Item Type | Name |
Concept
|
Acne Vulgaris
|
Concept
|
Acute Disease
|
Concept
|
Adenocarcinoma
|
Concept
|
Alcoholism
|
Concept
|
Amyloidosis
|
Concept
|
Abnormalities, Multiple
|
Concept
|
Bird Diseases
|
Concept
|
Breast Neoplasms
|
Concept
|
Bronchitis
|
Concept
|
Anxiety
|
Concept
|
Candidiasis
|
Concept
|
Anemia
|
Concept
|
Aortic Rupture
|
Concept
|
Arthritis, Rheumatoid
|
Concept
|
Asthma
|
Concept
|
Autoimmune Diseases
|
Concept
|
Conjunctivitis
|
Concept
|
Depressive Disorder
|
Concept
|
Attention Deficit Disorder with Hyperactivity
|
Concept
|
Bacterial Infections
|
Concept
|
DiGeorge Syndrome
|
Concept
|
Disseminated Intravascular Coagulation
|
Concept
|
Carcinoma, Renal Cell
|
Concept
|
Autistic Disorder
|
Concept
|
Bacterial Proteins
|
Concept
|
Mental Disorders
|
Concept
|
Bipolar Disorder
|
Concept
|
Bone Marrow Diseases
|
Concept
|
Carcinoma, Non-Small-Cell Lung
|
Concept
|
Cat Diseases
|
Concept
|
Cerebrovascular Disorders
|
Concept
|
Color Vision Defects
|
Concept
|
Child Development Disorders, Pervasive
|
Concept
|
Chromosome Deletion
|
Concept
|
Tourette Syndrome
|
Concept
|
Cognition Disorders
|
Concept
|
Cardiovascular Diseases
|
Concept
|
Carrier State
|
Concept
|
Goiter
|
Concept
|
Coronary Disease
|
Concept
|
Cross Infection
|
Concept
|
Cocarcinogenesis
|
Concept
|
Hemorrhagic Fevers, Viral
|
Concept
|
Communicable Diseases
|
Concept
|
Coronary Artery Disease
|
Concept
|
Dementia
|
Concept
|
Diabetes Mellitus, Type 1
|
Concept
|
Diabetes Mellitus, Type 2
|
Concept
|
Diabetic Retinopathy
|
Concept
|
Herpes Zoster
|
Concept
|
Horse Diseases
|
Concept
|
Cystic Fibrosis
|
Concept
|
Coronaviridae Infections
|
Concept
|
Disease
|
Concept
|
DNA-Binding Proteins
|
Concept
|
Depressive Disorder, Major
|
Concept
|
Dermatitis, Atopic
|
Concept
|
Dog Diseases
|
Concept
|
Diabetic Nephropathies
|
Concept
|
Immunologic Deficiency Syndromes
|
Concept
|
Congenital Hypothyroidism
|
Concept
|
Cytopathogenic Effect, Viral
|
Concept
|
Drug Hypersensitivity
|
Concept
|
Femoral Neck Fractures
|
Concept
|
Hemiplegia
|
Concept
|
Kidney Neoplasms
|
Concept
|
Leukemia
|
Concept
|
Hypertension
|
Concept
|
Deglutition Disorders
|
Concept
|
Chronic Disease
|
Concept
|
Eye Diseases
|
Concept
|
Eye Proteins
|
Concept
|
Macular Degeneration
|
Concept
|
Influenza in Birds
|
Concept
|
Influenza, Human
|
Concept
|
Employment
|
Concept
|
Microtubule-Associated Proteins
|
Concept
|
Muscle Hypotonia
|
Concept
|
Glaucoma, Open-Angle
|
Concept
|
Kidney Diseases
|
Concept
|
Obesity
|
Concept
|
Orthomyxoviridae Infections
|
Concept
|
Heart Failure
|
Concept
|
Dyslexia
|
Concept
|
Dysplastic Nevus Syndrome
|
Concept
|
Dystonia Musculorum Deformans
|
Concept
|
Hyperlipoproteinemia Type II
|
Concept
|
Hyperlipidemias
|
Concept
|
Hyperlipidemia, Familial Combined
|
Concept
|
Loneliness
|
Concept
|
Environmental Exposure
|
Concept
|
Hepatitis B
|
Concept
|
Inflammation
|
Concept
|
High Mobility Group Proteins
|
Concept
|
Membrane Proteins
|
Concept
|
Language Development Disorders
|
Concept
|
Hyperlipoproteinemias
|
Concept
|
Macular Edema
|
Concept
|
Nerve Tissue Proteins
|
Concept
|
Neutropenia
|
Concept
|
Pneumonia, Viral
|
Concept
|
Opportunistic Infections
|
Concept
|
Monosaccharide Transport Proteins
|
Concept
|
Pancreatic Neoplasms
|
Concept
|
Intellectual Disability
|
Concept
|
Mesothelioma
|
Concept
|
Migraine Disorders
|
Concept
|
Heat-Shock Proteins
|
Concept
|
Obsessive-Compulsive Disorder
|
Concept
|
Occupational Diseases
|
Concept
|
Ovarian Neoplasms
|
Concept
|
Lung Neoplasms
|
Concept
|
Sensation Disorders
|
Concept
|
Peripheral Nervous System Diseases
|
Concept
|
Shock, Septic
|
Concept
|
Metabolic Diseases
|
Concept
|
Muscle Proteins
|
Concept
|
Otitis Media
|
Concept
|
Pregnancy in Diabetics
|
Concept
|
Prostatic Neoplasms
|
Concept
|
Thrombocytopenia
|
Concept
|
Thromboembolism
|
Concept
|
Tobacco Use Disorder
|
Concept
|
Pleural Neoplasms
|
Concept
|
Pneumonia, Pneumocystis
|
Concept
|
Poultry Diseases
|
Concept
|
Proto-Oncogene Proteins
|
Concept
|
Proteins
|
Concept
|
Genetic Markers
|
Concept
|
Hirschsprung Disease
|
Concept
|
Hyperinsulinism
|
Concept
|
Hypothyroidism
|
Concept
|
Head and Neck Neoplasms
|
Concept
|
Repressor Proteins
|
Concept
|
Psychotic Disorders
|
Concept
|
Viral Core Proteins
|
Concept
|
Viral Matrix Proteins
|
Concept
|
Insulin Resistance
|
Concept
|
Respiratory Tract Infections
|
Concept
|
Reye Syndrome
|
Concept
|
Scleroderma, Systemic
|
Concept
|
Social Behavior Disorders
|
Concept
|
Respiratory Tract Diseases
|
Concept
|
Skin Pigmentation
|
Concept
|
Speech Disorders
|
Concept
|
Thyroiditis, Autoimmune
|
Concept
|
Hypersensitivity, Immediate
|
Concept
|
Hypertension, Pulmonary
|
Concept
|
Leukopenia
|
Concept
|
Body Mass Index
|
Concept
|
Testicular Neoplasms
|
Concept
|
Spondylitis, Ankylosing
|
Concept
|
Thinness
|
Concept
|
Syndrome
|
Concept
|
Urethritis
|
Concept
|
Zoonoses
|
Concept
|
Kidney Failure, Chronic
|
Concept
|
Viral Structural Proteins
|
Concept
|
Leukemia, Myeloid
|
Concept
|
Disease Transmission, Infectious
|
Concept
|
Sleep Apnea, Obstructive
|
Concept
|
Vascular Diseases
|
Concept
|
Viremia
|
Concept
|
Gangliosidosis, GM1
|
Concept
|
Neoplasms, Second Primary
|
Concept
|
Zebrafish Proteins
|
Concept
|
Lupus Erythematosus, Systemic
|
Concept
|
Multiple Myeloma
|
Concept
|
Multiple Sclerosis
|
Concept
|
Leukemia, Myeloid, Acute
|
Concept
|
Occupational Exposure
|
Concept
|
Post-Concussion Syndrome
|
Concept
|
Melanoma
|
Concept
|
Exfoliation Syndrome
|
Concept
|
tau Proteins
|
Concept
|
Neoplasm Recurrence, Local
|
Concept
|
Nerve Degeneration
|
Concept
|
Severe Acute Respiratory Syndrome
|
Concept
|
Severe Combined Immunodeficiency
|
Concept
|
Bronchial Hyperreactivity
|
Concept
|
RNA-Binding Proteins
|
Concept
|
Hypertrophy, Left Ventricular
|
Concept
|
Viral Nonstructural Proteins
|
Concept
|
Serotonin Plasma Membrane Transport Proteins
|
Concept
|
Respiratory Syncytial Virus Infections
|
Concept
|
Sepsis
|
Concept
|
Metabolic Syndrome
|
Concept
|
Multidrug Resistance-Associated Proteins
|
Concept
|
Genetic Association Studies
|
Concept
|
Fatal Outcome
|
Concept
|
Chronic Pain
|
Concept
|
Diagnostic and Statistical Manual of Mental Disorders
|
Concept
|
Renal Insufficiency, Chronic
|
Concept
|
Porcine Reproductive and Respiratory Syndrome
|
Concept
|
Cell Cycle Proteins
|
Concept
|
Proteinase Inhibitory Proteins, Secretory
|
Concept
|
Loss of Heterozygosity
|
Concept
|
Genetic Diseases, Inborn
|
Concept
|
Wnt Proteins
|
Concept
|
Peritonitis
|
Concept
|
Polycystic Ovary Syndrome
|
Concept
|
Pneumonia
|
Concept
|
Prenatal Exposure Delayed Effects
|
Concept
|
Pregnancy Complications
|
Concept
|
Recombinant Proteins
|
Concept
|
Respiratory Distress Syndrome, Newborn
|
Concept
|
Schizophrenia
|
Concept
|
Sleep Apnea Syndromes
|
Concept
|
Stress Disorders, Post-Traumatic
|
Concept
|
Tic Disorders
|
Concept
|
Tinnitus
|
Concept
|
Amyloidogenic Proteins
|
Concept
|
Cognitive Dysfunction
|
Concept
|
Skin Neoplasms
|
Concept
|
Viral Envelope Proteins
|
Concept
|
Adaptor Proteins, Signal Transducing
|
Concept
|
Dyslipidemias
|
Concept
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
Concept
|
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
|
Concept
|
HSP40 Heat-Shock Proteins
|
Concept
|
HIV Infections
|
Concept
|
Viral Proteins
|
Concept
|
Lung Diseases, Interstitial
|
Concept
|
Infectious Disease Transmission, Patient-to-Professional
|
Concept
|
GTP-Binding Proteins
|
Concept
|
Cholesterol Ester Transfer Proteins
|
Concept
|
Precursor Cell Lymphoblastic Leukemia-Lymphoma
|
Concept
|
Nucleocapsid Proteins
|
Concept
|
Homeodomain Proteins
|
Concept
|
Mood Disorders
|
Concept
|
Guillain-Barre Syndrome
|
Concept
|
Hearing Loss
|
Concept
|
Coronary Stenosis
|
Concept
|
Diabetes Complications
|
Concept
|
Chromosome Disorders
|
Concept
|
Tumor Suppressor Proteins
|
Concept
|
Mutant Proteins
|
Concept
|
Pulmonary Disease, Chronic Obstructive
|
Concept
|
Insulin Receptor Substrate Proteins
|
Concept
|
Immune Evasion
|
Concept
|
Haploinsufficiency
|
Concept
|
Vascular Stiffness
|
Concept
|
Intracellular Signaling Peptides and Proteins
|
Concept
|
Alzheimer Disease
|
Concept
|
Brain Neoplasms
|
Concept
|
Calcium-Binding Proteins
|
Concept
|
Carrier Proteins
|
Concept
|
Chromosome Aberrations
|
Concept
|
Cystitis
|
Concept
|
Diabetes Mellitus
|
Concept
|
Disease Models, Animal
|
Concept
|
Euphoria
|
Concept
|
Hemorrhage
|
Concept
|
Hyperglycemia
|
Concept
|
Hyperthyroxinemia
|
Concept
|
Infant, Newborn, Diseases
|
Concept
|
Lung Diseases, Obstructive
|
Concept
|
Neoplasm Proteins
|
Concept
|
Neoplasms
|
Concept
|
Neuroblastoma
|
Concept
|
Nuclear Proteins
|
Concept
|
Stuttering
|
Concept
|
Swine Diseases
|
Concept
|
Uveal Neoplasms
|
Concept
|
Virus Diseases
|
Concept
|
Hypertriglyceridemia
|
Concept
|
Neurofibrillary Tangles
|
Concept
|
Hidradenitis Suppurativa
|
Concept
|
Age of Onset
|
Concept
|
Neoplasm, Residual
|
Concept
|
Neurotoxicity Syndromes
|
Concept
|
Membrane Transport Proteins
|
Concept
|
Rare Diseases
|
Concept
|
Irritable Bowel Syndrome
|
Concept
|
Overweight
|
Concept
|
Dopamine Plasma Membrane Transport Proteins
|
Concept
|
Proto-Oncogene Proteins c-akt
|
Concept
|
Endophenotypes
|
Concept
|
GPI-Linked Proteins
|
Academic Article
|
Genetic aspects of early childhood stuttering.
|
Academic Article
|
Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)
|
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
|
Evidence of linkage between the serotonin transporter and autistic disorder.
|
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
|
Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers.
|
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 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
|
Computational issues in mapping variation affecting susceptibility to complex disorders: the chicken and the egg.
|
Academic Article
|
Relationship of insulin receptor substrate-1 and -2 genotypes to phenotypic features of polycystic ovary syndrome.
|
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
|
Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands.
|
Academic Article
|
Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder.
|
Academic Article
|
Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33.
|
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
|
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
|
Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder.
|
Academic Article
|
Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects.
|
Academic Article
|
Gene-based SNP mapping of a psychotic bipolar affective disorder linkage region on 22q12.3: association with HMG2L1 and TOM1.
|
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
|
The neutrophil alloantigen HNA-3a (5b) is located on choline transporter-like protein 2 and appears to be encoded by an R>Q154 amino acid substitution.
|
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
|
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
|
Segregation and linkage analyses of bipolar and major depressive illnesses in multigenerational pedigrees.
|
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
|
Lack of association between common single nucleotide polymorphisms in the TERT-CLPTM1L locus and breast cancer in women of African ancestry.
|
Academic Article
|
Bgl II RFLP at the human erythrocyte/HepG2-type glucose transporter (GLUT) locus on chromosome 1.
|
Academic Article
|
Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism.
|
Academic Article
|
Influenza A virus nucleoprotein exploits Hsp40 to inhibit PKR activation.
|
Academic Article
|
Segregation analysis of speech and language disorders.
|
Academic Article
|
Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior.
|
Academic Article
|
Parent-of-origin effects of the serotonin transporter gene associated with autism.
|
Academic Article
|
Glucose transporter gene and non-insulin-dependent diabetes.
|
Academic Article
|
Linkage analysis for psychiatric disorders. I. Basic concepts.
|
Academic Article
|
Lithium ion transport and affective disorders within families of bipolar patients. Identification of a major gene locus.
|
Academic Article
|
Variants affecting exon skipping contribute to complex traits.
|
Academic Article
|
Linkage analysis for psychiatric disorders. II. Methodological considerations.
|
Academic Article
|
Nonimmunoselected intrastrain genetic variation detected in pairs of high-yielding influenza A (H3N2) vaccine and parental viruses.
|
Academic Article
|
Influenza A virus haemagglutinin polymorphism: pleiotropic antigenic variants of A/Shanghai/11/87 (H3N2) virus selected as high yield reassortants.
|
Academic Article
|
Association of attention-deficit disorder and the dopamine transporter gene.
|
Academic Article
|
Stuttering: a complex behavioral disorder for our times?
|
Academic Article
|
Germline BAP1 mutations predispose to malignant mesothelioma.
|
Academic Article
|
Genetic linkage studies of thyroid peroxidase (TPO) gene in families with TPO deficiency.
|
Academic Article
|
Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.
|
Academic Article
|
Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.
|
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
|
Recombination of human influenza A viruses in nature.
|
Academic Article
|
Genetic relatedness between influenza A (H1N1) viruses isolated from humans and pigs.
|
Academic Article
|
Immunohistochemical and in situ hybridization studies of influenza A virus infection in human lungs.
|
Academic Article
|
Protection of mice against influenza A virus challenge by vaccination with baculovirus-expressed M2 protein.
|
Academic Article
|
Outcome in patients who require a gastrostomy after stroke.
|
Academic Article
|
Characterization of the surface proteins of influenza A (H5N1) viruses isolated from humans in 1997-1998.
|
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
|
Integration of cell line and clinical trial genome-wide analyses supports a polygenic architecture of Paclitaxel-induced sensory peripheral neuropathy.
|
Academic Article
|
NIH state-of-the-science conference statement: Preventing Alzheimer's disease and cognitive decline.
|
Academic Article
|
Genome-wide association study of Tourette's syndrome.
|
Academic Article
|
Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations.
|
Academic Article
|
National Institutes of Health State-of-the-Science Conference statement: preventing alzheimer disease and cognitive decline.
|
Academic Article
|
Influenza A(H1N1)pdm09 virus among healthy show pigs, United States.
|
Academic Article
|
Antigenic and genetic characteristics of swine-origin 2009 A(H1N1) influenza viruses circulating in humans.
|
Academic Article
|
Quantification of immunoreactive viral influenza proteins by immunoaffinity capture and isotope-dilution liquid chromatography-tandem mass spectrometry.
|
Academic Article
|
Genome-wide association study of obsessive-compulsive disorder.
|
Academic Article
|
Trans-population analysis of genetic mechanisms of ethnic disparities in neuroblastoma survival.
|
Academic Article
|
Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.
|
Academic Article
|
Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes.
|
Academic Article
|
Characterization of drug-resistant influenza A(H7N9) variants isolated from an oseltamivir-treated patient in Taiwan.
|
Academic Article
|
Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.
|
Academic Article
|
Influenza A virus neuraminidase protein enhances cell survival through interaction with carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) protein.
|
Academic Article
|
A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.
|
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
|
The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study.
|
Academic Article
|
Challenges in interpreting the evidence for genetic predictors of ototoxicity.
|
Academic Article
|
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
|
Academic Article
|
Adamantane resistance among influenza A viruses isolated early during the 2005-2006 influenza season in the United States.
|
Academic Article
|
An endoplasmic reticulum trafficking signal regulates surface expression of ß4 subunit of a voltage- and Ca²?-activated K? channel.
|
Academic Article
|
Obesity-associated variants within FTO form long-range functional connections with IRX3.
|
Academic Article
|
Genetic inactivation of p62 leads to accumulation of hyperphosphorylated tau and neurodegeneration.
|
Academic Article
|
Genetic variation associated with euphorigenic effects of d-amphetamine is associated with diminished risk for schizophrenia and attention deficit hyperactivity disorder.
|
Academic Article
|
Influenza A viral nucleoprotein interacts with cytoskeleton scaffolding protein a-actinin-4 for viral replication.
|
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
|
Psychiatrists' attitudes, knowledge, and experience regarding genetics: a preliminary study.
|
Academic Article
|
Identification of Influenza A/PR/8/34 Donor Viruses Imparting High Hemagglutinin Yields to Candidate Vaccine Viruses in Eggs.
|
Academic Article
|
Ethnic variation of TET2 SNP rs2454206 and association with clinical outcome in childhood AML: a report from the Children's Oncology Group.
|
Academic Article
|
Genetic resilience to amyloid related cognitive decline.
|
Academic Article
|
Transcription factor ETV1 is essential for rapid conduction in the heart.
|
Academic Article
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Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.
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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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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.
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A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.
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Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.
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Clinical and Genome-Wide Analysis of Cisplatin-Induced Peripheral Neuropathy in Survivors of Adult-Onset Cancer.
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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
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Classification of common human diseases derived from shared genetic and environmental determinants.
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Human Heat shock protein 40 (Hsp40/DnaJB1) promotes influenza A virus replication by assisting nuclear import of viral ribonucleoproteins.
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LNK deficiency promotes acute aortic dissection and rupture.
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Sex-specific genetic predictors of Alzheimer's disease biomarkers.
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Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.
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Multi-tissue transcriptome analyses identify genetic mechanisms underlying neuropsychiatric traits.
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Sex differences in the genetic predictors of Alzheimer's pathology.
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Genetic risk for major depressive disorder and loneliness in sex-specific associations with coronary artery disease.
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Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies.
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Influenza virus NS1- C/EBPß gene regulatory complex inhibits RIG-I transcription.
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Analysis of Genetically Regulated Gene Expression Identifies a Prefrontal PTSD Gene, SNRNP35, Specific to Military Cohorts.
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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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Alcohol and cigarette smoking consumption as genetic proxies for alcohol misuse and nicotine dependence.
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Fate or coincidence: do COPD and major depression share genetic risk factors?
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Pleiotropy of systemic lupus erythematosus risk alleles and cardiometabolic disorders: A phenome-wide association study and inverse-variance weighted meta-analysis.
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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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Leveraging electronic health records to inform genetic counseling practice surrounding psychiatric disorders.
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Pharmacogenomics of cisplatin-induced neurotoxicities: Hearing loss, tinnitus, and peripheral sensory neuropathy.
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The relationship between high density lipoprotein cholesterol and sepsis: A clinical and genetic approach.
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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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Autism Spectrum Disorder
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Concept
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SAP90-PSD95 Associated Proteins
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Concept
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Drug-Related Side Effects and Adverse Reactions
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Concept
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Familial Primary Pulmonary Hypertension
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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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Genetic and clinical determinants of telomere length.
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