Göran Brandberg

723 total citations
10 papers, 442 citations indexed

About

Göran Brandberg is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Göran Brandberg has authored 10 papers receiving a total of 442 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Surgery. Recurrent topics in Göran Brandberg's work include Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). Göran Brandberg is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). Göran Brandberg collaborates with scholars based in Sweden, France and United States. Göran Brandberg's co-authors include Raili Raininko, Orvar Eeg‐Olofsson, Ulrika von Döbeln, Niklas Darín, Eva Holmberg, Eva Kimber, Eva Lagberg Arkblad, Kerstin Berg, M. Tulinius and Margareta Nordling and has published in prestigious journals such as The American Journal of Human Genetics, The Journal of Pediatrics and Journal of Medical Genetics.

In The Last Decade

Göran Brandberg

10 papers receiving 433 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Göran Brandberg Sweden 8 244 116 96 80 74 10 442
Hanna Mierzewska Poland 15 444 1.8× 127 1.1× 49 0.5× 46 0.6× 126 1.7× 57 728
Noora Shahbeck Qatar 11 193 0.8× 143 1.2× 33 0.3× 35 0.4× 104 1.4× 14 426
Noboru Fueki Japan 10 207 0.8× 76 0.7× 35 0.4× 28 0.3× 65 0.9× 24 356
Christine í Dali Denmark 14 199 0.8× 56 0.5× 32 0.3× 18 0.2× 32 0.4× 28 532
Tarja Linnankivi Finland 14 424 1.7× 142 1.2× 41 0.4× 26 0.3× 85 1.1× 22 631
Krystyna Szymańska Poland 14 218 0.9× 177 1.5× 19 0.2× 49 0.6× 23 0.3× 48 485
K N Harikrishnan Australia 12 552 2.3× 249 2.1× 33 0.3× 51 0.6× 33 0.4× 16 722
Jeff Kobayashi Canada 9 102 0.4× 199 1.7× 47 0.5× 16 0.2× 79 1.1× 19 469
Monica Traverso Italy 13 348 1.4× 122 1.1× 30 0.3× 22 0.3× 38 0.5× 32 488
Takahito Inoue Japan 12 185 0.8× 124 1.1× 21 0.2× 27 0.3× 34 0.5× 30 604

Countries citing papers authored by Göran Brandberg

Since Specialization
Citations

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

Fields of papers citing papers by Göran Brandberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Göran Brandberg

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

All Works

10 of 10 papers shown
1.
Zhao, Jin, Jonatan Halvardson, Cecilia Zander, et al.. (2017). Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 177(1). 10–20. 32 indexed citations
2.
Halvardson, Jonatan, Jin Zhao, Ammar Zaghlool, et al.. (2016). Mutations in HECW2 are associated with intellectual disability and epilepsy. Journal of Medical Genetics. 53(10). 697–704. 48 indexed citations
3.
Pingault, Véronique, Asma Chaoui, Alain Verloès, et al.. (2014). Phenotypic similarities and differences in patients with a p.Met112Ile mutation in SOX10. American Journal of Medical Genetics Part A. 164(9). 2344–2350. 16 indexed citations
4.
Bjursell, Magnus, Henk J. Blom, Martin Engvall, et al.. (2011). Adenosine Kinase Deficiency Disrupts the Methionine Cycle and Causes Hypermethioninemia, Encephalopathy, and Abnormal Liver Function. The American Journal of Human Genetics. 89(4). 507–515. 91 indexed citations
5.
Arkblad, Eva Lagberg, Niklas Darín, Kerstin Berg, et al.. (2006). Multiplex ligation-dependent probe amplification improves diagnostics in spinal muscular atrophy. Neuromuscular Disorders. 16(12). 830–838. 92 indexed citations
6.
Brandberg, Göran, Raili Raininko, & Orvar Eeg‐Olofsson. (2003). Hypothalamic hamartoma with gelastic seizures in Swedish children and adolescents. European Journal of Paediatric Neurology. 8(1). 35–44. 73 indexed citations
7.
Wester, Ulf, Göran Brandberg, Margareta Larsson, Torsten Lönnerholm, & Göran Annerén. (2002). Chondrodysplasia punctata (CDP) with features of the tibia‐metacarpal type and maternal phenytoin treatment during pregnancy. Prenatal Diagnosis. 22(8). 663–668. 7 indexed citations
8.
Kyllerman, Mårten, Göran Brandberg, L Wiklund, & Jan‐Eric Månsson. (2002). Dysarthria, Progressive Parkinsonian Features and Symmetric Necrosis of Putamen in a Family with Painful Lipomas (Dercum Disease Variant). Neuropediatrics. 33(2). 69–72. 7 indexed citations
9.
Tentler, Dmitri, Göran Brandberg, Catalina Betancur, et al.. (2001). A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: Molecular analysis of the chromosome 7 breakpoint. American Journal of Medical Genetics. 105(8). 729–736. 16 indexed citations
10.
Hagenfeldt, Lars, et al.. (1990). 3-hydroxydicarboxylic aciduria—a fatty acid oxidation defect with severe prognosis. The Journal of Pediatrics. 116(3). 387–392. 60 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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