Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.

[1]  B. Beutler,et al.  The Serine Protease TMPRSS6 Is Required to Sense Iron Deficiency , 2008, Science.

[2]  N. Andrews,et al.  Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA) , 2008, Nature Genetics.

[3]  Peter M Visscher,et al.  Sizing up human height variation , 2008, Nature Genetics.

[4]  Jacques Fellay,et al.  WGAViewer: software for genomic annotation of whole genome association studies. , 2008, Genome research.

[5]  L. Liang,et al.  A genome-wide association study of global gene expression , 2007, Nature Genetics.

[6]  Manuel A. R. Ferreira,et al.  PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.

[7]  Simon C. Potter,et al.  Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls , 2007, Nature.

[8]  S. Navas-Carretero,et al.  The G277S transferrin mutation does not affect iron absorption in iron deficient women , 2007, European journal of nutrition.

[9]  C. V. van Duijn,et al.  Heritability of Serum Iron, Ferritin and Transferrin Saturation in a Genetically Isolated Population, the Erasmus Rucphen Family (ERF) Study , 2006, Human Heredity.

[10]  S. Henauw,et al.  Human transferrin G277S mutation and iron deficiency in pregnancy , 2006, British journal of haematology.

[11]  D. Clayton,et al.  Population structure, differential bias and genomic control in a large-scale, case-control association study , 2005, Nature Genetics.

[12]  M. Olivier.  A haplotype map of the human genome , 2003, Nature.

[13]  Margaret J. Wright,et al.  Brisbane Adolescent Twin Study: Outline of study methods and research projects , 2004 .

[14]  Sarah E Medland,et al.  A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q. , 2004, Twin research : the official journal of the International Society for Twin Studies.

[15]  Leena Peltonen,et al.  GenomEUtwin: A Strategy to Identify Genetic Influences on Health and Disease , 2003, Twin Research.

[16]  N. Martin,et al.  Relative importance of female‐specific and non‐female‐specific effects on variation in iron stores between women , 2003, British journal of haematology.

[17]  V. Felitti,et al.  Human transferrin G277S mutation: a risk factor for iron deficiency anaemia , 2001, British journal of haematology.

[18]  E. Beutler,et al.  Polymorphisms in the transferrin 5' flanking region associated with differences in total iron binding capacity: possible implications in iron homeostasis. , 2001, Blood cells, molecules & diseases.

[19]  D. Duffy,et al.  Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twins. , 2000, American journal of human genetics.

[20]  G. Abecasis,et al.  A general test of association for quantitative traits in nuclear families. , 2000, American journal of human genetics.

[21]  E. Beutler,et al.  The effect of transferrin polymorphisms on iron metabolism. , 1999, Blood cells, molecules & diseases.

[22]  P. Walter,et al.  The beta subunit of the signal recognition particle receptor is a transmembrane GTPase that anchors the alpha subunit, a peripheral membrane GTPase, to the endoplasmic reticulum membrane , 1995, The Journal of cell biology.

[23]  K. Lange,et al.  Programs for pedigree analysis: Mendel, Fisher, and dGene , 1988, Genetic epidemiology.