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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1963 3
1964 4
1965 3
1966 1
1967 6
1968 12
1969 14
1970 15
1971 17
1972 17
1973 26
1974 28
1975 16
1976 17
1977 26
1978 23
1979 17
1980 27
1981 21
1982 26
1983 27
1984 35
1985 44
1986 36
1987 86
1988 131
1989 138
1990 117
1991 159
1992 208
1993 195
1994 277
1995 251
1996 246
1997 262
1998 247
1999 239
2000 284
2001 261
2002 233
2003 224
2004 258
2005 305
2006 285
2007 257
2008 232
2009 266
2010 261
2011 263
2012 319
2013 288
2014 251
2015 320
2016 309
2017 283
2018 265
2019 253
2020 290
2021 271
2022 298
2023 254
2024 68

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9,001 results

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Page 1
Hereditary Diffuse Gastric Cancer Syndrome and the Role of CDH1: A Review.
Gamble LA, Heller T, Davis JL. Gamble LA, et al. JAMA Surg. 2021 Apr 1;156(4):387-392. doi: 10.1001/jamasurg.2020.6155. JAMA Surg. 2021. PMID: 33404644 Review.
This review aims to address the most current topics in management of the hereditary diffuse gastric cancer syndrome attributed to CDH1. OBSERVATIONS: Consensus management guidelines have broadened genetic testing criteria for CDH1. ...Further research is need …
This review aims to address the most current topics in management of the hereditary diffuse gastric cancer syndrome att …
Hereditary Cancer Syndromes: A Comprehensive Review with a Visual Tool.
Garutti M, Foffano L, Mazzeo R, Michelotti A, Da Ros L, Viel A, Miolo G, Zambelli A, Puglisi F. Garutti M, et al. Genes (Basel). 2023 Apr 30;14(5):1025. doi: 10.3390/genes14051025. Genes (Basel). 2023. PMID: 37239385 Free PMC article. Review.
Hereditary cancer syndromes account for nearly 10% of cancers even though they are often underdiagnosed. ...Herein, we searched the available literature to comprehensively review and categorize hereditary cancer syndromes affecting adults
Hereditary cancer syndromes account for nearly 10% of cancers even though they are often underdiagnosed. ...Herein, we
Hereditary Colorectal Cancer.
Hampel H, Kalady MF, Pearlman R, Stanich PP. Hampel H, et al. Hematol Oncol Clin North Am. 2022 Jun;36(3):429-447. doi: 10.1016/j.hoc.2022.02.002. Epub 2022 May 13. Hematol Oncol Clin North Am. 2022. PMID: 35577708 Review.
Around 10% to 16% of colorectal cancer patients have a pathogenic variant in a cancer susceptibility gene. ...The hereditary colorectal cancer syndromes can be divided into two major categories, the nonpolyposis and the polyposis conditions. ...
Around 10% to 16% of colorectal cancer patients have a pathogenic variant in a cancer susceptibility gene. ...The hereditar
ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
Syngal S, Brand RE, Church JM, Giardiello FM, Hampel HL, Burt RW; American College of Gastroenterology. Syngal S, et al. Am J Gastroenterol. 2015 Feb;110(2):223-62; quiz 263. doi: 10.1038/ajg.2014.435. Epub 2015 Feb 3. Am J Gastroenterol. 2015. PMID: 25645574 Free PMC article. Review.
This guideline presents recommendations for the management of patients with hereditary gastrointestinal cancer syndromes. The initial assessment is the collection of a family history of cancers and premalignant gastrointestinal conditions and should provide e …
This guideline presents recommendations for the management of patients with hereditary gastrointestinal cancer syndromes
Precancerous lesions of the stomach, gastric cancer and hereditary gastric cancer syndromes.
Gullo I, Grillo F, Mastracci L, Vanoli A, Carneiro F, Saragoni L, Limarzi F, Ferro J, Parente P, Fassan M. Gullo I, et al. Pathologica. 2020 Sep;112(3):166-185. doi: 10.32074/1591-951X-166. Pathologica. 2020. PMID: 33179620 Free PMC article. Review.
Gastric cancer accounts for about 6% of cancers worldwide, being the fifth most frequently diagnosed malignancy and the third leading cause of cancer related death. ...Furthermore, although most gastric cancers are sporadic, familial clustering is observed in up to …
Gastric cancer accounts for about 6% of cancers worldwide, being the fifth most frequently diagnosed malignancy and the third leading …
Deep intronic mutations and human disease.
Vaz-Drago R, Custódio N, Carmo-Fonseca M. Vaz-Drago R, et al. Hum Genet. 2017 Sep;136(9):1093-1111. doi: 10.1007/s00439-017-1809-4. Epub 2017 May 12. Hum Genet. 2017. PMID: 28497172 Review.
This review aims to highlight the importance of studying variation in deep intronic sequence as a cause of monogenic disorders as well as hereditary cancer syndromes....
This review aims to highlight the importance of studying variation in deep intronic sequence as a cause of monogenic disorders as well as …
Skin Cancer Associated Genodermatoses: A Literature Review.
Schierbeck J, Vestergaard T, Bygum A. Schierbeck J, et al. Acta Derm Venereol. 2019 Apr 1;99(4):360-369. doi: 10.2340/00015555-3123. Acta Derm Venereol. 2019. PMID: 30653245 Free article. Review.
Skin cancer has become the most common type of cancer worldwide as a result of environmental exposure and medical treatments. ...The disorders are described with clinical characteristics, genetics and management. The most common syndromes associated with basa …
Skin cancer has become the most common type of cancer worldwide as a result of environmental exposure and medical treatments. …
Advances in hereditary leiomyomatosis and renal cell carcinoma (HLRCC) research.
Ooi A. Ooi A. Semin Cancer Biol. 2020 Apr;61:158-166. doi: 10.1016/j.semcancer.2019.10.016. Epub 2019 Nov 2. Semin Cancer Biol. 2020. PMID: 31689495 Free PMC article. Review.
Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) is an autosomal dominant hereditary cancer syndrome with incomplete penetrance. ...HLRCC patients are genetically predisposed to develop skin leiomyomas, uterine fibroids, and the aggressiv
Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) is an autosomal dominant hereditary cancer syndrome
Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification.
Kamps R, Brandão RD, Bosch BJ, Paulussen AD, Xanthoulea S, Blok MJ, Romano A. Kamps R, et al. Int J Mol Sci. 2017 Jan 31;18(2):308. doi: 10.3390/ijms18020308. Int J Mol Sci. 2017. PMID: 28146134 Free PMC article. Review.
A number of clinical applications are reviewed, i.e., mutation detection in inherited cancer syndromes based on DNA-sequencing, detection of spliceogenic variants based on RNA-sequencing, DNA-sequencing to identify risk modifiers and application for pre-implantation …
A number of clinical applications are reviewed, i.e., mutation detection in inherited cancer syndromes based on DNA-sequencing …
DICER1 and Associated Conditions: Identification of At-risk Individuals and Recommended Surveillance Strategies.
Schultz KAP, Williams GM, Kamihara J, Stewart DR, Harris AK, Bauer AJ, Turner J, Shah R, Schneider K, Schneider KW, Carr AG, Harney LA, Baldinger S, Frazier AL, Orbach D, Schneider DT, Malkin D, Dehner LP, Messinger YH, Hill DA. Schultz KAP, et al. Clin Cancer Res. 2018 May 15;24(10):2251-2261. doi: 10.1158/1078-0432.CCR-17-3089. Epub 2018 Jan 17. Clin Cancer Res. 2018. PMID: 29343557 Free PMC article. Review.
Pathogenic germline DICER1 variants cause a hereditary cancer predisposition syndrome with a variety of manifestations. ...As DICER1 research expands, guidelines for screening and treatment will continue to be updated. Clin Cancer Res; 24(10); 2251-61. …
Pathogenic germline DICER1 variants cause a hereditary cancer predisposition syndrome with a variety of manifestations. …
9,001 results