Evidence map›Paper›PMID 37153872›Full record

ArticleHemaSphere2023

Genetic Subtypes and Outcome of Patients Aged 1 to 45 Years Old With Acute Lymphoblastic Leukemia in the NOPHO ALL2008 Trial.

Ulrika Norén-Nyström, Mette K Andersen, Gisela Barbany, Vaidas Dirse, Martine Eilert-Olsen, Marie Engvall, Arja Harila-Saari, Mats Heyman, Randi Hovland, Satu Häikiö and 13 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in HemaSphere, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

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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

23 authors.

Ulrika Norén-NyströmDepartment of Clinical Sciences, Pediatrics, Umeå University, Sweden.
Mette K AndersenDepartment of Clinical Genetics, University Hospital Rigshospitalet, Copenhagen, Denmark.
Gisela BarbanyDepartment of Molecular Medicine and Surgery, Karolinska Institutet, and Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.
Vaidas DirseHematology, Oncology and Transfusion Medicine Center, Vilnius University Hospital Santaros Klinikos, Lithuania.
Martine Eilert-OlsenSection for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, Norway.
Marie EngvallDepartment of Immunology, Genetics and Pathology, Uppsala University, Sweden.
Arja Harila-SaariDepartment of Women's and Children's Health, Uppsala University, Sweden.
Mats HeymanChildhood Cancer Research Unit, Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Randi HovlandDepartment for Medical Genetics, Haukeland University Hospital, Bergen, Norway.
Satu HäikiöDepartment of Genomics, Laboratory Division, Turku University Hospital, Finland.
Jón J JónssonDepartment of Genetics and Molecular Medicine, Landspitali, Reykjavik, Iceland.
Ritva KarhuLaboratory of Clinical Genetics, Fimlab Laboratories, Tampere, Finland.
Eigil KjeldsenDepartment of Hematology, Cancer Cytogenetics Section, Aarhus University Hospital, Denmark.
Anna NorbergDepartment of Medical Biosciences, Medical and Clinical Genetics, Umeå University, Sweden.
Birgitte S PreissDepartment of Pathology, Odense University Hospital, Denmark.
Kati PulkkinenLaboratory of Genetics, Eastern Finland Laboratory Centre, Kuopio, Finland.
Petter Quist-PaulsenDepartment of Hematology, St. Olav's Hospital, Trondheim University Hospital, Norway.
Hannele RäsänenNordlab Oulu Genetics laboratory, Oulu, Finland.
Kjeld SchmiegelowDepartment of Pediatrics and Adolescent Medicine, University Hospital Rigshospitalet, Copenhagen, Denmark.
Anne SeitsonenHUSLAB Laboratory of Genetics, University of Helsinki and Helsinki University Hospital, Finland.
Helene SjögrenDepartment of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Gothenburg, Sweden.
Pille TammurDepartment of Clinical Genetics, Tartu University Hospital, Estonia.
Bertil JohanssonDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID37153872
PMCPMC10162784

What OpenQuestion holds

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Registered trials

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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.