The DOI matches its Crossref record; 50 of the 50 references it cites were found in a registry or an index.
Solid form screening – A review
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Citations
Cites
Wold, S., Esbensen, K., & Geladi, P. (1987) · Chemometrics and Intelligent Laboratory Systems · doi:10.1016/0169-7439(87)80084-9 · Cited by 11,606
DREIDING: a generic force field for molecular simulations
Mayo, S. L., Olafson, B. D., & Goddard, W. A. (1990) · The Journal of Physical Chemistry · doi:10.1021/j100389a010 · Cited by 6,585
Amidon, G. L., Lennernäs, H., Shah, V. P., & Crison, J. R. (1995) · Pharmaceutical Research · doi:10.1023/a:1016212804288 · Cited by 5,430
Handbook of Chemometrics and Qualimetrics: Part A
(1998) · Data Handling in Science and Technology · doi:10.1016/s0922-3487(97)x8000-1 · Cited by 2,027
Characteristics and Significance of the Amorphous State in Pharmaceutical Systems
Hancock, B. C., & Zografi, G. (1997) · Journal of Pharmaceutical Sciences · doi:10.1021/js9601896 · Cited by 1,922
Encyclopedia of Pharmaceutical Technology
Swarbrick, J. (2013) · CRC Press eBooks · doi:10.1201/b19309 · Cited by 1,794
Amorphous pharmaceutical solids: preparation, characterization and stabilization
Yu, L. (2001) · Advanced Drug Delivery Reviews · doi:10.1016/s0169-409x(01)00098-9 · Cited by 1,405
What is the True Solubility Advantage for Amorphous Pharmaceuticals?
Hancock, B. C., & Parks, M. (2000) · Pharmaceutical Research · doi:10.1023/a:1007516718048 · Cited by 1,358
Polymorphism in Molecular Crystals
Bernstein, J. (2007) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780199236565.001.0001 · Cited by 1,346
Polymorphism in Pharmaceutical Solids
(2018) · CRC Press eBooks · doi:10.3109/9781420073225 · Cited by 1,099
Cited by
X-Ray Diffraction: Instrumentation and Applications
Bunaciu, A. A., Udriştioiu, E. G., & Aboul-Enein, H. Y. (2015) · Critical Reviews in Analytical Chemistry · doi:10.1080/10408347.2014.949616 · Cited by 953
De Beer, T., Burggraeve, A., Fonteyne, M., Saerens, L., Remon, J. P., & Vervaet, C. (2011) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2010.12.012 · Cited by 559
Pharmaceutical cocrystals: from serendipity to design to application
Kavanagh, O. N., Croker, D. M., Walker, G. M., & Zaworotko, M. J. (2019) · Drug Discovery Today · doi:10.1016/j.drudis.2018.11.023 · Cited by 323
Raman spectroscopy in pharmaceutical product design
Paudel, A., Raijada, D., & Rantanen, J. (2015) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2015.04.003 · Cited by 302
Self-citation
Metadata
- Authors
- AALTONEN, J., ALLESO, M., MIRZA, S., KORADIA, V, GORDON, K., & RANTANEN, J.
- Venue
- European Journal of Pharmaceutics and Biopharmaceutics
- Publisher
- Elsevier BV
- Published
- 2009-01
- Volume
- 71
- Issue
- 1
- Pages
- 23-37
- ISSN
- 0939-6411 (ISSN-L)
- OpenAlex
- W2086736722
- Cited by
- 276
- References
- 50
- FWCI
- 6.74
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Solid form screening – A review. https://app.cochat.ai/papers/10.1016/j.ejpb.2008.07.014
- The paper
- AALTONEN, J., ALLESO, M., MIRZA, S., KORADIA, V, GORDON, K., & RANTANEN, J. (2009). Solid form screening – A review. European Journal of Pharmaceutics and Biopharmaceutics. https://doi.org/10.1016/j.ejpb.2008.07.014
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.