Henrik Stranneheim

2.4k total citations
27 papers, 744 citations indexed

About

Henrik Stranneheim is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Henrik Stranneheim has authored 27 papers receiving a total of 744 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Clinical Biochemistry. Recurrent topics in Henrik Stranneheim's work include Genomics and Rare Diseases (7 papers), Metabolism and Genetic Disorders (7 papers) and Genomics and Phylogenetic Studies (6 papers). Henrik Stranneheim is often cited by papers focused on Genomics and Rare Diseases (7 papers), Metabolism and Genetic Disorders (7 papers) and Genomics and Phylogenetic Studies (6 papers). Henrik Stranneheim collaborates with scholars based in Sweden, Norway and France. Henrik Stranneheim's co-authors include Joakim Lundeberg, Anna Wedell, Sverker Lundin, Erik Pettersson, Daniel Klevebring, Nicole Lesko, Anna Wredenberg, Christoph Freyer, Daniel Nätt and Niclas Lindqvist and has published in prestigious journals such as Bioinformatics, PLoS ONE and Neurology.

In The Last Decade

Henrik Stranneheim

27 papers receiving 736 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Henrik Stranneheim Sweden	16	423	147	71	58	52	27	744
Maulilio J. Kipanyula Tanzania	14	536 1.3×	75 0.5×	24 0.3×	104 1.8×	125 2.4×	35	1.0k
Maya Sangesland United States	13	594 1.4×	65 0.4×	122 1.7×	30 0.5×	156 3.0×	26	1.0k
Alejandra García Chile	15	499 1.2×	77 0.5×	27 0.4×	46 0.8×	118 2.3×	43	957
Ryosuke Takii Japan	24	1.0k 2.4×	78 0.5×	14 0.2×	115 2.0×	99 1.9×	44	1.6k
Alex Rolfe United States	11	1.1k 2.6×	536 3.6×	40 0.6×	97 1.7×	50 1.0×	18	1.8k
Marie Craigon United Kingdom	12	514 1.2×	76 0.5×	20 0.3×	90 1.6×	168 3.2×	15	1.2k
Sebastian Meller Germany	20	528 1.2×	111 0.8×	17 0.2×	272 4.7×	42 0.8×	67	1.2k
Sandra Iurescia Italy	15	382 0.9×	87 0.6×	11 0.2×	33 0.6×	50 1.0×	31	740
Kathryn A. Rich United States	18	638 1.5×	143 1.0×	10 0.1×	82 1.4×	164 3.2×	21	1.5k
Atsushi Matsui Japan	20	392 0.9×	142 1.0×	8 0.1×	43 0.7×	333 6.4×	44	1.4k

Countries citing papers authored by Henrik Stranneheim

Since Specialization

Citations

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

Fields of papers citing papers by Henrik Stranneheim

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Henrik Stranneheim

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

All Works

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20 of 20 papers shown

Bruhn, Helene, K Naess, Sofia Ygberg, et al.. (2024). Novel Synonymous and Deep Intronic Variants Causing Primary and Secondary Pyruvate Dehydrogenase Complex Deficiency. Human Mutation. 2024. 1–16. 1 indexed citations

Stödberg, Tommy, et al.. (2023). Individualised human phenotype ontology gene panels improve clinical whole exome and genome sequencing analytical efficacy in a cohort of developmental and epileptic encephalopathies. Molecular Genetics & Genomic Medicine. 11(7). e2167–e2167. 2 indexed citations

Rasi, Chiara, Daniel Nilsson, Måns Magnusson, et al.. (2022). PatientMatcher: A customizable Python‐based open‐source tool for matching undiagnosed rare disease patients via the Matchmaker Exchange network. Human Mutation. 43(6). 708–716. 5 indexed citations

Magnusson, Måns, Jesper Eisfeldt, Daniel Nilsson, et al.. (2020). Loqusdb: added value of an observations database of local genomic variation. BMC Bioinformatics. 21(1). 273–273. 5 indexed citations

Naess, K, Helene Bruhn, Henrik Stranneheim, et al.. (2020). Clinical Presentation, Genetic Etiology, and Coenzyme Q10 Levels in 55 Children with Combined Enzyme Deficiencies of the Mitochondrial Respiratory Chain. The Journal of Pediatrics. 228. 240–251.e2. 8 indexed citations

Calvo‐Garrido, Javier, Camilla Maffezzini, F. Schober, et al.. (2019). SQSTM1/p62-Directed Metabolic Reprogramming Is Essential for Normal Neurodifferentiation. Stem Cell Reports. 12(4). 696–711. 36 indexed citations

Tegelberg, Saara, Jukka Kallijärvi, Janne Purhonen, et al.. (2017). Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model. Orphanet Journal of Rare Diseases. 12(1). 73–73. 18 indexed citations

Ygberg, Sofia, K Naess, Mats Eriksson, et al.. (2016). Biotin and Thiamine Responsive Basal Ganglia Disease – A vital differential diagnosis in infants with severe encephalopathy. European Journal of Paediatric Neurology. 20(3). 457–461. 17 indexed citations

Stranneheim, Henrik, Martin Engvall, K Naess, et al.. (2014). Rapid pulsed whole genome sequencing for comprehensive acute diagnostics of inborn errors of metabolism. BMC Genomics. 15(1). 1090–1090. 44 indexed citations

10.

Davanian, Haleh, Henrik Stranneheim, Tove Båge, et al.. (2012). Gene Expression Profiles in Paired Gingival Biopsies from Periodontitis-Affected and Healthy Tissues Revealed by Massively Parallel Sequencing. PLoS ONE. 7(9). e46440–e46440. 44 indexed citations

11.

Stranneheim, Henrik & Joakim Lundeberg. (2012). Stepping stones in DNA sequencing. Biotechnology Journal. 7(9). 1063–1073. 37 indexed citations

12.

Solnestam, Beata Werne, Henrik Stranneheim, Max Käller, et al.. (2012). Comparison of total and cytoplasmic mRNA reveals global regulation by nuclear retention and miRNAs. BMC Genomics. 13(1). 574–574. 33 indexed citations

13.

Stranneheim, Henrik, et al.. (2011). Scalable Transcriptome Preparation for Massive Parallel Sequencing. PLoS ONE. 6(7). e21910–e21910. 16 indexed citations

14.

Akan, Pelin, et al.. (2010). Design and assessment of binary DNA for nanopore sequencing. Genome Biology. 11(Suppl 1). P4–P4. 2 indexed citations

15.

Lundin, Sverker, Henrik Stranneheim, Erik Pettersson, Daniel Klevebring, & Joakim Lundeberg. (2010). Increased Throughput by Parallelization of Library Preparation for Massive Sequencing. PLoS ONE. 5(4). e10029–e10029. 99 indexed citations

16.

Ståhl, Patrik L., Henrik Stranneheim, Anna Asplund, et al.. (2010). Sun-Induced Nonsynonymous p53 Mutations Are Extensively Accumulated and Tolerated in Normal Appearing Human Skin. Journal of Investigative Dermatology. 131(2). 504–508. 35 indexed citations

17.

Stranneheim, Henrik, Max Käller, Tobias Allander, et al.. (2010). Classification of DNA sequences using Bloom filters. Bioinformatics. 26(13). 1595–1600. 43 indexed citations

18.

Nätt, Daniel, Niclas Lindqvist, Henrik Stranneheim, et al.. (2009). Inheritance of Acquired Behaviour Adaptations and Brain Gene Expression in Chickens. PLoS ONE. 4(7). e6405–e6405. 65 indexed citations

19.

Nätt, Daniel, et al.. (2009). Correction: Inheritance of Acquired Behaviour Adaptations and Brain Gene Expression in Chickens. PLoS ONE. 4(8). 11 indexed citations

20.

Stranneheim, Henrik, Lukas M. Orre, Janne Lehtiö, & Jenny Flygare. (2009). A comparison between protein profiles of B cell subpopulations and mantle cell lymphoma cells. Proteome Science. 7(1). 43–43. 6 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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