Göran Elinder

7.1k total citations · 2 hit papers
77 papers, 5.1k citations indexed

About

Göran Elinder is a scholar working on Hematology, Immunology and Infectious Diseases. According to data from OpenAlex, Göran Elinder has authored 77 papers receiving a total of 5.1k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Hematology, 21 papers in Immunology and 19 papers in Infectious Diseases. Recurrent topics in Göran Elinder's work include Autoimmune and Inflammatory Disorders Research (21 papers), Parvovirus B19 Infection Studies (17 papers) and Platelet Disorders and Treatments (12 papers). Göran Elinder is often cited by papers focused on Autoimmune and Inflammatory Disorders Research (21 papers), Parvovirus B19 Infection Studies (17 papers) and Platelet Disorders and Treatments (12 papers). Göran Elinder collaborates with scholars based in Sweden, United States and Italy. Göran Elinder's co-authors include Jan‐Inge Henter, Åke Öst, Shinsaku Imashuku, Olle Söder, Maurizio Aricò, Gritta Janka, Anita Aperia, Jan Andersson, Birger Andersson and Magnus Hansson and has published in prestigious journals such as The Lancet, Nature Genetics and Blood.

In The Last Decade

Göran Elinder

73 papers receiving 5.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Diagnostic guidelines for hemophagocytic lymphohistiocytosis. The FHL Study Group of the Histiocyte Society.

1991 617 citations Jan‐Inge Henter, Göran Elinder et al. profile →
Contemporary classification of histiocytic disorders

1997 597 citations Göran Elinder, Jan‐Inge Henter et al. Medical and Pediatric Oncology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Göran Elinder Sweden	31	3.2k	2.4k	2.2k	859	573	77	5.1k
R. Maarten Egeler Netherlands	27	3.8k 1.2×	2.5k 1.1×	2.8k 1.3×	849 1.0×	982 1.7×	63	6.4k
Jacek Winiarski Sweden	39	5.0k 1.6×	2.4k 1.0×	3.2k 1.4×	348 0.4×	712 1.2×	147	8.1k
David Webb United Kingdom	32	5.7k 1.8×	2.7k 1.2×	3.1k 1.4×	362 0.4×	635 1.1×	71	7.6k
Sheila Weitzman Canada	46	1.8k 0.6×	2.2k 0.9×	1.4k 0.6×	2.0k 2.4×	1.5k 2.6×	171	7.4k
Gritta Janka Germany	50	10.7k 3.4×	6.8k 2.9×	7.3k 3.3×	1.0k 1.2×	1.4k 2.4×	139	12.9k
Athimalaipet V Ramanan United Kingdom	35	2.4k 0.7×	1.1k 0.5×	1.2k 0.5×	134 0.2×	1.0k 1.8×	169	4.6k
Aytemiz Gürgey Türkiye	33	2.4k 0.8×	449 0.2×	541 0.2×	313 0.4×	303 0.5×	219	3.9k
AnnaCarin Horne Sweden	21	5.4k 1.7×	3.3k 1.4×	3.6k 1.6×	140 0.2×	735 1.3×	33	6.3k
Alexei A. Grom United States	48	5.0k 1.6×	1.8k 0.7×	3.6k 1.6×	152 0.2×	1.4k 2.5×	122	7.4k
Anne‐Marie Prieur France	26	4.1k 1.3×	269 0.1×	1.9k 0.9×	311 0.4×	1.2k 2.1×	55	6.6k

Countries citing papers authored by Göran Elinder

Since Specialization

Citations

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

Fields of papers citing papers by Göran Elinder

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Göran Elinder

This figure shows the co-authorship network connecting the top 25 collaborators of Göran Elinder. A scholar is included among the top collaborators of Göran Elinder 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 Göran Elinder. Göran Elinder 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

Carlsson, Göran, Göran Elinder, Helena Malmgren, et al.. (2009). Compound heterozygous HAX1 mutations in a Swedish patient with severe congenital neutropenia and no neurodevelopmental abnormalities. Pediatric Blood & Cancer. 53(6). 1143–1146. 10 indexed citations

Olén, Ola, Scott Montgomery, Göran Elinder, Anders Ekbom, & Jonas F. Ludvigsson. (2008). Increased risk of immune thrombocytopenic purpura among inpatients with coeliac disease. Scandinavian Journal of Gastroenterology. 43(4). 416–422. 20 indexed citations

Rajantie, Jukka, et al.. (2007). Does treatment of newly diagnosed idiopathic thrombocytopenic purpura reduce morbidity?. Archives of Disease in Childhood. 92(8). 704–707. 14 indexed citations

Rajantie, Jukka, et al.. (2006). Initial management of children with newly diagnosed idiopathic thrombocytopenic purpura in the Nordic countries. Acta Paediatrica. 95(6). 726–731. 7 indexed citations

Kimby, Eva, Ásgerður Sverrisdóttir, & Göran Elinder. (2004). Safety of rituximab therapy during the first trimester of pregnancy: a case history. European Journal Of Haematology. 72(4). 292–295. 99 indexed citations

Rosthøj, Steen, Iris Hedlund‐Treutiger, Jukka Rajantie, et al.. (2003). Duration and morbidity of newly diagnosed idiopathic thrombocytopenic purpura in children: a prospective nordic study of an unselected cohort. The Journal of Pediatrics. 143(3). 302–307. 92 indexed citations

Elinder, Göran, et al.. (2002). Centres for Clinical Education (CCE): Developing the Health Care Education of Tomorrow A Preliminary Report. Education for Health. 15(1). 10–18. 19 indexed citations

Skeppner, Gunnar, Anders Kreuger, & Göran Elinder. (2002). Transient Erythroblastopenia of Childhood: Prospective Study of 10 Patients With Special Reference to Viral Infections. Journal of Pediatric Hematology/Oncology. 24(4). 294–298. 19 indexed citations

Gustavsson, Peter, Emanuela Garelli, Sarah E. Ball, et al.. (1998). Identification of Microdeletions Spanning the Diamond-Blackfan Anemia Locus on 19q13 and Evidence for Genetic Heterogeneity. The American Journal of Human Genetics. 63(5). 1388–1395. 57 indexed citations

10.

Freedman, John, et al.. (1998). Directions for research in autoimmune thrombocytopenic purpura (ITP). Acta Paediatrica. 87(s424). 82–84. 6 indexed citations

11.

Hedlund‐Treutiger, Iris, J. Wahlström, & Göran Elinder. (1998). Role of the T cell receptor in idiopathic thrombocytopenic purpura (ITP). Acta Paediatrica. 87(s424). 46–50. 8 indexed citations

12.

Hedman, Anna M., et al.. (1997). Prevalence and treatment of chronic idiopathic thrombocytopenic purpura of childhood in Sweden. Acta Paediatrica. 86(2). 226–227. 31 indexed citations

13.

Gustavsson, Peter, Arie van Haeringen, Gil Tchernia, et al.. (1997). Diamond-Blackfan anaemia: genetic homogeneity for a gene on chromosome 19q13 restricted to 1.8 Mb. Nature Genetics. 16(4). 368–371. 73 indexed citations

14.

Henter, Jan‐Inge, et al.. (1996). Elevated circulating levels of interleukin‐1 receptor antagonist but not IL‐1 agonists in hemophagocytic lymphohistiocytosis. Medical and Pediatric Oncology. 27(1). 21–25. 4 indexed citations

15.

Henter, Jan‐Inge, et al.. (1996). Elevated circulating levels of interleukin-1 receptor antagonist but not IL-1 agonists in hemophagocytic lymphohistiocytosis. Medical and Pediatric Oncology. 27(1). 21–25. 37 indexed citations

16.

Åhlin, Anders, Martin de Boer, Dirk Roos, et al.. (1995). Prevalence, genetics and clinical presentation of chronic granulomatous disease in Sweden. Acta Paediatrica. 84(12). 1386–1394. 80 indexed citations

17.

Rabbani, Hodjattallah, Martin de Boer, Anders Åhlin, et al.. (1993). A 40‐base‐pair duplication in the gp91‐phox gene leading to X‐linked chronic granulomatous disease. European Journal Of Haematology. 51(4). 218–222. 11 indexed citations

18.

Henter, Jan‐Inge, et al.. (1993). Myelodysplasia Syndrome Following Epipodophyllotoxin Therapy in Familial Hemophagocyticlymphohistiocytosis. Pediatric Hematology and Oncology. 10(2). 163–168. 24 indexed citations

19.

Henter, Jan‐Inge, Anneka Ehrnst, Jan Andersson, & Göran Elinder. (1993). Familial hemophagocytic lymphohistiocytosis and viral infections. Acta Paediatrica. 82(4). 369–372. 101 indexed citations

20.

Henter, Jan‐Inge & Göran Elinder. (1991). Familial Hemophagocytic Lymphohistiocytosis: Clinical Review Based on the Findings in Seven Children. Acta Paediatrica. 80(3). 269–277. 48 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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