Mutlu Kartal‐Kaess

724 total citations
20 papers, 312 citations indexed

About

Mutlu Kartal‐Kaess is a scholar working on Hematology, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Mutlu Kartal‐Kaess has authored 20 papers receiving a total of 312 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Hematology, 9 papers in Molecular Biology and 4 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Mutlu Kartal‐Kaess's work include Hemophilia Treatment and Research (6 papers), Acute Myeloid Leukemia Research (4 papers) and Acute Lymphoblastic Leukemia research (4 papers). Mutlu Kartal‐Kaess is often cited by papers focused on Hemophilia Treatment and Research (6 papers), Acute Myeloid Leukemia Research (4 papers) and Acute Lymphoblastic Leukemia research (4 papers). Mutlu Kartal‐Kaess collaborates with scholars based in Germany, Switzerland and Sweden. Mutlu Kartal‐Kaess's co-authors include Anna Jauch, Axel Benner, Friedrich W. Cremer, Marc S. Raab, Dirk Hose, Hartmut Goldschmidt, Claus R. Bartram, Jelena Bila, Marion Moos and Alwin Krämer and has published in prestigious journals such as Genes & Development, Blood and International Journal of Molecular Sciences.

In The Last Decade

Mutlu Kartal‐Kaess

18 papers receiving 309 citations

Peers

Mutlu Kartal‐Kaess

HEMAT

ONCOL

PHEOH

GENET

Rika Kanezaki Japan

Patrizia Scaravaglio Italy

Jinjun Cheng United States

Juliana Godoy Assumpção Brazil

Carlo Dufour Italy

Stephanie A. Schnell United States

RB Jenkins United States

Véronique Della-Valle France

Alvin Soon Tiong Lim Singapore

Esther Gillert Germany

Rika Kanezaki Japan

Mutlu Kartal‐Kaess

163 ×1.0

HEMAT

198 ×1.4

47 ×0.8

ONCOL

69 ×1.2

PHEOH

78 ×1.8

GENET

Citations per year, relative to Mutlu Kartal‐Kaess Mutlu Kartal‐Kaess (= 1×) peers Rika Kanezaki

Countries citing papers authored by Mutlu Kartal‐Kaess

Since Specialization

Citations

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

Fields of papers citing papers by Mutlu Kartal‐Kaess

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mutlu Kartal‐Kaess. 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 Mutlu Kartal‐Kaess. The network helps show where Mutlu Kartal‐Kaess may publish in the future.

Co-authorship network of co-authors of Mutlu Kartal‐Kaess

This figure shows the co-authorship network connecting the top 25 collaborators of Mutlu Kartal‐Kaess. A scholar is included among the top collaborators of Mutlu Kartal‐Kaess 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 Mutlu Kartal‐Kaess. Mutlu Kartal‐Kaess 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

Carção, Manuel, Susanna Ranta, Heidi Glosli, et al.. (2025). Blood Group O Does Not Increase the Risk of Inhibitors in Severe Haemophilia A: Data from the PedNet Study Group. Haemophilia. 31(3). 419–423.

Kartal‐Kaess, Mutlu, Fernando Pinto, Veerle Labarque, et al.. (2024). Hemophilia B Leyden: characteristics and natural history in the International Pediatric Network of Hemophilia Management Registry. Journal of Thrombosis and Haemostasis. 23(3). 921–927. 1 indexed citations

Labarque, Veerle, Maria Elisa Mancuso, Mutlu Kartal‐Kaess, et al.. (2023). F8/F9 variants in the population-based PedNet Registry cohort compared with locus-specific genetic databases of the European Association for Haemophilia and Allied Disorders and the Centers for Disease Control and Prevention Hemophilia A or Hemophilia B Mutation Project. Research and Practice in Thrombosis and Haemostasis. 7(1). 100036–100036. 2 indexed citations

Ranta, Susanna, Jayashree Motwani, Jan Blatný, et al.. (2023). Dilemmas on emicizumab in children with haemophilia A: A survey of strategies from PedNet centres. Haemophilia. 29(5). 1291–1298. 8 indexed citations

Albisetti, Manuela, Alice Trinchero, Lukas Graf, et al.. (2023). “Hermes” - Hemophilia Related Mental Illness: A Cross-Sectional, Multicenter Study in Switzerland. Blood. 142(Supplement 1). 3741–3741.

Belle, Fabiën N., Christina Schindera, Tamara Diesch, et al.. (2022). Body image in adolescent survivors of childhood cancer: The role of chronic health conditions. Pediatric Blood & Cancer. 69(11). e29958–e29958. 7 indexed citations

Karow, Axel, Monika Haubitz, Elisabeth Oppliger Leibundgut, et al.. (2021). Targeting Telomere Biology in Acute Lymphoblastic Leukemia. International Journal of Molecular Sciences. 22(13). 6653–6653. 10 indexed citations

Bailey, Helen D., et al.. (2020). Parental occupational exposure to pesticides and risk of childhood cancer in Switzerland: a census-based cohort study. BMC Cancer. 20(1). 819–819. 14 indexed citations

Andersson, Nadine G., Veerle Labarque, Maria Elisa Mancuso, et al.. (2020). Novel F8 and F9 gene variants from the PedNet hemophilia registry classified according to ACMG/AMP guidelines. Human Mutation. 41(12). 2058–2072. 3 indexed citations

10.

Dantonello, Tobias M., Mutlu Kartal‐Kaess, Christoph Aebi, et al.. (2020). SARS-CoV-2 Infection During Induction Chemotherapy in a Child With High-risk T-Cell Acute Lymphoblastic Leukemia. Journal of Pediatric Hematology/Oncology. 43(6). e804–e807. 4 indexed citations

11.

Bochtler, Tilmann, Mutlu Kartal‐Kaess, Martin Granzow, et al.. (2018). Micronucleus formation in human cancer cells is biased by chromosome size. Genes Chromosomes and Cancer. 58(6). 392–395. 24 indexed citations

12.

Kartal‐Kaess, Mutlu, Tilmann Bochtler, Michael Kirsch, et al.. (2018). PPM1D Mutations Are Rare in De Novo and Therapy-Related Acute Myeloid Leukemia. Blood. 132(Supplement 1). 1472–1472. 3 indexed citations

13.

Bochtler, Tilmann, Martin Granzow, Friedrich Stölzel, et al.. (2017). Marker chromosomes can arise from chromothripsis and predict adverse prognosis in acute myeloid leukemia. Blood. 129(10). 1333–1342. 50 indexed citations

14.

Bochtler, Tilmann, Martin Granzow, Friedrich Stölzel, et al.. (2016). Marker Chromosomes Can Arise from Chromothripsis and Predict Adverse Prognosis in Acute Myeloid Leukemia. Blood. 128(22). 2869–2869. 3 indexed citations

15.

Cimmino, Luisa, Julian Jude, Yifang Hu, et al.. (2014). Pax5 loss imposes a reversible differentiation block in B-progenitor acute lymphoblastic leukemia. Genes & Development. 28(12). 1337–1350. 65 indexed citations

16.

Kartal‐Kaess, Mutlu, Luisa Cimmino, Simona Infantino, et al.. (2012). RNAi Screening Identifies A Novel Role for A-Kinase Anchoring Protein 12 (AKAP12) in B Cell Development and Function. Blood. 120(21). 855–855. 1 indexed citations

17.

Kartal‐Kaess, Mutlu, Joerg J Meerpohl, Alexandra Fischer, et al.. (2011). Analysis of Ribosomal Protein Genes Associated with Diamond Blackfan Anemia (DBA) In German DBA Patients and Their Relatives. Blood. 118(21). 729–729. 3 indexed citations

18.

Kartal‐Kaess, Mutlu, Eileen M. Shore, Meiqi Xu, et al.. (2010). Fibrodysplasia ossificans progressiva (FOP): watch the great toes!. European Journal of Pediatrics. 169(11). 1417–1421. 21 indexed citations

19.

Cremer, Friedrich W., Jelena Bila, Mutlu Kartal‐Kaess, et al.. (2005). Delineation of distinct subgroups of multiple myeloma and a model for clonal evolution based on interphase cytogenetics. Genes Chromosomes and Cancer. 44(2). 194–203. 74 indexed citations

20.

Cremer, Friedrich W., Mutlu Kartal‐Kaess, Dirk Hose, et al.. (2005). High incidence and intraclonal heterogeneity of chromosome 11 aberrations in patients with newly diagnosed multiple myeloma detected by multiprobe interphase FISH. Cancer Genetics and Cytogenetics. 161(2). 116–124. 19 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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