Claes Ladenvall

13.4k total citations
25 papers, 906 citations indexed

About

Claes Ladenvall is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Claes Ladenvall has authored 25 papers receiving a total of 906 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Epidemiology. Recurrent topics in Claes Ladenvall's work include Genetic Associations and Epidemiology (4 papers), Acute Myeloid Leukemia Research (3 papers) and Lymphoma Diagnosis and Treatment (3 papers). Claes Ladenvall is often cited by papers focused on Genetic Associations and Epidemiology (4 papers), Acute Myeloid Leukemia Research (3 papers) and Lymphoma Diagnosis and Treatment (3 papers). Claes Ladenvall collaborates with scholars based in Sweden, Finland and United States. Claes Ladenvall's co-authors include Christina Jern, Katarina Jood, Christian Blomstrand, Annika Rosengren, Per Ladenvall, Staffan Nilsson, Charlotte Ling, Anders H. Olsson, Leif Groop and Tina Rönn and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Diabetes and Stroke.

In The Last Decade

Claes Ladenvall

23 papers receiving 887 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Claes Ladenvall Sweden 14 325 222 220 194 138 25 906
Nihan Erginel‐Ünaltuna Türkiye 20 382 1.2× 186 0.8× 129 0.6× 180 0.9× 66 0.5× 87 1.1k
Jiao Lou China 24 554 1.7× 217 1.0× 152 0.7× 204 1.1× 171 1.2× 45 1.2k
Zoltán Szolnoki Hungary 20 308 0.9× 100 0.5× 77 0.3× 126 0.6× 49 0.4× 54 971
Nabila Bouatia‐Naji France 18 252 0.8× 314 1.4× 229 1.0× 256 1.3× 115 0.8× 49 1.0k
Andrew P. Boright Canada 13 404 1.2× 223 1.0× 106 0.5× 194 1.0× 32 0.2× 18 1.2k
Hugh S. Markus United Kingdom 12 160 0.5× 127 0.6× 129 0.6× 84 0.4× 72 0.5× 18 584
Ioanna Mosialou United States 12 552 1.7× 83 0.4× 138 0.6× 114 0.6× 70 0.5× 17 1.3k
Megan A. Evans United States 16 227 0.7× 161 0.7× 63 0.3× 189 1.0× 43 0.3× 31 1.0k
Tomonori Segawa Japan 18 389 1.2× 118 0.5× 111 0.5× 241 1.2× 50 0.4× 40 1.1k
Annie Poon United States 17 213 0.7× 154 0.7× 63 0.3× 106 0.5× 55 0.4× 28 876

Countries citing papers authored by Claes Ladenvall

Since Specialization
Citations

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

Fields of papers citing papers by Claes Ladenvall

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claes Ladenvall

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

All Works

20 of 20 papers shown
1.
Thörn, Ingrid, Millaray Marincevic, Claes Ladenvall, et al.. (2025). Single-cell sequencing reveals shared clonal signatures in nonmalignant B and tumor cells in T-prolymphocytic leukemia. PubMed. 2(2). 100076–100076.
2.
Eriksson, Anna, Lucy Mathot, Martin Rippin, et al.. (2023). Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia. Clinical Cancer Research. 29(15). 2826–2834. 3 indexed citations
3.
Vertemara, Jacopo, Claes Ladenvall, Anna Norberg, et al.. (2023). Novel pathological variants of NHP2 affect N-terminal domain flexibility, protein stability, H/ACA Ribonucleoprotein (RNP) complex formation and telomerase activity. Human Molecular Genetics. 32(19). 2901–2912. 2 indexed citations
4.
Baliakas, Panagiotis, Arielle R. Munters, Anders Kämpe, et al.. (2023). Integrating a Polygenic Risk Score into a clinical setting would impact risk predictions in familial breast cancer. Journal of Medical Genetics. 61(2). 150–154. 4 indexed citations
5.
6.
Alexsson, Andrei, Christer Sundström, Claes Ladenvall, et al.. (2021). PD-L1 and IDO1 are potential targets for treatment in patients with primary diffuse large B-cell lymphoma of the CNS. Acta Oncologica. 60(4). 531–538. 13 indexed citations
7.
Dahlberg, Johan, Claes Ladenvall, Roman Valls Guimerà, et al.. (2019). Arteria: An automation system for a sequencing core facility. GigaScience. 8(12). 3 indexed citations
8.
Ljungström, Viktor, Jakob Werner Hansen, Astrid Olsnes Kittang, et al.. (2016). Molecular Profiling In A Population Based Cohort Of Nordic Myelodysplastic Syndrome Patients. Haematologica. 101. 72–72. 1 indexed citations
9.
Prasad, Rashmi B., Peter Almgren, Ola Hansson, et al.. (2016). Excess maternal transmission of variants in the THADA gene to offspring with type 2 diabetes. Diabetologia. 59(8). 1702–1713. 14 indexed citations
10.
Tukiainen, Taru, Matti Pirinen, Antti‐Pekka Sarin, et al.. (2014). Chromosome X-Wide Association Study Identifies Loci for Fasting Insulin and Height and Evidence for Incomplete Dosage Compensation. PLoS Genetics. 10(2). e1004127–e1004127. 51 indexed citations
11.
Olsson, Anders H., Petr Volkov, Karl Bacos, et al.. (2014). Genome-Wide Associations between Genetic and Epigenetic Variation Influence mRNA Expression and Insulin Secretion in Human Pancreatic Islets. PLoS Genetics. 10(11). e1004735–e1004735. 132 indexed citations
12.
Zuydam, Natalie R. van, Benjamin F. Voight, Claes Ladenvall, et al.. (2013). Known SNPs in ADAMTS7, the 9p21 region and UBE2E interact with type 2 diabetes status to modify the risk of coronary artery disease in large populations. Diabetologia. 56. 76–77. 2 indexed citations
13.
Sharma, Amitabh, Natali Gulbahce, Samuel Pevzner, et al.. (2013). Network-based Analysis of Genome Wide Association Data Provides Novel Candidate Genes for Lipid and Lipoprotein Traits. Molecular & Cellular Proteomics. 12(11). 3398–3408. 22 indexed citations
14.
Olsson, Anders H., Jonathan L.S. Esguerra, Emilia Heimann, et al.. (2012). Reduced insulin secretion correlates with decreased expression of exocytotic genes in pancreatic islets from patients with type 2 diabetes. Molecular and Cellular Endocrinology. 364(1-2). 36–45. 96 indexed citations
15.
Olsson, Anders H., Tina Rönn, Claes Ladenvall, et al.. (2011). Two common genetic variants near nuclear-encoded OXPHOS genes are associated with insulin secretion in vivo. European Journal of Endocrinology. 164(5). 765–771. 20 indexed citations
16.
Jood, Katarina, Jonas ÅH Danielson, Claes Ladenvall, Christian Blomstrand, & Christina Jern. (2008). Fibrinogen gene variation and ischemic stroke. Journal of Thrombosis and Haemostasis. 6(6). 897–904. 30 indexed citations
17.
Ladenvall, Claes, Ann Gils, Katarina Jood, et al.. (2007). Thrombin Activatable Fibrinolysis Inhibitor Activation Peptide Shows Association With All Major Subtypes of Ischemic Stroke and With TAFI Gene Variation. Arteriosclerosis Thrombosis and Vascular Biology. 27(4). 955–962. 57 indexed citations
18.
Ladenvall, Claes, Katarina Jood, Christian Blomstrand, et al.. (2006). Serum C-Reactive Protein Concentration and Genotype in Relation to Ischemic Stroke Subtype. Stroke. 37(8). 2018–2023. 120 indexed citations
19.
Jood, Katarina, Per Ladenvall, Anna Tjärnlund‐Wolf, et al.. (2005). Fibrinolytic Gene Polymorphism and Ischemic Stroke. Stroke. 36(10). 2077–2081. 70 indexed citations
20.
Jood, Katarina, Claes Ladenvall, Annika Rosengren, Christian Blomstrand, & Christina Jern. (2005). Family History in Ischemic Stroke Before 70 Years of Age. Stroke. 36(7). 1383–1387. 149 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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2026