Tuva Barøy

672 total citations
21 papers, 333 citations indexed

About

Tuva Barøy is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Tuva Barøy has authored 21 papers receiving a total of 333 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 13 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Tuva Barøy's work include Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (5 papers) and Congenital heart defects research (3 papers). Tuva Barøy is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (5 papers) and Congenital heart defects research (3 papers). Tuva Barøy collaborates with scholars based in Norway, Czechia and United Kingdom. Tuva Barøy's co-authors include Eirik Frengen, Doriana Misceo, Madeleine Fannemel, Petter Strømme, Asbjørn Holmgren, Olaug K. Rødningen, Bjørn Tvedt, Vesna Bryn, Christeen Ramane J. Pedurupillay and Timothy Hughes and has published in prestigious journals such as Human Molecular Genetics, Gene and Orphanet Journal of Rare Diseases.

In The Last Decade

Tuva Barøy

20 papers receiving 306 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tuva Barøy Norway 12 221 161 44 30 29 21 333
Devon Lamb Thrush United States 10 218 1.0× 141 0.9× 54 1.2× 26 0.9× 25 0.9× 19 334
Ina Schanze Germany 11 201 0.9× 146 0.9× 26 0.6× 15 0.5× 19 0.7× 19 295
Ayelet Zerem Israel 11 180 0.8× 127 0.8× 42 1.0× 24 0.8× 18 0.6× 22 321
Adeline Ngoh United Kingdom 8 136 0.6× 175 1.1× 69 1.6× 35 1.2× 12 0.4× 15 367
Claire Guissart France 12 174 0.8× 73 0.5× 76 1.7× 32 1.1× 40 1.4× 22 301
Isabella Wimplinger Germany 6 226 1.0× 178 1.1× 34 0.8× 61 2.0× 17 0.6× 6 381
Enrico Alfei Italy 11 140 0.6× 160 1.0× 22 0.5× 58 1.9× 29 1.0× 25 333
Emily Tuttle United States 7 211 1.0× 113 0.7× 42 1.0× 19 0.6× 9 0.3× 10 314
Rocío Sánchez-Alcudia Spain 14 339 1.5× 72 0.4× 40 0.9× 21 0.7× 27 0.9× 18 418
Nicolas Chatron France 10 129 0.6× 123 0.8× 37 0.8× 30 1.0× 12 0.4× 44 263

Countries citing papers authored by Tuva Barøy

Since Specialization
Citations

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

Fields of papers citing papers by Tuva Barøy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tuva Barøy

This figure shows the co-authorship network connecting the top 25 collaborators of Tuva Barøy. A scholar is included among the top collaborators of Tuva Barøy 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 Tuva Barøy. Tuva Barøy 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.
Westbye, Alexander B., et al.. (2023). Clinical and Biochemical Characteristics of Untreated Adult Patients With Resistance to Thyroid Hormone Alpha. Journal of the Endocrine Society. 7(8). bvad089–bvad089. 5 indexed citations
2.
Erichsen, Anne Kjersti, et al.. (2022). A novel homozygous variant in the SPG7 gene presenting with childhood optic nerve atrophy. American Journal of Ophthalmology Case Reports. 26. 101400–101400. 2 indexed citations
3.
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
4.
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
5.
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
6.
Barøy, Tuva, Madeleine Fannemel, Doriana Misceo, et al.. (2015). A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms. Molecular Cytogenetics. 8(1). 31 indexed citations
7.
Amundsen, Silja Svanstrøm, Tuva Barøy, Svend Rand‐Hendriksen, et al.. (2015). Qualitative and quantitative analysis of FBN1 mRNA from 16 patients with Marfan Syndrome. BMC Medical Genetics. 16(1). 113–113. 8 indexed citations
8.
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
9.
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
10.
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
11.
Barøy, Tuva, et al.. (2013). Hyperphagia, Mild Developmental Delay But Apparently No Structural Brain Anomalies in a Boy Without SOX3 Expression. American Journal of Medical Genetics Part A. 161(5). 1137–1142. 9 indexed citations
12.
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
13.
14.
Floor, Karijn, et al.. (2012). A 1 Mb de novo deletion within 11q13.1q13.2 in a boy with mild intellectual disability and minor dysmorphic features. European Journal of Medical Genetics. 55(12). 695–699. 16 indexed citations
15.
Misceo, Doriana, Olaug K. Rødningen, Tuva Barøy, et al.. (2011). A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan–McDermid syndrome and hypergonadotropic hypogonadism. American Journal of Medical Genetics Part A. 155(2). 403–408. 30 indexed citations
16.
Barøy, Tuva, et al.. (2010). shRNA Expression Constructs Designed Directly from siRNA Oligonucleotide Sequences. Molecular Biotechnology. 45(2). 116–120. 4 indexed citations
17.
Barøy, Tuva, et al.. (2010). A de novo 15q13.2q13.3 deletion in a boy with an Angelman syndrome like phenotype. European Journal of Medical Genetics. 53(4). 221–224. 1 indexed citations
18.
Misceo, Doriana, Madeleine Fannemel, Tuva Barøy, et al.. (2009). SCA27 caused by a chromosome translocation: further delineation of the phenotype. Neurogenetics. 10(4). 371–374. 35 indexed citations
19.
Barøy, Tuva, Doriana Misceo, & Eirik Frengen. (2008). Strukturell variasjon i genomet bidrar til variasjon i egenskaper. Tidsskrift for Den Norske Laegeforening.
20.
Barøy, Tuva, Doriana Misceo, & Eirik Frengen. (2008). [Structural variation in the human genome contributes to variation of traits].. PubMed. 128(17). 1951–5. 8 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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