TGFBR1*6A and Cancer: A Meta-Analysis of 12 Case-Control Studies
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GWAS studies revealed genetic associations between germline variants in genes encoding TGF-β signaling molecules and susceptibilities to cancer and autoimmune disorders.
“GWAS studies revealed genetic associations between germline variants in genes encoding TGF-β signaling molecules and susceptibilities to cancer and autoimmune disorders396,397”
From TGFβ biology in cancer progression and immunotherapy (2021) · cites this paper as [397]
Cites
TGFBR1*6A and Cancer Risk: A Meta-Analysis of Seven Case-Control Studies
Kaklamani, V., Hou, N., Bian, Y., Reich, J., Offit, K., Michel, L. S., Rubinstein, W. S., RADEMAKER, A. W., & Pasche, B. (2003) · Journal of Clinical Oncology · doi:10.1200/jco.2003.11.524 · Cited by 107 · see citing works
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TGFβ biology in cancer progression and immunotherapy
Derynck, R., Turley, S. J., & Akhurst, R. J. (2021) · Nature Reviews Clinical Oncology · doi:10.1038/s41571-020-0403-1 · Cited by 944 · see citing works
Germline Allele-Specific Expression of <i>TGFBR1</i> Confers an Increased Risk of Colorectal Cancer
Valle, L., Serena-Acedo, T., Liyanarachchi, S., Hampel, H., Comeras, I., Li, Z., Zeng, Q., Zhang, H.-T., Pennison, M. J., Sadim, M., et al. (2008) · Science · doi:10.1126/science.1159397 · Cited by 141 · see citing works
Self-citationConcepts in Familial Colorectal Cancer: Where Do We Stand and What Is the Future?
Castells, A., Castellví–Bel, S., & Balaguer, F. (2009) · Gastroenterology · doi:10.1053/j.gastro.2009.06.015 · Cited by 61 · see citing works
- Authors
- Pasche, B., Kaklamani, V., Hou, N., Young, T., Rademaker, A., Peterlongo, P., Ellis, N., Offit, K., Caldes, T., Reiss, M., & Zheng, T.
- Affiliations
- Northwestern University (US)
- Memorial Sloan Kettering Cancer Center (US)
- Hospital Clínico San Carlos, Martin Lagos, Madrid, Spain
- Robert Wood Johnson Medical School, New Brunswick, NJ
- Yale University (US)
- ORCID
- Venue
- Journal of Clinical Oncology
- Published
- 2004-02-15
- Volume
- 22
- Issue
- 4
- Pages
- 756-758
- ISSN
- 0732-183X (ISSN-L)
- 1527-7755
- OpenAlex
- W2152601253
- Cited by
- 88
- References
- 1
- Citations by year
- 2022: 1 · 2021: 2 · 2020: 2 · 2019: 1 · 2018: 1 · 2016: 1 · 2015: 4 · 2014: 5 · 2013: 3 · 2012: 4
- FWCI
- 1.56
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Clinical Oncology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Avon Foundation for Women
- National Cancer Institute (CA89018, CA90386, P50CA089018, P50CA090386)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › BRCA gene mutations in cancer
- Keywords
- TGFBR1, TGF-beta type I receptor, genetic polymorphism, cancer susceptibility, case-control study
- MeSH terms
- Receptor, Transforming Growth Factor-beta Type I, Female, Gene Frequency, Humans, Neoplasms, Protein Serine-Threonine Kinases, Molecular Epidemiology, Receptors, Transforming Growth Factor beta, Genetic Predisposition to Disease, Activin Receptors, Type I
About these checks
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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