articles
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Apolipoprotein E e4 allele affects risk of hyperhomocysteinemia in the elderly Journal Articles
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Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations Journal Articles
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Assessing non-Mendelian inheritance in inherited axonopathies Journal Articles
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Assigning a probability for paternity in apparent cases of mutation. Journal Articles
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Association Between a Literature-Based Genetic Risk Score and Cardiovascular Events in Women Journal Articles
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Association between HLA Class I and Class II Alleles and the Outcome of West Nile Virus Infection: An Exploratory Study Journal Articles
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Association between high expression macrophage migration inhibitory factor (MIF) alleles and West Nile virus encephalitis Journal Articles
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Association between maternal childhood maltreatment and mother-infant attachment disorganization: Moderation by maternal oxytocin receptor gene and cortisol secretion Journal Articles
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Association between the seven-repeat allele of the dopamine-4 receptor gene (DRD4) and spontaneous food intake in pre-school children Journal Articles
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Association of BRM promoter polymorphisms and esophageal adenocarcinoma outcome Journal Articles
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Association of Granulomatosis With Polyangiitis (Wegener's) With HLA–DPB1*04 and SEMA6A Gene Variants: Evidence From Genome‐Wide Analysis Journal Articles
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Association of autism severity with a monoamine oxidase A functional polymorphism Journal Articles
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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
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Association of the CPT1B Gene with Skeletal Muscle Fat Infiltration in Afro‐Caribbean Men Journal Articles
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Association study between fibronectin and coronary heart disease Journal Articles
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Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn’s disease subjects Journal Articles
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Associations of the FTO rs9939609 variant with discrete body fat depots and dietary intake in a multi-ethnic cohort Journal Articles
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Atypical clinical course in juvenile metachromatic leukodystrophy involving novel arylsulfatase A gene mutations Journal Articles
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Autism and the X chromosome: No linkage to microsatellite loci detected using the affected sibling pair method Journal Articles
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BRCA2 Variants and cardiovascular disease in a multi-ethnic study Journal Articles
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Betaine aldehyde dehydrogenase polymorphism in spinach: Genetic and biochemical characterization Journal Articles
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Bi-allelic Loss of Human APC2, Encoding Adenomatous Polyposis Coli Protein 2, Leads to Lissencephaly, Subcortical Heterotopia, and Global Developmental Delay Journal Articles
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Biotinidase deficiency: Spectrum of molecular, enzymatic and clinical information from newborn screening Ontario, Canada (2007–2014) Journal Articles
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Birth weight interacts with a functional variant of the oxytocin receptor gene (OXTR) to predict executive functioning in children Journal Articles
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Bovine IFNGR2, IL12RB1, IL12RB2, and IL23R polymorphisms and MAP infection status Journal Articles
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Breast cancer prognostic significance of a single nucleotide polymorphism in the proximal androgen response element of the prostate specific antigen gene promoter Journal Articles
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CARD15 and IL23R influences Crohnʼs disease susceptibility but not disease phenotype in a Brazilian population Journal Articles
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CORRIGENDUM Journal Articles
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Caenorhabditis elegans SMA-10/LRIG Is a Conserved Transmembrane Protein that Enhances Bone Morphogenetic Protein Signaling Journal Articles
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Carrier frequency of the RSH/Smith‐Lemli‐Opitz IVS8‐1G>C mutation in African Americans Journal Articles
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Carving out turf in a biodiversity hotspot: multiple, previously unrecognized shrew species co‐occur onJavaIsland,Indonesia Journal Articles
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Case Report: Eosinophilic Esophagitis in a Patient With a Novel STAT1 Gain-of-Function Pathogenic Variant Journal Articles
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Characterization of Class I– and Class II–Like Major Histocompatibility Complex Loci in Pedigrees of North Atlantic Right Whales Journal Articles
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Characterization of Three Novel δ Chain Hemoglobin Variants and Two δ-Thalassemia Alleles Journal Articles
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Characterization of tumor necrosis factor–α block haplotypes associated with susceptibility to chronic venous leg ulcers in Caucasian patients Journal Articles
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Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesis Journal Articles
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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
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Clinical evaluation of a hemochromatosis next‐generation sequencing gene panel Journal Articles
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Codon Usage and Selection on Proteins Journal Articles
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Combining direct and indirect genetic methods to estimate dispersal for informing wildlife disease management decisions Journal Articles
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Common Low-Density Lipoprotein Receptor p.G116S Variant Has a Large Effect on Plasma Low-Density Lipoprotein Cholesterol in Circumpolar Inuit Populations Journal Articles
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Comorbidities and complications in adults with pyruvate kinase deficiency Journal Articles
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Comparative analysis of Shwachman-Diamond syndrome to other inherited bone marrow failure syndromes and genotype-phenotype correlation Journal Articles
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Compensatory neutral mutations and the evolution of RNA. Journal Articles
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Complications in the genotypic molecular diagnosis of pseudo arylsulfatase A deficiency Journal Articles
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Contemporary Gene Flow is a Major Force Shaping the Aspergillus fumigatus Population in Auckland, New Zealand Journal Articles
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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
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Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection Journal Articles
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DHCR7 nonsense mutations and characterisation of mRNA nonsense mediated decay in Smith-Lemli-Opitz syndrome Journal Articles
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DIVERSIFICATION OF SULAWESI MACAQUE MONKEYS: DECOUPLED EVOLUTION OF MITOCHONDRIAL AND AUTOSOMAL DNA Journal Articles
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DNA Marker Studies Show That Machado Joseph Disease is Not an Allele of The Huntingdon Disease Locus Journal Articles
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Decreased comfort food intake and allostatic load in adolescents carrying the A3669G variant of the glucocorticoid receptor gene Journal Articles
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Delayed prezygotic isolating mechanisms: evolution with a twist Journal Articles
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Demographic expansion and genetic load of the halophyte model plant Eutrema salsugineum Journal Articles
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Determination of lipoprotein(a) kringle repeat number from genomic DNA: copy number variation genotyping using qPCR Journal Articles
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Determining the cause of patchwork HBA1 and HBA2 genes: recurrent gene conversion or crossing over fixation events. Journal Articles
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Diagnosis of arylsulfatase A deficiency Journal Articles
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Differences in gluten metabolism among healthy volunteers, coeliac disease patients and first-degree relatives Journal Articles
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Differential permeability of rivers to raccoon gene flow corresponds to rabies incidence in Ontario, Canada Journal Articles
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Dinucleotide repeat polymorphism at the D21S65 locus Journal Articles
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Distinct Mechanisms of Action of theLozengeLocus inDrosophilaEye and Antennal Development are Suggested by the Analysis of Dominant Enhancers Journal Articles
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Divergence, hybridization, and recombination in the mitochondrial genome of the human pathogenic yeast Cryptococcus gattii Journal Articles
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Diversity, functional classification and genotyping of SHV β-lactamases in Klebsiella pneumoniae. Journal Articles
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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
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Drosophila RhoGAP68F is a putative GTPase activating protein for RhoA participating in gastrulation Journal Articles
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Effects of Nicotine Deprivation and Replacement on BOLD-fMRI Response to Smoking Cues as a Function of DRD4 VNTR Genotype Journal Articles
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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
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Environmental and allele‐specific influences on T cell receptor gene rearrangement: skewed α, δ and γ gene rearrangement patterns in chimeric mice Journal Articles
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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
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Evaluating the effects of historic bottleneck events: an assessment of microsatellite variability in the endangered, North Atlantic right whale Journal Articles
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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
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Evidence for genetic incompatibilities associated with post-zygotic reproductive isolation in the human fungal pathogenCryptococcus neoformans Journal Articles
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Evidence that Egfr Contributes to Cryptic Genetic Variation for Photoreceptor Determination in Natural Populations of Drosophila melanogaster Journal Articles
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Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA Journal Articles
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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction Journal Articles
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Exon-skipping in BCR/ABL is induced by ABL exon 2 Journal Articles
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Fetal growth interacts with multilocus genetic score reflecting dopamine signaling capacity to predict spontaneous sugar intake in children Journal Articles
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Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype Journal Articles
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Fetal hemoglobin in sickle cell anemia: Molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans Journal Articles
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Fine-Scale Patterns of Population Stratification Confound Rare Variant Association Tests Journal Articles
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Fixed-bin analysis for statistical evaluation of continuous distributions of allelic data from VNTR loci, for use in forensic comparisons. Journal Articles
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Founder effect for the T93MDHCR7mutation in Smith‐Lemli‐Opitz syndrome Journal Articles
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Fumarase deficiency: a rare disorder on the crossroads of clinical and metabolic genetics, neurology and cancer Journal Articles
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GENETIC HETEROGENEITY WITHIN ELECTROPHORETIC "ALLELES" OF XANTHINE DEHYDROGENASE IN DROSOPHILA PSEUDOOBSCURA Journal Articles
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GENIC VARIATION IN ABUNDANT SOLUBLE PROTEINS OF DROSOPHILA MELANOGASTER AND DROSOPHILA PSEUDOOBSCURA Journal Articles
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Gene duplication and divergence produce divergent MHC genotypes without disassortative mating Journal Articles
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Gene × Physical Activity Interactions in Obesity: Combined Analysis of 111,421 Individuals of European Ancestry Journal Articles
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Gene-Centric Meta-Analysis of Lipid Traits in African, East Asian and Hispanic Populations Journal Articles
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Genetic Differential Susceptibility to Socioeconomic Status and Childhood Obesogenic Behavior Journal Articles
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Genetic Diversity and Dispersal of Aspergillus fumigatus in Arctic Soils Journal Articles
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Genetic Diversity of Populations of Monilinia fructicola (Fungi, Ascomycota, Helotiales) from China Journal Articles
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Genetic Susceptibility to West Nile Virus and Dengue Journal Articles
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Genetic Variants Associated With Myocardial Infarction Risk Factors in Over 8000 Individuals From Five Ethnic Groups Journal Articles
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Genetic Variants and Susceptibility to Neurological Complications Following West Nile Virus Infection Journal Articles
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Genetic Variations of TAP1 Gene Exon 3 Affects Gene Expression and Escherichia coli F18 Resistance in Piglets Journal Articles
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Genetic analysis of inherited bone marrow failure syndromes from one prospective, comprehensive and population-based cohort and identification of novel mutations Journal Articles
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Genetic variation of the St. Lawrence beluga whale population assessed by DNA fingerprinting Journal Articles
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Genetically determined low maternal serum dopamine ?-hydroxylase levels and the etiology of autism spectrum disorders Journal Articles
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Genetics of microenvironmental canalization in
Arabidopsis thaliana Journal Articles
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Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets Journal Articles
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Genome-wide meta-analyses identify multiple loci associated with smoking behavior Journal Articles
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Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders Journal Articles
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Geographic Distribution of Mating Type Alleles of
Cryptococcus neoformans
in Four Areas of the United States Journal Articles
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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
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Gova/b alloantigen system on human platelets Journal Articles
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HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome Journal Articles
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Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family Journal Articles
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How well do you know your mutation? Complex effects of genetic background on expressivity, complementation, and ordering of allelic effects Journal Articles
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Human XPF controls TRF2 and telomere length maintenance through distinctive mechanisms Journal Articles
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Human milk fatty acid composition is associated with dietary, genetic, sociodemographic, and environmental factors in the CHILD Cohort Study Journal Articles
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Huntingtin is a scaffolding protein in the ATM oxidative DNA damage response complex Journal Articles
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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
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Identification of complex DNA polymorphisms based on variable number of tandem repeats (VNTR) and restriction site polymorphism Journal Articles
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Identification of restriction-fragment-length polymorphisms in genomic DNA of the lesser snow goose (Anser caerulescens caerulescens). Journal Articles
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Identification of two novel β°-thalassemia mutations in a filipino family: Frameshift codon 67 (− TG) and a β-globin gene deletion Journal Articles
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IgA and IgG antineutrophil cytoplasmic antibody engagement of Fc receptor genetic variants influences granulomatosis with polyangiitis Journal Articles
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Immunochip Analysis Identifies Multiple Susceptibility Loci for Systemic Sclerosis Journal Articles
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Implications of OPRM1 and CYP2B6 variants on treatment outcomes in methadone-maintained patients in Ontario: Exploring sex differences Journal Articles
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Increased FGF8 signaling promotes chondrogenic rather than osteogenic development in the embryonic skull Journal Articles
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Individual common variants exert weak effects on the risk for autism spectrum disorders Journal Articles
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Induction of antimicrobial activities in heterologous streptomycetes using alleles of the Streptomyces coelicolor gene absA1 Journal Articles
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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
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Investigation of the dopamine D5 receptor gene (DRD5) in adult attention deficit hyperactivity disorder Journal Articles
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Investigation on ERCC5 genetic polymorphisms and the development of gastric cancer in a Chinese population Journal Articles
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Is serotonin transporter polymorphism (5-HTTLPR) allele status a predictor for obsessive-compulsive disorder? A meta-analysis Journal Articles
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Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease Journal Articles
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Large-scale functional screen identifies genetic variants with splicing effects in modern and archaic humans Journal Articles
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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
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Linking Gene, Brain, and Behavior Journal Articles
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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
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Loss-of-Function
KCNE2
Variants Journal Articles
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Low genic variation in male-reproductive-tract proteins of Drosophila melanogaster and D. simulans. Journal Articles
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Lunatic Fringe-mediated Notch signaling is required for lung alveogenesis Journal Articles
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MHC Class I-Mediated Antigen Presentation and Induction of CD8+ Cytotoxic T-Cell Responses in Autoimmune Diabetes-Prone NOD Mice Journal Articles
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MOLECULAR AND PHARMACOLOGICAL CHARACTERISATION OF THE MSH-R ALLELES IN SWISS CATTLE BREEDS Conferences
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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
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Mesectodermal cell fate analysis in Drosophila midline mutants Journal Articles
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Mesenteric-portal Vein Thrombosis in a Patient with Hyperhomocysteinemia and Heterozygous for 20210A Prothrombin Allele Journal Articles
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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
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Metabolic Myopathies Discovered During Investigations of Statin Myopathy Journal Articles
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Metachromatic leukodystrophy: Multiple nonfunctional and pseudodeficiency alleles in a pedigree: Problems with diagnosis and counseling Journal Articles
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Mild β+-Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A) Journal Articles
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Mitochondrial recombination in natural populations of the button mushroom Agaricus bisporus Journal Articles
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Modeling Complex Disease with Demographic and Environmental Covariates and a Candidate Gene Marker Journal Articles
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Moderating effect of PLIN4 genetic variant on impulsivity traits in 5-year-old-children born small for gestational age Journal Articles
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Molecular Analysis of Phyllodes Tumors Reveals Distinct Changes in the Epithelial and Stromal Components Journal Articles
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Molecular basis of inherited human antithrombin deficiency Journal Articles
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Mutant Alleles at the Locus elav in Drosophila melanogaster lead to Nervous System Defects. A Developmental-Genetic Analysis Journal Articles
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Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly Journal Articles
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Mutations in TBCK, Encoding TBC1-Domain-Containing Kinase, Lead to a Recognizable Syndrome of Intellectual Disability and Hypotonia Journal Articles
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Mutations in the Chromatin Regulator Gene BRPF1 Cause Syndromic Intellectual Disability and Deficient Histone Acetylation Journal Articles
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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
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Mutations in the genestand still disrupt germ cell differentiation inDrosophila ovaries Journal Articles
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Mutual regulation of the Drosophila disconnected (disco) and Distal-less (Dll) genes contributes to proximal-distal patterning of antenna and leg Journal Articles
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New Locus for Skin Intrinsic Fluorescence in Type 1 Diabetes Also Associated With Blood and Skin Glycated Proteins Journal Articles
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Oncogenic events regulate tissue factor expression in colorectal cancer cells: implications for tumor progression and angiogenesis Journal Articles
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Oxytocin Receptor Polymorphisms are Differentially Associated with Social Abilities across Neurodevelopmental Disorders Journal Articles
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Parental and child genetic contributions to obesity traits in early life based on 83 loci validated in adults: the FAMILY study Journal Articles
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Patients with thalassemia in the United States Journal Articles
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Patterns of allele distribution in a hybrid population of the Cryptococcus neoformans species complex Journal Articles
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Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expression Journal Articles
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Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative. Journal Articles
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PhoPQ regulates acidic glycerophospholipid content of the
Salmonella
Typhimurium outer membrane Journal Articles
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Physical activity and genetic predisposition to obesity in a multiethnic longitudinal study Journal Articles
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Plasminogen Alleles Influence Susceptibility to Invasive Aspergillosis Journal Articles
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Polygenic Contribution in Individuals With Early-Onset Coronary Artery Disease Journal Articles
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Polymorphism in the
CETP
Gene Region, HDL Cholesterol, and Risk of Future Myocardial Infarction Journal Articles
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Population Genetic Structure of Aldabra Giant Tortoises Journal Articles
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Prediction of the excessive perioperative bleeding in patients undergoing coronary artery bypass grafting: Role of aspirin and platelet glycoprotein IIIa polymorphism Journal Articles
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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
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Prevalence of meconium ileus marks the severity of mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene Journal Articles
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Prostate Cancer Transcriptomic Regulation by the Interplay of Germline Risk Alleles, Somatic Mutations, and 3D Genomic Architecture Journal Articles
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Protein Z Levels, Protein Z G79A Polymorphism, and Prothrombotic Conditions Journal Articles
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Pseudomonas aeruginosa type IV minor pilins and PilY1 regulate virulence by modulating FimS-AlgR activity Journal Articles
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Quebec platelet disorder is linked to the urokinase plasminogen activator gene (PLAU) and increases expression of the linked allele in megakaryocytes Journal Articles
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Rank-based genome-wide analysis reveals the association of Ryanodine receptor-2 gene variants with childhood asthma among human populations Journal Articles
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Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes Journal Articles
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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
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Reconstructing the Prior Probabilities of Allelic Phylogenies Journal Articles
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Reduced hippocampus volume and memory performance in bipolar disorder patients carrying the BDNF val66met met allele Journal Articles
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Repellent Signaling by Slit Requires the Leucine-Rich Repeats Journal Articles
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Replication of an Egfr-Wing Shape Association in a Wild-Caught Cohort of Drosophila melanogaster Journal Articles
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Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample Journal Articles
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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
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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
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Role of Macrophage Migration Inhibitory Factor in Granulomatosis With Polyangiitis Conferences
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SLOS carrier frequency in Poland as determined by screening for Trp151X and Val326Leu DHCR7 mutations Journal Articles
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Secretory Phospholipase A2-IIA and Cardiovascular Disease Journal Articles
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Sequence variation at the major histocompatibility complex DRB loci in beluga ( Delphinapterus leucas ) and narwhal ( Monodon monoceros ) Journal Articles
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Sequence variation at the major histocompatibility complex locus DQ beta in beluga whales (Delphinapterus leucas) Journal Articles
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Sex-Specific Effect of Insulin-Dependent Diabetes 4 on Regulation of Diabetes Pathogenesis in the Nonobese Diabetic Mouse Journal Articles
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Significant differences in type IV pilin allele distribution among Pseudomonas aeruginosa isolates from cystic fibrosis (CF) versus non-CF patients Conferences
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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
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Single-Tube Multiplex-PCR Screen for Anti-3.7 and Anti-4.2 α-Globin Gene Triplications Journal Articles
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Sizing bands on autoradiograms: A study of precision for scoring DNA fingerprints Journal Articles
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Somatic cell hybridization studies on the genetic regulation and allelic mutations in metachromatic leukodystrophy Journal Articles
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Spatial heterogeneity in resources alters selective dynamics in
Drosophila melanogaster Journal Articles
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Spectrum of β-Thalassemia Mutations in Egypt Journal Articles
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Stabilizing selection on microsatellite allele length at arginine vasopressin 1a receptor and oxytocin receptor loci Journal Articles
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Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis Journal Articles
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Study of alleles of the second complement component (C2) on Canadian HLA haplotypes Journal Articles
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TATA-binding protein activates transcription when upstream of a GCN4-binding site in a novel yeast promoter. Journal Articles
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THE EFFECT OF COMBINING ALLELES INTO ELECTROPHORETIC CLASSES ON DETECTING LINKAGE DISEQUILIBRIUM Journal Articles
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THE Hb S/β+-Thalassemia Phenotype Demonstrates that the IVS-I (−2) (A>C) Mutation is a Mild β-Thalassemia Allele Journal Articles
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THE SAMPLING DISTRIBUTION OF LINKAGE DISEQUILIBRIUM Journal Articles
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TLR5 as an Anti-Inflammatory Target and Modifier Gene in Cystic Fibrosis Journal Articles
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The Brain-Derived Neurotrophic Factor Val66Met Polymorphism, Hippocampal Volume, and Cognitive Function in Geriatric Depression Journal Articles
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The E2F cell cycle regulator is required for Drosophila nurse cell DNA replication and apoptosis Journal Articles
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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
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The Effect of Vitamin E Supplementation on Cardiovascular Risk in Diabetic Individuals With Different Haptoglobin Phenotypes Journal Articles
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The Fat-Mass and Obesity-Associated (FTO) gene, physical activity, and risk of incident cardiovascular events in white women Journal Articles
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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
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The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease Journal Articles
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The distribution of nucleotide site differences between two finite sequences Journal Articles
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The environmental and genetic regulation of obake expressivity: morphogenetic fields as evolvable systems Journal Articles
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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
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The prospects for polymorphisms shared between species Journal Articles
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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
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The risks of breast and ovarian cancer associated with the Ashkenazi Jewish founder allele BRCA2 6174delT Journal Articles
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The sampling theory of neutral alleles and an urn model in population genetics Journal Articles
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The tissue polarity gene nemo carries out multiple roles in patterning during Drosophila development Journal Articles
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The variance of linkage disequilibrium between three loci in a finite population Journal Articles
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Thymic stromal lymphopoietin (TSLP) secretion from human nasal epithelium is a function of TSLP genotype Journal Articles
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Towards a genetic architecture of cryptic genetic variation and genetic assimilation: The contribution of K. G. Bateman Journal Articles
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Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders Journal Articles
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Treatment of a Lysosomal Storage Disease, Mucopolysaccharidosis VII, with Microencapsulated Recombinant Cells Journal Articles
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Trinucleotide repeat polymorphism within the human antithrombin gene (AT3): allele frequency data for three population groups Journal Articles
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Tryptophan hydroxylase polymorphisms in suicide victims Journal Articles
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Utilising red cell antigen genotyping and serological phenotyping in sickle cell disease patients to risk‐stratify patients for alloimmunisation risk Journal Articles
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Virulence of a Porphyromonas gingivalis W83 mutant defective in the prtH gene Journal Articles
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slit: an extracellular protein necessary for development of midline glia and commissural axon pathways contains both EGF and LRR domains. Journal Articles
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α1-Antitrypsin Deficiency Alleles in Cystic Fibrosis Lung Disease Journal Articles
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α+-Thalassemia Trait Caused by a Frameshift Mutation in Exon 2 of the α2-Globin Gene [HBA2 c.244delT] Journal Articles
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β-Thalassemia intermedia in a lebanese child due to homozygosity for the -88 (C→T) Mutation Journal Articles