Letter from the New Editor in Chief

por Tischkowitz, Marc
Publicado 2019

When to Consider Risk-Reducing Mastectomy in BRCA1/BRCA2 Mutation Carriers with Advanced Stage Ovarian Cancer: a Case Study Illustrating the Genetic Counseling Challenges

por Speight, Beverley, Tischkowitz, Marc
Publicado 2017

Clinical implications of germline mutations in breast cancer: TP53

por Schon, Katherine, Tischkowitz, Marc
Publicado 2017

Clinical implications of germline mutations in breast cancer genes: RECQL

por Bowden, A. Ramsay, Tischkowitz, Marc
Publicado 2019

BRCA1 and BRCA2 pathogenic variants and prostate cancer risk: systematic review and meta-analysis

por Nyberg, Tommy, Tischkowitz, Marc, Antoniou, Antonis C.
Publicado 2021

Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome

por Tischkowitz, Marc, Colas, Chrystelle, Pouwels, Sjaak, Hoogerbrugge, Nicoline
Publicado 2020

Update: variable implementation of the 2018 UKCGG/UKGTN guidelines for breast cancer gene panel tests offered by UK genetics services

por Wedderburn, Sarah, Archer, Stephanie, Tischkowitz, Marc, Hanson, Helen
Publicado 2021

Sporadic implementation of UK familial mammographic surveillance guidelines 15 years after original publication

por Evans, D. Gareth, Edwards, Maria, Duffy, Stephen W., Tischkowitz, Marc
Publicado 2019

Cancer incidence in relatives of British Fanconi Anaemia patients

por Tischkowitz, Marc, Easton, Douglas F, Ball, Jan, Hodgson, Shirley V, Mathew, Christopher G
Publicado 2008

Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update

por McGuigan, Anthony, Whitworth, James, Andreou, Avgi, Hearn, Timothy, Tischkowitz, Marc, Maher, Eamonn R.
Publicado 2022

RAD51C germline mutations in breast and ovarian cancer patients

por Akbari, Mohammad R, Tonin, Patricia, Foulkes, William D, Ghadirian, Parviz, Tischkowitz, Marc, Narod, Steven A
Publicado 2010

Consensus for genes to be included on cancer panel tests offered by UK genetics services: guidelines of the UK Cancer Genetics Group

por Taylor, Amy, Brady, Angela F, Frayling, Ian M, Hanson, Helen, Tischkowitz, Marc, Turnbull, Clare, Side, Lucy
Publicado 2018

p.Val804Met, the Most Frequent Pathogenic Mutation in RET, Confers a Very Low Lifetime Risk of Medullary Thyroid Cancer

por Loveday, Chey, Josephs, Katherine, Chubb, Daniel, Gunning, Adam, Izatt, Louise, Tischkowitz, Marc, Ellard, Sian, Turnbull, Clare
Publicado 2018

Risk of developing a second primary cancer in male breast cancer survivors: a systematic review and meta-analysis

por Allen, Isaac, Hassan, Hend, Sofianopoulou, Eleni, Eccles, Diana, Turnbull, Clare, Tischkowitz, Marc, Pharoah, Paul, Antoniou, Antonis C.
Publicado 2022

Risks of second non-breast primaries following breast cancer in women: a systematic review and meta-analysis

por Allen, Isaac, Hassan, Hend, Sofianopoulou, Eleni, Eccles, Diana, Turnbull, Clare, Tischkowitz, Marc, Pharoah, Paul, Antoniou, Antonis C.
Publicado 2023

Germ-line DICER1 mutations do not make a major contribution to the etiology of familial testicular germ cell tumours

por Sabbaghian, Nelly, Bahubeshi, Amin, Shuen, Andrew Y, Kanetsky, Peter A, Tischkowitz, Marc D, Nathanson, Katherine L, Foulkes, William D
Publicado 2013

Incorporating Truncating Variants in PALB2, CHEK2 and ATM into the BOADICEA Breast Cancer Risk Model

por Lee, Andrew J., Cunningham, Alex P., Tischkowitz, Marc, Simard, Jacques, Pharoah, Paul D., Easton, Douglas F., Antoniou, Antonis C.
Publicado 2016

Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working Group

por Bakhuizen, Jette J., Hanson, Helen, van der Tuin, Karin, Lalloo, Fiona, Tischkowitz, Marc, Wadt, Karin, Jongmans, Marjolijn C. J.
Publicado 2021

Contribution of the PALB2 c.2323C>T [p.Q775X] Founder mutation in well-defined breast and/or ovarian cancer families and unselected ovarian cancer cases of French Canadian descent

por Tischkowitz, Marc, Sabbaghian, Nelly, Hamel, Nancy, Pouchet, Carly, Foulkes, William D, Mes-Masson, Anne-Marie, Provencher, Diane M, Tonin, Patricia N
Publicado 2013

Assessing BRCA1 activity in DNA damage repair using human induced pluripotent stem cells as an approach to assist classification of BRCA1 variants of uncertain significance

por Ozgencil, Meryem, Barwell, Julian, Tischkowitz, Marc, Izatt, Louise, Kesterton, Ian, Simpson, Michael, Sharpe, Paul, de Sepulveda, Paulo, Voisset, Edwige, Solomon, Ellen
Publicado 2021