Bradley, Allan
University of Cambridge
26 papers on CoChatORCID 0000-0002-2349-8839
Most cited papers
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Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours
Donehower, L. A., Harvey, M., Slagle, B. L., McArthur, M. J., Montgomery, C. A., Butel, J. S., & Bradley, A. (1992) · Nature
Cancer-related Molecular PathwaysDevelopmental Biology and Gene Regulation
Cited by 4,649
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Identification of Mammalian microRNA Host Genes and Transcription Units
Rodriguez, A., Griffiths-Jones, S., Ashurst, J. L., & Bradley, A. (2004) · Genome Research
MicroRNA in disease regulationCancer-related molecular mechanisms research
Cited by 2,128
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Repair of double-strand breaks induced by CRISPR–Cas9 leads to large deletions and complex rearrangements
Kosicki, M., Tomberg, K., & Bradley, A. (2018) · Nature Biotechnology
CRISPR and Genetic EngineeringRNA regulation and disease
Cited by 1,883
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Requirement of bic/microRNA-155 for Normal Immune Function
Rodriguez, A., Vigorito, E., Clare, S., Warren, M. V., Couttet, P., Soond, D. R., van Dongen, S., Grocock, R. J., Das, P. P., Miska, E. A., et al. (2007) · Science
MicroRNA in disease regulationT-cell and B-cell Immunology
Cited by 1,833
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A conditional knockout resource for the genome-wide study of mouse gene function
Skarnes, W. C., Rosen, B., West, A. P., Koutsourakis, M., Bushell, W., Iyer, V., Mujica, A. O., Thomas, M., Harrow, J., Cox, T., et al. (2011) · Nature
CRISPR and Genetic EngineeringAnimal Genetics and Reproduction
Cited by 1,708
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Chk1 is an essential kinase that is regulated by Atr and required for the G 2 /M DNA damage checkpoint
Liu, Q., Guntuku, S., Cui, X.-S., Matsuoka, S., Cortez, D., Tamai, K., Luo, G., Carattini-Rivera, S., DeMayo, F., Bradley, A., et al. (2000) · Genes & Development
DNA Repair MechanismsCancer-related Molecular Pathways
Cited by 1,625
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p53 mutant mice that display early ageing-associated phenotypes
Tyner, S. D., Venkatachalam, S., Choi, J., Jones, S., Ghebranious, N., Igelmann, H., Lu, X., Soron, G., Cooper, B., Brayton, C., et al. (2002) · Nature
Genetics, Aging, and Longevity in Model OrganismsCancer-related Molecular Pathways
Cited by 1,459
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Rescue of embryonic lethality in Mdm2-deficient mice by absence of p53
Jones, S. N., Roe, A. E., Donehower, L. A., & Bradley, A. (1995) · Nature
Cancer-related Molecular PathwaysDevelopmental Biology and Gene Regulation
Cited by 1,280
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High-throughput discovery of novel developmental phenotypes
The International Mouse Phenotyping Consortium, Dickinson, M. E., Flenniken, A. M., Ji, X., Teboul, L., Wong, M. D., White, J. K., Meehan, T. F., Weninger, W. J., Westerberg, H., et al. (2016) · Nature
Genomics and Rare DiseasesZebrafish Biomedical Research Applications
Cited by 1,196
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Impaired Energy Homeostasis in C/EBPα Knockout Mice
Wang, N.-D., Finegold, M. J., Bradley, A., Ou, C. N., Abdelsayed, S. V., Wilde, M. D., Taylor, L. R., Wilson, D. R., & Darlington, G. J. (1995) · Science
Adipose Tissue and MetabolismMetabolism, Diabetes, and Cancer
Cited by 929
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Nonredundant roles of the mPer1 and mPer2 genes in the mammalian circadian clock.
Zheng, B., Albrecht, U., Kaasik, K., Sage, M., Lu, W., Vaishnav, S., Li, Q., Sun, Z. S., Eichele, G., Bradley, A., et al. (2001) · Cell
Circadian rhythm and melatoninPlant Molecular Biology Research
Cited by 900
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The mPer2 gene encodes a functional component of the mammalian circadian clock
Zheng, B., Larkin, D. W., Albrecht, U., Sun, Z. S., Sage, M., Eichele, G., Lee, C. C., & Bradley, A. (1999) · Nature
Circadian rhythm and melatoninSleep and Work-Related Fatigue
Cited by 718
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Functional analysis of activins during mammalian development
Matzuk, M. M., Kumar, T. R., Vassalli, A., Bickenbach, J. R., Roop, D. R., Jaenisch, R., & Bradley, A. (1995) · Nature
Developmental Biology and Gene RegulationCleft Lip and Palate Research
Cited by 578
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Spontaneous and carcinogen-induced tumorigenesis in p53-deficient mice.
Harvey, M., McArthur, M. J., Montgomery, C. A., Butel, J. S., Bradley, A., & Donehower, L. A. (1993) · Nature Genetics
Cancer-related Molecular PathwaysCarcinogens and Genotoxicity Assessment
Cited by 542
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Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes.
White, J. K., Gerdin, A.-K., Karp, N. A., Ryder, E., Buljan, M., Bussell, J. N., Salisbury, J., Clare, S., Ingham, N. J., Podrini, C., et al. (2013) · Cell
Genomics and Rare DiseasesAnimal Genetics and Reproduction
Cited by 509
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Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism
Nakatani, J., Tamada, K., Hatanaka, F., Ise, S., Ohta, H., Inoue, K., Tomonaga, S., Watanabe, Y., Chung, Y. J., Banerjee, R., et al. (2009) · Cell
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 482
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Butyrate greatly enhances derivation of human induced pluripotent stem cells by promoting epigenetic remodeling and the expression of pluripotency-associated genes.
Mali, P., Chou, B.-K., Yen, J., Ye, Z., Zou, J., Dowey, S., Brodsky, R. A., Ohm, J. E., Yu, W., Baylin, S. B., et al. (2010) · Stem Cells
Pluripotent Stem Cells ResearchEpigenetics and DNA Methylation
Cited by 417
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Overexpression of Mdm2 in mice reveals a p53-independent role for Mdm2 in tumorigenesis
Jones, S. N., Hancock, A. R., Vogel, H., Donehower, L. A., & Bradley, A. (1998) · Proceedings of the National Academy of Sciences
Cancer-related Molecular PathwaysHeat shock proteins research
Cited by 386
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An Expanded Oct4 Interaction Network: Implications for Stem Cell Biology, Development, and Disease
Pardo, M., Lang, B., Yu, L., Prosser, H., Bradley, A., Babu, M. M., & Choudhary, J. (2010) · Cell Stem Cell
Pluripotent Stem Cells ResearchDevelopmental Biology and Gene Regulation
Cited by 379
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Genetic Background Drives Transcriptional Variation in Human Induced Pluripotent Stem Cells
Rouhani, F., Kumasaka, N., de Brito, M. C., Bradley, A., Vallier, L., & Gaffney, D. (2014) · PLoS Genetics
Pluripotent Stem Cells ResearchEpigenetics and DNA Methylation
Cited by 294
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Effects of genetic background on tumorigenesis in p53‐deficient mice
Donehower, L. A., Harvey, M., Vogel, H., McArthur, M. J., Montgomery, C. A., Park, S. H., Thompson, T., Ford, R. J., & Bradley, A. (1995) · Molecular Carcinogenesis
Cancer-related Molecular PathwaysCarcinogens and Genotoxicity Assessment
Cited by 252
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Increased bone mass is an unexpected phenotype associated with deletion of the calcitonin gene
Hoff, A. O., Catala-Lehnen, P., Thomas, P. M., Priemel, M., Rueger, J. M., Nasonkin, I., Bradley, A., Hughes, M. R., Ordonez, N., Cote, G. J., et al. (2002) · Journal of Clinical Investigation
Bone Metabolism and DiseasesBone health and osteoporosis research
Cited by 209
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Cas9-induced large deletions and small indels are controlled in a convergent fashion
Kosicki, M., Allen, F., Steward, F., Tomberg, K., Pan, Y., & Bradley, A. (2022) · Nature Communications
CRISPR and Genetic EngineeringDNA Repair Mechanisms
Cited by 115
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Inter-homologue repair in fertilized human eggs?
Egli, D., Zuccaro, M. V., Kosicki, M., Church, G. M., Bradley, A., & Jasin, M. (2018) · Nature
CRISPR and Genetic EngineeringDNA Repair Mechanisms
Cited by 111
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