Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 45 Records) |
| Query Trace: Counseling and ATM[original query] |
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| Mutational profile of hereditary breast and ovarian cancer - Establishing genetic testing guidelines in a developing country. Current problems in cancer 2021 7 46 (1): 100767. Krivokuca Ana, Mihajlovic Milica, Susnjar Snezana, Spasojevic Ivana Bozovic, Minic Ivana, Popovic Lazar, Brankovic-Magic Mirja |
| 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 |
| Pathogenic Germline Variants in Cancer Susceptibility Genes in Children and Young Adults With Rhabdomyosarcoma. JCO precision oncology 2021 5 . Kim Jung, Light Nicholas, Subasri Vallijah, Young Erin L, Wegman-Ostrosky Talia, Barkauskas Donald A, Hall David, Lupo Philip J, Patidar Rajesh, Maese Luke D, Jones Kristine, Wang Mingyi, Tavtigian Sean V, Wu Dongjing, Shlien Adam, Telfer Frank, Goldenberg Anna, Skapek Stephen X, Wei Jun S, Wen Xinyu, Catchpoole Daniel, Hawkins Douglas S, Schiffman Joshua D, Khan Javed, Malkin David, Stewart Douglas |
| Genetic Variants in Patients With a Family History of Pancreatic Cancer: Impact of Multigene Panel Testing. Pancreas 2021 5 50 (4): 602-606. Zhu Huili, Welinsky Sara, Soper Emily R, Brown Karen L, Abul-Husn Noura S, Lucas Aimee |
| Germline molecular data in hereditary breast cancer in Brazil: Lessons from a large single-center analysis. PloS one 2021 2 16 (2): e0247363. Sandoval Renata Lazari, Leite Ana Carolina Rathsam, Barbalho Daniel Meirelles, Assad Daniele Xavier, Barroso Romualdo, Polidorio Natalia, Dos Anjos Carlos Henrique, de Miranda Andréa Discaciati, Ferreira Ana Carolina Salles de Mendonça, Fernandes Gustavo Dos Santos, Achatz Maria Isab |
| Clinical Impact of Pathogenic Germline Variants in Pancreatic Cancer: Results From a Multicenter, Prospective, Universal Genetic Testing Study. Clinical and translational gastroenterology 2021 Oct 12 (10): e00414. Uson Pedro L S, Samadder N Jewel, Riegert-Johnson Douglas, Boardman Lisa, Borad Mitesh J, Ahn Daniel, Sonbol Mohamad B, Faigel Douglas O, Fukami Norio, Pannala Rahul, Kunze Katie, Golafshar Michael, Klint Margaret, Esplin Edward D, Nussbaum Robert L, Stewart A Keith, Bekaii-Saab Tani |
| Germline Variants Identified in Patients with Early-onset Renal Cell Carcinoma Referred for Germline Genetic Testing. European urology oncology 2021 10 4 (6): 993-1000. Truong Hong, Sheikh Rania, Kotecha Ritesh, Kemel Yelena, Reisz Peter A, Lenis Andrew T, Mehta Nikita N, Khurram Aliya, Joseph Vijai, Mandelker Diana, Latham Alicia, Ceyhan-Birsoy Ozge, Ladanyi Marc, Shah Neil J, Walsh Michael F, Voss Martin H, Lee Chung-Han, Russo Paul, Coleman Jonathan A, Hakimi A Ari, Feldman Darren R, Stadler Zsofia K, Robson Mark E, Motzer Robert J, Offit Kenneth, Patil Sujata, Carlo Maria |
| Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women. The New England journal of medicine 2021 Jan . , Dorling Leila, Carvalho Sara, Allen Jamie, González-Neira Anna, Luccarini Craig, Wahlström Cecilia, Pooley Karen A, Parsons Michael T, Fortuno Cristina, Wang Qin, Bolla Manjeet K, Dennis Joe, Keeman Renske, Alonso M Rosario, Álvarez Nuria, Herraez Belen, Fernandez Victoria, Núñez-Torres Rocio, Osorio Ana, Valcich Jeanette, Li Minerva, Törngren Therese, Harrington Patricia A, Baynes Caroline, Conroy Don M, Decker Brennan, Fachal Laura, Mavaddat Nasim, Ahearn Thomas, Aittomäki Kristiina, Antonenkova Natalia N, Arnold Norbert, Arveux Patrick, Ausems Margreet G E M, Auvinen Päivi, Becher Heiko, Beckmann Matthias W, Behrens Sabine, Bermisheva Marina, Bia?kowska Katarzyna, Blomqvist Carl, Bogdanova Natalia V, Bogdanova-Markov Nadja, Bojesen Stig E, Bonanni Bernardo, Børresen-Dale Anne-Lise, Brauch Hiltrud, Bremer Michael, Briceno Ignacio, Brüning Thomas, Burwinkel Barbara, Cameron David A, Camp Nicola J, Campbell Archie, Carracedo Angel, Castelao Jose E, Cessna Melissa H, Chanock Stephen J, Christiansen Hans, Collée J Margriet, Cordina-Duverger Emilie, Cornelissen Sten, Czene Kamila, Dörk Thilo, Ekici Arif B, Engel Christoph, Eriksson Mikael, Fasching Peter A, Figueroa Jonine, Flyger Henrik, Försti Asta, Gabrielson Marike, Gago-Dominguez Manuela, Georgoulias Vassilios, Gil Fabian, Giles Graham G, Glendon Gord, Garcia Encarna B Gómez, Alnæs Grethe I Grenaker, Guénel Pascal, Hadjisavvas Andreas, Haeberle Lothar, Hahnen Eric, Hall Per, Hamann Ute, Harkness Elaine F, Hartikainen Jaana M, Hartman Mikael, He Wei, Heemskerk-Gerritsen Bernadette A M, Hillemanns Peter, Hogervorst Frans B L, Hollestelle Antoinette, Ho Weang Kee, Hooning Maartje J, Howell Anthony, Humphreys Keith, Idris Faiza, Jakubowska Anna, Jung Audrey, Kapoor Pooja Middha, Kerin Michael J, Khusnutdinova Elza, Kim Sung-Won, Ko Yon-Dschun, Kosma Veli-Matti, Kristensen Vessela N, Kyriacou Kyriacos, Lakeman Inge M M, Lee Jong Won, Lee Min Hyuk, Li Jingmei, Lindblom Annika, Lo Wing-Yee, Loizidou Maria A, Lophatananon Artitaya, Lubi?ski Jan, MacInnis Robert J, Madsen Michael J, Mannermaa Arto, Manoochehri Mehdi, Manoukian Siranoush, Margolin Sara, Martinez Maria Elena, Maurer Tabea, Mavroudis Dimitrios, McLean Catriona, Meindl Alfons, Mensenkamp Arjen R, Michailidou Kyriaki, Miller Nicola, Mohd Taib Nur Aishah, Muir Kenneth, Mulligan Anna Marie, Nevanlinna Heli, Newman William G, Nordestgaard Børge G, Ng Pei-Sze, Oosterwijk Jan C, Park Sue K, Park-Simon Tjoung-Won, Perez Jose I A, Peterlongo Paolo, Porteous David J, Prajzendanc Karolina, Prokofyeva Darya, Radice Paolo, Rashid Muhammad U, Rhenius Valerie, Rookus Matti A, Rüdiger Thomas, Saloustros Emmanouil, Sawyer Elinor J, Schmutzler Rita K, Schneeweiss Andreas, Schürmann Peter, Shah Mitul, Sohn Christof, Southey Melissa C, Surowy Harald, Suvanto Maija, Thanasitthichai Somchai, Tomlinson Ian, Torres Diana, Truong Thérèse, Tzardi Maria, Valova Yana, van Asperen Christi J, Van Dam Rob M, van den Ouweland Ans M W, van der Kolk Lizet E, van Veen Elke M, Wendt Camilla, Williams Justin A, Yang Xiaohong R, Yoon Sook-Yee, Zamora M Pilar, Evans D Gareth, de la Hoya Miguel, Simard Jacques, Antoniou Antonis C, Borg Åke, Andrulis Irene L, Chang-Claude Jenny, García-Closas Montserrat, Chenevix-Trench Georgia, Milne Roger L, Pharoah Paul D P, Schmidt Marjanka K, Spurdle Amanda B, Vreeswijk Maaike P G, Benitez Javier, Dunning Alison M, Kvist Anders, Teo Soo H, Devilee Peter, Easton Douglas |
| ATM c.7570G>C is a high-risk allele for breast cancer. International journal of cancer 2022 9 152 (3): 429-435. Kankuri-Tammilehto Minna, Tervasmäki Anna, Kraatari-Tiri Minna, Rahikkala Elisa, Pylkäs Katri, Kuismin Ou |
| 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 Cancer Risk in Women from Ghana Carrying Rare Germline Pathogenic Mutations. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2022 Jun . Ahearn Thomas U, Choudhury Parichoy Pal, Derkach Andriy, Wiafe-Addai Beatrice, Awuah Baffour, Yarney Joel, Edusei Lawrence, Titiloye Nicholas, Adjei Ernest, Vanderpuye Verna, Aitpillah Francis, Dedey Florence, Oppong Joseph, Osei-Bonsu Ernest Baawuah, Duggan Máire A, Brinton Louise A, Allen Jamie, Luccarini Craig, Baynes Caroline, Carvalho Sara, Dunning Alison M, Davis Lynn Brittny C, Chanock Stephen J, Hicks Belynda D, Yeager Meredith, Chatterjee Nilanjan, Biritwum Richard, Clegg-Lamptey Joe Nat, Nyarko Kofi, Wiafe Seth, Ansong Daniel, Easton Douglas F, Figueroa Jonine D, Garcia-Closas Montserr |
| Germline Pathogenic Variants Impact Clinicopathology of Advanced Lung Cancer. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2022 4 31 (7): 1450-1459. Mukherjee Semanti, Bandlamudi Chaitanya, Hellmann Matthew D, Kemel Yelena, Drill Esther, Rizvi Hira, Tkachuk Kaitlyn, Khurram Aliya, Walsh Michael F, Zauderer Marjorie G, Mandelker Diana, Topka Sabine, Zehir Ahmet, Srinivasan Preethi, Esai Selvan Myvizhi, Carlo Maria I, Cadoo Karen A, Latham Alicia, Hamilton Jada G, Liu Ying L, Lipkin Steven M, Belhadj Sami, Bond Gareth L, Gümü? Zeynep H, Klein Robert J, Ladanyi Marc, Solit David B, Robson Mark E, Jones David R, Kris Mark G, Vijai Joseph, Stadler Zsofia K, Amos Christopher I, Taylor Barry S, Berger Michael F, Rudin Charles M, Offit Kenne |
| Double heterozygous mutation in RAD50 and ATM genes in a Peruvian family with five cancer types: a case report. Revista de la Facultad de Ciencias Medicas (Cordoba, Argentina) 2022 3 79 (1): 53-56. Sánchez Castro Enrique Eduardo, Ziegler-Rodriguez Gonzalo, Castro Mujica María Del Carm |
| 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 |
| 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 |
| Frequency of germline pathogenic variants in breast cancer predisposition genes among young Turkish breast cancer patients. Breast cancer research and treatment 2023 8 . Aysun Dauti Isiklar, Lamiya Aliyeva, Ahmet Yesilyurt, Aykut Soyder, Gul Basar |
| 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 |
| New pathogenic germline variants identified in mesothelioma. Lung cancer (Amsterdam, Netherlands) 2023 3 179 107172. Belcaid Laila, Bertelsen Birgitte, Wadt Karin, Tuxen Ida, Spanggaard Iben, Højgaard Martin, Benn Sørensen Jens, Ravn Jesper, Lassen Ulrik, Cilius Nielsen Finn, Rohrberg Kristoffer, Westmose Yde Christi |
| 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 |
| Breast cancers in monoallelic MUTYH germline mutation carriers have clinicopathological features overlapping with those in BRCA1 germline mutation carriers. Breast cancer research and treatment 2023 12 . Aysenur Keske, Paul Weisman, Monica Ospina-Romero, Prachi Raut, Kelcy Smith-Simmer, Anna L Zakas, Christopher Flynn, Jin |
| Characteristics of familial pancreatic cancer families with additional colorectal carcinoma. Familial cancer 2023 1 . Lehman Bettina, Matthäi Elvira, Gercke Norman, Denzer Ulrike W, Figiel Jens, Hess Timo, Slater Emily P, Bartsch Detlef |
| 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 |
| Clinical implications of the family history in patients with lung cancer: a systematic review of the literature and a new cross-sectional/prospective study design (FAHIC: lung). Journal of translational medicine 2024 7 22 (1): 714. Fabrizio Citarella, Kazuki Takada, Priscilla Cascetta, Pierfilippo Crucitti, Roberta Petti, Bruno Vincenzi, Giuseppe Tonini, Francesco M Venanzi, Alessandra Bulotta, Sara Oresti, Carlo Greco, Sara Ramella, Lucio Crinò, Angelo Delmonte, Roberto Ferrara, Massimo Di Maio, Fiorella Gurrieri, Alessio Cortelli |
| Germline mutations of breast cancer susceptibility genes through expanded genetic analysis in unselected Colombian patients. Human genomics 2024 6 18 (1): 68. Diana Carolina Sierra-Díaz, Adrien Morel, Dora Janeth Fonseca-Mendoza, Nora Contreras Bravo, Nicolas Molano-Gonzalez, Mariana Borras, Isabel Munevar, Mauricio Lema, Henry Idrobo, Daniela Trujillo, Norma Serrano, Ana Isabel Orduz, Diego Lopera, Jaime González, Gustavo Rojas, Paula Londono-De Los Ríos, Ray Manneh, Rodrigo Cabrera, Wilson Rubiano, Jairo de la Peña, María Catalina Quintero, William Mantilla, Carlos M Restre |
| Targeted genotyping for recurring variants in cancer susceptibility genes in non-Ashkenazi Jewish patients with breast cancer diagnosed ?50 years. Cancer 2024 4 . Rinat Bernstein-Molho, Narmeen Abu Shhada, Yael Laitman, Iris Netzer, Shelley Shoval, Eitan Friedm |
| Cancer burden in individuals with single versus double pathogenic variants in cancer susceptibility genes. Genetics in medicine open 2024 12 2 101829. Nihat B Agaoglu, Brittany L Bychkovsky, Carolyn Horton, Min-Tzu Lo, Linda Polfus, Cassidy Carraway, Parichehr Hemyari, Colin Young, Marcy E Richardson, Rochelle Scheib, Judy E Garber, Huma Q Ra |
| Germline Variant Spectrum in Southern Italian High-Risk Hereditary Breast Cancer Patients: Insights from Multi-Gene Panel Testing. Current issues in molecular biology 2024 11 46 (11): 13003-13020. Valentina Rocca, Elisa Lo Feudo, Francesca Dinatolo, Serena Marianna Lavano, Anna Bilotta, Rosario Amato, Lucia D'Antona, Francesco Trapasso, Francesco Baudi, Emma Colao, Nicola Perrotti, Francesco Paduano, Rodolfo Iulia |
| 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 |
| Genetic Risk Factors for Early-Onset Merkel Cell Carcinoma. JAMA dermatology 2024 1 . Noreen Mohsin, Devin Hunt, Jia Yan, Austin J Jabbour, Paul Nghiem, Jaehyuk Choi, Yue Zhang, Alexandra F Freeman, Jenna R E Bergerson, Stefania Dell'Orso, Kristina Lachance, Rima Kulikauskas, Loren Collado, Wenjia Cao, Justin Lack, Morgan Similuk, Bryce A Seifert, Rajarshi Ghosh, Magdalena A Walkiewicz, Isaac Browne |
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