Vincent Barlogis

6.2k total citations
53 papers, 1.3k citations indexed

About

Vincent Barlogis is a scholar working on Immunology, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Vincent Barlogis has authored 53 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Immunology, 22 papers in Hematology and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Vincent Barlogis's work include Immunodeficiency and Autoimmune Disorders (16 papers), Hematopoietic Stem Cell Transplantation (12 papers) and Acute Lymphoblastic Leukemia research (12 papers). Vincent Barlogis is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (16 papers), Hematopoietic Stem Cell Transplantation (12 papers) and Acute Lymphoblastic Leukemia research (12 papers). Vincent Barlogis collaborates with scholars based in France, United Kingdom and United States. Vincent Barlogis's co-authors include Hérvè Chambost, Alexandre Fabre, Julie Berbis, Audrey Contet, Jean Donadieu, Nicolas Sirvent, Claire Galambrun, Pascal Auquier, Nizar Mahlaoui and Pascal Chastagner and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Experimental Medicine and Blood.

In The Last Decade

Vincent Barlogis

51 papers receiving 1.2k citations

Peers

Vincent Barlogis
Vincent Barlogis
Citations per year, relative to Vincent Barlogis Vincent Barlogis (= 1×) peers Michiko Kajiwara

Countries citing papers authored by Vincent Barlogis

Since Specialization
Citations

This map shows the geographic impact of Vincent Barlogis'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 Vincent Barlogis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vincent Barlogis more than expected).

Fields of papers citing papers by Vincent Barlogis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vincent Barlogis. 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 Vincent Barlogis. The network helps show where Vincent Barlogis may publish in the future.

Co-authorship network of co-authors of Vincent Barlogis

This figure shows the co-authorship network connecting the top 25 collaborators of Vincent Barlogis. A scholar is included among the top collaborators of Vincent Barlogis 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 Vincent Barlogis. Vincent Barlogis 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.
Mahlaoui, Nizar, Hassan Abolhassani, Koen van Aerde, et al.. (2025). Case Report: Activated PI3-kinase-δ syndrome and ovarian malignancies: a case series from the European ESID-APDS registry. Frontiers in Immunology. 16. 1572194–1572194. 1 indexed citations
2.
Ged, Cécile, Audrey Petit, Aïcha Salhi, et al.. (2024). Severe Perinatal Presentations of Günther’s Disease: Series of 20 Cases and Perspectives. Life. 14(1). 130–130. 1 indexed citations
4.
Marin‐Esteban, Viviana, Blandine Beaupain, Vincent Barlogis, et al.. (2021). Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity. Haematologica. 107(3). 765–769. 13 indexed citations
5.
Ducassou, Stéphane, Helder Fernandes, Hélène Savel, et al.. (2020). Prospective Evaluation of the First Option, Second-Line Therapy in Childhood Chronic Immune Thrombocytopenia: Splenectomy or Immunomodulation. The Journal of Pediatrics. 231. 223–230. 1 indexed citations
6.
Caye, Aurélie, Kevin Rouault‐Pierre, Marion Strullu, et al.. (2019). Despite mutation acquisition in hematopoietic stem cells, JMML-propagating cells are not always restricted to this compartment. Leukemia. 34(6). 1658–1668. 12 indexed citations
7.
Fabre, Alexandre, Tiphanie P. Vogel, Vincent Barlogis, et al.. (2018). STAT3 Gain of Function: A New Kid on the Block in Interstitial Lung Diseases. American Journal of Respiratory and Critical Care Medicine. 197(11). e22–e23. 21 indexed citations
8.
Saultier, Paul, Matthias Canault, Céline Falaise, et al.. (2018). Long-term management of leukocyte adhesion deficiency type III without hematopoietic stem cell transplantation. Haematologica. 103(6). e264–e267. 12 indexed citations
9.
Barlogis, Vincent, Nizar Mahlaoui, Pascal Auquier, et al.. (2017). Burden of Poor Health Conditions and Quality of Life in 656 Children with Primary Immunodeficiency. The Journal of Pediatrics. 194. 211–217.e5. 11 indexed citations
10.
Oudin, Claire, Pascal Auquier, Audrey Contet, et al.. (2015). Metabolic syndrome in adults who received hematopoietic stem cell transplantation for acute childhood leukemia: an LEA study. Bone Marrow Transplantation. 50(11). 1438–1444. 37 indexed citations
11.
Nicollas, R., et al.. (2013). Mastoïdite aiguë atypique révélant une leucémie de Burkitt chez une enfant de 7 mois. Archives de Pédiatrie. 20(12). 1317–1320. 3 indexed citations
12.
Berbis, Julie, Gérard Michel, Pascal Chastagner, et al.. (2013). A French Cohort of Childhood Leukemia Survivors: Impact of Hematopoietic Stem Cell Transplantation on Health Status and Quality of Life. Biology of Blood and Marrow Transplantation. 19(7). 1065–1072. 46 indexed citations
13.
Auquier, Pascal, Vincent Barlogis, Audrey Contet, et al.. (2013). Symptomatic osteonecrosis in childhood leukemia survivors: prevalence, risk factors and impact on quality of life in adulthood. Haematologica. 98(7). 1089–1097. 62 indexed citations
14.
Visentin, Silvia, et al.. (2013). La leishmaniose viscérale infantile, une cause de syndrome d’hémophagocytose lympho-histiocytaire facilement curable. Archives de Pédiatrie. 20(11). 1225–1229. 8 indexed citations
15.
Aladjidi, Nathalie, Raoul Santiago, Corinne Pondarré, et al.. (2012). Revisiting Splenectomy in Childhood Immune Thrombocytopenic Purpura in the Era of New Therapies: The French Experience. Journal of Blood Disorders & Transfusion. s3. 5 indexed citations
16.
Bosdure, E., et al.. (2011). Tuméfactions multiples chez un nouveau-né révélant une botryomycose. Archives de Pédiatrie. 18(2). 183–185. 1 indexed citations
17.
Beauté, Julien, Loïc Le Mignot, Nizar Mahlaoui, et al.. (2010). Epidemiology and Outcome of Invasive Fungal Diseases in Patients With Chronic Granulomatous Disease. The Pediatric Infectious Disease Journal. 30(1). 57–62. 74 indexed citations
18.
Barlogis, Vincent, Claude Lemarié, Claire Galambrun, et al.. (2010). Impact of Viable CD45 Cells Infused on Lymphocyte Subset Recovery after Unrelated Cord Blood Transplantation in Children. Biology of Blood and Marrow Transplantation. 17(1). 109–116. 5 indexed citations
19.
Rénard, C., Vincent Barlogis, Valérie Mialou, et al.. (2010). Lymphocyte subset reconstitution after unrelated cord blood or bone marrow transplantation in children. British Journal of Haematology. 152(3). 322–330. 55 indexed citations
20.
Moreau, Thomas, Boris Calmels, Vincent Barlogis, et al.. (2007). Potential Application of Gene Therapy to X-Linked Agammaglobulinemia. Current Gene Therapy. 7(4). 284–294. 10 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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