Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Death and PMS2[original query] |
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Population-based study of the association of variants in mismatch repair genes with prostate cancer risk and outcomes. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2010 Jan 19 (1): 1. Langeberg Wendy J, Kwon Erika M, Koopmeiners Joseph S, Ostrander Elaine A, Stanford Janet |
Comprehensive Genomic Profiling of 282 Pediatric Low- and High-Grade Gliomas Reveals Genomic Drivers, Tumor Mutational Burden, and Hypermutation Signatures. The oncologist 2017 9 22 (12): 1478-1490. Johnson Adrienne, Severson Eric, Gay Laurie, Vergilio Jo-Anne, Elvin Julia, Suh James, Daniel Sugganth, Covert Mandy, Frampton Garrett M, Hsu Sigmund, Lesser Glenn J, Stogner-Underwood Kimberly, Mott Ryan T, Rush Sarah Z, Stanke Jennifer J, Dahiya Sonika, Sun James, Reddy Prasanth, Chalmers Zachary R, Erlich Rachel, Chudnovsky Yakov, Fabrizio David, Schrock Alexa B, Ali Siraj, Miller Vincent, Stephens Philip J, Ross Jeffrey, Crawford John R, Ramkissoon Shakti |
The Relationship Between Mismatch Repair Deficiency and PD-L1 Expression in Breast Carcinoma. The American journal of surgical pathology 2017 9 42 (2): 183-191. Mills Anne M, Dill Erik A, Moskaluk Christopher A, Dziegielewski Jaroslaw, Bullock Tim N, Dillon Patrick |
Advantage of HSP110 (T17) marker inclusion for microsatellite instability (MSI) detection in colorectal cancer patients. Oncotarget 2018 7 9 (47): 28691-28701. Berardinelli Gustavo Noriz, Scapulatempo-Neto Cristovam, Durães Ronílson, Antônio de Oliveira Marco, Guimarães Denise, Reis Rui Manu |
Clinicopathological characteristics of POLE mutation in patients with non-small-cell lung cancer. Lung cancer (Amsterdam, Netherlands) 2018 Apr 118 57-61. Song Zhengbo, Cheng Guoping, Xu Chunwei, Wang Wenxian, Shao Yang, Zhang Yipi |
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study. JNCI cancer spectrum 2021 7 5 (2): . Kim Jung, Gianferante Matthew, Karyadi Danielle M, Hartley Stephen W, Frone Megan N, Luo Wen, Robison Leslie L, Armstrong Gregory T, Bhatia Smita, Dean Michael, Yeager Meredith, Zhu Bin, Song Lei, Sampson Joshua N, Yasui Yutaka, Leisenring Wendy M, Brodie Seth A, de Andrade Kelvin C, Fortes Fernanda P, Goldstein Alisa M, Khincha Payal P, Machiela Mitchell J, McMaster Mary L, Nickerson Michael L, Oba Leatrisse, Pemov Alexander, Pinheiro Maisa, Rotunno Melissa, Santiago Karina, Wegman-Ostrosky Talia, Diver W Ryan, Teras Lauren, Freedman Neal D, Hicks Belynda D, Zhu Bin, Wang Mingyi, Jones Kristine, Hutchinson Amy A, Dagnall Casey, Savage Sharon A, Tucker Margaret A, Chanock Stephen J, Morton Lindsay M, Stewart Douglas R, Mirabello Li |
Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study. The Lancet. Oncology 2021 6 22 (7): 1014-1022. Authors are not available |
Incidence, clinicopathologic, and genetic characteristics of mismatch repair gene-mutated glioblastomas. Journal of neuro-oncology 2021 Apr . Cho Yoon Ah, Kim Deokgeun, Lee Boram, Shim Joon Ho, Suh Yeon-L |
Germline variants predictive of tumor mutational burden and immune checkpoint inhibitor efficacy. iScience 2021 3 24 (3): 102248. Chatrath Ajay, Ratan Aakrosh, Dutta Anind |
Morphologic and Genomic Characteristics of Breast Cancers Occurring in Individuals with Lynch Syndrome. Clinical cancer research : an official journal of the American Association for Cancer Research 2021 10 28 (2): 404-413. Schwartz Christopher J, da Silva Edaise M, Marra Antonio, Gazzo Andrea M, Selenica Pier, Rai Vikas K, Mandelker Diana, Pareja Fresia, Misyura Maksym, D'Alfonso Timothy M, Brogi Edi, Drullinsky Pamela, Razavi Pedram, Robson Mark E, Drago Joshua Z, Wen Hannah Y, Zhang Liying, Weigelt Britta, Shia Jinru, Reis-Filho Jorge S, Zhang Ho |
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 |
Comparative Analysis of Mutational Patterns in Triple Negative Breast Cancer Before and after Neoadjuvant Chemotherapy in Patients with Residual Disease. Gene 2023 11 147980. Ashish Singh, Josh Thomas Georgy, Sakthi Dhananjayan, Elanthenral Sigamani, Ajoy Oommen John, Anjana Joel, Jagan Chandramohan, Rajadurai Abarna, Grace Rebekah, Selvamani Backianathan, Deepak Thomas Abraham, Mazhuvanchary Jacob Paul, Raju Titus Chacko, Marie Therese Manipadam, Rekha P |
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- Page last updated:Apr 22, 2024
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