Evidence map›Paper›PMID 30430080›Full record

ArticleFrontiers in oncology2018

GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in

Fabienne Lesueur, Noura Mebirouk, Yue Jiao, Laure Barjhoux, Muriel Belotti, Maïté Laurent, Mélanie Léone, Claude Houdayer, Brigitte Bressac-de Paillerets, Dominique Vaur and 29 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. International journal of molecular sciences · 2020
    Review
  9. Review
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

39 authors.

Fabienne LesueurINSERM, U900, Institut Curie, PSL Research University, Mines ParisTech, Paris, France.
Noura MebiroukINSERM, U900, Institut Curie, PSL Research University, Mines ParisTech, Paris, France.
Yue JiaoService de Génétique, Institut Curie, Paris, France.
Laure BarjhouxBiopathologie, Centre Léon Bérard, Lyon, France.
Muriel BelottiService de Génétique, Institut Curie, Paris, France.
Maïté LaurentService de Génétique, Institut Curie, Paris, France.
Mélanie LéoneHospices Civils de Lyon, Groupement Hospitalier EST, Bron, France.
Claude HoudayerService de Génétique, Institut Curie, Paris, France.
Brigitte Bressac-de PailleretsGustave Roussy, Université Paris-Saclay, Département de Biopathologie et INSERM U1186, Villejuif, France.
Dominique VaurDépartement de Biopathologie, Centre François Baclesse, Caen, France.
Hagay SobolInstitut Paoli Calmette, Département d'Anticipation et de Suivi des Cancers, Oncogénétique, Faculté de Médecine, Université d'Aix-Marseille, Marseille, France.
Catherine NoguèsInstitut Paoli Calmette, Département d'Anticipation et de Suivi des Cancers, Oncogénétique, Faculté de Médecine, Université d'Aix-Marseille, Marseille, France.
Michel LongyBiopathologie, Institut Bergonié, Bordeaux, France.
Isabelle MortemousqueService de Génétique, Hôpital Bretonneau, Tours, France.
Sandra Fert-FerrerService de Génétique, Centre Hospitalier de Chambéry, Chambéry, France.
Emmanuelle Mouret-FourmeService de Génétique, Institut Curie, Paris, France.
Pascal PujolService de Génétique Médicale et Oncogénétique, Hôpital Arnaud de Villeneuve, CHU Montpellier, INSERM 896, CRCM Val d'Aurelle, Montpellier, France.
Laurence Venat-BouvetService d'Oncologie Médicale, Hôpital Universitaire Dupuytren, Limoges, France.
Yves-Jean BignonUniversité Clermont Auvergne, INSERM, U1240, Centre Jean Perrin, Clermont-Ferrand, France.
Dominique LerouxDépartement de Génétique, CHU de Grenoble, Hôpital Couple-Enfant, Grenoble, France.
Isabelle CoupierService de Génétique Médicale et Oncogénétique, Hôpital Arnaud de Villeneuve, CHU Montpellier, INSERM 896, CRCM Val d'Aurelle, Montpellier, France.
Pascaline BerthetDépartement de Biopathologie, Centre François Baclesse, Caen, France.
Véronique MariUnité d'Oncogénétique, Centre Antoine Lacassagne, Nice, France.
Capucine DelnatteUnité d'Oncogénétique, Centre René Gauducheau, Nantes, France.
Paul GestaService d'Oncogénétique Régional Poitou-Charentes, Niort, France.
Marie-Agnès Collonge-RameService Génétique et Biologie du Développement-Histologie, CHU Hôpital Saint-Jacques, Besançon, France.
Sophie GiraudHospices Civils de Lyon, Groupement Hospitalier EST, Bron, France.
Valérie BonadonaUniversité Claude Bernard Lyon 1, Villeurbanne, France.
Amandine BaurandInstitut GIMI, CHU de Dijon et Centre de Lutte contre le Cancer Georges François Leclerc, Dijon, France.
Laurence FaivreInstitut GIMI, CHU de Dijon et Centre de Lutte contre le Cancer Georges François Leclerc, Dijon, France.
Bruno BuecherService de Génétique, Institut Curie, Paris, France.
Christine LassetUniversité Claude Bernard Lyon 1, Villeurbanne, France.
Marion Gauthier-VillarsService de Génétique, Institut Curie, Paris, France.
Francesca DamiolaBiopathologie, Centre Léon Bérard, Lyon, France.
Sylvie MazoyerINSERM, U1028, CNRS, UMR5292, Centre de Recherche en Neurosciences de Lyon, Lyon, France.
Sandrine M CaputoService de Génétique, Institut Curie, Paris, France.
Nadine AndrieuINSERM, U900, Institut Curie, PSL Research University, Mines ParisTech, Paris, France.
Dominique Stoppa-LyonnetService de Génétique, Institut Curie, Paris, France.
GEMO Study Collaborators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

BRCA1/2 mutation carriersbreast cancerDNA bankinggenetic epidemiologypathogenic variant (PV)

Identifiers

PMID30430080
PMCPMC6220051

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.