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Lancet Neurology, The, ISSN 1474-4422, 2015, Volume 14, Issue 12, pp. 1182 - 1195
Journal Article
Lancet Respiratory Medicine, The, ISSN 2213-2600, 2017, Volume 5, Issue 5, pp. 412 - 425
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 04/2011, Volume 20, Issue 8, pp. 1595 - 1609
Recessive mutations in the cartilage-associated protein (CRTAP), leucine proline-enriched proteoglycan 1 (LEPRE1) and peptidyl prolyl cis-trans isomerase B... 
MOLECULAR CHARACTERIZATION | PROLYL 3-HYDROXYLATION | BRUCK-SYNDROME | DOMAIN | CRTAP | CARBOXYL-TERMINAL PROPEPTIDE | PEPTIDE-BONDS | BIOCHEMISTRY & MOLECULAR BIOLOGY | COLLAGEN TRIPLE-HELIX | GENETICS & HEREDITY | PRO-ALPHA-1(I) CHAIN | IDENTIFICATION | Sequence Deletion | Proline - metabolism | Protein Disulfide-Isomerases - metabolism | Humans | Collagen Type I - secretion | Molecular Sequence Data | Osteogenesis Imperfecta - genetics | Infant | Femur - diagnostic imaging | Femur - abnormalities | Procollagen-Proline Dioxygenase - metabolism | Ribs - abnormalities | Ribs - diagnostic imaging | Base Sequence | Skull - abnormalities | Protein Stability | Child | Extracellular Matrix Proteins - metabolism | Infant, Newborn | Fibroblasts - metabolism | Amino Acid Sequence | Collagen Type I - metabolism | Hydroxylation | Extracellular Matrix Proteins - genetics | Cells, Cultured | Cyclophilins - genetics | Procollagen - metabolism | Osteogenesis Imperfecta - mortality | Membrane Glycoproteins - genetics | Radiography | Proline-Rich Protein Domains | Phenotype | Pedigree | Skull - diagnostic imaging | Adolescent | Protein Processing, Post-Translational | Proteoglycans - genetics | Peptidylprolyl isomerase | Proteoglycans | Fibroblasts | Osteogenesis imperfecta | Protein disulfide-isomerase | procollagen | Infants | Skin | Leucine | Mutation | Endoplasmic reticulum | Procollagen-proline dioxygenase
Journal Article
Nature Genetics, ISSN 1061-4036, 06/2016, Volume 48, Issue 6, pp. 624 - 633
Journal Article
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 1 - 7
Causes of the association between cognitive ability and health remain unknown, but may reflect a shared genetic aetiology. This study examines the causal... 
INTELLIGENCE | MULTIDISCIPLINARY SCIENCES | MIDLIFE | EDUCATIONAL-ATTAINMENT | HEIGHT | ASSOCIATION | CHILDHOOD | CORONARY-ARTERY-DISEASE | BLOOD-PRESSURE | AGE | DECLINE | Diabetes mellitus | Coronary vessels | Coronary artery | Cognitive ability | Cardiovascular disease | Blood pressure | Diabetes | Heart diseases | Educational attainment
Journal Article
Clinical Epigenetics, ISSN 1868-7075, 08/2018, Volume 10, Issue 1, pp. 101 - 8
Background: The biological mechanisms underlying frailty in older people are poorly understood. There is some evidence to suggest that DNA methylation patterns... 
Aging | Frailty | Epigenome-wide association study | Epigenetic age acceleration | TRIALS | PHENOTYPE | CANCER | ALL-CAUSE MORTALITY | SKELETAL-MUSCLE | OBESITY | ONCOLOGY | DISABILITY | WOMENS HEALTH | AGE | LIFE | Logistic regression | Usage | DNA | Aged | Research | Methylation | Health aspects | DNA methylation | Epigenetics | Phenotypes | Older people | CpG islands
Journal Article