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Phenylalanine hydroxylase deficiency
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Citations
Cited by
The complete European guidelines on phenylketonuria: diagnosis and treatment
van Wegberg, A. M. J., MacDonald, A., Ahring, K., Bélanger-Quintana, A., Blau, N., Bosch, A. M., Burlina, A., Campistol, J., Feillet, F., Giżewska, M., et al. (2017) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-017-0685-2 · Cited by 830
Treatment of a metabolic liver disease by in vivo genome base editing in adult mice
Villiger, L., Grisch-Chan, H. M., Lindsay, H., Ringnalda, F., Pogliano, C. B., Allegri, G., Fingerhut, R., Häberle, J., Matos, J., Robinson, M. D., et al. (2018) · Nature Medicine · doi:10.1038/s41591-018-0209-1 · Cited by 429
Is SOD1 loss of function involved in amyotrophic lateral sclerosis?
Saccon, R. A., Bunton-Stasyshyn, R. K. A., Fisher, E. M. C., & Fratta, P. (2013) · Brain · doi:10.1093/brain/awt097 · Cited by 317
Commensal bacteria and essential amino acids control food choice behavior and reproduction
Leitão-Gonçalves, R., Carvalho-Santos, Z., Francisco, A. P., Fioreze, G. T., Anjos, M., Baltazar, C., Elias, A. P., Itskov, P. M., Piper, M. D. W., & Ribeiro, C. (2017) · PLOS Biology · doi:10.1371/journal.pbio.2000862 · Cited by 315
Blau, N., Hennermann, J. B., Langenbeck, U., & Lichter-Konecki, U. (2011) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2011.08.017 · Cited by 262
Metadata
- Authors
- Mitchell, J. J., Trakadis, Y. J., & Scriver, C. R.
- Venue
- Genetics in Medicine
- Publisher
- Elsevier BV
- Published
- 2011-08
- Volume
- 13
- Issue
- 8
- Pages
- 607-617
- ISSN
- 1098-3600 (ISSN-L)
- OpenAlex
- W2098425369
- Cited by
- 536
- References
- 0
- FWCI
- 28.59
- Type
- journal article
- Language
- en
- Open access
- bronze
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Phenylalanine hydroxylase deficiency. https://app.cochat.ai/papers/10.1097/gim.0b013e3182141b48
- The paper
- Mitchell, J. J., Trakadis, Y. J., & Scriver, C. R. (2011). Phenylalanine hydroxylase deficiency. Genetics in Medicine. https://doi.org/10.1097/gim.0b013e3182141b48
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.
