Marie Meeths

1.9k total citations
22 papers, 730 citations indexed

About

Marie Meeths is a scholar working on Hematology, Immunology and Infectious Diseases. According to data from OpenAlex, Marie Meeths has authored 22 papers receiving a total of 730 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Hematology, 19 papers in Immunology and 7 papers in Infectious Diseases. Recurrent topics in Marie Meeths's work include Autoimmune and Inflammatory Disorders Research (21 papers), Immune Cell Function and Interaction (18 papers) and Parvovirus B19 Infection Studies (7 papers). Marie Meeths is often cited by papers focused on Autoimmune and Inflammatory Disorders Research (21 papers), Immune Cell Function and Interaction (18 papers) and Parvovirus B19 Infection Studies (7 papers). Marie Meeths collaborates with scholars based in Sweden, Norway and Denmark. Marie Meeths's co-authors include Jan‐Inge Henter, Yenan T. Bryceson, Samuel C. C. Chiang, Magnus Nordenskjöld, Stephanie M. Wood, AnnaCarin Horne, Carsten Heilmann, Henrik Hasle, Bianca Tesi and Magnus Sabel 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

Marie Meeths

22 papers receiving 725 citations

Peers

Marie Meeths

IMMUN

HEMAT

ONCOL

Marjorie Côte France

Eva Rudd Sweden

Satoshi Ikushima Japan

Yunze Zhao China

Catherine Schaffner United Kingdom

Stéphanie Rigaud United States

Osamu Tatsuzawa Japan

Juliette M. Lefebvre United States

Stefania Martini Italy

Christina Trambas Australia

Marjorie Côte France

Marie Meeths

336 ×0.7

IMMUN

308 ×0.7

HEMAT

175 ×0.7

56 ×0.7

21 ×0.3

ONCOL

Citations per year, relative to Marie Meeths Marie Meeths (= 1×) peers Marjorie Côte

Countries citing papers authored by Marie Meeths

Since Specialization

Citations

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

Fields of papers citing papers by Marie Meeths

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marie Meeths

This figure shows the co-authorship network connecting the top 25 collaborators of Marie Meeths. A scholar is included among the top collaborators of Marie Meeths 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 Marie Meeths. Marie Meeths is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Sekine, Takuya, et al.. (2024). CD8+ T Cell Biology in Cytokine Storm Syndromes. Advances in experimental medicine and biology. 1448. 129–144. 2 indexed citations

Jädersten, Martin, et al.. (2023). Malignancy-associated hemophagocytic lymphohistiocytosis in Sweden: incidence, clinical characteristics, and survival. Blood. 143(3). 233–242. 15 indexed citations

Horne, AnnaCarin, Tatiana von Bahr Greenwood, Samuel C. C. Chiang, et al.. (2021). Efficacy of Moderately Dosed Etoposide in Macrophage Activation Syndrome–Hemophagocytic Lymphohistiocytosis. The Journal of Rheumatology. 48(10). 1596–1602. 29 indexed citations

Meeths, Marie & Yenan T. Bryceson. (2021). Genetics and pathophysiology of haemophagocytic lymphohistiocytosis. Acta Paediatrica. 110(11). 2903–2911. 15 indexed citations

Ahlm, Clas, Bianca Tesi, Ingvar A. Bergdahl, et al.. (2019). Haploinsufficiency of UNC13D increases the risk of lymphoma. Cancer. 125(11). 1848–1854. 10 indexed citations

Tesi, Bianca, Peter Priftakis, Fredrik Lindgren, et al.. (2016). Successful Hematopoietic Stem Cell Transplantation in a Patient with LPS-Responsive Beige-Like Anchor (LRBA) Gene Mutation. Journal of Clinical Immunology. 36(5). 480–489. 28 indexed citations

Chiang, Samuel C. C., et al.. (2015). Cancer risk in relatives of patients with a primary disorder of lymphocyte cytotoxicity: a retrospective cohort study. The Lancet Haematology. 2(12). e536–e542. 23 indexed citations

Tesi, Bianca, Samuel C. C. Chiang, Dalia El‐Ghoneimy, et al.. (2015). Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense Mutations. Pediatric Blood & Cancer. 62(12). 2094–2100. 30 indexed citations

Meeths, Marie, et al.. (2014). Pathophysiology and spectrum of diseases caused by defects in lymphocyte cytotoxicity. Experimental Cell Research. 325(1). 10–17. 28 indexed citations

10.

Chiang, Samuel C. C., Marie Meeths, Bianca Tesi, et al.. (2014). An N-Terminal Missense Mutation in STX11 Causative of FHL4 Abrogates Syntaxin-11 Binding to Munc18-2. Frontiers in Immunology. 4. 515–515. 17 indexed citations

11.

Meeths, Marie, AnnaCarin Horne, Magnus Sabel, Yenan T. Bryceson, & Jan‐Inge Henter. (2014). Incidence and clinical presentation of primary hemophagocytic lymphohistiocytosis in Sweden. Pediatric Blood & Cancer. 62(2). 346–352. 60 indexed citations

12.

Cichocki, Frank, Heinrich Schlums, Hongchuan Li, et al.. (2014). Transcriptional regulation of Munc13-4 expression in cytotoxic lymphocytes is disrupted by an intronic mutation associated with a primary immunodeficiency. The Journal of Experimental Medicine. 211(6). 1079–1091. 29 indexed citations

13.

Hussein, Ayad Ahmed, Maher A. Sughayer, Rula Amarin, et al.. (2014). Hematopoietic stem cell transplantation of an adolescent with neurological manifestations of homozygous missense PRF1 mutation. Pediatric Blood & Cancer. 61(12). 2313–2315. 5 indexed citations

14.

Machaczka, Maciej, Monika Klimkowska, Samuel C. C. Chiang, et al.. (2012). Development of classical Hodgkin's lymphoma in an adult with biallelic STXBP2 mutations. Haematologica. 98(5). 760–764. 26 indexed citations

15.

Sieni, Elena, Valentina Cetica, Alessandra Santoro, et al.. (2011). Genotype–phenotype study of familial haemophagocytic lymphohistiocytosis type 3. Journal of Medical Genetics. 48(5). 343–352. 75 indexed citations

16.

Weitzman, Sheila, Stephanie M. Wood, Deepak Bansal, et al.. (2010). Unusual functional manifestations of a novel STX11 frameshift mutation in two infants with familial hemophagocytic lymphohistiocytosis type 4 (FHL4). Pediatric Blood & Cancer. 56(4). 654–657. 9 indexed citations

17.

Meeths, Marie, Miriam Entesarian, Waleed Al–Herz, et al.. (2010). Spectrum of clinical presentations in familial hemophagocytic lymphohistiocytosis type 5 patients with mutations in STXBP2. Blood. 116(15). 2635–2643. 89 indexed citations

18.

Meeths, Marie, Yenan T. Bryceson, Eva Rudd, et al.. (2009). Clinical presentation of Griscelli syndrome type 2 and spectrum of RAB27A mutations. Pediatric Blood & Cancer. 54(4). 563–572. 68 indexed citations

19.

Wood, Stephanie M., Marie Meeths, Samuel C. C. Chiang, et al.. (2009). Different NK cell–activating receptors preferentially recruit Rab27a or Munc13-4 to perforin-containing granules for cytotoxicity. Blood. 114(19). 4117–4127. 80 indexed citations

20.

Beutel, Karin, Marie Meeths, Niels Carlsen, et al.. (2008). Treatment of the X‐linked lymphoproliferative, Griscelli and Chédiak–Higashi syndromes by HLH directed therapy. Pediatric Blood & Cancer. 52(2). 268–272. 21 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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