HuGE Literature Finder
Records 1-30
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Germline and somatic mutations of multi-gene panel in Chinese patients with epithelial ovarian cancer: a prospective cohort study.
Journal of ovarian research 2019 Aug 12 (1): 80. Li Wenhui, Shao Di, Li Lei, Wu Ming, Ma Shuiqing, Tan Xianjie, Zhong Sen, Guo Fengming, Wang Zhe, Ye Mingz |
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The Spectrum of Mutations Predisposing to Familial Breast Cancer in Poland.
International journal of cancer 2019 Jun . Cybulski Cezary, Kluzniak Wojciech, Huzarski Tomasz, Wokolorczyk Dominika, Kashyap Aniruddh, Rusak Bogna, Stempa Klaudia, Gronwald Jacek, Szymiczek Agata, Bagherzadeh Maryam, Jakubowska Anna, Debniak Tadeusz, Lener Marcin, Rudnicka Helena, Szwiec Marek, Jarkiewicz-Tretyn Joanna, Stawicka Malgorzata, Domagala Pawel, Narod Steven A, Lubinski Jan, Akbari Mohammad R, |
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Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer.
Breast cancer research : BCR 2019 Apr 21 (1): 55. Weber-Lassalle Nana, Borde Julika, Weber-Lassalle Konstantin, Horváth Judit, Niederacher Dieter, Arnold Norbert, Kaulfuß Silke, Ernst Corinna, Paul Victoria G, Honisch Ellen, Klaschik Kristina, Volk Alexander E, Kubisch Christian, Rapp Steffen, Lichey Nadine, Altmüller Janine, Lepkes Louisa, Pohl-Rescigno Esther, Thiele Holger, Nürnberg Peter, Larsen Mirjam, Richters Lisa, Rhiem Kerstin, Wappenschmidt Barbara, Engel Christoph, Meindl Alfons, Schmutzler Rita K, Hahnen Eric, Hauke J |
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Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families.
BMC cancer 2019 Apr 19 (1): 313. Shahi Rajendra Bahadur, De Brakeleer Sylvia, Caljon Ben, Pauwels Ingrid, Bonduelle Maryse, Joris Sofie, Fontaine Christel, Vanhoeij Marian, Van Dooren Sonia, Teugels Erik, De Grève Jacqu |
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Germline mutations in 40 cancer susceptibility genes among Chinese patients with high hereditary risk breast cancer.
International journal of cancer 2019 Jan 144 (2): 281-289. Li Jun-Yan, Jing Ruilin, Wei Hongyi, Wang Minghao, Xiaowei Qi, Liu Haoxi, Jian Liu, Ou Jiang-Hua, Jiang Wei-Hua, Tian Fu-Guo, Sheng Yuan, Li Heng-Yu, Xu Hong, Zhang Rui-Shan, Guan Ai-Hua, Liu Ke, Jiang Hong-Chuan, Ren Yu, He Jian-Jun, Huang Weiwei, Liao Ning, Cai Xiangjun, Ming Jia, Ling Rui, Xu Yan, Hu Chun-Yan, Zhang Jianguo, Guo Baoliang, Ouyang Lizhi, Shuai Ping, Liu Zhenzhen, Zhong Ling, Zeng Zhen, Zhang Ting, Xuan Zhaoling, Tan Xuanni, Liang Junbin, Pan Qinwen, Chen Li, Zhang Fan, Fan Lin-Jun, Zhang Yi, Yang Xinhua, BoLi Jing, Chen Chongjian, Jiang J |
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Contribution of Massive Parallel Sequencing to Diagnosis of Hereditary Ovarian Cancer in the Czech Republic.
Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti 2019 32 (Supplementum2): 72-78. Soukupová Jana, Lhotová Klára, Zemánková Petra, Vocka Michal, Janatová Markéta, Stolarová Lenka, Borecká Marianna, Kleiblová Petra, Machácková Eva, Foretová Lenka, Koudová Monika, Lhota Filip, Tavandzis Spiros, Zikán Michal, Stránecký Viktor, Veselá Kamila, Panczak Aleš, Kotlas Jaroslav, Kleibl Zden |
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Fine mapping of 2q35 high-risk neuroblastoma locus reveals independent functional risk variants and suggests full-length BARD1 as tumor-suppressor.
International journal of cancer 2018 Aug . Cimmino Flora, Avitabile Marianna, Diskin Sharon J, Vaksman Zalman, Pignataro Piero, Formicola Daniela, Cardinale Antonella, Testori Alessandro, Koster Jan, de Torres Carmen, Devoto Marcella, Maris John M, Iolascon Achille, Capasso Mar |
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Variants of cancer susceptibility genes in Korean BRCA1/2 mutation-negative patients with high risk for hereditary breast cancer.
BMC cancer 2018 01 18 (1): 83. Park Ji Soo, Lee Seung-Tae, Nam Eun Ji, Han Jung Woo, Lee Jung-Yun, Kim Jieun, Kim Tae Il, Park Hyung Se |
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Mutations in BRCA1, BRCA2 and other breast and ovarian cancer susceptibility genes in Central and South American populations.
Biological research 2017 Oct 50 (1): 35. Jara Lilian, Morales Sebastian, de Mayo Tomas, Gonzalez-Hormazabal Patricio, Carrasco Valentina, Godoy Ra |
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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 |
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[Association between single nucleotide polymorphism of BARD1 gene and BRCA1 gene mutation in epithelial ovarian cancer].
Zhonghua fu chan ke za zhi 2017 Jun 52 (6): 403-410. Liu W L, Zhao J Z, Wang Z Z, Dong B, Hou Y Y, Wu X X, Guo Y |
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BARD1 Gene Polymorphisms Confer Nephroblastoma Susceptibility.
EBioMedicine 2017 Feb 16 101-105. Fu Wen, Zhu Jinhong, Xiong Si-Wei, Jia Wei, Zhao Zhang, Zhu Shi-Bo, Hu Jin-Hua, Wang Feng-Hua, Xia Huimin, He Jing, Liu Guo-Cha |
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Genomic analysis of inherited breast cancer among Palestinian women: Genetic heterogeneity and a founder mutation in TP53.
International journal of cancer 2017 08 141 (4): 750-756. Lolas Hamameh Suhair, Renbaum Paul, Kamal Lara, Dweik Dima, Salahat Mohammad, Jaraysa Tamara, Abu Rayyan Amal, Casadei Silvia, Mandell Jessica B, Gulsuner Suleyman, Lee Ming K, Walsh Tom, King Mary-Claire, Levy-Lahad Ephrat, Kanaan Moe |
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Germline multi-gene hereditary cancer panel testing in an unselected endometrial cancer cohort.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2016 Nov 29 (11): 1381-1389. Ring Kari L, Bruegl Amanda S, Allen Brian A, Elkin Eric P, Singh Nanda, Hartman Anne-Renee, Daniels Molly S, Broaddus Russell |
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Exome and deep sequencing of clinically aggressive neuroblastoma reveal somatic mutations that affect key pathways involved in cancer progression.
Oncotarget 2016 Mar . Lasorsa Vito Alessandro, Formicola Daniela, Pignataro Piero, Cimmino Flora, Calabrese Francesco Maria, Mora Jaume, Esposito Maria Rosaria, Pantile Marcella, Zanon Carlo, De Mariano Marilena, Longo Luca, Hogarty Michael D, de Torres Carmen, Tonini Gian Paolo, Iolascon Achille, Capasso Mar |
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Identification of germline alterations in breast cancer predisposition genes among Malaysian breast cancer patients using panel testing.
Clinical genetics 2016 Jan . Ng Pei Sze, Wen Wei Xiong, Fadlullah Muhammad Zaki Hidayatullah, Yoon Sook-Yee, Lee Sheau Yee, Thong Meow-Keong, Yip Cheng Har, Mohd Taib Nur Aishah, Teo Soo-Hwa |
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The Association between GWAS-identified BARD1 Gene SNPs and Neuroblastoma Susceptibility in a Southern Chinese Population.
International journal of medical sciences 2016 13 (2): 133-8. Zhang Ruizhong, Zou Yan, Zhu Jinhong, Zeng Xinhao, Yang Tianyou, Wang Fenghua, He Jing, Xia Huim |
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Inherited Mutations in Women With Ovarian Carcinoma.
JAMA oncology 2015 Dec 1-9. Norquist Barbara M, Harrell Maria I, Brady Mark F, Walsh Tom, Lee Ming K, Gulsuner Suleyman, Bernards Sarah S, Casadei Silvia, Yi Qian, Burger Robert A, Chan John K, Davidson Susan A, Mannel Robert S, DiSilvestro Paul A, Lankes Heather A, Ramirez Nilsa C, King Mary Claire, Swisher Elizabeth M, Birrer Michael |
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Prevalence of pathogenic mutations in cancer predisposition genes among pancreatic cancer patients.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2015 Oct . Hu Chunling, Hart Steven N, Bamlet William R, Moore Raymond M, Nandakumar Kannabiran, Eckloff Bruce W, Lee Yean K, Petersen Gloria M, McWilliams Robert R, Couch Fergus |
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Cancer predisposing BARD1 mutations affect exon skipping and are associated with overexpression of specific BARD1 isoforms.
Oncology reports 2015 Sep . Ratajska Magdalena, Matusiak Magdalena, Kuzniacka Alina, Wasag Bartosz, Brozek Izabela, Biernat Wojciech, Koczkowska Magdalena, Debniak Jaroslaw, Sniadecki Marcin, Kozlowski Piotr, Klonowska Katarzyna, Pilyugin Maxim, Wydra Dariusz, Laurent Geoff, Limon Janusz, Irminger-Finger Irmga |
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A Comparative Analysis of Breast and Ovarian Cancer-related Gene Mutations in Canadian and Saudi Arabian Patients with Breast Cancer.
Anticancer research 2015 May 35 (5): 2601-10. Amemiya Yutaka, Bacopulos Stephanie, Al-Shawarby Mohamed, Al-Tamimi Dalal, Naser Walid, Ahmed Ayesha, Khalifa Mahmoud, Slodkowska Elzbieta, Seth Ar |
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Candidate gene analysis of BRCA1/2 mutation-negative high-risk Russian breast cancer patients.
Cancer letters 2015 Apr 359 (2): 259-61. Sokolenko Anna P, Preobrazhenskaya Elena V, Aleksakhina Svetlana N, Iyevleva Aglaya G, Mitiushkina Natalia V, Zaitseva Olga A, Yatsuk Olga S, Tiurin Vladislav I, Strelkova Tatiana N, Togo Alexandr V, Imyanitov Evgeny |
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Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2015 Feb 33 (4): 304-11. Couch Fergus J, Hart Steven N, Sharma Priyanka, Toland Amanda Ewart, Wang Xianshu, Miron Penelope, Olson Janet E, Godwin Andrew K, Pankratz V Shane, Olswold Curtis, Slettedahl Seth, Hallberg Emily, Guidugli Lucia, Davila Jaime I, Beckmann Matthias W, Janni Wolfgang, Rack Brigitte, Ekici Arif B, Slamon Dennis J, Konstantopoulou Irene, Fostira Florentia, Vratimos Athanassios, Fountzilas George, Pelttari Liisa M, Tapper William J, Durcan Lorraine, Cross Simon S, Pilarski Robert, Shapiro Charles L, Klemp Jennifer, Yao Song, Garber Judy, Cox Angela, Brauch Hiltrud, Ambrosone Christine, Nevanlinna Heli, Yannoukakos Drakoulis, Slager Susan L, Vachon Celine M, Eccles Diana M, Fasching Peter |
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Inherited predisposition to breast cancer among African American women.
Breast cancer research and treatment 2015 Jan 149 (1): 31-9. Churpek Jane E, Walsh Tom, Zheng Yonglan, Moton Zakiya, Thornton Anne M, Lee Ming K, Casadei Silvia, Watts Amanda, Neistadt Barbara, Churpek Matthew M, Huo Dezheng, Zvosec Cecilia, Liu Fang, Niu Qun, Marquez Rafael, Zhang Jing, Fackenthal James, King Mary-Claire, Olopade Olufunmilayo |
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Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: the Polish population as an example.
Scientific reports 2015 5 10424. Klonowska Katarzyna, Ratajska Magdalena, Czubak Karol, Kuzniacka Alina, Brozek Izabela, Koczkowska Magdalena, Sniadecki Marcin, Debniak Jaroslaw, Wydra Dariusz, Balut Magdalena, Stukan Maciej, Zmienko Agnieszka, Nowakowska Beata, Irminger-Finger Irmgard, Limon Janusz, Kozlowski Pio |
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Prevalence of Germline Mutations in Genes Engaged in DNA Damage Repair by Homologous Recombination in Patients with Triple-Negative and Hereditary Non-Triple-Negative Breast Cancers.
PloS one 2015 10 (6): e0130393. Domagala Pawel, Jakubowska Anna, Jaworska-Bieniek Katarzyna, Kaczmarek Katarzyna, Durda Katarzyna, Kurlapska Agnieszka, Cybulski Cezary, Lubinski J |
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Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes.
European journal of human genetics : EJHG 2014 Nov 22 (11): 1305-13. Castéra Laurent, Krieger Sophie, Rousselin Antoine, Legros Angélina, Baumann Jean-Jacques, Bruet Olivia, Brault Baptiste, Fouillet Robin, Goardon Nicolas, Letac Olivier, Baert-Desurmont Stéphanie, Tinat Julie, Bera Odile, Dugast Catherine, Berthet Pascaline, Polycarpe Florence, Layet Valérie, Hardouin Agnes, Frébourg Thierry, Vaur Dominiq |
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A pilot study evaluating genetic alterations that drive tobacco- and betel quid-associated oral cancer in Northeast India.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2014 Sep 35 (9): 9317-30. Yadav Dhirendra Singh, Chattopadhyay Indranil, Verma Anand, Devi Thoudam Regina, Singh L C, Sharma Jagannath Dev, Kataki Amal Ch, Saxena Sunita, Kapur Suja |
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Targeted cancer exome sequencing reveals recurrent mutations in myeloproliferative neoplasms.
Leukemia 2014 May 28 (5): 1052-9. Tenedini E, Bernardis I, Artusi V, Artuso L, Roncaglia E, Guglielmelli P, Pieri L, Bogani C, Biamonte F, Rotunno G, Mannarelli C, Bianchi E, Pancrazzi A, Fanelli T, Malagoli Tagliazucchi G, Ferrari S, Manfredini R, Vannucchi A M, Tagliafico E, |
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Genome-wide pathway analysis in neuroblastoma.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2014 Apr 35 (4): 3471-85. Lee Young Ho, Kim Jae-Hoon, Song Gwan G |
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Germline and somatic mutations in homologous recombination genes predict platinum response and survival in ovarian, fallopian tube, and peritoneal carcinomas.
Clinical cancer research : an official journal of the American Association for Cancer Research 2014 Feb 20 (3): 764-75. Pennington Kathryn P, Walsh Tom, Harrell Maria I, Lee Ming K, Pennil Christopher C, Rendi Mara H, Thornton Anne, Norquist Barbara M, Casadei Silvia, Nord Alexander S, Agnew Kathy J, Pritchard Colin C, Scroggins Sheena, Garcia Rochelle L, King Mary-Claire, Swisher Elizabeth |
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A cross-sectional study of associations between nonsynonymous mutations of the BARD1 gene and breast cancer in Han Chinese women.
Asia-Pacific journal of public health / Asia-Pacific Academic Consortium for Public Health 2013 Jul 25 (4 Suppl): 8S-14S. Liu Hui, Zhang Hengwei, Sun Xianfu, He Yaning, Li Juntao, Guo Xuh |
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Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility.
Carcinogenesis 2013 Mar 34 (3): 605-11. Capasso Mario, Diskin Sharon J, Totaro Francesca, Longo Luca, De Mariano Marilena, Russo Roberta, Cimmino Flora, Hakonarson Hakon, Tonini Gian Paolo, Devoto Marcella, Maris John M, Iolascon Achil |
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The BARD1 Cys557Ser variant and risk of familial breast cancer in a South-American population.
Molecular biology reports 2012 Aug 39 (8): 8091-8. Gonzalez-Hormazabal Patricio, Reyes Jose M, Blanco Rafael, Bravo Teresa, Carrera Ignacio, Peralta Octavio, Gomez Fernando, Waugh Enrique, Margarit Sonia, Ibañez Gladys, Santos Jose L, Jara Lili |
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[Association between single nucleotide polymorphisms of BARD 1 gene and susceptibility of early-onset breast cancer in Uygur women in Xinjiang].
Zhonghua zhong liu za zhi [Chinese journal of oncology] 2012 May 34 (5): 341-7. Sun Gang, Wang Jiang-tao, Ma Bin-lin, Geng Zhong-li, Ren Guang-hui, Shan Mei-hui, Ma Bin, Ma Li-li, Wang Y |
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Replication of neuroblastoma SNP association at the BARD1 locus in African-Americans.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2012 Apr 21 (4): 658-63. Latorre Valeria, Diskin Sharon J, Diamond Maura A, Zhang Haitao, Hakonarson Hakon, Maris John M, Devoto Marcel |
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Lack of association between BARD1 Cys557Ser variant and breast cancer risk: a meta-analysis of 11,870 cases and 7,687 controls.
Journal of cancer research and clinical oncology 2011 Oct 137 (10): 1463-8. Ding Da-Peng, Zhang Ying, Ma Wen-Li, He Xiao-Feng, Wang Wei, Yu Hai-Lang, Guo Yu-Bo, Zheng Wen-Li |
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Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2011 May 20 (5): 1032-8. Spurdle Amanda B, Marquart Louise, McGuffog Lesley, Healey Sue, Sinilnikova Olga, Wan Fei, Chen Xiaoqing, Beesley Jonathan, Singer Christian F, Dressler Anne-Catharine, Gschwantler-Kaulich Daphne, Blum Joanne L, Tung Nadine, Weitzel Jeff, Lynch Henry, Garber Judy, Easton Douglas F, Peock Susan, Cook Margaret, Oliver Clare T, Frost Debra, Conroy Don, Evans D Gareth, Lalloo Fiona, Eeles Ros, Izatt Louise, Davidson Rosemarie, Chu Carol, Eccles Diana, Selkirk Christina G, Daly Mary, Isaacs Claudine, Stoppa-Lyonnet Dominique, Sinilnikova Olga M, Buecher Bruno, Belotti Muriel, Mazoyer Sylvie, Barjhoux Laure, Verny-Pierre Carole, Lasset Christine, Dreyfus Hélène, Pujol Pascal, Collonge-Rame Marie-Agnès, , Rookus Matti A, Verhoef Senno, Kriege Mieke, Hoogerbrugge Nicoline, Ausems Margreet G E M, van Os Theo A, Wijnen Juul, Devilee Peter, Meijers-Heijboer Hanne E J, Blok Marinus J, Heikkinen Tuomas, Nevanlinna Heli, Jakubowska Anna, Lubinski Jan, Huzarski Tomasz, Byrski Tomasz, Durocher Francine, Couch Fergus J, Lindor Noralane M, Wang Xianshu, Thomassen Mads, Domchek Susan, Nathanson Kate, Caligo Ma, Jernström Helena, Liljegren Annelie, Ehrencrona Hans, Karlsson Per, , Ganz Patricia A, Olopade Olufunmilayo I, Tomlinson Gail, Neuhausen Susan, Antoniou Antonis C, Chenevix-Trench Georgia, Rebbeck Timothy |
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A Large-scale genetic association study of esophageal adenocarcinoma risk.
Carcinogenesis 2010 Jul 31 (7): 1259-63. Liu Chen-Yu, Wu Michael C, Chen Feng, Ter-Minassian Monica, Asomaning Kofi, Zhai Rihong, Wang Zhaoxi, Su Li, Heist Rebecca S, Kulke Matthew H, Lin Xihong, Liu Geoffrey, Christiani David |
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Genetic variation in genes interacting with BRCA1/2 and risk of breast cancer in the Cypriot population.
Breast cancer research and treatment 2010 May 121 (1): 147-56. Loizidou Maria A, Cariolou Marios A, Neuhausen Susan L, Newbold Robert F, Bashiardes Evy, Marcou Yiola, Michael Thalia, Daniel Maria, Kakouri Eleni, Papadopoulos Panayiotis, Malas Simon, Hadjisavvas Andreas, Kyriacou Kyriac |
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Cancer predisposing missense and protein truncating BARD1 mutations in non-BRCA1 or BRCA2 breast cancer families.
Human mutation 2010 Mar 31 (3): E1175-85. De Brakeleer Sylvia, De Grève Jacques, Loris Remy, Janin Nicolas, Lissens Willy, Sermijn Erica, Teugels Er |
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Genetic susceptibility to distinct bladder cancer subphenotypes.
European urology 2010 Feb 57 (2): 283-92. Guey Lin T, García-Closas Montserrat, Murta-Nascimento Cristiane, Lloreta Josep, Palencia Laia, Kogevinas Manolis, Rothman Nathaniel, Vellalta Gemma, Calle M Luz, Marenne Gaëlle, Tardón Adonina, Carrato Alfredo, García-Closas Reina, Serra Consol, Silverman Debra T, Chanock Stephen, Real Francisco X, Malats Núria, |
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A gene-based risk score for lung cancer susceptibility in smokers and ex-smokers.
Postgraduate medical journal 2009 Oct 85 (1008): 515-24. Young R P, Hopkins R J, Hay B A, Epton M J, Mills G D, Black P N, Gardner H D, Sullivan R, Gamble G |
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Polymorphisms in HPV E6/E7 protein interacted genes and risk of cervical cancer in Chinese women: a case-control analysis.
Gynecologic oncology 2009 Aug 114 (2): 327-31. Zhou Xiaoyi, Han Suping, Wang Sumin, Chen Xiaojun, Dong Jing, Shi Xiaoyan, Xia Yankai, Wang Xinru, Hu Zhibin, Shen Hongbi |
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Explorative study to identify novel candidate genes related to oxaliplatin efficacy and toxicity using a DNA repair array.
British journal of cancer 2009 Jul 101 (2): 357-62. Kweekel D M, Antonini N F, Nortier J W R, Punt C J A, Gelderblom H, Guchelaar H |
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Modification of ovarian cancer risk by BRCA1/2-interacting genes in a multicenter cohort of BRCA1/2 mutation carriers.
Cancer research 2009 Jul 69 (14): 14. Rebbeck TR, Mitra N, Domchek SM, Wan F, Chuai S, Friebel TM, Panossian S, Spurdle A, Chenevix-Trench G, Singer CF, Pfeiler G, Neuhausen SL, Lynch HT, Garber JE, Weitzel JN, Isaacs C, Couch F, Narod SA, Rubinstein WS, Tomlinson GE, Ganz PA, Olopade OI, Tung N, Blum JL, Greenberg R, Nathanson KL, Daly MB |
Common variations in BARD1 influence susceptibility to high-risk neuroblastoma.
Nature genetics 2009 Jun 41 (6): 718-23. Capasso Mario, Devoto Marcella, Hou Cuiping, Asgharzadeh Shahab, Glessner Joseph T, Attiyeh Edward F, Mosse Yael P, Kim Cecilia, Diskin Sharon J, Cole Kristina A, Bosse Kristopher, Diamond Maura, Laudenslager Marci, Winter Cynthia, Bradfield Jonathan P, Scott Richard H, Jagannathan Jayanti, Garris Maria, McConville Carmel, London Wendy B, Seeger Robert C, Grant Struan F A, Li Hongzhe, Rahman Nazneen, Rappaport Eric, Hakonarson Hakon, Maris John |
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Polymorphisms in innate immunity genes and lung cancer risk in Xuanwei, China.
Environmental and molecular mutagenesis 2009 May 50 (4): 285-90. Shen Min, Vermeulen Roel, Rajaraman Preetha, Menashe Idan, He Xingzhou, Chapman Robert S, Yeager Meredith, Thomas Gilles, Burdett Laurie, Hutchinson Amy, Yuenger Jeff, Chanock Stephen, Lan Qi |
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The BARD1 Cys557Ser polymorphism and breast cancer risk: an Australian case-control and family analysis.
Breast cancer research and treatment 2009 May 115 (1): 145-50. Johnatty Sharon E, Beesley Jonathan, Chen Xiaoqing, Hopper John L, Southey Melissa C, Giles Graham G, Goldgar David E, Chenevix-Trench Georgia, Spurdle Amanda B, , |
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Genetic sequence variations of BRCA1-interacting genes AURKA, BAP1, BARD1 and DHX9 in French Canadian families with high risk of breast cancer.
Journal of human genetics 2009 Mar 54 (3): 152-61. Guénard Frédéric, Labrie Yvan, Ouellette Geneviève, Beauparlant Charles Joly, Durocher Francine, |
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Common genetic variation in candidate genes and susceptibility to subtypes of breast cancer.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2009 Jan 18 (1): 255-9. Mavaddat Nasim, Dunning Alison M, Ponder Bruce A J, Easton Douglas F, Pharoah Paul |
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Evaluating new candidate SNPs as low penetrance risk factors in sporadic breast cancer: a two-stage Spanish case-control study.
Gynecologic oncology 2009 Jan 112 (1): 210-4. Vega Ana, Salas Antonio, Milne Roger L, Carracedo Begoña, Ribas Gloria, Ruibal Alvaro, de León Antonio Cabrera, González-Hernández Ana, Benítez Javier, Carracedo Ang |
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Common single-nucleotide polymorphisms in DNA double-strand break repair genes and breast cancer risk.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2008 Dec 17 (12): 3482-9. Pooley Karen A, Baynes Caroline, Driver Kristy E, Tyrer Jonathan, Azzato Elizabeth M, Pharoah Paul D P, Easton Douglas F, Ponder Bruce A J, Dunning Alison |
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Polymorphism in the IL18 gene and epithelial ovarian cancer in non-Hispanic white women.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2008 Dec 17 (12): 3567-72. Palmieri Rachel T, Wilson Melanie A, Iversen Edwin S, Clyde Merlise A, Calingaert Brian, Moorman Patricia G, Poole Charles, Anderson A Rebecca, Anderson Stephanie, Anton-Culver Hoda, Beesley Jonathan, Hogdall Estrid, Brewster Wendy, Carney Michael E, Chen Xiaoqing, Chenevix-Trench Georgia, Chang-Claude Jenny, Cunningham Julie M, Dicioccio Richard A, Doherty Jennifer A, Easton Douglas F, Edlund Christopher K, Gayther Simon A, Gentry-Maharaj Aleksandra, Goode Ellen L, Goodman Marc T, Kjaer Susanne Kruger, Hogdall Claus K, Hopkins Michael P, Jenison Eric L, Blaakaer Jan, Lurie Galina, McGuire Valerie, Menon Usha, Moysich Kirsten B, Ness Roberta B, Pearce Celeste Leigh, Pharoah Paul D P, Pike Malcolm C, Ramus Susan J, Rossing Mary Anne, Song Honglin, Terada Keith Y, Vandenberg David, Vierkant Robert A, Wang-Gohrke Shan, Webb Penelope M, Whittemore Alice S, Wu Anna H, Ziogas Argyrios, Berchuck Andrew, Schildkraut Joellen M, , , |
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BARD1 variants are not associated with breast cancer risk in Australian familial breast cancer.
Breast cancer research and treatment 2008 Oct 111 (3): 505-9. Gorringe Kylie L, Choong David Y H, Visvader Jane E, Lindeman Geoffrey J, Campbell Ian |
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Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.
Carcinogenesis 2008 Oct 29 (10): 1938-43. Hosgood H Dean, Menashe Idan, Shen Min, Yeager Meredith, Yuenger Jeff, Rajaraman Preetha, He Xingzhou, Chatterjee Nilanjan, Caporaso Neil E, Zhu Yong, Chanock Stephen J, Zheng Tongzhang, Lan Qi |
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BARD1 and breast cancer in Poland.
Breast cancer research and treatment 2008 Jan 107 (1): 119-22. Jakubowska Anna, Cybulski Cezary, Szyma?ska Anna, Huzarski Tomasz, Byrski Tomasz, Gronwald Jacek, Debniak Tadeusz, Górski Bohdan, Kowalska Elzbieta, Narod Steven A, Lubi?ski J |
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Common non-synonymous polymorphisms in the BRCA1 Associated RING Domain (BARD1) gene are associated with breast cancer susceptibility: a case-control analysis.
Breast cancer research and treatment 2007 May 102 (3): 329-37. Huo Xiang, Hu Zhibin, Zhai Xiangjun, Wang Yan, Wang Shui, Wang Xuechen, Qin Jianwei, Chen Wenseng, Jin Guangfu, Liu Jiyong, Gao Jun, Wei Qingyi, Wang Xinru, Shen Hongbi |
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Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies.
Journal of medical genetics 2006 Nov 43 (11): 856-62. Karppinen S-M, Barkardottir R B, Backenhorn K, Sydenham T, Syrjäkoski K, Schleutker J, Ikonen T, Pylkäs K, Rapakko K, Erkko H, Johannesdottir G, Gerdes A-M, Thomassen M, Agnarsson B A, Grip M, Kallioniemi A, Kere J, Aaltonen L A, Arason A, Møller P, Kruse T A, Borg A, Winqvist |
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The BARD1 Cys557Ser variant and breast cancer risk in Iceland.
PLoS medicine 2006 Jul 3 (7): e217. Stacey Simon N, Sulem Patrick, Johannsson Oskar T, Helgason Agnar, Gudmundsson Julius, Kostic Jelena P, Kristjansson Kristleifur, Jonsdottir Thora, Sigurdsson Helgi, Hrafnkelsson Jon, Johannsson Jakob, Sveinsson Thorarinn, Myrdal Gardar, Grimsson Hlynur Niels, Bergthorsson Jon T, Amundadottir Laufey T, Gulcher Jeffrey R, Thorsteinsdottir Unnur, Kong Augustine, Stefansson Ka |
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BARD1 variants Cys557Ser and Val507Met in breast cancer predisposition.
European journal of human genetics : EJHG 2006 Feb 14 (2): 167-72. Vahteristo Pia, Syrjäkoski Kirsi, Heikkinen Tuomas, Eerola Hannaleena, Aittomäki Kristiina, von Smitten Karl, Holli Kaija, Blomqvist Carl, Kallioniemi Olli-Pekka, Nevanlinna He |
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SNP-SNP interactions in breast cancer susceptibility.
BMC cancer 2006 6 (): 114. Onay Venüs Ummiye, Briollais Laurent, Knight Julia A, Shi Ellen, Wang Yuanyuan, Wells Sean, Li Hong, Rajendram Isaac, Andrulis Irene L, Ozcelik Hil |
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Mutational analysis of BARD1 in familial breast cancer patients in Japan.
Cancer letters 2003 Oct 200 (1): 1-7. Ishitobi Makoto, Miyoshi Yasuo, Hasegawa Seiichi, Egawa Chiyomi, Tamaki Yasuhiro, Monden Morito, Noguchi Shinzabu |
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