Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 36 Records) |
Query Trace: Counseling and MSH2[original query] |
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Lynch Syndrome in high risk Ashkenazi Jews in Israel. Familial cancer 2013 Aug . Goldberg Y, Kedar I, Kariiv R, Halpern N, Plesser M, Hubert A, Kaduri L, Sagi M, Lerer I, Abeliovich D, Hamburger T, Nissan A, Goldshmidt H, Solar I, Geva R, Strul H, Rosner G, Baris H, Levi Z, Peretz T |
Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2-negative patients with early-onset breast cancer. Genetics in medicine : official journal of the American College of Medical Genetics 2015 Aug 17 (8): 630-8. Maxwell Kara N, Wubbenhorst Bradley, D'Andrea Kurt, Garman Bradley, Long Jessica M, Powers Jacquelyn, Rathbun Katherine, Stopfer Jill E, Zhu Jiajun, Bradbury Angela R, Simon Michael S, DeMichele Angela, Domchek Susan M, Nathanson Katherine |
Genetic features of Lynch syndrome in the Israeli population. Clinical genetics 2015 Jun 87 (6): 549-53. Goldberg Y, Barnes-Kedar I, Lerer I, Halpern N, Plesser M, Hubert A, Kadouri L, Goldshmidt H, Solar I, Strul H, Rosner G, Baris H N, Peretz T, Levi Z, Kariv |
Identification of germline genetic mutations in patients with pancreatic cancer. Cancer 2015 Oct . Salo-Mullen Erin E, O'Reilly Eileen M, Kelsen David P, Ashraf Asad M, Lowery Maeve A, Yu Kenneth H, Reidy Diane L, Epstein Andrew S, Lincoln Anne, Saldia Amethyst, Jacobs Lauren M, Rau-Murthy Rohini, Zhang Liying, Kurtz Robert C, Saltz Leonard, Offit Kenneth, Robson Mark E, Stadler Zsofia |
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 |
Prevalence of Lynch syndrome in unselected patients with endometrial or ovarian cancer. Archives of gynecology and obstetrics 2016 Nov 294 (6): 1299-1303. Kast Karin, Dobberschütz Catharina, Sadowski Carolin Eva, Pistorius Steffen, Wimberger Pauli |
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 |
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 |
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 |
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 |
HPV nonrelated endocervical adenocarcinoma in hereditary cancer syndromes. Tumori 2020 7 106 (6): NP67-NP72. Carnevali Ileana, Di Lauro Eleonora, Pensotti Valeria, Sahnane Nora, Leoni Eleonora, Formenti Giorgio, Ghezzi Fabio, Sessa Fausto, Tibiletti Maria Graz |
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 |
[A Case of High-Frequency Microsatellite Instability in Colorectal Cancer with MSH2 Mutation Detected Using Gene Panel Testing with a Next-Generation Sequencer]. Gan to kagaku ryoho. Cancer & chemotherapy 2020 7 47 (7): 1113-1115. Shimada Yoshifumi, Kameyama Hitoshi, Nakano Mae, Toshikawa Chie, Moro Kazuki, Tsuchida Junko, Arabiki Michiru, Matsumoto Akio, Tanaka Kana, Abe Kaoru, Oyanagi Hidehito, Tajima Yosuke, Nakano Masato, Hirose Yuki, Kano Yosuke, Ichikawa Hiroshi, Hanyu Takaaki, Takizawa Kazuyasu, Nagahashi Masayuki, Sakata Jun, Wakai Toshifu |
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 |
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma. JAMA oncology 2020 Mar . Mirabello Lisa, Zhu Bin, Koster Roelof, Karlins Eric, Dean Michael, Yeager Meredith, Gianferante Matthew, Spector Logan G, Morton Lindsay M, Karyadi Danielle, Robison Leslie L, Armstrong Gregory T, Bhatia Smita, Song Lei, Pankratz Nathan, Pinheiro Maisa, Gastier-Foster Julie M, Gorlick Richard, de Toledo Silvia Regina Caminada, Petrilli Antonio S, Patino-Garcia Ana, Lecanda Fernando, Gutierrez-Jimeno Miriam, Serra Massimo, Hattinger Claudia, Picci Piero, Scotlandi Katia, Flanagan Adrienne M, Tirabosco Roberto, Amary Maria Fernanda, Kurucu Nilgün, Ilhan Inci Ergurhan, Ballinger Mandy L, Thomas David M, Barkauskas Donald A, Mejia-Baltodano Gerardo, Valverde Patricia, Hicks Belynda D, Zhu Bin, Wang Mingyi, Hutchinson Amy A, Tucker Margaret, Sampson Joshua, Landi Maria T, Freedman Neal D, Gapstur Susan, Carter Brian, Hoover Robert N, Chanock Stephen J, Savage Sharon |
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 |
Multigene Panel Testing in Turkish Hereditary Cancer Syndrome Patients. Medeniyet medical journal 2022 6 37 (2): 150-158. Arslan Ates Esra, Turkyilmaz Ayberk, Alavanda Ceren, Yildirim Ozlem, Guney Ahmet Ilt |
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 |
Hereditary Gastric Cancer: Single-Gene or Multigene Panel Testing? A Mono-Institutional Experience. Genes 2023 5 14 (5): . Mariarosaria Calvello, Monica Marabelli, Sara Gandini, Elena Marino, Loris Bernard, Matteo Dal Molin, Giulia Di Cola, Cristina Zanzottera, Giovanni Corso, Nicola Fazio, Lorenzo Gervaso, Uberto Fumagalli Romario, Massimo Barberis, Aliana Guerrieri-Gonzaga, Lucio Bertario, Davide Serrano, Bernardo Bonan |
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 |
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- Page last updated:Apr 22, 2024
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