The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.
Germline mutations in the thyrotropin receptor gene cause non–autoimmune autosomal dominant hyperthyroidism
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Citations
Cites
The Metabolic Basis of Inherited Diseases
Winkelmann, R. K. (1972) · Archives of Dermatology · doi:10.1001/archderm.1972.01620110090032 · Cited by 1,769
Easy calculations of lod scores and genetic risks on small computers.
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Berridge, M. J. (1983) · Biochemical Journal · doi:10.1042/bj2120849 · Cited by 1,110
Two G Protein Oncogenes in Human Endocrine Tumors
Lyons, J., Landis, C. A., Harsh, G., Vallar, L., Grünewald, K., Feichtinger, H., Duh, Q.-Y., Clark, O. H., Kawasaki, E., Bourne, H. R., et al. (1990) · Science · doi:10.1126/science.2116665 · Cited by 1,037
The probable arrangement of the helices in G protein-coupled receptors.
Baldwin, J. M. (1993) · The EMBO Journal · doi:10.1002/j.1460-2075.1993.tb05814.x · Cited by 972
Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas
Parma, J., Duprez, L., Sande, J. V., Cochaux, P., Gervy, C., Mockel, J., Dumont, J., & Vassart, G. (1993) · Nature · doi:10.1038/365649a0 · Cited by 918
Self-citationROBBINS, L. (1993) · Cell · doi:10.1016/0092-8674(93)90572-8 · Cited by 876
Projection structure of rhodopsin
Schertler, G. F. X., Villa, C., & Henderson, R. (1993) · Nature · doi:10.1038/362770a0 · Cited by 762
Shenker, A., Laue, L., Kosugi, S., Merendino, J. J., Minegishi, T., & Cutler, G. B. (1993) · Nature · doi:10.1038/365652a0 · Cited by 745
Cited by
Aittomäki, K., Dieguez Lucena, J., Pakarinen, P., Sistonen, P., Tapanainen, J., Gromoll, J., Kaskikari, R., Sankila, E.-M., Lehväslaiho, H., Reyes Engel, A., et al. (1995) · Cell · doi:10.1016/0092-8674(95)90275-9 · Cited by 982
A Constitutively Active Mutant PTH-PTHrP Receptor in Jansen-Type Metaphyseal Chondrodysplasia
Schipani, E., Kruse, K., & Jüppner, H. (1995) · Science · doi:10.1126/science.7701349 · Cited by 685
The Thyrotropin (TSH)-Releasing Hormone Receptor: Interaction with TSH and Autoantibodies*
Rapoport, B., Chazenbalk, G. D., Jaume, J. C., & McLachlan, S. M. (1998) · Endocrine Reviews · doi:10.1210/edrv.19.6.0352 · Cited by 551
Isoforms of Mammalian Adenylyl Cyclase: Multiplicities of Signaling
Sunahara, R. K. (2002) · Molecular Interventions · doi:10.1124/mi.2.3.168 · Cited by 406
Genetics of congenital hypothyroidism
Park, S. M., & Chatterjee, V. K. K. (2005) · Journal of Medical Genetics · doi:10.1136/jmg.2004.024158 · Cited by 403
Metadata
- Authors
- Duprez, L., Parma, J., Van Sande, J., Allgeier, A., Leclère, J., Schvartz, C., Delisle, M.-J., Decoulx, M., Orgiazzi, J., Dumont, J., & Vassart, G.
- Venue
- Nature Genetics
- Published
- 1994-07
- Volume
- 7
- Issue
- 3
- Pages
- 396-401
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2059217527
- Cited by
- 379
- References
- 29
- FWCI
- 23.98
- Type
- journal article
- Language
- en
- Open access
- closed
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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
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- This page
- CoChat. (2026). Citation check: Germline mutations in the thyrotropin receptor gene cause non–autoimmune autosomal dominant hyperthyroidism. https://app.cochat.ai/papers/10.1038/ng0794-396
- The paper
- Duprez, L., Parma, J., Van Sande, J., Allgeier, A., Leclère, J., Schvartz, C., Delisle, M.-J., Decoulx, M., Orgiazzi, J., Dumont, J., & Vassart, G. (1994). Germline mutations in the thyrotropin receptor gene cause non–autoimmune autosomal dominant hyperthyroidism. Nature Genetics. https://doi.org/10.1038/ng0794-396
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.
