Kim Ramme

600 total citations
11 papers, 256 citations indexed

About

Kim Ramme is a scholar working on Immunology, Hematology and Genetics. According to data from OpenAlex, Kim Ramme has authored 11 papers receiving a total of 256 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Immunology, 5 papers in Hematology and 4 papers in Genetics. Recurrent topics in Kim Ramme's work include Immune Cell Function and Interaction (6 papers), Autoimmune and Inflammatory Disorders Research (4 papers) and Immunodeficiency and Autoimmune Disorders (3 papers). Kim Ramme is often cited by papers focused on Immune Cell Function and Interaction (6 papers), Autoimmune and Inflammatory Disorders Research (4 papers) and Immunodeficiency and Autoimmune Disorders (3 papers). Kim Ramme collaborates with scholars based in Sweden, Germany and Türkiye. Kim Ramme's co-authors include Jan‐Inge Henter, Magnus Nordenskjöld, Bengt Fadeel, Eva Rudd, Chengyun Zheng, Aytemiz Gürgey, Göran Carlsson, Jan Palmblad, Yenan T. Bryceson and Nevin Yalman and has published in prestigious journals such as Frontiers in Immunology, British Journal of Haematology and Journal of Medical Genetics.

In The Last Decade

Kim Ramme

11 papers receiving 250 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kim Ramme Sweden	6	180	146	82	69	40	11	256
Eva Rudd Sweden	8	333 1.9×	308 2.1×	166 2.0×	18 0.3×	39 1.0×	9	458
Marjorie Côte France	5	336 1.9×	308 2.1×	175 2.1×	14 0.2×	40 1.0×	6	468
Josefine Edner Sweden	5	224 1.2×	172 1.2×	98 1.2×	9 0.1×	17 0.4×	7	321
Funda Çipe Türkiye	9	114 0.6×	36 0.2×	31 0.4×	66 1.0×	15 0.4×	34	238
Lisa M. Ott de Bruin Netherlands	5	153 0.8×	118 0.8×	31 0.4×	50 0.7×	5 0.1×	8	273
Paige Tedrick United States	4	242 1.3×	234 1.6×	129 1.6×	11 0.2×	7 0.2×	6	333
Benedetta Ciambotti Italy	7	157 0.9×	183 1.3×	102 1.2×	6 0.1×	18 0.5×	7	248
Claudia Biondi Argentina	11	45 0.3×	135 0.9×	44 0.5×	97 1.4×	113 2.8×	47	362
Tuba Turul Özgür Türkiye	11	250 1.4×	53 0.4×	30 0.4×	101 1.5×	25 0.6×	21	324
Ute V. Solloch Germany	11	320 1.8×	193 1.3×	32 0.4×	30 0.4×	15 0.4×	17	453

Countries citing papers authored by Kim Ramme

Since Specialization

Citations

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

Fields of papers citing papers by Kim Ramme

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kim Ramme

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

All Works

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11 of 11 papers shown

Zetterström, Rolf, et al.. (2023). Case report: IKZF1-related early-onset CID is expected to be missed in TREC-based SCID screening but can be identified by determination of KREC levels. Frontiers in Immunology. 14. 1257581–1257581. 1 indexed citations

Mattsson, Kristin, et al.. (2019). Strong expression of p53 protein in bone marrow samples after hematopoietic stem cell transplantation indicates risk of relapse in pediatric acute lymphoblastic leukemia patients. Pediatric Transplantation. 23(4). e13408–e13408. 3 indexed citations

Sundin, Mikael, Per Marits, Kim Ramme, Antonios G.A. Kolios, & Jakob Nilsson. (2019). Severe combined immunodeficiency (SCID) presenting in childhood, with agammaglobulinemia, associated with novel compound heterozygous mutations in DCLRE1C. Clinical Immunology. 200. 16–18. 5 indexed citations

Gustafsson, Britt, et al.. (2018). Origins of STIL‐TAL1 fusion genes in children who later developed paediatric T‐cell acute lymphoblastic leukaemia: An investigation of neonatal blood spots. Pediatric Blood & Cancer. 65(11). e27310–e27310. 3 indexed citations

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

Horne, AnnaCarin, Kim Ramme, Eva Rudd, et al.. (2008). Characterization of PRF1, STX11 and UNC13D genotype‐phenotype correlations in familial hemophagocytic lymphohistiocytosis. British Journal of Haematology. 143(1). 75–83. 65 indexed citations

Ma, Daoxin, Eva Rudd, Josefine Edner, et al.. (2007). Sequence analysis of the SRGN, AP3B1, ARF6, and SH2D1A genes in familial hemophagocytic lymphohistiocytosis. Pediatric Blood & Cancer. 50(5). 1067–1069. 2 indexed citations

Carlsson, Göran, Malin Melin, Niklas Dahl, et al.. (2007). Kostmann syndrome or infantile genetic agranulocytosis, part two: understanding the underlying genetic defects in severe congenital neutropenia. Acta Paediatrica. 96(6). 813–819. 36 indexed citations

Karlsson, Jenny, Göran Carlsson, Kim Ramme, et al.. (2007). Low plasma levels of the protein pro‐LL‐37 as an early indication of severe disease in patients with chronic neutropenia. British Journal of Haematology. 137(2). 166–169. 30 indexed citations

10.

Rudd, Eva, Yenan T. Bryceson, Chengyun Zheng, et al.. (2007). Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis. Journal of Medical Genetics. 45(3). 134–141. 41 indexed citations

11.

Ramme, Kim, et al.. (1993). [Dermatofibrosis lenticularis disseminata with osteopoikilosis. Buschke-Olldendorff syndrome].. PubMed. 44(5). 312–4. 2 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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