Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits (Q28239018)

2

0 references

Marie-Pierre Dubé

9

0 references

Henry Völzke

20

0 references

Matthias Nauck

14

0 references

Charles Kooperberg

Louis-Philippe Lemieux Perreault

12

0 references

13

Louis-Philippe Lemieux Perreault

0 references

John D. Rioux

John D Rioux

16

0 references

Uwe Völker

Uwe Völker

Andrew Jackson O'Shaughnessy

19

0 references

4

Andrew O'Shaughnessy

0 references

Andreas Greinacher

21

Andreas Greinacher

0 references

Ulrike Peters

15

Ulrike Peters

0 references

Simon de Denus

8

Simon de Denus

0 references

Jean-Claude Tardif

23

Jean-Claude Tardif

0 references

Rebecca D. Jackson

11

Rebecca D Jackson

0 references

author name string

Paul L Auer

1

0 references

Ursula Schick

3

0 references

Ken Sin Lo

5

0 references

Nathalie Chami

6

0 references

Chris Carlson

7

0 references

Jeff Haessler

10

0 references

Frank Schmidt

17

0 references

Valérie Turcot

18

0 references

Li Hsu

22

0 references

George A Diaz

24

0 references

Alexander P Reiner

25

0 references

Guillaume Lettre

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

26

0 references

language of work or name

English

0 references

publication date

June 2014

0 references

published in

Nature Genetics

0 references

volume

46

0 references

issue

6

0 references

page(s)

629-34

0 references

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Lnk controls mouse hematopoietic stem cell self-renewal and quiescence through direct interactions with JAK2

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Genetics and beyond--the transcriptome of human monocytes and disease susceptibility

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A gain-of-function mutation of JAK2 in myeloproliferative disorders

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Immune thrombocytopenia: pathophysiologic and clinical update

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New gene functions in megakaryopoiesis and platelet formation

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A nonsynonymous LNK polymorphism associated with idiopathic erythrocytosis

29 September 2017

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Multiple loci are associated with white blood cell phenotypes

29 September 2017

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Induction of human fetal hemoglobin via the NRF2 antioxidant response signaling pathway

29 September 2017

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USF and NF-E2 cooperate to regulate the recruitment and activity of RNA polymerase II in the beta-globin gene locus

29 September 2017

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A common intracellular allosteric binding site for antagonists of the CXCR2 receptor

29 September 2017

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Expression of hepcidin and other iron-related genes in type 3 hemochromatosis due to a novel mutation in transferrin receptor-2.

29 September 2017

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Large-scale population study of human cell lines indicates that dosage compensation is virtually complete

29 September 2017

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Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization.

29 September 2017

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JAK2(V617F): Prevalence in a large Chinese hospital population

29 September 2017

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Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease

29 September 2017

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Design of the Women's Health Initiative clinical trial and observational study. The Women's Health Initiative Study Group

29 September 2017

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EKLF-driven PIT1 expression is critical for mouse erythroid maturation in vivo and in vitro.

29 September 2017

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Pooled DNA Resequencing of 68 Myocardial Infarction Candidate Genes in French Canadians

27 November 2018

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Cohort Profile: The Study of Health in Pomerania

27 November 2018

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Familial erythrocytosis genetically linked to erythropoietin receptor gene

27 November 2018

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Myelokathexis: chronic neutropenia with hyperplastic bone marrow and hypersegmented neutrophils in two siblings

27 November 2018

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12 December 2020

New TFR2 mutations in young Italian patients with hemochromatosis

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The JAK2V617F mutation is detectable at very low level in peripheral blood of healthy donors

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Effects of molgramostim, filgrastim and lenograstim in the treatment of myelokathexis

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Crossref

https://api.crossref.org/works/10.1038%2FNG.2962

7 January 2021

inferred from DOI database lookup

Design of the Women’s Health Initiative Clinical Trial and Observational Study

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2962

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG.2962

1 reference

1 reference

1 reference

PubMed publication ID

24777453

1 reference