Human Genome Epidemiology Literature Finder
|
Records 1 - 30 (of 35 Records) |
| Query Trace: Counseling and MSH6[original query] |
|---|
| Germline PMS2 mutation screened by mismatch repair protein immunohistochemistry of colorectal cancer in Japan. Cancer science 2016 Sep . Sugano Kokichi, Nakajima Takeshi, Sekine Shigeki, Taniguchi Hirokazu, Saito Shinya, Takahashi Masahiro, Ushiama Mineko, Sakamoto Hiromi, Yoshida Teruhi |
| Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population. Oncology reports 2016 Sep . Lagerstedt-Robinson Kristina, Rohlin Anna, Aravidis Christos, Melin Beatrice, Nordling Margareta, Stenmark-Askmalm Marie, Lindblom Annika, Nilbert M |
| A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America. BMC cancer 2017 9 17 (1): 623. Rossi Benedito Mauro, Palmero Edenir Inêz, López-Kostner Francisco, Sarroca Carlos, Vaccaro Carlos Alberto, Spirandelli Florencia, Ashton-Prolla Patricia, Rodriguez Yenni, de Campos Reis Galvão Henrique, Reis Rui Manuel, Escremim de Paula André, Capochin Romagnolo Luis Gustavo, Alvarez Karin, Della Valle Adriana, Neffa Florencia, Kalfayan Pablo German, Spirandelli Enrique, Chialina Sergio, Gutiérrez Angulo Melva, Castro-Mujica Maria Del Carmen, Sanchez de Monte Julio, Quispe Richard, da Silva Sabrina Daniela, Rossi Norma Teresa, Barletta-Carrillo Claudia, Revollo Susana, Taborga Ximena, Morillas L Lena, Tubeuf Hélène, Monteiro-Santos Erika Maria, Piñero Tamara Alejandra, Dominguez-Barrera Constantino, Wernhoff Patrik, Martins Alexandra, Hovig Eivind, Møller Pål, Dominguez-Valentin M |
| 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 |
| 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 Re?id, Alan Murat, Sanc? Muzaffer, Koç Alt |
| Impact of Patient Age on Molecular Alterations of Left-Sided Colorectal Tumors. The oncologist 2018 7 24 (3): 319-326. Puccini Alberto, Lenz Heinz-Josef, Marshall John L, Arguello David, Raghavan Derek, Korn W Michael, Weinberg Benjamin A, Poorman Kelsey, Heeke Arielle L, Philip Philip A, Shields Anthony F, Goldberg Richard M, Salem Mohamed |
| Comparison of screening strategies for Lynch syndrome in patients with newly diagnosed endometrial cancer: a prospective cohort study in China. Cancer communications (London, England) 2019 7 39 (1): 42. Chao Xiaopei, Li Lei, Wu Ming, Ma Shuiqing, Tan Xianjie, Zhong Sen, Bi Yalan, Lang Jing |
| Opportunistic testing of BRCA1, BRCA2 and mismatch repair genes improves the yield of phenotype driven hereditary cancer gene panels. International journal of cancer 2019 Mar . Feliubadaló Lídia, López-Fernández Adrià, Pineda Marta, Díez Orland, Del Valle Jesús, Gutiérrez-Enríquez Sara, Teulé Alex, González Sara, Stjepanovic Neda, Salinas Mónica, Capellá Gabriel, Brunet Joan, Lázaro Conxi, Balmaña Judith, |
| Colorectal cancer in Lynch syndrome associated with PMS2 and MSH6 mutations. International journal of colorectal disease 2019 12 35 (2): 351-353. Y?lmaz Ali, Mirili Cem, Bilici Mehmet, Tekin Salim Ba? |
| Penetrance of Colorectal Cancer Among Mismatch Repair Gene Mutation Carriers: A Meta-Analysis. JNCI cancer spectrum 2020 9 4 (5): pkaa027. Wang Cathy, Wang Yan, Hughes Kevin S, Parmigiani Giovanni, Braun Daniel |
| Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer. Genes, chromosomes & cancer 2020 7 59 (12): 697-701. Schubert Stephanie A, Ruano Dina, Tiersma Yvonne, Drost Mark, de Wind Niels, Nielsen Maartje, van Hest Liselotte P, Morreau Hans, de Miranda Noel F C C, van Wezel T |
| Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patients. Human genetics 2020 7 140 (2): 321-331. Horiuchi Yasue, Matsubayashi Hiroyuki, Kiyozumi Yoshimi, Nishimura Seiichiro, Higashigawa Satomi, Kado Nobuhiro, Nagashima Takeshi, Mizuguchi Maki, Ohnami Sumiko, Arai Makoto, Urakami Kenichi, Kusuhara Masatoshi, Yamaguchi K |
| 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 |
| Lynch Syndrome Germline Mutations in Breast Cancer: Next Generation Sequencing Case-Control Study of 1,263 Participants. Frontiers in oncology 2020 6 10 666. Nikitin Aleksey G, Chudakova Daria A, Enikeev Rafael F, Sakaeva Dina, Druzhkov Maxim, Shigapova Leyla H, Brovkina Olga I, Shagimardanova Elena I, Gusev Oleg A, Gordiev Marat |
| Gene Panel Tumor Testing in Ovarian Cancer Patients Significantly Increases the Yield of Clinically Actionable Germline Variants beyond BRCA1/BRCA2. Cancers 2020 10 12 (10): . Barbosa Ana, Pinto Pedro, Peixoto Ana, Guerra Joana, Pinto Carla, Santos Catarina, Pinheiro Manuela, Escudeiro Carla, Bartosch Carla, Silva João, Teixeira Manuel |
| Observed evidence for guideline-recommended genes in predicting prostate cancer risk from a large population-based cohort. The Prostate 2021 7 81 (13): 1002-1008. Wei Jun, Yang Wancai, Shi Zhuqing, Lu Lucy, Wang Qiang, Resurreccion W Kyle, Engelmann Valentina, Zheng S Lilly, Hulick Peter J, Cooney Kathleen A, Isaacs William B, Helfand Brian T, Lu Jim, Xu Jianfe |
| Lynch Syndrome in Thai Endometrial Cancer Patients. Asian Pacific journal of cancer prevention : APJCP 2021 5 22 (5): 1477-1483. Manchana Tarinee, Ariyasriwatana Chai, Triratanachat Surang, Phowthongkum Pras |
| A novel founder MSH2 deletion in Ethiopian Jews is mainly associated with early-onset colorectal cancer. Familial cancer 2021 4 21 (2): 181-188. Kedar I, Walsh L, Levi G Reznick, Lieberman S, Shtaya A Abu, Nathan S Naftaly, Lagovsky I, Tomashov-Matar R, Goldenberg M, Basel-Salmon L, Katz L, Aleme O, Peretz T Yablonski, Hubert A, Rothstein D, Castellvi-Bel S, Walsh T, King M C, Pritchard C C, Levi Z, Half E, Laish I, Goldberg |
| An effective algorithm to detect the possibility of being MSI phenotype in endometrial cancer given the BMI status and histological subtype: a statistical study. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2022 5 24 (9): 1809-1817. González Villa Isabel, González Dávila Enrique Francisco, Afonso Idaira Jael Expósito, Blanco Leynis Isabel Martínez, Ferrer Juan Francisco Loro, Galván Juan José Cabre |
| 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 |
| Lynch Syndrome Identification in Saudi Cohort of Endometrial Cancer Patients Screened by Universal Approach. International journal of molecular sciences 2022 10 23 (20): . Bu Rong, Siraj Abdul K, Parvathareddy Sandeep Kumar, Iqbal Kaleem, Azam Saud, Qadri Zeeshan, Al-Rasheed Maha, Haqawi Wael, Diaz Mark, Alobaisi Khadija, Annaiyappanaidu Padmanaban, Siraj Nabil, AlHusaini Hamed, Alomar Osama, Al-Badawi Ismail A, Al-Dayel Fouad, Al-Kuraya Khawla |
| 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 |
| Uncommon variants detected via hereditary cancer panel and suggestions for genetic counseling. Mutation research 2023 7 827 111831. Zeynep Özdemir, Ezgi Çevik, Ömür Berna Çakmak Öksüzo?lu, Mutlu Do?an, Öztürk Ate?, Ece Esin, ?rem Bilgetekin, Umut Demirci, Ça?lar Köseo?lu, Alper Topal, Nuri Karadurmu?, Haktan Ba??? Erdem, Taha Bah |
| Evaluation of genetic alterations in hereditary cancer susceptibility genes in the Ashkenazi Jewish women community of Mexico. Frontiers in genetics 2023 2 14 1094260. Díaz-Velásquez Clara Estela, Gitler Rina, Antoniano Adriana, Kershenovich Sefchovich Ronny, De La Cruz-Montoya Aldo Hugo, Martínez-Gregorio Héctor, Rojas-Jiménez Ernesto Arturo, Cortez Cardoso Penha Ricardo, Terrazas Luis Ignacio, Wegman-Ostrosky Talia, Levi-Lahad Ephrat, Zabaleta Jovanny, Perdomo Sandra, Vaca-Paniagua Feli |
| Association of Reported Candidate Monogenic Genes With Lung Cancer Risk. Clinical lung cancer 2023 2 . Rifkin Andrew S, Less Ethan M, Wei Jun, Shi Zhuqing, Zheng Siqun Lilly, Helfand Brian T, Hulick Peter J, Krantz Seth B, Xu Jianfe |
| Germline genetic testing reveals pathogenic variants in uterine serous carcinoma patients. Gynecologic oncology reports 2024 9 55 101498. Katelyn Tondo-Steele, Kara J Milliron, Jean H Siedel, Shitanshu Uppal, Sofia D Merajver, Karen McLe |
| Performance evaluation of predictive models for detecting MMR gene mutations associated with Lynch syndrome in cancer patients in a Chinese cohort in Taiwan. International journal of cancer 2024 7 . Fei-Hung Hung, Hung-Pin Peng, Chen-Fang Hung, Ling-Ling Hsieh, An-Suei Yang, Yong Alison Wa |
| Prevalence of Potentially Pathogenic Germline Variants Among Adult Patients in the Philippines With Solid Malignancies Who Underwent Tumor Genomic Profiling. JCO global oncology 2024 6 10 e2400019. Paula Isabel Franco, Jose Jasper Andal, Daphne Chua Ang, Frances Victoria Q |
| Multi-ethnic heterozygote frequencies of cancer susceptibility genes to inform counseling of reproductive risk. Genetics in medicine : official journal of the American College of Medical Genetics 2024 11 101246. Jacquelyn Powers, Heather Wachtel, Erica Trujillo, Heena Desai, Ryan Hausler, Laura Conway, Bradley Wubbenhorst, , , Susan M Domchek, Katherine L Nathanson, Kara N Maxwe |
| A new subtype of Lynch syndrome associated with MSH2 c.354T>A (p. Y118*) identified in a Chinese family: case report and literature review. Frontiers in genetics 2024 10 15 1440179. Lan Zhong, Wenxiang Wang, Yuanqiong Duan, Liang Song, Zhanghuan Li, Kaixuan Yang, Qintong Li, Rutie Y |
- Page last reviewed:Feb 1, 2024
- Content source: