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Author Details

Chris Van Geet
1989
148
36
PMIDPaper TitleJournal TitlePublished Year
36790527Ribosome dysfunction underlies SLFN14-related thrombocytopenia.Blood2023
37601858Hydroxyurea treatment for adult sickle cell anemia patients in Kinshasa.EJHaem2023
37014748Clinical and biological profile of Sickle Cell Anemia children in a rural area in Central Africa.Hematology2023
36696193Clinical application of multigene panel testing for bleeding, thrombotic, and platelet disorders: a 3-year Belgian experience.J Thromb Haemost2023
36799251Monitoring of SARS-CoV-2 concentration and circulation of variants of concern in wastewater of Leuven, Belgium.2023
36525434Clinical and laboratory characterization of adult sickle cell anemia patients in Kinshasa.PLoS One2022
35971883Methylome analysis for haemophilia A intron 22 inversion patients with and without inhibitors: A pilot study.Haemophilia2022
35819088Value of DNA testing in the diagnosis of sickle-cell anemia in childhood in an environment with a high prevalence of other causes of anemia.J Clin Lab Anal2022
36067238Urban rats as carriers of invasive Salmonella Typhimurium sequence type 313, Kisangani, Democratic Republic of Congo.PLoS Neglected Tropical Diseases2022
34476343The EHA Research Roadmap: Platelet Disorders.Hemasphere2021
34348454Combined transcriptome and proteome profiling of SRC kinase activity in healthy and E527K defective megakaryocytes.Haematologica2021
33075815Unravelling the disease mechanism for TSPYL1 deficiency.Hum Mol Genet2020
32166874Bortezomib for autoimmune hemolytic anemia after intestinal transplantation.Pediatric Transplantation2020
33079472Clinical 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.J Thromb Haemost2020
31240161A novel missense variant in <i>SLC18A2</i> causes recessive brain monoamine vesicular transport disease and absent serotonin in platelets.JIMD Rep2019
31624776Blood platelet research in autism spectrum disorders: In search of biomarkers.Res Pract Thromb Haemost2019
30467204Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopenia.Haematologica2019
31204551De novo variant in tyrosine kinase SRC causes thrombocytopenia: case report of a second family.Platelets2019
29391254Abnormal differentiation of B cells and megakaryocytes in patients with Roifman syndrome.J Allergy Clin Immunol2018
30194525Renal Replacement Therapy in children with severe developmental disability: guiding questions for decision-making.Eur J Pediatr2018
278660143D Multi-segment foot kinematics in children: A developmental study in typically developing boys.2017
28637664Expanded repertoire of <i>RASGRP2</i> variants responsible for platelet dysfunction and severe bleeding.Blood2017
28545593PIGO deficiency: palmoplantar keratoderma and novel mutations.Orphanet J Rare Dis2017
28895773GATA1 gene variants associated with thrombocytopenia and anemia.Platelets2017
28759637Pituitary adenylate cyclase-activating polypeptide (PACAP) in zebrafish models of nephrotic syndrome.PLoS One2017
28540435Validation of the Child HCAHPS survey to measure pediatric inpatient experience of care in Flanders.European Journal of Pediatrics2017
28082341The transcription factor GATA1 regulates NBEAL2 expression through a long-distance enhancer.Haematologica2017
27757173Methylome analysis for spina bifida shows <i>SOX18</i> hypomethylation as a risk factor with evidence for a complex (epi)genetic interplay to affect neural tube development.Clin Epigenetics2016
27251128Severe anaemia associated with Plasmodium falciparum infection in children: consequences for additional blood sampling for research.Malaria Journal2016
27286886Microbiological, clinical and molecular findings of non-typhoidal Salmonella bloodstream infections associated with malaria, Oriental Province, Democratic Republic of the Congo.BMC Infectious Diseases2016
27050435Distribution and Function of PACAP and Its Receptors in the Healthy and Nephrotic Kidney.Nephron2016
26912466A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss.Blood2016
27084890A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.Blood2016
26819647Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects.Clin Epigenetics2016
26936507A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies.Sci Transl Med2016
26267676Platelet abnormalities in nephrotic syndrome.Pediatr Nephrol2016
26449951Invasive Salmonella Infections at Multiple Surveillance Sites in the Democratic Republic of the Congo, 2011-2014.Clin Infect Dis2015
25931131Staphylococcus aureus nasal carriage among healthcare workers in Kisangani, the Democratic Republic of the Congo.European Journal of Clinical Microbiology and Infectious Diseases2015
25565354DNA methylation analysis of Homeobox genes implicates HOXB7 hypomethylation as risk factor for neural tube defects.Epigenetics2015
25949529Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders.Genome Med2015
25758343Pituitary adenylate cyclase-activating polypeptide deficiency associated with increased platelet count and aggregability in nephrotic syndrome.J Thromb Haemost2015
26349489Nutri-epigenomic Studies Related to Neural Tube Defects: Does Folate Affect Neural Tube Closure Via Changes in DNA Methylation?Mini Rev Med Chem2015
26500752Platelet studies in autism spectrum disorder patients and first-degree relatives.Mol Autism2015
24551225Frequency of severe malaria and invasive bacterial infections among children admitted to a rural hospital in Burkina Faso.PLoS ONE2014
25258084Transcriptional diversity during lineage commitment of human blood progenitors.Science2014
24390128Clinical practice: immune thrombocytopenia in paediatrics.European Journal of Pediatrics2014
23975545Epidemic increase in Salmonella bloodstream infection in children, Bwamanda, the Democratic Republic of Congo.Eur J Clin Microbiol Infect Dis2014
24186861MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.Hum Mutat2014
23971719Novel GATA1 mutation in residue D218 leads to macrothrombocytopenia and clinical bleeding problems.Platelets2014
24418119Accuracy of PfHRP2 versus Pf-pLDH antigen detection by malaria rapid diagnostic tests in hospitalized children in a seasonal hyperendemic malaria transmission area in Burkina Faso.Malaria Journal2014
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