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skip to content advertisement menu explore journals get published about bmc login my account search search all bmc articles search hereditary cancer in clinical practice menu home about articles submission guidelines search submit a manuscript articles recent most accessed content type: research | 5 june 2018 high frequency of pathogenic non-founder germline mutations in brca1 and brca2 in families with breast and ovarian cancer in a founder population authors: j. maksimenko, a. irmejs, g. trofimovičs, d. bērziņa, e. skuja, g. purkalne, e. miklaševičs and j. gardovskis content type: research | 10 may 2018 patient and provider perspectives on adherence to and care coordination of lynch syndrome surveillance recommendations: findings from qualitative interviews authors: jennifer l. schneider, katrina a. b. goddard, kristin r. muessig, james v. davis, alan f. rope, jessica e. hunter, susan k. peterson, louise s. acheson, sapna syngal, georgia l. wiesner and jacob a. reiss content type: research | 27 april 2018 platinum-based neoadjuvant chemotherapy in brca1-positive breast cancer: a retrospective cohort analysis and literature review authors: nikolai havn sæther, elina skuja, arvids irmejs, jelena maksimenko, edvins miklasevics, gunta purkalne and janis gardovskis content type: research | 24 april 2018 challenges in recruiting african-american women for a breast cancer genetics study authors: amanda j. compadre, melinda e. simonson, katy gray, gail runnells, susan kadlubar and kristin k. zorn content type: case report | 7 march 2018 cdkn2a founder mutation in pancreatic ductal adenocarcinoma patients without cutaneous features of familial atypical multiple mole melanoma (fammm) syndrome authors: carol cremin, sarah howard, lyly le, aly karsan, david f. schaeffer, daniel renouf and kasmintan a. schrader most recent articles rss view all articles content type: review | 1 august 2015 the role of brca1 and brca2 mutations in prostate, pancreatic and stomach cancers authors: helen cavanagh and katherine m.a. rogers content type: review | 12 august 2013 germline deletions in the epcam gene as a cause of lynch syndrome – literature review authors: katarzyna tutlewska, jan lubinski and grzegorz kurzawski content type: review | 11 september 2013 hereditary breast cancer: ever more pieces to the polygenic puzzle authors: natalia bogdanova, sonja helbig and thilo dörk content type: review | 19 april 2016 palb2: research reaching to clinical outcomes for women with breast cancer authors: melissa c. southey, ingrid winship and tú nguyen-dumont content type: research | 28 august 2014 mutation analysis of palb2 in brca1 and brca2 -negative breast and/or ovarian cancer families from eastern ontario, canada authors: taila hartley, luca cavallone, nelly sabbaghian, rachel silva-smith, nancy hamel, olga aleynikova, erika smith, valerie hastings, pedro pinto, marc tischkowitz, eva tomiak and william d foulkes most accessed articles rss view all articles article publication charges author discount all authors submitting to hereditary cancer in clinical practice are eligible for partial coverage of the journal’s article-processing charge (apc). this discount must be requested before the view publication charges page by emailing the journal development editor at [email protected] for a code. authors will not have to pay the full apc themselves if the article is accepted. aims and scope hereditary cancer in clinical practice is an open access journal that publishes articles of interest for the cancer genetics community and serves as a discussion forum for the development appropriate healthcare strategies. cancergenetics encompasses a wide variety of disciplines and knowledge in the field is rapidly growing, especially as the amount of information linking genetic differences to inherited cancer predispositions continues expanding. with the increased knowledge of genetic variability and how this relates to cancer risk there is a growing demand not only to disseminate this information into clinical practice but also to enable competent debate concerning how such information is managed and what it implies for patient care. topics covered by the journal include but are not limited to: original research articles on any aspect of inherited predispositions to cancer. reviews of inherited cancer predispositions. application of molecular and cytogenetic analysis to clinical decision making. clinical aspects of the management of hereditary cancers. genetic counselling issues associated with cancer genetics. the role of registries in improving health care of patients with an inherited predisposition to cancer. meet the editors-in-chief jan lubinski is a professor of medicine and head of the international hereditary cancer center (organized in 1992) of pomeranian medical university in szczecin, poland. the center conducted the first world-wide population screening for cancer family syndromes in a 1.7 million region of west-pomerania, poland in 2000-2001. it has a network of outpatient clinics covering almost the entire country as well as a cancer bio-bank with biological samples and clinical data from 250,000 cancer cases and appropriate controls, which includes registries of thousands of mutation carriers. rodney j scott graduated from the university of western australia, australia with a phd in cellular biology and subsequently worked in the department of pathology and laboratory medicine at the university of texas in houston and then at the centre for teaching and learning at the university of basel, switzerland. since 1999 prof. scott has been a visiting professor at the international hereditary cancer center in szczecin, poland and more recently has been appointed as a adjunct professor at the universiti kebangsaan malaysia. society affiliations hereditary cancer in clinical practice is the official journal of the international hereditary cancer centre and is published under the auspices of international union against canc er. the polish ministry of science and higher education and west pomeranian voivodeship (województwo zachodniopomorskie) provide funds for the publication of articles in this journal. advertisement submit a manuscript editorial board sign up for article alerts and news from this journal follow follow us on twitter 2017 journal metrics speed 81 days from submission to first decision 9 days from acceptance to publication citation impact 1.590 - 2-year impact factor 1.575 - 5-year impact factor 0.81 - source normalized impact per paper (snip) 0.848 - scimago journal rank (sjr) usage 160,434 downloads 1069.0 usage factor social media impact 48 mentions more about our metrics advertisement hereditary cancer in clinical practice issn: 1897-4287 contact us submission enquiries: [email protected] general enquiries: [email protected] explore journals get published about bmc read more on our blogs receive bmc newsletters manage article alerts language editing for authors scientific editing for authors policies accessibility press center contact us leave feedback careers follow bmc bmc twitter page bmc facebook page bmc google plus page bmc weibo page by using this website, you agree to our terms and conditions , privacy statement and cookies policy. manage the cookies we use in the preference centre. © 2018 biomed central ltd unless otherwise stated. part of springer nature .