Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 63 Records) |
Query Trace: Breast Neoplasms and MSH6[original query] |
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Mutation Rates in Cancer Susceptibility Genes in Patients With Breast Cancer With Multiple Primary Cancers. JCO precision oncology 2020 9 4 . Maxwell Kara N, Wenz Brandon M, Kulkarni Abha, Wubbenhorst Bradley, D'Andrea Kurt, Weathers Benita, Goodman Noah, Vijai Joseph, Lilyquist Jenna, Hart Steven N, Slavin Thomas P, Schrader Kasmintan A, Ravichandran Vignesh, Thomas Tinu, Hu Chunling, Robson Mark E, Peterlongo Paolo, Bonanni Bernardo, Ford James M, Garber Judy E, Neuhausen Susan L, Shah Payal D, Bradbury Angela R, DeMichele Angela M, Offit Kenneth, Weitzel Jeffrey N, Couch Fergus J, Domchek Susan M, Nathanson Katherine |
Heritable Susceptibility to Breast Cancer among African-American Women in the Detroit Research on Cancer Survivors Study. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2020 9 29 (11): 2369-2375. Purrington Kristen S, Raychaudhuri Sreejata, Simon Michael S, Clark Julie, Ratliff Valerie, Dyson Gregory, Craig Douglas B, Boerner Julie L, Beebe-Dimmer Jennifer L, Schwartz Ann |
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, Kizilboga Akgun Tugba, Yildiz Jale, Enc Feruze, Kir Gozde, Canbek Sezin, Kilic Ali, Zemheri Ebru, Ezberci Fikret, Ozcelik Melike, Dinler Doganay Gizem, Doganay Leve |
Lynch Syndrome Germline Mutations in Breast Cancer: Next Generation Sequencing Case-Control Study of 1,263 Participants. Frontiers in oncology 2020 6 10 666. Nikitin Aleksey G, Chudakova Daria A, Enikeev Rafael F, Sakaeva Dina, Druzhkov Maxim, Shigapova Leyla H, Brovkina Olga I, Shagimardanova Elena I, Gusev Oleg A, Gordiev Marat |
Investigating the Link between Lynch Syndrome and Breast Cancer. European journal of breast health 2020 4 16 (2): 106-109. Sheehan Megan, Heald Brandie, Yanda Courtney, Kelly Erinn Downs, Grobmyer Stephen, Eng Charis, Kalady Matthew, Pederson Hol |
Rare Germline Genetic Variants and the Risks of Epithelial Ovarian Cancer. Cancers 2020 Oct 12 (10): . Pavanello Marina, Chan Isaac Hy, Ariff Amir, Pharoah Paul Dp, Gayther Simon A, Ramus Susan |
Multigene panel testing results in patients with multiple breast cancer primaries. The breast journal 2020 Jan . Corredor Jessica, Woodson Ashley H, Gutierrez Barrera Angelica, Arun Ba |
Germline variants in hereditary breast cancer genes are associated with early age at diagnosis and family history in Guatemalan breast cancer. Breast cancer research and treatment 2021 7 189 (2): 533-539. Ren Megan, Orozco Anali, Shao Kang, Albanez Anaseidy, Ortiz Jeremy, Cao Boyang, Wang Lusheng, Barreda Lilian, Alvarez Christian S, Garland Lisa, Wu Dongjing, Chung Charles C, Wang Jiahui, Frone Megan, Ralon Sergio, Argueta Victor, Orozco Roberto, Gharzouzi Eduardo, Dean Micha |
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 |
Exonic sequencing and MLH3 gene expression analysis of breast cancer patients. Cellular and molecular biology (Noisy-le-Grand, France) 2021 12 67 (3): 35-43. Khailany Rozhgar A, Ozaslan Mehm |
[Difference analysis of somatic mutations between deficient mismatch repair and proficient mismatch repair gene related with colorectal cancer]. Zhonghua zhong liu za zhi [Chinese journal of oncology] 2021 10 43 (10): 1088-1093. Tang X J, Yang M Y, Zhu L Z, Xu D, Yuan |
Morphologic and Genomic Characteristics of Breast Cancers Occurring in Individuals with Lynch Syndrome. Clinical cancer research : an official journal of the American Association for Cancer Research 2021 10 28 (2): 404-413. Schwartz Christopher J, da Silva Edaise M, Marra Antonio, Gazzo Andrea M, Selenica Pier, Rai Vikas K, Mandelker Diana, Pareja Fresia, Misyura Maksym, D'Alfonso Timothy M, Brogi Edi, Drullinsky Pamela, Razavi Pedram, Robson Mark E, Drago Joshua Z, Wen Hannah Y, Zhang Liying, Weigelt Britta, Shia Jinru, Reis-Filho Jorge S, Zhang Ho |
Predicted Chemotherapy Benefit for Breast Cancer Patients With Germline Pathogenic Variants in Cancer Susceptibility Genes. JNCI cancer spectrum 2021 1 5 (1): . Kurian Allison W, Ward Kevin C, Abrahamse Paul, Hamilton Ann S, Katz Steven |
Looking beyond the cytogenetics in haematological malignancies: decoding the role of tandem repeats in DNA repair genes. Molecular biology reports 2022 9 49 (11): 10293-10305. Bhattacharya Priyanjali, Patel Trupti |
Multi-gene panel testing increases germline predisposing mutations' detection in a cohort of breast/ovarian cancer patients from Southern Italy. Frontiers in medicine 2022 9 894358. Nunziato Marcella, Di Maggio Federica, Pensabene Matilde, Esposito Maria Valeria, Starnone Flavio, De Angelis Carmine, Calabrese Alessandra, D'Aiuto Massimiliano, Botti Gerardo, De Placido Sabino, D'Argenio Valeria, Salvatore Frances |
Pathogenicity Reclassification of Genetic Variants Related to Early-Onset Breast Cancer among Women of Mongoloid Origin. Asian Pacific journal of cancer prevention : APJCP 2022 6 23 (6): 2027-2033. Gervas Polina, Molokov Aleksey, Babyshkina Nataliya, Kiselev Artem, Zarubin Aleksei, Yumov Evgeny, Pisareva Lubov, Choynzonov Evgeny, Cherdyntseva Nadez |
Identification of hereditary breast and ovarian cancer germline variants in Granada (Spain): NGS perspective. Molecular genetics and genomics : MGG 2022 4 297 (3): 859-871. Molina-Zayas María, Garrido-Navas Carmen, García-Puche Jose Luis, Barwell Julian, Pedrinaci Susana, Atienza Margarita Martínez, García-Linares Susana, de Haro-Muñoz Tomás, Lorente Jose Antonio, Serrano M Jose, Poyatos-Andújar Anton |
Breast and Ovarian Cancer Penetrance Estimates Derived From Germline Multiple-Gene Sequencing Results in Women. JCO precision oncology 2022 2 1 1-12. Kurian Allison W, Hughes Elisha, Handorf Elizabeth A, Gutin Alexander, Allen Brian, Hartman Anne-Renee, Hall Michael |
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 |
No Evidence of Increased Risk of Breast Cancer in Women With Lynch Syndrome Identified by Multigene Panel Testing. JCO precision oncology 2022 1 4 51-60. Stoll Jessica, Rosenthal Eric, Cummings Shelly, Willmott Jamie, Bernhisel Ryan, Kupfer Sonia |
Uncommon variants detected via hereditary cancer panel and suggestions for genetic counseling. Mutation research 2023 7 827 111831. Zeynep Özdemir, Ezgi Çevik, Ömür Berna Çakmak Öksüzo?lu, Mutlu Do?an, Öztürk Ate?, Ece Esin, ?rem Bilgetekin, Umut Demirci, Ça?lar Köseo?lu, Alper Topal, Nuri Karadurmu?, Haktan Ba??? Erdem, Taha Bah |
Risk of Syndrome-Associated Cancers Among First-Degree Relatives of Patients With Pancreatic Ductal Adenocarcinoma With Pathogenic or Likely Pathogenic Germline Variants. JAMA oncology 2023 5 . Xuan Chen, Margaret A Meyer, Jennifer L Kemppainen, Masayasu Horibe, Shruti Chandra, Shounak Majumder, Gloria M Petersen, Kari G Ra |
Pathogenic variants among females with breast cancer and a non-breast cancer reveal opportunities for cancer interception. Breast cancer research and treatment 2023 3 . Bychkovsky Brittany L, Lo Min-Tzu, Yussuf Amal, Horton Carrie, Hemyari Parichehr, LaDuca Holly, Garber Judy E, Scheib Rochelle, Rana Huma |
Evaluation of genetic alterations in hereditary cancer susceptibility genes in the Ashkenazi Jewish women community of Mexico. Frontiers in genetics 2023 2 14 1094260. Díaz-Velásquez Clara Estela, Gitler Rina, Antoniano Adriana, Kershenovich Sefchovich Ronny, De La Cruz-Montoya Aldo Hugo, Martínez-Gregorio Héctor, Rojas-Jiménez Ernesto Arturo, Cortez Cardoso Penha Ricardo, Terrazas Luis Ignacio, Wegman-Ostrosky Talia, Levi-Lahad Ephrat, Zabaleta Jovanny, Perdomo Sandra, Vaca-Paniagua Feli |
Systematic review of reported association studies of monogenic genes and bladder cancer risk and confirmation analysis in a large population cohort. BJUI compass 2023 2 4 (2): 156-163. Mian Abrar, Wei Jun, Shi Zhuqing, Rifkin Andrew S, Zheng S Lilly, Glaser Alexander P, Kearns James T, Helfand Brian T, Xu Jianfe |
Exome Sequencing Reveals Novel Germline Variants in Breast Cancer Patients in the Southernmost Region of Thailand. Journal of personalized medicine 2023 11 13 (11): . Panupong Sukpan, Surasak Sangkhathat, Hutcha Sriplung, Wison Laochareonsuk, Pongsakorn Choochuen, Nasuha Auseng, Weerawan Khoonjan, Rusta Salaeh, Kornchanok Thangnaphadol, Kasemsun Wanawanakorn, Kanyanatt Kanokwiro |
Mutations of TP53 and genes related to homologous recombination repair in breast cancer with germline BRCA1/2 mutations. Human genomics 2023 1 17 (1): 2. Kim Jinyong, Jeong Kyeonghun, Jun Hyeji, Kim Kwangsoo, Bae Jeong Mo, Song Myung Geun, Yi Hanbaek, Park Songyi, Woo Go-Un, Lee Dae-Won, Kim Tae-Yong, Lee Kyung-Hun, Im Seock- |
Frequency of Pathogenic Germline Mutations in Early and Late Onset Familial Breast Cancer Patients Using Multi-Gene Panel Sequencing: An Egyptian Study. Genes 2023 1 14 (1): . Nassar Auhood, Zekri Abdel-Rahman N, Kamel Mahmoud M, Elberry Mostafa H, Lotfy Mai M, Seadawy Mohamed G, Hassan Zeinab K, Soliman Hany K, Lymona Ahmed M, Youssef Amira Salah El-D |
The Clinical and Genetic Landscape of Hereditary Cancer: Experience from a Single Clinical Diagnostic Laboratory. Cancer genomics & proteomics 2024 8 21 (5): 448-463. Nikolaos Tsoulos, Konstantinos Agiannitopoulos, Kevisa Potska, Anastasia Katseli, Christina Ntogka, Georgia Pepe, Dimitra Bouzarelou, Athanasios Papathanasiou, Dimitrios Grigoriadis, Georgios N Tsaousis, Helen Gogas, Theodore Troupis, Konstantinos Papazisis, Ioannis Natsiopoulos, Vassileios Venizelos, Kyriakos Amarantidis, Stylianos Giassas, Christos Papadimitriou, Elena Fountzilas, Maroulio Stathoulopoulou, Anna Koumarianou, Grigorios Xepapadakis, Alexandru Blidaru, Daniela Zob, Oana Voinea, Mustafa Özdo?an, Mahmut Çerkez Ergören, Alinta Hegmane, Eirini Papadopoulou, George Nasioulas, Christos Markopoul |
Double Heterozygosity for Germline Mutations in Chinese Breast Cancer Patients. Cancers 2024 7 16 (14): . Ava Kwong, Cecilia Y S Ho, Chun-Hang Au, Edmond S K |
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