Evidence map›Paper›PMID 31558678›Full record

ArticleHaematologica2020

Genetic and phenotypic characterization of indolent T-cell lymphoproliferative disorders of the gastrointestinal tract.

Craig R Soderquist, Nupam Patel, Vundavalli V Murty, Shane Betman, Nidhi Aggarwal, Ken H Young, Luc Xerri, Rebecca Leeman-Neill, Suzanne K Lewis, Peter H Green and 6 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

38 citing papers in PubMed, 75 citations in OpenAlex.

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  19. Extranodal T- and NK-cell lymphomas.Virchows Archiv : an international journal of pathology · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 8 institutions in 3 countries.

Craig R SoderquistDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York Presbyterian Hospital, New York, NY, USA crs2130@cumc.columbia.edu gb96@cumc.columbia.edu.
Nupam PatelDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York Presbyterian Hospital, New York, NY, USA.
Vundavalli V MurtyDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York Presbyterian Hospital, New York, NY, USA.
Shane BetmanDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York Presbyterian Hospital, New York, NY, USA.
Nidhi AggarwalDepartment of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Ken H YoungDepartment of Hematopathology, MD Anderson Cancer Center, Houston, TX, USA.
Luc XerriDepartment of Bio-Pathology, Institut Paoli-Calmettes, Aix-Marseille University, Marseille, France.
Rebecca Leeman-NeillDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York Presbyterian Hospital, New York, NY, USA.
Suzanne K LewisDepartment of Medicine, Celiac Disease Center, Columbia University Irving Medical Center, New York Presbyterian Hospital, New York, NY, USA.
Peter H GreenDepartment of Medicine, Celiac Disease Center, Columbia University Irving Medical Center, New York Presbyterian Hospital, New York, NY, USA.
Susan HsiaoDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York Presbyterian Hospital, New York, NY, USA.
Mahesh M MansukhaniDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York Presbyterian Hospital, New York, NY, USA.
Eric D HsiPathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
Laurence de LevalInstitute of Pathology, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
Bachir AlobeidDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York Presbyterian Hospital, New York, NY, USA.
Govind BhagatDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York Presbyterian Hospital, New York, NY, USA crs2130@cumc.columbia.edu gb96@cumc.columbia.edu.
Columbia University · USNew York Hospital Queens · USNewYork–Presbyterian Hospital · USAix-Marseille Université · FRCleveland Clinic · USThe University of Texas MD Anderson Cancer Center · USUniversity of Lausanne · CHUniversity of Pittsburgh Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Indolent T-cell lymphoproliferative disorders of the gastrointestinal tract are rare clonal T-cell diseases that more commonly occur in the intestines and have a protracted clinical course. Different immunophenotypic subsets have been described, but the molecular pathogenesis and cell of origin of these lymphocytic proliferations is poorly understood. Hence, we performed targeted next-generation sequencing and comprehensive immunophenotypic analysis of ten indolent T-cell lymphoproliferative disorders of the gastrointestinal tract, which comprised CD4

Indexed as

Lymphoproliferative DisordersT-LymphocytesGastrointestinal TractHumansImmunophenotypingPhenotype

Identifiers

PMID31558678
PMCPMC7327650
OpenAlexW2976359641

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.