HuGE Literature Finder
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Early detection of duodenal cancer by upper GI-endoscopy in Lynch syndrome. International journal of cancer 2021 Jul . Vangala Deepak B, Ladigan-Badura Swetlana, Engel Christoph, Hüneburg Robert, Perne Claudia, Bucksch Karolin, Nattermann Jacob, Steinke-Lange Verena, Rahner Nils, Weitz Jürgen, Kloor Matthias, Tomann Judith, Canbay Ali, Nguyen Huu-Phuc, Strassburg Christian, Möslein Gabriele, Morak Monika, Holinski-Feder Elke, Büttner Reinhard, Aretz Stefan, Loeffler Markus, Schmiegel Wolff, Pox Christian, Schulmann Karsten, |
Characterization and Clinical Outcomes of DNA Mismatch Repair-deficient Small Bowel Adenocarcinoma. Clinical cancer research : an official journal of the American Association for Cancer Research 2020 Nov . Latham Alicia, Shia Jinru, Patel Zalak, Reidy-Lagunes Diane L, Segal Neil H, Yaeger Rona, Ganesh Karuna, Connell Louise, Kemeny Nancy E, Kelsen David P, Hechtman Jaclyn F, Nash Garrett M, Paty Philip B, Zehir Ahmet, Tkachuk Kaitlyn, Sheikh Rania, Markowitz Arnold J, Mandelker Diana, Offit Kenneth, Berger Michael F, Cercek Andrea, Garcia-Aguilar Julio, Saltz Leonard B, Weiser Martin R, Stadler Zsofia |
Lynch syndrome identification in a Brazilian cohort of endometrial cancer screened by a universal approach. Gynecologic oncology 2020 Jul . Rosa Reginaldo Cruz Alves, Santis Jessica Oliveira, Teixeira Lorena Alves, Molfetta Greice Andreotti, Dos Santos Jennifer Thalita Targino, Ribeiro Vanessa Dos Santos, Chahud Fernando, Ribeiro-Silva Alfredo, Brunaldi Mariângela Ottoboni, Silva Wilson Araújo, Ferraz Victor Evangelista de Far |
Targeted Next-Generation Sequencing of MLH1, MSH2, and MSH6 Genes in Patients with Endometrial Carcinoma under 50 Years of Age Balkan medical journal 2019 01 36 (1): 37-42. Özdemir Taha Resid, Alan Murat, Sanci Muzaffer, Koç Alt |
Rare germline alterations in cancer-related genes associated with the risk of multiple primary tumor development. Journal of molecular medicine (Berlin, Germany) 2017 Jan . Villacis Rolando A R, Basso Tatiane R, Canto Luisa M, Pinheiro Maísa, Santiago Karina M, Giacomazzi Juliana, de Paula Cláudia A A, Carraro Dirce M, Ashton-Prolla Patrícia, Achatz Maria I, Rogatto Silvia |
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 |
Genetic variants within the hTERT gene and the risk of colorectal cancer in Lynch syndrome. Genes & cancer 2015 Nov 6 (11-12): 445-51. Win Aung Ko, Clendenning Mark, Crawford William, Rosty Christophe, Preston Susan G, Southey Melissa C, Parry Susan, Giles Graham G, Macrae Finlay A, Winship Ingrid M, Baron John A, Hopper John L, Jenkins Mark A, Buchanan Daniel |
Colon and endometrial cancers with mismatch repair deficiency can arise from somatic, rather than germline, mutations. Gastroenterology 2014 Dec 147 (6): 1308-1316.e1. Haraldsdottir Sigurdis, Hampel Heather, Tomsic Jerneja, Frankel Wendy L, Pearlman Rachel, de la Chapelle Albert, Pritchard Colin |
Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients. Genetics in medicine : official journal of the American College of Medical Genetics 2014 Nov 16 (11): 830-7. LaDuca Holly, Stuenkel A J, Dolinsky Jill S, Keiles Steven, Tandy Stephany, Pesaran Tina, Chen Elaine, Gau Chia-Ling, Palmaer Erika, Shoaepour Kamelia, Shah Divya, Speare Virginia, Gandomi Stephanie, Chao Elizabe |
Design and validation of an oligonucleotide microarray for the detection of genomic rearrangements associated with common hereditary cancer syndromes. Journal of experimental & clinical cancer research : CR 2014 33 74. Mancini-DiNardo Debora, Judkins Thaddeus, Woolstenhulme Nick, Burton Collin, Schoenberger Jeremy, Ryder Matthew, Murray Adam, Gutin Natalia, Theisen Aaron, Holladay Jayson, Craft Jonathan, Arnell Christopher, Moyes Kelsey, Roa Benjam |
ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing. The Journal of molecular diagnostics : JMD 2012 Jul 14 (4): 357-66. Pritchard Colin C, Smith Christina, Salipante Stephen J, Lee Ming K, Thornton Anne M, Nord Alex S, Gulden Cassandra, Kupfer Sonia S, Swisher Elizabeth M, Bennett Robin L, Novetsky Akiva P, Jarvik Gail P, Olopade Olufunmilayo I, Goodfellow Paul J, King Mary-Claire, Tait Jonathan F, Walsh T |
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- Page last updated:Jun 22, 2022
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