ArticleEuropean journal of human genetics : EJHG2023
Reply to Letter by Tellier et al., 'Scientific refutation of ESHG statement on embryo selection'.
Francesca Forzano, Olga Antonova, Angus Clarke, Guido de Wert, Sabine Hentze, Yalda Jamshidi, Yves Moreau, Markus Perola, Inga Prokopenko, Andrew Read and 6 more
Erratum issuedAbstract readLetterComment
In one paragraphArticle in European journal of human genetics : EJHG, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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
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 registryThe 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 literatureWho cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
5 · Who and what moneyAuthors and funding
16 authors.
Francesca ForzanoClinical Genetics Department, Guy's and St Thomas NHS Foundation Trust, London, UK. francesca.forzano@nhs.net.ORCID 0000-0001-5632-0052 Angus ClarkeDivision of Cancer and Genetics, School of Medicine, Cardiff University, Cardiff, Wales, UK.ORCID 0000-0002-1200-9286 Sabine HentzePractice for Human Genetics, Heidelberg, Germany.
Yalda JamshidiGenetics Research Centre, Molecular and Clinical Sciences Institute, St George's University of London, London, UK.ORCID 0000-0003-0151-6482 Yves MoreauUniversity of Leuven ESAT-STADIUS, B-3001, Leuven, Belgium.
Markus PerolaFinnish Institute for Health and Welfare (THL), Biomedicum 1, Haartmaninkatu 8, 00290, Helsinki, Finland.
Inga ProkopenkoDepartment of Clinical & Experimental Medicine, University of Surrey, Guildford, UK.
Andrew ReadCentre for Genomic Medicine, St Mary's Hospital, M13 0JH, Manchester, England.
Alexandre ReymondCenter for Integrative Genomics, University of Lausanne, CH- 1015, Lausanne, Switzerland.ORCID 0000-0003-1030-8327 Vigdis StefansdottirDepartment of Genetics and Molecular Medicine, Landspitali University Hospital, Reykjavik, Iceland.ORCID 0000-0003-4451-3126 Carla van ElSection Community Genetics, Department of Clinical Genetics and Amsterdam Public Health Research Institute, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0003-2201-2320 Maurizio GenuardiUOC Genetica Medica, Dipartimento di Scienze di Laboratorio e Infettivologiche, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.ORCID 0000-0002-7410-8351 Executive Committee of the European Society of Human Genetics
Public and Professional Policy Committee of the European Society of Human Genetics
Funding
No grant is acknowledged in the PubMed record.
6 · The paper itselfAbstract
PubMed holds no abstract for this paper.
Identifiers
PMID36450798
PMCPMC9995443
What OpenQuestion holds
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