Human Genome Epidemiology Literature Finder
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Records 1 - 20 (of 20 Records) |
| Query Trace: Ovarian Neoplasms and FANCM[original query] |
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| Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer. Proceedings of the National Academy of Sciences of the United States of America 2014 Oct 111 (42): 15172-7. Kiiski Johanna I, Pelttari Liisa M, Khan Sofia, Freysteinsdottir Edda S, Reynisdottir Inga, Hart Steven N, Shimelis Hermela, Vilske Sara, Kallioniemi Anne, Schleutker Johanna, Leminen Arto, Bützow Ralf, Blomqvist Carl, Barkardottir Rosa B, Couch Fergus J, Aittomäki Kristiina, Nevanlinna He |
| Patterns and functional implications of rare germline variants across 12 cancer types. Nature communications 2015 6 10086. Lu Charles, Xie Mingchao, Wendl Michael C, Wang Jiayin, McLellan Michael D, Leiserson Mark D M, Huang Kuan-Lin, Wyczalkowski Matthew A, Jayasinghe Reyka, Banerjee Tapahsama, Ning Jie, Tripathi Piyush, Zhang Qunyuan, Niu Beifang, Ye Kai, Schmidt Heather K, Fulton Robert S, McMichael Joshua F, Batra Prag, Kandoth Cyriac, Bharadwaj Maheetha, Koboldt Daniel C, Miller Christopher A, Kanchi Krishna L, Eldred James M, Larson David E, Welch John S, You Ming, Ozenberger Bradley A, Govindan Ramaswamy, Walter Matthew J, Ellis Matthew J, Mardis Elaine R, Graubert Timothy A, Dipersio John F, Ley Timothy J, Wilson Richard K, Goodfellow Paul J, Raphael Benjamin J, Chen Feng, Johnson Kimberly J, Parvin Jeffrey D, Ding |
| Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer. JAMA oncology 2016 Dec . Neidhardt Guido, Hauke Jan, Ramser Juliane, Groß Eva, Gehrig Andrea, Müller Clemens R, Kahlert Anne-Karin, Hackmann Karl, Honisch Ellen, Niederacher Dieter, Heilmann-Heimbach Stefanie, Franke André, Lieb Wolfgang, Thiele Holger, Altmüller Janine, Nürnberg Peter, Klaschik Kristina, Ernst Corinna, Ditsch Nina, Jessen Frank, Ramirez Alfredo, Wappenschmidt Barbara, Engel Christoph, Rhiem Kerstin, Meindl Alfons, Schmutzler Rita K, Hahnen Er |
| Germline whole exome sequencing and large-scale replication identifies FANCM as a likely high grade serous ovarian cancer susceptibility gene. Oncotarget 2017 (31): 50930-50940. Dicks Ed, Song Honglin, Ramus Susan J, Oudenhove Elke Van, Tyrer Jonathan P, Intermaggio Maria P, Kar Siddhartha, Harrington Patricia, Bowtell David D, Group Aocs Study, Cicek Mine S, Cunningham Julie M, Fridley Brooke L, Alsop Jennifer, Jimenez-Linan Mercedes, Piskorz Anna, Goranova Teodora, Kent Emma, Siddiqui Nadeem, Paul James, Crawford Robin, Poblete Samantha, Lele Shashi, Sucheston-Campbell Lara, Moysich Kirsten B, Sieh Weiva, McGuire Valerie, Lester Jenny, Odunsi Kunle, Whittemore Alice S, Bogdanova Natalia, Dürst Matthias, Hillemanns Peter, Karlan Beth Y, Gentry-Maharaj Aleksandra, Menon Usha, Tischkowitz Marc, Levine Douglas, Brenton James D, Dörk Thilo, Goode Ellen L, Gayther Simon A, Pharoah D P Pa |
| CHEK2 c.1100delC mutation is associated with an increased risk for male breast cancer in Finnish patient population. BMC cancer 2017 Sep 17 (1): 620. Hallamies Sanna, Pelttari Liisa M, Poikonen-Saksela Paula, Jekunen Antti, Jukkola-Vuorinen Arja, Auvinen Päivi, Blomqvist Carl, Aittomäki Kristiina, Mattson Johanna, Nevanlinna He |
| FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population. Breast cancer research and treatment 2017 Jul . Kiiski Johanna I, Tervasmäki Anna, Pelttari Liisa M, Khan Sofia, Mantere Tuomo, Pylkäs Katri, Mannermaa Arto, Tengström Maria, Kvist Anders, Borg Åke, Kosma Veli-Matti, Kallioniemi Anne, Schleutker Johanna, Bützow Ralf, Blomqvist Carl, Aittomäki Kristiina, Winqvist Robert, Nevanlinna He |
| Reanalysis of BRCA1/2 negative high risk ovarian cancer patients reveals novel germline risk loci and insights into missing heritability. PloS one 2017 12 (6): e0178450. Stafford Jaime L, Dyson Gregory, Levin Nancy K, Chaudhry Sophia, Rosati Rita, Kalpage Hasini, Wernette Courtney, Petrucelli Nancie, Simon Michael S, Tainsky Michael |
| Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia. American journal of human genetics 2018 8 103 (2): 200-212. Kasak Laura, Punab Margus, Nagirnaja Liina, Grigorova Marina, Minajeva Ave, Lopes Alexandra M, Punab Anna Maria, Aston Kenneth I, Carvalho Filipa, Laasik Eve, Smith Lee B, , Conrad Donald F, Laan Mar |
| The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants. International journal of cancer 2018 11 144 (11): 2683-2694. Schubert Stephanie, van Luttikhuizen Jana L, Auber Bernd, Schmidt Gunnar, Hofmann Winfried, Penkert Judith, Davenport Colin F, Hille-Betz Ursula, Wendeburg Lena, Bublitz Janin, Tauscher Marcel, Hackmann Karl, Schröck Evelin, Scholz Caroline, Wallaschek Hannah, Schlegelberger Brigitte, Illig Thomas, Steinemann Dor |
| Multigene panel testing beyond BRCA1/2 in breast/ovarian cancer Spanish families and clinical actionability of findings. Journal of cancer research and clinical oncology 2018 10 144 (12): 2495-2513. Bonache Sandra, Esteban Irene, Moles-Fernández Alejandro, Tenés Anna, Duran-Lozano Laura, Montalban Gemma, Bach Vanessa, Carrasco Estela, Gadea Neus, López-Fernández Adrià, Torres-Esquius Sara, Mancuso Francesco, Caratú Ginevra, Vivancos Ana, Tuset Noemí, Balmaña Judith, Gutiérrez-Enríquez Sara, Diez Orla |
| FANCM and RECQL genetic variants and breast cancer susceptibility: relevance to South Poland and West Ukraine. BMC medical genetics 2018 1 19 (1): 12. Nguyen-Dumont Tú, Myszka Aleksander, Karpinski Pawel, Sasiadek Maria M, Akopyan Hayane, Hammet Fleur, Tsimiklis Helen, Park Daniel J, Pope Bernard J, Slezak Ryszard, Kitsera Nataliya, Siekierzynska Aleksandra, Southey Melissa |
| 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 |
| Analysis of polymorphisms in genes associated with the FA/BRCA pathway in three patients with multiple primary malignant neoplasms. Artificial cells, nanomedicine, and biotechnology 2019 Dec 47 (1): 1101-1112. Wang Le, Wang Hao, Wang Ting, Liu Jinhui, Chen Wei, Wang Yamin, Chen Chao, Zhu Hongli, Dai Pengg |
| Recurrent moderate-risk mutations in Finnish breast and ovarian cancer patients. International journal of cancer 2019 Mar . Nurmi Anna, Muranen Taru A, Pelttari Liisa M, Kiiski Johanna I, Heikkinen Tuomas, Lehto Sini, Kallioniemi Anne, Schleutker Johanna, Bützow Ralf, Blomqvist Carl, Aittomäki Kristiina, Nevanlinna He |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
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