Original language | English |
---|---|
Pages (from-to) | 811-812 |
Number of pages | 2 |
Journal | Gen. Med. |
Volume | 22 |
Issue number | 4 |
DOIs | |
Publication status | Published - 2020 |
Keywords
- DNA mismatch repair protein MSH2
- MutL protein homolog 1
- age
- breast cancer
- cancer diagnosis
- cancer registry
- cancer risk
- cancer screening
- clinical practice
- gender
- genetic analysis
- genetic association
- genetic variability
- hereditary nonpolyposis colorectal cancer
- heterozygote
- human
- Letter
- mismatch repair
- MSH2 gene
- patient coding
- practice guideline
- prospective study
- risk assessment
- genetics
- information processing
- Colorectal Neoplasms, Hereditary Nonpolyposis
- Data Management
- DNA Mismatch Repair
- Humans
- MutL Protein Homolog 1
- Prospective Studies
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Response to Dominguez-Valentin M et al. 2019: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database : Genetics in Medicine. / Tolva, G.; Gandini, S.; Marabelli, M. et al.
In: Gen. Med., Vol. 22, No. 4, 2020, p. 811-812.Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - Response to Dominguez-Valentin M et al. 2019: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
T2 - Genetics in Medicine
AU - Tolva, G.
AU - Gandini, S.
AU - Marabelli, M.
AU - Calvello, M.
AU - Guerrieri-Gonzaga, A.
AU - Bertario, L.
AU - Bonanni, B.
N1 - Cited By :1 Export Date: 5 March 2021 CODEN: GEMEF Correspondence Address: Tolva, G.; Division of Cancer Prevention and Genetics, Italy; email: gianluca.tolva@ieo.it Chemicals/CAS: DNA mismatch repair protein MSH2, 153700-72-2; MutL protein homolog 1, 155577-96-1; MutL Protein Homolog 1 References: Dominguez-Valentin, M., Sampson, J., Seppälä, T., Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: Findings from the Prospective Lynch Syndrome Database (2019) Genet Med, , https://doi.org/10.1038/s41436-019-0596-9, Jul 24, Epub ahead of print; Win, A.K., Lindor, N.M., Jenkins, M.A., Risk of breast cancer in Lynch syndrome: a systematic review (2013) Breast Cancer Res., 15; Win, A.K., Young, J.P., Lindor, N.M., Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study (2012) J Clin Oncol, 30, pp. 958-964; Engel, C., Loeffler, M., Steinke, V., Risks of less common cancers in proven mutation carriers with lynch syndrome (2012) J Clin Oncol, 30, pp. 4409-4415; Pande, M., Wei, C., Chen, J., Cancer spectrum in DNA mismatch repair gene mutation carriers: results from a hospital based Lynch syndrome registry (2012) Fam Cancer, 11, pp. 441-447; Win, A.K., Lindor, N.M., Young, J.P., Risks of primary extracolonic cancers following colorectal cancer in Lynch syndrome (2012) J Natl Cancer Inst, 104, pp. 1363-1372; Win, A.K., Lindor, N.M., Winship, I., Risks of Colorectal and Other Cancers After Endometrial Cancer for Women With Lynch Syndrome (2013) J Natl Cancer Inst, 105, pp. 274-279; Harkness, E.F., Barrow, E., Newton, K., Lynch syndrome caused by MLH1 mutations is associated with an increased risk of breast cancer: a cohort study (2015) J Med Genet, 52, pp. 553-556; Goldberg, M., Bell, K., Aronson, M., Association between the Lynch syndrome gene MSH2 and breast cancer susceptibility in a Canadian familial cancer registry (2017) J Med Genet, 54, pp. 742-746; Therkildsen, C., Ladelund, S., Smith-Hansen, L., Towards gene- and gender-based risk estimates in Lynch syndrome; age-specific incidences for 13 extra-colorectal cancer types (2017) Br J Cancer, 117, pp. 1702-1710; Møller, P., Seppälä, T.T., Bernstein, I., Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database (2018) Gut., 67, pp. 1306-1316; Møller, P., Seppälä, T., Bernstein, I., Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the Prospective Lynch Syndrome Database (2017) Gut., 66, pp. 464-472; Stjepanovic, N., Moreira, L., Carneiro, F., Hereditary gastrointestinal cancers: ESMO clinical practice guidelines for diagnosis, treatment and follow-up (2019) Ann Oncol, 30, pp. 1558-1571; Gupta, S., Provenzale, D., Llor, X., NCCN guidelines insights: genetic/familial high-risk assessment: colorectal, version 2.2019 (2019) J Natl Compr Cancer Netw, 17, pp. 1032-1041
PY - 2020
Y1 - 2020
KW - DNA mismatch repair protein MSH2
KW - MutL protein homolog 1
KW - age
KW - breast cancer
KW - cancer diagnosis
KW - cancer registry
KW - cancer risk
KW - cancer screening
KW - clinical practice
KW - gender
KW - genetic analysis
KW - genetic association
KW - genetic variability
KW - hereditary nonpolyposis colorectal cancer
KW - heterozygote
KW - human
KW - Letter
KW - mismatch repair
KW - MSH2 gene
KW - patient coding
KW - practice guideline
KW - prospective study
KW - risk assessment
KW - genetics
KW - information processing
KW - Colorectal Neoplasms, Hereditary Nonpolyposis
KW - Data Management
KW - DNA Mismatch Repair
KW - Humans
KW - MutL Protein Homolog 1
KW - Prospective Studies
U2 - 10.1038/s41436-019-0716-6
DO - 10.1038/s41436-019-0716-6
M3 - Article
VL - 22
SP - 811
EP - 812
JO - Gen. Med.
JF - Gen. Med.
SN - 1098-3600
IS - 4
ER -