About: Heritability of Serum Iron, Ferritin and Transferrin Saturation in a Genetically Isolated Population, the Erasmus Rucphen Family (ERF) Study

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About: Heritability of Serum Iron, Ferritin and Transferrin Saturation in a Genetically Isolated Population, the Erasmus Rucphen Family (ERF) Study Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у 2006 (uk) im Jahr 2006 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57309176-D59CEFC8-1448-4043-A4BB-5C9446408770
publication date	2006-01-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q57309176-1701280D-C3FE-408D-8F72-746C982CF7B3 wds:Q57309176-21B91DED-873A-477A-99C5-D1643CE502CD wds:Q57309176-2B8CE462-1B09-452A-BA0B-B6D5199BBE8D wds:Q57309176-5982C043-48FB-4428-8F6C-7FED39F824F7 wds:Q57309176-5E4AC8C9-509A-403F-9A1D-CD39695B682D wds:Q57309176-9BC6369E-EB6E-4072-818C-B8D9228878DD wds:Q57309176-BBD676F4-C93D-4BAB-AB17-0B37A5955E25 wds:Q57309176-E9C57C54-F236-4814-9E49-2361B6597BAA
cites work	Juvenile hemochromatosis locus maps to chromosome 1q. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22. Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USA. Multipoint quantitative-trait linkage analysis in general pedigrees Iron imports. I. Intestinal iron absorption and its regulation Hyperferritinemia, iron overload, and multiple metabolic alterations identify patients at risk for nonalcoholic steatohepatitis
author name string	wds:Q57309176-5181D8D7-ADB7-4600-91A3-1C25480E384F wds:Q57309176-8C1C0F06-9791-426F-9650-E7AE0DF62556 wds:Q57309176-C1298A68-6755-4FEB-B229-3553EEA7C1D5 wds:Q57309176-F07A0C65-5F6D-4DFC-8394-79224BBB4514
author name string	H.A.P. Pols B.A. Oostra O.T. Njajou D.W. Swinkels
rdfs:label	Heritability of Serum Iron, Ferritin and Transferrin Saturation in a Genetically Isolated Population, the Erasmus Rucphen Family (ERF) Study (en) Heritability of Serum Iron, Ferritin and Transferrin Saturation in a Genetically Isolated Population, the Erasmus Rucphen Family (ERF) Study (nl)
skos:prefLabel	Heritability of Serum Iron, Ferritin and Transferrin Saturation in a Genetically Isolated Population, the Erasmus Rucphen Family (ERF) Study (en) Heritability of Serum Iron, Ferritin and Transferrin Saturation in a Genetically Isolated Population, the Erasmus Rucphen Family (ERF) Study (nl)
name	Heritability of Serum Iron, Ferritin and Transferrin Saturation in a Genetically Isolated Population, the Erasmus Rucphen Family (ERF) Study (en) Heritability of Serum Iron, Ferritin and Transferrin Saturation in a Genetically Isolated Population, the Erasmus Rucphen Family (ERF) Study (nl)
author	wds:Q57309176-6E213EDA-7E3F-4EC5-8B35-3C8C2DDE19AB wds:Q57309176-795E8DBC-8B21-4898-B03C-654E79916CC0 wds:Q57309176-AE3757EE-FBA7-4328-A6B4-05DAF382362C wds:Q57309176-EF77A110-38A0-4D2D-A146-6040496DF845
author	Cornelia M. van Duijn Yurii S. Aulchenko M. Carola Zillikens Behrooz Z. Alizadeh
title	wds:Q57309176-C0547B4C-2A17-4A3E-A900-868647E4868D
title	Heritability of Serum Iron, Ferritin and Transferrin Saturation in a Genetically Isolated Population, the Erasmus Rucphen Family (ERF) Study (en)
page(s)	wds:Q57309176-963E891C-D343-4FAC-BCA9-37EE4DC77DB6
page(s)	222-228
instance of	wds:Q57309176-10025883-7B13-4A5F-9332-AE4D3AFC64FF
instance of	scholarly article
main subject	wds:Q57309176-812F0902-B710-4C72-80E5-4EE1D37E9DF5
main subject	heritability
PubMed ID	wds:Q57309176-5A854EB9-DE2D-41C4-BF92-4185F1E96B13
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16877869
PubMed ID	16877869
published in	wds:Q57309176-036CC616-4E50-4378-AD1D-28AAE9E7D4A0
published in	Human Heredity
issue	wds:Q57309176-98A665E7-61FE-44E9-9B6C-4C3D8CD95EF5
volume	wds:Q57309176-4B3F4DA3-0806-4CC3-9AAE-9CFB078901EA
issue	4
volume	61
DOI	wds:Q57309176-08603914-2E40-480C-BCDF-6266A4B608B9
DOI	http://dx.doi.org/10.1159/000094777
DOI	10.1159/000094777
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57309176
is cites work of	Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits A genome-wide association analysis of serum iron concentrations Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Genome-wide association study identifies variants in PMS1 associated with serum ferritin in a Chinese population A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis Human helminth co-infection: no evidence of common genetic control of hookworm and Schistosoma mansoni infection intensity in a Brazilian community Genome-wide admixture and association study of serum iron, ferritin, transferrin saturation and total iron binding capacity in African Americans Gender and iron genes may modify associations between brain iron and memory in healthy aging Variables Related to Iron Status and Genetic Background Among Korean Populations: Ironing Out the Differences Heritability and demographic analyses in the large isolated population of Val Borbera suggest advantages in mapping complex traits genes COMBINING INDIVIDUAL PARTICIPANT DATA AND SUMMARY STATISTICS FROM BOTH CONTINUOUSLY VALUED AND BINARY VARIABLES TO ESTIMATE REGRESSION PARAMETERS Genetic variants influencing biomarkers of nutrition are not associated with cognitive capability in middle-aged and older adults Breaking loops in large complex pedigrees Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study Common Variants and Haplotypes in the TF, TNF-α, and TMPRSS6 Genes Are Associated with Iron Status in a Female Black South African Population Associations between Common Variants in Iron-Related Genes with Haematological Traits in Populations of African Ancestry. A critical evaluation of results from genome-wide association studies of micronutrient status and their utility in the practice of precision nutrition An Analytic Solution to the Computation of Power and Sample Size for Genetic Association Studies under a Pleiotropic Mode of Inheritance The association of HFE gene H63D polymorphism with endurance athlete status and aerobic capacity: novel findings and a meta-analysis
is cites work of	wds:Q28943352-031E611A-5B91-42E9-9BE5-5AED70E331B4 wds:Q33579535-DC6E68F2-98D3-4D36-95AF-933DA3875B20 wds:Q34097695-F7F7C701-5852-40F4-9DA2-9FD7C7D73972 wds:Q37399509-B6881633-44B6-45B4-8E5F-75D561E682D6 wds:Q43546360-44915124-9184-4A85-B619-7C66638E67ED wds:Q57599172-3D5AECFA-2ECA-49BA-B2CE-4C160F8126D3 wds:Q21142722-589EE93A-F209-47BE-82B5-D7EF6F479C3E wds:Q34597837-F2401DA4-2B81-4C22-B524-110826E834F8 wds:Q37082253-6BBBCC2D-5B43-4D32-B222-C5899608FA42 wds:Q36953067-3D567E9D-F6E0-42A1-ADDD-2D96CD6292EF wds:Q40266390-81E07A36-8216-4311-A0E6-B8AEF6AD534F wds:Q33669191-BE647DCA-F0F8-4F59-8554-88A0ADBCD306 wds:Q36058819-777C3F4C-3329-4C08-9DC1-10979F107FF1 wds:Q37276849-A33AEEE8-720A-4B1C-961A-9510042D6A62 wds:Q92293557-C69AC8FA-65EC-433D-80AD-7D4C1FFCB48B

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