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

Authors: Brandie Heald and Charis Eng

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):O2

Content type: Oral presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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A breast cancer prediction model incorporating familial and personal risk factors

Authors: Jack Cuzick

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A29

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Genome wide association identified colorectal cancer susceptibility loci and colorectal cancer risk in Lynch syndrome

Authors: Mala Pande, Marsha L Frazier, Patrick M Lynch, Russell Broaddus and Christopher I Amos

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):P16

Content type: Poster presentation Published on: 25 May 2010

This article is part of a Supplement: Volume 8 Supplement 1
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Rehabilitating the sick role: post-surgical experiences of high risk women who undergo risk reducing mastectomy

Authors: N Hallowell, L Heiniger, B Baylock, M Price and P Butow

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A6

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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A Familial Adenomatous Polyposis (FAP) patient education conference and its impact on patients and families

Authors: Devki S Saraiya, Thuy M Vu, Robert L Askew, Susan K Peterson, Miguel A Rodriguez-Bigas and Patrick M Lynch

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):P20

Content type: Poster presentation Published on: 25 May 2010

This article is part of a Supplement: Volume 8 Supplement 1
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Iron as diagnostic marker of cancer

Authors: Grzegorz Sukiennicki, Magdalena Muszyńska, Katarzyna Jaworska-Bieniek, Katarzyna Kaczmarek, Wojciech Marciniak, Marcin Lener, Katarzyna Durda, Tomasz Gromowski, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Oleg Oszurek, Cezary Cybulski, Tadeusz Dębniak, Antoni Morawski, Anna Jakubowska…

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 2):A5

Content type: Meeting abstract Published on: 26 November 2015

This article is part of a Supplement: Volume 13 Supplement 2
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Searching for BRCA3 by exome sequencing

Authors: I Makunin, M Stark, M Gartside and G Chenevix-Trench

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A68

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Correction to: Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients

An amendment to this paper has been published and can be accessed via the original article.

Authors: Muhammad Usman Rashid, Noor Muhammad, Faiz Ali Khan, Umara Shehzad, Humaira Naeemi, Naila Malkani and Ute Hamann

Citation: Hereditary Cancer in Clinical Practice 2021 19:4

Content type: Correction Published on: 7 January 2021

The original article was published in Hereditary Cancer in Clinical Practice 2020 18:25
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The InSiGHT approach to classification of mismatch repair gene variants

Authors: JP Plazzer

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A72

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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A report of a family with an MSH2 mutation and prostate cancer

Authors: Erin A Mundt, Sara C Knapke and Robert Hopkin

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):P29

Content type: Poster presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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Factors associated with genetic testing distress in patients tested for Lynch Syndrome or Hereditary Breast and Ovarian Cancer Syndrome

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

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):P33

Content type: Poster presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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Cancer predisposing BARD1 mutations in breast-ovarian cancer families

Authors: Magdalena Ratajska, Magdalena Matusiak, Izabela Brożek, Maciej Stukan, Marcin Śniadecki, Jarosław Dębniak, Dariusz Wydra and Janusz Limon

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 4):A10

Content type: Meeting abstract Published on: 10 December 2012

This article is part of a Supplement: Volume 10 Supplement 4
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Microsatellite instability in colorectal adenomas and hyperplastic polyps in Lynch syndrome

Authors: Matthew B Yurgelun, Ajay Goel, C Richard Boland and Elena M Stoffel

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):O4

Content type: Oral presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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Reclassifying ovarian cancer: origins, subtypes and resistance to therapy

Authors: DDL Bowtell

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A35

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Correction: When is a mutation not a mutation: the case of the c.594-2A>C splice variant in a woman harbouring another BRCA1 mutation in trans

Authors: Michelle Wong-Brown, Mary McPhillips, Margaret Gleeson, Allan D. Spigelman, Cliff J. Meldrum, Susan Dooley and Rodney J. Scott

Citation: Hereditary Cancer in Clinical Practice 2022 20:20

Content type: Correction Published on: 30 May 2022

The original article was published in Hereditary Cancer in Clinical Practice 2016 14:6
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Dissecting genetic pathways in schwannomatosis and malignant rhabdoid tumour

Authors: E Algar

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A8

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Aggressive gastric cancer in a patient with an APC mutation and a monoallelic MYH mutation

Authors: Paul Wise, Duveen Sturgeon and Reid Ness

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):P22

Content type: Poster presentation Published on: 25 May 2010

This article is part of a Supplement: Volume 8 Supplement 1
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BRCA1 testing in Lithuania

Authors: Ramunas Janavicius

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 4):A9

Content type: Meeting abstract Published on: 10 December 2012

This article is part of a Supplement: Volume 10 Supplement 4
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Copper as diagnostic marker of cancers

Authors: Magdalena Muszyńska, Wojciech Marciniak, Katarzyna Jaworska-Bieniek, Katarzyna Kaczmarek, Grzegorz Sukiennicki, Marcin Lener, Katarzyna Durda, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Oleg Oszurek, Cezary Cybulski, Tadeusz Dębniak, Antoni Morawski, Anna Jakubowska and Jan Lubiński

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 2):A7

Content type: Meeting abstract Published on: 26 November 2015

This article is part of a Supplement: Volume 13 Supplement 2
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Male breast cancer in the prophylactics programme by the Ministry of Health of Poland

Authors: Artur Barczyk

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 4):A12

Content type: Meeting abstract Published on: 10 December 2012

This article is part of a Supplement: Volume 10 Supplement 4
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Identification of breast cancer susceptibility genes using whole exome sequencing

Authors: E Thompson, M Doyle, J Ellul, J Li and I Campbell

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A41

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Vitamins A, E and D and cancer risk in BRCA1 carriers

Authors: K Kąklewski, D Gackowski, K Durda, T Huzarski, J Gronwald, T Dębniak, A Tołłoczko, O Ashuryk and A Jakubowska

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A10

Content type: Meeting abstract Published on: 20 April 2012

This article is part of a Supplement: Volume 10 Supplement 3
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Pharmacogenetics of FAC chemotherapy side effects in breast cancer patients

Authors: Karolina Tecza, Jolanta Pamula-Pilat, Joanna Lanuszewska and Ewa Grzybowska

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 2):A10

Content type: Meeting abstract Published on: 26 November 2015

This article is part of a Supplement: Volume 13 Supplement 2
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Linking of Utah genealogies to outpatient colonoscopy records defines familial aggregation of colorectal polyps and cancer

Authors: Therese MF Tuohy, Richard Pimentel, Kerry Rowe, Randall Burt and Geraldine Mineau

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):P24

Content type: Poster presentation Published on: 25 May 2010

This article is part of a Supplement: Volume 8 Supplement 1
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Copper transport system and response to ovarian cancer chemotherapy

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

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 2):A9

Content type: Meeting abstract Published on: 26 November 2015

This article is part of a Supplement: Volume 13 Supplement 2
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Loss of MSH6 and PMS2 immunohistochemical staining in tumour tissue of two individuals with a germline PMS2 mutation

Authors: E Edwards, M Bowman, M Walsh and J Kirk

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A76

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Primary treatment patterns in women recruited to the Australian Ovarian Cancer Study

Authors: J Hung, S Fereday, P Harnett, D Giles, B Gao, N Traficante, G Chenevix-Trench, A Green, P Webb, D Bowtell and A DeFazio

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A80

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Population Screening of CHEK2 Mutations in Poland

Authors: Cezary Cybulski, Tomasz Huzarski, Jowita Huzarska, Tomasz Byrski, Jacek Gronwald, Oleg Oszurek, Jolanta Grajczyk, Ligia Sikora and Jan Lubiński

Citation: Hereditary Cancer in Clinical Practice 2006 4:57

Content type: Commentary Published on: 15 January 2006
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Defining the overlap between sporadic and attenuated familial adenoma risk

Authors: Thérèse M Tuohy, Deborah W Neklason, Kenneth M Boucher, Richard G Pimentel, Kerry G Rowe, Geraldine P Mineau and Randall W Burt

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):P37

Content type: Poster presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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GWAS markers in diagnostics of breast cancer risk

Authors: Anna Jakubowska

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 4):A14

Content type: Meeting abstract Published on: 10 December 2012

This article is part of a Supplement: Volume 10 Supplement 4
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Shortcuts to genetic characterization of polyposis patients in a high-risk registry

Authors: Michelle W Done, Deborah Neklason, Randall Burt and Thérèse Tuohy

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):O8

Content type: Oral presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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Reflex microsatellite instability & immunohistochemistry testing practices & follow-up of abnormal results at U.S. cancer programs

Authors: Laura C Beamer, Marcia Grant, Deborah J MacDonald, Heather Hampel, Kathleen Blazer, Carin Huizenga and Jeffrey N Weitzel

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):P2

Content type: Poster presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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Whole genome sequencing in the study of disease and application in personalised medicine

Authors: A Kumarasuriyar

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A39

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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When is it best to test? Attitudes of health professionals regarding genetic testing for Familial Adenomatous Polyposis (FAP)

Authors: E Lynch, RE Duncan, F Macrae and M Delatycki

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A43

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Effects of X-ray irradiation on methylation levels of p16, MGMT and APC genes in sporadic colorectal carcinoma and corresponding normal colonic mucosa

Authors: Łukasz Krakowczyk, Joanna K Strzelczyk, Sławomir Blamek, Adam Maciejewski, Stanisław Półtorak and Andrzej Wiczkowski

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A12

Content type: Meeting abstract Published on: 20 April 2012

This article is part of a Supplement: Volume 10 Supplement 3
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Juvenile Polyps: a large pediatric cohort

Authors: Victor L Fox, Stephen Perros, Hongyu Jiang and Jeffrey Goldsmith

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):O2

Content type: Oral presentation Published on: 25 May 2010

This article is part of a Supplement: Volume 8 Supplement 1
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Pathological diagnosis of ovarian cancer

Authors: Hilda High and Michael Friedlander

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A82

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Selecting women for breast cancer chemoprevention and what agents should be used

Authors: J Cuzick

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A10

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Functional in silico analysis of missense mutations in the MSH6 gene

Authors: Katarzyna Gajdel and Grzegorz Kurzawski

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 1):A10

Content type: Meeting abstract Published on: 9 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Large genomic rearrangements in BRCA1 and BRCA2 genes in breast and ovarian cancer families in Poland

Authors: Helena Bielecka and Bohdan Górski

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 1):A1

Content type: Meeting abstract Published on: 12 January 2012

This article is part of a Supplement: Volume 10 Supplement 1
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Large genomic rearrangements in BRCA1 and BRCA2 genes in breast and ovarian cancer families in Poland

Authors: Helena Bielecka and Bohdan Górski

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A2

Content type: Meeting abstract Published on: 20 April 2012

This article is part of a Supplement: Volume 10 Supplement 3
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Hereditary non-polyposis colorectal cancer: barriers to and facilitators of screening and disease management

Authors: Kathy Watkins, Christine Way, Jacqueline Stokes, Robert Meadus, Mary Jane Esplen, Jane Green, Valerie Ludlow and Patrick Parfrey

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):P39

Content type: Poster presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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Systemic therapy for hereditary cancer

Authors: Evgeny N Imyanitov

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 4):A16

Content type: Meeting abstract Published on: 10 December 2012

This article is part of a Supplement: Volume 10 Supplement 4
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Is the whole greater than the sum of its parts?

Authors: L Andrews and J Duffy

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A45

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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IDH1 mutation analysis – an example of putative glioma marker

Authors: Marzena Lewandowska, T Szylberg, K Roszkowski, J Furtak, W Windorbska, J Rytlewska and W Jóźwicki

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A14

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 role of selected egzo- and endogenic agents on preinitiation process of bladder cancer

Authors: A Iwaniuk, M Owczarek, M Pietrusiński, E Borkowska, M Rozniecki, M Borowiec, M Sosnowski, J Kocki and B Kałużewski

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 2):A14

Content type: Meeting abstract Published on: 26 November 2015

This article is part of a Supplement: Volume 13 Supplement 2
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Atypical presentation of Lynch Syndrome: a case report

Authors: Shanna Gustafson, Whitney Ducaine and Dana Zakalik

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):P10

Content type: Poster presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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Hereditary Cancer in Clinical Practice transfers to BioMed Central

Authors: Jan Lubiński, Rolf H Sijmons and Rodney J Scott

Citation: Hereditary Cancer in Clinical Practice 2009 7:1

Content type: Editorial Published on: 26 January 2009
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The A148T variant of CDKN2A gene in bladder cancer

Authors: E Borkowska, A Jedrzejczyk, A Kruk, M Traczyk, M Pietrusiński, P Marks and B Kaluzewski

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 2):A11

Content type: Meeting abstract Published on: 1 June 2011

This article is part of a Supplement: Volume 9 Supplement 2
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Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancer

Authors: Deborah W Neklason, Therese M Tuohy, Jeffery Stevens, Brith Otterud, Lisa Baird, Richard A Kerber, Wade S Samowitz, Scott K Kuwada, Mark F Leppert and Randall W Burt

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):O4

Content type: Oral presentation Published on: 25 May 2010

This article is part of a Supplement: Volume 8 Supplement 1
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