Evidence map›Paper›PMID 36534659›Full record

ArticlePloS one2022

Novel THPO variant in hereditary thrombocytopenia: A potential candidate variant for predisposition to myeloid neoplasm.

Seok Ryun Kwon, Man Jin Kim, Young-Eun Lee, Jiwon Yun, Da-Jeong Jeong, Jae Hyeon Park, Sunghoon Kwon, Dong Soon Lee

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 83% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 2 institutions in 1 country.

Seok Ryun KwonDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.ORCID 0000-0001-5873-6916
Man Jin KimDepartment of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.
Young-Eun LeeDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Jiwon YunDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Da-Jeong JeongDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Jae Hyeon ParkDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.ORCID 0000-0003-0261-2185
Sunghoon KwonDepartment of Electrical and Computer Engineering, Seoul National University, Seoul, Korea.
Dong Soon LeeDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.ORCID 0000-0002-7085-9270
Seoul National University · KRSeoul National University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary thrombocytopenia is a heterogeneous group of congenital disorders with a wide range of symptoms depending on the severity of platelet dysfunction or thrombocytopenia. Because of its clinical phenotypes and the bone marrow morphology associated with this condition, hereditary thrombocytopenia can be misdiagnosed as primary immune thrombocytopenia and myelodysplastic syndrome. Therefore, genetic evidence is necessary for the accurate diagnosis of hereditary thrombocytopenia. Refractory cytopenia of childhood is a subgroup of myelodysplastic syndrome that was added to the World Health Organization classification in 2008. To investigate the germline and somatic variants associated with refractory cytopenia of childhood, we performed targeted multigene sequencing in three patients with refractory cytopenia of childhood. Of the three patients, one progressed from megakaryocytic hypoplasia with thrombocytopenia, and targeted multigene sequencing revealed THPO variants in this patient and his sister. We propose that the monoallelic deletion of THPO is a potential candidate for germline predisposition to myeloid malignancy.

Indexed as

Myelodysplastic SyndromesMyeloproliferative DisordersNeoplasmsThrombocytopeniaDisease SusceptibilityHumansIsoxazoles4,5,6,7-tetrahydroisoxazolo(4,5-c)pyridin-3-olIsoxazoles

Identifiers

PMID36534659
PMCPMC9762605
OpenAlexW4311914315

What OpenQuestion holds

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LicenceCC BY
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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.