Evidence map›Paper›PMID 38233595›Full record

ArticleNature genetics2024

Inherited polygenic effects on common hematological traits influence clonal selection on JAK2

Jing Guo, Klaudia Walter, Pedro M Quiros, Muxin Gu, E Joanna Baxter, John Danesh, Emanuele Di Angelantonio, David Roberts, Paola Guglielmelli, Claire N Harrison and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Nature genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
8.3field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Genetic influences on haematopoiesis.Nature reviews. Genetics · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Molecular profiling in MPN: who should have it and why?Hematology. American Society of Hematology. Education Program · 2024
    Review
  12. Myeloproliferative Neoplasms: Challenging Dogma.Journal of clinical medicine · 2024
    Review
  13. Article
  14. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 7 institutions in 3 countries.

Jing GuoWellcome Sanger Institute, Hinxton, UK.ORCID 0000-0003-1923-6614
Klaudia WalterWellcome Sanger Institute, Hinxton, UK.ORCID 0000-0003-4448-0301
Pedro M QuirosWellcome Sanger Institute, Hinxton, UK.
Muxin GuWellcome Sanger Institute, Hinxton, UK.
E Joanna BaxterInstituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain.
John DaneshWellcome Sanger Institute, Hinxton, UK.
Emanuele Di AngelantonioNational Institute for Health Research Blood and Transplant Research Unit in Donor Health and Genomics, University of Cambridge, Cambridge, UK.
David RobertsNational Institute for Health Research Blood and Transplant Research Unit in Donor Health and Genomics, University of Cambridge, Cambridge, UK.
Paola GuglielmelliDepartment of Experimental and Clinical Medicine, Center for Research and Innovation of Myeloproliferative Neoplasms (CRIMM), AOU Careggi, University of Florence, Florence, Italy.ORCID 0000-0003-1809-284X
Claire N HarrisonDepartment of Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Anna L GodfreyCambridge University Hospitals NHS Trust, Cambridge, UK.
Anthony R GreenWellcome-MRC Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, Cambridge, UK.
George S VassiliouWellcome-MRC Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, Cambridge, UK.ORCID 0000-0003-4337-8022
Dragana VuckovicWellcome Sanger Institute, Hinxton, UK.
Jyoti NangaliaWellcome Sanger Institute, Hinxton, UK. jn5@sanger.ac.uk.ORCID 0000-0001-7122-4608
Nicole SoranzoWellcome Sanger Institute, Hinxton, UK. ns6@sanger.ac.uk.ORCID 0000-0003-1095-3852
University of Cambridge · GBWellcome/MRC Cambridge Stem Cell Institute · GBWellcome Sanger Institute · GBCambridge University Hospitals NHS Foundation Trust · GBGuy's and St Thomas' NHS Foundation Trust · GBInstituto de Investigación Sanitaria del Principado de Asturias · ESUniversity of Florence · IT

Funding

Medical Research Council MC_PC_17230Wellcome Trust
6 · The paper itself

Abstract

Myeloproliferative neoplasms (MPNs) are chronic cancers characterized by overproduction of mature blood cells. Their causative somatic mutations, for example, JAK2

Indexed as

Myeloproliferative DisordersNeoplasmsGenetic Risk ScoreHumansJanus Kinase 2MutationPhenotypeJAK2 protein, humanJanus Kinase 2

Identifiers

PMID38233595
PMCPMC10864174
OpenAlexW4390947885

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.