Research
A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome
Els van Riel, Margreet GEM Ausems, Frans BL Hogervorst, Irma Kluijt, Marielle E van Gijn, Jeanne van Echtelt, Karen Scheidel-Jacobse, Eric FAM Hennekam, Rein P Stulp, Yvonne J Vos, G Johan A Offerhaus, Fred H Menko, Johan JP Gille
Hereditary Cancer in Clinical Practice 2010, 8:7 (12 August 2010)
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Research
Cancer and Lhermitte-Duclos disease are common in Cowden syndrome patients
Douglas L Riegert-Johnson, Ferga C Gleeson, Maegan Roberts, Krysta Tholen, Lauren Youngborg, Melvin Bullock, Lisa A Boardman
Hereditary Cancer in Clinical Practice 2010, 8:6 (17 June 2010)
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Research
MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer
Bente A Talseth-Palmer, Mary McPhillips, Claire Groombridge, Allan Spigelman, Rodney J Scott
Hereditary Cancer in Clinical Practice 2010, 8:5 (21 May 2010)
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Research
BRCA1 mutations in women with familial or early-onset breast cancer and BRCA2 mutations in familial cancer in Estonia
Kristiina Tamboom, Krista Kaasik, Jelena Ar avskaja, Mare Tekkel, Aili Lilleorg, Peeter Padrik, Andres Metspalu, Toomas Veidebaum
Hereditary Cancer in Clinical Practice 2010, 8:4 (9 April 2010)
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Research
Surveillance of FAP: a prospective blinded comparison of capsule endoscopy and other GI imaging to detect small bowel polyps
Paul Tescher, Finlay A Macrae, Tony Speer, Damien Stella, Robert Gibson, Jason A Tye-Din, Geeta Srivatsa, Ian T Jones, Kaye Marion
Hereditary Cancer in Clinical Practice 2010, 8:3 (4 April 2010)
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Research
High penetrances of BRCA1 and BRCA2 mutations confirmed in a prospective series
Pål Møller, Lovise Mæhle, Lars F Engebretsen, Trond Ludvigsen, Christoffer Jonsrud, Jaran Apold, Anita Vabø, Neal Clark
Hereditary Cancer in Clinical Practice 2010, 8:2 (19 January 2010)
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Research
Is no news good news? Inconclusive genetic test results in BRCA1 and BRCA2 from patients and professionals' perspectives
Audrey Ardern-Jones, Regina Kenen, Elly Lynch, Rebecca Doherty, Rosalind Eeles
Hereditary Cancer in Clinical Practice 2010, 8:1 (12 January 2010)
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Research
Cancer risk in MLH1, MSH2 and MSH6 mutation carriers; different risk profiles may influence clinical management
Dewkoemar Ramsoekh, Anja Wagner, Monique E van Leerdam, Dennis Dooijes, Carli MJ Tops, Ewout W Steyerberg, Ernst J Kuipers
Hereditary Cancer in Clinical Practice 2009, 7:17 (23 December 2009)
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Research
Penetrance of HNPCC-related cancers in a retrolective cohort of 12 large Newfoundland families carrying a MSH2 founder mutation: an evaluation using modified segregation models
Karen A Kopciuk, Yun-Hee Choi, Elena Parkhomenko, Patrick Parfrey, John McLaughlin, Jane Green, Laurent Briollais
Hereditary Cancer in Clinical Practice 2009, 7:16 (28 October 2009)
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Research
Risk perception after genetic counseling in patients with increased risk of cancer
Johanna Rantala, Ulla Platten, Gunilla Lindgren, Bo Nilsson, Brita Arver, Annika Lindblom, Yvonne Brandberg
Hereditary Cancer in Clinical Practice 2009, 7:15 (23 August 2009)
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Research
Penetrance of colorectal cancer among MLH1/MSH2 carriers participating in the colorectal cancer familial registry in Ontario
Yun-Hee Choi, Michelle Cotterchio, Gail McKeown-Eyssen, Monga Neerav, Bharati Bapat, Kevin Boyd, Steven Gallinger, John McLaughlin, Melyssa Aronson, Laurent Briollais
Hereditary Cancer in Clinical Practice 2009, 7:14 (23 August 2009)
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Research
Molecular genetics analysis of hereditary breast and ovarian cancer patients in India
Nagasamy Soumittra, Balaiah Meenakumari, Tithi Parija, Veluswami Sridevi, Karunakaran N Nancy, Rajaraman Swaminathan, Kamalalayam R Rajalekshmy, Urmila Majhi, Thangarajan Rajkumar
Hereditary Cancer in Clinical Practice 2009, 7:13 (6 August 2009)
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Case report
Unusual presentation of Lynch Syndrome
Veronica PCC Yu, Marco Novelli, Stewart J Payne, Sam Fisher, Rebecca A Barnetson, Ian M Frayling, Ann Barrett, David Goudie, Audrey Ardern-Jones, Ros Eeles, Susan Shanley
Hereditary Cancer in Clinical Practice 2009, 7:12 (3 June 2009)
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Research
Factors associated with testicular self-examination among unaffected men from multiple-case testicular cancer families
Susan T Vadaparampil, Richard P Moser, Jennifer Loud, June A Peters, Mark H Greene, Larissa Korde
Hereditary Cancer in Clinical Practice 2009, 7:11 (29 May 2009)
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Letter to the Editor
Early-onset breast cancer in a Lebanese family with Lynch syndrome due to MSH2 gene mutation
Riad Akoum, Albert Ghaoui, Emile Brihi, Maroun Ghabash, Nicolas Hajjar
Hereditary Cancer in Clinical Practice 2009, 7:10 (28 May 2009)
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Research
Australian clinicians and chemoprevention for women at high familial risk for breast cancer
Louise A Keogh, John L Hopper, Doreen Rosenthal, Kelly-Anne Phillips
Hereditary Cancer in Clinical Practice 2009, 7:9 (4 May 2009)
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Commentary
Breast cancer therapy for BRCA1 carriers: moving towards platinum standard?
Evgeny N Imyanitov
Hereditary Cancer in Clinical Practice 2009, 7:8 (20 April 2009)
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Research
Survival in Norwegian BRCA1 mutation carriers with breast cancer
Anne Irene Hagen, Steinar Tretli, Lovise Mæhle, Jaran Apold, Nina Vedå, Pål Møller
Hereditary Cancer in Clinical Practice 2009, 7:7 (14 April 2009)
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Research
Standard psychological consultations and follow up for women at increased risk of hereditary breast cancer considering prophylactic mastectomy
Murly BM Tan, Eveline MA Bleiker, Marian BE Menke-Pluymers, Arthur R Van Gool, Silvia van Dooren, Bert N Van Geel, Madeleine MA Tilanus-Linthorst, Karina CM Bartels, Jan GM Klijn, Cecile TM Brekelmans, Caroline Seynaeve
Hereditary Cancer in Clinical Practice 2009, 7:6 (31 March 2009)
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Research
High frequency of BRCA1, but not CHEK2 or NBS1 (NBN), founder mutations in Russian ovarian cancer patients
Evgeny N Suspitsin, Nathalia Yu Sherina, Daria N Ponomariova, Anna P Sokolenko, Aglaya G Iyevleva, Tatyana V Gorodnova, Olga A Zaitseva, Olga S Yatsuk, Alexandr V Togo, Nathalia N Tkachenko, Grigory A Shiyanov, Oksana S Lobeiko, Nadezhda Yu Krylova, Dmitry E Matsko, Sergey Ya Maximov, Adel F Urmancheyeva, Nathalia V Porhanova, Evgeny N Imyanitov
Hereditary Cancer in Clinical Practice 2009, 7:5 (25 February 2009)
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