Davidoff, Andrew M.
St. Jude Children's Research Hospital
16 papers on CoChatORCID 0000-0001-7900-2794
Most cited papers
- Verified
Adenovirus-Associated Virus Vector–Mediated Gene Transfer in Hemophilia B
Nathwani, A. C., Tuddenham, E. G. D., Rangarajan, S., Rosales, C., McIntosh, J., Linch, D. C., Chowdary, P., Riddell, A., Pie, A. J., Harrington, C., et al. (2011) · New England Journal of Medicine
Hemophilia Treatment and ResearchVirus-based gene therapy research
Cited by 1,864
- Verified
Long-Term Safety and Efficacy of Factor IX Gene Therapy in Hemophilia B
Nathwani, A. C., Reiss, U. M., Tuddenham, E. G. D., Rosales, C., Chowdary, P., McIntosh, J., Della Peruta, M., Lheriteau, E., Patel, N., Raj, D., et al. (2014) · New England Journal of Medicine
Hemophilia Treatment and ResearchVirus-based gene therapy research
Cited by 1,273
- Verified
Long-term Safety and Efficacy Following Systemic Administration of a Self-complementary AAV Vector Encoding Human FIX Pseudotyped With Serotype 5 and 8 Capsid Proteins
Nathwani, A. C., Rosales, C., McIntosh, J., Rastegarlari, G., Nathwani, D., Raj, D., Nawathe, S., Waddington, S. N., Bronson, R., Jackson, S., et al. (2011) · Molecular Therapy
Virus-based gene therapy researchHemophilia Treatment and Research
Cited by 345
- Verified
Therapeutic levels of FVIII following a single peripheral vein administration of rAAV vector encoding a novel human factor VIII variant
McIntosh, J., Lenting, P. J., Rosales, C., Lee, D., Rabbanian, S., Raj, D., Patel, N., Tuddenham, E. G. D., Christophe, O. D., McVey, J. H., et al. (2013) · Blood
Hemophilia Treatment and ResearchVirus-based gene therapy research
Cited by 278
- Verified
Sex significantly influences transduction of murine liver by recombinant adeno-associated viral vectors through an androgen-dependent pathway
Davidoff, A. M., Ng, C. Y. C., Zhou, J., Spence, Y., & Nathwani, A. C. (2003) · Blood
Virus-based gene therapy researchRNA Interference and Gene Delivery
Cited by 244
- Verified
MicroRNA-21 promotes glioblastoma tumorigenesis by down-regulating insulin-like growth factor-binding protein-3 (IGFBP3)
Yang, C. H., Yue, J., Pfeffer, S. R., Fan, M., Paulus, E., Hosni-Ahmed, A., Sims, M., Qayyum, S., Davidoff, A. M., Handorf, C. R., et al. (2014) · Journal of Biological Chemistry
MicroRNA in disease regulationGlioma Diagnosis and Treatment
Cited by 164
- Verified
Bioengineered AAV Capsids with Combined High Human Liver Transduction In Vivo and Unique Humoral Seroreactivity
Paulk, N. K., Pekrun, K., Zhu, E., Nygaard, S., Li, B., Xu, J., Chu, K., Leborgne, C., Dane, A. P., Haft, A., et al. (2018) · Molecular Therapy
Virus-based gene therapy researchRNA Interference and Gene Delivery
Cited by 161
- Verified
Good manufacturing practice production of self-complementary serotype 8 adeno-associated viral vector for a hemophilia B clinical trial
Allay, J. A., Sleep, S., Long, S., Tillman, D. M., Clark, R., Carney, G., Fagone, P., McIntosh, J. H., Nienhuis, A. W., Davidoff, A. M., et al. (2011) · Human Gene Therapy
Virus-based gene therapy researchHemophilia Treatment and Research
Cited by 152
- Verified
Learning and Age-Related Changes in Genome-wide H2A.Z Binding in the Mouse Hippocampus
Stefanelli, G., Azam, A. B., Walters, B. J., Brimble, M. A., Gettens, C. P., Bouchard-Cannon, P., Cheng, H.-Y. M., Davidoff, A. M., Narkaj, K., Day, J. J., et al. (2018) · Cell Reports
Genomics and Chromatin DynamicsMemory and Neural Mechanisms
Cited by 98
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Systemic errors in quantitative polymerase chain reaction titration of self-complementary adeno-associated viral vectors and improved alternative methods
Fagone, P., Wright, J. F., Nathwani, A. C., Nienhuis, A. W., Davidoff, A. M., & Gray, J. T. (2012) · Human Gene Therapy Methods
Virus-based gene therapy researchMolecular Biology Techniques and Applications
Cited by 97
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Enhancing transduction of the liver by adeno-associated viral vectors
Nathwani, A. C., Cochrane, M., McIntosh, J., Ng, C. Y. C., Zhou, J., Gray, J. T., & Davidoff, A. M. (2009) · Gene Therapy
Virus-based gene therapy researchRNA Interference and Gene Delivery
Cited by 77
- Verified
Successful attenuation of humoral immunity to viral capsid and transgenic protein following AAV-mediated gene transfer with a non-depleting CD4 antibody and cyclosporine
McIntosh, J. H., Cochrane, M., Cobbold, S., Waldmann, H., Nathwani, S. A., Davidoff, A. M., & Nathwani, A. C. (2012) · Gene Therapy
Virus-based gene therapy researchRNA Interference and Gene Delivery
Cited by 70
- Verified
GO-8: Preliminary Results of a Phase I/II Dose Escalation Trial of Gene Therapy for Haemophilia a Using a Novel Human Factor VIII Variant
Nathwani, A. C., Tuddenham, E., Chowdary, P., McIntosh, J., Lee, D., Rosales, C., Phillips, M., Pie, J., Junfang, Z., Meagher, M. M., et al. (2018) · Blood
Hemophilia Treatment and ResearchVirus-based gene therapy research
Cited by 52
- Verified
Preventing packaging of translatable P5-associated DNA contaminants in recombinant AAV vector preps
Brimble, M. A., Cheng, P.-H., Winston, S. M., Reeves, I. L., Souquette, A., Spence, Y., Zhou, J., Wang, Y.-D., Morton, C. L., Valentine, M., et al. (2022) · Molecular Therapy - Methods & Clinical Development
Virus-based gene therapy researchRNA Interference and Gene Delivery
Cited by 30
- Verified
Assessing interactions for fixed-dose drug combinations in tumor xenograft studies
Wu, J., Tracey, L., & Davidoff, A. M. (2012) · Journal of Biopharmaceutical Statistics
Statistical Methods in Clinical TrialsOptimal Experimental Design Methods
Cited by 21
- Verified
Our journey to successful gene therapy for hemophilia B
Nathwani, A. C., Nienhuis, A. W., & Davidoff, A. M. (2014) · Human Gene Therapy
Hemophilia Treatment and ResearchVirus-based gene therapy research
Cited by 15
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