Anna Norberg

438 total citations
16 papers, 274 citations indexed

About

Anna Norberg is a scholar working on Molecular Biology, Physiology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Anna Norberg has authored 16 papers receiving a total of 274 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Physiology and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Anna Norberg's work include Telomeres, Telomerase, and Senescence (7 papers), DNA Repair Mechanisms (3 papers) and Cardiac electrophysiology and arrhythmias (3 papers). Anna Norberg is often cited by papers focused on Telomeres, Telomerase, and Senescence (7 papers), DNA Repair Mechanisms (3 papers) and Cardiac electrophysiology and arrhythmias (3 papers). Anna Norberg collaborates with scholars based in Sweden, Finland and United States. Anna Norberg's co-authors include Irina Golovleva, Jenni Jonasson, Eva‐Lena Stattin, Kristina Cederquist, Monica Holmberg, Björn‐Anders Jonsson, Herbert Sandström, Andrew F. Irvine, Masanori Mishima and Stacy Month and has published in prestigious journals such as Blood, Human Molecular Genetics and Oikos.

In The Last Decade

Anna Norberg

15 papers receiving 268 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna Norberg Sweden 9 123 116 66 34 30 16 274
Lenka Mrázová Czechia 12 181 1.5× 93 0.8× 56 0.8× 45 1.3× 39 1.3× 33 308
Martin A. Haagmans Netherlands 7 157 1.3× 41 0.4× 28 0.4× 52 1.5× 43 1.4× 11 301
Georg Kern Austria 12 199 1.6× 49 0.4× 36 0.5× 68 2.0× 19 0.6× 17 313
Peter Heim Germany 6 141 1.1× 207 1.8× 20 0.3× 15 0.4× 75 2.5× 7 335
Mohsen Karbasiyan Germany 6 245 2.0× 83 0.7× 35 0.5× 15 0.4× 97 3.2× 9 445
Carlos E. Speck‐Martins Brazil 11 137 1.1× 25 0.2× 11 0.2× 63 1.9× 58 1.9× 23 314
Anne Gläser Germany 9 212 1.7× 80 0.7× 62 0.9× 11 0.3× 75 2.5× 15 332
Andrea Johnson United States 9 144 1.2× 36 0.3× 39 0.6× 93 2.7× 18 0.6× 20 323
Cristina Dias United Kingdom 11 172 1.4× 21 0.2× 17 0.3× 34 1.0× 143 4.8× 16 359
Emily Bonkowski United States 4 118 1.0× 37 0.3× 10 0.2× 37 1.1× 72 2.4× 11 277

Countries citing papers authored by Anna Norberg

Since Specialization
Citations

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

Fields of papers citing papers by Anna Norberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Norberg

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

All Works

16 of 16 papers shown
1.
2.
Kvarnung, Malin, Maria Pettersson, Maryam Rafati, et al.. (2024). Identification of biallelic POLA2 variants in two families with an autosomal recessive telomere biology disorder. European Journal of Human Genetics. 33(5). 580–587. 2 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.
Böhm, Stefanie, Helena Malmgren, Anna Norberg, et al.. (2020). Biallelic mutations in WRAP53 result in dysfunctional telomeres, Cajal bodies and DNA repair, thereby causing Hoyeraal–Hreidarsson syndrome. Cell Death and Disease. 11(4). 238–238. 22 indexed citations
5.
Norberg, Anna. (2019). aminorberg/SDM-comparison: Norberg et al. (2019). Zenodo (CERN European Organization for Nuclear Research). 1 indexed citations
6.
Norberg, Anna, Sofie Degerman, Katariina Hannula‐Jouppi, et al.. (2018). Characterization of an X-chromosome-linked telomere biology disorder in females with DKC1 mutation. Leukemia. 33(1). 275–278. 4 indexed citations
7.
Trotta, Luca, Anna Norberg, Mervi Taskinen, et al.. (2018). Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders. Orphanet Journal of Rare Diseases. 13(1). 139–139. 10 indexed citations
8.
Norberg, Anna, Anna Rosén, Klas Raaschou‐Jensen, et al.. (2018). Novel variants in Nordic patients referred for genetic testing of telomere-related disorders. European Journal of Human Genetics. 26(6). 858–867. 15 indexed citations
9.
Winbo, Annika, Eva‐Lena Stattin, Anna Norberg, et al.. (2017). Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis. BMC Medical Genetics. 18(1). 74–74. 5 indexed citations
10.
Stattin, Eva‐Lena, Kristina Cederquist, Jenni Jonasson, et al.. (2015). Genetic screening in sudden cardiac death in the young can save future lives. International Journal of Legal Medicine. 130(1). 59–66. 50 indexed citations
11.
Ueda, Yutaka, Rodrigo T. Calado, Anna Norberg, et al.. (2014). A mutation in the H/ACA box of telomerase RNA component gene (TERC) in a young patient with myelodysplastic syndrome. BMC Medical Genetics. 15(1). 68–68. 18 indexed citations
12.
Jönsson, Frida, Marie Burstedt, Ola Sandgren, Anna Norberg, & Irina Golovleva. (2013). Novel mutations in CRB1 and ABCA4 genes cause Leber congenital amaurosis and Stargardt disease in a Swedish family. European Journal of Human Genetics. 21(11). 1266–1271. 17 indexed citations
13.
Irvine, Andrew F., Anna Norberg, Stacy Month, et al.. (2013). Congenital dyserythropoietic anemia type III (CDA III) is caused by a mutation in kinesin family member, KIF23. Blood. 121(23). 4791–4799. 67 indexed citations
14.
Stattin, Eva‐Lena, Annika Winbo, Kristina Cederquist, et al.. (2012). Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing. BMC Cardiovascular Disorders. 12(1). 95–95. 22 indexed citations
15.
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
16.
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

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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