1. BRCA1 and BRCA2 families and the risk of skin cancer

   • Ophira M. Ginsburg
   • Charmaine Kim-Sing
   • Hereditary Breast Cancer Clinical Study Group

   OriginalPaper 01 September 2010 Pages: 489 - 493

2. Predicting BRCA1 and BRCA2 gene mutation carriers: comparison of PENN II model to previous study

   • Noralane M. Lindor
   • Kiley J. Johnson
   • Fergus Couch

   OriginalPaper 29 May 2010 Pages: 495 - 502

   

3. Breast cancer susceptibility variants alter risk in familial ovarian cancer

   • A. Latif
   • H. J. McBurney
   • W. G. Newman

   OriginalPaper 26 May 2010 Pages: 503 - 506

4. Comprehensive BRCA1 and BRCA2 mutation analyses and review of French Canadian families with at least three cases of breast cancer

   • Luca Cavallone
   • Suzanna L. Arcand
   • Patricia N. Tonin

   OriginalPaper 08 August 2010 Pages: 507 - 517

   

5. Complete BRCA mutation screening in breast and ovarian cancer predisposition families from a North-Eastern Romanian population

   • Lucian Negura
   • Nancy Uhrhammer
   • Yves-Jean Bignon

   OriginalPaper 22 June 2010 Pages: 519 - 523

6. Can a phenotype for recessive inheritance in breast cancer be defined?

   • Carolina Ellberg
   • Göran Jönsson
   • Håkan Olsson

   OriginalPaper 13 June 2010 Pages: 525 - 530

   

7. PALB2: a novel inactivating mutation in a Italian breast cancer family

   • Cristina Balia
   • Elisa Sensi
   • Maria Adelaide Caligo

   BriefCommunication 18 September 2010 Pages: 531 - 536

   

8. Screening for large genomic rearrangements of the BRIP1 and CHK1 genes in Finnish breast cancer families

   • Szilvia Solyom
   • Katri Pylkäs
   • Robert Winqvist

   OriginalPaper 22 June 2010 Pages: 537 - 540

9. BRCA1 mutations and colorectal cancer in Poland

   • Janina Suchy
   • Cezary Cybulski
   • Steven A. Narod

   OriginalPaper 23 September 2010 Pages: 541 - 544

10. The contribution of breast cancer pathology to statistical models to predict mutation risk in BRCA carriers

    • Ana Cristina Vargas
    • Leonard Da Silva
    • Sunil R. Lakhani

    OriginalPaper 25 June 2010 Pages: 545 - 553

    

11. Magnetic resonance colonography for colorectal cancer screening in patients with Lynch syndrome gene mutation

    • Eu Jin Lim
    • Christopher Leung
    • Finlay Macrae

    OriginalPaper 22 May 2010 Pages: 555 - 561

    

12. Frequency of extracolonic tumors in Brazilian families with Lynch syndrome: analysis of a hereditary colorectal cancer institutional registry

    • Felipe Carneiro da Silva
    • Ligia Petrolini de Oliveira
    • Fábio de Oliveira Ferreira

    OriginalPaper 10 August 2010 Pages: 563 - 570

    

13. Selective COX-2 inhibition affects fatty acids, but not COX mRNA expression in patients with FAP

    • Kari Almendingen
    • Laila N. Larsen
    • Lars Aabakken

    OriginalPaper Open access 01 July 2010 Pages: 571 - 580

14. FAP, gastric cancer, and genetic counseling featuring children and young adults: a family study and review

    • Henry T. Lynch
    • Carrie Snyder
    • Jason Foster

    OriginalPaper 08 June 2010 Pages: 581 - 588

    

15. MYH biallelic mutation can inactivate the two genetic pathways of colorectal cancer by APC or MLH1 transversions

    • Jérémie H. Lefevre
    • Chrystelle Colas
    • Yann Parc

    BriefCommunication 18 July 2010 Pages: 589 - 594

    

16. Papillary thyroid cancer in a patient with MUTYH-associated polyposis (MAP)

    • Muhammad Ali Pervaiz
    • Amanda Eppolito
    • Karen Schmidt

    BriefCommunication 13 July 2010 Pages: 595 - 597

17. A functional varient in microRNA-146a is associated with risk of esophageal squamous cell carcinoma in Chinese Han

    • Hong Guo
    • Kai Wang
    • Yun Bai

    OriginalPaper 01 August 2010 Pages: 599 - 603

18. CDH1 gene mutations do not contribute in hereditary diffuse gastric cancer in Poland

    • Anna Jakubowska
    • Małgorzata Ławniczak
    • Jan Lubiński

    OriginalPaper Open access 15 September 2010 Pages: 605 - 608

19. Peutz-Jeghers syndrome: a study of long-term surgical morbidity and causes of mortality

    • Y. Nancy You
    • Bruce G. Wolff
    • Rui Qin

    OriginalPaper 23 June 2010 Pages: 609 - 616

    

20. Pancreatic cancer risk counselling and screening: impact on perceived risk and psychological functioning

    • Christine Maheu
    • Andrea Vodermaier
    • Mary Jane Esplen

    OriginalPaper 10 July 2010 Pages: 617 - 624

21. Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations

    • Xiaohong Rose Yang
    • Xueying Liang
    • Alisa M. Goldstein

    OriginalPaper 24 June 2010 Pages: 625 - 633

    

22. Clinical and molecular characterization of Brazilian families with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation

    • Israel Gomy
    • Greice Andreotti Molfetta
    • Wilson Araujo Silva Jr.

    OriginalPaper 22 June 2010 Pages: 635 - 642

    

23. A novel mutation of the Succinate Dehydrogenase B Gene in a Korean Family with Pheochromocytoma

    • Sang Ah Lee
    • Eun Hee Kim
    • Woo Je Lee

    OriginalPaper 20 June 2010 Pages: 643 - 646

    

24. Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits

    • C. R. M. Lammens
    • E. M. A. Bleiker
    • S. Verhoef

    OriginalPaper Open access 25 July 2010 Pages: 647 - 654

    

25. Thymoma associated with malignancies may herald a hereditary cancer syndrome

    • Omid Saeed Tehrani
    • Emily Q. Chen
    • Abdul W. Mughal

    Letter 24 August 2010 Pages: 655 - 657

    

26. Similarities in solar ultraviolet irradiance and other environmental factors may explain much of the family link between uveal melanoma and other cancers

    • William B. Grant
    • Johan E. Moan
    • Asta Juzeniene

    Letter 15 August 2010 Pages: 659 - 660

27. Hereditary predisposition rather than environmental factor are likely to explain the familial link between uveal melanoma and other cancers

    • M. H. Abdel-Rahman
    • R. Pilarski

    Letter 25 August 2010 Pages: 661 - 662

28. Contribution of CDKN2A/P16 ^INK4A , P14 ^ARF , CDK4 and BRCA1/2 germline mutations in individuals with suspected genetic predisposition to uveal melanoma

    • B. Buecher
    • M. Gauthier-Villars
    • D. Stoppa-Lyonnet

    OriginalPaper 15 September 2010 Pages: 663 - 667

29. Disclosing cancer genetic information within families: perspectives of counselees and their at-risk relatives

    • Afsaneh Hayat Roshanai
    • Claudia Lampic
    • Karin Nordin

    OriginalPaper 25 June 2010 Pages: 669 - 679

    

30. Real world experience with cancer genetic counseling via telephone

    • Rebecca Sutphen
    • Barbara Davila
    • Joanne Armstrong

    OriginalPaper 27 August 2010 Pages: 681 - 689

    

31. Communicating genetic risk information within families: a review

    • Mel Wiseman
    • Caroline Dancyger
    • Susan Michie

    OriginalPaper 18 September 2010 Pages: 691 - 703

32. Report of the Combined Meeting of the International Society for Gastrointestinal Hereditary Tumours, the Human Variome Project and the National Cancer Institute Colon Cancer Family Registry, Duesseldorf, Germany, 24 June 2009

    • Maija Kohonen-Corish
    • Thomas K. Weber
    • the Meeting Participants

    Report 08 June 2010 Pages: 705 - 711

33. Abstracts 3rd Biennial Meeting of InSiGHT (International Society for Gastrointestinal Hereditary Tumours)

    Events 18 June 2010 Pages: 713 - 748