| Item Type | Name |
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Concept
|
Acne Vulgaris
|
|
Concept
|
Air
|
|
Concept
|
Acclimatization
|
|
Concept
|
Adenosine Deaminase
|
|
Concept
|
Adenosine Diphosphate
|
|
Concept
|
Haplorhini
|
|
Concept
|
Abnormalities, Multiple
|
|
Concept
|
Bird Diseases
|
|
Concept
|
Birds
|
|
Concept
|
Biology
|
|
Concept
|
Adenosine Triphosphate
|
|
Concept
|
Cats
|
|
Concept
|
Aortic Rupture
|
|
Concept
|
Chromosome Banding
|
|
Concept
|
Chromosomes, Human, Pair 11
|
|
Concept
|
Chromosomes, Human, Pair 2
|
|
Concept
|
Chromosomes, Human, Pair 6
|
|
Concept
|
Apomorphine
|
|
Concept
|
Analysis of Variance
|
|
Concept
|
Antarctic Regions
|
|
Concept
|
Chromosomes, Human, Pair 8
|
|
Concept
|
Arthritis, Rheumatoid
|
|
Concept
|
Cytogenetics
|
|
Concept
|
Anti-Inflammatory Agents
|
|
Concept
|
Cell Differentiation
|
|
Concept
|
Attention Deficit Disorder with Hyperactivity
|
|
Concept
|
Awards and Prizes
|
|
Concept
|
Bayes Theorem
|
|
Concept
|
DiGeorge Syndrome
|
|
Concept
|
Autoradiography
|
|
Concept
|
Bone Marrow Examination
|
|
Concept
|
Ethics, Medical
|
|
Concept
|
Ferrets
|
|
Concept
|
Chromosomes, Human, Pair 1
|
|
Concept
|
Chromosomes, Human, Pair 15
|
|
Concept
|
Chromosomes, Human, Pair 21
|
|
Concept
|
Chromosomes, Human, Pair 3
|
|
Concept
|
Cerebellum
|
|
Concept
|
Chromosomes, Human, Pair 12
|
|
Concept
|
Chromosome Deletion
|
|
Concept
|
Chromosomes, Human, Pair 13
|
|
Concept
|
Chromosomes, Human, Pair 22
|
|
Concept
|
Codon
|
|
Concept
|
Chromosomes, Human, Pair 5
|
|
Concept
|
Chromosomes, Human, Pair 7
|
|
Concept
|
Cold Temperature
|
|
Concept
|
Chromosomes, Human, Pair 20
|
|
Concept
|
Coronary Artery Disease
|
|
Concept
|
Indians, North American
|
|
Concept
|
Congenital Hypothyroidism
|
|
Concept
|
Chiroptera
|
|
Concept
|
Dogs
|
|
Concept
|
Ducks
|
|
Concept
|
Chromosomes, Human, Pair 10
|
|
Concept
|
Chromosomes, Human, Pair 19
|
|
Concept
|
Chromosomes, Human, Pair 9
|
|
Concept
|
Exons
|
|
Concept
|
Family
|
|
Concept
|
Health Expenditures
|
|
Concept
|
Cost-Benefit Analysis
|
|
Concept
|
Dextroamphetamine
|
|
Concept
|
DNA, Satellite
|
|
Concept
|
Influenza in Birds
|
|
Concept
|
Introns
|
|
Concept
|
Mice, Inbred C3H
|
|
Concept
|
Geese
|
|
Concept
|
Genetics, Behavioral
|
|
Concept
|
Disabled Persons
|
|
Concept
|
Dyslexia
|
|
Concept
|
Family Characteristics
|
|
Concept
|
Genetics, Medical
|
|
Concept
|
Genetics, Population
|
|
Concept
|
Iodides
|
|
Concept
|
Language Development Disorders
|
|
Concept
|
Pharmacogenetics
|
|
Concept
|
Mammals
|
|
Concept
|
Mice, Transgenic
|
|
Concept
|
Poultry
|
|
Concept
|
Monosaccharide Transport Proteins
|
|
Concept
|
NADP
|
|
Concept
|
Mice, Inbred BALB C
|
|
Concept
|
Mice, Inbred C57BL
|
|
Concept
|
Cricetinae
|
|
Concept
|
Nuclear Family
|
|
Concept
|
Poultry Diseases
|
|
Concept
|
Primates
|
|
Concept
|
Hirschsprung Disease
|
|
Concept
|
Rabbits
|
|
Concept
|
Quail
|
|
Concept
|
Virology
|
|
Concept
|
Reye Syndrome
|
|
Concept
|
Potassium Channels
|
|
Concept
|
Receptors, GABA-A
|
|
Concept
|
Ribonucleoproteins
|
|
Concept
|
Health Knowledge, Attitudes, Practice
|
|
Concept
|
Speech Disorders
|
|
Concept
|
Swine
|
|
Concept
|
Humans
|
|
Concept
|
Warfarin
|
|
Concept
|
Tamoxifen
|
|
Concept
|
Marriage
|
|
Concept
|
Gangliosidosis, GM1
|
|
Concept
|
Deoxyribonucleases, Type II Site-Specific
|
|
Concept
|
Bias
|
|
Concept
|
Campylobacter jejuni
|
|
Concept
|
Rats, Sprague-Dawley
|
|
Concept
|
Human Genome Project
|
|
Concept
|
Postmenopause
|
|
Concept
|
Mice, Obese
|
|
Concept
|
Mites
|
|
Concept
|
RNA-Binding Proteins
|
|
Concept
|
Health Care Costs
|
|
Concept
|
TNF Receptor-Associated Factor 6
|
|
Concept
|
Mice, Knockout
|
|
Concept
|
Receptors, AMPA
|
|
Concept
|
Serotonin Plasma Membrane Transport Proteins
|
|
Concept
|
Telomerase
|
|
Concept
|
Antineoplastic Agents, Alkylating
|
|
Concept
|
Multidrug Resistance-Associated Proteins
|
|
Concept
|
Cystic Fibrosis Transmembrane Conductance Regulator
|
|
Concept
|
Protein Folding
|
|
Concept
|
Systems Biology
|
|
Concept
|
Proteomics
|
|
Concept
|
Songbirds
|
|
Concept
|
Parents
|
|
Concept
|
3' Untranslated Regions
|
|
Concept
|
Potassium Channels, Inwardly Rectifying
|
|
Concept
|
Promoter Regions, Genetic
|
|
Concept
|
Mice
|
|
Concept
|
Adiposity
|
|
Concept
|
Rats
|
|
Concept
|
Neanderthals
|
|
Concept
|
Finches
|
|
Concept
|
Adaptor Proteins, Signal Transducing
|
|
Concept
|
Insulin-Secreting Cells
|
|
Concept
|
Regulatory Elements, Transcriptional
|
|
Concept
|
Temperature
|
|
Concept
|
Zebrafish
|
|
Concept
|
Large-Conductance Calcium-Activated Potassium Channel alpha Subunits
|
|
Concept
|
Selection Bias
|
|
Concept
|
Multivariate Analysis
|
|
Concept
|
Hominidae
|
|
Concept
|
Phylogeography
|
|
Concept
|
ATP-Binding Cassette Transporters
|
|
Concept
|
Coronary Angiography
|
|
Concept
|
GTP-Binding Proteins
|
|
Concept
|
Cholesterol Ester Transfer Proteins
|
|
Concept
|
Molecular Epidemiology
|
|
Concept
|
Receptors, Kainic Acid
|
|
Concept
|
CD4 Lymphocyte Count
|
|
Concept
|
Untranslated Regions
|
|
Concept
|
Chromosome Disorders
|
|
Concept
|
KCNQ1 Potassium Channel
|
|
Concept
|
Metabolomics
|
|
Concept
|
Insulin Receptor Substrate Proteins
|
|
Concept
|
RNA, Small Interfering
|
|
Concept
|
Siblings
|
|
Concept
|
Drug Discovery
|
|
Concept
|
Calcium-Binding Proteins
|
|
Concept
|
Chickens
|
|
Concept
|
Chromosomes, Human
|
|
Concept
|
Chromosomes, Human, Pair 16
|
|
Concept
|
Chromosomes, Human, Pair 18
|
|
Concept
|
DNA Restriction Enzymes
|
|
Concept
|
Electrophoresis, Agar Gel
|
|
Concept
|
Genetic Counseling
|
|
Concept
|
Hemagglutinins
|
|
Concept
|
Horses
|
|
Concept
|
Immunochemistry
|
|
Concept
|
Membrane Potentials
|
|
Concept
|
Mothers
|
|
Concept
|
Patient Compliance
|
|
Concept
|
Rats, Mutant Strains
|
|
Concept
|
Stuttering
|
|
Concept
|
Cost of Illness
|
|
Concept
|
Ribonucleoproteins, Small Nuclear
|
|
Concept
|
Computational Biology
|
|
Concept
|
Unnecessary Procedures
|
|
Concept
|
Genomics
|
|
Concept
|
Potassium Channels, Voltage-Gated
|
|
Concept
|
Membrane Transport Proteins
|
|
Concept
|
MicroRNAs
|
|
Concept
|
Chromosomes, Human, X
|
|
Concept
|
Irritable Bowel Syndrome
|
|
Concept
|
Dopamine Plasma Membrane Transport Proteins
|
|
Concept
|
Excitatory Amino Acid Transporter 3
|
|
Concept
|
Large-Conductance Calcium-Activated Potassium Channel beta Subunits
|
|
Concept
|
Multilocus Sequence Typing
|
|
Concept
|
HapMap Project
|
|
Concept
|
B7 Antigens
|
|
Academic Article
|
cDNA sequence and localization of polymorphic human cytosolic phosphoenolpyruvate carboxykinase gene (PCK1) to chromosome 20, band q13.31: PCK1 is not tightly linked to maturity-onset diabetes of the young.
|
|
Academic Article
|
Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)
|
|
Academic Article
|
The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16.
|
|
Academic Article
|
Genome-wide search for asthma susceptibility loci in a founder population. The Collaborative Study on the Genetics of Asthma.
|
|
Academic Article
|
Allele-sharing models: LOD scores and accurate linkage tests.
|
|
Academic Article
|
Human influenza A (H1N2) viruses isolated from China.
|
|
Academic Article
|
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus.
|
|
Academic Article
|
Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers.
|
|
Academic Article
|
Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans.
|
|
Academic Article
|
Genetic characterization of the pathogenic influenza A/Goose/Guangdong/1/96 (H5N1) virus: similarity of its hemagglutinin gene to those of H5N1 viruses from the 1997 outbreaks in Hong Kong.
|
|
Academic Article
|
Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations.
|
|
Academic Article
|
Role of calpain-10 gene variants in familial type 2 diabetes in Caucasians.
|
|
Academic Article
|
Risk of influenza A (H5N1) infection among poultry workers, Hong Kong, 1997-1998.
|
|
Academic Article
|
Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma.
|
|
Academic Article
|
Infection of a child in Hong Kong by an influenza A H3N2 virus closely related to viruses circulating in European pigs.
|
|
Academic Article
|
Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families.
|
|
Academic Article
|
Methods for analysis and visualization of SNP genotype data for complex diseases.
|
|
Academic Article
|
Lack of evidence for human-to-human transmission of avian influenza A (H9N2) viruses in Hong Kong, China 1999.
|
|
Academic Article
|
Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians.
|
|
Academic Article
|
Genome scan for loci linked to mite sensitivity: the Collaborative Study on the Genetics of Asthma (CSGA).
|
|
Academic Article
|
Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus.
|
|
Academic Article
|
Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33.
|
|
Academic Article
|
Genome-wide scan for metabolic syndrome and related quantitative traits in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25.
|
|
Academic Article
|
Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees.
|
|
Academic Article
|
Polymorphisms of GLUT2 and GLUT4 genes. Use in evaluation of genetic susceptibility to NIDDM in blacks.
|
|
Academic Article
|
Mapping genes influencing type 2 diabetes risk and BMI in Japanese subjects.
|
|
Academic Article
|
Genome-wide scan for type 2 diabetes loci in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25.
|
|
Academic Article
|
Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q.
|
|
Academic Article
|
Haplotype structure and phylogenetic shadowing of a hypervariable region in the CAPN10 gene.
|
|
Academic Article
|
Genetic epidemiology of diabetes.
|
|
Academic Article
|
Combined analysis of three whole genome linkage scans for Ankylosing Spondylitis.
|
|
Academic Article
|
Relationship of EGFR mutations, expression, amplification, and polymorphisms to epidermal growth factor receptor inhibitors in the NCI60 cell lines.
|
|
Academic Article
|
Confirmed locus on chromosome 11p and candidate loci on 6q and 8p for the triglyceride and cholesterol traits of combined hyperlipidemia.
|
|
Academic Article
|
Gene-based SNP mapping of a psychotic bipolar affective disorder linkage region on 22q12.3: association with HMG2L1 and TOM1.
|
|
Academic Article
|
Prevention and control of influenza: recommendations of the Advisory Committee on Immunization Practices (ACIP).
|
|
Academic Article
|
Quality of life in paediatric lupus.
|
|
Academic Article
|
Insulin gene mutations as a cause of permanent neonatal diabetes.
|
|
Academic Article
|
Polygenic virulence factors involved in pathogenesis of 1997 Hong Kong H5N1 influenza viruses in mice.
|
|
Academic Article
|
Evidence for a susceptibility locus on chromosome 10p15 in early-onset obsessive-compulsive disorder.
|
|
Academic Article
|
Evaluation of genetic variation contributing to differences in gene expression between populations.
|
|
Academic Article
|
Population-specific GSTM1 copy number variation.
|
|
Academic Article
|
Prevention and control of influenza: recommendations of the Advisory Committee on Immunization Practices (ACIP).
|
|
Academic Article
|
Genetic variants in the calpain-10 gene and the development of type 2 diabetes in the Japanese population.
|
|
Academic Article
|
Genomewide significant linkage to stuttering on chromosome 12.
|
|
Academic Article
|
Human genetics: an expression of interest.
|
|
Academic Article
|
No bias in linkage analysis.
|
|
Academic Article
|
Rational inferences about departures from Hardy-Weinberg equilibrium.
|
|
Academic Article
|
Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.
|
|
Academic Article
|
Common polymorphisms of calpain-10 are associated with abdominal obesity in subjects at high risk of type 2 diabetes.
|
|
Academic Article
|
Obesity and hyperinsulinemia in a family with pancreatic agenesis and MODY caused by the IPF1 mutation Pro63fsX60.
|
|
Academic Article
|
Fine mapping and positional candidate studies on chromosome 5p13 identify multiple asthma susceptibility loci.
|
|
Academic Article
|
SCAN: SNP and copy number annotation.
|
|
Academic Article
|
Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases?
|
|
Academic Article
|
Genetic variations in GRIA1 on chromosome 5q33 related to asparaginase hypersensitivity.
|
|
Academic Article
|
Genetic bases of the temperature-sensitive phenotype of a master donor virus used in live attenuated influenza vaccines: A/Leningrad/134/17/57 (H2N2).
|
|
Academic Article
|
A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2.
|
|
Academic Article
|
The missing association: sequencing-based discovery of novel SNPs in VKORC1 and CYP2C9 that affect warfarin dose in African Americans.
|
|
Academic Article
|
Platinum sensitivity-related germline polymorphism discovered via a cell-based approach and analysis of its association with outcome in ovarian cancer patients.
|
|
Academic Article
|
Lack of association between common single nucleotide polymorphisms in the TERT-CLPTM1L locus and breast cancer in women of African ancestry.
|
|
Academic Article
|
Genome-wide meta-analysis for severe diabetic retinopathy.
|
|
Academic Article
|
Meta-analysis of 23 type 2 diabetes linkage studies from the International Type 2 Diabetes Linkage Analysis Consortium.
|
|
Academic Article
|
Genome-wide ancestry association testing identifies a common European variant on 6q14.1 as a risk factor for asthma in African American subjects.
|
|
Academic Article
|
Bgl II RFLP at the human erythrocyte/HepG2-type glucose transporter (GLUT) locus on chromosome 1.
|
|
Academic Article
|
Linkage disequilibrium in the human insulin/insulin-like growth factor II region of human chromosome II.
|
|
Academic Article
|
Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism.
|
|
Academic Article
|
Multiple Taq I RFLPs at the human manganese superoxide dismutase (S0D2) locus on chromosome 6.
|
|
Academic Article
|
Genetic architecture of transcript-level variation in humans.
|
|
Academic Article
|
Prolonged shedding of amantadine-resistant influenzae A viruses by immunodeficient patients: detection by polymerase chain reaction-restriction analysis.
|
|
Academic Article
|
Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior.
|
|
Academic Article
|
Restriction fragment polymorphisms of the HLA-DR, HLA-DQ, and insulin gene regions in IDDM: the GAW5 data.
|
|
Academic Article
|
Comprehensive evaluation of the contribution of X chromosome genes to platinum sensitivity.
|
|
Academic Article
|
Parent-of-origin effects of the serotonin transporter gene associated with autism.
|
|
Academic Article
|
Lack of significant person-to-person spread of swine influenza-like virus following fatal infection in an immunocompromised child.
|
|
Academic Article
|
Nucleotide sequences of the neuraminidase genes of influenza A/Leningrad/134/57 (H2N2) virus and two of its live, attenuated, cold-adapted variants.
|
|
Academic Article
|
Isolation of a cDNA clone encoding a KATP channel-like protein expressed in insulin-secreting cells, localization of the human gene to chromosome band 21q22.1, and linkage studies with NIDDM.
|
|
Academic Article
|
Apa I and Sst I RFLPs at the insulin-like growth factor II (IGF2) locus on chromosome 11.
|
|
Academic Article
|
Influenza A virus haemagglutinin polymorphism: pleiotropic antigenic variants of A/Shanghai/11/87 (H3N2) virus selected as high yield reassortants.
|
|
Academic Article
|
Genetic stability of cold-adapted A/Leningrad/134/47/57 (H2N2) influenza virus: sequence analysis of live cold-adapted reassortant vaccine strains before and after replication in children.
|
|
Academic Article
|
Stuttering: a complex behavioral disorder for our times?
|
|
Academic Article
|
Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews.
|
|
Academic Article
|
FstSNP-HapMap3: a database of SNPs with high population differentiation for HapMap3.
|
|
Academic Article
|
A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene.
|
|
Academic Article
|
A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.
|
|
Academic Article
|
Identification of novel germline polymorphisms governing capecitabine sensitivity.
|
|
Academic Article
|
Inheritance of human platelet thermolabile phenol sulfotransferase (TL PST) activity.
|
|
Academic Article
|
The 31-cM region of chromosome 11 including the obesity gene tubby and ATP-sensitive potassium channel genes, SUR1 and Kir6.2, does not contain a major susceptibility locus for NIDDM in 127 non-Hispanic white affected sibships.
|
|
Academic Article
|
Locus on chromosome 6p linked to elevated HDL cholesterol serum levels and to protection against premature atherosclerosis in a kindred with familial hypercholesterolemia.
|
|
Academic Article
|
Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21.
|
|
Academic Article
|
GEL: a novel genotype calling algorithm using empirical likelihood.
|
|
Academic Article
|
Genetic studies of stuttering in a founder population.
|
|
Academic Article
|
Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.
|
|
Academic Article
|
Reconstructability analysis as a tool for identifying gene-gene interactions in studies of human diseases.
|
|
Academic Article
|
Germline polymorphisms discovered via a cell-based, genome-wide approach predict platinum response in head and neck cancers.
|
|
Academic Article
|
Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.
|
|
Academic Article
|
Can recovery from stuttering be considered a genetically milder subtype of stuttering?
|
|
Academic Article
|
Localization of MODY3 to a 5-cM region of human chromosome 12.
|
|
Academic Article
|
Amantadine-resistant influenza A in nursing homes. Identification of a resistant virus prior to drug use.
|
|
Academic Article
|
Avian-to-human transmission of H9N2 subtype influenza A viruses: relationship between H9N2 and H5N1 human isolates.
|
|
Academic Article
|
Long term trends in the evolution of H(3) HA1 human influenza type A.
|
|
Academic Article
|
Protection of mice against influenza A virus challenge by vaccination with baculovirus-expressed M2 protein.
|
|
Academic Article
|
Influenza-associated deaths among children in the United States, 2003-2004.
|
|
Academic Article
|
Endocytic trafficking signals in KCNMB2 regulate surface expression of a large conductance voltage and Ca(2+)-activated K+ channel.
|
|
Academic Article
|
Prevention and control of influenza. Recommendations of the Advisory Committee on Immunization Practices (ACIP), 2007.
|
|
Academic Article
|
Effectiveness of influenza vaccination of day care children in reducing influenza-related morbidity among household contacts.
|
|
Academic Article
|
Integration of cell line and clinical trial genome-wide analyses supports a polygenic architecture of Paclitaxel-induced sensory peripheral neuropathy.
|
|
Academic Article
|
In vitro evolution of H5N1 avian influenza virus toward human-type receptor specificity.
|
|
Academic Article
|
Fine mapping of breast cancer genome-wide association studies loci in women of African ancestry identifies novel susceptibility markers.
|
|
Academic Article
|
Genome-wide association study of Tourette's syndrome.
|
|
Academic Article
|
Influenza-associated hospitalizations in the United States.
|
|
Academic Article
|
Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations.
|
|
Academic Article
|
A genome-wide association study of breast cancer in women of African ancestry.
|
|
Academic Article
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National Institutes of Health State-of-the-Science Conference statement: preventing alzheimer disease and cognitive decline.
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Academic Article
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Effect of receptor binding domain mutations on receptor binding and transmissibility of avian influenza H5N1 viruses.
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Academic Article
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A distinct lineage of influenza A virus from bats.
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Influenza A(H1N1)pdm09 virus among healthy show pigs, United States.
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A genome-wide integrative study of microRNAs in human liver.
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Genetic analysis of avian influenza A viruses isolated from domestic waterfowl in live-bird markets of Hanoi, Vietnam, preceding fatal H5N1 human infections in 2004.
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Quantification of immunoreactive viral influenza proteins by immunoaffinity capture and isotope-dilution liquid chromatography-tandem mass spectrometry.
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Effects of passage history and sampling bias on phylogenetic reconstruction of human influenza A evolution.
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Genome-wide interrogation of longitudinal FEV1 in children with asthma.
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Poly-omic prediction of complex traits: OmicKriging.
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Integrative analyses of genetic variation, epigenetic regulation, and the transcriptome to elucidate the biology of platinum sensitivity.
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Clinical drug response can be predicted using baseline gene expression levels and in vitro drug sensitivity in cell lines.
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A nondegenerate code of deleterious variants in Mendelian loci contributes to complex disease risk.
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Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes.
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Characterization of drug-resistant influenza A(H7N9) variants isolated from an oseltamivir-treated patient in Taiwan.
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Immunogenicity and reactogenicity of 1 versus 2 doses of trivalent inactivated influenza vaccine in vaccine-naive 5-8-year-old children.
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Genetic analysis of human H2N2 and early H3N2 influenza viruses, 1957-1972: evidence for genetic divergence and multiple reassortment events.
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Identification of molecular markers associated with alteration of receptor-binding specificity in a novel genotype of highly pathogenic avian influenza A(H5N1) viruses detected in Cambodia in 2013.
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Influenza A virus neuraminidase protein enhances cell survival through interaction with carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) protein.
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Inactivated and live attenuated influenza vaccines in young children--how do they compare?
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The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study.
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Identification of a variant in KDR associated with serum VEGFR2 and pharmacodynamics of Pazopanib.
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Academic Article
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Immunogenicity and efficacy of Russian live attenuated and US inactivated influenza vaccines used alone and in combination in nursing home residents.
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Academic Article
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Surveillance of resistance to adamantanes among influenza A(H3N2) and A(H1N1) viruses isolated worldwide.
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Academic Article
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Highly pathogenic avian influenza A(H7N3) virus in poultry workers, Mexico, 2012.
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Academic Article
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Institutional Profile: University of Chicago Center for Personalized Therapeutics: research, education and implementation science.
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Academic Article
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An endoplasmic reticulum trafficking signal regulates surface expression of ß4 subunit of a voltage- and Ca²?-activated K? channel.
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Anti-ganglioside antibody induction by swine (A/NJ/1976/H1N1) and other influenza vaccines: insights into vaccine-associated Guillain-Barré syndrome.
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Influenza A viral nucleoprotein interacts with cytoskeleton scaffolding protein a-actinin-4 for viral replication.
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Influenza activity - United States, 2013-14 season and composition of the 2014-15 influenza vaccines.
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Academic Article
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Comparative immunogenicity and cross-clade protective efficacy of mammalian cell-grown inactivated and live attenuated H5N1 reassortant vaccines in ferrets.
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Academic Article
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Characterization of reverse genetics-derived cold-adapted master donor virus A/Leningrad/134/17/57 (H2N2) and reassortants with H5N1 surface genes in a mouse model.
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Genetic factors affecting gene transcription and catalytic activity of UDP-glucuronosyltransferases in human liver.
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Academic Article
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A genome-wide sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13.
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A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology.
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Beyond type 2 diabetes, obesity and hypertension: an axis including sleep apnea, left ventricular hypertrophy, endothelial dysfunction, and aortic stiffness among Mexican Americans in Starr County, Texas.
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Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.
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Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines.
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STAMS: STRING-assisted module search for genome wide association studies and application to autism.
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Variants in WFS1 and Other Mendelian Deafness Genes Are Associated with Cisplatin-Associated Ototoxicity.
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Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer.
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Academic Article
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A novel coronavirus associated with severe acute respiratory syndrome.
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Academic Article
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Classification of common human diseases derived from shared genetic and environmental determinants.
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LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins.
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Academic Article
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Shared Genetic Control of Brain Activity During Sleep and Insulin Secretion: A Laboratory-Based Family Study.
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Up For A Challenge (U4C): Stimulating innovation in breast cancer genetic epidemiology.
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Academic Article
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Relationship between very low low-density lipoprotein cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: A US-based cross-sectional observational study using electronic health records.
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Gene and MicroRNA Perturbations of Cellular Response to Pemetrexed Implicate Biological Networks and Enable Imputation of Response in Lung Adenocarcinoma.
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Sex-specific genetic predictors of Alzheimer's disease biomarkers.
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Critical Evaluation of Data Requires Rigorous but Broadly Based Statistical Inference.
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Diagnostic Algorithms to Study Post-Concussion Syndrome Using Electronic Health Records: Validating a Method to Capture an Important Patient Population.
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Clinical and Genome-wide Analysis of Cisplatin-induced Tinnitus Implicates Novel Ototoxic Mechanisms.
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Complex Simplicity and Hirschsprung's Disease.
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Inferred divergent gene regulation in archaic hominins reveals potential phenotypic differences.
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Clinical evaluation of germline polymorphisms associated with capecitabine toxicity in breast cancer: TBCRC-015.
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Automated Phenotyping Tool for Identifying Developmental Language Disorder Cases in Health Systems Data (APT-DLD): A New Research Algorithm for Deployment in Large-Scale Electronic Health Record Systems.
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Genetic variants and functional pathways associated with resilience to Alzheimer's disease.
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A Transcriptome-Wide Association Study Identifies Candidate Susceptibility Genes for Pancreatic Cancer Risk.
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A transcriptome-wide association study of Alzheimer's disease using prediction models of relevant tissues identifies novel candidate susceptibility genes.
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Academic Article
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A transcriptome-wide association study identifies novel candidate susceptibility genes for prostate cancer risk.
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Academic Article
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Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes.
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Academic Article
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Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension.
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Academic Article
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Polygenic transcriptome risk scores (PTRS) can improve portability of polygenic risk scores across ancestries.
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Academic Article
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Exploration of an alternative to body mass index to characterize the relationship between height and weight for prediction of metabolic phenotypes and cardiovascular outcomes.
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Academic Article
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Predicted expression of genes involved in the thiopurine metabolic pathway and azathioprine discontinuation due to myelotoxicity.
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Academic Article
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Two polymorphic gene loci associated with treprostinil dose in pulmonary arterial hypertension.
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Academic Article
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Discerning asthma endotypes through comorbidity mapping.
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Academic Article
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Exploring the genetics of rhythmic perception and musical engagement in the Vanderbilt Online Musicality Study.
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Concept
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Gastrointestinal Microbiome
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Concept
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Sequestosome-1 Protein
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Concept
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Alpha-Ketoglutarate-Dependent Dioxygenase FTO
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Concept
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Perilipin-1
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Concept
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Peroxisome-Targeting Signal 1 Receptor
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Concept
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Human Genetics
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Concept
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NAV1.5 Voltage-Gated Sodium Channel
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Concept
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Sulfonylurea Receptors
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Academic Article
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Genetic and clinical determinants of telomere length.
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Academic Article
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Genetic Variants Associated With Hidradenitis Suppurativa.
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Academic Article
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Association between APOL1 risk variants and the occurrence of sepsis in Black patients hospitalized with infections: a retrospective cohort study.
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Academic Article
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Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI.
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Academic Article
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Characterizing genetic profiles for high triglyceride levels in U.S. patients of African ancestry.
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