HuGE Literature Finder
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| Association of Reported Candidate Monogenic Genes With Lung Cancer Risk. Clinical lung cancer 2023 2 . Rifkin Andrew S, Less Ethan M, Wei Jun, Shi Zhuqing, Zheng Siqun Lilly, Helfand Brian T, Hulick Peter J, Krantz Seth B, Xu Jianfe |
| Beyond BRCA: Patterns of risk-reducing surgery for non-BRCA, homologous recombination repair pathway gene variant carriers. Gynecologic oncology 2023 2 170 234-240. Lee Sarah S, Karpel Hannah C, Oh Cheongeun, Smith Julia, Pothuri Bhava |
| Characterization of BRCA Deficiency in Ovarian Cancer. Cancers 2023 3 15 (5): . Barbero Giovanna, Zuntini Roberta, Magini Pamela, Desiderio Laura, Bonaguro Michela, Perrone Anna Myriam, Rubino Daniela, Grippa Mina, De Leo Antonio, Ceccarelli Claudio, Godino Lea, Miccoli Sara, Ferrari Simona, Santini Donatella, De Iaco Pierandrea, Zamagni Claudio, Innella Giovanni, Turchetti Danie |
| Homologous Recombination Repair Gene Mutations to Predict Olaparib Plus Bevacizumab Efficacy in the First-Line Ovarian Cancer PAOLA-1/ENGOT-ov25 Trial. JCO precision oncology 2023 1 7 e2200258. Pujade-Lauraine Eric, Brown Jessica, Barnicle Alan, Wessen Jonathan, Lao-Sirieix Pierre, Criscione Steven W, du Bois Andreas, Lorusso Domenica, Romero Ignacio, Petru Edgar, Yoshida Hiroyuki, Vergote Ignace, Colombo Nicoletta, Hietanen Sakari, Provansal Magali, Schmalfeldt Barbara, Pignata Sandro, Martín Lorente Cristina, Berton Dominique, Runnebaum Ingo B, Ray-Coquard Isabel |
| Molecular Genetic Characteristics of FANCI, a Proposed New Ovarian Cancer Predisposing Gene. Genes 2023 2 14 (2): . Fierheller Caitlin T, Alenezi Wejdan M, Serruya Corinne, Revil Timothée, Amuzu Setor, Bedard Karine, Subramanian Deepak N, Fewings Eleanor, Bruce Jeffrey P, Prokopec Stephenie, Bouchard Luigi, Provencher Diane, Foulkes William D, El Haffaf Zaki, Mes-Masson Anne-Marie, Tischkowitz Marc, Campbell Ian G, Pugh Trevor J, Greenwood Celia M T, Ragoussis Jiannis, Tonin Patricia |
| 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 |
| Prevalence of germline mutations in cancer susceptibility genes in Chinese patients with renal cell carcinoma. Translational andrology and urology 2023 3 12 (2): 308-319. Feng Huayi, Cao Shouqing, Ouyang Qing, Li Huaikang, Li Xiubin, Chen Ke, Zhang Xiangyi, Huang Yan, Zhang Xu, Ma X |
| Prevalence of Pathogenic Germline Mutations in 13 Hereditary Cancer-Related Genes in Breast Cancer Patients in Narathiwat Province, Thailand. Asian Pacific journal of cancer prevention : APJCP 2023 2 24 (2): 525-530. Sukpan Panupong, Kanokwiroon Kanyanatt, Sriplung Hutcha, Laochareonsuk Wison, Choochuen Pongsakorn, Auseng Nasuha, Wanawanakorn Kasemsun, Sangkhathat Suras |
| The impact of coding germline variants on contralateral breast cancer risk and survival. American journal of human genetics 2023 2 110 (3): 475-486. Morra Anna, Mavaddat Nasim, Muranen Taru A, Ahearn Thomas U, Allen Jamie, Andrulis Irene L, Auvinen Päivi, Becher Heiko, Behrens Sabine, Blomqvist Carl, Bojesen Stig E, Bolla Manjeet K, Brauch Hiltrud, Camp Nicola J, Carvalho Sara, Castelao Jose E, Cessna Melissa H, Chang-Claude Jenny, Chenevix-Trench Georgia, , Czene Kamila, Decker Brennan, Dennis Joe, Dörk Thilo, Dorling Leila, Dunning Alison M, Ekici Arif B, Eriksson Mikael, Evans D Gareth, Fasching Peter A, Figueroa Jonine D, Flyger Henrik, Gago-Dominguez Manuela, García-Closas Montserrat, Geurts-Giele Willemina R R, Giles Graham G, Guénel Pascal, Gündert Melanie, Hahnen Eric, Hall Per, Hamann Ute, Harrington Patricia A, He Wei, Heikkilä Päivi, Hooning Maartje J, Hoppe Reiner, Howell Anthony, Humphreys Keith, , Jakubowska Anna, Jung Audrey Y, Keeman Renske, Kristensen Vessela N, Lubi?ski Jan, Mannermaa Arto, Manoochehri Mehdi, Manoukian Siranoush, Margolin Sara, Mavroudis Dimitrios, Milne Roger L, Mulligan Anna Marie, Newman William G, Park-Simon Tjoung-Won, Peterlongo Paolo, Pharoah Paul D P, Rhenius Valerie, Saloustros Emmanouil, Sawyer Elinor J, Schmutzler Rita K, Shah Mitul, Spurdle Amanda B, Tomlinson Ian, Truong Thérèse, van Veen Elke M, Vreeswijk Maaike P G, Wang Qin, Wendt Camilla, Yang Xiaohong R, Nevanlinna Heli, Devilee Peter, Easton Douglas F, Schmidt Marjanka |
| Inherited rare variants in homologous recombination and neurodevelopmental genes are associated with increased risk of neuroblastoma. EBioMedicine 2022 Dec 87 104395. Bonfiglio Ferdinando, Lasorsa Vito Alessandro, Cantalupo Sueva, D'Alterio Giuseppe, Aievola Vincenzo, Boccia Angelo, Ardito Martina, Furini Simone, Renieri Alessandra, Morini Martina, Stainczyk Sabine, Westermann Frank, Paolella Giovanni, Eva Alessandra, Iolascon Achille, Capasso Mar |
| Whole-Exome Sequencing Among Chinese Patients With Hereditary Diffuse Gastric Cancer. JAMA network open 2022 Dec 5 (12): e2245836. Liu Ze-Xian, Zhang Xiao-Long, Zhao Qi, Chen Yungchang, Sheng Hui, He Cai-Yun, Sun Yu-Ting, Lai Ming-Yu, Wu Min-Qing, Zuo Zhi-Xiang, Wang Wei, Zhou Zhi-Wei, Wang Feng-Hua, Li Yu-Hong, Xu Rui-Hua, Qiu Miao-Zh |
| Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci. Journal of the National Cancer Institute 2022 Oct . DeVries Amber A, Dennis Joe, Tyrer Jonathan P, Peng Pei-Chen, Coetzee Simon G, Reyes Alberto L, Plummer Jasmine T, Davis Brian D, Chen Stephanie S, Dezem Felipe Segato, Aben Katja K H, Anton-Culver Hoda, Antonenkova Natalia N, Beckmann Matthias W, Beeghly-Fadiel Alicia, Berchuck Andrew, Bogdanova Natalia V, Bogdanova-Markov Nadja, Brenton James D, Butzow Ralf, Campbell Ian, Chang-Claude Jenny, Chenevix-Trench Georgia, Cook Linda S, DeFazio Anna, Doherty Jennifer A, Dörk Thilo, Eccles Diana M, Eliassen A Heather, Fasching Peter A, Fortner Renée T, Giles Graham G, Goode Ellen L, Goodman Marc T, Gronwald Jacek, , , Håkansson Niclas, Hildebrandt Michelle A T, Huff Chad, Huntsman David G, Jensen Allan, Kar Siddhartha, Karlan Beth Y, Khusnutdinova Elza K, Kiemeney Lambertus A, Kjaer Susanne K, Kupryjanczyk Jolanta, Labrie Marilyne, Lambrechts Diether, Le Nhu D, Lubi?ski Jan, May Taymaa, Menon Usha, Milne Roger L, Modugno Francesmary, Monteiro Alvaro N, Moysich Kirsten B, Odunsi Kunle, Olsson Håkan, Pearce Celeste L, Pejovic Tanja, Ramus Susan J, Riboli Elio, Riggan Marjorie J, Romieu Isabelle, Sandler Dale P, Schildkraut Joellen M, Setiawan V Wendy, Sieh Weiva, Song Honglin, Sutphen Rebecca, Terry Kathryn L, Thompson Pamela J, Titus Linda, Tworoger Shelley S, Van Nieuwenhuysen Els, Edwards Digna Velez, Webb Penelope M, Wentzensen Nicolas, Whittemore Alice S, Wolk Alicja, Wu Anna H, Ziogas Argyrios, Freedman Matthew L, Lawrenson Kate, Pharoah Paul D P, Easton Douglas F, Gayther Simon A, Jones Michelle |
| DNA methylation of the immediate upstream region of BRCA1 major transcription start sites is an independent favorable prognostic factor in patients with high-grade serous ovarian cancer. Gynecologic oncology 2022 Oct . Ebata Takahiro, Yamashita Satoshi, Takeshima Hideyuki, Yoshida Hiroshi, Kawata Yoshiko, Kino Nao, Yasugi Toshiharu, Terao Yasuhisa, Yonemori Kan, Kato Tomoyasu, Ushijima Toshika |
| Development and Validation of the PREMMplus Model for Multigene Hereditary Cancer Risk Assessment. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2022 Aug JCO2200120. Yurgelun Matthew B, Uno Hajime, Furniss C Sloane, Ukaegbu Chinedu, Horiguchi Miki, Yussuf Amal, LaDuca Holly, Chittenden Anu, Garber Judy E, Syngal Sap |
| 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 |
| Breast Cancer Risk in Women from Ghana Carrying Rare Germline Pathogenic Mutations. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2022 Jun . Ahearn Thomas U, Choudhury Parichoy Pal, Derkach Andriy, Wiafe-Addai Beatrice, Awuah Baffour, Yarney Joel, Edusei Lawrence, Titiloye Nicholas, Adjei Ernest, Vanderpuye Verna, Aitpillah Francis, Dedey Florence, Oppong Joseph, Osei-Bonsu Ernest Baawuah, Duggan Máire A, Brinton Louise A, Allen Jamie, Luccarini Craig, Baynes Caroline, Carvalho Sara, Dunning Alison M, Davis Lynn Brittny C, Chanock Stephen J, Hicks Belynda D, Yeager Meredith, Chatterjee Nilanjan, Biritwum Richard, Clegg-Lamptey Joe Nat, Nyarko Kofi, Wiafe Seth, Ansong Daniel, Easton Douglas F, Figueroa Jonine D, Garcia-Closas Montserr |
| Concurrent BRAFV600E and BRCA Mutations in MSS Metastatic Colorectal Cancer: Prevalence and Case Series of mCRC patients with prolonged OS. Cancer treatment and research communications 2022 Apr 32 100569. Cannon Timothy Lewis, Randall Jamie N, Sokol Ethan S, Alexander Sonja M, Wadlow Raymond C, Winer Arthur A, Barnett Daniel M, Rayes Danny L, Nimeiri Halla S, McGregor Kimberly |
| [Oncogénétique dans les cancers de l'ovaire]. La Revue du praticien 2022 7 72 (6): 639-641. Desseignés Camille, Benusiglio Patri |
| AZD5305 More Tolerable than Earlier PARP Agents. Cancer discovery 2022 5 12 (7): 1602. Authors are not available |
| Characterization of genetic predisposition to molecular subtypes of breast cancer in Brazilian patients. Frontiers in oncology 2022 12 976959. Paixão Daniele, Torrezan Giovana Tardin, Santiago Karina Miranda, Formiga Maria Nirvana, Ahuno Samuel Terkper, Dias-Neto Emmanuel, Tojal da Silva Israel, Foulkes William D, Polak Paz, Carraro Dirce Mar |
| 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 |
| Comprehensive Analysis of the Expression and Prognosis for RAD51 Family in Human Breast Cancer. International journal of general medicine 2022 15 4925-4936. Shi Yaqin, Shen Meng, Xu Mengdan, Tao Min, Chen Kai, Zhu Qingqi |
| 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 |
| Influence of germline test results on surgical decision making in women with invasive breast cancer. Cancer genetics 2022 7 266-267 81-85. Vargason Ashlee B, Turner Clesson E, Shriver Craig D, Ellsworth Rachel |
| Multigene Panel Testing in Turkish Hereditary Cancer Syndrome Patients. Medeniyet medical journal 2022 6 37 (2): 150-158. Arslan Ates Esra, Turkyilmaz Ayberk, Alavanda Ceren, Yildirim Ozlem, Guney Ahmet Ilt |
| 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 |
| Risk-reducing surgery in unaffected individuals receiving cancer genetic testing in an integrated health care system. Cancer 2022 6 128 (16): 3090-3098. Knerr Sarah, Guo Boya, Mittendorf Kathleen F, Feigelson Heather Spencer, Gilmore Marian J, Jarvik Gail P, Kauffman Tia L, Keast Erin, Lynch Frances L, Muessig Kristin R, Okuyama Sonia, Veenstra David L, Zepp Jamilyn M, Goddard Katrina A B, Devine Be |
| Somatic inactivation of breast cancer predisposition genes in tumors associated with pathogenic germline variants. Journal of the National Cancer Institute 2022 10 115 (2): 181-189. Lim Belle W X, Li Na, Mahale Sakshi, McInerny Simone, Zethoven Magnus, Rowley Simone M, Huynh Joanne, Wang Theresa, Lee Jue Er Amanda, Friedman Mia, Devereux Lisa, Scott Rodney J, Sloan Erica K, James Paul A, Campbell Ian |
| Spectrum of Germline Mutations Within Fanconi Anemia-Associated Genes Across Populations of Varying Ancestry. JNCI cancer spectrum 2022 8 5 (1): . Chan Sock Hoai, Ni Ying, Li Shao-Tzu, Teo Jing Xian, Ishak Nur Diana Binte, Lim Weng Khong, Ngeow Joan |
| Targeted molecular profiling of epithelial ovarian cancer from Italian BRCA wild-type patients with a BRCA and PARP pathways gene panel. Experimental and molecular pathology 2022 9 128 104833. Salvati Annamaria, Carnevali Ileana, Alexandrova Elena, Facchi Sofia, Ronchi Susanna, Libera Laura, Sahnane Nora, Memoli Domenico, Lamberti Jessica, Amabile Sonia, Pepe Stefano, Tarallo Roberta, Sessa Fausto, Weisz Alessandro, Tibiletti Maria Grazia, Rizzo Frances |
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- Page last updated:Mar 31, 2023
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