Editorial
Hereditary Cancer in Clinical Practice transfers to BioMed Central
Jan Lubi ski, Rolf H Sijmons, Rodney J Scott
Hereditary Cancer in Clinical Practice 2009, 7:1 (26 January 2009)
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Case report
Large family with both parents affected by distinct BRCA1 mutations: implications for genetic testing
Anna P Sokolenko, Dmitry A Voskresenskiy, Aglaya G Iyevleva, Elena M Bit-Sava, Nadezhda I Gutkina, Maxim S Anisimenko, Nathalia Yu Sherina, Nathalia V Mitiushkina, Yulia M Ulibina, Olga S Yatsuk, Olga A Zaitseva, Evgeny N Suspitsin, Alexandr V Togo, Valery A Pospelov, Sergey P Kovalenko, Vladimir F Semiglazov, Evgeny N Imyanitov
Hereditary Cancer in Clinical Practice 2009, 7:2 (26 January 2009)
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Research
Genetic variants in MUTYH are not associated with endometrial cancer risk
Katie A Ashton, Anthony Proietto, Geoffrey Otton, Ian Symonds, Rodney J Scott
Hereditary Cancer in Clinical Practice 2009, 7:3 (26 January 2009)
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Research
The contribution of CHEK2 to the TP53-negative Li-Fraumeni phenotype
Marielle WG Ruijs, Annegien Broeks, Fred H Menko, Margreet GEM Ausems, Anja Wagner, Rogier Oldenburg, Hanne Meijers-Heijboer, Laura J van't Veer, Senno Verhoef
Hereditary Cancer in Clinical Practice 2009, 7:4 (17 February 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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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
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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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
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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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
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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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
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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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
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 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
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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