Cathérine Heijmans

3.3k total citations
25 papers, 305 citations indexed

About

Cathérine Heijmans is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Cathérine Heijmans has authored 25 papers receiving a total of 305 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 16 papers in Hematology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Cathérine Heijmans's work include Hemoglobinopathies and Related Disorders (17 papers), Iron Metabolism and Disorders (14 papers) and Prenatal Screening and Diagnostics (5 papers). Cathérine Heijmans is often cited by papers focused on Hemoglobinopathies and Related Disorders (17 papers), Iron Metabolism and Disorders (14 papers) and Prenatal Screening and Diagnostics (5 papers). Cathérine Heijmans collaborates with scholars based in Belgium, Democratic Republic of the Congo and United States. Cathérine Heijmans's co-authors include Alina Ferster, Phu-Quoc Lê, Laurence Dedeken, Sophie Huybrechts, Christine Devalck, Laurence Rozen, Anna Vanderfaeillie, Béatrice Gulbis, André Efira and Marie‐Françoise Dresse and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Cathérine Heijmans

24 papers receiving 300 citations

Peers

Cathérine Heijmans
Elineema Meda Tanzania
Cathérine Heijmans
Citations per year, relative to Cathérine Heijmans Cathérine Heijmans (= 1×) peers Elineema Meda

Countries citing papers authored by Cathérine Heijmans

Since Specialization
Citations

This map shows the geographic impact of Cathérine Heijmans's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Cathérine Heijmans with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cathérine Heijmans more than expected).

Fields of papers citing papers by Cathérine Heijmans

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cathérine Heijmans. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Cathérine Heijmans. The network helps show where Cathérine Heijmans may publish in the future.

Co-authorship network of co-authors of Cathérine Heijmans

This figure shows the co-authorship network connecting the top 25 collaborators of Cathérine Heijmans. A scholar is included among the top collaborators of Cathérine Heijmans based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Cathérine Heijmans. Cathérine Heijmans is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Mercier, Nathalie, et al.. (2024). A new case of sodium‐dependent multivitamin transporter defect occurring as a life‐threatening condition responsive to early vitamin supplementation and literature review. Molecular Genetics & Genomic Medicine. 12(2). e2388–e2388. 4 indexed citations
2.
Gulbis, Béatrice, Fleur Samantha Benghiat, Bénédicte Brichard, et al.. (2021). Factors Influencing Change in MCV and Age at Transplantation in the Belgian Sickle Cell Disease Registry. Blood. 138(Supplement 1). 4171–4171. 1 indexed citations
3.
Dedeken, Laurence, et al.. (2019). Successful transition from paediatric to adult care in sickle cell disease. Dépôt institutionnel de l'Université libre de Bruxelles (Université Libre de Bruxelles). 40(6). 495–501. 1 indexed citations
4.
Dedeken, Laurence, Phu-Quoc Lê, Laurence Rozen, et al.. (2018). AutomatedRBCexchange compared to manual exchange transfusion for children with sickle cell disease is cost‐effective and reduces iron overload. Transfusion. 58(6). 1356–1362. 20 indexed citations
5.
Lê, Phu-Quoc, Alina Ferster, Laurence Dedeken, et al.. (2017). Neonatal screening improves sickle cell disease clinical outcome in Belgium. Journal of Medical Screening. 25(2). 57–63. 12 indexed citations
6.
Lê, Phu-Quoc, Béatrice Gulbis, Laurence Dedeken, et al.. (2015). Survival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment. Pediatric Blood & Cancer. 62(11). 1956–1961. 122 indexed citations
7.
Blumental, Sophie, M. Lambermont, Cathérine Heijmans, et al.. (2015). First Documented Transmission of Trypanosoma cruzi Infection through Blood Transfusion in a Child with Sickle-Cell Disease in Belgium. PLoS neglected tropical diseases. 9(10). e0003986–e0003986. 16 indexed citations
8.
Dedeken, Laurence, Phu-Quoc Lê, Cathérine Heijmans, et al.. (2014). Reduction of the Six-Minute Walk Distance in Children with Sickle Cell Disease Is Correlated with Silent Infarct: Results from a Cross-Sectional Evaluation in a Single Center in Belgium. PLoS ONE. 9(10). e108922–e108922. 12 indexed citations
9.
Aloni, Michel Ntetani, Phu-Quoc Lê, Cathérine Heijmans, et al.. (2014). A pilot study of manual chronic partial exchange transfusion in children with sickle disease. Hematology. 20(5). 284–288. 5 indexed citations
10.
Dedeken, Laurence, Phu-Quoc Lê, Laurence Rozen, et al.. (2014). Clinical Benefit and Costs’ Evaluation of Erythocytapheresis Compared to Manual Exchange Transfusion for Children with Sickle Cell Disease: A Single Center Experience. Blood. 124(21). 4091–4091. 2 indexed citations
11.
Aloni, Michel Ntetani, Pauline Lecerf, Phu-Quoc Lê, et al.. (2014). Is Pica under-reported in children with sickle cell disease? A pilot study in a Belgian cohort. Hematology. 20(7). 429–432. 10 indexed citations
12.
Rozen, Laurence, Sophie Huybrechts, Laurence Dedeken, et al.. (2013). Transient leukemia in a newborn without Down syndrome: case report and review of the literature. European Journal of Pediatrics. 173(12). 1643–1647. 11 indexed citations
13.
Lê, Phu-Quoc, Laurence Dedeken, Béatrice Gulbis, et al.. (2013). Low Sickle Cell Disease Mortality In Belgium and Benefit From Hydroxyurea Therapy. Blood. 122(21). 2231–2231. 1 indexed citations
14.
Heijmans, Cathérine, et al.. (2012). Les complications respiratoires de la drépanocytose chez les enfants : le syndrome thoracique aigu Respiratory complications of sickle cell anemia in children : the acute chest syndrome. 1 indexed citations
15.
Damry, Nasroolla, et al.. (2011). Unusual clinical manifestation of lymphangiomatosis. SHILAP Revista de lepidopterología. 94(4). 206–206. 1 indexed citations
16.
Goffin, Laurence, Sophie Huybrechts, Cathérine Heijmans, et al.. (2011). Various aspects of Kikuchi disease in three children: systemic or self-limited disease?. Pediatric Rheumatology. 9(S1). 1 indexed citations
17.
Dedeken, Laurence, Phu-Quoc Lê, Nadira Azzi, et al.. (2011). Hematopoietic Stem Cell Transplantation for Sickle Cell Disease in Childhood: A Single Center Experience with 45 Patients. Blood. 118(21). 3103–3103. 2 indexed citations
18.
Aloni, Michel Ntetani, Pauline Lecerf, Cathérine Heijmans, et al.. (2010). Pica In Children with Sickle Cell Disease. Blood. 116(21). 4807–4807.
19.
Lê, Phu-Quoc, Béatrice Gulbis, Christiane Vermylen, et al.. (2010). Possible Dose Adjustment of Hydroxyurea In Young Patients with Sickle Cell Disease and Followed In the Belgian Registry. Blood. 116(21). 4823–4823. 1 indexed citations
20.
Lê, Phu-Quoc, Alina Ferster, Frédéric Cotton, et al.. (2010). Sickle cell disease from Africa to Belgium, from neonatal screening to clinical management.. PubMed. 70(5-6). 467–70. 16 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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