Bo Isomaa

25.1k total citations · 1 hit paper
36 papers, 2.6k citations indexed

About

Bo Isomaa is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism and Surgery. According to data from OpenAlex, Bo Isomaa has authored 36 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 17 papers in Endocrinology, Diabetes and Metabolism and 12 papers in Surgery. Recurrent topics in Bo Isomaa's work include Pancreatic function and diabetes (11 papers), Genetic Associations and Epidemiology (10 papers) and Diabetes and associated disorders (8 papers). Bo Isomaa is often cited by papers focused on Pancreatic function and diabetes (11 papers), Genetic Associations and Epidemiology (10 papers) and Diabetes and associated disorders (8 papers). Bo Isomaa collaborates with scholars based in Finland, Sweden and United States. Bo Isomaa's co-authors include Leif Groop, Valeriya Lyssenko, Peter Almgren, Anna Jonsson, Marja‐Riitta Taskinen, Peter M. Nilsson, David Altshuler, Nicolò Pulizzi, Göran Berglund and Carol Forsblom and has published in prestigious journals such as New England Journal of Medicine, PLoS ONE and Diabetes Care.

In The Last Decade

Bo Isomaa

36 papers receiving 2.6k 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.

Clinical Risk Factors, DNA Variants, and the Development of Type 2 Diabetes

2008 649 citations Valeriya Lyssenko, Anna Jonsson et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bo Isomaa Finland	21	1.2k	1.1k	850	787	381	36	2.6k
Kun‐san Xiang China	28	706 0.6×	986 0.9×	1.5k 1.7×	738 0.9×	472 1.2×	118	3.2k
Anna Jonsson Denmark	20	793 0.6×	871 0.8×	791 0.9×	547 0.7×	471 1.2×	40	2.2k
Sayuko Kobes United States	31	1.3k 1.0×	620 0.6×	1.2k 1.4×	544 0.7×	678 1.8×	86	3.3k
Steven C. Elbein United States	28	804 0.7×	1.0k 0.9×	1.2k 1.4×	867 1.1×	859 2.3×	63	3.1k
James L. Rosenzweig United States	22	630 0.5×	1.9k 1.7×	708 0.8×	717 0.9×	341 0.9×	34	2.8k
Steven Hunter United Kingdom	26	476 0.4×	1.3k 1.2×	447 0.5×	584 0.7×	497 1.3×	101	2.7k
Leen M. ‘t Hart Netherlands	30	663 0.5×	775 0.7×	1.5k 1.8×	818 1.0×	424 1.1×	98	3.0k
Assumpta Caixàs Spain	31	540 0.4×	783 0.7×	381 0.4×	753 1.0×	688 1.8×	149	2.8k
Michal Anděl Czechia	28	484 0.4×	481 0.4×	598 0.7×	595 0.8×	449 1.2×	118	2.2k
L. Groop Sweden	30	652 0.5×	1.3k 1.2×	1.1k 1.3×	873 1.1×	1.1k 3.0×	57	3.5k

Countries citing papers authored by Bo Isomaa

Since Specialization

Citations

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

Fields of papers citing papers by Bo Isomaa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bo Isomaa

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

Kettunen, Jarno L. T., Elina Rantala, Om Prakash Dwivedi, et al.. (2021). A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY. Diabetologia. 65(4). 632–643. 13 indexed citations

Haljas, Kadri, Liisa Hakaste, Jari Lahti, et al.. (2018). The associations of daylight and melatonin receptor 1B gene rs10830963 variant with glycemic traits: the prospective PPP-Botnia study. Annals of Medicine. 51(1). 58–67. 10 indexed citations

Abels, Mia, Matteo Riva, Hedvig Bennet, et al.. (2015). CART is a novel glucose-dependent peptide with antidiabetic actions in humans. Diabetologia. 58. 1 indexed citations

Alyass, Akram, Peter Almgren, Mikael Åkerlund, et al.. (2014). Modelling of OGTT curve identifies 1 h plasma glucose level as a strong predictor of incident type 2 diabetes: results from two prospective cohorts. Diabetologia. 58(1). 87–97. 106 indexed citations

Ahlqvist, Emma, Filippo Turrini, Stefan Lang, et al.. (2012). A common variant upstream of the PAX6 gene influences islet function in man. STM:n Hallinnonalan avoin julkaisuarkisto (Julkari). 1 indexed citations

Jonsson, Anna, et al.. (2012). Effect of a common variant of the PCSK2 gene on reduced insulin secretion. Diabetologia. 55(12). 3245–3251. 14 indexed citations

Reinbothe, Thomas, Sami Alkayyali, Emma Ahlqvist, et al.. (2012). The human L-type calcium channel Cav1.3 regulates insulin release and polymorphisms in CACNA1D associate with type 2 diabetes. Diabetologia. 56(2). 340–349. 58 indexed citations

Andersen, Mette K., et al.. (2012). Family history of Type 1 diabetes affects insulin secretion in patients with ‘Type 2’ diabetes. Diabetic Medicine. 30(5). e163–9. 6 indexed citations

Räikkönen, Katri, et al.. (2011). Association between depressive symptoms and metabolic syndrome is not explained by antidepressant medication: Results from the PPP-Botnia Study. Annals of Medicine. 44(3). 279–288. 34 indexed citations

10.

Reiling, Erwin, Valeriya Lyssenko, Jolanda M.A. Boer, et al.. (2011). Codon 72 polymorphism (rs1042522) of TP53 is associated with changes in diastolic blood pressure over time. European Journal of Human Genetics. 20(6). 696–700. 20 indexed citations

11.

Vassy, Jason L., Peter Shrader, Anna Jonsson, et al.. (2011). Association between parental history of diabetes and type 2 diabetes genetic risk scores in the PPP-Botnia and Framingham Offspring Studies. Diabetes Research and Clinical Practice. 93(2). e76–e79. 20 indexed citations

12.

Guey, Lin T., Jasmina Kravić, Olle Melander, et al.. (2011). Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants. Genetic Epidemiology. 35(4). 236–246. 78 indexed citations

13.

Ahlqvist, Emma, Fabiola Turrini, Stefan Lang, et al.. (2011). A common variant upstream of the PAX6 gene influences islet function in man. Diabetologia. 55(1). 94–104. 27 indexed citations

14.

Olsson, Anders H., et al.. (2010). A common variant near the PRL gene is associated with increased adiposity in males. Molecular Genetics and Metabolism. 102(1). 78–81. 20 indexed citations

15.

Rönn, Tina, Pernille Poulsen, Bo Isomaa, et al.. (2009). Genetic Variation in ATP5O Is Associated with Skeletal Muscle ATP50 mRNA Expression and Glucose Uptake in Young Twins. PLoS ONE. 4(3). e4793–e4793. 22 indexed citations

16.

Fredriksson, J. Magnus, Dragi Anevski, Peter Almgren, et al.. (2007). Variation in GYS1 Interacts with Exercise and Gender to Predict Cardiovascular Mortality. PLoS ONE. 2(3). e285–e285. 13 indexed citations

17.

Saxena, Richa, Paul I.W. de Bakker, Vamsi K. Mootha, et al.. (2006). Comprehensive Association Testing of Common Mitochondrial DNA Variation in Metabolic Disease. The American Journal of Human Genetics. 79(1). 54–61. 150 indexed citations

18.

Isomaa, Bo, et al.. (2002). Onset of glucose intolerance in MODY3 Pro291fsInsC mutation carrierscoincides with pubertal years - a prospective follow-up study. Diabetologia. 45. 129–129. 2 indexed citations

19.

Isomaa, Bo, et al.. (2001). The metabolic syndrome influences the risk of chronic complications in patients with Type II diabetes. Diabetologia. 44(9). 1148–1154. 213 indexed citations

20.

Groop, Leif, Carol Forsblom, Mikko Lehtovirta, et al.. (1996). Metabolic consequences of a family history of NIDDM (the Botnia study): evidence for sex-specific parental effects. Diabetes. 45(11). 1585–1593. 77 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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