Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 51 Records) |
| Query Trace: Breast Neoplasms and PMS2[original query] |
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| Multigene Panel Testing Increases the Number of Loci Associated with Gastric Cancer Predisposition. Cancers 2019 9 11 (9): . Tedaldi Gianluca, Pirini Francesca, Tebaldi Michela, Zampiga Valentina, Cangini Ilaria, Danesi Rita, Arcangeli Valentina, Ravegnani Mila, Abou Khouzam Raefa, Molinari Chiara, Oliveira Carla, Morgagni Paolo, Saragoni Luca, Bencivenga Maria, Ulivi Paola, Amadori Dino, Martinelli Giovanni, Falcini Fabio, Ranzani Guglielmina Nadia, Calistri Danie |
| Retesting of women who are negative for a BRCA1 and BRCA2 mutation using a 20-gene panel. Journal of medical genetics 2019 12 57 (6): 380-384. Lerner-Ellis Jordan, Sopik Victoria, Wong Andrew, Lázaro Conxi, Narod Steven A, Charames George |
| Landscape of Germline Mutations in DNA Repair Genes for Breast Cancer in Latin America: Opportunities for PARP-Like Inhibitors and Immunotherapy. Genes 2019 10 10 (10): . Urbina-Jara Laura Keren, Rojas-Martinez Augusto, Martinez-Ledesma Emmanuel, Aguilar Dione, Villarreal-Garza Cynthia, Ortiz-Lopez Roc |
| Lynch Syndrome Germline Mutations in Breast Cancer: Next Generation Sequencing Case-Control Study of 1,263 Participants. Frontiers in oncology 2020 6 10 666. Nikitin Aleksey G, Chudakova Daria A, Enikeev Rafael F, Sakaeva Dina, Druzhkov Maxim, Shigapova Leyla H, Brovkina Olga I, Shagimardanova Elena I, Gusev Oleg A, Gordiev Marat |
| Investigating the Link between Lynch Syndrome and Breast Cancer. European journal of breast health 2020 4 16 (2): 106-109. Sheehan Megan, Heald Brandie, Yanda Courtney, Kelly Erinn Downs, Grobmyer Stephen, Eng Charis, Kalady Matthew, Pederson Hol |
| Comparison of BRCA versus non-BRCA germline mutations and associated somatic mutation profiles in patients with unselected breast cancer. Aging 2020 Feb 12 . Chen Bo, Zhang Guochun, Li Xuerui, Ren Chongyang, Wang Yulei, Li Kai, Mok Hsiaopei, Cao Li, Wen Lingzhu, Jia Minghan, Li Cheukfai, Guo Liping, Wei Guangnan, Lin Jiali, Li Yingzi, Zhang Yuchen, Han-Zhang Han, Liu Jing, Lizaso Analyn, Liao Ni |
| Genetic Variants Detected Using Cell-Free DNA from Blood and Tumor Samples in Patients with Inflammatory Breast Cancer. International journal of molecular sciences 2020 Feb 21 (4): . Winn Jennifer S, Hasse Zachary, Slifker Michael, Pei Jianming, Arisi-Fernandez Sebastian M, Talarchek Jacqueline N, Obeid Elias, Baldwin Donald A, Gong Yulan, Ross Eric, Cristofanilli Massimo, Alpaugh R Katherine, Fernandez Sandra |
| Cancer Previvors in an Active Duty Service Women Population: An Opportunity for Prevention and Increased Force Readiness. Military medicine 2020 . Lovejoy Leann A, Turner Clesson E, Shriver Craig D, Ellsworth Rachel |
| Multigene panel testing results in patients with multiple breast cancer primaries. The breast journal 2020 Jan . Corredor Jessica, Woodson Ashley H, Gutierrez Barrera Angelica, Arun Ba |
| Case-case analysis addressing ascertainment bias for multigene panel testing implicates BRCA1 and PALB2 in endometrial cancer. Human mutation 2021 7 42 (10): 1265-1278. Johnatty Sharon E, Pesaran Tina, Dolinsky Jill, Yussuf Amal, LaDuca Holly, James Paul A, O'Mara Tracy A, Spurdle Amanda |
| Landscape of somatic mutations in breast cancer: new opportunities for targeted therapies in Saudi Arabian patients. Oncotarget 2021 Mar 12 (7): 686-697. Barakeh Duna H, Aljelaify Rasha, Bashawri Yara, Almutairi Amal, Alqubaishi Fatimah, Alnamnakani Mohammed, Almubarak Latifa, Al Naeem Abdulrahman, Almushawah Fatema, Alrashed May, Abedalthagafi Mal |
| Characteristics of Germline Non-BRCA Mutation Status of High-Risk Breast Cancer Patients in China and Correlation with High-Risk Factors and Multigene Testing Suggestions. Frontiers in genetics 2021 12 12 674094. Su Yifan, Yao Qianlan, Xu Yuyin, Yu Chengli, Zhang Jing, Wang Qian, Li Jiwei, Shi Di, Yu Baohua, Zeng Yupeng, Zhu Xiaoli, Bai Qianming, Zhou Xiaoy |
| [Difference analysis of somatic mutations between deficient mismatch repair and proficient mismatch repair gene related with colorectal cancer]. Zhonghua zhong liu za zhi [Chinese journal of oncology] 2021 10 43 (10): 1088-1093. Tang X J, Yang M Y, Zhu L Z, Xu D, Yuan |
| 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 |
| Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia. PloS one 2021 16 (1): e0245362. Boujemaa Maroua, Hamdi Yosr, Mejri Nesrine, Romdhane Lilia, Ghedira Kais, Bouaziz Hanen, El Benna Houda, Labidi Soumaya, Dallali Hamza, Jaidane Olfa, Ben Nasr Sonia, Haddaoui Abderrazek, Rahal Khaled, Abdelhak Sonia, Boussen Hamouda, Boubaker Mohamed Sam |
| Predicted Chemotherapy Benefit for Breast Cancer Patients With Germline Pathogenic Variants in Cancer Susceptibility Genes. JNCI cancer spectrum 2021 1 5 (1): . Kurian Allison W, Ward Kevin C, Abrahamse Paul, Hamilton Ann S, Katz Steven |
| Multi-Gene Mutation Profiling by Targeted Next-Generation Sequencing in Premenopausal Breast Cancer. Genes 2022 Jul 13 (8): . Zografos Eleni, Andrikopoulou Angeliki, Papatheodoridi Alkistis Maria, Kaparelou Maria, Bletsa Garyfalia, Liontos Michalis, Dimopoulos Meletios-Athanasios, Zagouri Flo |
| Pathogenicity Reclassification of Genetic Variants Related to Early-Onset Breast Cancer among Women of Mongoloid Origin. Asian Pacific journal of cancer prevention : APJCP 2022 6 23 (6): 2027-2033. Gervas Polina, Molokov Aleksey, Babyshkina Nataliya, Kiselev Artem, Zarubin Aleksei, Yumov Evgeny, Pisareva Lubov, Choynzonov Evgeny, Cherdyntseva Nadez |
| Breast and Ovarian Cancer Penetrance Estimates Derived From Germline Multiple-Gene Sequencing Results in Women. JCO precision oncology 2022 2 1 1-12. Kurian Allison W, Hughes Elisha, Handorf Elizabeth A, Gutin Alexander, Allen Brian, Hartman Anne-Renee, Hall Michael |
| Clinical and psychological implications of secondary and incidental findings in cancer susceptibility genes after exome sequencing in patients with rare disorders. Journal of medical genetics 2022 11 . Carrasco Estela, López-Fernández Adrià, Codina-Sola Marta, Valenzuela Irene, Cueto-González A M, Villacampa Guillermo, Navarro Victor, Torres-Esquius Sara, Palau Dolors, Cruellas Mara, Torres Maite, Perez-Dueñas Belen, Abulí Anna, Diez Orland, Sábado-Álvarez Constantino, García-Arumí Elena, Tizzano Eduardo F, Moreno Lucas, Balmaña Judi |
| The prevalence of germline pathogenic variants in Estonian colorectal cancer patients: results from routine clinical setting 2016-2021. Frontiers in genetics 2022 11 13 1020543. Roht Laura, Tooming Mikk, Rekker Kadri, Roomere Hanno, Toome Kadri, Murumets Ülle, Šamarina Ustina, Õunap Katrin, Kahre Tii |
| Increased Co-Occurrence of Pathogenic Variants in Hereditary Breast and Ovarian Cancer and Lynch Syndromes: A Consequence of Multigene Panel Genetic Testing? International journal of molecular sciences 2022 10 23 (19): . Infante Mar, Arranz-Ledo Mónica, Lastra Enrique, Abella Luis Enrique, Ferreira Raquel, Orozco Marta, Hernández Lara, Martínez Noemí, Durán Merced |
| No Evidence of Increased Risk of Breast Cancer in Women With Lynch Syndrome Identified by Multigene Panel Testing. JCO precision oncology 2022 1 4 51-60. Stoll Jessica, Rosenthal Eric, Cummings Shelly, Willmott Jamie, Bernhisel Ryan, Kupfer Sonia |
| Co-Occurrence of Germline Genomic Variants and Copy Number Variations in Hereditary Breast and Colorectal Cancer Patients. Genes 2023 8 14 (8): . Luiza Côrtes, Tatiane Ramos Basso, Rolando André Rios Villacis, Jeferson Dos Santos Souza, Mads Malik Aagaard Jørgensen, Maria Isabel Achatz, Silvia Regina Rogat |
| Uncommon variants detected via hereditary cancer panel and suggestions for genetic counseling. Mutation research 2023 7 827 111831. Zeynep Özdemir, Ezgi Çevik, Ömür Berna Çakmak Öksüzo?lu, Mutlu Do?an, Öztürk Ate?, Ece Esin, ?rem Bilgetekin, Umut Demirci, Ça?lar Köseo?lu, Alper Topal, Nuri Karadurmu?, Haktan Ba??? Erdem, Taha Bah |
| 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 |
| Comprehensive profiling of pathogenic germline large genomic rearrangements in a pan-cancer analysis. Molecular oncology 2023 4 . Sun Zhe, Bai Chujie, Su Miaoyi, Tang Haimeng, Wu Xiaoying, Wang Yue, Bao Hua, Liu Xunbiao, Wu Xue, Shao Yang, Xu B |
| Pilot study of gene mutations associated with Lynch syndrome in Slovak patients with breast cancer. Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti 2023 4 36 (2): 130-134. L Krasni?anová, R Saade, P Priš?áková, H Gbelcová, K Ka?avská, M Karaba, J Benca, M Mego, V Repis |
| Pathogenic variants among females with breast cancer and a non-breast cancer reveal opportunities for cancer interception. Breast cancer research and treatment 2023 3 . Bychkovsky Brittany L, Lo Min-Tzu, Yussuf Amal, Horton Carrie, Hemyari Parichehr, LaDuca Holly, Garber Judy E, Scheib Rochelle, Rana Huma |
| 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 |
- Page last reviewed:Oct 1, 2023
- Page last updated:Nov 30, 2023
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