Human Genome Epidemiology Literature Finder
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Records 1 - 19 (of 19 Records) |
| Query Trace: Disease and FANCM[original query] |
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| Exome resequencing identifies potential tumor-suppressor genes that predispose to colorectal cancer. Human mutation 2013 Jul 34 (7): 1026-34. Smith Christopher G, Naven Marc, Harris Rebecca, Colley James, West Hannah, Li Ning, Liu Yuan, Adams Richard, Maughan Timothy S, Nichols Laura, Kaplan Richard, Wagner Michael J, McLeod Howard L, Cheadle Jeremy |
| FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome. International journal of cancer 2016 Aug . Kiiski Johanna I, Fagerholm Rainer, Tervasmäki Anna, Pelttari Liisa M, Khan Sofia, Jamshidi Maral, Mantere Tuomo, Pylkäs Katri, Bartek Jiri, Bartkova Jirina, Mannermaa Arto, Tengström Maria, Kosma Veli-Matti, Winqvist Robert, Kallioniemi Anne, Aittomäki Kristiina, Blomqvist Carl, Nevanlinna He |
| [Association between clinical outcome and gene mutation in children with Fanconi anemia]. Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2016 Aug 18 (8): 742-5. Chang Li-Xian, Ren Ruan-Ruan, Yang Wen-Yu, Zhang Jia-Yuan, Wan Yang, Liu Tian-Feng, Zhang Li, Chen Xiao-Juan, Zhu Shuai, Ruan Min, Chen Xia, Liu Xiao-Ming, Qi Ben-Quan, Zhang Ran-Ran, Zou Yao, Chen Yu-Mei, Zhu Xiao-F |
| 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 |
| Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility. Genetics in medicine : official journal of the American College of Medical Genetics 2017 8 20 (4): 452-457. Catucci Irene, Osorio Ana, Arver Brita, Neidhardt Guido, Bogliolo Massimo, Zanardi Federica, Riboni Mirko, Minardi Simone, Pujol Roser, Azzollini Jacopo, Peissel Bernard, Manoukian Siranoush, De Vecchi Giovanna, Casola Stefano, Hauke Jan, Richters Lisa, Rhiem Kerstin, Schmutzler Rita K, Wallander Karin, Törngren Therese, Borg Åke, Radice Paolo, Surrallés Jordi, Hahnen Eric, Ehrencrona Hans, Kvist Anders, Benitez Javier, Peterlongo Pao |
| A possible role of FANCM mutations in male breast cancer susceptibility: Results from a multicenter study in Italy. Breast (Edinburgh, Scotland) 2018 Apr 38 92-97. Silvestri Valentina, Rizzolo Piera, Zelli Veronica, Valentini Virginia, Zanna Ines, Bianchi Simonetta, Tibiletti Maria Grazia, Varesco Liliana, Russo Antonio, Tommasi Stefania, Coppa Anna, Capalbo Carlo, Calistri Daniele, Viel Alessandra, Cortesi Laura, Manoukian Siranoush, Bonanni Bernardo, Montagna Marco, Palli Domenico, Radice Paolo, Peterlongo Paolo, Ottini Lau |
| 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 |
| 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 |
| 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 |
| 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 |
A Genome-Wide Association Study for Hypertensive Kidney Disease in Korean Men.
Genes 2021 May 12 (5): . Kim Hye-Rim, Jin Hyun-Seok, Eom Yong-B |
| 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 |
| Novel Bi-Allelic Variants of FANCM Cause Sertoli Cell-Only Syndrome and Non-Obstructive Azoospermia. Frontiers in genetics 2022 1 12 799886. Zhang Yuxiang, Li Peng, Liu Nachuan, Jing Tao, Ji Zhiyong, Yang Chao, Zhao Liangyu, Tian Ruhui, Chen Huixing, Huang Yuhua, Zhi Erlei, Ou Ningjing, Bai Haowei, Zhou Yuchuan, Li Zheng, Yao Chenche |
| 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 |
| 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 |
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