Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Counseling and STK11[original query] |
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| STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome. Human mutation 2014 Jul 35 (7): 851-8. Wang Zhiqing, Wu Baoping, Mosig Rebecca A, Chen Yulan, Ye Fei, Zhang Yali, Gong Wei, Gong Lanbo, Huang Fei, Wang Xinying, Nie Biao, Zheng Haoxuan, Cui Miao, Wang Yadong, Wang Juan, Chen Chudi, Polydorides Alexandros D, Zhang David Y, Martignetti John A, Jiang |
| Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond. JAMA oncology 2015 Apr 1 (1): 23-32. Hansford Samantha, Kaurah Pardeep, Li-Chang Hector, Woo Michelle, Senz Janine, Pinheiro Hugo, Schrader Kasmintan A, Schaeffer David F, Shumansky Karey, Zogopoulos George, Santos Teresa Almeida, Claro Isabel, Carvalho Joana, Nielsen Cydney, Padilla Sarah, Lum Amy, Talhouk Aline, Baker-Lange Katie, Richardson Sue, Lewis Ivy, Lindor Noralane M, Pennell Erin, MacMillan Andree, Fernandez Bridget, Keller Gisella, Lynch Henry, Shah Sohrab P, Guilford Parry, Gallinger Steven, Corso Giovanni, Roviello Franco, Caldas Carlos, Oliveira Carla, Pharoah Paul D P, Huntsman David |
| Prevalence of deleterious germline variants in risk genes including BRCA1/2 in consecutive ovarian cancer patients (AGO-TR-1). PloS one 2017 10 12 (10): e0186043. Harter Philipp, Hauke Jan, Heitz Florian, Reuss Alexander, Kommoss Stefan, Marmé Frederik, Heimbach André, Prieske Katharina, Richters Lisa, Burges Alexander, Neidhardt Guido, de Gregorio Nikolaus, El-Balat Ahmed, Hilpert Felix, Meier Werner, Kimmig Rainer, Kast Karin, Sehouli Jalid, Baumann Klaus, Jackisch Christian, Park-Simon Tjoung-Won, Hanker Lars, Kröber Sandra, Pfisterer Jacobus, Gevensleben Heidrun, Schnelzer Andreas, Dietrich Dimo, Neunhöffer Tanja, Krockenberger Mathias, Brucker Sara Y, Nürnberg Peter, Thiele Holger, Altmüller Janine, Lamla Josefin, Elser Gabriele, du Bois Andreas, Hahnen Eric, Schmutzler Ri |
| Prenatal diagnosis in a hereditary Peutz-Jeghers syndrome family with high cancer risk. BMC medical genetics 2018 5 19 (1): 66. Wang Zhiqing, Liu Shu, Liu Siping, Wang Yadong, Chen Junsheng, Wu Baopi |
| High risk and early onset of cancer in Chinese patients with Peutz-Jeghers syndrome. Frontiers in oncology 2022 8 12 900516. Wang Zhiqing, Wang Zhi, Wang Ying, Wu Jianhua, Yu Zonglin, Chen Chudi, Chen Junsheng, Wu Baoping, Chen |
| 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 |
| Preimplantation genetic testing in two Danish couples affected by Peutz-Jeghers syndrome. Scandinavian journal of gastroenterology 2022 10 58 (3): 314-318. Byrjalsen Anna, Roos Laura, Diemer Tue, Karstensen John Gásdal, Løssl Kristine, Jelsig Anne Mar |
| Molecular characteristics of young-onset colorectal cancer in Vietnamese patients. Asia-Pacific journal of clinical oncology 2022 Jan . Do Minh Duc, Nguyen Thinh Huu, Le Khuong Thai, Le Linh Hoang Gia, Nguyen Bac Hoang, Le Kien Trung, Doan Thao Phuong Thi, Ho Chuong Quoc, Nguyen Hoai-Nghia, Tran Tuan Diep, Vu Hoang A |
| Universal Genetic Testing for Newly Diagnosed Invasive Breast Cancer. JAMA network open 2024 9 7 (9): e2431427. Zoulikha Rezoug, Stephanie P Totten, David Szlachtycz, Adrienne Atayan, Kristen Mohler, Sophie Albert, Leila Feng, Brianna Lemieux Anglin, Zhen Shen, Daniel Jimenez, Nancy Hamel, Nicholas Meti, Khashayar Esfahani, Jean-François Boileau, Ipshita Prakash, Mark Basik, Sarkis Meterissian, Francine Tremblay, David Fleiszer, Dawn Anderson, George Chong, Stephanie M Wong, William D Foulk |
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