Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Melanoma and MSH6[original query] |
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| Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes. Familial cancer 2008 7 (4): 331-7. Magnusson Susanne, Borg Ake, Kristoffersson Ulf, Nilbert Mef, Wiebe Thomas, Olsson Håk |
| Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations. Human genetics 2016 Jul . Yang Xiaohong R, Rotunno Melissa, Xiao Yanzi, Ingvar Christian, Helgadottir Hildur, Pastorino Lorenza, van Doorn Remco, Bennett Hunter, Graham Cole, Sampson Joshua N, Malasky Michael, Vogt Aurelie, Zhu Bin, Bianchi-Scarra Giovanna, Bruno William, Queirolo Paola, Fornarini Giuseppe, Hansson Johan, Tuominen Rainer, Burdett Laurie, Hicks Belynda, Hutchinson Amy, Jones Kristine, Yeager Meredith, Chanock Stephen J, Landi Maria Teresa, Höiom Veronica, Olsson Håkan, Gruis Nelleke, Ghiorzo Paola, Tucker Margaret A, Goldstein Alisa |
| A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families. Hereditary cancer in clinical practice 2018 11 16 16. Karimi Masoud, von Salomé Jenny, Aravidis Christos, Silander Gustav, Askmalm Marie Stenmark, Henriksson Isabelle, Gebre-Medhin Samuel, Frödin Jan-Erik, Björck Erik, Lagerstedt-Robinson Kristina, Lindblom Annika, Tham Em |
| Microsatellite Instability Is Associated With the Presence of Lynch Syndrome Pan-Cancer. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2018 10 37 (4): 286-295. Latham Alicia, Srinivasan Preethi, Kemel Yelena, Shia Jinru, Bandlamudi Chaitanya, Mandelker Diana, Middha Sumit, Hechtman Jaclyn, Zehir Ahmet, Dubard-Gault Marianne, Tran Christina, Stewart Carolyn, Sheehan Margaret, Penson Alexander, DeLair Deborah, Yaeger Rona, Vijai Joseph, Mukherjee Semanti, Galle Jesse, Dickson Mark A, Janjigian Yelena, O'Reilly Eileen M, Segal Neil, Saltz Leonard B, Reidy-Lagunes Diane, Varghese Anna M, Bajorin Dean, Carlo Maria I, Cadoo Karen, Walsh Michael F, Weiser Martin, Aguilar Julio Garcia, Klimstra David S, Diaz Luis A, Baselga Jose, Zhang Liying, Ladanyi Marc, Hyman David M, Solit David B, Robson Mark E, Taylor Barry S, Offit Kenneth, Berger Michael F, Stadler Zsofia |
| Whole Exome Sequencing Identifies Candidate Genes Associated with Hereditary Predisposition to Uveal Melanoma. Ophthalmology 2019 Nov . Abdel-Rahman Mohamed H, Sample Klarke M, Pilarski Robert, Walsh Tomas, Grosel Timothy, Kinnamon Daniel, Boru Getachew, Massengill James B, Schoenfield Lynn, Kelly Ben, Gordon David, Johansson Peter, DeBenedictis Meghan J, Singh Arun, Casadei Silvia, Davidorf Frederick H, White Peter, Stacey Andrew W, Scarth James, Fewings Ellie, Tischkowitz Marc, King Mary-Claire, Hayward Nicholas K, Cebulla Colleen |
| Co-Occurrence of Familial Non-Medullary Thyroid Cancer (FNMTC) and Hereditary Non-Polyposis Colorectal Cancer (HNPCC) Associated Tumors-A Cohort Study. Frontiers in endocrinology 2021 7 12 653401. Aswath Kshama, Welch James, Gubbi Sriram, Veeraraghavan Padmasree, Avadhanula Shirisha, Gara Sudheer Kumar, Dikoglu Esra, Merino Maria, Raffeld Mark, Xi Liqiang, Kebebew Electron, Klubo-Gwiezdzinska Joan |
| Germline variants predictive of tumor mutational burden and immune checkpoint inhibitor efficacy. iScience 2021 3 24 (3): 102248. Chatrath Ajay, Ratan Aakrosh, Dutta Anind |
| Differential Expression of the TLR4 Gene in Pan-Cancer and Its Related Mechanism. Frontiers in cell and developmental biology 2021 10 9 700661. Hu Jialing, Xu Jiasheng, Feng Xiaojin, Li Yiran, Hua Fuzhou, Xu Guoh |
| Significance of the Multi-gene Panel myRisk in Japan. Anticancer research 2022 7 42 (8): 4097-4102. Hayashi Saori, Kubo Makoto, Matsuzaki Sawako, Kai Masaya, Morisaki Takafumi, Yamada Mai, Kaneshiro Kazuhisa, Takao Yuka, Shimazaki Akiko, Nagayoshi Kinuko, Mizuuchi Yusuke, Nakamura Masafu |
| Pancreatic Cancer with Mutation in BRCA1/2, MLH1, and APC Genes: Phenotype Correlation and Detection of a Novel Germline BRCA2 Mutation. Genes 2022 2 13 (2): . Vietri Maria Teresa, D'Elia Giovanna, Caliendo Gemma, Albanese Luisa, Signoriello Giuseppe, Napoli Claudio, Molinari Anna Mar |
| Risk of Syndrome-Associated Cancers Among First-Degree Relatives of Patients With Pancreatic Ductal Adenocarcinoma With Pathogenic or Likely Pathogenic Germline Variants. JAMA oncology 2023 5 . Xuan Chen, Margaret A Meyer, Jennifer L Kemppainen, Masayasu Horibe, Shruti Chandra, Shounak Majumder, Gloria M Petersen, Kari G Ra |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 01, 2023
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