Monica Holmberg

1.3k total citations
29 papers, 1.0k citations indexed

About

Monica Holmberg is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Monica Holmberg has authored 29 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 16 papers in Cellular and Molecular Neuroscience and 4 papers in Neurology. Recurrent topics in Monica Holmberg's work include Genetic Neurodegenerative Diseases (12 papers), Mitochondrial Function and Pathology (11 papers) and DNA Repair Mechanisms (4 papers). Monica Holmberg is often cited by papers focused on Genetic Neurodegenerative Diseases (12 papers), Mitochondrial Function and Pathology (11 papers) and DNA Repair Mechanisms (4 papers). Monica Holmberg collaborates with scholars based in Sweden, Finland and United States. Monica Holmberg's co-authors include Gösta Holmgren, Mika Scheinin, Elin Larsson, Lars Forsgren, Lars Forsgren, Angelica Nordin, Anna‐Lena Ström, Veronica Fagerholm, Jan Minde and Göran Leonardsson and has published in prestigious journals such as PLoS ONE, Scientific Reports and Genome Research.

In The Last Decade

Monica Holmberg

29 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Monica Holmberg Sweden 19 720 673 254 95 79 29 1.0k
Hirohide Sawada Japan 14 380 0.5× 485 0.7× 122 0.5× 71 0.7× 166 2.1× 32 960
Francesca Cavalcanti Italy 20 1.0k 1.4× 974 1.4× 408 1.6× 113 1.2× 34 0.4× 43 1.3k
Nicol Birsa United Kingdom 15 153 0.2× 786 1.2× 265 1.0× 51 0.5× 143 1.8× 17 1.1k
So Yoen Choi South Korea 17 158 0.2× 510 0.8× 244 1.0× 64 0.7× 105 1.3× 22 813
Hiroyuki Morino Japan 20 564 0.8× 685 1.0× 494 1.9× 124 1.3× 163 2.1× 78 1.2k
Luigia Atorino Italy 7 320 0.4× 598 0.9× 348 1.4× 43 0.5× 277 3.5× 8 1.4k
Barbara Castellotti Italy 25 757 1.1× 987 1.5× 670 2.6× 305 3.2× 189 2.4× 65 1.8k
Coro Paisán‐Ruiz United States 19 322 0.4× 479 0.7× 472 1.9× 237 2.5× 166 2.1× 34 1.1k
Ezgi Öztürk Australia 16 340 0.5× 250 0.4× 113 0.4× 104 1.1× 60 0.8× 32 837
Katrin S. Lindenberg Germany 14 817 1.1× 942 1.4× 295 1.2× 34 0.4× 121 1.5× 32 1.2k

Countries citing papers authored by Monica Holmberg

Since Specialization
Citations

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

Fields of papers citing papers by Monica Holmberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Monica Holmberg

This figure shows the co-authorship network connecting the top 25 collaborators of Monica Holmberg. A scholar is included among the top collaborators of Monica Holmberg 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 Monica Holmberg. Monica Holmberg 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.
Jönsson, Frida, et al.. (2021). EYS mutations and implementation of minigene assay for variant classification in EYS-associated retinitis pigmentosa in northern Sweden. Scientific Reports. 11(1). 7696–7696. 5 indexed citations
2.
Lindsten, Hans, et al.. (2016). The High Level of Aberrant Splicing of ISCU in Slow-Twitch Muscle May Involve the Splicing Factor SRSF3. PLoS ONE. 11(10). e0165453–e0165453. 6 indexed citations
3.
Nordin, Angelica, Elin Larsson, & Monica Holmberg. (2011). The defective splicing caused by the ISCU intron mutation in patients with myopathy with lactic acidosis is repressed by PTBP1 but can be derepressed by IGF2BP1. Human Mutation. 33(3). 467–470. 33 indexed citations
4.
Nordin, Angelica, Elin Larsson, Lars‐Eric Thornell, & Monica Holmberg. (2010). Tissue-specific splicing of ISCU results in a skeletal muscle phenotype in myopathy with lactic acidosis, while complete loss of ISCU results in early embryonic death in mice. Human Genetics. 129(4). 371–378. 35 indexed citations
5.
Blomstedt, Patric, Marwan Hariz, Stephen Tisch, et al.. (2009). A family with a hereditary form of torsion dystonia from Northern Sweden treated with bilateral pallidal deep brain stimulation. Movement Disorders. 24(16). 2415–2419. 8 indexed citations
6.
Minde, Jan, Thomas Andersson, Inger Nennesmo, et al.. (2008). A novel NGFB point mutation: a phenotype study of heterozygous patients. Journal of Neurology Neurosurgery & Psychiatry. 80(2). 188–195. 29 indexed citations
7.
Larsson, Elin, et al.. (2008). Nerve growth factor R221W responsible for insensitivity to pain is defectively processed and accumulates as proNGF. Neurobiology of Disease. 33(2). 221–228. 32 indexed citations
8.
Minde, Jan, Olle Svensson, Monica Holmberg, Göran Solders, & Göran Toolanen. (2006). Orthopedic aspects of familial insensitivity to pain due to a novel nerve growth factor beta mutation. Acta Orthopaedica. 77(2). 198–202. 35 indexed citations
9.
Ström, Anna‐Lena, Lars Forsgren, & Monica Holmberg. (2005). Identification and characterization of Spinocerebellar Ataxia Type 7 (SCA7) isoform SCA7b in mice. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1731(3). 149–153. 3 indexed citations
10.
Norberg, Anna, Lars Forsgren, Dan Holmberg, & Monica Holmberg. (2005). Exclusion of the juvenile myoclonic epilepsy gene EFHC1 as the cause of migraine on chromosome 6, but association to two rare polymorphisms in MEP1A and RHAG. Neuroscience Letters. 396(2). 137–142. 7 indexed citations
11.
Ström, Anna‐Lena, Lars Forsgren, & Monica Holmberg. (2005). A role for both wild-type and expanded ataxin-7 in transcriptional regulation. Neurobiology of Disease. 20(3). 646–655. 39 indexed citations
12.
Einarsdóttir, Elísabet, Ingegerd Söderström, Anna Löfgren‐Burström, et al.. (2003). The CTLA4 region as a general autoimmunity factor: An extended pedigree provides evidence for synergy with the HLA locus in the etiology of type 1 diabetes mellitus, Hashimoto's thyroiditis and Graves' disease. European Journal of Human Genetics. 11(1). 81–84. 48 indexed citations
13.
14.
Jonasson, Jenni, et al.. (2002). Cloning and expression analysis of the murine homolog of the spinocerebellar ataxia type 7 (SCA7) gene. Gene. 285(1-2). 91–99. 18 indexed citations
15.
Jonasson, Jenni, Anna‐Lena Ström, Patricia Hart, et al.. (2002). Expression of ataxin-7 in CNS and non-CNS tissue of normal and SCA7 individuals. Acta Neuropathologica. 104(1). 29–37. 24 indexed citations
16.
Xu, Chennian, Monica Holmberg, Annette Oturai, et al.. (2001). Linkage analysis suggests a region of importance for multiple sclerosis in 3p14–13. Genes and Immunity. 2(8). 451–454. 3 indexed citations
17.
Holmberg, Monica, Mika Scheinin, Hitoshi Kurose, & Riitta Miettinen. (1999). Adrenergic α2C-receptors reside in rat striatal GABAergic projection neurons: comparison of radioligand binding and immunohistochemistry. Neuroscience. 93(4). 1323–1333. 50 indexed citations
18.
Lindblad, K, M L Savontaus, Giovanni Stévanin, et al.. (1996). An expanded CAG repeat sequence in spinocerebellar ataxia type 7.. Genome Research. 6(10). 965–971. 85 indexed citations
19.
Holmberg, Monica, et al.. (1995). Localization of autosomal dominant cerebellar ataxia associated with retinal degeneration and anticipation to chromosome 3p12-p21.1. Human Molecular Genetics. 4(8). 1441–1445. 57 indexed citations
20.

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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