Heidi Anderson

1.3k total citations
41 papers, 777 citations indexed

About

Heidi Anderson is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Heidi Anderson has authored 41 papers receiving a total of 777 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 15 papers in Genetics and 6 papers in Cell Biology. Recurrent topics in Heidi Anderson's work include Genetic and phenotypic traits in livestock (6 papers), Human-Animal Interaction Studies (6 papers) and Mesenchymal stem cell research (5 papers). Heidi Anderson is often cited by papers focused on Genetic and phenotypic traits in livestock (6 papers), Human-Animal Interaction Studies (6 papers) and Mesenchymal stem cell research (5 papers). Heidi Anderson collaborates with scholars based in United States, Finland and Netherlands. Heidi Anderson's co-authors include Jonas Donner, Leena Valmu, Johanna Nystedt, Suvi Natunen, Saara Laitinen, Annamari Heiskanen, Tero Satomaa, Hannes Lohi, Jaakko Pohjoismäki and Tia Hirvonen and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Genome Research.

In The Last Decade

Heidi Anderson

38 papers receiving 752 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Heidi Anderson United States 15 373 266 149 97 85 41 777
Jessica A. Lehoczky United States 16 548 1.5× 203 0.8× 52 0.3× 96 1.0× 119 1.4× 33 903
So Gun Hong United States 20 685 1.8× 323 1.2× 85 0.6× 23 0.2× 130 1.5× 60 989
Sudha Srinivasan United States 16 824 2.2× 589 2.2× 104 0.7× 192 2.0× 133 1.6× 25 1.5k
Klaus Olek Germany 13 497 1.3× 393 1.5× 62 0.4× 46 0.5× 46 0.5× 20 1.0k
Cecilia Dyer United States 10 605 1.6× 527 2.0× 156 1.0× 33 0.3× 68 0.8× 16 941
Verónica Domínguez Spain 16 530 1.4× 180 0.7× 49 0.3× 306 3.2× 93 1.1× 32 1.1k
Yukiteru Ouji Japan 19 553 1.5× 39 0.1× 88 0.6× 163 1.7× 105 1.2× 55 988
María J. García‐García United States 15 834 2.2× 252 0.9× 25 0.2× 134 1.4× 70 0.8× 25 1.0k
Katarina Truvé Sweden 15 258 0.7× 167 0.6× 40 0.3× 19 0.2× 22 0.3× 17 542
William B. Solomon United States 13 1.2k 3.2× 387 1.5× 207 1.4× 42 0.4× 89 1.0× 32 1.7k

Countries citing papers authored by Heidi Anderson

Since Specialization
Citations

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

Fields of papers citing papers by Heidi Anderson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heidi Anderson

This figure shows the co-authorship network connecting the top 25 collaborators of Heidi Anderson. A scholar is included among the top collaborators of Heidi Anderson 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 Heidi Anderson. Heidi Anderson 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.
Kartzinel, Tyler R., Timothy J. Divoll, Bethan L. Littleford‐Colquhoun, et al.. (2025). Global Availability of Plant DNA Barcodes as Genomic Resources to Support Basic and Policy‐Relevant Biodiversity Research. Molecular Ecology. 34(7). e17712–e17712. 4 indexed citations
2.
Abitbol, Marie, Heidi Anderson, Paolo Ferrari, et al.. (2024). Classification of feline hypertrophic cardiomyopathy-associated gene variants according to the American College of Medical Genetics and Genomics guidelines. Frontiers in Veterinary Science. 11. 1327081–1327081. 8 indexed citations
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Anderson, Heidi, Meredith T. Morris, Victoria C. Yan, et al.. (2023). Enolase Inhibitors as Early Lead Therapeutics against Trypanosoma brucei. Pathogens. 12(11). 1290–1290.
5.
6.
Gupta, Aditi, Shellie D. Ellis, Crystal Burkhardt, et al.. (2022). Implementing a home-based virtual hypertension programme—a pilot feasibility study. Family Practice. 40(2). 414–422. 8 indexed citations
7.
Anderson, Heidi, Stephen Davison, Kaisa Kyöstilä, et al.. (2022). Genetic epidemiology of blood type, disease and trait variants, and genome-wide genetic diversity in over 11,000 domestic cats. PLoS Genetics. 18(6). e1009804–e1009804. 11 indexed citations
8.
Wilkins, Heather, Xiaowan Wang, Scott J. Koppel, et al.. (2021). Bioenergetic and inflammatory systemic phenotypes in Alzheimer’s disease APOE ε4‐carriers. Aging Cell. 20(5). e13356–e13356. 12 indexed citations
9.
Bannasch, Danika L., Thomas R. Famula, Jonas Donner, et al.. (2021). The effect of inbreeding, body size and morphology on health in dog breeds. SHILAP Revista de lepidopterología. 8(1). 12–12. 44 indexed citations
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Anderson, Heidi, et al.. (2020). Effects of Distal Mutations on Prolyl-Adenylate Formation of Escherichia coli Prolyl-tRNA Synthetase. The Protein Journal. 39(5). 542–553. 6 indexed citations
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Dreger, Dayna L., Angela M. Hughes, Balasubramanian Ganesan, et al.. (2019). True Colors: Commercially-acquired morphological genotypes reveal hidden allele variation among dog breeds, informing both trait ancestry and breed potential. PLoS ONE. 14(10). e0223995–e0223995. 21 indexed citations
14.
Donner, Jonas, Heidi Anderson, Stephen Davison, et al.. (2018). Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs. PLoS Genetics. 14(4). e1007361–e1007361. 70 indexed citations
15.
Donner, Jonas, Maria Kaukonen, Heidi Anderson, et al.. (2016). Genetic Panel Screening of Nearly 100 Mutations Reveals New Insights into the Breed Distribution of Risk Variants for Canine Hereditary Disorders. PLoS ONE. 11(8). e0161005–e0161005. 41 indexed citations
16.
Nystedt, Johanna, Matti Korhonen, Heidi Anderson, et al.. (2016). Expression of neural cell adhesion molecule and polysialic acid in human bone marrow-derived mesenchymal stromal cells. Stem Cell Research & Therapy. 7(1). 113–113. 23 indexed citations
17.
Leshchiner, Ignaty, Kristen Alexa, Peter B. Kelsey, et al.. (2012). Mutation mapping and identification by whole-genome sequencing. Genome Research. 22(8). 1541–1548. 109 indexed citations
18.
Hirvonen, Tia, Heli Suila, Ilja Ritamo, et al.. (2011). The i Blood Group Antigen as a Marker for Umbilical Cord Blood-Derived Mesenchymal Stem Cells. Stem Cells and Development. 21(3). 455–464. 12 indexed citations
19.
Suila, Heli, Timo Hirvonen, Annamari Heiskanen, et al.. (2010). Are globoseries glycosphingolipids SSEA-3 and -4 markers for stem cells derived from human umbilical cord blood?. Journal of Molecular Cell Biology. 3(2). 99–107. 42 indexed citations
20.
Tolvanen, Martti, Pauli J. Ojala, Petri Törönen, et al.. (2008). Interspliced transcription chimeras: Neglected pathological mechanism infiltrating gene accession queries?. Journal of Biomedical Informatics. 42(2). 382–389. 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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