Evidence map›Paper›PMID 32443704›Full record

ArticleCancers2020

Germline Mutation in

Maisa Pinheiro, Fernanda Cristina Sulla Lupinacci, Karina Miranda Santiago, Sandra Aparecida Drigo, Fabio Albuquerque Marchi, Carlos Eduardo Fonseca-Alves, Sonia Cristina da Silva Andrade, Mads Malik Aagaard, Tatiane Ramos Basso, Mariana Bisarro Dos Reis and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. 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
0.7field-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. Family-Based Study RevealsInternational journal of molecular sciences · 2026
    Article
  2. Review
  3. Article
  4. Article
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

17 authors at 8 institutions in 4 countries.

Maisa PinheiroFaculty of Medicine, Sao Paulo State University, UNESP, Botucatu SP 18618-687, Brazil.ORCID 0000-0002-9112-1179
Fernanda Cristina Sulla LupinacciInternational Research Center, A.C. Camargo Cancer Center, São Paulo SP 01508-010, Brazil.
Karina Miranda SantiagoInternational Research Center, A.C. Camargo Cancer Center, São Paulo SP 01508-010, Brazil.ORCID 0000-0002-6326-7795
Sandra Aparecida DrigoDepartment of Surgery and Orthopedics, Experimental Research Unity, Faculty of Medicine, São Paulo State University, UNESP, Botucatu SP 18618-687, Brazil.ORCID 0000-0001-6747-6642
Fabio Albuquerque MarchiInternational Research Center, A.C. Camargo Cancer Center, São Paulo SP 01508-010, Brazil.
Carlos Eduardo Fonseca-AlvesDepartment of Veterinary Surgery and Anesthesiology, São Paulo State University, UNESP, Botucatu SP 18618-681, Brazil.ORCID 0000-0002-6702-6139
Sonia Cristina da Silva AndradeDepartment of Genetics and Evolutionary Biology, University of São Paulo, USP, São Paulo SP 05508-090, Brazil.ORCID 0000-0002-1302-5261
Mads Malik AagaardDepartment of Clinical Genetics, Vejle University Hospital, 7100 Vejle, Denmark.ORCID 0000-0003-4742-7047
Tatiane Ramos BassoInternational Research Center, A.C. Camargo Cancer Center, São Paulo SP 01508-010, Brazil.
Mariana Bisarro Dos ReisInternational Research Center, A.C. Camargo Cancer Center, São Paulo SP 01508-010, Brazil.
Rolando André Rios VillacisDepartment of Genetics and Morphology, Institute of Biological Sciences, University of Brasília, UnB, Brasília DF 70910-900, Brazil.
Martin RofféInternational Research Center, A.C. Camargo Cancer Center, São Paulo SP 01508-010, Brazil.ORCID 0000-0001-7247-3067
Glaucia Noeli Maroso HajjInternational Research Center, A.C. Camargo Cancer Center, São Paulo SP 01508-010, Brazil.
Igor JurisicaKrembil Research Institute, UHN, University of Toronto, Toronto, ON M5G 2C4, Canada.ORCID 0000-0002-2507-946X
Luiz Paulo KowalskiInternational Research Center, A.C. Camargo Cancer Center, São Paulo SP 01508-010, Brazil.
Maria Isabel AchatzCancer Genetics Unit, Centro de Oncologia, Hospital Sirio Libanês, São Paulo SP 01308-050, Brazil.ORCID 0000-0001-6894-1219
Silvia Regina RogattoDepartment of Clinical Genetics, Vejle University Hospital, Institute of Regional Health Research, University of Southern Denmark, 5000 Odense, Denmark.ORCID 0000-0003-4637-5687
AC Camargo Hospital · BRUniversidade Estadual Paulista (Unesp) · BRHospital Sírio-Libanês · BRUniversidade de Brasília · BRUniversidade de São Paulo · BRUniversity of Southern Denmark · DKUniversity of Toronto · CAVejle Sygehus · DK

Funding

Coordination for the Improvement of Higher Education Personnel (CAPES) 8195/14-5National Council for Scientific and Technological Development (CNPq) 481132/2012-0São Paulo Research Foundation (FAPESP) 2012/12714-5, 2013/0186-7, 2014/03983-8
6 · The paper itself

Abstract

Multiple primary thyroid cancer (TC) and breast cancer (BC) are commonly diagnosed, and the lifetime risk for these cancers is increased in patients with a positive family history of both TC and BC. Although this phenotype is partially explained by

Indexed as

breast cancerexome sequencingfamilial cancerfunctional analysisMUS81thyroid cancer

Identifiers

PMID32443704
PMCPMC7281423
OpenAlexW3027277977

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.