HuGE Literature Finder
Records
1
-
30
| Landscape of somatic mutations in breast cancer: new opportunities for targeted therapies in Saudi Arabian patients. Oncotarget 2021 Mar 12 (7): 686-697. Barakeh Duna H, Aljelaify Rasha, Bashawri Yara, Almutairi Amal, Alqubaishi Fatimah, Alnamnakani Mohammed, Almubarak Latifa, Al Naeem Abdulrahman, Almushawah Fatema, Alrashed May, Abedalthagafi Mal |
| Germline pathogenic variant spectrum in 25 cancer susceptibility genes in Turkish breast and colorectal cancer patients and elderly controls. International journal of cancer 2020 Jul . Akcay Izzet Mehmet, Celik Elifnaz, Agaoglu Nihat Bugra, Alkurt Gizem, Akgun Tugba Kizilboga, Yildiz Jale, Enc Feruze, Kir Gozde, Canbek Sezin, Kilic Ali, Zemheri Ebru, Ezberci Fikret, Özcelik Melike, Doganay Gizem Dinler, Doganay Leve |
| Correlation of MLH1 polymorphisms, survival statistics, in silico assessment and gene downregulation with clinical outcomes among breast cancer cases. Molecular biology reports 2019 Nov . Malik Saima Shakil, Zia Ayisha, Mubarik Sumaira, Masood Nosheen, Rashid Sajid, Sherrard Alice, Khan Muhammad Bilal, Khadim Muhammad Tah |
| Germline mutations in Thai patients with nonmucinous epithelial ovarian cancer. World journal of clinical oncology 2019 Nov 10 (11): 358-368. Manchana Tarinee, Phowthongkum Prasit, Teerapakpinyo Chinacho |
| High prevalence of the MLH1 V384D germline mutation in patients with HER2-positive luminal B breast cancer. Scientific reports 2019 Jul 9 (1): 10966. Lee Seung Eun, Lee Hye Seung, Kim Kyoung-Yeon, Park Jung-Hoon, Roh Hanseong, Park Ha Young, Kim Wan-Se |
| Genetic analysis of subsequent second primary malignant neoplasms in long-term pancreatic cancer survivors suggests new potential hereditary genetic alterations. Cancer management and research 2019 11 599-609. Lovecek Martin, Janatova Marketa, Skalicky Pavel, Zemanek Tomas, Havlik Roman, Ehrmann Jiri, Strouhal Ondrej, Zemankova Petra, Lhotova Klara, Borecka Marianna, Soukupova Jana, Svebisova Hana, Soucek Pavel, Hlavac Viktor, Kleibl Zdenek, Neoral Cestmir, Melichar Bohuslav, Mohelnikova-Duchonova Beatri |
| 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 |
| Frequency of pathogenic germline mutations in cancer susceptibility genes in breast cancer patients. Medical oncology (Northwood, London, England) 2018 Apr 35 (6): 81. Kaur Raman Preet, Shafi Gowhar, Benipal Raja Paramjeet Singh, Munshi Anja |
| Somatic mutations in early onset luminal breast cancer. Oncotarget 2018 Apr 9 (32): 22460-22479. Encinas Giselly, Sabelnykova Veronica Y, de Lyra Eduardo Carneiro, Hirata Katayama Maria Lucia, Maistro Simone, de Vasconcellos Valle Pedro Wilson Mompean, de Lima Pereira Gláucia Fernanda, Rodrigues Lívia Munhoz, de Menezes Pacheco Serio Pedro Adolpho, de Gouvêa Ana Carolina Ribeiro Chaves, Geyer Felipe Correa, Basso Ricardo Alves, Pasini Fátima Solange, Del Pilar Esteves Diz Maria, Brentani Maria Mitzi, Guedes Sampaio Góes João Carlos, Chammas Roger, Boutros Paul C, Koike Folgueira Maria Aparecida Azeve |
| Elucidating therapeutic molecular targets in premenopausal Asian women with recurrent breast cancers. NPJ breast cancer 2018 4 19. Yap Yoon-Sim, Singh Angad P, Lim John H C, Ahn Jin-Hee, Jung Kyung-Hae, Kim Jeongeun, Dent Rebecca A, Ng Raymond C H, Kim Sung-Bae, Chiang Derek |
| High frequency of pathogenic non-founder germline mutations in BRCA1 and BRCA2 in families with breast and ovarian cancer in a founder population. Hereditary cancer in clinical practice 2018 16 12. Maksimenko J, Irmejs A, Trofimovi?s G, B?rzi?a D, Skuja E, Purkalne G, Miklaševi?s E, Gardovskis |
| Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer. JAMA oncology 2017 Sep 3 (9): 1190-1196. Couch Fergus J, Shimelis Hermela, Hu Chunling, Hart Steven N, Polley Eric C, Na Jie, Hallberg Emily, Moore Raymond, Thomas Abigail, Lilyquist Jenna, Feng Bingjian, McFarland Rachel, Pesaran Tina, Huether Robert, LaDuca Holly, Chao Elizabeth C, Goldgar David E, Dolinsky Jill |
| Network Meta-Analysis on the Effects of DNA Damage Response-Related Gene Mutations on Overall Survival of Breast Cancer Based on TCGA Database. Journal of cellular biochemistry 2017 May . Liu Chang, Chang Hong, Li Xiao-Han, Qi Ya-Fei, Wang Jin-Ou, Zhang Ying, Yang Xiang-Ho |
| Mutational profiling of brain metastasis from breast cancer: matched pair analysis of targeted sequencing between brain metastasis and primary breast cancer. Oncotarget 2015 Oct . Lee Ji Yun, Park Kyunghee, Lim Sung Hee, Kim Hae Su, Yoo Kwai Han, Jung Ki Sun, Song Haa-Na, Hong Mineui, Do In-Gu, Ahn TaeJin, Lee Se Kyung, Bae Soo Youn, Kim Seok Won, Lee Jeong Eon, Nam Seok Jin, Kim Duk-Hwan, Jung Hae Hyun, Kim Ji-Yeon, Ahn Jin Seok, Im Young-Hyuck, Park Yeon H |
| Lynch syndrome caused by MLH1 mutations is associated with an increased risk of breast cancer: a cohort study. Journal of medical genetics 2015 Aug 52 (8): 553-6. Harkness Elaine F, Barrow Emma, Newton Katy, Green Kate, Clancy Tara, Lalloo Fiona, Hill James, Evans D Gare |
| 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 |
| Risk of secondary malignancy (including breast) in patients with mismatch-repair protein deficiency. The American journal of surgical pathology 2014 Nov 38 (11): 1494-500. Clay Michael R, Allison Kimberly H, Folkins Ann K, Longacre Teri |
| 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 |
| Polymorphisms in DNA repair genes, recreational physical activity and breast cancer risk. International journal of cancer. Journal international du cancer 2014 Feb 134 (3): 654-63. McCullough Lauren E, Santella Regina M, Cleveland Rebecca J, Millikan Robert C, Olshan Andrew F, North Kari E, Bradshaw Patrick T, Eng Sybil M, Terry Mary Beth, Shen Jing, Crew Katherine D, Rossner Pavel, Teitelbaum Susan L, Neugut Alfred I, Gammon Marilie |
| Assessing SNP-SNP interactions among DNA repair, modification and metabolism related pathway genes in breast cancer susceptibility. PloS one 2014 8 (6): e64896. Sapkota Yadav, Mackey John R, Lai Raymond, Franco-Villalobos Conrado, Lupichuk Sasha, Robson Paula J, Kopciuk Karen, Cass Carol E, Yasui Yutaka, Damaraju Sambasivar |
| Factors modifying the risk for developing acute skin toxicity after whole-breast intensity modulated radiotherapy. BMC cancer 2014 14 711. De Langhe Sofie, Mulliez Thomas, Veldeman Liv, Remouchamps Vincent, van Greveling Annick, Gilsoul Monique, De Schepper Eline, De Ruyck Kim, De Neve Wilfried, Thierens Hube |
| 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 |
| Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome. Journal of the National Cancer Institute 2013 Feb . Win AK, Lindor NM, Winship I, Tucker KM, Buchanan DD, Young JP, Rosty C, Leggett B, Giles GG, Goldblatt J, Macrae FA, Parry S, Kalady MF, Baron JA, Ahnen DJ, Marchand LL, Gallinger S, Haile RW, Newcomb PA, Hopper JL, Jenkins MA |
| BRCA1, TP53, and CHEK2 germline mutations in uterine serous carcinoma. Cancer 2013 Jan 119 (2): 332-8. Pennington Kathryn P, Walsh Tom, Lee Ming, Pennil Christopher, Novetsky Akiva P, Agnew Kathy J, Thornton Anne, Garcia Rochelle, Mutch David, King Mary-Claire, Goodfellow Paul, Swisher Elizabeth |
| Colorectal cancer susceptibility variants alter risk of breast cancer in a Chinese Han population. Genetics and molecular research : GMR 2013 12 (4): 6268-74. Wei W, Jiang M, Luo L, Li Z, Wang P, Dong W |
| Risks of less common cancers in proven mutation carriers with lynch syndrome. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2012 Oct . Engel C, Loeffler M, Steinke V, Rahner N, Holinski-Feder E, Dietmaier W, Schackert HK, Goergens H, von Knebel Doeberitz M, Goecke TO, Schmiegel W, Buettner R, Moeslein G, Letteboer TG, García EG, Hes FJ, Hoogerbrugge N, Menko FH, van Os TA, Sijmons RH, Wagner A, Kluijt I, Propping P, Vasen HF |
| Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2012 Mar 30 (9): 958-64. Win Aung Ko, Young Joanne P, Lindor Noralane M, Tucker Katherine M, Ahnen Dennis J, Young Graeme P, Buchanan Daniel D, Clendenning Mark, Giles Graham G, Winship Ingrid, Macrae Finlay A, Goldblatt Jack, Southey Melissa C, Arnold Julie, Thibodeau Stephen N, Gunawardena Shanaka R, Bapat Bharati, Baron John A, Casey Graham, Gallinger Steven, Le Marchand Loïc, Newcomb Polly A, Haile Robert W, Hopper John L, Jenkins Mark |
| Evidence for breast cancer as an integral part of Lynch syndrome. Genes, chromosomes & cancer 2012 Jan 51 (1): 83-91. Buerki Nicole, Gautier Lucienne, Kovac Michal, Marra Giancarlo, Buser Mauro, Mueller Hansjakob, Heinimann Ka |
| Association between genetic polymorphisms in the XRCC1, XRCC3, XPD, GSTM1, GSTT1, MSH2, MLH1, MSH3, and MGMT genes and radiosensitivity in breast cancer patients. International journal of radiation oncology, biology, physics 2011 Sep 81 (1): 52-8. Mangoni Monica, Bisanzi Simonetta, Carozzi Francesca, Sani Cristina, Biti Giampaolo, Livi Lorenzo, Barletta Emanuela, Costantini Adele Seniori, Gorini Giusep |
| Genetic polymorphisms of multiple DNA repair pathways impact age at diagnosis and TP53 mutations in breast cancer. Carcinogenesis 2011 Jun . Smith TR, Liu-Mares W, Van Emburgh BO, Levine EA, Allen GO, Hill JW, Reis IM, Kresty LA, Pegram MD, Miller MS, Hu JJ |
- Page last reviewed:Oct 1, 2021
- Page last updated:Jan 12, 2022
- Content source: