Asbjørn Holmgren

1.1k total citations
18 papers, 711 citations indexed

About

Asbjørn Holmgren is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Asbjørn Holmgren has authored 18 papers receiving a total of 711 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Sensory Systems. Recurrent topics in Asbjørn Holmgren's work include Genetics and Neurodevelopmental Disorders (5 papers), Genetic Syndromes and Imprinting (4 papers) and Genomics and Rare Diseases (3 papers). Asbjørn Holmgren is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Genetic Syndromes and Imprinting (4 papers) and Genomics and Rare Diseases (3 papers). Asbjørn Holmgren collaborates with scholars based in Norway, United States and Sweden. Asbjørn Holmgren's co-authors include Doriana Misceo, Eirik Frengen, Yongfeng Guo, Melinka A. Butenko, Wenche Kristiansen, Steven E. Clark, Chun‐Lin Shi, Grethe‐Elisabeth Stenvik, Reidunn B. Aalen and Tuva Barøy and has published in prestigious journals such as PLoS ONE, The Plant Cell and Human Molecular Genetics.

In The Last Decade

Asbjørn Holmgren

18 papers receiving 694 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Asbjørn Holmgren Norway 12 442 250 102 96 73 18 711
Catalin N. Topala Netherlands 11 411 0.9× 84 0.3× 218 2.1× 234 2.4× 52 0.7× 11 949
Zhenle Zang China 17 262 0.6× 51 0.2× 31 0.3× 53 0.6× 77 1.1× 29 510
Shu Zhu China 15 516 1.2× 70 0.3× 23 0.2× 131 1.4× 152 2.1× 39 820
Sung-Min Hwang South Korea 11 231 0.5× 207 0.8× 53 0.5× 28 0.3× 42 0.6× 24 615
Kenju Hara Japan 15 385 0.9× 30 0.1× 21 0.2× 138 1.4× 265 3.6× 40 778
Alison Hugill United Kingdom 12 484 1.1× 38 0.2× 14 0.1× 203 2.1× 30 0.4× 14 767
Qiusheng Tong United States 15 1.1k 2.5× 30 0.1× 182 1.8× 52 0.5× 200 2.7× 17 1.3k
Ricco Lindner Germany 13 419 0.9× 18 0.1× 39 0.4× 56 0.6× 210 2.9× 17 604
Anna Maria Salvatore Italy 16 359 0.8× 24 0.1× 34 0.3× 20 0.2× 67 0.9× 22 588
L. Wuarin United States 10 278 0.6× 90 0.4× 7 0.1× 67 0.7× 143 2.0× 11 593

Countries citing papers authored by Asbjørn Holmgren

Since Specialization
Citations

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

Fields of papers citing papers by Asbjørn Holmgren

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Asbjørn Holmgren

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

All Works

18 of 18 papers shown
1.
Holmgren, Asbjørn, Ibrahim A. Akkouh, Kevin S. O’Connell, et al.. (2024). Bipolar patients display stoichiometric imbalance of gene expression in post-mortem brain samples. Molecular Psychiatry. 29(4). 1128–1138. 2 indexed citations
2.
Misceo, Doriana, Inger‐Lise Mero, Arvind Y. M. Sundaram, et al.. (2023). Novel Loss of Function Variants in CENPF Including a Large Intragenic Deletion in Patients with Strømme Syndrome. Genes. 14(11). 1985–1985. 1 indexed citations
3.
Holmgren, Asbjørn, et al.. (2022). Mapping the expression of an ANK3 isoform associated with bipolar disorder in the human brain. Translational Psychiatry. 12(1). 45–45. 2 indexed citations
4.
Gunnes, Gjermund, Asbjørn Holmgren, Janne E. Reseland, et al.. (2019). STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone. Cell Calcium. 85. 102110–102110. 10 indexed citations
5.
Akkouh, Ibrahim A., Silje Skrede, Asbjørn Holmgren, et al.. (2019). Exploring lithium’s transcriptional mechanisms of action in bipolar disorder: a multi-step study. Neuropsychopharmacology. 45(6). 947–955. 29 indexed citations
6.
Gunnes, Gjermund, Robert H. Lee, William E. Louch, et al.. (2018). STIM1 R304W causes muscle degeneration and impaired platelet activation in mice. Cell Calcium. 76. 87–100. 23 indexed citations
7.
Strømme, Petter, Stefan Groeneweg, Elaine C. Souza, et al.. (2018). Mutated Thyroid Hormone Transporter OATP1C1 Associates with Severe Brain Hypometabolism and Juvenile Neurodegeneration. Thyroid. 28(11). 1406–1415. 58 indexed citations
8.
Pedurupillay, Christeen Ramane J., Silja Svanstrøm Amundsen, Tuva Barøy, et al.. (2016). Clinical and molecular characteristics in three families with biallelic mutations in IGHMBP2. Neuromuscular Disorders. 26(9). 570–575. 21 indexed citations
9.
Barøy, Tuva, Christeen Ramane J. Pedurupillay, Yngve Thomas Bliksrud, et al.. (2016). A novel mutation in FBXL4 in a Norwegian child with encephalomyopathic mitochondrial DNA depletion syndrome 13. European Journal of Medical Genetics. 59(6-7). 342–346. 17 indexed citations
10.
Chiang, Samuel C. C., Tuva Barøy, Asbjørn Holmgren, et al.. (2016). Novel PIGT Variant in Two Brothers: Expansion of the Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 Phenotype. Genes. 7(12). 108–108. 17 indexed citations
11.
Pedurupillay, Christeen Ramane J., Tuva Barøy, Asbjørn Holmgren, et al.. (2015). Kaufman oculocerebrofacial syndrome in sisters with novel compound heterozygous mutation in UBE3B. American Journal of Medical Genetics Part A. 167(3). 657–663. 11 indexed citations
12.
Barøy, Tuva, Janet Koster, Petter Strømme, et al.. (2015). A novel type of rhizomelic chondrodysplasia punctata, RCDP5, is caused by loss of the PEX5 long isoform. Human Molecular Genetics. 24(20). 5845–5854. 57 indexed citations
13.
Koht, Jeanette, Gia Tuong Tran, Doriana Misceo, et al.. (2014). Spastic Paraplegia Type 7 Is Associated with Multiple Mitochondrial DNA Deletions. PLoS ONE. 9(1). e86340–e86340. 43 indexed citations
14.
Fannemel, Madeleine, Tuva Barøy, Asbjørn Holmgren, et al.. (2014). Haploinsufficiency of XPO1 and USP34 by a de novo 230 kb deletion in 2p15, in a patient with mild intellectual disability and cranio-facial dysmorphisms. European Journal of Medical Genetics. 57(9). 513–519. 28 indexed citations
15.
Dahm, Anders Erik Astrup, Giovanni Luca Tiscia, Asbjørn Holmgren, et al.. (2014). Genetic variations in the annexin A5 gene and the risk of pregnancy‐related venous thrombosis. Journal of Thrombosis and Haemostasis. 13(3). 409–413. 9 indexed citations
16.
Misceo, Doriana, Asbjørn Holmgren, William E. Louch, et al.. (2014). A Dominant STIM1 Mutation Causes Stormorken Syndrome. Human Mutation. 35(5). 556–564. 118 indexed citations
17.
Barøy, Tuva, Doriana Misceo, Petter Strømme, et al.. (2013). Haploinsufficiency of two histone modifier genes on 6p22.3, ATXN1 and JARID2, is associated with intellectual disability. Orphanet Journal of Rare Diseases. 8(1). 3–3. 13 indexed citations
18.
Stenvik, Grethe‐Elisabeth, Yongfeng Guo, Chun‐Lin Shi, et al.. (2008). The EPIP Peptide of INFLORESCENCE DEFICIENT IN ABSCISSION Is Sufficient to Induce Abscission inArabidopsisthrough the Receptor-Like Kinases HAESA and HAESA-LIKE2  . The Plant Cell. 20(7). 1805–1817. 252 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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