Anna Letko

665 total citations
46 papers, 334 citations indexed

About

Anna Letko is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Anna Letko has authored 46 papers receiving a total of 334 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 18 papers in Genetics and 13 papers in Cell Biology. Recurrent topics in Anna Letko's work include Neurological diseases and metabolism (12 papers), melanin and skin pigmentation (8 papers) and Genetic and phenotypic traits in livestock (7 papers). Anna Letko is often cited by papers focused on Neurological diseases and metabolism (12 papers), melanin and skin pigmentation (8 papers) and Genetic and phenotypic traits in livestock (7 papers). Anna Letko collaborates with scholars based in Switzerland, United States and Germany. Anna Letko's co-authors include Cord Drögemüller, Irene M. Häfliger, Tosso Leeb, Vidhya Jagannathan, James R. Mickelson, Katie M. Minor, Christine Flury, C. Schelling, Peter J. Dickinson and S. M. Schmutz and has published in prestigious journals such as Bioinformatics, Scientific Reports and BMC Genomics.

In The Last Decade

Anna Letko

40 papers receiving 325 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 Letko Switzerland 12 152 140 77 36 36 46 334
Bibaswan Ghoshal Canada 7 87 0.6× 248 1.8× 64 0.8× 8 0.2× 12 0.3× 7 509
Kenzi Oshima Japan 14 54 0.4× 311 2.2× 174 2.3× 28 0.8× 59 1.6× 29 573
Irene M. Häfliger Switzerland 13 240 1.6× 143 1.0× 57 0.7× 12 0.3× 11 0.3× 60 391
D. Shalhevet United States 7 52 0.3× 131 0.9× 27 0.4× 18 0.5× 18 0.5× 15 448
Yu‐Ten Ju Taiwan 13 134 0.9× 200 1.4× 52 0.7× 6 0.2× 6 0.2× 36 448
Carla García‐Morales United Kingdom 12 55 0.4× 214 1.5× 39 0.5× 28 0.8× 10 0.3× 19 475
Valerie E. Vancollie United Kingdom 8 60 0.4× 162 1.2× 51 0.7× 17 0.5× 10 0.3× 12 278
Ulla Gustafson Sweden 7 221 1.5× 203 1.4× 84 1.1× 3 0.1× 33 0.9× 7 500
Hadriano M. Lacerda Spain 13 74 0.5× 232 1.7× 71 0.9× 27 0.8× 3 0.1× 16 463

Countries citing papers authored by Anna Letko

Since Specialization
Citations

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

Fields of papers citing papers by Anna Letko

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Letko

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Letko. A scholar is included among the top collaborators of Anna Letko 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 Letko. Anna Letko 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.
Häfliger, Irene M., et al.. (2025). Rare phenotypes of white coat color in Simmental calves: genetic causes of syndromic forms of albinism and depigmentation. Molecular Genetics and Genomics. 300(1). 91–91.
2.
Letko, Anna, et al.. (2024). Whole genome sequencing reveals candidate causal genetic variants for spastic syndrome in Holstein cattle. Scientific Reports. 14(1). 31188–31188.
3.
Letko, Anna, Pascale Quignon, Jonas Donner, et al.. (2024). A RETREG1 variant is associated with hereditary sensory and autonomic neuropathy with acral self‐mutilation in purebred German Spitz. Animal Genetics. 55(6). 810–819.
4.
Letko, Anna, et al.. (2024). Congenital syndromic Chiari-like malformation (CSCM) in Holstein cattle: towards unravelling of possible genetic causes. Acta veterinaria Scandinavica. 66(1). 29–29. 2 indexed citations
5.
Grest, Paula, Anna Letko, Vidhya Jagannathan, et al.. (2023). Independent COL17A1 Variants in Cats with Junctional Epidermolysis Bullosa. Genes. 14(10). 1835–1835.
6.
Letko, Anna, et al.. (2023). Identification of genomic regions associated with differences in fleece type in Huacaya and Suri alpacas (Vicugna pacos). Animal Genetics. 55(1). 163–167. 2 indexed citations
7.
Letko, Anna, et al.. (2021). Genetic evaluation of small ruminant lentivirus susceptibility in Valais blacknose sheep. Animal Genetics. 52(5). 781–782. 3 indexed citations
8.
Häfliger, Irene M., et al.. (2021). A frameshift insertion in FA2H causes a recessively inherited form of ichthyosis congenita in Chianina cattle. Molecular Genetics and Genomics. 296(6). 1313–1322. 8 indexed citations
9.
Letko, Anna, et al.. (2020). Ear type in sheep is associated with the MSRB3 locus. Animal Genetics. 51(6). 968–972. 14 indexed citations
10.
Häfliger, Irene M., Anna Letko, Leonardo Murgiano, & Cord Drögemüller. (2020). De novo stop‐lost germline mutation in FGFR3 causes severe chondrodysplasia in the progeny of a Holstein bull. Animal Genetics. 51(3). 466–469. 3 indexed citations
11.
Lischer, Heidi E. L., Irene Keller, Irene M. Häfliger, et al.. (2020). New genomic features of the polled intersex syndrome variant in goats unraveled by long‐read whole‐genome sequencing. Animal Genetics. 51(3). 439–448. 20 indexed citations
12.
Letko, Anna, Vidhya Jagannathan, Kaspar Matiasek, et al.. (2020). Whole Genome Sequencing Indicates Heterogeneity of Hyperostotic Disorders in Dogs. Genes. 11(2). 163–163. 1 indexed citations
13.
Häfliger, Irene M., et al.. (2020). A Heterozygous Missense Variant in the COL5A2 in Holstein Cattle Resembling the Classical Ehlers–Danlos Syndrome. Animals. 10(11). 2002–2002. 9 indexed citations
14.
Letko, Anna, et al.. (2020). A de novo variant in OTX2 in a lamb with otocephaly. Acta veterinaria Scandinavica. 62(1). 5–5. 1 indexed citations
15.
Letko, Anna, et al.. (2020). Compound heterozygous PLA2G6 loss-of-function variants in Swaledale sheep with neuroaxonal dystrophy. Molecular Genetics and Genomics. 296(1). 235–242. 4 indexed citations
16.
Letko, Anna, Irene M. Häfliger, Timothy Geraghty, et al.. (2020). Deleterious AGXT Missense Variant Associated with Type 1 Primary Hyperoxaluria (PH1) in Zwartbles Sheep. Genes. 11(10). 1147–1147. 3 indexed citations
17.
Letko, Anna, et al.. (2019). A de novo in‐frame duplication in the COL1A2 gene in a Lagotto Romagnolo dog with osteogenesis imperfecta. Animal Genetics. 50(6). 786–787. 8 indexed citations
18.
Letko, Anna, Elisabeth Dietschi, Vidhya Jagannathan, et al.. (2019). A Missense Variant in SCN8A in Alpine Dachsbracke Dogs Affected by Spinocerebellar Ataxia. Genes. 10(5). 362–362. 9 indexed citations
19.
Grahofer, Alexander, Anna Letko, Irene M. Häfliger, et al.. (2019). Chromosomal imbalance in pigs showing a syndromic form of cleft palate. BMC Genomics. 20(1). 349–349. 15 indexed citations
20.
Becker, Doreen, Katie M. Minor, Anna Letko, et al.. (2017). A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs. BMC Genomics. 18(1). 662–662. 17 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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