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Bowel cancer chemoprevention - ready for the clinic?

Authors: J Burn

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A12

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Selenium and cancer – what have we learned from epidemiology and molecular epidemiology studies?

Authors: Ewa Jablonska, Jolanta Gromadzinska and Wojciech Wasowicz

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 1):A12

Content type: Meeting abstract Published on: 9 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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CHEK2 mutations as markers for high risk of breast cancer

Authors: Cezary Cybulski, Dominika Wokołorczyk, Anna Jakubowska, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Tadeusz Dębniak, Bohdan Górski, P Blecharz, S A Narod and Jan Lubiński

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A4

Content type: Meeting abstract Published on: 20 April 2012

This article is part of a Supplement: Volume 10 Supplement 3
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The spectrum of mutations in families with breast and ovarian cancer from the region of Saxony, Germany

Authors: Michalina Tomys, Marzena Skrzypczak-Zielinska, Marzena Jasinowska, Andrzej Plawski and Ursula Froster

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 1):A2

Content type: Meeting abstract Published on: 9 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Overview of genetic markers for hereditary colorectal cancer

Authors: Rodney J Scott

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 4):A22

Content type: Meeting abstract Published on: 10 December 2012

This article is part of a Supplement: Volume 10 Supplement 4
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Correction to: Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis

Authors: Karin Wallander, Håkan Thonberg, Daniel Nilsson and Emma Tham

Citation: Hereditary Cancer in Clinical Practice 2021 19:47

Content type: Correction Published on: 16 November 2021

The original article was published in Hereditary Cancer in Clinical Practice 2021 19:46
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The CHEK 2 GENE mutations and the risk of Gastric cancer

Authors: Urszula Teodorczyk, Cezary Cybulski, Anna Jakubowska, Teresa Starzyńska, Małgorzata Ławniczak, Katarzyna Ferenc, Krzysztof Marlicz, Zbigniew Banaszkiewicz, Rafał Wiśniowski and Jan Lubiński

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 1):A10

Content type: Meeting abstract Published on: 12 January 2012

This article is part of a Supplement: Volume 10 Supplement 1
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A genome-wide association study to identify genetic markers associated with endometrial cancer grade

Authors: T O’Mara, D Duffy, DJ Thompson, S Ahmed, K Ferguson, CS Healey, G Montgomery, M Shah, J Morrison, PP Pharoah, AM Dunning, PM Webb, DF Easton and AB Spurdle

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A47

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Observation of the cancer patient journey: a learning curve for Genetic Counsellors

Authors: JA Taylor and KJ Mann

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A51

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Blood and serum samples collection and storage for further selenium measurements

Authors: Magdalena Muszyńska, Grzegorz Sukiennicki, Anna Jakubowska and Jan Lubiński

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A16

Content type: Meeting abstract Published on: 20 April 2012

This article is part of a Supplement: Volume 10 Supplement 3
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DNA methylation in tumor-adjacent normal tissue in the course of head and neck squamous cell carcinoma as an epigenetic field for cancerization

Authors: Joanna Katarzyna Strzelczyk, Łukasz Krakowczyk, Anna Płachetka, Grażyna Izdebska-Straszak and Andrzej Wiczkowski

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A20

Content type: Meeting abstract Published on: 20 April 2012

This article is part of a Supplement: Volume 10 Supplement 3
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Contribution of genetic variation within SuprMam1 and SuprMam2 to breast cancer susceptibility

Authors: M Ratnadiwakara, M Rooke, R Williams and AC Blackburn

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A90

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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"It's not even about her it's about the whole family": accounts of participation in a family cancer study

Authors: H Shipman and A Clarke

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A14

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Letter to the Editors on the van Oostrom's Paper

Authors: Sung-Won Kim, Dong-Young Noh and Jae-Gahb Park

Citation: Hereditary Cancer in Clinical Practice 2004 2:197

Content type: Letter to the editor Published on: 15 December 2004
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The risk of breast cancer in women with a CHEK2 mutation

Authors: Cezary Cybulski, Dominika Wokołorczyk, Anna Jakubowska, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Tadeusz Dębniak, Bohdan Górski, Steven A Narod and Jan Lubiński

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 1):A5

Content type: Meeting abstract Published on: 12 January 2012

This article is part of a Supplement: Volume 10 Supplement 1
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Folic acid and cancer risk in BRCA1 carriers

Authors: Katarzyna Durda, Anna Jakubowska, Krzysztof Kąklewski, Katarzyna Jaworska, Satish Gupta, Tomasz Byrski, Tomasz Huzarski, Jacek Gronwald, Cezary Cybulski, Tadeusz Dębniak, Aleksandra Tołoczko, Oleg Ashuryk and Jan Lubiński

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A6

Content type: Meeting abstract Published on: 20 April 2012

This article is part of a Supplement: Volume 10 Supplement 3
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Genetic polymorphisms and ovarian cancer risk and response to paclitaxel/cisplatin chemotherapy

Authors: Karolina Tecza, Jolanta Pamula-Pilat, Zofia Kolosza, Natalia Radlak and Ewa Grzybowska

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 1):A4

Content type: Meeting abstract Published on: 9 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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DNA testing for high risk of prostate cancer

Authors: Dominika Wokołorczyk

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 1):A12

Content type: Meeting abstract Published on: 12 January 2012

This article is part of a Supplement: Volume 10 Supplement 1
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An audit of treatment focussed BRCA1/2 mutation testing at an integrated Familial Cancer Clinic

Authors: A Lewis, L Cicciarelli, D Pandey, CM Lovett, R Driessen, S Sawyer, MA Young and G Mitchell

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A49

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Making a good model better - evaluation of the NSW Combined Family Cancer Clinic meetings

Authors: Lynne Purser, Kathy Tucker, Kristine Barlow-Stewart and Kate Dunlop

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A53

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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The case of the youngest infant with hepatoblastoma with APC gene mutation

Authors: Maryna Krawczuk-Rybak, Anna Jakubiuk-Tomaszuk, Elżbieta Skiba and Andrzej Pławski

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A18

Content type: Meeting abstract Published on: 20 April 2012

This article is part of a Supplement: Volume 10 Supplement 3
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Factors influencing effective acquisition of primary care patients for cancer early diagnostics

Authors: Paweł Żuk, Artur Prusaczyk, Anna Kołak, Małgorzata Kalisz and Tomasz Włodarczyk

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 2):A18

Content type: Meeting abstract Published on: 26 November 2015

This article is part of a Supplement: Volume 13 Supplement 2
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Linkage to chromosome 2q32.2-q35 in families with serrated neoplasia

Authors: Aedan Roberts, Derek Nancarrow, Daniel D Buchanan, Mark Clendenning, David Duggan, Diane McKeone, Rhiannon Walters, Michael D Walsh, Bruce W Young, Jeremy R Jass and Joanne P Young

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):O8

Content type: Oral presentation Published on: 25 May 2010

This article is part of a Supplement: Volume 8 Supplement 1
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Clinicopathologic and genetic features of young patients with colorectal cancer

Authors: Melyssa Aronson, Steve Gallinger, Heidi Rothenmund, Kara Semotiuk, Spring Holter, Terri Berk, Aaron Pollett, Zane Cohen, Bharati Bapat, Hyeja Kim and Robert Gryfe

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):P2

Content type: Poster presentation Published on: 25 May 2010

This article is part of a Supplement: Volume 8 Supplement 1
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Correction to: Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants

Authors: Krithika Murali, Tanya M. Dwarte, Mehrdad Nikfarjam, Katherine M. Tucker, Rhys B. Vaughan, Marios Efthymiou, Allison Collins, Allan D. Spigelman, Lucinda Salmon, Amber L. Johns, David B. Williams, Martin B. Delatycki, Thomas John and Alina Stoita

Citation: Hereditary Cancer in Clinical Practice 2021 19:37

Content type: Correction Published on: 8 September 2021

The original article was published in Hereditary Cancer in Clinical Practice 2021 19:33
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Identification of a novel disease-associated variant in the BRCA1 3’UTR that introduces a functional miR-103 target site

Authors: BL Brewster, F Rossiello, JD French, SL Edwards, EM Wong, P Whiley, N Waddell, X Chen, B Bove, AB Spurdle, P Radice, AK Godwin, MC Southey, MA Brown and P Peterlongo

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A88

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Peer live supervision in the familial cancer setting

Authors: M Kentwell, A Sexton, L Hodgkin, Y Bylstra, M Bogwitz, K Mann, J Taylor, M Sahhar, F Pearce, I Winship and GJ Lindeman

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A16

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Genomic imbalance in endometrial hyperplasia and cancer

Authors: Michal Bednarek, Maria Constantinou, Lukasz Kepczynski, Agata Shiar Kassassir, Anna Sobczuk, Maria Wieszczycka, Jacek Suzin and Bogdan Kaluzewski

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 1):A16

Content type: Meeting abstract Published on: 9 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Serrated polyposis syndrome and colonoscopic surveillance: who is it safe to follow?

Authors: S Parry, S Woodall, G Willdridge, MD Walsh, DD Buchanan, C Rosty and JP Young

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A20

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Rapid test for detection of high risk of breast cancer

Authors: K Durda, K Jaworska, A Jakubowska, T Dębniak and B Górski

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 1):A7

Content type: Meeting abstract Published on: 12 January 2012

This article is part of a Supplement: Volume 10 Supplement 1
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Selenium (Se) and the risk of breast, ovarian and prostate cancers

Authors: Katarzyna Jaworska, Anna Jakubowska, Katarzyna Durda, Tomasz Huzarski, Pablo Serrano-Fernandez, Grzegorz Sukiennicki, Magdalena Muszyńska, Tomasz Byrski, Jacek Gronwald, Satish Gupta, K Kaczmarek and Jan Lubiński

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A8

Content type: Meeting abstract Published on: 20 April 2012

This article is part of a Supplement: Volume 10 Supplement 3
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Familial risk and diagnosis of colorectal cancer in young individuals

Authors: Pavel Elsakov

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 1):A6

Content type: Meeting abstract Published on: 9 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Cumulative small effect genetic markers and the detection of advanced colorectal neoplasias by population screening

Authors: A Kurlapska, P Serrano-Fernández, T Starzyńska, E Małecka-Panas, G A Dąbrowski, T Dębniak, G Kurzawski, J Suchy, W Rogoza-Mateja, R J Scott and J Lubiński

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 4):A26

Content type: Meeting abstract Published on: 10 December 2012

This article is part of a Supplement: Volume 10 Supplement 4
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HOXB13 mutations and prostate cancer in Poland

Authors: Wojciech Kluźniak, Dominika Wokołorczyk, Jan Lubiński and Cezary Cybulski

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 4):A30

Content type: Meeting abstract Published on: 10 December 2012

This article is part of a Supplement: Volume 10 Supplement 4
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East meets west: cross-cultural ethnic focussed genetic-counselling

Authors: Risha Zia and Lesley Andrews

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A55

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Mind the gap: challenges in the clinical management of Lynch syndrome families

Authors: Carin R Huizenga, Arelis E Martir-Negron, Kathleen R Blazer, Julie O Culver, Deborah J MacDonald and Jeffrey N Weitzel

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):P16

Content type: Poster presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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Assessing and addressing ongoing information and support needs among individuals with Lynch syndrome

Authors: Anna M Leininger, Mia Resner and Carrie A Zabel

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):P20

Content type: Poster presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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Intramucosal adenocarcinoma arising within a colonic polypoid ganglioneuroma in a 21 year old female with Cowden syndrome

Authors: Anu Chittenden, Joel E Goldberg, Jason L Hornick and Elena M Stoffel

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):P4

Content type: Poster presentation Published on: 25 May 2010

This article is part of a Supplement: Volume 8 Supplement 1
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A state-wide population-based program for detection of Lynch syndrome based upon immunohistochemical and molecular testing of colorectal tumours

Authors: L Schofield, F Grieu, J Goldblatt, B Amanuel and B Iacopetta

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A18

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Mismatch repair gene mutations and cancer risks: an update

Authors: AK Win, JL Hopper and MA Jenkins

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A22

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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BRCA1 mutation- oncological treatment- reconstructive surgery of the breast- pregnancy: diagnostic and therapeutic procedures in a 28 year old patient diagnosed with a tumor in the left breast with a BRCA1 mutation

Authors: Ewa Kilar

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 1):A9

Content type: Meeting abstract Published on: 12 January 2012

This article is part of a Supplement: Volume 10 Supplement 1
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Retrospective analysis of patients with hereditary non- polyposis colorectal cancer (HNPCC)

Authors: Banaszkiewicz Zbigniew, Pawel Jarmocik, Marcin Mrozowski and Arkadiusz Jawien

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 1):A8

Content type: Meeting abstract Published on: 9 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Prostate cancer screening based on genotyping for high risk founder alleles

Authors: Cezary Cybulski, Dominika Wokołorczyk, Wojciech Kluźniak and Jan Lubiński

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 4):A28

Content type: Meeting abstract Published on: 10 December 2012

This article is part of a Supplement: Volume 10 Supplement 4
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Case study: positive outcomes from a negative

Authors: R Williams and K Tucker

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A57

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Pathogenic germline TP53 mutations in adult sarcoma patients; implications for treatment and screening – description of an upcoming project

Authors: K Mahendran, M Ballinger, J Kirk, D Thomas and M Tattersall

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A61

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Awareness and uptake of genetic testing among individuals at-risk for hereditary colon cancer

Authors: Jan T Lowery, Al Marcus, Nora Horick, Dianne Finkelstein and Dennis J Ahnen

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):P22

Content type: Poster presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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Neoadjuvant therapy with cisplatin in BRCA1-positive breast cancer patients

Authors: T Byrski, J Gronwald, T Huzarski, RA Dent, D Zuziak, R Wiśniowski, E Marczyk, P Blecharz, O Szurek, C Cybulski, T Dębniak, B Górski, J Lubiński and S Narod

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 2):A4

Content type: Meeting abstract Published on: 1 June 2011

This article is part of a Supplement: Volume 9 Supplement 2
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Impact of mismatch repair (MMR) genetic test result on perceived cancer risk and cancer screening

Authors: Monica Dandapani, Margery Rosenblatt, Anu Chittenden, Rowena Mercado, Judy E Garber, Sapna Syngal and Elena M Stoffel

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):P6

Content type: Poster presentation Published on: 25 May 2010

This article is part of a Supplement: Volume 8 Supplement 1
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Targeting oncogenes in advanced melanoma

Authors: GA McArthur

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A24

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Clinical management of women in BRCAX families: issues and controversies

Authors: G Mitchell

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A1

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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