Andrew Dahl

1.5k total citations
15 papers, 450 citations indexed

About

Andrew Dahl is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Andrew Dahl has authored 15 papers receiving a total of 450 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Cancer Research. Recurrent topics in Andrew Dahl's work include Genetic Associations and Epidemiology (3 papers), Genetic and phenotypic traits in livestock (3 papers) and Genetic Mapping and Diversity in Plants and Animals (3 papers). Andrew Dahl is often cited by papers focused on Genetic Associations and Epidemiology (3 papers), Genetic and phenotypic traits in livestock (3 papers) and Genetic Mapping and Diversity in Plants and Animals (3 papers). Andrew Dahl collaborates with scholars based in United States, United Kingdom and Australia. Andrew Dahl's co-authors include Noah Zaitlen, Fernando Arena, Melanie May, David Barker, Charles E. Schwartz, Lisbeth Tranebjærg, Vesna Ponjavic, Sten Andréasson, Roger E. Stevenson and Chun Ye and has published in prestigious journals such as Nature Communications, Nature Genetics and The American Journal of Human Genetics.

In The Last Decade

Andrew Dahl

15 papers receiving 443 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andrew Dahl United States	9	241	207	37	27	27	15	450
Yoshinori Shirai Japan	11	266 1.1×	130 0.6×	8 0.2×	16 0.6×	7 0.3×	49	511
Dean Phelan Australia	11	188 0.8×	180 0.9×	39 1.1×	51 1.9×	5 0.2×	15	398
Brian P. Perry United States	12	137 0.6×	233 1.1×	6 0.2×	79 2.9×	6 0.2×	27	509
Haipeng Zhu China	11	254 1.1×	38 0.2×	8 0.2×	8 0.3×	22 0.8×	22	398
Ahmad Usman Zafar Pakistan	11	347 1.4×	53 0.3×	7 0.2×	113 4.2×	10 0.4×	30	471
Margaret R. Starostik United States	7	340 1.4×	102 0.5×	5 0.1×	17 0.6×	9 0.3×	10	502
Rini Pauly United States	9	171 0.7×	90 0.4×	14 0.4×	2 0.1×	7 0.3×	31	335
Eeva-Marja Sankila Finland	7	474 2.0×	318 1.5×	8 0.2×	129 4.8×	3 0.1×	16	978
Atteeq U. Rehman United States	12	373 1.5×	93 0.4×	8 0.2×	315 11.7×	6 0.2×	19	588

Countries citing papers authored by Andrew Dahl

Since Specialization

Citations

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

Fields of papers citing papers by Andrew Dahl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew Dahl

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew Dahl. A scholar is included among the top collaborators of Andrew 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 Andrew Dahl. Andrew 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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15 of 15 papers shown

Dahl, Andrew, et al.. (2024). A scalable and robust variance components method reveals insights into the architecture of gene-environment interactions underlying complex traits. The American Journal of Human Genetics. 111(7). 1462–1480. 2 indexed citations

Dahl, Andrew, Michael Thompson, Morten Dybdahl Krebs, et al.. (2023). Phenotype integration improves power and preserves specificity in biobank-based genetic studies of major depressive disorder. Nature Genetics. 55(12). 2082–2093. 23 indexed citations

Sandor, Cynthia, Andrew Dahl, Michael Lawton, et al.. (2022). Universal clinical Parkinson’s disease axes identify a major influence of neuroinflammation. Genome Medicine. 14(1). 129–129. 6 indexed citations

Celona, Barbara, Fleur C. Garton, Joel Mefford, et al.. (2021). Comprehensive cell type decomposition of circulating cell-free DNA with CelFiE. Nature Communications. 12(1). 2717–2717. 33 indexed citations

Keys, Kevin L., Angel C. Y. Mak, Marquitta J. White, et al.. (2020). On the cross-population generalizability of gene expression prediction models. PLoS Genetics. 16(8). e1008927–e1008927. 31 indexed citations

Liu, Xuanyao, Joel Mefford, Andrew Dahl, et al.. (2020). GBAT: a gene-based association test for robust detection of trans-gene regulation. Genome biology. 21(1). 211–211. 12 indexed citations

Hernandez, Ryan D., et al.. (2019). Ultrarare variants drive substantial cis heritability of human gene expression. Nature Genetics. 51(9). 1349–1355. 68 indexed citations

Steinsaltz, David, Andrew Dahl, & Kenneth W. Wachter. (2018). Statistical properties of simple random-effects models for genetic heritability. Electronic Journal of Statistics. 12(1). 321–356. 7 indexed citations

Berlanga‐Taylor, Antonio J., Katharine Plant, Andrew Dahl, et al.. (2018). Genomic Response to Vitamin D Supplementation in the Setting of a Randomized, Placebo-Controlled Trial. EBioMedicine. 31. 133–142. 25 indexed citations

10.

Hernandez, Ryan D., et al.. (2018). Singleton Variants Dominate the Genetic Architecture of Human Gene Expression. SSRN Electronic Journal. 6 indexed citations

11.

Hernandez, Ryan D., et al.. (2018). Singleton Variants Dominate the Genetic Architecture of Human Gene Expression. SSRN Electronic Journal. 3 indexed citations

12.

Dahl, Andrew, et al.. (2017). Detecting Clusters in Atom Probe Data with Gaussian Mixture Models. Microscopy and Microanalysis. 23(2). 269–278. 26 indexed citations

13.

Dahl, Andrew, Valentina Iotchkova, Amelie Baud, et al.. (2016). A multiple-phenotype imputation method for genetic studies. Nature Genetics. 48(4). 466–472. 65 indexed citations

14.

Tranebjærg, Lisbeth, Charles E. Schwartz, Sten Andréasson, et al.. (1995). A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.. Journal of Medical Genetics. 32(4). 257–263. 136 indexed citations

15.

Goldschmidt, Peter G. & Andrew Dahl. (1976). Demoflush Estimating Population in Seasonal Resort Communities. Growth and Change. 7(2). 44–48. 7 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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