Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 55 Records) |
| Query Trace: Neoplasms and FANCM[original query] |
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| Recommendations for Preventive Care for Women with Rare Genetic Cause of Breast and Ovarian Cancer. Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti 2019 8 32 (Supplementum2): 6-13. Foretová Lenka, Navrátilová Marie, Svoboda Marek, Vaší?ková Petra, S?ahlová Eva Hrabincová, Házová Jana, Kleiblová Petra, Kleibl Zden?k, Machá?ková Eva, Palácová Markéta, Petráková Katarí |
| A Patient Affected with Serous Ovarian/Peritoneal Carcinoma Carrying the FANCM Mutation. Case reports in oncological medicine 2019 6 2019 9357924. Nikolaidi Adamantia, Konstantopoulou Irene, Pistalmantzian Nikolaos, Fostira Florentia, Yannoukakos Drakoulis, Athanasiadis Ili |
| Identifying sequence variants contributing to hereditary breast and ovarian cancer in BRCA1 and BRCA2 negative breast and ovarian cancer patients. Scientific reports 2019 12 9 (1): 19986. Jarhelle Elisabeth, Riise Stensland Hilde Monica Frostad, Hansen Geir Åsmund Myge, Skarsfjord Siri, Jonsrud Christoffer, Ingebrigtsen Monica, Strømsvik Nina, Van Ghelue Marij |
| The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer. NPJ breast cancer 2019 5 38. Figlioli Gisella, Bogliolo Massimo, Catucci Irene, Caleca Laura, Lasheras Sandra Viz, Pujol Roser, Kiiski Johanna I, Muranen Taru A, Barnes Daniel R, Dennis Joe, Michailidou Kyriaki, Bolla Manjeet K, Leslie Goska, Aalfs Cora M, , Adank Muriel A, Adlard Julian, Agata Simona, Cadoo Karen, Agnarsson Bjarni A, Ahearn Thomas, Aittomäki Kristiina, Ambrosone Christine B, Andrews Lesley, Anton-Culver Hoda, Antonenkova Natalia N, Arndt Volker, Arnold Norbert, Aronson Kristan J, Arun Banu K, Asseryanis Ella, Auber Bernd, Auvinen Päivi, Azzollini Jacopo, Balmaña Judith, Barkardottir Rosa B, Barrowdale Daniel, Barwell Julian, Beane Freeman Laura E, Beauparlant Charles Joly, Beckmann Matthias W, Behrens Sabine, Benitez Javier, Berger Raanan, Bermisheva Marina, Blanco Amie M, Blomqvist Carl, Bogdanova Natalia V, Bojesen Anders, Bojesen Stig E, Bonanni Bernardo, Borg Ake, Brady Angela F, Brauch Hiltrud, Brenner Hermann, Brüning Thomas, Burwinkel Barbara, Buys Saundra S, Caldés Trinidad, Caliebe Almuth, Caligo Maria A, Campa Daniele, Campbell Ian G, Canzian Federico, Castelao Jose E, Chang-Claude Jenny, Chanock Stephen J, Claes Kathleen B M, Clarke Christine L, Collavoli Anita, Conner Thomas A, Cox David G, Cybulski Cezary, Czene Kamila, Daly Mary B, de la Hoya Miguel, Devilee Peter, Diez Orland, Ding Yuan Chun, Dite Gillian S, Ditsch Nina, Domchek Susan M, Dorfling Cecilia M, Dos-Santos-Silva Isabel, Durda Katarzyna, Dwek Miriam, Eccles Diana M, Ekici Arif B, Eliassen A Heather, Ellberg Carolina, Eriksson Mikael, Evans D Gareth, Fasching Peter A, Figueroa Jonine, Flyger Henrik, Foulkes William D, Friebel Tara M, Friedman Eitan, Gabrielson Marike, Gaddam Pragna, Gago-Dominguez Manuela, Gao Chi, Gapstur Susan M, Garber Judy, García-Closas Montserrat, García-Sáenz José A, Gaudet Mia M, Gayther Simon A, , Giles Graham G, Glendon Gord, Godwin Andrew K, Goldberg Mark S, Goldgar David E, Guénel Pascal, Gutierrez-Barrera Angelica M, Haeberle Lothar, Haiman Christopher A, Håkansson Niclas, Hall Per, Hamann Ute, Harrington Patricia A, Hein Alexander, Heyworth Jane, Hillemanns Peter, Hollestelle Antoinette, Hopper John L, Hosgood H Dean, Howell Anthony, Hu Chunling, Hulick Peter J, Hunter David J, Imyanitov Evgeny N, , Isaacs Claudine, Jakimovska Milena, Jakubowska Anna, James Paul, Janavicius Ramunas, Janni Wolfgang, John Esther M, Jones Michael E, Jung Audrey, Kaaks Rudolf, Karlan Beth Y, Khusnutdinova Elza, Kitahara Cari M, Konstantopoulou Irene, Koutros Stella, Kraft Peter, Lambrechts Diether, Lazaro Conxi, Le Marchand Loic, Lester Jenny, Lesueur Fabienne, Lilyquist Jenna, Loud Jennifer T, Lu Karen H, Luben Robert N, Lubinski Jan, Mannermaa Arto, Manoochehri Mehdi, Manoukian Siranoush, Margolin Sara, Martens John W M, Maurer Tabea, Mavroudis Dimitrios, Mebirouk Noura, Meindl Alfons, Menon Usha, Miller Austin, Montagna Marco, Nathanson Katherine L, Neuhausen Susan L, Newman William G, Nguyen-Dumont Tu, Nielsen Finn Cilius, Nielsen Sarah, Nikitina-Zake Liene, Offit Kenneth, Olah Edith, Olopade Olufunmilayo I, Olshan Andrew F, Olson Janet E, Olsson Håkan, Osorio Ana, Ottini Laura, Peissel Bernard, Peixoto Ana, Peto Julian, Plaseska-Karanfilska Dijana, Pocza Timea, Presneau Nadege, Pujana Miquel Angel, Punie Kevin, Rack Brigitte, Rantala Johanna, Rashid Muhammad U, Rau-Murthy Rohini, Rennert Gad, Lejbkowicz Flavio, Rhenius Valerie, Romero Atocha, Rookus Matti A, Ross Eric A, Rossing Maria, Rudaitis Vilius, Ruebner Matthias, Saloustros Emmanouil, Sanden Kristin, Santamariña Marta, Scheuner Maren T, Schmutzler Rita K, Schneider Michael, Scott Christopher, Senter Leigha, Shah Mitul, Sharma Priyanka, Shu Xiao-Ou, Simard Jacques, Singer Christian F, Sohn Christof, Soucy Penny, Southey Melissa C, Spinelli John J, Steele Linda, Stoppa-Lyonnet Dominique, Tapper William J, Teixeira Manuel R, Terry Mary Beth, Thomassen Mads, Thompson Jennifer, Thull Darcy L, Tischkowitz Marc, Tollenaar Rob A E M, Torres Diana, Troester Melissa A, Truong Thérèse, Tung Nadine, Untch Michael, Vachon Celine M, van Rensburg Elizabeth J, van Veen Elke M, Vega Ana, Viel Alessandra, Wappenschmidt Barbara, Weitzel Jeffrey N, Wendt Camilla, Wieme Greet, Wolk Alicja, Yang Xiaohong R, Zheng Wei, Ziogas Argyrios, Zorn Kristin K, Dunning Alison M, Lush Michael, Wang Qin, McGuffog Lesley, Parsons Michael T, Pharoah Paul D P, Fostira Florentia, Toland Amanda E, Andrulis Irene L, Ramus Susan J, Swerdlow Anthony J, Greene Mark H, Chung Wendy K, Milne Roger L, Chenevix-Trench Georgia, Dörk Thilo, Schmidt Marjanka K, Easton Douglas F, Radice Paolo, Hahnen Eric, Antoniou Antonis C, Couch Fergus J, Nevanlinna Heli, Surrallés Jordi, Peterlongo Pao |
| Prevalence and clinical implications of germline predisposition gene mutations in patients with acute myeloid leukemia. Scientific reports 2020 9 10 (1): 14297. Kim Borahm, Yun Woobin, Lee Seung-Tae, Choi Jong Rok, Yoo Keon Hee, Koo Hong Hoe, Jung Chul Won, Kim Sun H |
| Subsequent Neoplasm Risk Associated With Rare Variants in DNA Damage Response and Clinical Radiation Sensitivity Syndrome Genes in the Childhood Cancer Survivor Study. JCO precision oncology 2020 4 . Morton Lindsay M, Karyadi Danielle M, Hartley Stephen W, Frone Megan N, Sampson Joshua N, Howell Rebecca M, Neglia Joseph P, Arnold Michael A, Hicks Belynda D, Jones Kristine, Zhu Bin, Dagnall Casey L, Karlins Eric, Yeager Meredith S, Leisenring Wendy M, Yasui Yutaka, Turcotte Lucie M, Smith Susan A, Weathers Rita E, Miller Jeremy, Sigel Byron S, Merino Diana M, Berrington de Gonzalez Amy, Bhatia Smita, Robison Leslie L, Tucker Margaret A, Armstrong Gregory T, Chanock Stephen |
| Contribution of Inherited DNA-Repair Gene Mutations to Hormone-Sensitive and Castrate-Resistant Metastatic Prostate Cancer and Implications for Clinical Outcome. JCO precision oncology 2019 3 . Yadav Siddhartha, Hart Steven N, Hu Chunling, Hillman David, Lee Kun Y, Gnanaolivu Rohan, Na Jie, Polley Eric C, Couch Fergus J, Kohli Mani |
| High-Throughput Sequencing of Gastric Cancer Patients: Unravelling Genetic Predispositions Towards an Early-Onset Subtype. Cancers 2020 7 12 (7): . Machlowska Julita, Kapusta Przemys?aw, Baj Jacek, Morsink Folkert H M, Wo?kow Pawe?, Maciejewski Ryszard, Offerhaus G Johan A, Sitarz Robe |
| Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients. Cancers 2020 4 12 (4): . Del Valle Jesús, Rofes Paula, Moreno-Cabrera José Marcos, López-Dóriga Adriana, Belhadj Sami, Vargas-Parra Gardenia, Teulé Àlex, Cuesta Raquel, Muñoz Xavier, Campos Olga, Salinas Mónica, de Cid Rafael, Brunet Joan, González Sara, Capellá Gabriel, Pineda Marta, Feliubadaló Lídia, Lázaro Con |
| A comprehensive analysis of candidate genes in familial pancreatic cancer families reveals a high frequency of potentially pathogenic germline variants. EBioMedicine 2020 3 53 102675. Earl Julie, Galindo-Pumariño Cristina, Encinas Jessica, Barreto Emma, Castillo Maria E, Pachón Vanessa, Ferreiro Reyes, Rodríguez-Garrote Mercedes, González-Martínez Silvia, Ramon Y Cajal Teresa, Diaz Luis Robles, Chirivella-Gonzalez Isabel, Rodriguez Montse, de Castro Eva Martínez, García-Seisdedos David, Muñoz Gloria, Rosa Juan Manuel Rosa, Marquez Mirari, Malats Nuría, Carrato Alfre |
| Analysis of 11 candidate genes in 849 adult patients with suspected hereditary cancer predisposition. Genes, chromosomes & cancer 2020 Oct . Cavaillé Mathias, Uhrhammer Nancy, Privat Maud, Ponelle-Chachuat Flora, Gay-Bellile Mathilde, Lepage Mathis, Molnar Ioana, Viala Sandrine, Bidet Yannick, Bignon Yves-Je |
| Next-generation Sequencing Reveals Age-dependent Genetic Underpinnings in Lung adenocarcinoma. Journal of Cancer 2022 4 13 (5): 1565-1572. Wu Xiaonan, Zhao Jun, Yang Ling, Nie Xin, Wang Zheng, Zhang Ping, Li Chao, Hu Xueqing, Tang Min, Yi Yuting, Du Xinhua, Xia Xuefeng, Guan Yanfang, Yu Zicheng, Gu Wenguang, Quan Xiangming, Li Lin, Shi Ho |
| Mutational spectrum of breast cancer susceptibility genes among women ascertained in a cancer risk clinic in Northeast Brazil. Breast cancer research and treatment 2022 3 193 (2): 485-494. Felix Gabriela E S, Guindalini Rodrigo Santa Cruz, Zheng Yonglan, Walsh Tom, Sveen Elisabeth, Lopes Taisa Manuela Machado, Côrtes Juliana, Zhang Jing, Carôzo Polyanna, Santos Irlânia, Bonfim Thaís Ferreira, Garicochea Bernardo, Toralles Maria Betânia Pereira, Meyer Roberto, Netto Eduardo Martins, Abe-Sandes Kiyoko, King Mary-Claire, de Oliveira Nascimento Ivana Lucia, Olopade Olufunmilayo |
| 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 |
| Canonical and uncanonical pathogenic germline variants in colorectal cancer patients by next-generation sequencing in a European referral center. ESMO open 2022 11 7 (6): 100607. Poliani L, Greco L, Barile M, Dal Buono A, Bianchi P, Basso G, Giatti V, Genuardi M, Malesci A, Laghi L, |
| 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 |
| Genomic characterization of metastatic castration-resistant prostate cancer patients undergoing PSMA radioligand therapy: A single-center experience. The Prostate 2022 Oct . Satapathy Swayamjeet, Das Chandan K, Aggarwal Piyush, Sood Ashwani, Parihar Ashwin S, Singh Shrawan K, Mittal Bhagwant |
| Comprehensive Comparative Molecular Characterization of Young and Old Lung Cancer Patients. Frontiers in oncology 2022 1 11 806845. Hu Mingming, Tan Jinjing, Liu Zhentian, Li Lifeng, Zhang Hongmei, Zhao Dan, Li Baolan, Gao Xuan, Che Nanying, Zhang Tongm |
| Prevalence of FANCM germline variants in BRCA1/2 negative breast and/or ovarian cancer patients from Pakistan. Familial cancer 2022 Jul . Rashid Muhammad Usman, Muhammad Noor, Shehzad Umara, Khan Faiz Ali, Loya Asif, Hamann U |
| Prevalence and clinical implications of germline pathogenic variants in cancer predisposing genes in young patients across sarcoma subtypes. Journal of medical genetics 2023 8 . Nathalia de Angelis de Carvalho, Karina Miranda Santiago, Joyce Maria Lisboa Maia, Felipe D'Almeida Costa, Maria Nirvana Formiga, Diogo Cordeiro de Queiroz Soares, Daniele Paixão, Celso Abdon Lopes de Mello, Cecilia Maria Lima da Costa, José Claudio Casali da Rocha, Barbara Rivera, Dirce Maria Carraro, Giovana Tardin Torrez |
| A comprehensive analysis of Fanconi anemia genes in Chinese patients with high-risk hereditary breast cancer. Journal of cancer research and clinical oncology 2023 8 . Qiao-Yan Zhu, Pu-Chun Li, Yi-Fan Zhu, Jia-Ni Pan, Rong Wang, Xiao-Lin Li, Wei-Wu Ye, Xiao-Wen Ding, Xiao-Jia Wang, Wen-Ming C |
| Germ line variants in patients with acute myeloid leukemia without a suspicion of hereditary hematologic malignancy syndrome. Blood advances 2023 7 . Francesca Guijarro, Mònica López-Guerra, Jordi Morata, Alex Bataller, Sara Paz, Josep Maria Cornet-Masana, Antònia Banús-Mulet, Laia Cuesta-Casanovas, Josep Maria Carbó, Sandra Castaño-Díez, Carlos Jiménez-Vicente, Albert Cortés-Bullich, Ana Triguero, Alexandra Martínez-Roca, Daniel Esteban, Marta Gómez-Hernando, José Ramón Álamo Moreno, Irene López-Oreja, Marta Garrote, Ruth Muñoz Risueño, Raul Tonda, Ivo G Gut, Dolors Colomer, Marina Díaz-Beya, Jordi Este |
| New pathogenic germline variants identified in mesothelioma. Lung cancer (Amsterdam, Netherlands) 2023 3 179 107172. Belcaid Laila, Bertelsen Birgitte, Wadt Karin, Tuxen Ida, Spanggaard Iben, Højgaard Martin, Benn Sørensen Jens, Ravn Jesper, Lassen Ulrik, Cilius Nielsen Finn, Rohrberg Kristoffer, Westmose Yde Christi |
| 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 |
| Whole exome sequencing and replication for breast cancer among Hispanic/Latino women identifies FANCM as a susceptibility gene for estrogen-receptor-negative breast cancer. medRxiv : the preprint server for health sciences 2023 2 . Nierenberg Jovia L, Adamson Aaron W, Hu Donglei, Huntsman Scott, Patrick Carmina, Li Min, Steele Linda, Tong Barry, Shieh Yiwey, Fejerman Laura, Gruber Stephen B, Haiman Christopher A, John Esther M, Kushi Lawrence H, Torres-Mejía Gabriela, Ricker Charité, Weitzel Jeffrey N, Ziv Elad, Neuhausen Susan |
| Association of FANCM Mutations with Familial and Early-Onset Breast Cancer Risk in a South American Population. International journal of molecular sciences 2023 2 24 (4): . Morales-Pison Sebastian, Morales-González Sarai, Fernandez-Ramires Ricardo, Tapia Julio C, Maldonado Edio, Calaf Gloria M, Jara Lili |
| Analysis of clinical and genomic profiles of therapy-related myeloid neoplasm in Korea. Human genomics 2023 2 17 (1): 13. Yun Jiwon, Song Hyojin, Kim Sung-Min, Kim Soonok, Kwon Seok Ryun, Lee Young Eun, Jeong Dajeong, Park Jae Hyeon, Kwon Sunghoon, Yun Hongseok, Lee Dong So |
| FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women. European journal of human genetics : EJHG 2023 1 . Figlioli Gisella, Billaud Amandine, Ahearn Thomas U, Antonenkova Natalia N, Becher Heiko, Beckmann Matthias W, Behrens Sabine, Benitez Javier, Bermisheva Marina, Blok Marinus J, Bogdanova Natalia V, Bonanni Bernardo, Burwinkel Barbara, Camp Nicola J, Campbell Archie, Castelao Jose E, Cessna Melissa H, Chanock Stephen J, , Czene Kamila, Devilee Peter, Dörk Thilo, Engel Christoph, Eriksson Mikael, Fasching Peter A, Figueroa Jonine D, Gabrielson Marike, Gago-Dominguez Manuela, García-Closas Montserrat, González-Neira Anna, Grassmann Felix, Guénel Pascal, Gündert Melanie, Hadjisavvas Andreas, Hahnen Eric, Hall Per, Hamann Ute, Harrington Patricia A, He Wei, Hillemanns Peter, Hollestelle Antoinette, Hooning Maartje J, Hoppe Reiner, Howell Anthony, Humphreys Keith, , Jager Agnes, Jakubowska Anna, Khusnutdinova Elza K, Ko Yon-Dschun, Kristensen Vessela N, Lindblom Annika, Lissowska Jolanta, Lubi?ski Jan, Mannermaa Arto, Manoukian Siranoush, Margolin Sara, Mavroudis Dimitrios, Newman William G, Obi Nadia, Panayiotidis Mihalis I, Rashid Muhammad U, Rhenius Valerie, Rookus Matti A, Saloustros Emmanouil, Sawyer Elinor J, Schmutzler Rita K, Shah Mitul, Sironen Reijo, Southey Melissa C, Suvanto Maija, Tollenaar Rob A E M, Tomlinson Ian, Truong Thérèse, van der Kolk Lizet E, van Veen Elke M, Wappenschmidt Barbara, Yang Xiaohong R, Bolla Manjeet K, Dennis Joe, Dunning Alison M, Easton Douglas F, Lush Michael, Michailidou Kyriaki, Pharoah Paul D P, Wang Qin, Adank Muriel A, Schmidt Marjanka K, Andrulis Irene L, Chang-Claude Jenny, Nevanlinna Heli, Chenevix-Trench Georgia, Evans D Gareth, Milne Roger L, Radice Paolo, Peterlongo Pao |
| Prevalence of germline variants in Brazilian pancreatic carcinoma patients. Scientific reports 2024 9 14 (1): 21083. Lívia Munhoz Rodrigues, Simone Maistro, Maria Lucia Hirata Katayama, Vinícius Marques Rocha, Rossana Veronica Mendoza Lopez, Edia Filomena di Tullio Lopes, Fernanda Toledo Gonçalves, Cintia Fridman, Pedro Adolpho de Menezes Pacheco Serio, Luciana Rodrigues Carvalho Barros, Luiz Antonio Senna Leite, Vanderlei Segatelli, Maria Del Pilar Estevez-Diz, Rodrigo Santa Cruz Guindalini, Ulysses Ribeiro Junior, Maria Aparecida Azevedo Koike Folguei |
| Comparative sequencing study of mismatch repair and homology-directed repair genes in endometrial cancer and breast cancer patients from Kazakhstan. International journal of cancer 2024 10 . Ying Zheng, Natalia Vdovichenko, Peter Schürmann, Dhanya Ramachandran, Robert Geffers, Lisa-Marie Speith, Natalia Bogdanova, Julia Enßen, Natalia Dubrowinskaja, Tatyana Yugay, Zura Berkutovna Yessimsiitova, Nurzhan Turmanov, Peter Hillemanns, Thilo Dö |
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