German National Case Collection for familial pancreatic Cancer (FaPaCa) - acceptance and psychological aspects of a pancreatic cancer screening program

by Frederike S. Franke, Elvira Matthäi, Emily P. Slater, Christoph Schicker, Johannes Kruse, Detlef K. Bartsch
Published 2018-11-01

The prevalence of hereditary hemorrhagic telangiectasia in Juvenile Polyposis syndrome patients with <it>SMAD4</it> mutations

by O’Malley Margaret, LaGuardia Lisa, Kalady Matthew, Parambil Joe, Leach Brandie, Eng Charis, Church James, Burke Carol
Published 2011-03-01

Awareness and uptake of genetic testing among individuals at-risk for hereditary colon cancer

by Lowery Jan T, Marcus Al, Horick Nora, Finkelstein Dianne, Ahnen Dennis J
Published 2011-03-01

High frequency of pathogenic non-founder germline mutations in BRCA1 and BRCA2 in families with breast and ovarian cancer in a founder population

by J. Maksimenko, A. Irmejs, G. Trofimovičs, D. Bērziņa, E. Skuja, G. Purkalne, E. Miklaševičs, J. Gardovskis
Published 2018-06-01

BRCA mutation screening and patterns among high-risk Lebanese subjects

by Chantal Farra, Christelle Dagher, Rebecca Badra, Miza Salim Hammoud, Raafat Alameddine, Johnny Awwad, Muhieddine Seoud, Jaber Abbas, Fouad Boulos, Nagi El Saghir, Deborah Mukherji
Published 2019-01-01

Meeting abstracts from the Annual Conference on Hereditary Cancers 2015

by Ella R. Thompson, Michelle Wong-Brown, Simone M. Rowley, Susan Dooley, Na Lil, Michael Hipwell, Simone McInerny, Cliff Meldrum, Lisa Devereux, David Mossman, Alison H. Trainer, Briar-Rose Millar, Gillian Mitchell, Cate Smith, Paul A. James, Ian G. Campbell, Rodney J. Scott, Katarzyna Klonowska, Anna Jakubowska, Jelena Maksimenko, Arvids Irmejs, Miki Nakazawa-Miklasevica, Inga Melbarde-Gorkusa, Genadijs Trofimovics, Janis Gardovskis, Edvins Miklasevics, Karolina Tęcza, Jolanta Pamuła-Piłat, Joanna Łanuszewska, Ewa Grzybowska, Edvins Miklasevics, M. Szwiec, J. Tomiczek-Szwiec, M. Gełej, C. Cybulski, T. Huzarski, E. Kilar, Małgorzata Oczko-Wojciechowska, Michał Świerniak, Jolanta Krajewska, Małgorzata Kowalska, Tomasz Tyszkiewicz, Agnieszka Pawlaczek, Michał Jarząb, Monika Kowal, Dagmara Rusinek, Jadwiga Zebracka-Gala, Agnieszka Czarniecka, Barbara Jarzab, Andrzej Plawski, Paweł Borun, Joanna Szczepinska, Monika Siolek, Beata Kozak-Klonowska, Katarzyna Kaczmarek, Magdalena Muszyńska, Wojciech Marciniak, Grzegorz Sukiennicki, Marcin Lener, Katarzyna Durda, Katarzyna Jaworska-Bieniek, Tomasz Gromowski, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Oleg Oszurek, Cezary Cybulski, Tadeusz Dębniak, Antoni Morawski, Anna Jakubowska, Jan Lubiński, Grzegorz Sukiennicki, Magdalena Muszyńska, Wojciech Marciniak, Katarzyna Kaczmarek, Marcin Lener, Katarzyna Durda, Katarzyna Jaworska-Bieniek, Tomasz Gromowski, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Oleg Oszurek, Cezary Cybulski, Tadeusz Dębniak, Antoni Morawski, Anna Jakubowska, Jan Lubiński, Michał Post
Published 2017-10-01

Functional polymorphisms in the TERT promoter are associated with risk of serious ovarian and breast cancer

by Beesley Jonathan, Pickett Hilda, Johnatty Sharon, Chen Xiaoqing, Li Jun, Rider David, Stutz Michael, Lambrecht Diether, Chang-Claude Jenny, Dork Thilo, Goodman Marc, Kiemmney Bart, Bandera Elisa, Kelemen Linda, Wang-Gorke Shan, Campbell Ian, Gayther Simon, Ramus Susan, Goode Ellen, Reddel Roger, Chenevix-Trench Georgia
Published 2012-04-01

Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (F...

by Marta Ramírez-Calvo, Zaida García-Casado, Antonio Fernández-Serra, Inmaculada de Juan, Sarai Palanca, Silvestre Oltra, José Luis Soto, Adela Castillejo, Víctor M Barbera, Ma José Juan-Fita, Ángel Segura, Isabel Chirivella, Ana Beatriz Sánchez, Isabel Tena, Carolina Chaparro, Dolores Salas, José Antonio López-Guerrero
Published 2019-01-01

A qualitative study of barriers to genetic counseling and potential for mobile technology education among women with ovarian cancer

by Rachel Isaksson Vogel, Kristin Niendorf, Heewon Lee, Sue Petzel, Hee Yun Lee, Melissa A. Geller
Published 2018-07-01

Linkage to chromosome 2q32.2-q35 in families with serrated neoplasia

by Roberts Aedan, Nancarrow Derek, Buchanan Daniel D, Clendenning Mark, Duggan David, McKeone Diane, Walters Rhiannon, Walsh Michael D, Young Bruce W, Jass Jeremy R, Young Joanne P
Published 2010-05-01

Motivators and barriers of tamoxifen use as risk-reducing medication amongst women at increased breast cancer risk: a systematic literature review

by B. Meiser, W. K. T. Wong, M. Peate, C. Julian-Reynier, J. Kirk, G. Mitchell
Published 2017-09-01

A Lowering of Breast and Ovarian Cancer Risk in Women with a BRCA1 Mutation by Selenium Supplementation of Diet

by Huzarski Tomasz, Byrski Tomasz, Gronwald Jacek, Kowalska Elżbieta, Zajączek Stanisław, Górski Bohdan, Huzarska Jowita, Cybulski Cezary, Narod Steven A, Lubiński Jan
Published 2006-01-01

Von Hippel-Lindau Disease

by Hes Frederik J, Höppener Jo WM, Luijt Rob, Lips Cornelis JM
Published 2005-11-01

ARLTS1 polymorphisms and basal cell carcinoma of the skin

by Li Xuchen, Gast Andreas, Rudnai Peter, Gurzau Eugene, Koppova Kvetoslava, Hemminki Kari, Kumar Rajiv
Published 2007-03-01

Validation study of risk prediction models for female relatives of Australian women with breast cancer

by MacInnis R, Dite G, Bickerstaffe A, Dowty J, Aujard K, Apicella C, Phillips K, Weideman P, Hopper J
Published 2012-04-01

Pathological diagnosis of ovarian cancer

by High Hilda, Friedlander Michael
Published 2012-04-01

A Counselling Model for BRCA1/2 Genetic Susceptibility Testing

by van Oostrom Iris, Tibben Aad
Published 2004-02-01

Comparison of family health history to personal genomic screening for risk assessment of colon cancer

by Heald Brandie, Eng Charis
Published 2011-03-01

Childhood Adrenocortical Tumours: a Review

by Marques-Pereira Rosana, DeLacerda Luiz, Lacerda Hadriano M, Michalkiewicz Edson, Sandrini Fabiano, Sandrini Romolo
Published 2006-05-01

Encyclopaedia of tumour-associated familial disorders. Part I: from AIMAH to CHIME syndrome

by Sijmons Rolf H
Published 2008-02-01