Human Genome Epidemiology Literature Finder
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Query Trace: Breast Neoplasms and FANCM[original query] |
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Mutational analysis of FANCL, FANCM and the recently identified FANCI suggests that among the 13 known Fanconi Anemia genes, only FANCD1/BRCA2 plays a major role in high-risk breast cancer predisposition. Carcinogenesis 2009 Nov 30 (11): 1898-902. García María J, Fernández Victoria, Osorio Ana, Barroso Alicia, Fernández Fernando, Urioste Miguel, Benítez Javi |
Polymorphic variations in the FANCA gene in high-risk non-BRCA1/2 breast cancer individuals from the French Canadian population. Molecular oncology 2013 Feb 7 (1): 85-100. Litim Nadhir, Labrie Yvan, Desjardins Sylvie, Ouellette Geneviève, Plourde Karine, Belleau Pascal, , Durocher Franci |
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 |
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor. Human molecular genetics 2015 Sep 24 (18): 5345-55. Peterlongo Paolo, Catucci Irene, Colombo Mara, Caleca Laura, Mucaki Eliseos, Bogliolo Massimo, Marin Maria, Damiola Francesca, Bernard Loris, Pensotti Valeria, Volorio Sara, Dall'Olio Valentina, Meindl Alfons, Bartram Claus, Sutter Christian, Surowy Harald, Sornin Valérie, Dondon Marie-Gabrielle, Eon-Marchais Séverine, Stoppa-Lyonnet Dominique, Andrieu Nadine, Sinilnikova Olga M, , Mitchell Gillian, James Paul A, Thompson Ella, , , Marchetti Marina, Verzeroli Cristina, Tartari Carmen, Capone Gabriele Lorenzo, Putignano Anna Laura, Genuardi Maurizio, Medici Veronica, Marchi Isabella, Federico Massimo, Tognazzo Silvia, Matricardi Laura, Agata Simona, Dolcetti Riccardo, Puppa Lara Della, Cini Giulia, Gismondi Viviana, Viassolo Valeria, Perfumo Chiara, Mencarelli Maria Antonietta, Baldassarri Margherita, Peissel Bernard, Roversi Gaia, Silvestri Valentina, Rizzolo Piera, Spina Francesca, Vivanet Caterina, Tibiletti Maria Grazia, Caligo Maria Adelaide, Gambino Gaetana, Tommasi Stefania, Pilato Brunella, Tondini Carlo, Corna Chiara, Bonanni Bernardo, Barile Monica, Osorio Ana, Benitez Javier, Balestrino Luisa, Ottini Laura, Manoukian Siranoush, Pierotti Marco A, Renieri Alessandra, Varesco Liliana, Couch Fergus J, Wang Xianshu, Devilee Peter, Hilbers Florentine S, van Asperen Christi J, Viel Alessandra, Montagna Marco, Cortesi Laura, Diez Orland, Balmaña Judith, Hauke Jan, Schmutzler Rita K, Papi Laura, Pujana Miguel Angel, Lázaro Conxi, Falanga Anna, Offit Kenneth, Vijai Joseph, Campbell Ian, Burwinkel Barbara, Kvist Anders, Ehrencrona Hans, Mazoyer Sylvie, Pizzamiglio Sara, Verderio Paolo, Surralles Jordi, Rogan Peter K, Radice Pao |
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 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 |
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 |
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 |
Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia. Genetics in medicine : official journal of the American College of Medical Genetics 2017 8 20 (4): 458-463. Bogliolo Massimo, Bluteau Dominique, Lespinasse James, Pujol Roser, Vasquez Nadia, d'Enghien Catherine Dubois, Stoppa-Lyonnet Dominique, Leblanc Thierry, Soulier Jean, Surrallés Jor |
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 |
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 |
Mutational analysis of candidate genes in Israeli male breast cancer cases. Breast cancer research and treatment 2018 3 170 (2): 399-404. Schayek Hagit, Korach Hila, Laitman Yael, Bernstein-Molho Rinat, Friedman Eit |
Correlation of FANCM expression with clinical factors in luminal B breast cancer. Breast cancer (Tokyo, Japan) 2018 Jan . Wang Yiran, Wang Junnan, Long Fei, Wang Ning, Zhang Bingbing, Han Huan, Wang Yaj |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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