Brigitte Strahm

6.6k total citations
78 papers, 1.7k citations indexed

About

Brigitte Strahm is a scholar working on Hematology, Immunology and Molecular Biology. According to data from OpenAlex, Brigitte Strahm has authored 78 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Hematology, 23 papers in Immunology and 20 papers in Molecular Biology. Recurrent topics in Brigitte Strahm's work include Hematopoietic Stem Cell Transplantation (27 papers), Acute Myeloid Leukemia Research (26 papers) and Immunodeficiency and Autoimmune Disorders (13 papers). Brigitte Strahm is often cited by papers focused on Hematopoietic Stem Cell Transplantation (27 papers), Acute Myeloid Leukemia Research (26 papers) and Immunodeficiency and Autoimmune Disorders (13 papers). Brigitte Strahm collaborates with scholars based in Germany, Italy and Switzerland. Brigitte Strahm's co-authors include David Malkin, Franco Locatelli, Charlotte M. Niemeyer, Bernd Gruhn, Peter Bader, Miriam Erlacher, Carsten Speckmann, Bernhard Kremens, Thomas Vraetz and Friedhelm Hildebrandt and has published in prestigious journals such as Blood, The Journal of Immunology and Cochrane Database of Systematic Reviews.

In The Last Decade

Brigitte Strahm

74 papers receiving 1.6k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Brigitte Strahm Germany 24 835 499 439 311 200 78 1.7k
Masue Imaizumi Japan 25 818 1.0× 886 1.8× 423 1.0× 220 0.7× 357 1.8× 101 2.0k
Gabriele Strauß Germany 17 636 0.8× 249 0.5× 200 0.5× 302 1.0× 158 0.8× 42 1.2k
Miharu Yabe Japan 21 565 0.7× 509 1.0× 235 0.5× 134 0.4× 240 1.2× 84 1.3k
Mirjana Kočova United States 18 436 0.5× 388 0.8× 744 1.7× 506 1.6× 153 0.8× 89 2.5k
Roberto Gastaldi Italy 24 351 0.4× 542 1.1× 138 0.3× 313 1.0× 160 0.8× 73 1.7k
A Okano Japan 17 439 0.5× 283 0.6× 372 0.8× 190 0.6× 229 1.1× 40 1.3k
Rashmi Sood United States 15 739 0.9× 373 0.7× 191 0.4× 113 0.4× 84 0.4× 24 1.3k
Beverly W. Baron United States 20 313 0.4× 502 1.0× 623 1.4× 118 0.4× 140 0.7× 55 1.8k
Enrico Balleari Italy 23 735 0.9× 368 0.7× 439 1.0× 117 0.4× 150 0.8× 71 1.8k
Jean‐Antoine Ribeil France 26 871 1.0× 701 1.4× 277 0.6× 204 0.7× 65 0.3× 79 2.0k

Countries citing papers authored by Brigitte Strahm

Since Specialization
Citations

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

Fields of papers citing papers by Brigitte Strahm

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brigitte Strahm

This figure shows the co-authorship network connecting the top 25 collaborators of Brigitte Strahm. A scholar is included among the top collaborators of Brigitte Strahm 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 Brigitte Strahm. Brigitte Strahm 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.
Weiss, Julia Miriam, Irene González-Menéndez, Geoffroy Andrieux, et al.. (2025). PUMA-induced apoptosis drives bone marrow failure and genomic instability in telomerase-deficient mice. Cell Death and Differentiation. 33(1). 38–50.
2.
Strahm, Brigitte, et al.. (2024). The different faces of GATA2 deficiency: implications for therapy and surveillance. Frontiers in Oncology. 14. 1423856–1423856. 2 indexed citations
3.
Masetti, Riccardo, Francesco Baccelli, Davide Leardini, et al.. (2023). Venetoclax-based therapies in pediatric advanced MDS and relapsed/refractory AML: a multicenter retrospective analysis. Blood Advances. 7(16). 4366–4370. 20 indexed citations
4.
Reinhardt, Dirk, André Baruchel, Henrik Hasle, et al.. (2023). Treatment of Molecular Relapses in Pediatric AML Saves Toxicities Prior to Hematopoietic Stem Cell Transplantation (HSCT) - Results of AMoRe2017 Trial. Blood. 142(Supplement 1). 1521–1521.
5.
Cesaro, Simone, Jean Donadieu, Marco Cipolli, et al.. (2022). Stem Cell Transplantation in Patients Affected by Shwachman-Diamond Syndrome: Expert Consensus and Recommendations From the EBMT Severe Aplastic Anaemia Working Party. Transplantation and Cellular Therapy. 28(10). 637–649. 7 indexed citations
6.
Heredia, Cristina Díaz de, Dorine Bresters, Lawrence Faulkner, et al.. (2021). Recommendations on hematopoietic stem cell transplantation for patients with Diamond–Blackfan anemia. On behalf of the Pediatric Diseases and Severe Aplastic Anemia Working Parties of the EBMT. Bone Marrow Transplantation. 56(12). 2956–2963. 10 indexed citations
7.
Willasch, André, Hermann Kreyenberg, Nona Shayegi, et al.. (2014). Monitoring of Hematopoietic Chimerism after Transplantation for Pediatric Myelodysplastic Syndrome: Real-Time or Conventional Short Tandem Repeat PCR in Peripheral Blood or Bone Marrow?. Biology of Blood and Marrow Transplantation. 20(12). 1918–1925. 27 indexed citations
8.
9.
Yoshimi, Ayami, Brigitte Strahm, Irith Baumann, et al.. (2013). Hematopoietic Stem Cell Transplantation in Children and Young Adults with Secondary Myelodysplastic Syndrome and Acute Myelogenous Leukemia after Aplastic Anemia. Biology of Blood and Marrow Transplantation. 20(3). 425–429. 10 indexed citations
10.
Baumann, In go, Monika Führer, Barbara De Moerloose, et al.. (2011). Immunosuppressive therapy with anti-thymocyte globin and cyclosporine A in patients with refractory cytopenia in childhood. Bone Marrow Transplantation. 46. 1 indexed citations
11.
Bartsch, Ingrid, Kirstin Sandrock, François Lanza, et al.. (2011). Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay. Thrombosis and Haemostasis. 106(9). 475–483. 30 indexed citations
12.
Rohr, Jan, Karin Beutel, Andrea Maul‐Pavicic, et al.. (2010). Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases. Haematologica. 95(12). 2080–2087. 89 indexed citations
13.
Strahm, Brigitte, et al.. (2006). Defibrotide for the treatment of hepatic veno‐occlusive disease in children. Pediatric Blood & Cancer. 48(7). 700–704. 38 indexed citations
14.
Bader, Peter, Charlotte M. Niemeyer, André Willasch, et al.. (2005). Children with myelodysplastic syndrome (MDS) and increasing mixed chimaerism after allogeneic stem cell transplantation have a poor outcome which can be improved by pre‐emptive immunotherapy. British Journal of Haematology. 128(5). 649–658. 28 indexed citations
15.
Yoshimi, Ayami, Charlotte M. Niemeyer, Ulrich Duffner, et al.. (2005). Chimaerism analyses and subsequent immunological intervention after stem cell transplantation in patients with juvenile myelomonocytic leukaemia. British Journal of Haematology. 129(4). 542–549. 32 indexed citations
16.
Dormann, Sabine, et al.. (2004). Life-threatening complications of transient abnormal myelopoiesis in neonates with Down syndrome. European Journal of Pediatrics. 163(7). 374–377. 16 indexed citations
17.
Baumann, Irith, Brigitte Strahm, Eva Bergstraesser, et al.. (2003). Immunosuppressive therapy for children with refractory anemia. mediaTUM (Technical University of Munich). 1 indexed citations
18.
Brandau, Oliver, Volker Schuster, Michael Weiss, et al.. (1999). Epstein--Barr Virus-Negative Boys With Non-Hodgkin Lymphoma Are Mutated in the Sh2D1A Gene, as Are Patients With X-Linked Lymphoproliferative Disease (XLP). Human Molecular Genetics. 8(13). 2407–2413. 81 indexed citations
19.
Vollmer, Martin, et al.. (1998). Two novel mutations of the gene for Kir 1.1 (ROMK) in neonatal Bartter syndrome. Pediatric Nephrology. 12(1). 69–71. 34 indexed citations
20.
Neumann, H., Brigitte Strahm, B Bender, et al.. (1997). Concise clinical report. Late occurrence of cysts in autosomal dominant medullary cystic kidney disease. Nephrology Dialysis Transplantation. 12(6). 1242–1246. 23 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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