Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 39 Records) |
Query Trace: Syndrome and CDH1[original query] |
---|
Germline CDH1 mutations are a significant contributor to the high frequency of early-onset diffuse gastric cancer cases in New Zealand M?ori. Familial cancer 2018 Mar . Hakkaart Christopher, Ellison-Loschmann Lis, Day Robert, Sporle Andrew, Koea Jonathan, Harawira Pauline, Cheng Soo, Gray Michelle, Whaanga Tracey, Pearce Neil, Guilford Par |
Low risk of invasive lobular carcinoma of the breast in carriers of BRCA1 (hereditary breast and ovarian cancer) and TP53 (Li-Fraumeni syndrome) germline mutations. The breast journal 2018 11 25 (1): 16-19. Ditchi Yoan, Broudin Chloé, El Dakdouki Yolla, Muller Marie, Lavaud Pernelle, Caron Olivier, Lejri Donia, Baynes Caroline, Mathieu Marie-Christine, Salleron Julia, Benusiglio Patrick |
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 |
Next Generation Sequencing Reveals Novel Mutations in Mismatch Repair Genes and Other Cancer Predisposition Genes in Asian Patients with Suspected Lynch Syndrome. Clinical colorectal cancer 2019 7 18 (4): e324-e334. Ow Samuel G W, Tan Kar Tong, Yang Henry, Yap Hui-Ling, Sapari Nur Sabrina Binte, Ong Pei Yi, Soong Richie, Lee Soo-Ch |
A new mutL homolog 1 c.1896+5G>A germline mutation detected in a Lynch syndrome-associated lung and gastric double primary cancer patient. Molecular genetics & genomic medicine 2019 Jun e787. Chen Xuyuan, Li Xiang, Liang Hongsen, Wei Lichun, Cui Qiang, Yao Ming, Wu |
Endoscopic Ultrasound Has Limited Utility in Diagnosis of Gastric Cancer in Carriers of CDH1 Mutations. Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 2019 5 18 (2): 505-508.e1. Kumar Shria, Katona Bryson W, Long Jessica M, Domchek Susan, Rustgi Anil K, Roses Robert, Ginsberg Gregory |
Associations of CDH1 germline variant location and cancer phenotype in families with hereditary diffuse gastric cancer (HDGC). Journal of medical genetics 2019 2 56 (6): 370-379. Lo Winifred, Zhu Bin, Sabesan Arvind, Wu Ho-Hsiang, Powers Astin, Sorber Rebecca A, Ravichandran Sarangan, Chen Ina, McDuffie Lucas A, Quadri Humair S, Beane Joal D, Calzone Kathleen, Miettinen Markku M, Hewitt Stephen M, Koh Christopher, Heller Theo, Wacholder Sholom, Rudloff U |
Identification of germline pathogenic variants in DNA damage repair genes by a next-generation sequencing multigene panel in BRCAX patients. Clinical biochemistry 2019 Nov . Rodríguez-Balada Marta, Roig Bàrbara, Melé Mireia, Albacar Cinta, Serrano Sara, Salvat Mònica, Querol Montserrat, Borràs Joan, Martorell Lourdes, Gumà Jos |
Characteristics of cancer susceptibility genes mutations in 282 patients with gastric adenocarcinoma. Chinese journal of cancer research = Chung-kuo yen cheng yen chiu 2020 9 32 (4): 508-515. Ji Ke, Ao Sheng, He Liu, Zhang Lijiao, Feng Li, Lyu Guoqi |
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 |
Hereditary Diffuse Gastric Cancer: A Comparative Cohort Study According to Pathogenic Variant Status. Cancers 2020 12 12 (12): . Marwitz Tim, Hüneburg Robert, Spier Isabel, Lau Jan-Frederic, Kristiansen Glen, Lingohr Philipp, Kalff Jörg C, Aretz Stefan, Nattermann Jacob, Strassburg Christian |
Cancer predisposition and germline CTNNA1 variants. European journal of medical genetics 2021 8 64 (10): 104316. Lobo Silvana, Benusiglio Patrick R, Coulet Florence, Boussemart Lise, Golmard Lisa, Spier Isabel, Hüneburg Robert, Aretz Stefan, Colas Chrystelle, Oliveira Car |
Second Primary Cancers After Gastric Cancer, and Gastric Cancer as Second Primary Cancer. Clinical epidemiology 2021 7 13 515-525. Zheng Guoqiao, Sundquist Kristina, Sundquist Jan, Chen Tianhui, Försti Asta, Hemminki Akseli, Hemminki Ka |
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 |
Exome sequencing in BRCA1-2 candidate familias: the contribution of other cancer susceptibility genes. Frontiers in oncology 2021 11 649435. Doddato Gabriella, Valentino Floriana, Giliberti Annarita, Papa Filomena Tiziana, Tita Rossella, Bruno Lucia Pia, Resciniti Sara, Fallerini Chiara, Benetti Elisa, Palmieri Maria, Mencarelli Maria Antonietta, Fabbiani Alessandra, Bruttini Mirella, Orrico Alfredo, Baldassarri Margherita, Fava Francesca, Lopergolo Diego, Lo Rizzo Caterina, Lamacchia Vittoria, Mannucci Sara, Pinto Anna Maria, Curr Aurora, Mancini Virginia, , , Mari Francesca, Renieri Alessandra, Ariani Frances |
Geographical Distribution of E-cadherin Germline Mutations in the Context of Diffuse Gastric Cancer: A Systematic Review. Cancers 2021 4 13 (6): . Corso Giovanni, Corso Federica, Bellerba Federica, Carneiro Patrícia, Seixas Susana, Cioffi Antonio, La Vecchia Carlo, Magnoni Francesca, Bonanni Bernardo, Veronesi Paolo, Gandini Sara, Figueiredo Joa |
The results of multigene panel sequencing in Slovak HBOC families. Neoplasma 2021 Mar . Konecny Michal, Kosova Klaudia, Tilandyova Petra, Wachsmannova Lenka, Baldovic Marian, Krajcovic Juraj, Patlevicova Andrea, Markus Jan, Ciernikova So |
CDH1 germline mutations in healthy individuals from families with the hereditary diffuse gastric cancer syndrome. Journal of medical genetics 2021 12 59 (4): 313-317. Corso Giovanni, Magnoni Francesca, Massari Giulia, Trovato Cristina Maria, De Scalzi Alessandra Margherita, Vicini Elisa, Bonanni Bernardo, Veronesi Paolo, Galimberti Viviana, Bagnardi Vincen |
Surveillance and Surgical Considerations in Hereditary Diffuse Gastric Cancer. Gastrointestinal endoscopy clinics of North America 2021 11 32 (1): 163-175. Gamble Lauren A, Davis Jeremy |
[Hereditary gastric cancer syndromes and their association with specific histological subtypes]. Bulletin du cancer 2022 8 . Dardenne Antoine, Sirmai Laura, Metras Julie, Enea Diana, Svrcek Magali, Benusiglio Patrick |
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 |
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes. The Lancet. Oncology 2022 11 24 (1): 91-106. Garcia-Pelaez José, Barbosa-Matos Rita, Lobo Silvana, Dias Alexandre, Garrido Luzia, Castedo Sérgio, Sousa Sónia, Pinheiro Hugo, Sousa Liliana, Monteiro Rita, Maqueda Joaquin J, Fernandes Susana, Carneiro Fátima, Pinto Nádia, Lemos Carolina, Pinto Carla, Teixeira Manuel R, Aretz Stefan, Bajalica-Lagercrantz Svetlana, Balmaña Judith, Blatnik Ana, Benusiglio Patrick R, Blanluet Maud, Bours Vincent, Brems Hilde, Brunet Joan, Calistri Daniele, Capellá Gabriel, Carrera Sergio, Colas Chrystelle, Dahan Karin, de Putter Robin, Desseignés Camille, Domínguez-Garrido Elena, Egas Conceição, Evans D Gareth, Feret Damien, Fewings Eleanor, Fitzgerald Rebecca C, Coulet Florence, Garcia-Barcina María, Genuardi Maurizio, Golmard Lisa, Hackmann Karl, Hanson Helen, Holinski-Feder Elke, Hüneburg Robert, Krajc Mateja, Lagerstedt-Robinson Kristina, Lázaro Conxi, Ligtenberg Marjolijn J L, Martínez-Bouzas Cristina, Merino Sonia, Michils Geneviève, Novakovi? Srdjan, Patiño-García Ana, Ranzani Guglielmina Nadia, Schröck Evelin, Silva Inês, Silveira Catarina, Soto José L, Spier Isabel, Steinke-Lange Verena, Tedaldi Gianluca, Tejada María-Isabel, Woodward Emma R, Tischkowitz Marc, Hoogerbrugge Nicoline, Oliveira Car |
Inherited Cancer Susceptibility Gene Sequence Variations Among Patients With Appendix Cancer. JAMA oncology 2022 11 9 (1): 95-101. Holowatyj Andreana N, Washington Mary K, Tavtigian Sean V, Eng Cathy, Horton Carol |
Frequency of CDH1, CTNNA1 and CTNND1 Germline Variants in Families with Diffuse and Mixed Gastric Cancer. Cancers 2023 9 15 (17): . Joana Guerra, Carla Pinto, Pedro Pinto, Manuela Pinheiro, Catarina Santos, Ana Peixoto, Carla Escudeiro, Ana Barbosa, Miguel Porto, Inês Francisco, Paula Lopes, Ana Raquel Isidoro, Ana Luísa Cunha, Cristina Albuquerque, Isabel Claro, Carla Oliveira, João Silva, Manuel R Teixei |
Clinical implication of CDH1 mutations in genetic testing for diffuse gastric cancer patients. Oncology 2023 9 . Giovanni Corso, Cristina Maria Trovato, Salvatore Petitto, Antonia Girardi, Alessandra Margherita De Scalzi, Beatrice Bianchi, Francesca Magnoni, Antonio Cioffi, Viviana Galimberti, Paolo Veronesi, Giovanni Mazzarol, Patrick Maisonneu |
Germline CDH1 variants in hereditary diffuse gastric cancer syndrome with focus on younger women. Journal of cancer research and clinical oncology 2023 8 . Giovanni Corso, Giovanni Comelli, Paolo Veronesi, Beatrice Bianchi, Salvatore Petitto, Andrea Polizzi, Antonia Girardi, Antonio Cioffi, Carlo La Vecchia, Vincenzo Bagnardi, Francesca Magno |
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 |
Molecular genetic investigation of hereditary breast and ovarian cancer patients in the Southern Transdanubian region: widening the mutation spectrum and searching for new pathogenic variants using next-generation methods. Pathology oncology research : POR 2024 8 30 1611813. László Baráti, Anita Maász, Alexandra Mikó, Éva Bércesi, Sultan Al Kalbani, Judit Bene, Sebestyén Kovács, László Mangel, Kinga Hadzsi |
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 |
CDH1 Genotype Exploration in Women With Hereditary Lobular Breast Cancer Phenotype. JAMA network open 2024 4 7 (4): e247862. Giovanni Corso, Elena Marino, Cristina Zanzottera, Carla Oliveira, Loris Bernard, Debora Macis, Joana Figueiredo, Joana Pereira, Patrícia Carneiro, Giulia Massari, Massimo Barberis, Alessandra Margherita De Scalzi, Sergio Vincenzo Taormina, Elham Sajjadi, Claudia Sangalli, Sara Gandini, Oriana D'Ecclesiis, Cristina Maria Trovato, Anna Rotili, Filippo Pesapane, Luca Nicosia, Carlo La Vecchia, Viviana Galimberti, Elena Guerini-Rocco, Bernardo Bonanni, Paolo Verone |
- Page last reviewed:Feb 1, 2024
- Content source: