Magnus Jöud

1.8k total citations
9 papers, 280 citations indexed

About

Magnus Jöud is a scholar working on Hematology, Physiology and Molecular Biology. According to data from OpenAlex, Magnus Jöud has authored 9 papers receiving a total of 280 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Hematology, 5 papers in Physiology and 3 papers in Molecular Biology. Recurrent topics in Magnus Jöud's work include Blood groups and transfusion (6 papers), Erythrocyte Function and Pathophysiology (5 papers) and HIV Research and Treatment (3 papers). Magnus Jöud is often cited by papers focused on Blood groups and transfusion (6 papers), Erythrocyte Function and Pathophysiology (5 papers) and HIV Research and Treatment (3 papers). Magnus Jöud collaborates with scholars based in Sweden and United States. Magnus Jöud's co-authors include Martin L. Olsson, Jill R. Storry, Björn Nilsson, Britt Thuresson, Ram Ajore, Birgitta Nilsson Sojka, Bo Åkerström, Marie McConkey, David M. Raiser and Gordon Saksena and has published in prestigious journals such as Nature Genetics, Scientific Reports and EMBO Molecular Medicine.

In The Last Decade

Magnus Jöud

9 papers receiving 275 citations

Peers

Magnus Jöud

HEMAT

PHYSI

MB

GENET

Núria Nogués Spain

RS Weinberg United States

Xianguo Xu China

Hatsue Tsuneyama Japan

Kalin Mayberry United States

Yvonne Lisa Behrens Germany

Chiara Antoniani France

Manan Shah Australia

Carrie Lin United States

Don Lavelle United States

Núria Nogués Spain

Magnus Jöud

240 ×1.4

HEMAT

142 ×1.2

PHYSI

58 ×0.5

MB

72 ×1.1

GENET

104 ×2.0

GENET

Citations per year, relative to Magnus Jöud Magnus Jöud (= 1×) peers Núria Nogués

Countries citing papers authored by Magnus Jöud

Since Specialization

Citations

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

Fields of papers citing papers by Magnus Jöud

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Magnus Jöud

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

All Works

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9 of 9 papers shown

1.

Kander, Thomas, et al.. (2022). ABO and RhD blood group are not associated with mortality and morbidity in critically ill patients; a multicentre observational study of 29 512 patients. BMC Anesthesiology. 22(1). 91–91. 6 indexed citations

2.

Jöud, Magnus, et al.. (2018). Identification of human glycosyltransferase genes expressed in erythroid cells predicts potential carbohydrate blood group loci. Scientific Reports. 8(1). 6040–6040. 11 indexed citations

3.

Ajore, Ram, David M. Raiser, Marie McConkey, et al.. (2017). Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP 53 mutations. EMBO Molecular Medicine. 9(4). 498–507. 75 indexed citations

4.

Jöud, Magnus, Ram Ajore, Sunitha Vege, et al.. (2017). SMIM1 variants rs1175550 and rs143702418 independently modulate Vel blood group antigen expression. Scientific Reports. 7(1). 40451–40451. 17 indexed citations

5.

Ajore, Ram, David M. Raiser, Marie McConkey, et al.. (2017). Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with. DSpace@MIT (Massachusetts Institute of Technology). 1 indexed citations

6.

Jöud, Magnus, et al.. (2016). Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project. Blood Advances. 1(3). 240–249. 110 indexed citations

7.

Storry, Jill R., Magnus Jöud, Britt Thuresson, et al.. (2013). INTEGRATIVE GENOMICS IDENTIFIES SMIM1 AS THE LOCUS OF A NOVEL ERYTHROCYTE MEMBRANE PROTEIN AND THE VEL BLOOD GROUP SYSTEM. Vox Sanguinis. 105. 29–29. 1 indexed citations

8.

Storry, Jill R., Magnus Jöud, Britt Thuresson, et al.. (2013). Homozygosity for a null allele of SMIM1 defines the Vel-negative blood group phenotype. Nature Genetics. 45(5). 537–541. 56 indexed citations

9.

Thuresson, Britt, Julia S. Westman, Magnus Jöud, & Martin L. Olsson. (2010). A P-1/P-2-Specific Polymorphism Found In A Novel A4Galt Transcript: The Missing Link Between P-K And P1 Histo-Blood Group Antigens. Lund University Publications (Lund University). 3 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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