ArticleBlood advances2018
Phenotype description and response to thrombopoietin receptor agonist in
Abstract readCase Reports
In one paragraph
Article in Blood advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.
0numbers the graph read from it
0cells of the map it votes in
21citing 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.
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.
Who cites it
21 citing papers in PubMed.
- Eltrombopag for the treatment of inherited thrombocytopenias: a phase II clinical trial.Haematologica · 2020Trial
- Thrombopoietin receptor agonists in inherited thrombocytopenias: an evolving mosaic of evidence.Research and practice in thrombosis and haemostasis · 2026Article
- Bleeding Disorders in Children With Genetic Diseases: A Narrative Review.Acta paediatrica (Oslo, Norway : 1992) · 2026Review
- Negative cooperativity regulates ligand activation of DIAPH1 and other diaphanous related formins.Communications biology · 2025Article
- Genetics of inherited thrombocytopenias.Blood · 2022Review
- Treatment of inherited thrombocytopenias.Haematologica · 2022Review
- Review
- Human deafness-associated variants alter the dynamics of key molecules in hair cell stereocilia F-actin cores.Human genetics · 2022Review
- Late-onset hearing loss case associated with a heterozygous truncating variant of DIAPH1.Clinical genetics · 2022Article
- Expanding the genetic spectrum of TUBB1-related thrombocytopenia.Blood advances · 2021Article
- Formins in Human Disease.Cells · 2021Review
- Variable Autoinhibition among Deafness-Associated Variants of Diaphanous 1 (DIAPH1).Biochemistry · 2021Article
- Inherited Platelet Disorders: An Updated Overview.International journal of molecular sciences · 2021Review
- Role of Thrombopoietin Receptor Agonists in Inherited Thrombocytopenia.International journal of molecular sciences · 2021Review
- Clinical management, ethics and informed consent related to multi-gene panel-based high throughput sequencing testing for platelet disorders: Communication from the SSC of the ISTH.Journal of thrombosis and haemostasis : JTH · 2020Article
- Inherited thrombocytopenias: history, advances and perspectives.Haematologica · 2020Review
- The integrity of cochlear hair cells is established and maintained through the localization of Dia1 at apical junctional complexes and stereocilia.Cell death & disease · 2020Article
- Article
- Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders.Blood · 2019Article
- Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
20 authors.
Sarah K WestburySchool of Cellular and Molecular Medicine and.ORCID 0000-0002-0950-8148
Kate DownesNIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom.
Claire BurneyUniversity Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom.
Maria L LozanoServicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, IMIB-Arrixaca, CIBERER-U765, Murcia, Spain.
Samya G ObajiDepartment of Haematology, School of Medicine, Cardiff University, Cardiff, United Kingdom.
Cheng Hock TohRoald Dahl Haemostasis and Thrombosis Centre, Royal Liverpool University Hospital, Liverpool, United Kingdom.
Teresa SevivasServiço de Sangue, Medicina Transfusional e Imunohemoterapia do Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
Neil V MorganInstitute of Cardiovascular Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
Wendy N ErberNIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom.
Carly KempsterDepartment of Haematology, University of Cambridge, Cambridge Biomedical Campus, Cambridge, United Kingdom.
Samantha F MooreSchool of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, United Kingdom.
Chantal ThysDepartment of Cardiovascular Sciences, Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium.
Sofia PapadiaNIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom.ORCID 0000-0002-9222-3812
Willem H OuwehandNIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom.
NIHR BioResource–Rare Diseases
Michael A LaffanNIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom.
Keith GomezNIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom.ORCID 0000-0002-8934-0700
Kathleen FresonNIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom.
Jose RiveraServicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, IMIB-Arrixaca, CIBERER-U765, Murcia, Spain.
Andrew D MumfordSchool of Cellular and Molecular Medicine and.
Funding
British Heart Foundation FS/16/20/32005British Heart Foundation PG/13/36/30275British Heart Foundation PG/16/3/31833Medical Research Council MR/J011711/1Medical Research Council MR/K023489/1Wellcome Trust
Abstract
PubMed holds no abstract for this paper.
Indexed as
Genetic Association StudiesPhenotypeAdaptor Proteins, Signal TransducingAdolescentAdultAgedBiomarkersChildChild, PreschoolFemaleForminsHumansMaleMiddle AgedPedigreeReceptors, ThrombopoietinAdaptor Proteins, Signal TransducingBiomarkersDIAPH1 protein, humanForminsReceptors, Thrombopoietin
Identifiers
What OpenQuestion holds
Textmetadata
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.