Item Type | Name |
Concept
|
Alleles
|
Concept
|
Amino Acid Sequence
|
Concept
|
Base Sequence
|
Concept
|
DNA, Recombinant
|
Concept
|
Gene Frequency
|
Concept
|
Genes, Regulator
|
Concept
|
Gene Expression Regulation
|
Concept
|
Genes, Dominant
|
Concept
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Genes, Viral
|
Concept
|
Genes
|
Concept
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Genes, Recessive
|
Concept
|
Oncogenes
|
Concept
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Gene Amplification
|
Concept
|
Molecular Sequence Data
|
Concept
|
Repetitive Sequences, Nucleic Acid
|
Concept
|
Sequence Homology, Nucleic Acid
|
Concept
|
Genome
|
Concept
|
Sequence Homology, Amino Acid
|
Concept
|
Gene Library
|
Concept
|
Genes, Tumor Suppressor
|
Concept
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Genome, Viral
|
Concept
|
Genomic Library
|
Concept
|
Gene Expression
|
Concept
|
Genes, Reporter
|
Concept
|
Consensus Sequence
|
Concept
|
Gene Deletion
|
Concept
|
Genes, X-Linked
|
Concept
|
Gene Regulatory Networks
|
Concept
|
Genetic Pleiotropy
|
Concept
|
Exome
|
Concept
|
Gene-Environment Interaction
|
Concept
|
Gene Expression Profiling
|
Concept
|
Regulatory Elements, Transcriptional
|
Concept
|
Genome, Human
|
Concept
|
Gene Expression Regulation, Leukemic
|
Concept
|
Sequence Homology
|
Concept
|
Gene Knockdown Techniques
|
Concept
|
Gene Dosage
|
Concept
|
Protein Sorting Signals
|
Concept
|
Transcriptome
|
Concept
|
Epistasis, Genetic
|
Concept
|
Gene Expression Regulation, Neoplastic
|
Concept
|
Conserved Sequence
|
Concept
|
Polymorphism, Single Nucleotide
|
Concept
|
Quantitative Trait Loci
|
Concept
|
Genetic Loci
|
Concept
|
Nucleotide Motifs
|
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
|
Genetic variation in neuraminidase genes of influenza A (H3N2) viruses.
|
Academic Article
|
Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)
|
Academic Article
|
Identification of microsatellite markers near the human genes encoding the beta-cell ATP-sensitive K+ channel and linkage studies with NIDDM in Japanese.
|
Academic Article
|
Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1)
|
Academic Article
|
Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle.
|
Academic Article
|
The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16.
|
Academic Article
|
Two different mutations in the thyroid peroxidase gene of a large inbred Amish kindred: power and limits of homozygosity mapping.
|
Academic Article
|
Hypertriglyceridemia and the apolipoprotein CIII gene locus: lack of association with the variant insulin response element in Italian school children.
|
Academic Article
|
An approach for identifying simple sequence repeat DNA polymorphisms near cloned cDNAs and genes. Linkage studies of the islet amyloid polypeptide/amylin and liver glycogen synthase genes and NIDDM.
|
Academic Article
|
Accurate inference of relationships in sib-pair linkage studies.
|
Academic Article
|
Linkage studies in NIDDM with markers near the sulphonylurea receptor gene.
|
Academic Article
|
The genetics of asthma. Mapping genes for complex traits in founder populations.
|
Academic Article
|
Human influenza A (H1N2) viruses isolated from China.
|
Academic Article
|
Genetic inheritance of body mass index in African-American and African families.
|
Academic Article
|
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus.
|
Academic Article
|
Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom.
|
Academic Article
|
Mutations in the coding region of the neurogenin 3 gene (NEUROG3) are not a common cause of maturity-onset diabetes of the young in Japanese subjects.
|
Academic Article
|
beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4 (NEUROD4) in Japanese patients with MODY.
|
Academic Article
|
A calpain-10 gene polymorphism is associated with reduced muscle mRNA levels and insulin resistance.
|
Academic Article
|
Genetic factors in autoimmune thyroid disease analyzed by restriction fragment length polymorphisms of candidate genes.
|
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
|
Insulin resistance is attenuated in women with polycystic ovary syndrome with the Pro(12)Ala polymorphism in the PPARgamma gene.
|
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
|
Challenges in identifying genetic variation affecting susceptibility to type 2 diabetes: examples from studies of the calpain-10 gene.
|
Academic Article
|
Beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3beta gene (HNF3B) in Japanese patients with maturity-onset diabetes of the young.
|
Academic Article
|
No diabetes-associated mutations in the coding region of the hepatocyte nuclear factor-4gamma gene (HNF4G) in Japanese patients with MODY.
|
Academic Article
|
A statistical method for identification of polymorphisms that explain a linkage result.
|
Academic Article
|
Genome-wide approaches for identifying interacting susceptibility regions for asthma.
|
Academic Article
|
Variation within the type 2 diabetes susceptibility gene calpain-10 and polycystic ovary syndrome.
|
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
|
Evidence for gene-environment interactions in a linkage study of asthma and smoking exposure.
|
Academic Article
|
Genetic Analysis Workshop II: results of segregation analyses using POINTER and linkage analyses using LIPED.
|
Academic Article
|
Genome scan for loci linked to mite sensitivity: the Collaborative Study on the Genetics of Asthma (CSGA).
|
Academic Article
|
Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population.
|
Academic Article
|
Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus.
|
Academic Article
|
Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder.
|
Academic Article
|
The allelic architecture of human disease genes: common disease-common variant...or not?
|
Academic Article
|
Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33.
|
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
|
Antigenic and genetic variation in influenza A (H1N1) virus isolates recovered from a persistently infected immunodeficient child.
|
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
|
Gender-specific differences in expression in human lymphoblastoid cell lines.
|
Academic Article
|
Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder.
|
Academic Article
|
Association of the calpain-10 gene with type 2 diabetes in Europeans: results of pooled and meta-analyses.
|
Academic Article
|
Relationship of EGFR mutations, expression, amplification, and polymorphisms to epidermal growth factor receptor inhibitors in the NCI60 cell lines.
|
Academic Article
|
Patterns of linkage disequilibrium in the type 2 diabetes gene calpain-10.
|
Academic Article
|
Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects.
|
Academic Article
|
SNPs meet CNVs in genome-wide association studies: HGV2007 meeting report.
|
Academic Article
|
Gene-based SNP mapping of a psychotic bipolar affective disorder linkage region on 22q12.3: association with HMG2L1 and TOM1.
|
Academic Article
|
Insulin gene mutations as a cause of permanent neonatal diabetes.
|
Academic Article
|
Evaluation of genetic variation contributing to differences in gene expression between populations.
|
Academic Article
|
Population-specific GSTM1 copy number variation.
|
Academic Article
|
Prediction of CYP3A4 enzyme activity using haplotype tag SNPs in African Americans.
|
Academic Article
|
Genetic variants in the calpain-10 gene and the development of type 2 diabetes in the Japanese population.
|
Academic Article
|
Human genetics: an expression of interest.
|
Academic Article
|
Rational inferences about departures from Hardy-Weinberg equilibrium.
|
Academic Article
|
Identification of genetic variants and gene expression relationships associated with pharmacogenes in humans.
|
Academic Article
|
Expression and alternative splicing of folate pathway genes in HapMap lymphoblastoid cell lines.
|
Academic Article
|
The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population.
|
Academic Article
|
Insulin-receptor and apolipoprotein genes contribute to development of NIDDM in Chinese Americans.
|
Academic Article
|
Variation in the perilipin gene (PLIN) affects glucose and lipid metabolism in non-Hispanic white women with and without polycystic ovary syndrome.
|
Academic Article
|
Obesity and hyperinsulinemia in a family with pancreatic agenesis and MODY caused by the IPF1 mutation Pro63fsX60.
|
Academic Article
|
The insulin gene and susceptibility to IDDM.
|
Academic Article
|
SCAN: SNP and copy number annotation.
|
Academic Article
|
Chemotherapeutic drug susceptibility associated SNPs are enriched in expression quantitative trait loci.
|
Academic Article
|
Disease associations. Chance, artifact, or susceptibility genes?
|
Academic Article
|
Population differences in microRNA expression and biological implications.
|
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
|
Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue.
|
Academic Article
|
Linkage disequilibrium in the human insulin/insulin-like growth factor II region of human chromosome II.
|
Academic Article
|
On sharing quantitative trait GWAS results in an era of multiple-omics data and the limits of genomic privacy.
|
Academic Article
|
Genetic risk factors for type 2 diabetes: a trans-regulatory genetic architecture?
|
Academic Article
|
Mixed effects modeling of proliferation rates in cell-based models: consequence for pharmacogenomics and cancer.
|
Academic Article
|
PACdb: a database for cell-based pharmacogenomics.
|
Academic Article
|
Antigenic drift in influenza virus H3 hemagglutinin from 1968 to 1980: multiple evolutionary pathways and sequential amino acid changes at key antigenic sites.
|
Academic Article
|
Identification of microsatellite markers near the human ob gene and linkage studies in NIDDM-affected sib pairs.
|
Academic Article
|
Identification of a functional polymorphism of the human type 5 17beta-hydroxysteroid dehydrogenase gene associated with polycystic ovary syndrome.
|
Academic Article
|
Four RFLPs of the human insulin receptor gene: PstI, KpnI, RsaI (2 RFLPs).
|
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
|
Insulin-gene sharing in sib pairs with insulin-dependent diabetes mellitus: no evidence for linkage.
|
Academic Article
|
Glucose transporter gene and non-insulin-dependent diabetes.
|
Academic Article
|
Linkage analysis for psychiatric disorders. I. Basic concepts.
|
Academic Article
|
Copy number polymorphisms and anticancer pharmacogenomics.
|
Academic Article
|
Next generation analytic tools for large scale genetic epidemiology studies of complex diseases.
|
Academic Article
|
Lithium ion transport and affective disorders within families of bipolar patients. Identification of a major gene locus.
|
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
|
Nonimmunoselected intrastrain genetic variation detected in pairs of high-yielding influenza A (H3N2) vaccine and parental viruses.
|
Academic Article
|
Association of attention-deficit disorder and the dopamine transporter gene.
|
Academic Article
|
Concordant gene expression in leukemia cells and normal leukocytes is associated with germline cis-SNPs.
|
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
|
Linkage of familial dysalbuminemic hyperthyroxinemia to the albumin gene in a large Amish kindred.
|
Academic Article
|
Comprehensive survey of SNPs in the Affymetrix exon array using the 1000 Genomes dataset.
|
Academic Article
|
Linkage studies on NIDDM and the insulin and insulin-receptor genes.
|
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 Diabetic Retinopathy Genes through a Genome-Wide Association Study among Mexican-Americans from Starr County, Texas.
|
Academic Article
|
A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.
|
Academic Article
|
Four RFLPs of the human insulin receptor gene: PstI, KpnI, RsaI (2 RFLPs).
|
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
|
HLA and mate choice in humans.
|
Academic Article
|
Mapping diabetes-susceptibility genes. Lessons learned from search for DNA marker for maturity-onset diabetes of the young.
|
Academic Article
|
Genetic linkage studies of thyroid peroxidase (TPO) gene in families with TPO deficiency.
|
Academic Article
|
Variation in the calpain-10 gene affects blood glucose levels in the British population.
|
Academic Article
|
Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21.
|
Academic Article
|
A genome-wide approach to identify genetic variants that contribute to etoposide-induced cytotoxicity.
|
Academic Article
|
Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies.
|
Academic Article
|
Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.
|
Academic Article
|
Evolution of highly pathogenic H5N1 avian influenza viruses in Vietnam between 2001 and 2007.
|
Academic Article
|
Reconstructability analysis as a tool for identifying gene-gene interactions in studies of human diseases.
|
Academic Article
|
Genome-wide local ancestry approach identifies genes and variants associated with chemotherapeutic susceptibility in African Americans.
|
Academic Article
|
Genetic architecture of microRNA expression: implications for the transcriptome and complex traits.
|
Academic Article
|
Variation of apolipoprotein-B gene is associated with obesity, high blood cholesterol levels, and increased risk of coronary heart disease.
|
Academic Article
|
[The association of non-insulin-dependent diabetes mellitus with the genes responsible for carbohydrate and lipid metabolism in the Chinese].
|
Academic Article
|
Comparative studies of wild-type and 'cold-mutant' (temperature sensitive) influenza viruses: geneology of the matrix (M) and non-structural (NS) proteins in recombinant cold-adapted H3N2 viruses.
|
Academic Article
|
Comparative studies of wild-type and cold-mutant (temperature-sensitive) influenza viruses: nonrandom reassortment of genes during preparation of live virus vaccine candidates by recombination at 25 degrees between recent H3N2 and H1N1 epidemic strains and cold-adapted A/An Arbor/6/60.
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Academic Article
|
Comparative studies of wild-type and cold-mutant (temperature-sensitive) influenza virus: detection of mutations in all genes of the A/Ann Arbor/6/60 (H2N2) mutant vaccine donor strain.
|
Academic Article
|
Genetic stability of A/Ann Arbor/6/60 cold-mutant (temperature-sensitive) live influenza virus genes: analysis by oligonucleotide mapping of recombinant vaccine strains before and after replication in volunteers.
|
Academic Article
|
Recombination of human influenza A viruses in nature.
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Academic Article
|
Human trials with wild-type H1N1 and recombinant H3N2-H1N1 influenza A viruses of 1977-1978.
|
Academic Article
|
Avian-to-human transmission of H9N2 subtype influenza A viruses: relationship between H9N2 and H5N1 human isolates.
|
Academic Article
|
Genetic relatedness between influenza A (H1N1) viruses isolated from humans and pigs.
|
Academic Article
|
Predicting the evolution of human influenza A.
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Academic Article
|
Characterization of the surface proteins of influenza A (H5N1) viruses isolated from humans in 1997-1998.
|
Academic Article
|
Endocytic trafficking signals in KCNMB2 regulate surface expression of a large conductance voltage and Ca(2+)-activated K+ channel.
|
Academic Article
|
Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants.
|
Academic Article
|
Genetic compatibility and virulence of reassortants derived from contemporary avian H5N1 and human H3N2 influenza A viruses.
|
Academic Article
|
Essential role of sequestosome 1/p62 in regulating accumulation of Lys63-ubiquitinated proteins.
|
Academic Article
|
A distinct lineage of influenza A virus from bats.
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Academic Article
|
Characterization of the reconstructed 1918 Spanish influenza pandemic virus.
|
Academic Article
|
Comprehensive genetic analysis of cytarabine sensitivity in a cell-based model identifies polymorphisms associated with outcome in AML patients.
|
Academic Article
|
Identification of A/H5N1 influenza viruses using a single gene diagnostic microarray.
|
Academic Article
|
A genome-wide integrative study of microRNAs in human liver.
|
Academic Article
|
Antigenic and genetic characteristics of swine-origin 2009 A(H1N1) influenza viruses circulating in humans.
|
Academic Article
|
An influenza A (H1N1) virus, closely related to swine influenza virus, responsible for a fatal case of human influenza.
|
Academic Article
|
Characterization of an avian influenza A (H5N1) virus isolated from a child with a fatal respiratory illness.
|
Academic Article
|
Trans-population analysis of genetic mechanisms of ethnic disparities in neuroblastoma survival.
|
Academic Article
|
Genome-wide interrogation of longitudinal FEV1 in children with asthma.
|
Academic Article
|
pRRophetic: an R package for prediction of clinical chemotherapeutic response from tumor gene expression levels.
|
Academic Article
|
Integrative analyses of genetic variation, epigenetic regulation, and the transcriptome to elucidate the biology of platinum sensitivity.
|
Academic Article
|
Clinical drug response can be predicted using baseline gene expression levels and in vitro drug sensitivity in cell lines.
|
Academic Article
|
A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.
|
Academic Article
|
Genetic analysis of human H2N2 and early H3N2 influenza viruses, 1957-1972: evidence for genetic divergence and multiple reassortment events.
|
Academic Article
|
The antigenicity and evolution of influenza H1 haemagglutinin, from 1950-1957 and 1977-1983: two pathways from one gene.
|
Academic Article
|
Influenza A virus nucleoprotein induces apoptosis in human airway epithelial cells: implications of a novel interaction between nucleoprotein and host protein Clusterin.
|
Academic Article
|
Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies.
|
Academic Article
|
Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus.
|
Academic Article
|
Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium.
|
Academic Article
|
Genome-wide identification of microRNA expression quantitative trait loci.
|
Academic Article
|
SCAN database: facilitating integrative analyses of cytosine modification and expression QTL.
|
Academic Article
|
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
|
Academic Article
|
An endoplasmic reticulum trafficking signal regulates surface expression of ß4 subunit of a voltage- and Ca²?-activated K? channel.
|
Academic Article
|
Identifying plausible genetic models based on association and linkage results: application to type 2 diabetes.
|
Academic Article
|
Obesity-associated variants within FTO form long-range functional connections with IRX3.
|
Academic Article
|
Guidelines for investigating causality of sequence variants in human disease.
|
Academic Article
|
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.
|
Academic Article
|
Genetic factors affecting gene transcription and catalytic activity of UDP-glucuronosyltransferases in human liver.
|
Academic Article
|
A genome-wide sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13.
|
Academic Article
|
A gene-based association method for mapping traits using reference transcriptome data.
|
Academic Article
|
Imputing Gene Expression in Uncollected Tissues Within and Beyond GTEx.
|
Academic Article
|
Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues.
|
Academic Article
|
STAMS: STRING-assisted module search for genome wide association studies and application to autism.
|
Academic Article
|
Variants in WFS1 and Other Mendelian Deafness Genes Are Associated with Cisplatin-Associated Ototoxicity.
|
Academic Article
|
Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer.
|
Academic Article
|
Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal.
|
Academic Article
|
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.
|
Academic Article
|
Clinical and Genome-Wide Analysis of Cisplatin-Induced Peripheral Neuropathy in Survivors of Adult-Onset Cancer.
|
Academic Article
|
Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation.
|
Academic Article
|
Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics.
|
Academic Article
|
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.
|
Academic Article
|
Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma.
|
Academic Article
|
Human Heat shock protein 40 (Hsp40/DnaJB1) promotes influenza A virus replication by assisting nuclear import of viral ribonucleoproteins.
|
Academic Article
|
An integrative functional genomics framework for effective identification of novel regulatory variants in genome-phenome studies.
|
Academic Article
|
LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins.
|
Academic Article
|
Gene and MicroRNA Perturbations of Cellular Response to Pemetrexed Implicate Biological Networks and Enable Imputation of Response in Lung Adenocarcinoma.
|
Academic Article
|
De novo pattern discovery enables robust assessment of functional consequences of non-coding variants.
|
Academic Article
|
GRIK5 Genetically Regulated Expression Associated with Eye and Vascular Phenomes: Discovery through Iteration among Biobanks, Electronic Health Records, and Zebrafish.
|
Academic Article
|
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.
|
Academic Article
|
A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data.
|
Academic Article
|
Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.
|
Academic Article
|
Multi-tissue transcriptome analyses identify genetic mechanisms underlying neuropsychiatric traits.
|
Academic Article
|
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.
|
Academic Article
|
Inferred divergent gene regulation in archaic hominins reveals potential phenotypic differences.
|
Academic Article
|
APOE e4-specific associations of VEGF gene family expression with cognitive aging and Alzheimer's disease.
|
Academic Article
|
Combining clinical and candidate gene data into a risk score for azathioprine-associated leukopenia in routine clinical practice.
|
Academic Article
|
Influenza virus NS1- C/EBPß gene regulatory complex inhibits RIG-I transcription.
|
Academic Article
|
Analysis of Genetically Regulated Gene Expression Identifies a Prefrontal PTSD Gene, SNRNP35, Specific to Military Cohorts.
|
Academic Article
|
The regulatory genome constrains protein sequence evolution: implications for the search for disease-associated genes.
|
Academic Article
|
A Transcriptome-Wide Association Study Identifies Candidate Susceptibility Genes for Pancreatic Cancer Risk.
|
Academic Article
|
A unified framework for joint-tissue transcriptome-wide association and Mendelian randomization analysis.
|
Academic Article
|
Three dimensional modeling of biologically relevant fluid shear stress in human renal tubule cells mimics in vivo transcriptional profiles.
|
Academic Article
|
Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients.
|
Academic Article
|
Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.
|
Academic Article
|
A transcriptome-wide association study identifies novel blood-based gene biomarker candidates for Alzheimer's disease risk.
|
Academic Article
|
A transcriptome-wide association study of Alzheimer's disease using prediction models of relevant tissues identifies novel candidate susceptibility genes.
|
Academic Article
|
A transcriptome-wide association study identifies novel candidate susceptibility genes for prostate cancer risk.
|
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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Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension.
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Predicted expression of genes involved in the thiopurine metabolic pathway and azathioprine discontinuation due to myelotoxicity.
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Two polymorphic gene loci associated with treprostinil dose in pulmonary arterial hypertension.
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Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome.
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Concept
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Gene Editing
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Multi-ancestry meta-analysis of tobacco use disorder prioritizes novel candidate risk genes and reveals associations with numerous health outcomes.
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