The emerging landscape of breast cancer susceptibility

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Items 201–300 of 487

1. Deep exploration of PARP inhibitors in breast cancer: monotherapy and combination therapy
   Zheling Chen, Xiao Wang, Xiao Li, Yucheng Zhou, Ke Chen · 2021 · Journal of International Medical Research
2. Exome sequencing identifies a recurrent variant in SERPINA3 associating with hereditary susceptibility to breast cancer
   Susanna Koivuluoma, Anna Tervasmäki, Saila Kauppila, Robert Winqvist, Timo A. Kumpula, Outi Kuismin, Jukka S. Moilanen, Katri Pylkäs · 2020 · European Journal of Cancer
3. Germline and somatic KLLN alterations in breast cancer dysregulate G2 arrest
   Emily A. Nizialek, Charissa Peterson, Jessica L. Mester, Erinn Downes-Kelly, Charis Eng · 2013 · Human Molecular Genetics
4. Targeting the CINful genome: Strategies to overcome tumor heterogeneity
   Chelsea E. Cunningham, Mackenzie J. MacAuley, Garima Yadav, Frederick S. Vizeacoumar, Andrew Freywald, Franco J. Vizeacoumar · 2019 · Progress in Biophysics and Molecular Biology
5. Design Considerations for Massively Parallel Sequencing Studies of Complex Human Disease
   Bing Feng, Sean V. Tavtigian, Melissa C. Southey, David E. Goldgar · 2011 · PLoS ONE
6. Evaluation of a 27-gene inherited cancer panel across 630 consecutive patients referred for testing in a clinical diagnostic laboratory
   Sabrina A. Gardner, Katelyn S. Weymouth, Wei S. Kelly, Ekaterina A. Bogdanova, Wenjie Chen, Daniel S. Lupu, Joshua A. Suhl, Qiandong Zeng, Ute Geigenmüller, Debbie Boles et al. · 2018 · Hereditary Cancer in Clinical Practice
7. Expression and prognostic significance of Fanconi anemia group D2 protein and breast cancer type 1 susceptibility protein in familial and sporadic breast cancer
   Feng Liang, Feng Jin · 2019 · Oncology Letters
8. The rs9340799 polymorphism of the estrogen receptor alpha (ESR1) gene and its association with breast cancer susceptibility
   Shing Cheng Tan, Teck Yew Low, Ezanee Azlina Mohamad Hanif, Mohamad Ayub Khan Sharzehan, Hamed Kord‐Varkaneh, Md Asiful Islam · 2021 · Scientific Reports
9. Family-specific, novel, deleterious germline variants provide a rich resource to identify genetic predispositions for BRCAx familial breast cancer
   Hongxiu Wen, Yeong C. Kim, Carrie Snyder, Fengxia Xiao, Elizabeth A. Fleissner, Dina Becirovic, Jiangtao Luo, Bradley M. Downs, Simon Sherman, Kenneth H. Cowan et al. · 2014 · BMC Cancer
10. An Integrative Genomics Approach for Associating GWAS Information with Triple-Negative Breast Cancer
    Chindo Hicks, Ranjit Kumar, Antonio Pannuti, Kandis V. Backus, Alexandra Shaye Brown, Jesus Monico, Lucio Miele · 2013 · Cancer Informatics
11. Personalized Prognosis and Diagnosis of Type 2 Diabetes – Vision or Fiction?
    Günter A. Müller · 2010 · Pharmacology
12. Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families
    Aðalgeir Arason, Haukur Gunnarsson, Guðrún Jóhannesdóttir, Kristján Jónasson, Pär‐Ola Bendahl, Elizabeth M. Gillanders, Bjarni Agnar Agnarsson, Goran G. Jonsson, Katri Pylkäs, Aki Mustonen et al. · 2010 · Breast Cancer Research
13. CZECANCA: CZEch CAncer paNel for Clinical Application – Design and Optimization of the Targeted Sequencing Panel for the Identification of Cancer Susceptibility in High-risk Individuals from the Czech Republic
    Jana Soukupová, Petra Zemánková, Petra Kleiblová, Markéta Janatová, Zdeněk Kleibl · 2016 · Klinicka onkologie
14. Half of germline pathogenic and likely pathogenic variants found on panel tests do not fulfil NHS testing criteria
    Tala Andoni, Jennifer M. Wiggins, Rachel Robinson, Ruth S. Charlton, Michael Sandberg, Rosalind A. Eeles · 2022 · Scientific Reports
15. Mutational analysis of telomere genes in BRCA1/2-negative breast cancer families with very short telomeres
    Kira Yanowsky, Alicia Barroso, Ana Osório, Miguel Urioste, Javier J. Benitez, Beatriz Martínez–Delgado · 2012 · Breast Cancer Research and Treatment
16. Utility of Matrix Metalloproteinases in the Diagnosis, Monitoring and Prognosis of Ovarian Cancer Patients
    Aleksandra Kicman, Marek Niczyporuk, Monika Kulesza, Joanna Motyka, Sławomir Ławicki · 2022 · Cancer Management and Research
17. Mutation Analysis of the RAD51C and RAD51D Genes in High-Risk Ovarian Cancer Patients and Families from the Czech Republic
    Markéta Janatová, Jana Soukupová, Jana Stribrna, Petra Kleiblová, Michal Vočka, Petra Boudova, Zdeněk Kleibl, Petr Pohlreich · 2015 · PLoS ONE
18. Identification of sequence polymorphisms in the mitochondrial displacement loop as risk factors for sporadic and familial breast cancer
    Meng Cheng, Zhanjun Guo, Haiping Li, Zheng Li, Chunxiao Li, Cuizhi Geng · 2014 · Tumor Biology
19. Evidence against PALB2 involvement in Icelandic breast cancer susceptibility
    Haukur Gunnarsson, Aðalgeir Arason, Elizabeth M. Gillanders, Bjarni Agnar Agnarsson, Guðrún Jóhannesdóttir, Oskar T. Johannsson, Rosa Bjork Barkardottir · 2008 · Journal of Negative Results in BioMedicine
20. Rare missense mutations in RECQL and POLG associate with inherited predisposition to breast cancer
    Anna Tervasmäki, Tuomo Mantere, Jaana M. Hartikainen, Saila Kauppila, Hang‐Mao Lee, Susanna Koivuluoma, Mervi Grip, Peeter Karihtala, Arja Jukkola‐Vuorinen, Arto Mannermaa et al. · 2018 · International Journal of Cancer
21. Familial Breast Cancer: Disease Related Gene Mutations and Screening Strategies for Chinese Population
    Lu Hua Shen, Shizhen Zhang, Kaiyue Wang, Xiaochen Wang · 2021 · Frontiers in Oncology
22. The Fanconi anemia pathway: Insights from somatic cell genetics using DT40 cell line
    Minoru Takata, Masamichi Ishiai, Hiroyuki Kitao · 2009 · Mutation research. Fundamental and molecular mechanisms of mutagenesis
23. Associations between breast density and a panel of single nucleotide polymorphisms linked to breast cancer risk: a cohort study with digital mammography
    Brad M. Keller, Anne Marie McCarthy, Jinbo Chen, Katrina Armstrong, Emily F. Conant, Susan M. Domchek, Despina Kontos B · 2015 · BMC Cancer
24. Analysis of DNA Repair–Related Genes in Breast Cancer Reveals CUL4A Ubiquitin Ligase as a Novel Biomarker of Trabectedin Response
    María J. García, Laura Paula Saucedo-Cuevas, Iván Muñoz‐Repeto, Victoria Fernández, María J. Robles, Samuel Domingo, José Palacios, Miguel Aracil, Antonio Nieto, Juan Carlos Tercero et al. · 2013 · Molecular Cancer Therapeutics
25. Characterization of three alternative transcripts of the BRCA1 gene in patients with breast cancer and a family history of breast and/or ovarian cancer who tested negative for pathogenic mutations
    G. Gambino, M. Tancredi, Elisabetta Falaschi, P. Aretini, M. Caligo · 2015 · International Journal of Molecular Medicine
26. Unique Features of Germline Variation in Five Egyptian Familial Breast Cancer Families Revealed by Exome Sequencing
    Yeong C. Kim, Amr S. Soliman, Jian Cui, Mohamed Ramadan, Ahmed Hablas, Mohamed Ibrahim Abouelhoda, Nehal Hussien, Ola Sayed Ahmed, Abdel‐Rahman N. Zekri, Ibrahim A. Seifeldin et al. · 2017 · PLoS ONE
27. Elucidating the Underlying Functional Mechanisms of Breast Cancer Susceptibility Through Post-GWAS Analyses
    Mahdi Rivandi, John W.M. Martens, Antoinette Hollestelle · 2018 · Frontiers in Genetics
28. Joint Analysis of Multiple Traits in Rare Variant Association Studies
    Zhenchuan Wang, Xuexia Wang, Qiuying Sha, Shuanglin Zhang · 2016 · Annals of Human Genetics
29. The highly prevalent BRCA2 mutation c.2808_2811del (3036delACAA) is located in a mutational hotspot and has multiple origins
    Mar Infante, M. Duran, Alberto Acedo, Eva María Sánchez-Tapia, Beatriz Díez‐Gómez, A. Barroso, M. Garcia-Gonzalez, Lídia Feliubadaló, Adriana Lasa, Miguel de la Hoya et al. · 2013 · Carcinogenesis
30. Tumour spectrum in non-BRCA hereditary breast cancer families in Sweden
    Wendt, Camilla, Lindblom, Annika, Arver, Brita, von Wachenfeldt, Anna, Margolin, Sara · 2015 · Hereditary Cancer in Clinical Practice
31. Breast Cancer
    France Labrèche, Mark S. Goldberg, Dana Hashim, Elisabete Weiderpass · 2020 · Springer eBooks
32. A Knowledge Base for Teaching Biology Situated in the Context of Genetic Testing
    Paul van der Zande, Arend Jan Waarlo, Mieke Brekelmans, Sanne Floor Akkerman, Jan D. H. M. Vermunt · 2010 · International Journal of Science Education
33. Breast cancer genetic susceptibility: With focus in Saudi Arabia
    Fawaz Dabea Alshammari · 2019 · Journal of Oncological Sciences
34. Germline mutations of multiple breast cancer-related genes are differentially associated with triple-negative breast cancers and prognostic factors
    Chihiro Hata, Hirofumi Nakaoka, Yu Xiang, Dong Wang, Anping Yang, Dahai Liu, Fang Liu, Qingfeng Zou, Wei Li, Ke Zheng et al. · 2020 · Journal of Human Genetics
35. Predictive polymorphisms for breast cancer in postmenopausal Mexican women
    Mónica Sierra-Martínez, Leticia Hernandez Cadena, José Rubén García-Sánchez, Gustavo Acosta‐Altamirano, Carmen Palacios‐Reyes, Patricia García Alonso-Themann, Liliana García‐Ortiz, Laura Itzel Quintas Granados, Octavio Daniel Reyes‐Hernández · 2016 · Journal of Cancer Research and Therapeutics
36. Germline copy number variations associated with breast cancer susceptibility in a Japanese population
    Yutaka Suehiro, Takae Okada, Naoya Shikamoto, Yibo Zhan, Kohei Sakai, Naoko Okayama, M. Nishioka, Tomoko Furuya, Atsunori Oga, Shigeto Kawauchi et al. · 2012 · Tumor Biology
37. Low‐frequency nonsynonymous variants in FKBPL and ARPC1B genes are associated with breast cancer risk in Chinese women
    Wen Zhou, Yue Jiang, Meng Zhu, Dong Hang, Jiaping Chen, Jing Zhou, Juncheng Dai, Hongxia Ma, Zhibin Hu, Guangfu Jin et al. · 2016 · Molecular Carcinogenesis
38. Breast cancer family history and allele-specific DNA methylation in the legacy girls study
    Hui-Chen Wu, Catherine Do, Irene Louise Andrulis, Esther M. John, Mary Beryl Daly, Saundra S. Buys, Wendy K. Chung, Julia A. Knight, Angela R. Bradbury, Theresa H.M. Keegan et al. · 2018 · Epigenetics
39. Integrative analysis of common genes and driver mutations implicated in hormone stimulation for four cancers in women
    Salma Begum Bhyan, YongKiat Wee, Yining Liu, Scott F. Cummins, Min Zhao · 2019 · PeerJ
40. In vitro model for DNA double‐strand break repair analysis in breast cancer reveals cell type–specific associations with age and prognosis
    Miriam Deniz, Julia Kaufmann, Andreea Stahl, Theresa Gundelach, Wolfgang Janni, Isabell Hoffmann, Marlen Keimling, Stephanie Hampp, Michaela Ihle, Lisa Wiesmüller · 2016 · The FASEB Journal
41. New cancer susceptibility loci: Population and familial risks
    Kari Hemminki, Asta Försti, Justo Lorenzo Bermejo · 2008 · International Journal of Cancer
42. Biological Basis of Breast Cancer-Related Disparities in Precision Oncology Era
    Anca-Narcisa Neagu, Pathea Shawnae Bruno, Kaya R. Johnson, Gabriella Ballestas, Costel C. Darie · 2024 · International Journal of Molecular Sciences
43. Murine Double Minute Clone 2 309T/G and 285G/C Promoter Single Nucleotide Polymorphism as a Risk Factor for Breast Cancer: A Polish Experience
    Piotr Piotrowski, Margarita Lianeri, Błażej Rubiś, Hanna Knuła, Maria Rybczyńska, Sylwia Grodecka-Gazdecka, Paweł Piotr Jagodziński · 2012 · The International Journal of Biological Markers
44. Rad51 paralogs and the risk of unselected breast cancer: A case-control study
    Peter Grešner, Ewa Jabłońska, Jolanta Gromadzińska · 2020 · PLoS ONE
45. Chasing the origin of 23 recurrent BRCA1 mutations in Pakistani breast and ovarian cancer patients
    Muhammad Usman Rashid, Noor Muhammad, Humaira Naeemi, Umara Shehzad, Ute Hamann · 2022 · International Journal of Cancer
46. Mutation screening of the MERIT40 gene encoding a novel BRCA1 and RAP80 interacting protein in breast cancer families
    Szilvia Sólyom, Jeffrey Patterson-Fortin, Katri Pylkäs, Roger A. Greenberg, Robert Winqvist · 2009 · Breast Cancer Research and Treatment
47. Adaptive clustering and adaptive weighting methods to detect disease associated rare variants
    Qiuying Sha, Shuaicheng Wang, Shuanglin Zhang · 2012 · European Journal of Human Genetics
48. Gene-expression patterns in peripheral blood classify familial breast cancer susceptibility
    Stephen Piccolo, Irene Louise Andrulis, Adam Louis Cohen, Thomas A. Conner, Philip J. Moos, Avrum E. Spira, Saundra S. Buys, William Evan Johnson, Andrea H. Bild · 2015 · BMC Medical Genomics
49. PHIP- a novel candidate breast cancer susceptibility locus on 6q14.1
    Xiang Jiao, NBCS Collaborators, kConFab/AOCS Investigators, Christos Aravidis, Rajeshwari Marikkannu, Johanna Rantala, Simone Picelli, Tatjana Adamović, Tao Liu, Paula T. Maguire et al. · 2017 · Oncotarget
50. Discovery of rare coding variants in OGDHL and BRCA2 in relation to breast cancer risk in Chinese women
    Xingyi Guo, Jirong Long, Zhishan Chen, Xiao‐Ou Shu, Yong‐Bing Xiang, Wanqing Wen, Chenjie Zeng, Yu‐Tang Gao, Qiuyin Cai, Wei Zheng · 2019 · International Journal of Cancer
51. IGFBP1 and IGFBP3 polymorphisms predict circulating IGFBP-3 levels among women from high-risk breast cancer families
    Ann H. Rosendahl, Maria Hietala, Maria Henningson, Hakan Lars Olsson, Helena Jernström · 2010 · Breast Cancer Research and Treatment
52. Low penetrance alleles as risk modifiers in familial and sporadic breast cancer
    Eva Esteban Cardeñosa, Inmaculada de Juan Jiménez, Sarai Palanca Suela, Isabel Chirivella, Ángel Segura Huerta, Ana Santaballa Beltrán, María Casals El Busto, Eva Barragán-González, Óscar Fuster, José D. Bermúdez et al. · 2012 · Familial Cancer
53. New, fast and cheap prediction tests for BRCA1 gene mutations identification in clinical samples
    Aleksandra Gajda, Agnieszka Potęga, Agata Kowalczyk, Sławomir Sęk, Sebastian Zięba, Artur Kowalik, Andrzej Kudelski, Anna Maria Nowicka · 2023 · Scientific Reports
54. Integrative analyses reveal signaling pathways underlying familial breast cancer susceptibility
    Stephen Piccolo, Laura M. Hoffman, Thomas A. Conner, Gajendra Shrestha, Adam Louis Cohen, Jeffrey R. Marks, Leigh A. Neumayer, Cori Agarwal, Mary C. Beckerle, Irene Louise Andrulis et al. · 2016 · Molecular Systems Biology
55. The Rare Variant rs35356162 in UHRF1BP1 Increases Bladder Cancer Risk in Han Chinese Population
    Junlong Wu, Meilin Wang, Haitao Chen, Jianfeng Xu, Guiming Zhang, Chengyuan Gu, Qiang Ding, Qingyi Wei, Yao Zhu, Dingwei Ye · 2020 · Frontiers in Oncology
56. Mutation analysis of the AATF gene in breast cancer families
    Maria K. Haanpää, Mervi Reiman, Jenni Nikkilä, Hannele Erkko, Katri Pylkäs, Robert Winqvist · 2009 · BMC Cancer
57. Identification of low-frequency variants of UGT1A3 associated with bladder cancer risk by next-generation sequencing
    Rui Zheng, Mulong Du, Yuqiu Ge, Fang Gao, Junyi Xin, Qiang Lv, Chao Qin, Yao Zhu, Chengyuan Gu, Mengyun Wang et al. · 2021 · Oncogene
58. Kernel-Machine Testing Coupled with a Rank-Truncation Method for Genetic Pathway Analysis
    Qi Yan, Hemant K. Tiwari, Nengjun Yi, Wan‐Yu Lin, Guimin Gao, Xiang‐Yang Lou, Xiangqin Cui, Nianjun Liu · 2014 · Genetic Epidemiology
59. FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets
    Bernard J. Pope, Tú Nguyen‐Dumont, Fabrice Odefrey, Fleur Hammet, Russell N. Bell, Kayoko Tao, Sean V. Tavtigian, David E. Goldgar, Andrew J. Lonie, Melissa C. Southey et al. · 2013 · BMC Bioinformatics
60. Contrasting epistatic interactions between rat quantitative trait loci controlling mammary cancer development
    Géraldine Piessevaux, Virginie Lella, Michèle Rivière, Daniel Stieber, Pierre Luc Dreze, Josiane Szpirer, Claude Szpirer · 2008 · Mammalian Genome
61. Connecting the Dots: Interplay between Ubiquitylation and SUMOylation at DNA Double-Strand Breaks
    Jiang-bo Tang, R. A. Greenberg · 2010 · Genes & Cancer
62. Breast cancer risk associated with genes encoding DNA repair MRN complex: a study from Punjab, Pakistan
    Rabbia Tariq Khan, Ayesha Siddique, Naeem Shahid, Samina Khokher, Warda Fatima · 2018 · Breast Cancer
63. Association between 15 known or potential breast cancer susceptibility genes and breast cancer risks in Chinese women
    Fenfen Fu, Dongjie Zhang, Li Hu, Senthil K. Sundaram, Dingge Ying, Ying Zhang, Shuna Fu, Juan Zhang, Lu Yao, Ye Xu et al. · 2021 · Cancer Biology and Medicine
64. p.Ala541Thr variant of MEN1 gene: A non deleterious polymorphism or a pathogenic mutation?
    Cécile Nozières, Chang Xian Zhang, Alexandre Buffet, S. Dupasquier, Rosa Vargas‐Poussou, Marine Guillaud-Bataille, Martine Cordier–Bussat, Philippe B Ruszniewski, Sophie Christin‐Maître, Arnaud Murat et al. · 2014 · Annales d Endocrinologie
65. Differences of Variable Number Tandem Repeats in XRCC5 Promoter Are Associated with Increased or Decreased Risk of Breast Cancer in BRCA Gene Mutation Carriers
    Jian Cui, Jiangtao Luo, Yeong C. Kim, Carrie Snyder, Dina Becirovic, Bradley M. Downs, Henry T. Lynch, San Ming Wang · 2016 · Frontiers in Oncology
66. Application of composite resin for single-appointment anterior and posterior diastema closure.
    Alton M. Lacy · 1998 · PubMed
67. Testing an optimally weighted combination of common and/or rare variants with multiple traits
    Zhenchuan Wang, Qiuying Sha, Shurong Fang, Kui Zhang, Shuanglin Zhang · 2018 · PLoS ONE
68. Integrating PARP inhibitors into the management of breast cancer: where are we?
    Hamdy A. Azim, Loay Mohamed Hassan Kassem, Hatem A. Azim · 2021 · Chinese Clinical Oncology
69. Impact of Neoantigen Expression and T-Cell Activation on Breast Cancer Survival
    Wenjing Li, Amei Amei, Francis Bui, Saba Norouzifar, Lingeng Lu, Zuoheng Wang · 2021 · Cancers
70. Epidemiology and Risk Factors of Breast Cancer
    Tabassum Zafar, Ab Qayoom Naik, Manoj Kumar, Vinoy K. Shrivastava · 2022 · Springer eBooks
71. Update on genetic predisposition to breast cancer
    Munaza Ahmed, Fiona I. Lalloo, D. Gareth Evans · 2009 · Expert Review of Anticancer Therapy
72. The Influence of Common Polymorphisms on Breast Cancer
    Diana Eccles, William Tapper · 2010 · Cancer treatment and research
73. Transcriptomic analysis revealed potential regulatory biomarkers and repurposable drugs for breast cancer treatment
    Most Shornale Akter, Md. Helal Uddin, Sheikh Atikur Rahman, Md. Arju Hossain, Md. Ashiqur Rahman Ashik, Nurun Nesa Zaman, Omar Faruk, Md. Sanwar Hossain, Anzana Parvin, Md Habibur Rahman · 2024 · Cancer Reports
74. Screening of Finnish RAD51Cfounder mutations in prostate and colorectal cancer patients
    Liisa M. Pelttari, Riikka Nurminen, Alexandra E. Gylfe, Lauri A. Aaltonen, Johanna Schleutker, Heli A. Nevanlinna · 2012 · BMC Cancer
75. Biomarkers associated with different types of cancer as a potential candidate for early diagnosis of oncological disorders
    Arpana Parihar, Surbhi Jain, Dipesh Singh Parihar, Pushpesh Ranjan, Raju Khan · 2021 · Elsevier eBooks
76. Disease-driven detection of differential inherited SNP modules from SNP network
    Chuanxing Li, Yongsheng Li, Juan Xu, Junying Lv, Ye Ma, Tingting Shao, Binsheng Gong, Renjie Tan, Yun Xiao, Xia Li · 2011 · Gene
77. Evaluation of the germline single nucleotide polymorphism rs583522 in the TNFAIP3 gene as a prognostic marker in esophageal cancer
    Tarik Ghadban, Magdalena Schmidt-Yang, Faik Güntac Uzunoglu, Daniel R. Perez, Alexander T. El Gammal, Jameel Miro, Ulrich Friedrich Wellner, Klaus Pantel, Jakob Robert Izbicki, Yogesh Kumar Vashist · 2015 · Cancer Genetics
78. Critical Analysis of Genome-Wide Association Studies: Triple Negative Breast Cancer Quae Exempli Causa
    Maria-Ancuţa Jurj, Mihail Buse, Alina‐Andreea Zimța, Angelo Paradiso, Schuyler Safi Korban, Laura Pop, Ioana Berindan‐Neagoe · 2020 · International Journal of Molecular Sciences
79. Breast Radiation Therapy–Related Treatment Outcomes in Patients With or Without Germline Mutations on Multigene Panel Testing
    Bhavana V. Chapman, Diane Liu, Yu Shen, Oluwafikayo O. Olamigoke, David S. Lakomy, Angelica M. Gutierrez‐Barrera, Shane Richard Stecklein, Gabriel Oliveira Sawakuchi, Scott J. Bright, Isabelle Bedrosian et al. · 2021 · International Journal of Radiation Oncology*Biology*Physics
80. An unusual BRCA2 allele carrying two splice site mutations
    Mario P. Colombo, Carla Barbara Ripamonti, Valeria Pensotti, Claudia Foglia, Bernard Peissel, Marco Alessandro Pierotti, Siranoush Manoukian, Paolo Radice · 2009 · Annals of Oncology
81. Replication of genome-wide discovered breast cancer risk loci in the Cypriot population
    Maria A. Loizidou, Andreas Hadjisavvas, John P. A. Ioannidis, Kyriacos C. Kyriacou · 2011 · Breast Cancer Research and Treatment
82. Association detection between ordinal trait and rare variants based on adaptive combination of P values
    Meida Wang, Weijun Ma, Ying Zhou · 2017 · Journal of Human Genetics
83. Genetic dissection of the BRCA2 promoter and transcriptional impact of DNA variants
    Eugenia Fraile‐Bethencourt, Alberto Valenzuela‐Palomo, Beatriz Díez‐Gómez, Mar Infante, Mercedes Durán, Germán Marcos, Enrique Lastra, Susana Gómez‐Barrero, Eladio A. Velasco · 2018 · Breast Cancer Research and Treatment
84. Single nucleotide polymorphisms in the mitochondrial displacement loop and age-at-onset of familial breast cancer
    Haiping Lee, Cuizhi Geng, Meng Cheng, Zheng Lee, Zhanjun Guo · 2016 · Mitochondrial DNA Part A
85. A Rare Variant Association Test Based on Combinations of Single-Variant Tests
    Qiuying Sha, Shuanglin Zhang · 2014 · Genetic Epidemiology
86. Biomarkers in Breast Cancer
    Serena Bertozzi, Ambrogio Pietro Londero, Luca Seriau, Roberta Di Vora, Carla Cedolini, Laura Mariuzzi · 2018 · InTech eBooks
87. The Landscape of BRCA Mutations among Egyptian Women with Breast Cancer
    Hamdy A. Azim, Samah Aly Loutfy, Hatem A. Azim, Nermin S. Kamal, Nasra F. Abdel Fattah, Mostafa Hamed Elberry, Mohamed R. Abdelaziz, Marwa Abdelsalam, Madonna A. Fekry, Kyrillus Samaan Shohdy et al. · 2023 · Oncology and Therapy
88. Mutation analysis of RAD51L1 (RAD51B/REC2) in multiple-case, non-BRCA1/2 breast cancer families
    kConFab, Julie Johnson, Sue C. Healey, Kum Kum Khanna, Georgia Chenevix‐Trench · 2011 · Breast Cancer Research and Treatment
89. Next-generation sequencing of BRCA1 and BRCA2 in breast cancer patients and control subjects
    Lubomir Balabanski, G Antov, Ivanka Istalianova Dimova, Samuil Lyubomirov Ivanov, M Nacheva, I. Gavrilov, Desislava Valentinova Nesheva, Blaga Borisova Rukova, Savina Petrova Hadjidekova, Maxim Malinov et al. · 2014 · Molecular and Clinical Oncology
90. Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies?
    JooYong Park, Ji‐Yeob Choi, Jaesung Choi, Seokang Chung, Nan Song, Sue K. Park, Wonshik Han, Dong‐Young Noh, Sei-Hyun Ahn, Jong Won Lee et al. · 2021 · Cancers
91. Genetic Counseling and the Advanced Practice Oncology Nursing Role in a Hereditary Cancer Prevention Clinic: Hereditary Breast Cancer Focus (Part I)
    Carrie Snyder, Jane F. Lynch, Henry T. Lynch · 2009 · The Breast Journal
92. Genome instability in blood cells of a BRCA1 + breast cancer family
    Fengxia Xiao, Yeong C. Kim, Carrie Snyder, Hongxiu Wen, Pei Xian Chen, Jiangtao Luo, Dina Becirovic, Bradley M. Downs, Kenneth H. Cowan, Henry T. Lynch et al. · 2014 · BMC Cancer
93. TOPBP1 , CLSPN and PALB2 genes in familial breast cancer susceptibility
    Hannele Erkko · 2008
94. Detecting association of rare and common variants based on cross-validation prediction error
    Xinlan Yang, Shuaichen Wang, Shuanglin Zhang, Qiuying Sha · 2017 · Genetic Epidemiology
95. Detection of novel germline mutations in six breast cancer predisposition genes by targeted next-generation sequencing
    Li Dong, Nan Wu, Shaojing Wang, Yanan Cheng, Lei Han, Jing Zhao, Xinxin Long, Kun Mu, Menghui Li, Lijuan Wei et al. · 2018 · Human Mutation
96. Genome-wide long non-coding RNA association study on Han Chinese women identifies lncHSAT164 as a novel susceptibility gene for breast cancer
    Jingkai Xu, Guozheng Li, Zhi Li, Wenjing Li, Runsheng Chen, Bo Zhang, Xuejun Zhang · 2021 · Chinese Medical Journal
97. Two founder BRCA2 mutations predispose to breast cancer in young women
    Mar Infante, Mercedes Durán, Adriana Lasa, Alberto Acedo, Miguel de la Hoya, Eva Esteban‐Cardeñosa, David J. Sanz, Lucía Pérez‐Cabornero, Enrique Lastra, Cristina Miner et al. · 2009 · Breast Cancer Research and Treatment
98. Breast Cancer Prevention
    Patricia A. Thompson, Christina M. Laukaitis, Alison Stopeck · 2013 · Springer eBooks
99. Considerations for Comprehensive Assessment of Genetic Predisposition in Familial Breast Cancer
    Henry T. Lynch, Carrie Synder, San Ming Wang · 2014 · The Breast Journal
100. A new mutation of BRCA2 gene in an Italian healthy woman with familial breast cancer history
     Maurizio Pisanò, Valeria Mezzolla, Maria Maddalena Galante, Giovanni Alemanno, Corrado Manca, Vito Lorusso, Antonio Malvası, Andrea Tinelli · 2010 · Familial Cancer