The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.
Evidence That Lymphangiomyomatosis Is Caused by TSC2 Mutations: Chromosome 16p13 Loss of Heterozygosity in Angiomyolipomas and Lymph Nodes from Women with Lymphangiomyomatosis
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Citations
Cites
Mutation and cancer: statistical study of retinoblastoma
Knudson, A. G. (1971) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.68.4.820 · Cited by 7,612
Identification of the Tuberous Sclerosis Gene TSC1 on Chromosome 9q34
Slegtenhorst, M. V., Hoogt, R. D., Hermans, C., Nellist, M., Janssen, B., Verhoef, S., Lindhout, D., Ouweland, A. V. D., Halley, D., Young, J., et al. (1997) · Science · doi:10.1126/science.277.5327.805 · Cited by 1,648
Self-citationIdentification and characterization of the tuberous sclerosis gene on chromosome 16
(1993) · Cell · doi:10.1016/0092-8674(93)90618-z · Cited by 1,645
Whole genome amplification from a single cell: implications for genetic analysis.
Zhang, L., Cui, X., Schmitt, K., Hubert, R., Navidi, W., & Arnheim, N. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.13.5847 · Cited by 896
Hemminki, A., Tomlinson, I., Markie, D., Järvinen, H., Sistonen, P., Björkqvist, A.-M., Knuutila, S., Salovaara, R., Bodmer, W., Shibata, D., et al. (1997) · Nature Genetics · doi:10.1038/ng0197-87 · Cited by 491
Taylor, J. R., Ryu, J., Colby, T. V., & Raffin, T. A. (1990) · New England Journal of Medicine · doi:10.1056/nejm199011013231807 · Cited by 460
Somatic mutation of the MEN1 gene in parathyroid tumours
Heppner, C., Kester, M. B., Agarwal, S. K., Debelenko, L. V., Emmert-Buck, M. R., Guru, S. C., Manickam, P., Olufemi, S.-E., Skarulis, M. C., Doppman, J. L., et al. (1997) · Nature Genetics · doi:10.1038/ng0897-375 · Cited by 415
Loss of heterozygosity on chromosome 16p13.3 in hamartomas from tuberous sclerosis patients
Green, A. J., Smith, M., & Yates, J. R. W. (1994) · Nature Genetics · doi:10.1038/ng0294-193 · Cited by 364
Review and hypotheses: somatic mosaicism: observations related to clinical genetics.
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Pulmonary lymphangiomyomatosis. A review.
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Cited by
Tuberous Sclerosis Complex Consensus Conference: Revised Clinical Diagnostic Criteria
Roach, E. S., Gomez, M. R., & Northrup, H. (1998) · Journal of Child Neurology · doi:10.1177/088307389801301206 · Cited by 1,081
Molecular targets for cancer therapy in the PI3K/AKT/mTOR pathway
Polivka, J., & Janku, F. (2014) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2013.12.004 · Cited by 765
Contemporary Diagnosis and Management of Renal Angiomyolipoma
Nelson, C. P., & Sanda, M. G. (2002) · Journal of Urology · doi:10.1016/s0022-5347(05)64440-0 · Cited by 420
Perivascular epithelioid cell neoplasms: pathology and pathogenesis
Folpe, A. L., & Kwiatkowski, D. J. (2010) · Human Pathology · doi:10.1016/j.humpath.2009.05.011 · Cited by 401
Contemporary Diagnosis and Management of Renal Angiomyolipoma
NELSON, C. P., & SANDA, M. G. (2002) · The Journal of Urology · doi:10.1097/00005392-200210010-00004 · Cited by 384
Metadata
- Authors
- Smolarek, T. A., Wessner, L. L., McCormack, F. X., Mylet, J. C., Menon, A. G., & Henske, E. P.
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 1998-04
- Volume
- 62
- Issue
- 4
- Pages
- 810-815
- ISSN
- 0002-9297 (ISSN-L)
- OpenAlex
- W2044670696
- Cited by
- 314
- References
- 30
- FWCI
- 6.02
- Type
- journal article
- Language
- en
- Open access
- bronze
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- This page
- CoChat. (2026). Citation check: Evidence That Lymphangiomyomatosis Is Caused by TSC2 Mutations: Chromosome 16p13 Loss of Heterozygosity in Angiomyolipomas and Lymph Nodes from Women with Lymphangiomyomatosis. https://app.cochat.ai/papers/10.1086/301804
- The paper
- Smolarek, T. A., Wessner, L. L., McCormack, F. X., Mylet, J. C., Menon, A. G., & Henske, E. P. (1998). Evidence That Lymphangiomyomatosis Is Caused by TSC2 Mutations: Chromosome 16p13 Loss of Heterozygosity in Angiomyolipomas and Lymph Nodes from Women with Lymphangiomyomatosis. The American Journal of Human Genetics. https://doi.org/10.1086/301804
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.
