(Q24655591)

47

0 references

Christian Gieger

50

0 references

Alexander Teumer

18

0 references

Vilmundur Gudnason

51

0 references

Stefania Bandinelli

34

0 references

Luigi Ferrucci

54

0 references

Nicole Soranzo

4

0 references

Eric Boerwinkle

28

0 references

Cornelia M. van Duijn

52

0 references

André Uitterlinden

38

0 references

Abbas Dehghan

10

0 references

Christa Meisinger

46

0 references

Gudny Eiriksdottir

25

0 references

Thor Aspelund

12

0 references

Albert Hofman

30

0 references

Bruce M. Psaty

53

0 references

Matthias Nauck

48

0 references

Josef Coresh

36

0 references

Augusto Rendon

Augusto Rendon

24

0 references

Andrew E Jaffe

Andrew Jaffe

15

0 references

Janine F Felix

Janine F Felix

23

0 references

Albert V. Smith

Albert V Smith

5

0 references

Jerome I Rotter

29

Jerome I Rotter

0 references

Mary Cushman

60

Mary Cushman

0 references

Tamara B. Harris

61

Tamara B Harris

0 references

Andreas Greinacher

56

Andreas Greinacher

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Willem H. Ouwehand

44

Willem H Ouwehand

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Lenore J Launer

40

Lenore J Launer

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Andrew Singleton

35

Andrew B Singleton

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Jack Guralnik

20

Jack M Guralnik

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Thomas Lumley

37

Thomas Lumley

0 references

Jacqueline C M Witteman

58

Jacqueline C M Witteman

0 references

Dena G. Hernandez

32

Dena G Hernandez

0 references

L. Adrienne Cupples

41

L Adrienne Cupples

0 references

Tim Spector

49

Tim D Spector

0 references

Caroline S. Fox

19

Caroline S Fox

0 references

Toshiko Tanaka

14

Toshiko Tanaka

0 references

Christopher J O'Donnell

57

Christopher J O'Donnell

0 references

Ben A Oostra

42

Ben A Oostra

0 references

Kenneth M Rice

22

Kenneth Rice

0 references

Georg B Ehret

21

Georg B Ehret

0 references

Nicole L. Glazer

9

Nicole L Glazer

0 references

Michael Marmot

6

Michael A Nalls

0 references

Joshua C Bis

16

Joshua C M Bis

0 references

Germaine C. Verwoert

17

Germaine C Verwoert

0 references

Santhi K Ganesh

1

Santhi K Ganesh

0 references

Aravinda Chakravarti

55

Aravinda Chakravarti

0 references

Ming-Huei Chen

7

Ming-Huei Chen

0 references

Neil A Zakai

2

Neil A Zakai

0 references

Brigitte Kühnel

11

Brigitte Kuhnel

0 references

Kushang V Patel

27

Kushang V Patel

0 references

Jennifer Sambrook

31

Jennifer G Sambrook

0 references

Jing-Ping Lin

62

Jing-Ping Lin

0 references

Susan L Furth

59

Susan Furth

0 references

Daniel Levy

26

Daniel Levy

0 references

author name string

Frank J A van Rooij

3

0 references

Anna Kottgen

8

0 references

Qiong Yang

13

0 references

Gang Zheng

33

0 references

Janine M Vangils

39

0 references

Jaap-Jan Zwaginga

43

0 references

Swee-Lay Thein

ER stress controls iron metabolism through induction of hepcidin

45

0 references

language of work or name

English

0 references

publication date

November 2009

0 references

published in

Nature Genetics

0 references

volume

41

0 references

issue

11

0 references

page(s)

1191-8

0 references

cites work

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Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA)

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Newly identified genetic risk variants for celiac disease related to the immune response

7 April 2017

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Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia

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Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study

7 April 2017

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Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

7 April 2017

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The definition of anemia: what is the lower limit of normal of the blood hemoglobin concentration?

7 April 2017

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The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding

7 April 2017

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A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

7 April 2017

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Principal components analysis corrects for stratification in genome-wide association studies

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7 April 2017

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Identification of a gene responsible for familial Wolff-Parkinson-White syndrome

7 April 2017

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Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts

7 April 2017

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Genome-wide association study of blood pressure and hypertension

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Genomic control for association studies

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Genome-wide association study identifies eight loci associated with blood pressure

7 April 2017

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lumi: a pipeline for processing Illumina microarray

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The genetic association database

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Human fetal hemoglobin expression is regulated by the developmental stage-specific repressor BCL11A.

7 April 2017

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Genetic complexity in sickle cell disease

28 September 2017

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Stat5 regulates cellular iron uptake of erythroid cells via IRP-2 and TfR-1.

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Promoter polymorphism of the erythropoietin gene in severe diabetic eye and kidney complications

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A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.

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Imputation-based analysis of association studies: candidate regions and quantitative traits

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Hepcidin antimicrobial peptide transgenic mice exhibit features of the anemia of inflammation

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Genomewide scans of red cell indices suggest linkage on chromosome 6q23.

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Diffuse large B-cell lymphoma subgroups have distinct genetic profiles that influence tumor biology and improve gene-expression-based survival prediction

28 September 2017

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Influence of flow properties of blood upon viscosity-hematocrit relationships

28 September 2017

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Progression through key stages of haemopoiesis is dependent on distinct threshold levels of c-Myb.

28 September 2017

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Hemochromatosis due to mutations in transferrin receptor 2.

28 September 2017

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Anemia as a risk factor for cardiovascular disease in The Atherosclerosis Risk in Communities (ARIC) study

28 September 2017

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Cytokine signaling and hematopoietic homeostasis are disrupted in Lnk-deficient mice

28 September 2017

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Abnormal mesoderm patterning in mouse embryos mutant for the SH2 tyrosine phosphatase Shp-2.

28 September 2017

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Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis

28 September 2017

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Genetic and environmental causes of variation in basal levels of blood cells

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Haematocrit: relationships with blood lipids, blood pressure and other cardiovascular risk factors.

30 May 2018

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Mortality and anaemia in women

30 May 2018

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Genetic and environmental influences on the size and number of cells in the blood

30 May 2018

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Partial deficiency of erythrocyte spectrin in hereditary spherocytosis

30 May 2018

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A prospective study of anemia status, hemoglobin concentration, and mortality in an elderly cohort: the Cardiovascular Health Study.

30 May 2018

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21 January 2018

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Determinants and characteristics of mean corpuscular volume and hemoglobin concentration in white HFE C282Y homozygotes in the hemochromatosis and iron overload screening study.

21 January 2018

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The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humans.

21 January 2018

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Evidence for a gene influencing haematocrit on chromosome 6q23-24: genomewide scan in the Framingham Heart Study

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Increased Risk of Acute Myocardial Infarction in Carriers of the Hemochromatosis Gene Cys282Tyr Mutation

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c-Myb and p300 regulate hematopoietic stem cell proliferation and differentiation

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Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11.

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Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia

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P-selectin glycoprotein ligand-1 is expressed on endothelial cells and mediates monocyte adhesion to activated endothelium

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Genotypic and phenotypic characterization of Noonan syndrome: New data and review of the literature

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Sequence-based polymorphisms in members of the apoptosis Bcl-2 gene family and their association with hematocrit level.

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Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy

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Heterozygosity for a hereditary hemochromatosis gene is associated with cardiovascular death in women

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Hepcidin: a new tool in the management of anaemia in patients with chronic kidney disease?

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Evidence for additional blood pressure correlates in adults 20-56 years old

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12 December 2020

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Hematocrit and the risk of cardiovascular disease--the Framingham study: a 34-year follow-up

1 reference

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Mean red cell volume as a correlate of blood pressure

1 reference

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Genetic and environmental causes of variation in basal levels of blood cells

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7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG.466

1 reference

Dimensions Publication ID

1008124875

0 references

1 reference

1 reference

PubMed publication ID

19862010

1 reference