Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: Syndrome and NBN[original query] |
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Cancer risk of heterozygotes with the NBN founder mutation. Journal of the National Cancer Institute 2007 Dec 99 (24): 1875-80. Seemanová Eva, Jarolim Petr, Seeman Pavel, Varon Raymonda, Digweed Martin, Swift Michael, Sperling Ka |
Variations in the NBN/NBS1 gene and the risk of breast cancer in non-BRCA1/2 French Canadian families with high risk of breast cancer. BMC cancer 2009 9 (1): 181. Desjardins Sylvie, Beauparlant Joly Charles, Labrie Yvan, Ouellette Geneviève, Durocher Francine, |
NBN 657del5 heterozygous mutations and colorectal cancer risk in the Czech Republic. Mutation research 2009 Jun 666 (1-2): 64-7. Pardini Barbara, Naccarati Alessio, Polakova Veronika, Smerhovsky Zdenek, Hlavata Ivona, Soucek Pavel, Novotny Jan, Vodickova Ludmila, Tomanova Vera, Landi Stefano, Vodicka Pav |
Heterozygous germ-line mutations in the NBN gene predispose to medulloblastoma in pediatric patients. Acta neuropathologica 2010 Mar 119 (3): 325-34. Ciara El?bieta, Piekutowska-Abramczuk Dorota, Popowska Ewa, Grajkowska Wies?awa, Barszcz S?awomir, Perek Danuta, Dembowska-Bagi?ska Bo?enna, Perek-Polnik Marta, Kowalewska Ewa, Czaj?ska Aneta, Syczewska Ma?gorzata, Czornak Kamila, Krajewska-Walasek Ma?gorzata, Roszkowski Marcin, Chrzanowska Krystyna |
High prevalence of the NBN gene mutation c.657-661del5 in Southeast Germany. Journal of applied genetics 2010 51 (2): 211-4. Maurer M H, Hoffmann K, Sperling K, Varon |
Role of 657del5 NBN mutation and 7p12.2 (IKZF1), 9p21 (CDKN2A), 10q21.2 (ARID5B) and 14q11.2 (CEBPE) variation and risk of childhood ALL in the Polish population. Leukemia research 2011 Nov 35 (11): 1534-6. Pastorczak Agata, Górniak Patryk, Sherborne Amy, Hosking Fay, Treli?ska Joanna, Lejman Monika, Szczepa?ski Tomasz, Borowiec Maciej, Fendler Wojciech, Kowalczyk Jerzy, Houlston Richard S, M?ynarski Wojcie |
[Heterozygous carriers of Slavic mutation 657del5 of NBN gene in patients with colorectal cancer]. Casopís lékar?? c?eských 2011 150 (2): 97-9. Seemanová Eva, Hoch Jirí, Seeman Pav |
Identification of a novel NBN truncating mutation in a family with hereditary prostate cancer. Familial cancer 2012 Aug . Zuhlke KA, Johnson AM, Okoth LA, Stoffel EM, Robbins CM, Tembe WA, Salinas CA, Zheng SL, Xu J, Carpten JD, Lange EM, Isaacs WB, Cooney KA |
Association of the nibrin gene (NBN) variants with breast cancer. Biomedical reports 2016 Mar 4 (3): 369-373. Uzunoglu Hakan, Korak Tugcan, Ergul Emel, Uren Nihal, Sazci Ali, Utkan N Zafer, Kargi Ertu?rul, Triyaki Ça?ri, Yirmibesoglu Okt |
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 |
Germline cancer susceptibility gene variants, somatic second hits, and survival outcomes in patients with resected pancreatic cancer. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Jul . Yurgelun Matthew B, Chittenden Anu B, Morales-Oyarvide Vicente, Rubinson Douglas A, Dunne Richard F, Kozak Margaret M, Qian Zhi Rong, Welch Marisa W, Brais Lauren K, Da Silva Annacarolina, Bui Justin L, Yuan Chen, Li Tingting, Li Wanwan, Masuda Atsuhiro, Gu Mancang, Bullock Andrea J, Chang Daniel T, Clancy Thomas E, Linehan David C, Findeis-Hosey Jennifer J, Doyle Leona A, Thorner Aaron R, Ducar Matthew D, Wollison Bruce M, Khalaf Natalia, Perez Kimberly, Syngal Sapna, Aguirre Andrew J, Hahn William C, Meyerson Matthew L, Fuchs Charles S, Ogino Shuji, Hornick Jason L, Hezel Aram F, Koong Albert C, Nowak Jonathan A, Wolpin Brian |
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, Vo?ka Michal, Janatová Markéta, Stola?ová Lenka, Borecká Marianna, Kleiblová Petra, Machá?ková Eva, Foretová Lenka, Koudová Monika, Lhota Filip, Tavandzis Spiros, Zikán Michal, Stránecký Viktor, Veselá Kamila, Panczak Aleš, Kotlas Jaroslav, Kleibl Zden |
Recommendations for Preventive Care for Women with Rare Genetic Cause of Breast and Ovarian Cancer. Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti 2019 8 32 (Supplementum2): 6-13. Foretová Lenka, Navrátilová Marie, Svoboda Marek, Vaší?ková Petra, S?ahlová Eva Hrabincová, Házová Jana, Kleiblová Petra, Kleibl Zden?k, Machá?ková Eva, Palácová Markéta, Petráková Katarí |
Cancer Susceptibility Mutations in Patients With Urothelial Malignancies. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2019 12 38 (5): 406-414. Carlo Maria I, Ravichandran Vignesh, Srinavasan Preethi, Bandlamudi Chaitanya, Kemel Yelena, Ceyhan-Birsoy Ozge, Mukherjee Semanti, Mandelker Diana, Chaim Joshua, Knezevic Andrea, Rana Satshil, Fnu Zarina, Breen Kelsey, Arnold Angela G, Khurram Aliya, Tkachuk Kaitlyn, Cipolla Catharine K, Regazzi Ashley, Hakimi A Ari, Al-Ahmadie Hikmat, Dalbagni Guido, Cadoo Karen A, Walsh Michael F, Teo Min-Yuen, Funt Samuel A, Coleman Jonathan A, Bochner Bernard H, Iyer Gopa, Solit David B, Stadler Zsofia K, Zhang Liying, Rosenberg Jonathan E, Taylor Barry S, Robson Mark E, Berger Michael F, Vijai Joseph, Bajorin Dean F, Offit Kenne |
Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population. BMC medical genomics 2020 Feb 13 (1): 21. da Costa E Silva Carvalho Simone, Cury Nathalia Moreno, Brotto Danielle Barbosa, de Araujo Luiza Ferreira, Rosa Reginaldo Cruz Alves, Texeira Lorena Alves, Plaça Jessica Rodrigues, Marques Adriana Aparecida, Peronni Kamila Chagas, Ruy Patricia de Cássia, Molfetta Greice Andreotti, Moriguti Julio Cesar, Carraro Dirce Maria, Palmero Edenir Inêz, Ashton-Prolla Patricia, de Faria Ferraz Victor Evangelista, Silva Wilson Arau |
Identification of Germline Mutations in Melanoma Patients with Early Onset, Double Primary Tumors, or Family Cancer History by NGS Analysis of 217 Genes. Biomedicines 2020 Oct 8 (10): . Stolarova Lenka, Jelinkova Sandra, Storchova Radka, Machackova Eva, Zemankova Petra, Vocka Michal, Kodet Ondrej, Kral Jan, Cerna Marta, Volkova Zuzana, Janatova Marketa, Soukupova Jana, Stranecky Viktor, Dundr Pavel, Foretova Lenka, Macurek Libor, Kleiblova Petra, Kleibl Zden |
Detection of Germline Variants in 450 Breast/Ovarian Cancer Families with a Multi-Gene Panel Including Coding and Regulatory Regions. International journal of molecular sciences 2021 Jul 22 (14): . Guglielmi Chiara, Scarpitta Rosa, Gambino Gaetana, Conti Eleonora, Bellè Francesca, Tancredi Mariella, Cervelli Tiziana, Falaschi Elisabetta, Cosini Cinzia, Aretini Paolo, Congregati Caterina, Marino Marco, Patruno Margherita, Pilato Brunella, Spina Francesca, Balestrino Luisa, Tenedini Elena, Carnevali Ileana, Cortesi Laura, Tagliafico Enrico, Tibiletti Maria Grazia, Tommasi Stefania, Ghilli Matteo, Vivanet Caterina, Galli Alvaro, Caligo Maria Adelai |
Pancreatic Cancer with Mutation in BRCA1/2, MLH1, and APC Genes: Phenotype Correlation and Detection of a Novel Germline BRCA2 Mutation. Genes 2022 2 13 (2): . Vietri Maria Teresa, D'Elia Giovanna, Caliendo Gemma, Albanese Luisa, Signoriello Giuseppe, Napoli Claudio, Molinari Anna Mar |
Germline Genetic NBN Variation and Predisposition to B-cell Acute Lymphoblastic Leukemia in Children. Research square 2023 7 . Jun Yang, Carolin Escherich, Wenan Chen, Yizhen Li, Wenjian Yang, Rina Nishii, Zhenhua Li, Elizabeth Raetz, Meenakshi Devidas, Gang Wu, Kim Nichols, Hiroto Inaba, Ching-Hon Pui, Sima Jeha, Bruce Camitta, Eric Larsen, Stephen Hunger, Mignon L |
Investigating the prevalence of pathogenic variants in Saudi Arabian patients with familial cancer using a multigene next generation sequencing panel. Oncotarget 2023 6 14 580-594. Musa AlHarbi, Nahla Ali Mobark, Wael Abdel Rahman AlJabarat, Hadeel ElBardis, Ebtehal AlSolme, Abdullah Bany Hamdan, Ali H AlFakeeh, Fatimah AlMushawah, Fawz AlHarthi, Abdullah A AlSharm, Ali Abdullah O Balbaid, Naji AlJohani, Alicia Y Zhou, Heather A Robinson, Saleh A Alqahtani, Malak Abedalthaga |
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- Page last updated:Apr 22, 2024
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