HuGE Literature Finder
Records 1-30
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Differences in Genomic Alterations Between Brain Metastases and Primary Tumors.
Neurosurgery 2020 Dec . Dono Antonio, Takayasu Takeshi, Yan Yuanqing, Bundrant Bethany E, Arevalo Octavio, Lopez-Garcia Carlos A, Esquenazi Yoshua, Ballester Leomar |
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Association between genetic variants at 9p21 locus with risk of breast cancer: A systematic review and meta-analysis.
Pathology, research and practice 2020 Jul 216 (7): 152987. Abdeahad Hossein, Bahrami Afsane, Saeedi Nikoo, Shabani Mohammad, Pezeshki Milad, Khazaei Majid, Shafiee Mojtaba, Ghorbani Elnaz, Ferns Gordon A, Soleimanpour Saman, Rahmani Farzad, Soleimani Atena, Fiuji Hamid, Ryzhikov Mikhail, Avan Amir, Mahdi Hassanian Sey |
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Comparison of mutation profile between primary phyllodes tumors of the breast and their paired local recurrences.
Polish journal of pathology : official journal of the Polish Society of Pathologists 2020 71 (1): 7-12. Mitus Jerzy, Adamczyk Agnieszka, Majchrzyk Kaja, Kowalik Artur, Rys Janusz, Niemiec Joan |
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Identification of CDKN2A variants in breast cancer patients in Pakistan.
Genes & genetic systems 2019 Jun . Khan Ranjha, Aftab Ayesha, Tabassum Sobia, Hussain Hafiz Muhammad Jafar, Hameed Abdul, Mahmood Humera, Munir Faiza, Bukhari Ihtish |
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Genomic and Transcriptomic Landscape of Triple-Negative Breast Cancers: Subtypes and Treatment Strategies.
Cancer cell 2019 Feb . Jiang Yi-Zhou, Ma Ding, Suo Chen, Shi Jinxiu, Xue Mengzhu, Hu Xin, Xiao Yi, Yu Ke-Da, Liu Yi-Rong, Yu Ying, Zheng Yuanting, Li Xiangnan, Zhang Chenhui, Hu Pengchen, Zhang Jing, Hua Qi, Zhang Jiyang, Hou Wanwan, Ren Luyao, Bao Ding, Li Bingying, Yang Jingcheng, Yao Ling, Zuo Wen-Jia, Zhao Shen, Gong Yue, Ren Yi-Xing, Zhao Ya-Xin, Yang Yun-Song, Niu Zhenmin, Cao Zhi-Gang, Stover Daniel G, Verschraegen Claire, Kaklamani Virginia, Daemen Anneleen, Benson John R, Takabe Kazuaki, Bai Fan, Li Da-Qiang, Wang Peng, Shi Leming, Huang Wei, Shao Zhi-Mi |
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Large-scale meta-analysis of mutations identified in panels of breast/ovarian cancer-related genes - Providing evidence of cancer predisposition genes.
Gynecologic oncology 2019 Feb . Suszynska Malwina, Klonowska Katarzyna, Jasinska Anna J, Kozlowski Pio |
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Genetic polymorphisms of diabetes-related genes, their interaction with diabetes status, and breast cancer incidence and mortality: The Long Island Breast Cancer Study Project.
Molecular carcinogenesis 2019 03 58 (3): 436-446. Parada Humberto, Cleveland Rebecca J, North Kari E, Stevens June, Teitelbaum Susan L, Neugut Alfred I, Santella Regina M, Martinez Maria E, Gammon Marilie |
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Evaluation of the two polymorphisms rs1801133 in MTHFR and rs10811661 in CDKN2A/B in breast cancer.
Journal of cellular biochemistry 2018 Oct . Hesari Amirreza, Maleksabet Amir, Tirkani Abolfazl Nosrati, Ghazizadeh Hamideh, Iranifar Elmira, Mohagheg Fatoalah, Anoshrvani Ali Arash, Ghasemi Faez |
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Association of Breast and Ovarian Cancers With Predisposition Genes Identified by Large-Scale Sequencing.
JAMA oncology 2018 Aug . Lu Hsiao-Mei, Li Shuwei, Black Mary Helen, Lee Shela, Hoiness Robert, Wu Sitao, Mu Wenbo, Huether Robert, Chen Jefferey, Sridhar Srijani, Tian Yuan, McFarland Rachel, Dolinsky Jill, Tippin Davis Brigette, Mexal Sharon, Dunlop Charles, Elliott Aar |
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Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity.
Breast cancer research : BCR 2018 Aug 20 (1): 87. Penkert Judith, Schmidt Gunnar, Hofmann Winfried, Schubert Stephanie, Schieck Maximilian, Auber Bernd, Ripperger Tim, Hackmann Karl, Sturm Marc, Prokisch Holger, Hille-Betz Ursula, Mark Dorothea, Illig Thomas, Schlegelberger Brigitte, Steinemann Dor |
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Mutations in BRCA1, BRCA2, and PALB2, and a panel of 50 cancer-associated genes in pancreatic ductal adenocarcinoma.
Scientific reports 2018 May 8 (1): 8105. Takeuchi Shoko, Doi Manami, Ikari Naoki, Yamamoto Masakazu, Furukawa To |
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Genetic heterogeneity and actionable mutations in HER2-positive primary breast cancers and their brain metastases.
Oncotarget 2018 Apr 9 (29): 20617-20630. De Mattos-Arruda Leticia, Ng Charlotte K Y, Piscuoglio Salvatore, Gonzalez-Cao Maria, Lim Raymond S, De Filippo Maria R, Fusco Nicola, Schultheis Anne M, Ortiz Carolina, Viteri Santiago, Arias Alexandra, Macedo Gabriel S, Oliveira Mafalda, Gomez Patricia, Teixidó Cristina, Nuciforo Paolo, Peg Vicente, Saura Cristina, Ramon Y Cajal Santiago, Casas Francesc Tresserra, Weigelt Britta, Cortes Javier, Seoane Joan, Reis-Filho Jorge |
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A genetic variant in CDKN2A/B gene is associated with the increased risk of breast cancer.
Journal of clinical laboratory analysis 2017 Mar . ShahidSales Soodabeh, Mehramiz Mehraneh, Ghasemi Faezeh, Aledavood Amir, Shamsi Mehri, Hassanian Seyed Mahdi, Ghayour-Mobarhan Majid, Avan Am |
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Next-generation sequencing of circulating tumor DNA to predict recurrence in triple-negative breast cancer patients with residual disease after neoadjuvant chemotherapy.
NPJ breast cancer 2017 3 24. Chen Yu-Hsiang, Hancock Bradley A, Solzak Jeffrey P, Brinza Dumitru, Scafe Charles, Miller Kathy D, Radovich Mil |
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Mutational Profile of Metastatic Breast Cancers: A Retrospective Analysis.
PLoS medicine 2016 Dec 13 (12): e1002201. Lefebvre Celine, Bachelot Thomas, Filleron Thomas, Pedrero Marion, Campone Mario, Soria Jean-Charles, Massard Christophe, Lévy Christelle, Arnedos Monica, Lacroix-Triki Magali, Garrabey Julie, Boursin Yannick, Deloger Marc, Fu Yu, Commo Frédéric, Scott Véronique, Lacroix Ludovic, Dieci Maria Vittoria, Kamal Maud, Diéras Véronique, Gonçalves Anthony, Ferrerro Jean-Marc, Romieu Gilles, Vanlemmens Laurence, Mouret Reynier Marie-Ange, Théry Jean-Christophe, Le Du Fanny, Guiu Séverine, Dalenc Florence, Clapisson Gilles, Bonnefoi Hervé, Jimenez Marta, Le Tourneau Christophe, André Fabri |
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Targeted next-generation sequencing detects a high frequency of potentially actionable mutations in metastatic breast cancers.
Experimental and molecular pathology 2016 Apr 100 (3): 421-425. Muller Kristen E, Marotti Jonathan D, de Abreu Francine B, Peterson Jason D, Miller Todd W, Chamberlin Mary D, Tsongalis Gregory J, Tafe Laura |
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Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2-negative patients with early-onset breast cancer.
Genetics in medicine : official journal of the American College of Medical Genetics 2015 Aug 17 (8): 630-8. Maxwell Kara N, Wubbenhorst Bradley, D'Andrea Kurt, Garman Bradley, Long Jessica M, Powers Jacquelyn, Rathbun Katherine, Stopfer Jill E, Zhu Jiajun, Bradbury Angela R, Simon Michael S, DeMichele Angela, Domchek Susan M, Nathanson Katherine |
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Prevalence of germline mutations in cancer predisposition genes in patients with pancreatic cancer.
Gastroenterology 2015 Mar 148 (3): 556-64. Grant Robert C, Selander Iris, Connor Ashton A, Selvarajah Shamini, Borgida Ayelet, Briollais Laurent, Petersen Gloria M, Lerner-Ellis Jordan, Holter Spring, Gallinger Stev |
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Analysis of sequence variants in the 3'UTR of CDKN2A gene in melanoma patients.
Contemporary oncology (Poznan?, Poland) 2015 19 (4): 276-9. Przyby?a Anna, Lamperska Katarzyna, Mackiewicz Andrz |
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Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers.
Carcinogenesis 2014 Dec 35 (12): 2698-705. Li Wen-Qing, Pfeiffer Ruth M, Hyland Paula L, Shi Jianxin, Gu Fangyi, Wang Zhaoming, Bhattacharjee Samsiddhi, Luo Jun, Xiong Xiaoqin, Yeager Meredith, Deng Xiang, Hu Nan, Taylor Philip R, Albanes Demetrius, Caporaso Neil E, Gapstur Susan M, Amundadottir Laufey, Chanock Stephen J, Chatterjee Nilanjan, Landi Maria Teresa, Tucker Margaret A, Goldstein Alisa M, Yang Xiaohong |
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Increased prevalence of lung, breast, and pancreatic cancers in addition to melanoma risk in families bearing the cyclin-dependent kinase inhibitor 2A mutation: implications for genetic counseling.
Journal of the American Academy of Dermatology 2014 Nov 71 (5): 888-95. Potrony Miriam, Puig-Butillé Joan Anton, Aguilera Paula, Badenas Celia, Carrera Cristina, Malvehy Josep, Puig Susa |
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Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2014 Jul 32 (19): 2001-9. Kurian Allison W, Hare Emily E, Mills Meredith A, Kingham Kerry E, McPherson Lisa, Whittemore Alice S, McGuire Valerie, Ladabaum Uri, Kobayashi Yuya, Lincoln Stephen E, Cargill Michele, Ford James |
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Unique molecular signatures as a hallmark of patients with metastatic breast cancer: implications for current treatment paradigms.
Oncotarget 2014 May 5 (9): 2349-54. Wheler Jennifer J, Parker Barbara A, Lee Jack J, Atkins Johnique T, Janku Filip, Tsimberidou Apostolia M, Zinner Ralph, Subbiah Vivek, Fu Siqing, Schwab Richard, Moulder Stacy, Valero Vicente, Schwaederle Maria, Yelensky Roman, Miller Vincent A, Stephens M Philip J, Meric-Bernstam Funda, Kurzrock Razel |
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Breast cancer subtypes and previously established genetic risk factors: a bayesian approach.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2014 Jan 23 (1): 84-97. O'Brien Katie M, Cole Stephen R, Engel Lawrence S, Bensen Jeannette T, Poole Charles, Herring Amy H, Millikan Robert |
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Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients.
BMC medical genetics 2014 15 (1): 55. Silva Felipe C, Lisboa Bianca Cg, Figueiredo Marcia Cp, Torrezan Giovana T, Santos Erika Mm, Krepischi Ana C, Rossi Benedito M, Achatz Maria I, Carraro Dirce |
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Evaluating genome-wide association study-identified breast cancer risk variants in African-American women.
PloS one 2013 8 (4): e58350. Long Jirong, Zhang Ben, Signorello Lisa B, Cai Qiuyin, Deming-Halverson Sandra, Shrubsole Martha J, Sanderson Maureen, Dennis Joe, Michailidou Kyriaki, Michailiou Kyriaki, Easton Douglas F, Shu Xiao-Ou, Blot William J, Zheng W |
Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk.
PLoS genetics 2013 9 (3): e1003173. Gaudet Mia M, Kuchenbaecker Karoline B, Vijai Joseph, Klein Robert J, Kirchhoff Tomas, McGuffog Lesley, Barrowdale Daniel, Dunning Alison M, Lee Andrew, Dennis Joe, Healey Sue, Dicks Ed, Soucy Penny, Sinilnikova Olga M, Pankratz Vernon S, Wang Xianshu, Eldridge Ronald C, Tessier Daniel C, Vincent Daniel, Bacot Francois, Hogervorst Frans B L, Peock Susan, Stoppa-Lyonnet Dominique, , Peterlongo Paolo, Schmutzler Rita K, Nathanson Katherine L, Piedmonte Marion, Singer Christian F, Thomassen Mads, , Hansen Thomas v O, Neuhausen Susan L, Blanco Ignacio, Greene Mark H, Garber Judith, Weitzel Jeffrey N, Andrulis Irene L, Goldgar David E, D'Andrea Emma, Caldes Trinidad, Nevanlinna Heli, Osorio Ana, van Rensburg Elizabeth J, Arason Adalgeir, Rennert Gad, van den Ouweland Ans M W, van der Hout Annemarie H, Kets Carolien M, Aalfs Cora M, Wijnen Juul T, Ausems Margreet G E M, , , Frost Debra, Ellis Steve, Fineberg Elena, Platte Radka, Evans D Gareth, Jacobs Chris, Adlard Julian, Tischkowitz Marc, Porteous Mary E, Damiola Francesca, , Golmard Lisa, Barjhoux Laure, Longy Michel, Belotti Muriel, Ferrer Sandra Fert, Mazoyer Sylvie, Spurdle Amanda B, Manoukian Siranoush, Barile Monica, Genuardi Maurizio, Arnold Norbert, Meindl Alfons, Sutter Christian, Wappenschmidt Barbara, Domchek Susan M, Pfeiler Georg, Friedman Eitan, Jensen Uffe Birk, Robson Mark, Shah Sohela, Lazaro Conxi, Mai Phuong L, Benitez Javier, Southey Melissa C, Schmidt Marjanka K, Fasching Peter A, Peto Julian, Humphreys Manjeet K, Wang Qin, Michailidou Kyriaki, Sawyer Elinor J, Burwinkel Barbara, Guénel Pascal, Bojesen Stig E, Milne Roger L, Brenner Hermann, Lochmann Magdalena, , Aittomäki Kristiina, Dörk Thilo, Margolin Sara, Mannermaa Arto, Lambrechts Diether, Chang-Claude Jenny, Radice Paolo, Giles Graham G, Haiman Christopher A, Winqvist Robert, Devillee Peter, García-Closas Montserrat, Schoof Nils, Hooning Maartje J, Cox Angela, Pharoah Paul D P, Jakubowska Anna, Orr Nick, González-Neira Anna, Pita Guillermo, Alonso M Rosario, Hall Per, Couch Fergus J, Simard Jacques, Altshuler David, Easton Douglas F, Chenevix-Trench Georgia, Antoniou Antonis C, Offit Kenne |
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Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers.
Breast cancer research : BCR 2012 14 (1): R33. Antoniou Antonis C, Kuchenbaecker Karoline B, Soucy Penny, Beesley Jonathan, Chen Xiaoqing, McGuffog Lesley, Lee Andrew, Barrowdale Daniel, Healey Sue, Sinilnikova Olga M, Caligo Maria A, Loman Niklas, Harbst Katja, Lindblom Annika, Arver Brita, Rosenquist Richard, Karlsson Per, Nathanson Kate, Domchek Susan, Rebbeck Tim, Jakubowska Anna, Lubinski Jan, Jaworska Katarzyna, Durda Katarzyna, Z?owowcka-Per?owska El?bieta, Osorio Ana, Durán Mercedes, Andrés Raquel, Benítez Javier, Hamann Ute, Hogervorst Frans B, van Os Theo A, Verhoef Senno, Meijers-Heijboer Hanne E J, Wijnen Juul, Gómez Garcia Encarna B, Ligtenberg Marjolijn J, Kriege Mieke, Collée J Margriet, Ausems Margreet G E M, Oosterwijk Jan C, Peock Susan, Frost Debra, Ellis Steve D, Platte Radka, Fineberg Elena, Evans D Gareth, Lalloo Fiona, Jacobs Chris, Eeles Ros, Adlard Julian, Davidson Rosemarie, Cole Trevor, Cook Jackie, Paterson Joan, Douglas Fiona, Brewer Carole, Hodgson Shirley, Morrison Patrick J, Walker Lisa, Rogers Mark T, Donaldson Alan, Dorkins Huw, Godwin Andrew K, Bove Betsy, Stoppa-Lyonnet Dominique, Houdayer Claude, Buecher Bruno, de Pauw Antoine, Mazoyer Sylvie, Calender Alain, Léoné Mélanie, Bressac-de Paillerets Brigitte, Caron Olivier, Sobol Hagay, Frenay Marc, Prieur Fabienne, Ferrer Sandra U, Mortemousque Isabelle, Buys Saundra, Daly Mary, Miron Alexander, Terry Mary U, Hopper John L, John Esther M, Southey Melissa, Goldgar David, Singer Christian F, Fink-Retter Anneliese, Tea Muy-Kheng, Kaulich Daphne U, Hansen Thomas V, Nielsen Finn C, Barkardottir Rosa B, Gaudet Mia, Kirchhoff Tomas, Joseph Vijai, Dutra-Clarke Ana, Offit Kenneth, Piedmonte Marion, Kirk Judy, Cohn David, Hurteau Jean, Byron John, Fiorica James, Toland Amanda E, Montagna Marco, Oliani Cristina, Imyanitov Evgeny, Isaacs Claudine, Tihomirova Laima, Blanco Ignacio, Lazaro Conxi, Teulé Alex, Valle J Del, Gayther Simon A, Odunsi Kunle, Gross Jenny, Karlan Beth Y, Olah Edith, Teo Soo-Hwang, Ganz Patricia A, Beattie Mary S, Dorfling Cecelia M, van Rensburg Elizabeth U, Diez Orland, Kwong Ava, Schmutzler Rita K, Wappenschmidt Barbara, Engel Christoph, Meindl Alfons, Ditsch Nina, Arnold Norbert, Heidemann Simone, Niederacher Dieter, Preisler-Adams Sabine, Gadzicki Dorothea, Varon-Mateeva Raymonda, Deissler Helmut, Gehrig Andrea, Sutter Christian, Kast Karin, Fiebig Britta, Schäfer Dieter, Caldes Trinidad, de la Hoya Miguel, Nevanlinna Heli, Muranen Taru A, Lespérance Bernard, Spurdle Amanda B, Neuhausen Susan L, Ding Yuan C, Wang Xianshu, Fredericksen Zachary, Pankratz Vernon S, Lindor Noralane M, Peterlongo Paolo, Manoukian Siranoush, Peissel Bernard, Zaffaroni Daniela, Bonanni Bernardo, Bernard Loris, Dolcetti Riccardo, Papi Laura, Ottini Laura, Radice Paolo, Greene Mark H, Loud Jennifer T, Andrulis Irene L, Ozcelik Hilmi, Mulligan Anna U, Glendon Gord, Thomassen Mads, Gerdes Anne-Marie, Jensen Uffe B, Skytte Anne-Bine, Kruse Torben A, Chenevix-Trench Georgia, Couch Fergus J, Simard Jacques, Easton Douglas F, , , , , |
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Can a phenotype for recessive inheritance in breast cancer be defined?
Familial cancer 2010 Dec 9 (4): 525-30. Ellberg Carolina, Jönsson Göran, Olsson Håk |
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Contribution of CDKN2A/P16 ( INK4A ), P14 (ARF), CDK4 and BRCA1/2 germline mutations in individuals with suspected genetic predisposition to uveal melanoma.
Familial cancer 2010 Dec 9 (4): 663-7. Buecher B, Gauthier-Villars M, Desjardins L, Lumbroso-Le Rouic L, Levy C, De Pauw A, Bombled J, Tirapo C, Houdayer C, Bressac-de Paillerets B, Stoppa-Lyonnet |
- Page last reviewed:Oct 1, 2020
- Page last updated:May 05, 2021
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