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An update of clinical issues from InSIGHT 2011

Authors: L Lipton

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A9

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Impact of genetic testing on risk-reducing behavior in women at risk for hereditary gynecologic cancer syndromes

Authors: Matthew B Yurgelun, Rowena Mercado, Margery Rosenblatt, Judy E Garber, Sapna Syngal and Elena M Stoffel

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):P23

Content type: Poster presentation Published on: 25 May 2010

This article is part of a Supplement: Volume 8 Supplement 1
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Pathological complete response to neoadjuvant cisplatin in BRCA1-positive breast cancer patients

Authors: Tomasz Byrski, Tomasz Huzarski, Rebecca Dent, Elzbieta Marczyk, Marek Jasiowka, Jacek Gronwald, Jerzy Jakubowicz, Cezary Cybulski, Rafal Wisniowski, Dariusz Godlewski, Jan Lubinski and Steven A Narod

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 2):A8

Content type: Meeting abstract Published on: 26 November 2015

This article is part of a Supplement: Volume 13 Supplement 2
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Colorectal tumour BRAF V600E and MLH1 promoter methylation status in the assessment of mismatch repair gene sequence variants of unknown clinical significance

Authors: M Parsons, B Thompson, D Goldgar, J Hopper, M Jenkins, D Buchanan, J Young and A Spurdle

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A75

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 for Cancer Family Syndromes in the West Pomeranian Region of Poland

Authors: Jacek Gronwald, Andrzej Raczyński, Mariusz Tarhoni, Mirosław Blachowski, Tomasz Huzarski, Tomasz Byrski, Aleksandra Tołoczko-Grabarek, Tadeusz Dębniak, Cezary Cybulski, Jowita Huzarska, Oleg Oszurek and Jan Lubiński

Citation: Hereditary Cancer in Clinical Practice 2006 4:56

Content type: Commentary Published on: 15 January 2006
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Do NSAIDs suppress polyps in MUTYH-associated polyposis? A case report

Authors: Duveen Sturgeon, Alan J Herline and Paul E Wise

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):P36

Content type: Poster presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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Constitutional methylation of cancer-related and selenoprotein coding genes in breast carcinoma in Polish population

Authors: Satish Gupta, Katarzyna Jaworska, Anna Jakubowska, Tomasz K Wojdacz, Lise Lotte Hansen and Jan Lubiński

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 4):A13

Content type: Meeting abstract Published on: 10 December 2012

This article is part of a Supplement: Volume 10 Supplement 4
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Design considerations for massively parallel sequencing studies of common familial cancers

Authors: BJ Feng, SV Tavtigian, MC Southey and DE Goldgar

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A38

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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An audit of families with unreported or misreported cancers verified through a population-based cancer registry: implications for providing cancer risk assessment and management advice by a Familial Cancer Centre

Authors: M Kentwell, M Bogwitz, L Donoghue and T McArdle

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A42

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Identification of new genetic alterations in MLH1, MSH2 and MSH6 using IHC and HRM analysis in Lynch syndrome-suspected patients

Authors: A Mazurek, A Fiszer-Kierzkowska and M Budryk

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A11

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 curious case of a woman with two BRCA1 mutations in trans

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

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 2):A11

Content type: Meeting abstract Published on: 26 November 2015

This article is part of a Supplement: Volume 13 Supplement 2
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Mutation-negative FAP patients with mRNA defects of APC

Authors: Michelle W Condie, Therese MF Tuohy, Patricia Shires, Randall W Burt and Deborah W Neklason

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):O1

Content type: Oral presentation Published on: 25 May 2010

This article is part of a Supplement: Volume 8 Supplement 1
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State-wide population screening for Lynch syndrome? Improved ascertainment of at risk families

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

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A77

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Integrated genomic analysis and functional characterisation of novel oncogenes in ovarian cancer

Authors: SJ Davis, KJ Simpson, IG Campbell and KL Gorringe

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A81

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 Lowering of Breast and Ovarian Cancer Risk in Women with a BRCA1 Mutation by Selenium Supplementation of Diet

Authors: Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Elżbieta Kowalska, Stanisław Zajączek, Bohdan Górski, Jowita Huzarska, Cezary Cybulski, Steven A Narod and Jan Lubiński

Citation: Hereditary Cancer in Clinical Practice 2006 4:58

Content type: Commentary Published on: 15 January 2006
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A case of late breast cancer metastases to both suprarenal glands 28 years after mastectomy

Authors: T Banasiewicz, Ł Krokowicz, M Biczysko, M Janicka-Jedyńska, A Pławski, J Paszkowski, P Gronek, B Stawny and M Drews

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A1

Content type: Meeting abstract Published on: 20 April 2012

This article is part of a Supplement: Volume 10 Supplement 3
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Late presentation of cancer in compound heterozygote PMS2 mutation carrier

Authors: Paulien P van Galen, Renee Perrier and Francois P Bernier

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):P38

Content type: Poster presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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BRCA1 mutation in the Triple- Negative Breast Cancer Group

Authors: Jelena Maksimenko, Arvids Irmejs, Genadijs Trofimovics and Edvins Miklasevics

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 4):A15

Content type: Meeting abstract Published on: 10 December 2012

This article is part of a Supplement: Volume 10 Supplement 4
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Clinical practice improvement in the genetics clinic

Authors: S Greening

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A44

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 genetics of melanoma

Authors: T Debniak

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 2):A10

Content type: Meeting abstract Published on: 1 June 2011

This article is part of a Supplement: Volume 9 Supplement 2
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Gastrointestinal polyposis and PTEN mutations: an under-acknowledged diagnostic criterion

Authors: Brandie Heald, Jessica Mester and Charis Eng

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):O3

Content type: Oral presentation Published on: 25 May 2010

This article is part of a Supplement: Volume 8 Supplement 1
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Bone density loss after risk reducing salpingo-oophorectomy

Authors: L Andrews, B Zielony and C White

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A79

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Benign serous ovarian tumour: a redefining moment?

Authors: Sally Hunter, Kylie Gorringe, Michael Anglesio, Raghwa Sharma, Blake Gilks, Anna deFazio, David Huntsman and Ian Campbell

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A83

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Lynch syndrome mutations in Poland and the Baltic States

Authors: Dagmara Dymerska, Jan Lubinski and Grzegorz Kurzawski

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 1):A11

Content type: Meeting abstract Published on: 9 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Spectrum of tumors in the families with Hereditary Breast Ovarian Cancer syndrome carrying germline mutations in BRCA1 and 2 genes

Authors: M Budryk, J Pamuła-Piłat, K Tęcza and E Grzybowska

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 1):A2

Content type: Meeting abstract Published on: 12 January 2012

This article is part of a Supplement: Volume 10 Supplement 1
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Neoadjuvant chemotherapy with Cisplatin in BRCA1 mutation carriers – results of treatment

Authors: T Byrski, J Gronwald, T Huzarski, E Marczyk, P Blecharz, O Ashuryk, C Cybulski, D Zuziak, R Wiśniowski, D Godlewski, SA Narod and J Lubiński

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A3

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 insights into breast cancer risk

Authors: Michelle Wong-Brown, Kelly Avery-Kiejda and Rodney J Scott

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 1):A1

Content type: Meeting abstract Published on: 9 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Cisplatin in breast cancer treatment in BRCA1 carriers

Authors: Jacek Gronwald, Tomasz Byrski, Jan Lubinski and Steven A Narod

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 4):A17

Content type: Meeting abstract Published on: 10 December 2012

This article is part of a Supplement: Volume 10 Supplement 4
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Genetic alterations and field defect in head and neck squamous cell carcinoma

Authors: J K Strzelczyk, Ł Krakowczyk, M Kwaśniewski, A Płachetka, K Gołąbek, K Chwiałkowska, A Maciejewski and A Wiczkowski

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 4):A21

Content type: Meeting abstract Published on: 10 December 2012

This article is part of a Supplement: Volume 10 Supplement 4
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Audit of adherence to GI screening recommendations for Lynch Syndrome Patients

Authors: Lucinda Hossack, Omid Zarghom, Gillian Mitchell, Mary Shanahan, Craig Lynch, Alexander Heriot and Alex Boussioutas

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A50

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Prospective clinical trials on correlations between macro-/ microelements and vitamins and cancer risk

Authors: Jan Lubinski

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A15

Content type: Meeting abstract Published on: 20 April 2012

This article is part of a Supplement: Volume 10 Supplement 3
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Allel RET+3 : T a medullary thyroid cancer

Authors: A Pławski and M Podralska

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 2):A12

Content type: Meeting abstract Published on: 1 June 2011

This article is part of a Supplement: Volume 9 Supplement 2
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Cancer occurrence during follow-up of the CAPP2 study -aspirin use for up to four years significantly reduces Lynch syndrome cancers for up to several years after completion of therapy

Authors: John Burn, John C Mathers, Anne-Marie Gerdes, MarieLuise Bisgaard, Gareth Evans, Diana Eccles, Annika Lindblom, Findlay Macrae, Eamonn R Maher, Jukka-Pekka Mecklin, Gabriela Moslein, Sylviane Olschwang, Raj Ramesar, Hans FA Vasen, Juul Wijnen, Gail Barker…

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):O5

Content type: Oral presentation Published on: 25 May 2010

This article is part of a Supplement: Volume 8 Supplement 1
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Correction to: Overview on population screening for carriers with germline mutations in mismatch repair (MMR) genes in China

Authors: Min Zhang and Tianhui Chen

Citation: Hereditary Cancer in Clinical Practice 2021 19:27

Content type: Correction Published on: 17 May 2021

The original article was published in Hereditary Cancer in Clinical Practice 2021 19:26
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The use of the Illumina FFPE Restoration Protocol to obtain suitable quality DNA for SNP-based CGH– a pilot study

Authors: AN Hosein, S Cocciardi, J Jayanthan, S Song, P Simpson and G Chenevix-Trench

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A85

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Risk-reducing surgery for breast and ovarian cancer risks - where are we now?

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

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A13

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Erratum to: Dear Readers

Authors: Evgeny N. Imyanitov

Citation: Hereditary Cancer in Clinical Practice 2007 5:56

Content type: Erratum Published on: 15 March 2007

The original article was published in Hereditary Cancer in Clinical Practice 2006 4:193
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The influence of selenium concentration and variations in selenoprotein genes on the CHEK2-dependent cancers

Authors: Satish Gupta, Magdalena Muszynska, Katarzyna Jaworska-Bieniek, Grzegorz Sukiennicki, Katarzyna Kaczmarek, Anna Jakubowska and Jan Lubinski

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 1):A13

Content type: Meeting abstract Published on: 9 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Why choose the treatment with cisplatin for BRCA1 breast cancers patients?

Authors: T Byrski, T Huzarski, E Marczyk, P Blecharz, J Gronwald, O Ashuryk, C Cybulski, T Dębniak, D Zuziak, D Godlewski, J Kladny, J Lubinski and SA Narod

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 1):A4

Content type: Meeting abstract Published on: 12 January 2012

This article is part of a Supplement: Volume 10 Supplement 1
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Genome-wide association studies identify new melanoma susceptibility loci

Authors: Tadeusz Dębniak

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A5

Content type: Meeting abstract Published on: 20 April 2012

This article is part of a Supplement: Volume 10 Supplement 3
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BRCA1 founder mutations and ovarian cancer in Belarus

Authors: A Savanevich, A Ashuryk, J Lubinski and J Gronwald

Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 1):A3

Content type: Meeting abstract Published on: 9 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Diagnostic microarray test for a genetic predisposition to hereditary nonpolyposis colorectal cancer (HNPCC)

Authors: M Kaszuba, A Sikorski, J Odważna and J Wojciechowicz

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 4):A23

Content type: Meeting abstract Published on: 10 December 2012

This article is part of a Supplement: Volume 10 Supplement 4
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Sebaceous neoplasms in Lynch syndrome

Authors: Monica Dandapani, Anu Chittenden, Aaron J Stunkel, Margery Rosenblatt, Sapna Syngal and Elena M Stoffel

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):P7

Content type: Poster presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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Prospective observation of breast/ovarian cancer risk in BRCA1 carriers depending on serum selenium level optimized with diet

Authors: J Lubiński, T Huzarski, A Jakubowska, J Gronwald, K Jaworska, M Muszyńska, G Sukiennicki, K Durda, C Cybulski, T Dębniak, A Tołoczko, O Oszurek, P Serrano-Fernandez, R Scott and S Narod

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 1):A11

Content type: Meeting abstract Published on: 12 January 2012

This article is part of a Supplement: Volume 10 Supplement 1
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‘Next-generation’ genome wide association studies

Authors: J Hopper, E Makalic, D Schmidt, M Bui, J Stone, M Kapuscinski, D Park, M Jenkins and M Southey

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A48

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Use of unit standard paragraphs and letters in: 1. Australian Familial Cancer Centres 2. One Centre’s experience at Southern Health

Authors: C Smyth, C Holding, C Hunt, S O’Connell, E Johnson, N Gelfand and M Harris

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A52

Content type: Meeting abstract Published on: 12 April 2012

This article is part of a Supplement: Volume 10 Supplement 2
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Serum concentration of iron as predictor of cancer risk among BRCA1 mutation carriers

Authors: Grzegorz Sukiennicki, Magdalena Muszyńska, Tomasz Huzarski, Jacek Gronwald, Cezary Cybulski, Tadeusz Dębniak, Aleksandra Tołoczko-Grabarek, Oleg Ashuryk, Anna Jakubowska, Antoni Morawski and Jan Lubiński

Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 3):A21

Content type: Meeting abstract Published on: 20 April 2012

This article is part of a Supplement: Volume 10 Supplement 3
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Post-surgical surveillance in Lynch syndrome--a Cleveland Clinic experience

Authors: Susan Fay, Ellen McGannon and James M Church

Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):P13

Content type: Poster presentation Published on: 10 March 2011

This article is part of a Supplement: Volume 9 Supplement 1
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A predictive model of metachronous colorectal cancer occurrence in Lynch syndrome

Authors: Lucio Bertario, Paola Sala, Paolo Radice, Stefano Signoroni, Giovanni Ballardini, Emanuele Meroni and Antonio Russo

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):O7

Content type: Oral presentation Published on: 25 May 2010

This article is part of a Supplement: Volume 8 Supplement 1
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Colorectal cancer risk in patients with inflammatory bowel disease and Lynch syndrome

Authors: Melyssa Aronson, Joanne Stempak, Mark Silverberg, Kara Semotiuk, Robert Gryfe and Steven Gallinger

Citation: Hereditary Cancer in Clinical Practice 2010 8(Suppl 1):P1

Content type: Poster presentation Published on: 25 May 2010

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