Cohort profile: 1958 British birth cohort (National Child Development Study).
about
Association of the FCRL3 gene with rheumatoid arthritis: a further example of population specificity?The prevalence of metabolic syndrome and metabolically healthy obesity in Europe: a collaborative analysis of ten large cohort studiesIndependent and population-specific association of risk variants at the IRGM locus with Crohn's diseaseGenome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controlsPhosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damageGermline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomasGenome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetesA unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individualsDeciphering the impact of common genetic variation on lung cancer risk: a genome-wide association studyA human type 1 diabetes susceptibility locus maps to chromosome 21q22.3IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel diseaseCommon 5p15.33 and 6p21.33 variants influence lung cancer riskA genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinomaData Safe Havens in health research and healthcareLong working hours and alcohol use: systematic review and meta-analysis of published studies and unpublished individual participant dataChronic Pain in Children and Adolescents: Diagnosis and Treatment of Primary Pain Disorders in Head, Abdomen, Muscles and JointsA genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathyLoci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemiaInherited variation in immune genes and pathways and glioblastoma riskThe CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma25-Hydroxyvitamin D and pre-clinical alterations in inflammatory and hemostatic markers: a cross sectional analysis in the 1958 British Birth CohortGenetics and epigenetics of rheumatoid arthritisSearch for new loci and low-frequency variants influencing glioma risk by exome-array analysisDataSHIELD: taking the analysis to the data, not the data to the analysisPopulation genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) ConsortiumThe role of longitudinal cohort studies in epigenetic epidemiology: challenges and opportunitiesEvaluation of genetic markers as instruments for Mendelian randomization studies on vitamin DParticipant identification in genetic association studies: improved methods and practical implicationsAge and gender differences in physical capability levels from mid-life onwards: the harmonisation and meta-analysis of data from eight UK cohort studiesA genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemiaCommon variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma riskVariation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphomaCommon variation at 3p22.1 and 7p15.3 influences multiple myeloma riskA genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3)Identification of ZNF313/RNF114 as a novel psoriasis susceptibility geneA genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemiaThe Dunedin Multidisciplinary Health and Development Study: overview of the first 40 years, with an eye to the futureEuropean birth cohorts offer insights on environmental factors affecting human development and healthGenome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk lociA genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.
P2860
Q21195657-1E50EFA9-6214-4A8A-902D-A5DB1191CCE2Q21256400-A13BCF41-CEF3-4B7B-9AE7-F8F7FC174669Q22242868-F604CAE9-B8AE-4E58-A413-A20E3DFA7315Q24550675-2A1287CD-9813-4884-B31C-C97D74A30D70Q24603171-8B1E0B17-EED7-429D-81F5-23A43D12AB14Q24617520-4EC60597-98A0-4D17-912F-DC7663723989Q24632382-94B84D7F-A1AC-44E5-A0CB-C25AA854CA5DQ24644474-16401D13-F14B-4B66-B01C-61CD22813B07Q24644661-5DCB4C91-45D0-4A4A-B208-2E20AB5AA256Q24644978-CFD21B43-986C-4F4F-86A5-462D0F5B8E45Q24645890-EED6C3C2-2F83-4121-AAAA-8FC63F9BE190Q24646182-C0A2F2C7-7DA1-4BEB-AC9A-97EC1B899981Q24657797-245AD970-106B-4D0F-9FA7-4B28426AAA50Q26827422-D094DF9D-16E0-4C3C-92C9-410964B4CC02Q27010041-BF739D7F-B477-49E9-B4BF-12460FCD0676Q28069591-7C023D1A-6068-4CB5-AA98-FA51789CA657Q28242687-1F64E392-BC57-49B2-B207-1E615EB30877Q28255265-C5368DC4-D1E3-490C-8489-B21B83652770Q28383820-0FFC9D5B-CA0B-46E2-BC95-4B2AAE38A4EBQ28391289-48090335-87E8-45AC-BE50-D0C16AB719D6Q28474061-6E8789D5-5F4C-4699-979C-E236F2F30538Q28534348-9210ECF2-98B7-4A3A-AB81-EA90AF232421Q28606408-81A7780D-4ADC-4E0E-90E0-E514C60D7864Q28649310-D1717DCA-9D6C-4535-8A13-FD0927B40CF9Q28681745-46A30909-F8C8-4865-94A9-0DEB76B65BF9Q28727710-51166548-3FCA-48FD-A487-29D23B3CD608Q28729831-8F849FC2-C69D-4EE6-9963-975C323CF271Q28741674-0ABF75A3-C29A-42C5-A355-45D524585D7FQ28742632-73848678-4EA5-4B62-AB6A-342F9F89B172Q28943318-500FF4CF-5DA6-4CE4-9C0D-ECF658FAE3C2Q28943335-7B0AC380-1705-4AB0-B885-431C005C2F86Q28943378-B0354EFE-9629-4C3C-8EA8-DC2D69827010Q28943395-E6D9CCC9-B8EA-4E29-B3AB-7E673AA6103DQ28943455-4CCCCC83-3DA1-4EDB-AAE4-53DA02156DD3Q28943483-494E9CB3-4917-42DB-B7E2-38CDFBB6FF59Q28943555-D9153502-A317-4343-BDD0-CBA7B0713C71Q29030027-8F4F85C4-F700-409D-804D-E44C96848F4EQ29109857-6ADA5E47-6DA9-4791-83D4-0D9D8094755EQ29248527-0D27F56C-2F5C-4755-8C3F-0F73A54F4531Q29417036-C9C4F468-9304-4B40-B84C-B126BAA03AD7
P2860
Cohort profile: 1958 British birth cohort (National Child Development Study).
description
2005 nî lūn-bûn
@nan
2005 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Cohort profile: 1958 British birth cohort (National Child Development Study).
@ast
Cohort profile: 1958 British birth cohort (National Child Development Study).
@en
Cohort profile: 1958 British birth cohort
@nl
type
label
Cohort profile: 1958 British birth cohort (National Child Development Study).
@ast
Cohort profile: 1958 British birth cohort (National Child Development Study).
@en
Cohort profile: 1958 British birth cohort
@nl
prefLabel
Cohort profile: 1958 British birth cohort (National Child Development Study).
@ast
Cohort profile: 1958 British birth cohort (National Child Development Study).
@en
Cohort profile: 1958 British birth cohort
@nl
P356
P1476
Cohort profile: 1958 British birth cohort (National Child Development Study).
@en
P2093
Chris Power
P356
10.1093/IJE/DYI183
P50
P577
2005-09-09T00:00:00Z