Genetic Predisposition to DiseaseDisease SusceptibilityGenetic LinkagePolymorphism, Single NucleotideGenotypeChromosome MappingHaplotypesAllelesLod ScoreLinkage DisequilibriumMicrobial Sensitivity TestsGenome-Wide Association StudyCase-Control StudiesBRCA1 ProteinGene FrequencyGenetic MarkersPolymorphism, GeneticBRCA2 ProteinGenes, BRCA1PedigreeGenetic TestingChromosomes, Human, Pair 6Microsatellite RepeatsPhenotypeGenome, HumanAnti-Bacterial AgentsMutationFamily HealthGenetic Association StudiesGenetic VariationGenetic LociChromosomes, Human, Pair 1SchizophreniaGerm-Line MutationGenes, RetinoblastomaChromosomes, Human, Pair 2Age of OnsetHeterozygoteGenetic HeterogeneityBreast NeoplasmsAsian Continental Ancestry GroupDiabetes Mellitus, Type 1Chromosomes, Human, Pair 13Genes, BRCA2Models, GeneticNuclear FamilyNeoplastic Syndromes, HereditaryPolymerase Chain ReactionMolecular Sequence DataChromosomes, Human, Pair 5Retinoblastoma ProteinEndosomal Sorting Complexes Required for TransportQuantitative Trait LociFamilyRisk FactorsEuropean Continental Ancestry GroupLupus Erythematosus, SystemicChromosomes, Human, Pair 20DNA Mutational AnalysisChromosomes, Human, Pair 10Carrier ProteinsEpistasis, GeneticDrug Resistance, BacterialNod2 Signaling Adaptor ProteinTranscription FactorsMice, CongenicDNA-Binding ProteinsDrug Resistance, MicrobialChromosomes, Human, Pair 17Protein Tyrosine Phosphatase, Non-Receptor Type 22PsoriasisPenetranceRetinoblastomaSequence Analysis, DNABase SequenceMice, Inbred C57BLExonsAutistic DisorderHLA-DRB1 ChainsMultifactorial InheritanceChromosomes, Human, Pair 3HLA AntigensNeuronal Migration DisordersNeoplasm ProteinsOvarian NeoplasmsAntifungal AgentsDisease Models, AnimalHeterozygote DetectionChromosomes, Human, Pair 7Crohn DiseaseDiabetes Mellitus, Type 2Neuregulin-1Animals, CongenicMajor Histocompatibility ComplexChromosomes, Human, Pair 12Mutation, MissenseCrosses, GeneticBipolar DisorderParagangliomaChromosomes, Human, Pair 11