Items where Subject is "QH426 Genetics"
- Library of Congress Subject Areas (23005)
- Q Science (4645)
- QH Natural history (166)
- QH426 Genetics (27)
- QH Natural history (166)
- Q Science (4645)
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Allum, N., Allansdottir, A., Gaskell, G. , Hampel, J., Jackson, J., Moldovan, A., Priest, S., Stares, S. & Stoneman, P. (2017). Religion and the public ethics of stem-cell research: Attitudes in Europe, Canada and the United States. PLoS One, 12(4), article number e0176274. doi: 10.1371/journal.pone.0176274
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Chatterjee, S., Debnath, R., Biswas, S. ORCID: 0000-0002-6770-9845 & Bairagi, A. K. (2024). Prediction of RNA Secondary Structure Using Butterfly Optimization Algorithm. Human-Centric Intelligent Systems, 4, pp. 220-240. doi: 10.1007/s44230-024-00062-6
Coutts, F., Palmos, A. B., Duarte, R. R. R. , de Jong, S., Lewis, C. M., Dima, D. ORCID: 0000-0002-2598-0952 & Powell, T. R. (2018). The polygenic nature of telomere length and the anti-ageing properties of lithium. Neuropsychopharmacology, 44(4), pp. 757-765. doi: 10.1038/s41386-018-0289-0
Cowell, R. (2009). Efficient maximum likelihood pedigree reconstruction. Theoretical Population Biology, 76(4), pp. 285-291. doi: 10.1016/j.tpb.2009.09.002
Cowell, R. (2009). Validation of an STR peak area model. Forensic Science International: Genetics, 3(3), pp. 193-199. doi: 10.1016/j.fsigen.2009.01.006
Cowell, R. (2013). A simple greedy algorithm for reconstructing pedigrees. Theoretical Population Biology, 83(1), pp. 55-63. doi: 10.1016/j.tpb.2012.11.002
Cowell, R., Graversen, T., Lauritzen, S. L. & Mortera, J. (2014). Analysis of forensic DNA mixtures with artefacts. Journal of the Royal Statistical Society. Series C: Applied Statistics, 64(1), pp. 1-48. doi: 10.1111/rssc.12071
Cowell, R., Lauritzen, S. L. & Mortera, J. (2011). Probabilistic expert systems for handling artifacts in complex DNA mixtures. Forensic Science International: Genetics, 5(3), pp. 202-209. doi: 10.1016/j.fsigen.2010.03.008
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Dujon, A. M., Aktipis, A., Alix‐Panabières, C. , Amend, S. R., Boddy, A. M., Brown, J. S., Capp, J-P., DeGregori, J., Ewald, P., Gatenby, R., Gerlinger, M., Giraudeau, M., Hamede, R. R., Hansen, E., Kareva, I., Maley, C. C., Marusyk, A., McGranahan, N., Metzger, M. J., Nedelcu, A. M., Noble, R. ORCID: 0000-0002-8057-4252, Nunney, L., Pienta, K. J., Polyak, K., Pujol, P., Read, A. F., Roche, B., Sebens, S., Solary, E., Staňková, K., Swain Ewald, H., Thomas, F. & Ujvari, B. (2020). Identifying key questions in the ecology and evolution of cancer. Evolutionary Applications, 14(4), pp. 877-892. doi: 10.1111/eva.13190
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Fastman, Y., Noble, R. ORCID: 0000-0002-8057-4252, Recker, M. & Dzikowski, R. (2012). Erasing the epigenetic memory and beginning to switch--the onset of antigenic switching of var genes in Plasmodium falciparum. PLoS One, 7(3), article number e34168. doi: 10.1371/journal.pone.0034168
Finer, S., Martin, H. C., Khan, A. , Hunt, K. A., MacLaughlin, B., Ahmed, Z., Ashcroft, R. ORCID: 0000-0001-6065-4717, Durham, C., MacArthur, D. G., McCarthy, M. I., Robson, J., Trivedi, B., Griffiths, C., Wright, J., Trembath, R. C. & van Heel, D. A. (2019). Cohort Profile: East London Genes & Health (ELGH), a community based population genomics and health study of British-Bangladeshi and British-Pakistani people. International Journal of Epidemiology, 49(1), 20-21I. doi: 10.1101/426163
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Huntjens, B. ORCID: 0000-0002-4864-0723, Ctori, I. ORCID: 0000-0003-1523-4996, Mahroo, O. A. , Williams, K. M. & Hammond, C. J. (2016). Classification and heritability of macular pigment spatial profile phenotypes using two-wavelength fundus autofluorescence. Acta Ophthalmologica, 94, doi: 10.1111/j.1755-3768.2016.0526
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Jadva, V. ORCID: 0000-0003-0922-0694, Shaw, K., Bay, B. , Poulsen, M., Ingerslev, J., Petersen, M. R., Fedder, J. & Kesmodel, U. S. (2024). The experiences of parents with a child born following pre-implantation genetic testing. Fertility and Sterility, 122(4), pp. 740-743. doi: 10.1016/j.fertnstert.2024.05.141
Jimeno, A., Jimenez-Ruiz, E. ORCID: 0000-0002-9083-4599, Lee, V. , Gaudan, S., Berlanga, R. & Rebholz-Schuhmann, D. (2008). Assessment of disease named entity recognition on a corpus of annotated sentences. BMC Bioinformatics, 9(S3), article number S3. doi: 10.1186/1471-2105-9-s3-s3
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Lemant, J., Le Sueur, C., Manojlović, V. & Noble, R. ORCID: 0000-0002-8057-4252 (2022). Robust, Universal Tree Balance Indices. Systematic Biology, 71(5), pp. 1210-1224. doi: 10.1093/sysbio/syac027
Liatsis, P., Nazarboland, M. A., Goulermas, J. Y. , Zeng, X. J. & Milonidis, E. (2008). Automating the processing of cDNA microarray images. International Journal of Intelligent Systems Technologies and Applications, 5(1-2), pp. 115-144. doi: 10.1504/ijista.2008.018170
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Mamouei, M. H., Budidha, K. ORCID: 0000-0002-6329-8399, Baishya, N. ORCID: 0000-0002-2231-6132 , Qassem, M. & Kyriacou, P. A. ORCID: 0000-0002-2868-485X (2020). Comparison of wavelength selection methods for in-vitro estimation of lactate: a new unconstrained, genetic algorithm-based wavelength selection. Scientific Reports, 10(1), article number 16905. doi: 10.1038/s41598-020-73406-4
Mamouei, M. H., Qassem, M., Budidha, K. ORCID: 0000-0002-6329-8399 , Baishya, N., Vadgama, P. & Kyriacou, P. A. ORCID: 0000-0002-2868-485X (2019). Comparison of a Genetic Algorithm Variable Selection and Interval Partial Least Squares for quantitative analysis of lactate in PBS. 2019 41st Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC), pp. 3239-3242. doi: 10.1109/embc.2019.8856765
Marris, C. (2018). Genomic technologies in the bioeconomy: Introduction. In: Gibbon, S., Prainsack, B., Hilgartner, S. & Lamoreaux, J. (Eds.), Genomic technologies in the bioeconomy: Introduction. (pp. 57-62). London: Routledge. doi: 10.4324/9781315451695
Mayor, Charlie (2012). The classification of gene products in the molecular biology domain: Realism, objectivity, and the limitations of the Gene Ontology. (Unpublished Doctoral thesis, City University London)
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Packer, A., Corbett, A., Arathimos, R. , Ballard, C., Aarsland, D., Hampshire, A., Dima, D. ORCID: 0000-0002-2598-0952, Creese, B., Malanchini, M. & Powell, T. R. (2023). Limited evidence of a shared genetic relationship between C-reactive protein levels and cognitive function in older UK adults of European ancestry. Frontiers in Dementia, 2, article number 1093223. doi: 10.3389/frdem.2023.1093223
Pozarickij, A., Williams, C., Hysi, P. G. , Guggenheim, J. A., Aslam, T., Barman, S. A., Barrett, J. H., Bishop, P., Blows, P., Bunce, C., Carare, R. O., Chakravarthy, U., Chan, M., Chua, S. Y. L., Crabb, D. P. ORCID: 0000-0001-8754-3902, Cumberland, P. M., Day, A., Desai, P., Dhillon, B., Dick, A. D., Egan, C., Ennis, S., Foster, P., Fruttiger, M., Gallacher, J. E. J., Garway-Heath, D. F., Gibson, J., Gore, D., Hammond, C. J., Hardcastle, A., Harding, S. P., Hogg, R. E., Keane, P. A., Khaw, S. P. T., Khawaja, A. P., Lascaratos, G., Lotery, A. J., Mac Gillivray, T., Mackie, S., Martin, K., McGaughey, M., McGuinness, B., McKay, G. J., McKibbin, M., Mitry, D., Moore, T., Morgan, J. E., Muthy, Z. A., O’Sullivan, E., Owen, C. G., Patel, P., Paterson, E., Peto, T., Petzold, A., Rahi, J. S., Rudnikca, A. R., Self, J., Sivaprasad, S., Steel, D., Stratton, I., Strouthidis, N., Sudlow, C., Thomas, D., Trucco, E., Tufail, A., Vitart, V., Vernon, S. A., Viswanathan, A. C., Williams, K., Woodside, J. V., Yates, M. M., Yip, J. & Zheng, Y. (2019). Quantile regression analysis reveals widespread evidence for gene-environment or gene-gene interactions in myopia development. Communications Biology, 2(1), article number 167. doi: 10.1038/s42003-019-0387-5
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Rutledge, G. A. ORCID: 0000-0002-2093-4543, Pratt, S. G., Richer, S. P. , Huntjens, B. ORCID: 0000-0002-4864-0723, Perry, C. B., Pratt, G. & Podella, C. (2020). Foveal macular pigment dip in offspring of age-related macular degeneration patients is inversely associated with omega-3 index. BMC Ophthalmology, 20(1), article number 473. doi: 10.1186/s12886-020-01742-0
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Smederevac, S., Sadikovic, S., Colovic, P. , Vucinic, N., Milutinovic, A., Riemann, R., Corr, P. J. ORCID: 0000-0002-7618-0058, Prinz, M. & Budimlija, Z. (2022). Quantitative behavioral genetic and molecular genetic foundations of the approach and avoidance strategies. Current Psychology, 42(17), pp. 14268-14282. doi: 10.1007/s12144-022-02724-9
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Wilson, B. J., Islam, R., Francis, J. , Grimshaw, J. M., Permaul, J. A., Allanson, J. E., Blaine, S., Graham, I. D., Meschino, W. S., Ramsay, C. R. & Carroll, J. C. (2016). Supporting genetics in primary care: investigating how theory can inform professional education. European Journal of Human Genetics, 24(11), pp. 1541-1546. doi: 10.1038/ejhg.2016.68
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Zhou, F. ORCID: 0000-0002-9851-8312, Butterworth, A. S. & Asimit, J. L. (2022). Flashfm-ivis: interactive visualisation for fine-mapping of multiple quantitative traits. In: Human Heredity. 50th European Mathematical Genetics Meeting (EMGM) 2022, 21-22 Apr 2022, Cambridge, United Kingdom. doi: 10.1159/000524615
Zhou, F. ORCID: 0000-0002-9851-8312, Butterworth, A. S. & Asimit, J. L. (2022). Flashfm-ivis: interactive visualization for fine-mapping of multiple quantitative traits. Bioinformatics, 38(17), pp. 4238-4242. doi: 10.1093/bioinformatics/btac453