Andy Dahl

870 total citations
17 papers, 287 citations indexed

About

Andy Dahl is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Andy Dahl has authored 17 papers receiving a total of 287 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 10 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Andy Dahl's work include Genetic Associations and Epidemiology (16 papers), Bioinformatics and Genomic Networks (8 papers) and Genetic Mapping and Diversity in Plants and Animals (7 papers). Andy Dahl is often cited by papers focused on Genetic Associations and Epidemiology (16 papers), Bioinformatics and Genomic Networks (8 papers) and Genetic Mapping and Diversity in Plants and Animals (7 papers). Andy Dahl collaborates with scholars based in United States, United Kingdom and Germany. Andy Dahl's co-authors include Noah Zaitlen, Jonathan Flint, Na Cai, Kenneth S. Kendler, Andrew J. Schork, Kenneth W. Wachter, Sriram Sankararaman, David Steinsaltz, Silviu‐Alin Bacanu and Khiem Nguyen and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Andy Dahl

15 papers receiving 283 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andy Dahl United States	9	195	91	35	20	20	17	287
Lide Han United States	9	159 0.8×	51 0.6×	33 0.9×	22 1.1×	27 1.4×	16	328
Daniel J. Weiner United States	7	174 0.9×	98 1.1×	32 0.9×	26 1.3×	12 0.6×	10	310
Aleix Arnau‐Soler United Kingdom	6	77 0.4×	46 0.5×	53 1.5×	58 2.9×	25 1.3×	8	249
Nicolás W. Martín Australia	7	77 0.4×	74 0.8×	31 0.9×	7 0.3×	13 0.7×	10	210
Sylvanus Toikumo United States	7	51 0.3×	34 0.4×	13 0.4×	23 1.1×	17 0.8×	16	145
Erin Macdonald-Dunlop United Kingdom	4	56 0.3×	106 1.2×	15 0.4×	16 0.8×	14 0.7×	6	211
Judit García‐González United States	11	68 0.3×	57 0.6×	7 0.2×	33 1.6×	19 0.9×	20	298
Robert Loughnan United States	8	67 0.3×	49 0.5×	27 0.8×	15 0.8×	6 0.3×	20	183
Fiona A. Hagenbeek Netherlands	10	42 0.2×	75 0.8×	9 0.3×	20 1.0×	21 1.1×	19	204

Countries citing papers authored by Andy Dahl

Since Specialization

Citations

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

Fields of papers citing papers by Andy Dahl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andy Dahl

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

All Works

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17 of 17 papers shown

Mefford, Joel, F. Zhang, Richard Border, et al.. (2025). Beyond predictive R: Quantile regression and non-equivalence tests reveal complex relationships of traits and polygenic scores. The American Journal of Human Genetics. 112(6). 1363–1375.

Appadurai, Vivek, Richard Border, Noah Zaitlen, et al.. (2025). The relationship between genotype- and phenotype-based estimates of genetic liability to psychiatric disorders, in practice and in theory. The American Journal of Human Genetics. 113(1). 184–201.

Saitou, Marie, et al.. (2024). Allele frequency impacts the cross-ancestry portability of gene expression prediction in lymphoblastoid cell lines. The American Journal of Human Genetics. 111(12). 2814–2825. 1 indexed citations

Thompson, Michael, Joel Mefford, Tanushree Haldar, et al.. (2024). Characterizing the genetic architecture of drug response using gene-context interaction methods. Cell Genomics. 4(12). 100722–100722. 4 indexed citations

Chen, Minhui & Andy Dahl. (2024). A robust model for cell type-specific interindividual variation in single-cell RNA sequencing data. Nature Communications. 15(1). 5229–5229. 2 indexed citations

Alvarez, Marcus, Silviu‐Alin Bacanu, Andrew J. Schork, et al.. (2023). Deep learning-based phenotype imputation on population-scale biobank data increases genetic discoveries. Nature Genetics. 55(12). 2269–2276. 29 indexed citations

Tang, David, et al.. (2023). Factorizing polygenic epistasis improves prediction and uncovers biological pathways in complex traits. The American Journal of Human Genetics. 110(11). 1875–1887. 4 indexed citations

Border, Richard, Georgios Athanasiadis, Alfonso Buil, et al.. (2022). Cross-trait assortative mating is widespread and inflates genetic correlation estimates. Science. 378(6621). 754–761. 71 indexed citations

Krebs, Morten Dybdahl, et al.. (2021). Abstracts. Genetic Epidemiology. 45(7). 741–807. 1 indexed citations

10.

Sheppard, Brooke, Nadav Rappoport, Po‐Ru Loh, et al.. (2021). A model and test for coordinated polygenic epistasis in complex traits. Proceedings of the National Academy of Sciences. 118(15). 10 indexed citations

11.

Steinsaltz, David, Andy Dahl, & Kenneth W. Wachter. (2020). On Negative Heritability and Negative Estimates of Heritability. Genetics. 215(2). 343–357. 24 indexed citations

12.

Dahl, Andy, Khiem Nguyen, Na Cai, et al.. (2020). A Robust Method Uncovers Significant Context-Specific Heritability in Diverse Complex Traits. The American Journal of Human Genetics. 106(1). 71–91. 43 indexed citations

13.

Dahl, Andy & Noah Zaitlen. (2020). Genetic Influences on Disease Subtypes. Annual Review of Genomics and Human Genetics. 21(1). 413–435. 16 indexed citations

14.

Dahl, Andy, Vincent Guillemot, Joel Mefford, Hugues Aschard, & Noah Zaitlen. (2019). Adjusting for Principal Components of Molecular Phenotypes Induces Replicating False Positives. Genetics. 211(4). 1179–1189. 10 indexed citations

15.

Dahl, Andy, Na Cai, Arthur Ko, et al.. (2019). Reverse GWAS: Using genetics to identify and model phenotypic subtypes. PLoS Genetics. 15(4). e1008009–e1008009. 26 indexed citations

16.

Peterson, Roseann E., Na Cai, Andy Dahl, et al.. (2019). MOLECULAR GENETIC ANALYSIS SUBDIVIDED BY ADVERSITY EXPOSURE SUGGESTS ETIOLOGIC HETEROGENEITY IN MAJOR DEPRESSION. European Neuropsychopharmacology. 29. S792–S793. 1 indexed citations

17.

Peterson, Roseann E., Na Cai, Andy Dahl, et al.. (2018). Molecular Genetic Analysis Subdivided by Adversity Exposure Suggests Etiologic Heterogeneity in Major Depression. American Journal of Psychiatry. 175(6). 545–554. 45 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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