Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program D Taliun*, DN Harris*, MD Kessler*, J Carlson*, ZA Szpiech*, R Torres*, ... Nature 590 (7845), 290-299, 2021 | 1422 | 2021 |
Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans J Carlson, AE Locke, M Flickinger, M Zawistowski, S Levy, RM Myers, ... Nature communications 9 (1), 1-13, 2018 | 139 | 2018 |
A Community-Maintained Standard Library of Population Genetic Models JR Adrion, CB Cole, N Dukler, JG Galloway, AL Gladstein, G Gower, ... eLife 9, e54967, 2020 | 128 | 2020 |
Quantifying and contextualizing the impact of bioRxiv preprints through automated social media audience segmentation J Carlson, K Harris PLoS Biology 18 (9), e3000860, 2020 | 58 | 2020 |
The Mutationathon highlights the importance of reaching standardization in estimates of pedigree-based germline mutation rates LA Bergeron, S Besenbacher, T Turner, CJ Versoza, RJ Wang, AL Price, ... Elife 11, e73577, 2022 | 41 | 2022 |
Counter the weaponization of genetics research by extremists J Carlson, BM Henn, DR Al-Hindi, S Ramachandran Nature 610 (7932), 444-447, 2022 | 28 | 2022 |
Helmsman: fast and efficient mutation signature analysis for massive sequencing datasets J Carlson, JZ Li, S Zöllner BMC genomics 19, 1-5, 2018 | 23 | 2018 |
Inferring evolutionary dynamics of mutation rates through the lens of mutation spectrum variation J Carlson, WS DeWitt, K Harris Current Opinion in Genetics & Development 62, 50-57, 2020 | 21 | 2020 |
The apportionment of citations: a scientometric analysis of Lewontin 1972 J Carlson, K Harris Philosophical Transactions of the Royal Society B 377 (1852), 20200409, 2022 | 8 | 2022 |
The effect of mutation subtypes on the allele frequency spectrum and population genetics inference K Liao, J Carlson, S Zöllner G3: Genes, Genomes, Genetics 13 (4), jkad035, 2023 | 1 | 2023 |
Confounding Fuels Hereditarian Fallacies JW Benning, J Carlson, RG Shaw, A Harpak bioRxiv, 2024 | | 2024 |
Frequency and spectrum of mutations in human sperm measured using duplex sequencing correlate with trio-based de novo mutation analyses J Axelsson, D LeBlanc, H Shojaeisaadi, MJ Meier, DM Fitzgerald, ... medRxiv, 2024.02. 13.24302689, 2024 | | 2024 |
Typological Thinking in Human Genomics Research Contributes to the Production and Prominence of Scientific Racism KA Bird, J Carlson Frontiers in Genetics 15, 1345631, 2024 | | 2024 |
Clark (2023) and the Persistence of Hereditarian Fallacies JW Benning*, J Carlson*, R Shaw, A Harpak, [*contributed equally] bioRxiv, 2023.11. 01.565061, 2023 | | 2023 |
Mapping the Landscape of Mutation Rate Heterogeneity in the Human Genome: Approaches and Applications J Carlson | | 2018 |