ArticleHaematologica2018
Natural history of GATA2 deficiency in a survey of 79 French and Belgian patients.
Open access · goldAbstract readMulticenter Study
In one paragraph
Article in Haematologica, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 110 papers, 3 of them syntheses that pooled it.
0numbers the graph read from it
0cells of the map it votes in
110citing papers in PubMed, 3 pooled it
7.5field-weighted citation impact, top 2% of its field
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
110 citing papers in PubMed, 3 syntheses or guidelines pooled it, 174 citations in OpenAlex.
- Prognostic significance of GATA2 in patients with MDS/AML: a systematic review and meta-analysis.Annals of hematology · 2024Pooled it
- GATA2 deficiency and hemophagocytic lymphohistiocytosis (HLH): a systematic review of reported cases.BMC infectious diseases · 2024Pooled it
- Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review.Genetics in medicine : official journal of the American College of Medical Genetics · 2024Pooled it
- Fungal Infections in Disorders of Inborn Errors of Immunity.Clinical reviews in allergy & immunology · 2026Review
- [Clinical characteristics and prognosis of myelodysplastic neoplasms with GATA2 mutations].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2026Article
- Hemophagocytic Lymphohistiocytosis Triggered byClinical case reports · 2026Article
- Review
- GATA2 Deficiency Syndrome: A Case Series and Literature Review.Journal of clinical immunology · 2026Review
- Common cutaneous signs unmasking a severe hematological disorder: GATA2 deficiency.Dermatology online journal · 2026Article
- Myelodysplastic syndrome progress to acute myeloid leukemia: new insights and updates.Frontiers in immunology · 2026Review
- Long-term outcome after allogeneic stem cell transplantation for GATA2 deficiency: An analysis of 67 adults and children from France and Belgium.British journal of haematology · 2026Article
- Co-occurrence of GATA2 deficiency and probable constitutional mosaic STAG2 alteration in a young adult with myelodysplastic syndrome: a case report.Frontiers in medicine · 2026Article
- Article
- Human iPSCs-based modeling unveils SETBP1 as a driver of chromatin rewiring in GATA2 deficiency.Nature communications · 2025Article
- GATA2 Mediates Macrophage Proliferation During Atherosclerosis.Journal of the American Heart Association · 2025Article
- Whole-Genome Sequencing Reveals a NovelCancers · 2025Article
- GATA2 mutation is associated with immune dysfunction and increased Mycobacterium haemophilum susceptibility in immunocompromised individuals.JCI insight · 2025Article
- Germline and somatic genetic landscape of pediatric myelodysplastic syndromes.Haematologica · 2025Review
- Acquired Bernard-Soulier syndrome as the presenting feature of GATA2-related myeloid neoplasm in an adolescent: an insight into the mechanisms underlying the platelet defect.Haematologica · 2025Article
- Age-dependent phenotypic and molecular evolution of pediatric MDS arising from GATA2 deficiency.Blood cancer journal · 2025Article
50 more citing papers are in PubMed but not listed here.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
33 authors at 18 institutions in 3 countries.
Jean DonadieuDepartment of Paediatric Haematology and Oncology, Registre National des Neutropénies Chroniques, AP-HP Trousseau Hospital, Paris, France.
Marie LamantDepartment of Paediatric Haematology and Immunology, CHU Toulouse, France.
Claire FieschiDepartment of Clinical Immunology Assistance Publique - Hôpitaux de Paris (AP-HP) Saint-Louis Hospital, France.
Flore Sicre de FontbruneDepartment of Haematology and Bone Marrow Transplantation, AP-HP Saint-Louis Hospital, Paris, France.
Aurélie CayeGenetic Laboratory, AP-HP Robert Debré Hospital, Paris, France.
Marie OuacheeDepartment of Haematology, AP-HP Robert Debré Hospital, Paris, France.
Blandine BeaupainFrench Neutropenia Registry, AP-HP Trousseau Hospital, Paris, France.
Jacinta BustamanteLaboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR 1163, Necker-Enfants Malades Hospital, Paris, France.
Hélène A PoirelCentre for Human Genetics, Cliniques Universitaires Saint-Luc & Human Molecular Genetics (GEHU), de Duve Institute -Université Catholique de Louvain, Brussels, Belgium.
Bertrand IsidorDepartment of Genetics, CHU Nantes, France.
Eric Van Den NesteDepartment of Haematology, St Luc Hospital, Brussels, Belgium.
Antoine NeelDepartment of Internal Medicine, CHU Nantes, France.
Stanislas NimubonaDepartment of Haematology, CHU de Rennes, France.
Fabienne ToutainDepartment of Paediatric Haematology and Oncology, CHU de Rennes, France.
Vincent BarlogisDepartment of Paediatric Haematology, CHU de Marseille, Hopital La Timone, Université Aix-Marseille, France.
Nicolas SchleinitzInternal Medicine, CHU de Marseille, Hopital La Timone, Université Aix-Marseille, France.
Thierry LeblancDepartment of Haematology, AP-HP Robert Debré Hospital, Paris, France.
Pierre RohrlichDepartment of Haematology, CHU de Besançon, France.
Felipe SuarezDepartment of Haematology, AP-HP Necker-Enfants Malades, INSERM UMR 1163 and CNRS ERL 8254 Institut Imagine, Sorbonne Paris Cité, Université Paris Descartes, France.
Dana RantaDepartment of Haematology, CHU de Nancy, France.
Wadih Abou ChahlaDepartment of Paediatric Haematology, CHU de Lille, France.
Bénédicte BrunoDepartment of Paediatric Haematology, CHU de Lille, France.
Louis TerriouDepartment of Internal Medicine and Immunology, CHU Lille, France.
Sylvie FrancoisDepartment of Haematology, CHU d'Angers, France.
Bruno LioureDepartment of Haematology, CHU de Strasbourg, France.
Guido AhleDepartment of Neurology, Hôpitaux Civils de Colmar, France.
Françoise BachelerieInflammation Chimiokines et Immunopathologie, INSERM, Faculté de Médecine, Université Paris-Sud, Université Paris-Saclay, Clamart, France.
Claude PreudhommeLaboratory of Haematology, CHU de Lille, France.
Eric DelabesseLaboratory of Haematology, IUCT-Oncopole, Toulouse, France.
Hélène CaveGenetic Laboratory, AP-HP Robert Debré Hospital, Paris, France.
Christine Bellanné-ChantelotDepartment of Genetics, AP-HP Pitié Salpêtrière Hospital, Faculté de Médecine Sorbonne Université, Paris, France.
Marlène PasquetDepartment of Paediatric Haematology and Immunology, CHU Toulouse, France pasquet.m@chu-toulouse.fr.
French GATA2 study group
Assistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Universitaire de Lille · FRCentre Hospitalier Universitaire de Rennes · FRHôpital Armand-Trousseau · FRHôpital de la Timone · FRHôpital Robert-Debré · FRUniversité Paris Cité · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Toulouse · FRCliniques Universitaires Saint-Luc · BEHôpital Saint-Louis · FRHopitaux Civils de Colmar · FRInserm · FRInstitut universitaire du cancer de Toulouse Oncopole · FRUniversité Paris-Saclay · FR
Funding
No grant is acknowledged in the PubMed record.
Abstract
Heterozygous germline
Indexed as
Germ-Line MutationYoung AdultAdolescentAdultBelgiumChildChild, PreschoolFranceGATA2 DeficiencyHematologic NeoplasmsHematopoietic Stem Cell TransplantationHumansInfantInfant, NewbornInfectionsMiddle Aged
Identifiers
What OpenQuestion holds
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Read underepoch 390
Registered trials
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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.