Freyja Imsland

2.2k total citations
14 papers, 632 citations indexed

About

Freyja Imsland is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Freyja Imsland has authored 14 papers receiving a total of 632 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Cell Biology. Recurrent topics in Freyja Imsland's work include Genetic and phenotypic traits in livestock (5 papers), Genomics and Chromatin Dynamics (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Freyja Imsland is often cited by papers focused on Genetic and phenotypic traits in livestock (5 papers), Genomics and Chromatin Dynamics (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Freyja Imsland collaborates with scholars based in Sweden, United States and France. Freyja Imsland's co-authors include Leif Andersson, Michèle Tixier‐Boichard, David Gourichon, Carl‐Johan Rubin, Agathe Vieaud, Finn Hallböök, Bertrand Bed’Hom, Henrik Boije, Dominic Wright and Jennifer R. S. Meadows and has published in prestigious journals such as Nature Genetics, PLoS ONE and PLoS Genetics.

In The Last Decade

Freyja Imsland

14 papers receiving 609 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Freyja Imsland 418 235 144 121 113 14 632
U. Philipp 310 0.7× 275 1.2× 88 0.6× 75 0.6× 176 1.6× 39 735
L. V. Millon 649 1.6× 396 1.7× 288 2.0× 29 0.2× 112 1.0× 32 1.0k
T. Hasegawa 364 0.9× 181 0.8× 46 0.3× 52 0.4× 155 1.4× 22 523
Doreen Schwochow 481 1.2× 197 0.8× 55 0.4× 102 0.8× 100 0.9× 7 669
Christine Flury 767 1.8× 137 0.6× 101 0.7× 78 0.6× 72 0.6× 39 895
Gus Cothran 264 0.6× 121 0.5× 60 0.4× 51 0.4× 141 1.2× 12 504
Hironaga Kakoi 735 1.8× 426 1.8× 44 0.3× 85 0.7× 126 1.1× 75 946
Chungang Feng 530 1.3× 306 1.3× 134 0.9× 265 2.2× 33 0.3× 41 789
Gérard Guérin 640 1.5× 410 1.7× 225 1.6× 72 0.6× 335 3.0× 30 1.1k
G. Dolf 547 1.3× 261 1.1× 73 0.5× 55 0.5× 25 0.2× 63 857

Countries citing papers authored by Freyja Imsland

Since Specialization
Citations

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

Fields of papers citing papers by Freyja Imsland

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Freyja Imsland

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

All Works

14 of 14 papers shown
1.
Staiger, Elizabeth A., Markus Sällman Almén, Marta Promerová, et al.. (2017). The evolutionary history of the DMRT3 ‘Gait keeper’ haplotype. Animal Genetics. 48(5). 551–559. 15 indexed citations
2.
Imsland, Freyja, et al.. (2017). Association analysis of KIT, MITF, and PAX3 variants with white markings in Spanish horses. Animal Genetics. 48(3). 349–352. 18 indexed citations
3.
Eriksson, S., Lisa Andersson, Freyja Imsland, et al.. (2016). Conformation Traits and Gaits in the Icelandic Horse are Associated with Genetic Variants inMyostatin(MSTN). Journal of Heredity. 107(5). 431–437. 7 indexed citations
4.
Imsland, Freyja, Kelly A. McGowan, Carl‐Johan Rubin, et al.. (2015). Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses. Nature Genetics. 48(2). 152–158. 59 indexed citations
5.
Velie, Brandon D., Freyja Imsland, Lisa Andersson, et al.. (2015). Frequencies of polymorphisms in myostatin vary in Icelandic horses according to the use of the horses. Animal Genetics. 46(4). 467–468. 2 indexed citations
6.
Imsland, Freyja, et al.. (2015). The importance of the DMRT3 ‘Gait keeper’ mutation on riding traits and gaits in Standardbred and Icelandic horses. Livestock Science. 176. 33–39. 14 indexed citations
7.
Promerová, Marta, Leif Andersson, Leif Andersson, et al.. (2014). Worldwide frequency distribution of the ‘Gait keeper’ mutation in the DMRT3 gene. Animal Genetics. 45(2). 274–282. 75 indexed citations
8.
Sundström, Elisabeth, Freyja Imsland, Sofia Mikko, et al.. (2012). Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses. BMC Genomics. 13(1). 365–365. 38 indexed citations
9.
Imsland, Freyja, Chungang Feng, Henrik Boije, et al.. (2012). The Rose-comb Mutation in Chickens Constitutes a Structural Rearrangement Causing Both Altered Comb Morphology and Defective Sperm Motility. PLoS Genetics. 8(6). e1002775–e1002775. 102 indexed citations
10.
Wang, Yanqiang, Yu Gao, Freyja Imsland, et al.. (2012). The Crest Phenotype in Chicken Is Associated with Ectopic Expression of HOXC8 in Cranial Skin. PLoS ONE. 7(4). e34012–e34012. 49 indexed citations
11.
Boije, Henrik, Mohammad Harun‐Or‐Rashid, Freyja Imsland, et al.. (2012). Sonic Hedgehog-Signalling Patterns the Developing Chicken Comb as Revealed by Exploration of the Pea-comb Mutation. PLoS ONE. 7(12). e50890–e50890. 19 indexed citations
12.
Bellone, Rebecca R., George W. Forsyth, Tosso Leeb, et al.. (2010). Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses. Briefings in Functional Genomics. 9(3). 193–207. 36 indexed citations
13.
Wright, Dominic, Henrik Boije, Jennifer R. S. Meadows, et al.. (2009). Copy Number Variation in Intron 1 of SOX5 Causes the Pea-comb Phenotype in Chickens. PLoS Genetics. 5(6). e1000512–e1000512. 195 indexed citations
14.
Böðvarsdóttir, Sigríður Klara, et al.. (2009). 64,XX, SRY-, and ZFY-Negative Icelandic Horse Likely to Be True Hermaphrodite. Journal of Equine Veterinary Science. 29(10). 734–738. 3 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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