Evidence map›Paper›PMID 36387175›Full record

ArticleFrontiers in oncology2022

Mono- and biallelic germline variants of DNA glycosylase genes in colon adenomatous polyposis families from two continents.

Alisa Petriina Olkinuora, Andrea Constanza Mayordomo, Anni Katariina Kauppinen, María Belén Cerliani, Mariana Coraglio, Ávila Karina Collia, Alejandro Gutiérrez, Karin Alvarez, Alessandra Cassana, Francisco Lopéz-Köstner and 9 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Aflatoxin BEnvironmental and molecular mutagenesis · 2025
    Article
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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

19 authors at 9 institutions in 3 countries.

Alisa Petriina OlkinuoraDepartment of Medical and Clinical Genetics, Medicum, University of Helsinki, Helsinki, Finland.
Andrea Constanza MayordomoPrograma de Cáncer Hereditario (Pro.Can.He.), Hospital Italiano de Buenos Aires, Ciudad Autónoma de Buenos Aires, Argentina.
Anni Katariina KauppinenDepartment of Medical and Clinical Genetics, Medicum, University of Helsinki, Helsinki, Finland.
María Belén CerlianiInstituto Multidisciplinario de Biología Celular (IMBICE), Comisión de Investigaciones Científicas de la provincia de Buenos Aires (CICPBA)-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)-Universidad Nacional de La Plata (UNLP), Buenos Aires, Argentina.
Mariana CoraglioUnidad de Proctología, Hospital de Gastroenterología "Dr. Carlos Bonorino Udaondo", Ciudad Autónoma, de Buenos Aires, Argentina.
Ávila Karina ColliaUnidad de Proctología, Hospital de Gastroenterología "Dr. Carlos Bonorino Udaondo", Ciudad Autónoma, de Buenos Aires, Argentina.
Alejandro GutiérrezUnidad de Proctología, Hospital de Gastroenterología "Dr. Carlos Bonorino Udaondo", Ciudad Autónoma, de Buenos Aires, Argentina.
Karin AlvarezCentro de cáncer, Clínica Universidad de Los Andes, Santiago, Chile.
Alessandra CassanaUnidad de Coloproctología, Clínica Las Condes, Santiago de Chile, Chile.
Francisco Lopéz-KöstnerCentro de cáncer, Clínica Universidad de Los Andes, Santiago, Chile.
Federico JaukServicio de Anatomía Patológica, Hospital Italiano de Buenos Aires, Ciudad Autónoma de Buenos Aires, Argentina.
Hernán García-RivelloServicio de Anatomía Patológica, Hospital Italiano de Buenos Aires, Ciudad Autónoma de Buenos Aires, Argentina.
Ari RistimäkiApplied Tumor Genomics Research Program, Research Programs Unit, University of Helsinki, Helsinki, Finland.
Laura KoskenvuoDepartment of Gastroenterological Surgery, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Anna LepistöApplied Tumor Genomics Research Program, Research Programs Unit, University of Helsinki, Helsinki, Finland.
Taina Tuulikki NieminenDepartment of Medical and Clinical Genetics, Medicum, University of Helsinki, Helsinki, Finland.
Carlos Alberto VaccaroPrograma de Cáncer Hereditario (Pro.Can.He.), Hospital Italiano de Buenos Aires, Ciudad Autónoma de Buenos Aires, Argentina.
Walter Hernán PavicicPrograma de Cáncer Hereditario (Pro.Can.He.), Hospital Italiano de Buenos Aires, Ciudad Autónoma de Buenos Aires, Argentina.
Päivi PeltomäkiDepartment of Medical and Clinical Genetics, Medicum, University of Helsinki, Helsinki, Finland.
University of Helsinki · FIHospital Italiano de Buenos Aires · ARUniversidad de Los Andes, Chile · CLClínica Las Condes · CLComisión de Investigaciones Científicas · ARHelsinki University Hospital · FIHospital District of Helsinki and Uusimaa · FIInstituto Multidisciplinario de Biología Celular · ARInstituto Universitario Hospital Italiano · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, biallelic germline variants of the DNA glycosylase genes

Indexed as

DNA glycosylaseexome sequencinggermline variantMUTYHNEIL1NTHL1OGG1polyposis

Identifiers

PMID36387175
PMCPMC9650540
OpenAlexW4307706231

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.