In one paragraphArticle in Genes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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
1 · What the graph read from itWhat 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
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what moneyAuthors and funding
12 authors.
Rabia AkramNeurochemicalbiology and Genetics Laboratory (NGL), Department of Physiology, Faculty of Life Sciences, Government College University, Faisalabad 38000, Pakistan.ORCID 0000-0001-9416-6391 Haseeb AnwarNeurochemicalbiology and Genetics Laboratory (NGL), Department of Physiology, Faculty of Life Sciences, Government College University, Faisalabad 38000, Pakistan.ORCID 0000-0001-8438-9700 Humaira MuzaffarNeurochemicalbiology and Genetics Laboratory (NGL), Department of Physiology, Faculty of Life Sciences, Government College University, Faisalabad 38000, Pakistan.ORCID 0000-0003-2172-8474 Valentina TurchettiDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK.
Tracy LauDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK.ORCID 0000-0003-0514-1729 Barbara VonaInstitute of Human Genetics, University Medical Center Göttingen, 37073 Göttingen, Germany.ORCID 0000-0002-6719-3447 Ehtisham Ul Haq MakhdoomNeurochemicalbiology and Genetics Laboratory (NGL), Department of Physiology, Faculty of Life Sciences, Government College University, Faisalabad 38000, Pakistan.ORCID 0000-0002-4865-6194 Javed IqbalDepartment of Neurology, Allied Hospital, Faisalabad Medical University, Faisalabad 38000, Pakistan.
Shahid Mahmood BaigHuman Molecular Genetics Laboratory, Health Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE) College, Faisalabad 38000, Pakistan.ORCID 0000-0002-0683-5872 Ghulam HussainNeurochemicalbiology and Genetics Laboratory (NGL), Department of Physiology, Faculty of Life Sciences, Government College University, Faisalabad 38000, Pakistan.ORCID 0000-0001-9090-7789 Stephanie EfthymiouDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK.ORCID 0000-0003-4900-9877 Henry HouldenDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK.
Funding
Medical Research Council G0601943Medical Research Council MR/S005021/1The Wellcome Trust, The MRC, The MSA Trust, The National Institute for Health Research University College London Hospitals Biomedical Research Centre NIHR-BRC), The Michael J Fox Foundation (MJFF), The Fidelity Trust, Rosetrees Trust, The Dolby Family fun WT093205MA, WT104033AIA; MR/S01165X/1, MR/S005021/1, G0601943Wellcome Trust
6 · The paper itselfAbstract
PubMed holds no abstract for this paper.
Indexed as
ConsanguinityMyelin-Associated GlycoproteinPedigreeSpastic Paraplegia, HereditaryExome SequencingHomozygoteHumansMutationPakistanMyelin-Associated Glycoproteincerebellar ataxiaMAGPakistanspastic paraplegiaSPG75
Identifiers
PMID39336794
PMCPMC11431006
What OpenQuestion holds
Textmetadata
LicenceCC BY
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