| Item Type | Name |
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Concept
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Aged, 80 and over
|
|
Concept
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Adolescent
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Concept
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Aged
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Concept
|
Amino Acid Sequence
|
|
Concept
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Adult
|
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Concept
|
Apolipoproteins E
|
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Concept
|
Chromosomes, Human, Pair 11
|
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Concept
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Chromosomes, Human, Pair 6
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Concept
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Community Pharmacy Services
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Concept
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Aryl Hydrocarbon Hydroxylases
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Concept
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Base Sequence
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Concept
|
Bayes Theorem
|
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Concept
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Body Height
|
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Concept
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Bernard-Soulier Syndrome
|
|
Concept
|
Child
|
|
Concept
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Developmental Disabilities
|
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Concept
|
Chromosomes, Human, Pair 12
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|
Concept
|
Diabetes Mellitus, Type 1
|
|
Concept
|
Cystic Fibrosis
|
|
Concept
|
Child, Preschool
|
|
Concept
|
Gastric Mucosa
|
|
Concept
|
Chromosomes, Human, Pair 17
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|
Concept
|
Chromosomes, Human, Pair 19
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|
Concept
|
Chromosomes, Human, Pair 9
|
|
Concept
|
Drug Interactions
|
|
Concept
|
Micrognathism
|
|
Concept
|
Hexokinase
|
|
Concept
|
Infant
|
|
Concept
|
Pharmacogenetics
|
|
Concept
|
Estrogens
|
|
Concept
|
Prothrombin
|
|
Concept
|
Molecular Sequence Data
|
|
Concept
|
Ovariectomy
|
|
Concept
|
Middle Aged
|
|
Concept
|
Nucleotides
|
|
Concept
|
Ovarian Neoplasms
|
|
Concept
|
Patient Readmission
|
|
Concept
|
Patients
|
|
Concept
|
Phosphorylation
|
|
Concept
|
Population Surveillance
|
|
Concept
|
Prostatic Neoplasms
|
|
Concept
|
Gallbladder Neoplasms
|
|
Concept
|
Glycine
|
|
Concept
|
Risk Factors
|
|
Concept
|
Xenopus
|
|
Concept
|
Inpatients
|
|
Concept
|
Regulatory Sequences, Nucleic Acid
|
|
Concept
|
Retinitis Pigmentosa
|
|
Concept
|
Risk
|
|
Concept
|
Humans
|
|
Concept
|
Body Mass Index
|
|
Concept
|
Multicenter Studies as Topic
|
|
Concept
|
Hereditary Sensory and Motor Neuropathy
|
|
Concept
|
Proportional Hazards Models
|
|
Concept
|
Risk Assessment
|
|
Concept
|
Glutamic Acid
|
|
Concept
|
RNA Splice Sites
|
|
Concept
|
Professional Role
|
|
Concept
|
Prostate-Specific Antigen
|
|
Concept
|
Menopause
|
|
Concept
|
Neoplasm Recurrence, Local
|
|
Concept
|
Point Mutation
|
|
Concept
|
Mice, Knockout
|
|
Concept
|
Community Health Planning
|
|
Concept
|
Disease Progression
|
|
Concept
|
BRCA1 Protein
|
|
Concept
|
Mutation, Missense
|
|
Concept
|
Disclosure
|
|
Concept
|
Cystic Fibrosis Transmembrane Conductance Regulator
|
|
Concept
|
In Situ Hybridization, Fluorescence
|
|
Concept
|
Gene-Environment Interaction
|
|
Concept
|
Internationality
|
|
Concept
|
Amino Acid Substitution
|
|
Concept
|
Platelet Glycoprotein GPIb-IX Complex
|
|
Concept
|
BRCA2 Protein
|
|
Concept
|
Adenomatous Polyposis Coli Protein
|
|
Concept
|
Promoter Regions, Genetic
|
|
Concept
|
Mice
|
|
Concept
|
Glutamate Carboxypeptidase II
|
|
Concept
|
Apolipoprotein E4
|
|
Concept
|
Logistic Models
|
|
Concept
|
Electronic Health Records
|
|
Concept
|
Reproducibility of Results
|
|
Concept
|
Patient Satisfaction
|
|
Concept
|
Survival Rate
|
|
Concept
|
Odds Ratio
|
|
Concept
|
Patient Selection
|
|
Concept
|
Mucin-1
|
|
Concept
|
Tumor Suppressor Proteins
|
|
Concept
|
Morpholinos
|
|
Concept
|
Genome-Wide Association Study
|
|
Concept
|
Comparative Genomic Hybridization
|
|
Concept
|
Alzheimer Disease
|
|
Concept
|
Enhancer Elements, Genetic
|
|
Concept
|
Factor V
|
|
Concept
|
Lymphoma, Non-Hodgkin
|
|
Concept
|
Lysine
|
|
Concept
|
Neoplasm Invasiveness
|
|
Concept
|
Patient Transfer
|
|
Concept
|
Phenotype
|
|
Concept
|
Predictive Value of Tests
|
|
Concept
|
Prospective Studies
|
|
Concept
|
Genetic Predisposition to Disease
|
|
Concept
|
Telomere-Binding Proteins
|
|
Concept
|
Young Adult
|
|
Academic Article
|
Cytogenetic and array-CGH characterization of a complex de novo rearrangement involving duplication and deletion of 9p and clinical findings in a 4-month-old female.
|
|
Academic Article
|
Bernard-Soulier syndrome: common ancestry in two African American families with the GP Ib alpha Leu129Pro mutation.
|
|
Academic Article
|
Multicenter development and validation of a risk stratification tool for ward patients.
|
|
Academic Article
|
Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.
|
|
Academic Article
|
Targeted prostate cancer screening in BRCA1 and BRCA2 mutation carriers: results from the initial screening round of the IMPACT study.
|
|
Academic Article
|
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
|
|
Academic Article
|
History repeats itself: the family medication history and pharmacogenomics.
|
|
Academic Article
|
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus.
|
|
Academic Article
|
Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
|
|
Academic Article
|
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.
|
|
Academic Article
|
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.
|
|
Academic Article
|
Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms.
|
|
Academic Article
|
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
|
|
Academic Article
|
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
|
Academic Article
|
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.
|
|
Academic Article
|
Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers.
|
|
Academic Article
|
Hematologic toxicity in BRCA1 and BRCA2 mutation carriers during chemotherapy: A retrospective matched cohort study.
|
|
Academic Article
|
Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness.
|
|
Academic Article
|
Characterization of the Cancer Spectrum in Men With Germline BRCA1 and BRCA2 Pathogenic Variants: Results From the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA).
|
|
Academic Article
|
Germline HOXB13 G84E mutation carriers and risk to twenty common types of cancer: results from the UK Biobank.
|
|
Academic Article
|
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
|
|
Academic Article
|
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
|
|
Academic Article
|
Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
|
|
Academic Article
|
The Contribution of Pharmacogenetic Drug Interactions to 90-Day Hospital Readmissions: Preliminary Results from a Real-World Healthcare System.
|
|
Academic Article
|
Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk.
|
|
Academic Article
|
Effect Modification by Social Determinants of Pharmacogenetic Medication Interactions on 90-Day Hospital Readmissions within an Integrated U.S. Healthcare System.
|
|
Concept
|
Cytochrome P450 Family 2
|
|
Concept
|
Dimensional Measurement Accuracy
|
|
Concept
|
Carcinogenesis
|
|
Concept
|
Ataxia Telangiectasia Mutated Proteins
|
|
Academic Article
|
Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2.
|
|
Academic Article
|
Cancer-associated thrombosis by cancer sites and inherited factors in a prospective population-based cohort.
|