subject area of
- A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy Journal Article
- A MODEL SYSTEM FOR ANALYSIS OF FAMILY RESEMBLANCE IN EXTENDED KINSHIPS OF TWINS Journal Article
- A POLYMORPHIC HUMAN MYOSIN HEAVY-CHAIN LOCUS IS LINKED TO AN ANONYMOUS SINGLE COPY LOCUS (D17S1) AT 17P13 Journal Article
- A fast and accurate method for detection of IBD shared haplotypes in genome-wide SNP data Journal Article
- A functional mutation in the terminal exon of elastin in severe, early-onset chronic obstructive pulmonary disease Journal Article
- A new locus for autosomal dominant Stargardt-like disease maps to chromosome 4 Journal Article
- A new locus for dominant drusen and macular degeneration maps to chromosome 6q14 Journal Article
- A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease Journal Article
- Analytic power calculation for QTL linkage analysis of small pedigrees Journal Article
- Assembling a time bomb - cytochrome c oxidase and disease Journal Article
- Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt disease. Journal Article
- Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice Journal Article
- Exclusion of candidate genes and loci for multiple Lentigines syndrome Journal Article
- FAMILIAL AND INDIVIDUAL INFLUENCES ON BLOOD-PRESSURE Journal Article
- Gene mutations and genomic rearrangements in the mouse as a result of transposon mobilization from chromosomal concatemers Journal Article
- Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family Journal Article
- Idiopathic Scoliosis Families Highlight Actin-Based and Microtubule-Based Cellular Projections and Extracellular Matrix in Disease Etiology Journal Article
- Mapping of an autoimmunity susceptibility locus (AIS1) to chromosome 1p31.3-p32.2 Journal Article
- Modeling Extended Twin Family Data II: Power Associated With Different Family Structures Journal Article
- Nominal association with CHRNA4 variants and nicotine dependence Journal Article
- Our Tangled Family Tree: New Genomic Methods Offer Insight into the Legacy of Archaic Admixture Journal Article
- Quantification of Inbreeding Due to Distant Ancestors and Its Detection Using Dense Single Nucleotide Polymorphism Data Journal Article
- Targeted expression of a dominant-negative fibroblast growth factor (FGF) receptor in gonadotropin-releasing hormone (GnRH) neurons reduces FGF responsiveness and the size of GnRH neuronal population Journal Article
- The ABCR gene in recessive and dominant Stargardt diseases: A genetic pathway in macular degeneration Journal Article
- The familial aggregation of depressive symptoms, antisocial behavior, and alcohol abuse Journal Article
- The genetics of children's oral reading performance Journal Article
- The importance of family-based sampling for biobanks. Journal Article
- The role of pleiotropy vs signaller-receiver gene epistasis in life history trade-offs: dissecting the genomic architecture of organismal design in social systems Journal Article