Nuclear Family
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Subject Areas on Research
- A genomewide screen in multiplex rheumatoid arthritis families suggests genetic overlap with other autoimmune diseases.
- A genomic screen of autism: evidence for a multilocus etiology.
- A large sample of finnish diabetic sib-pairs reveals no evidence for a non-insulin-dependent diabetes mellitus susceptibility locus at 2qter.
- A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
- African-American Fathers' Perspectives on Facilitators and Barriers to Father-Son Sexual Health Communication.
- Analysis of association between Alzheimer disease and the K variant of butyrylcholinesterase (BCHE-K).
- Association Between Parental HPV Knowledge and Intentions to Have Their Daughters Vaccinated.
- Association test for X-linked QTL in family-based designs.
- Associations Between Fathers' and Sons' Sexual Risk in Rural Kenya: The Potential for Intergenerational Transmission.
- Autism or a related developmental disability.
- Barber-led sexual health education intervention for Black male adolescents and their fathers.
- Black Fathers' Preferences for Sexual Health Interventions with their Adolescent Sons.
- Comparing age-related macular degeneration phenotype in probands from singleton and multiplex families.
- Complete genomic screen for disease susceptibility loci in nuclear families.
- Correct splicing despite mutation of the invariant first nucleotide of a 5' splice site: a possible basis for disparate clinical phenotypes in siblings with adenosine deaminase deficiency.
- Daughters and Mothers Against Breast Cancer (DAMES): main outcomes of a randomized controlled trial of weight loss in overweight mothers with breast cancer and their overweight daughters.
- De novo partial duplication of chromosome 7p in a male with autistic disorder.
- Diagnosis of mitochondrial trifunctional protein deficiency in a blood spot from the newborn screening card by tandem mass spectrometry and DNA analysis.
- Disputes over memory ownership: What memories are disputed?
- Does HLA-dependent chimerism underlie the pathogenesis of juvenile dermatomyositis?
- Elevated antisaccade error rate as an intermediate phenotype for psychosis across diagnostic categories.
- False positive rates in a genomic screen for complex quantitative traits.
- Familial chordoma, a tumor of notochordal remnants, is linked to chromosome 7q33.
- Familial dermatomyositis.
- Father-Son Communication About Consistent and Correct Condom Use.
- Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: potential genetic and phenotypic heterogeneity.
- Focal segmental glomerulosclerosis: a need for caution in live-related renal transplantation.
- Genetic linkage analysis of complex genetic traits by using affected sibling pairs.
- Grade-of-membership sibpair linkage analysis maps IDDM11 to chromosome 14q24.3-q31.
- Granulocyte colony-stimulating factor after allogeneic bone marrow transplantation.
- Health care utilization of families of carpenters with alcohol or substance abuse-related diagnoses.
- Heritable individual-specific and allele-specific chromatin signatures in humans.
- Human Papillomavirus Awareness in Haiti: Preparing for a National HPV Vaccination Program.
- Hypospadias in sons of women exposed to diethylstilbestrol in utero.
- Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia.
- Informative missingness in genetic association studies: case-parent designs.
- Interpretation of simultaneous linkage and family-based association tests in genome screens.
- Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.
- Long-term follow-up of cutaneous changes in siblings with mandibuloacral dysplasia who were originally considered to have hereditary sclerosing poikiloderma.
- Mapping genes for NIDDM. Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) Study.
- Mixed leukocyte culture reactivity and graft-versus-host disease in HLA-identical marrow transplantation for leukemia.
- Mothers' preferences and willingness to pay for vaccinating daughters against human papillomavirus.
- Multiple risk factors in the development of externalizing behavior problems: group and individual differences.
- No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.
- Older Parents Benefit More in Health Outcome From Daughters' Than Sons' Emotional Care in China.
- Ordered subset analysis in genetic linkage mapping of complex traits.
- Parent experience of caring for neonates with seizures.
- Principal Sources of Information African American Fathers Draw Upon to Inform their Sons about Sex and Sexual Health Risks.
- SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families.
- Screening the genome for rheumatoid arthritis susceptibility genes: a replication study and combined analysis of 512 multicase families.
- Searching for epistatic interactions in nuclear families using conditional linkage analysis.
- Sequential sib-pair and association studies to detect genes in quantitative traits.
- The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects.
- The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes.
- The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci.
- Turnings and adaptations in resilient daughters of battered women
- Twins Dispute Memory Ownership: A New False Memory Phenomenon
- Two identical triplet sisters carrying a germline BRCA1 gene mutation acquire very similar breast cancer somatic mutations at multiple other sites throughout the genome.
- Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs.
- Values that Fathers Communicate to Sons about Sex, Sexuality, Relationships, and Marriage.