407 total citations 10 papers, 302 citations indexed
About
Ivemark Bi is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Surgery.
According to data from OpenAlex, Ivemark Bi has authored 10 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Pediatrics, Perinatology and Child Health, 3 papers in Genetics and 2 papers in Surgery. Recurrent topics in Ivemark Bi's work include Pediatric Urology and Nephrology Studies (3 papers), Congenital Diaphragmatic Hernia Studies (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Ivemark Bi is often cited by papers focused on Pediatric Urology and Nephrology Studies (3 papers), Congenital Diaphragmatic Hernia Studies (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Ivemark Bi collaborates with scholars based in . Ivemark Bi's co-authors include J Hellström, Göran Anneroth, K. Lindblom, Ulf Rudhe, M. Fraccaro, J. Lindsten, L. Tiepolo, P Zetterqvist, Maj Hultén and Jon Jonasson and has published in prestigious journals such as PubMed.
In The Last Decade
Ivemark Bi
10 papers
receiving
240 citations
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late)
cites ·
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This map shows the geographic impact of Ivemark Bi'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 Ivemark Bi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ivemark Bi more than expected).
This network shows the impact of papers produced by Ivemark Bi. 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 Ivemark Bi. The network helps show where Ivemark Bi may publish in the future.
Co-authorship network of co-authors of Ivemark Bi
This figure shows the co-authorship network connecting the top 25 collaborators of Ivemark Bi.
A scholar is included among the top collaborators of Ivemark Bi 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 Ivemark Bi. Ivemark Bi is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
All Works
10 of 10 papers shown
1.
Fraccaro, M., Maj Hultén, Ivemark Bi, et al.. (1972). Structural abnormalities of chromosome 18. 3. Two G-18 translocations, one identified AS 22-18.. PubMed. 15(2). 93–8.3 indexed citations
2.
Anneroth, Göran & Ivemark Bi. (1971). Histochemical localization of lipids in the human gingival epithelium and their relation to the dry mass concentration.. PubMed. 22(1). 7–18.5 indexed citations
3.
Fraccaro, M., Maj Hultén, Ivemark Bi, et al.. (1971). Structural abnormalities of chromosome 18. I. A case of 18q-, with autopsy findings.. PubMed. 14(4). 275–80.5 indexed citations
4.
Anneroth, Göran & Ivemark Bi. (1970). Histochemical localization of lipids in human dental pulp.. PubMed. 63(11). 747–55.1 indexed citations
Rudhe, Ulf, et al.. (1959). Congenital hypoplasia of the right pulmonary artery associated with myomatosis of the lung.. PubMed. Suppl 245. 323–30.2 indexed citations
7.
Bi, Ivemark, et al.. (1958). Renal dysplasia and pyelonephritis in infants and children. I.. PubMed. 66(3). 255–63.38 indexed citations
8.
Bi, Ivemark & K. Lindblom. (1958). Arterial ruptures in the adult polycystic kidney.. PubMed. 115(1-2). 100–10.4 indexed citations
9.
Bi, Ivemark, et al.. (1958). Renal dysplasia and urinary-tract infection.. PubMed. 115(1-2). 58–65.11 indexed citations
10.
Bi, Ivemark. (1955). Implications of agenesis of the spleen on the pathogenesis of conotruncus anomalies in childhood; an analysis of the heart malformations in the splenic agenesis syndrome, with fourteen new cases.. PubMed. 44(Suppl 104). 7–110.145 indexed citations
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