Linkage to chromosome 11p12 in two Maltese families with a highly penetrant form of osteoporosis

No abstract is available for this paper.

• Publication year

  2007

• Venue

  European Journal of Human Genetics

• Publication date

  2007-07-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1038/sj.ejhg.5201814PMID 17377523
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• High-density SNP analysis of 642 Caucasian families with rheumatoid arthritis identifies two new linkage regions on 11p12 and 2q33

  2006cited by this paper
• Screening of tumor necrosis factor receptor-associated factor 6 as a candidate gene for inflammatory bowel disease

  2006cited by this paper
• TNFRSF11B gene variants and bone mineral density in postmenopausal women in Malta.

  2006cited by this paper
• Mechanistic insight into osteoclast differentiation in osteoimmunology

  2005cited by this paper
• CD44 is a determinant of inflammatory bone loss

  2005cited by this paper
• Osteoporosis, inflammation and ageing

  2005cited by this paper
• easyLINKAGE: a PERL script for easy and automated two-/multi-point linkage analyses

  2005cited by this paper
• RANKing c-Jun in osteoclast development.

  2004cited by this paper
• A locus for autosomal dominant keratoconus maps to human chromosome 3p14–q13

  2004cited by this paper
• Standards and guidelines for performing central dual-energy x-ray absorptiometry in premenopausal women, men, and children.

  2004cited by this paper
• Confirmation of linkage to chromosome 1q for peak vertebral bone mineral density in premenopausal white women.

  2004cited by this paper
• A genome-wide linkage scan for bone mineral density in an extended sample: evidence for linkage on 11q23 and Xq27

  2004cited by this paper
• Replication in genetic studies of complex traits

  2004cited by this paper
• Quantitative Trait Loci on Chromosomes 2p, 4p, and 13q Influence Bone Mineral Density of the Forearm and Hip in Mexican Americans

  2003cited by this paper
• Why PLoS Became a Publisher

  2003cited by this paper
• Genome-wide search in Finnish families with inflammatory bowel disease provides evidence for novel susceptibility loci

  2003cited by this paper
• Linkage of Osteoporosis to Chromosome 20p12 and Association to BMP2

  2003cited by this paper
• Suggestive Linkage of 2p22-25 and 11q12-13 with Low Bone Mineral Density at the Lumbar Spine in the Irish Population

  2003cited by this paper
• Associations of polymorphisms in the vitamin D receptor gene (BsmI and FokI) with bone mineral density in postmenopausal women in Malta

  2003cited by this paper
• Searching for osteoporosis genes in the post-genome era: progress and challenges

  2003cited by this paper
• Comparison of genome screens for two independent cohorts provides replication of suggestive linkage of bone mineral density to 3p21 and 1p36.

  2003cited by this paper
• Impaired osteoblastic differentiation, reduced bone formation, and severe osteoporosis in noggin-overexpressing mice.

  2003cited by this paper
• A RANK/TRAF6-dependent Signal Transduction Pathway Is Essential for Osteoclast Cytoskeletal Organization and Resorptive Function*

  2002cited by this paper
• Coeliac disease: follow‐up linkage study provides further support for existence of a susceptibility locus on chromosome 11p11

  2001cited by this paper
• Variance component linkage analysis indicates a QTL for femoral neck bone mineral density on chromosome 1p36.

  2001cited by this paper
• Genome Screen for Quantitative Trait Loci Underlying Normal Variation in Femoral Structure

  2001cited by this paper
• Genomewide scans of complex human diseases: true linkage is hard to find.

  2001cited by this paper
• Evidence for a Major Gene for Bone Mineral Density in Idiopathic Osteoporotic Families

  2000cited by this paper
• A cholesterol-lowering gene maps to chromosome 13q.

  2000cited by this paper
• Positional Cloning of Disease Genes: Advantages of Genetic Isolates

  1999cited by this paper
• TRAF6 deficiency results in osteopetrosis and defective interleukin-1, CD40, and LPS signaling.

  1999cited by this paper
• Suggestive Linkage of the Parathyroid Receptor Type 1 to Osteoporosis

  1999cited by this paper
• Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutation.

  1998cited by this paper
• First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q

  1998cited by this paper
• Linkage of a QTL Contributing to Normal Variation in Bone Mineral Density to Chromosome 11q12–13

  1998cited by this paper
• Allele-sharing models: LOD scores and accurate linkage tests.

  1997cited by this paper
• Linkage of a gene causing high bone mass to human chromosome 11 (11q12-13)

  1997cited by this paper
• Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13.

  1996cited by this paper
• A simple salting out procedure for extracting DNA from human nucleated cells.

  1988cited by this paper

• Skeletal abnormalities, pediatric-onset severe osteoporosis, and multiple fragility fractures in a patient with a novel CTNNB1 de novo variant

  2024cites this paper
• Replication Study Confirms the Association of the Common rs1800629 Variant of the TNFα Gene with Postmenopausal Osteoporosis Susceptibility in the Han Chinese Population

  2018cites this paper
• Genetic association study identified a 20 kb regulatory element in WLS associated with osteoporosis and bone mineral density in Han Chinese

  2017cites this paper
• Clinical and genetic findings in early-onset primary osteoporosis

  2012cites this paper
• Selected Works in Bioinformatics

  2011cites this paper
• Family Based Studies in Complex Disorders: The Use of Bioinformatics Software for Data Analysis in Studies on Osteoporosis

  2011cites this paper
• A genome-wide association analysis implicates SOX6 as a candidate gene for wrist bone mass

  2010cites this paper
• Osteoporosis as an Hereditary Disease

  2010cites this paper
• Genetics of osteoporosis.

  2010cites this paper
• Variants within protectin (CD59) and CD44 genes linked to an inherited haplotype in a family with coeliac disease.

  2009cites this paper
• Effects of a synonymous variant in exon 9 of the CD44 gene on pre-mRNA splicing in a family with osteoporosis.

  2009influential citation
• Genetic studies of osteoporosis in Malta : a review

  2009cites this paper
• Quantitative trait loci, genes, and polymorphisms that regulate bone mineral density in mouse.

  2009cites this paper
• Molecular genetic studies of gene identification for osteoporosis

  2008cites this paper