Human Genome Epidemiology Literature Finder
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Records 1 - 29 (of 29 Records) |
| Query Trace: Neoplasms and SLX4[original query] |
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| Mutation analysis of the SLX4/FANCP gene in hereditary breast cancer. Breast cancer research and treatment 2011 Dec 130 (3): 1021-8. Landwehr Rosa, Bogdanova Natalia V, Antonenkova Natalia, Meyer Andreas, Bremer Michael, Park-Simon Tjoung-Won, Hillemanns Peter, Karstens Johann H, Schindler Detlev, Dörk Thi |
| Analysis of the novel fanconi anemia gene SLX4/FANCP in familial breast cancer cases. Human mutation 2013 Jan 34 (1): 70-3. Bakker Janine L, van Mil Saskia E, Crossan Gerry, Sabbaghian Nelly, De Leeneer Kim, Poppe Bruce, Adank Muriel, Gille Hans, Verheul Henk, Meijers-Heijboer Hanne, de Winter Johan P, Claes Kathleen, Tischkowitz Marc, Waisfisz Quint |
| Analysis of SLX4/FANCP in non-BRCA1/2-mutated breast cancer families. BMC cancer 2012 12 (1): 84. Fernández-Rodríguez Juana, Quiles Francisco, Blanco Ignacio, Teulé Alex, Feliubadaló Lídia, Valle Jesús Del, Salinas Mónica, Izquierdo Angel, Darder Esther, Schindler Detlev, Capellá Gabriel, Brunet Joan, Lázaro Conxi, Pujana Miguel Ang |
| Low prevalence of SLX4 loss-of-function mutations in non-BRCA1/2 breast and/or ovarian cancer families. European journal of human genetics : EJHG 2012 Dec . de Garibay GR, Díaz A, Gaviña B, Romero A, Garre P, Vega A, Blanco A, Tosar A, Díez O, Pérez-Segura P, Díaz-Rubio E, Caldés T, de la Hoya M |
| Assessment of SLX4 Mutations in Hereditary Breast Cancers. PloS one 2013 8 (6): e66961. Shah Sohela, Kim Yonghwan, Ostrovnaya Irina, Murali Rajmohan, Schrader Kasmintan A, Lach Francis P, Sarrel Kara, Rau-Murthy Rohini, Hansen Nichole, Zhang Liyng, Kirchhoff Tomas, Stadler Zsofia, Robson Mark, Vijai Joseph, Offit Kenneth, Smogorzewska Aga |
| Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data. PloS one 2013 8 (12): e81503. Mosley Jonathan D, Van Driest Sara L, Larkin Emma K, Weeke Peter E, Witte John S, Wells Quinn S, Karnes Jason H, Guo Yan, Bastarache Lisa, Olson Lana M, McCarty Catherine A, Pacheco Jennifer A, Jarvik Gail P, Carrell David S, Larson Eric B, Crosslin David R, Kullo Iftikhar J, Tromp Gerard, Kuivaniemi Helena, Carey David J, Ritchie Marylyn D, Denny Josh C, Roden Dan |
| Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2014 Jul 32 (19): 2001-9. Kurian Allison W, Hare Emily E, Mills Meredith A, Kingham Kerry E, McPherson Lisa, Whittemore Alice S, McGuire Valerie, Ladabaum Uri, Kobayashi Yuya, Lincoln Stephen E, Cargill Michele, Ford James |
| A low-frequency haplotype spanning SLX4/FANCP constitutes a new risk locus for early-onset breast cancer (<60 years) and is associated with reduced DNA repair capacity. International journal of cancer 2018 02 142 (4): 757-768. Surowy Harald, Varga Dominic, Burwinkel Barbara, Marmé Frederik, Sohn Christof, Luedeke Manuel, Rinckleb Antje, Maier Christiane, Deissler Helmut, Volcic Meta, Wiesmüller Lisa, Hasenburg Annette, Klar Maximilian, Hoegel Josef, Vogel Walth |
| Multigene panel testing beyond BRCA1/2 in breast/ovarian cancer Spanish families and clinical actionability of findings. Journal of cancer research and clinical oncology 2018 10 144 (12): 2495-2513. Bonache Sandra, Esteban Irene, Moles-Fernández Alejandro, Tenés Anna, Duran-Lozano Laura, Montalban Gemma, Bach Vanessa, Carrasco Estela, Gadea Neus, López-Fernández Adrià, Torres-Esquius Sara, Mancuso Francesco, Caratú Ginevra, Vivancos Ana, Tuset Noemí, Balmaña Judith, Gutiérrez-Enríquez Sara, Diez Orla |
| Mutation Spectrum of Cancer-Associated Genes in Patients With Early Onset of Colorectal Cancer. Frontiers in oncology 2019 8 9 673. Zhunussova Gulnur, Afonin Georgiy, Abdikerim Saltanat, Jumanov Abai, Perfilyeva Anastassiya, Kaidarova Dilyara, Djansugurova Ley |
| High-Throughput Sequencing of Gastric Cancer Patients: Unravelling Genetic Predispositions Towards an Early-Onset Subtype. Cancers 2020 7 12 (7): . Machlowska Julita, Kapusta Przemys?aw, Baj Jacek, Morsink Folkert H M, Wo?kow Pawe?, Maciejewski Ryszard, Offerhaus G Johan A, Sitarz Robe |
| Frequency of heterozygous germline pathogenic variants in genes for Fanconi anemia in patients with non-BRCA1/BRCA2 breast cancer: a meta-analysis. Breast cancer research and treatment 2020 Jun . Alter Blanche P, Best Ana |
| Population-based targeted sequencing of 54 candidate genes identifies PALB2 as a susceptibility gene for high-grade serous ovarian cancer. Journal of medical genetics 2020 6 58 (5): 305-313. Song Honglin, Dicks Ed M, Tyrer Jonathan, Intermaggio Maria, Chenevix-Trench Georgia, Bowtell David D, Traficante Nadia, Group Aocs, Brenton James, Goranova Teodora, Hosking Karen, Piskorz Anna, van Oudenhove Elke, Doherty Jen, Harris Holly R, Rossing Mary Anne, Duerst Matthias, Dork Thilo, Bogdanova Natalia V, Modugno Francesmary, Moysich Kirsten, Odunsi Kunle, Ness Roberta, Karlan Beth Y, Lester Jenny, Jensen Allan, Krüger Kjaer Susanne, Høgdall Estrid, Campbell Ian G, Lázaro Conxi, Pujara Miguel Angel, Cunningham Julie, Vierkant Robert, Winham Stacey J, Hildebrandt Michelle, Huff Chad, Li Donghui, Wu Xifeng, Yu Yao, Permuth Jennifer B, Levine Douglas A, Schildkraut Joellen M, Riggan Marjorie J, Berchuck Andrew, Webb Penelope M, Group Opal Study, Cybulski Cezary, Gronwald Jacek, Jakubowska Anna, Lubinski Jan, Alsop Jennifer, Harrington Patricia, Chan Isaac, Menon Usha, Pearce Celeste L, Wu Anna H, de Fazio Anna, Kennedy Catherine J, Goode Ellen, Ramus Susan, Gayther Simon, Pharoah Pa |
| A Novel Risk Stratification System for Thyroid Nodules With Indeterminate Cytology-A Pilot Cohort Study. Frontiers in endocrinology 2020 3 11 53. Gomes-Lima Cristiane J, Auh Sungyoung, Thakur Shilpa, Zemskova Marina, Cochran Craig, Merkel Roxanne, Filie Armando C, Raffeld Mark, Patel Snehal B, Xi Liqiang, Wartofsky Leonard, Burman Kenneth D, Klubo-Gwiezdzinska Joan |
| Clinical management and genomic profiling of pediatric low-grade gliomas in Saudi Arabia. PloS one 2020 1 15 (1): e0228356. Mobark Nahla A, Alharbi Musa, Alhabeeb Lamees, AlMubarak Latifa, Alaljelaify Rasha, AlSaeed Mariam, Almutairi Amal, Alqubaishi Fatmah, Ahmad Maqsood, Al-Banyan Ayman, Alotabi Fahad E, Barakeh Duna, AlZahrani Malak, Al-Khalidi Hisham, Ajlan Abdulrazag, Ramkissoon Lori A, Ramkissoon Shakti H, Abedalthagafi Mal |
| Increased Cancer Prevalence in Peripartum Cardiomyopathy. JACC. CardioOncology 2021 8 1 (2): 196-205. Pfeffer Tobias J, Schlothauer Stella, Pietzsch Stefan, Schaufelberger Maria, Auber Bernd, Ricke-Hoch Melanie, List Manuel, Berliner Dominik, Abou Moulig Valeska, König Tobias, Arany Zolt, Sliwa Karen, Bauersachs Johann, Hilfiker-Kleiner Deni |
| Precision Oncology of High-Grade Ovarian Cancer Defined through Targeted Sequencing. Cancers 2021 10 13 (20): . Wessman Sandra, Fuentes Beatriz Bohorquez, Törngren Therese, Kvist Anders, Kokaraki Georgia, Menkens Hanna, Hjerpe Elisabet, Hugo Ythalo, Petta Tirzah Braz, Borg Åke, Carlson Joseph |
| Spectrum of Germline Mutations Within Fanconi Anemia-Associated Genes Across Populations of Varying Ancestry. JNCI cancer spectrum 2022 8 5 (1): . Chan Sock Hoai, Ni Ying, Li Shao-Tzu, Teo Jing Xian, Ishak Nur Diana Binte, Lim Weng Khong, Ngeow Joan |
| Mutational spectrum of breast cancer susceptibility genes among women ascertained in a cancer risk clinic in Northeast Brazil. Breast cancer research and treatment 2022 3 193 (2): 485-494. Felix Gabriela E S, Guindalini Rodrigo Santa Cruz, Zheng Yonglan, Walsh Tom, Sveen Elisabeth, Lopes Taisa Manuela Machado, Côrtes Juliana, Zhang Jing, Carôzo Polyanna, Santos Irlânia, Bonfim Thaís Ferreira, Garicochea Bernardo, Toralles Maria Betânia Pereira, Meyer Roberto, Netto Eduardo Martins, Abe-Sandes Kiyoko, King Mary-Claire, de Oliveira Nascimento Ivana Lucia, Olopade Olufunmilayo |
| New insights on familial colorectal cancer type X syndrome. Scientific reports 2022 2 12 (1): 2846. Garcia Felipe Antonio de Oliveira, de Andrade Edilene Santos, de Campos Reis Galvão Henrique, da Silva Sábato Cristina, Campacci Natália, de Paula Andre Escremin, Evangelista Adriane Feijó, Santana Iara Viana Vidigal, Melendez Matias Eliseo, Reis Rui Manuel, Palmero Edenir In |
| Malignant pleural mesothelioma: Germline variants in DNA repair genes may steer tailored treatment. European journal of cancer (Oxford, England : 1990) 2022 1 163 44-54. Sculco Marika, La Vecchia Marta, Aspesi Anna, Pinton Giulia, Clavenna Michela G, Casalone Elisabetta, Allione Alessandra, Grosso Federica, Libener Roberta, Muzio Alberto, Rena Ottavio, Baietto Guido, Parini Sara, Boldorini Renzo, Giachino Daniela, Papotti Mauro, Scagliotti Giorgio V, Migliore Enrica, Mirabelli Dario, Moro Laura, Magnani Corrado, Ferrante Daniela, Matullo Giuseppe, Dianzani Ir |
| Germline Sequencing Analysis to Inform Clinical Gene Panel Testing for Aggressive Prostate Cancer. JAMA oncology 2023 9 . Burcu F Darst, Ed Saunders, Tokhir Dadaev, Xin Sheng, Peggy Wan, Loreall Pooler, Lucy Y Xia, Stephen Chanock, Sonja I Berndt, Ying Wang, Alpa V Patel, Demetrius Albanes, Stephanie J Weinstein, Vincent Gnanapragasam, Chad Huff, Fergus J Couch, Alicja Wolk, Graham G Giles, Tu Nguyen-Dumont, Roger L Milne, Mark M Pomerantz, Julie A Schmidt, Ruth C Travis, Timothy J Key, Konrad H Stopsack, Lorelei A Mucci, William J Catalona, Beth Marosy, Kurt N Hetrick, Kimberly F Doheny, Robert J MacInnis, Melissa C Southey, Rosalind A Eeles, Fredrik Wiklund, David V Conti, Zsofia Kote-Jarai, Christopher A Haim |
| Genomic analyses of germline and somatic variation in high-grade serous ovarian cancer. Journal of ovarian research 2023 7 16 (1): 141. A W Adamson, Y C Ding, L Steele, L A Leong, R Morgan, M T Wakabayashi, E S Han, T H Dellinger, P S Lin, A A Hakim, S Wilczynski, C D Warden, S Tao, V Bedell, M C Cristea, S L Neuhaus |
| Genomic Analyses of Germline and Somatic Variation in High-Grade Serous Ovarian Cancer. Research square 2023 3 . Adamson Aaron W, Ding Yuan Chun, Steele Linda, Leong Lucile A, Morgan Robert, Wakabayashi Mark T, Han Ernest S, Dellinger Thanh H, Lin Paul S, Hakim Amy A, Wilczynski Sharon, Warden Charles D, Tao Shu, Bedell Victoria, Cristea Mihaela C, Neuhausen Susan |
| Germline pathogenic variants in patients with early onset neuroendocrine neoplasms. Endocrine-related cancer 2023 3 . Riechelmann Rachel Pimenta, Donadio Mauro D, Jesus Victor Hugo F de, de Carvalho Nathalia de Angelis, Santiago Karina Miranda, Barros Milton J, Lopes Laura, Santos Gabriel Oliveira Dos, Formiga Maria Nirvana, Carraro Dirce Maria, Torrezan Giovana Tard |
| The ctDNA-based postoperative molecular residual disease status in different subtypes of early-stage breast cancer. Gland surgery 2023 1 11 (12): 1924-1935. Yang Yang, Zhang Jie, Li Jiao-Yang, Xu Lu, Wang Si-Ning, Zhang Jun-Qi, Xun Zhou, Xia Yu, Cao Jian-Bo, Liu Yang, Shi Li-Yan, Li Wei, Shi Yong-Lei, He Yuan-Ge, Gu De-Jian, Yu Zheng-Yuan, Chen Kai, Lan Ji |
| Prognostic value of genomic mutation signature associated with immune microenvironment in southern Chinese patients with esophageal squamous cell carcinoma. Cancer immunology, immunotherapy : CII 2024 6 73 (8): 141. Yue Zhou, Li Chu, Shuyan Li, Xiao Chu, Jianjiao Ni, Shanshan Jiang, Yechun Pang, Danru Zheng, Yujuan Lu, Fangcen Lan, Xiuyu Cai, Xi Yang, Zhengfei Z |
| Alterations in DNA Damage Repair Genes Before and After Neoadjuvant Cisplatin-based Chemotherapy in Muscle-invasive Bladder Cancer. European urology open science 2024 12 71 38-48. Ursula Lemberger, Büsra Ernhofer, Sigurd Krieger, Andreas Bruchbacher, André Oszwald, Ekaterina Laukhtina, Andrea Haitl, Melanie R Hassler, Bernhard Englinger, Eva Compérat, Shahrokh F Shari |
| Comparative sequencing study of mismatch repair and homology-directed repair genes in endometrial cancer and breast cancer patients from Kazakhstan. International journal of cancer 2024 10 . Ying Zheng, Natalia Vdovichenko, Peter Schürmann, Dhanya Ramachandran, Robert Geffers, Lisa-Marie Speith, Natalia Bogdanova, Julia Enßen, Natalia Dubrowinskaja, Tatyana Yugay, Zura Berkutovna Yessimsiitova, Nurzhan Turmanov, Peter Hillemanns, Thilo Dö |
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