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Publication
Validation of CZECANCA (CZEch CAncer paNel for Clinical Application) for targeted NGS-based analysis of hereditary cancer syndromes.   Soukupova Jana et al. PloS one 2018 13(4) e0195761
Development of a Web-based Family Intervention for BRCA Carriers and Their Biological Relatives: Acceptability, Feasibility, and Usability Study.   Katapodi Maria C et al. JMIR cancer 2018 Apr 4(1) e7
Understanding of multigene test results among males undergoing germline testing for inherited prostate cancer: Implications for genetic counseling.   Giri Veda N et al. The Prostate 2018 Apr
Factors Influencing Clinical Follow-Up for Individuals with a Personal History of Breast and/or Ovarian Cancer and Previous Uninformative BRCA1 and BRCA2 Testing.   Chadwell Sarah E et al. Journal of genetic counseling 2018 Mar
Hereditary cancer gene panel test reports: wide heterogeneity suggests need for standardization.   Makhnoon Sukh et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Mar
Psychological impact of multi-gene cancer panel testing in patients with a clinical suspicion of hereditary cancer across Spain.   Esteban I et al. Psycho-oncology 2018 Mar
Evaluating and improving the implementation of a community-based hereditary cancer screening program.   Greenberg Samantha et al. Journal of community genetics 2018 Mar
A population-based analysis of germline BRCA1 and BRCA2 testing among ovarian cancer patients in an era of histotype-specific approaches to ovarian cancer prevention.   Hanley Gillian E et al. BMC cancer 2018 Mar 18(1) 254
Patient-Centered Care in Breast Cancer Genetic Clinics.   Brédart Anne et al. International journal of environmental research and public health 2018 Feb 15(2)
Men seeking counselling in a Breast Cancer Risk Evaluation Clinic.   Freitas Ana Catarina et al. Ecancermedicalscience 2018 12804
Colorectal cancer survivors' interest in genetic testing for hereditary cancer: implications for universal tumor screening.   Cragun Deborah et al. Genetic testing and molecular biomarkers 2012 Jun 16(6) 493-9
Colorectal cancer survivors undergoing genetic testing for hereditary non-polyposis colorectal cancer: motivational factors and psychosocial functioning.   Esplen M J et al. Clinical genetics 2007 Nov 72(5) 394-401
Identification of genetic variants for clinical management of familial colorectal tumors.   Dominguez-Valentin Mev et al. BMC medical genetics 2018 Feb 19(1) 26
Patient communication of cancer genetic test results in a diverse population.   Ricker Charité N et al. Translational behavioral medicine 2018 Jan 8(1) 85-94
Parental attitudes and expectations towards receiving genomic test results in healthy children.   Kulchak Rahm Alanna et al. Translational behavioral medicine 2018 Jan 8(1) 44-53
Risk management adherence following genetic testing for hereditary cancer syndromes: a Singaporean experience.   Courtney Eliza et al. Familial cancer 2018 Jan
Reproductive Decision Support: Preferences and Needs of Couples at Risk for Hereditary Cancer and Clinical Geneticists.   Reumkens Kelly et al. Journal of genetic counseling 2018 Jan
Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds.   Dominguez-Valentin Mev et al. Hereditary cancer in clinical practice 2018 164
MSH6 and PMS2 germ-line pathogenic variants implicated in Lynch syndrome are associated with breast cancer.   Roberts Maegan E et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Jan
Improving attendance to genetic counselling services for gynaecological oncology patients.   Pokharel Hanoon P et al. Gynecologic oncology research and practice 2018 52
BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway.   Heramb Cecilie et al. Hereditary cancer in clinical practice 2018 163
Evaluation of a 27-gene inherited cancer panel across 630 consecutive patients referred for testing in a clinical diagnostic laboratory.   Gardner Sabrina A et al. Hereditary cancer in clinical practice 2018 161
Factors influencing the decision to share cancer genetic results among family members: an in-depth interview study of women in an Asian setting.   Li Shao-Tzu et al. Psycho-oncology 2018 Jan
Investigating barriers to genetic counseling and germline mutation testing in women with suspected hereditary breast and ovarian cancer syndrome and Lynch syndrome.   Shaw Josephine et al. Patient education and counseling 2017 Dec
Managing Variant Interpretation Discrepancies in Hereditary Cancer: Clinical Practice, Concerns, and Desired Resources.   Zirkelbach Ellen et al. Journal of genetic counseling 2017 Dec
Evaluation of Breast Cancer Patients with Genetic Risk in a University Hospital: Before and After the Implementation of a Heredofamilial Cancer Unit.  Lobo Miriam et al. Journal of genetic counseling 2017 Dec
Professionals' knowledge, attitude and referral behaviour of preimplantation genetic diagnosis for hereditary breast and ovarian cancer.   Gietel-Habets J J G et al. Reproductive biomedicine online 2017 Dec
Adaptation of couples living with a high risk of breast/ovarian cancer and the association with risk-reducing surgery.   Shapira Rachel et al. Familial cancer 2017 Dec
Observed frequency and challenges of variant reclassification in a hereditary cancer clinic.   Macklin Sarah et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Dec
Hereditary gynaecologic cancers in Nepal: a proposed model of care to serve high risk populations in developing countries.   Pokharel Hanoon P et al. Hereditary cancer in clinical practice 2017 1512
High-Risk Palliative Care Patients' Knowledge and Attitudes about Hereditary Cancer Testing and DNA Banking.   Quillin John M et al. Journal of genetic counseling 2017 Dec
Decision making and experiences of young adults undergoing presymptomatic genetic testing for familial cancer: a longitudinal grounded theory study.  Godino Lea et al. European journal of human genetics : EJHG 2017 Nov
Germline Genetic Features of Young Individuals with Colorectal Cancer.   Stoffel Elena M et al. Gastroenterology 2017 Nov
Investigating Uncertainty in Genetic Counseling Encounters: Managing Information About Genetic Cancer Risk.   Rauscher Emily A et al. Journal of health communication 2017 Nov 1-9
Development of a high risk pancreatic screening clinic using 3.0 T MRI.   Barnes Chad A et al. Familial cancer 2017 Nov
Prevalence and detection of psychosocial problems in cancer genetic counseling.   Eijzenga W et al. Familial cancer 2015 Dec 14(4) 629-36
Identification of hereditary cancer in the general population: development and validation of a screening questionnaire for obtaining the family history of cancer.   Campacci Natalia et al. Cancer medicine 2017 Oct
Emotional impact on the results of BRCA1 and BRCA2 genetic test: an observational retrospective study.   Mella Sara et al. Hereditary cancer in clinical practice 2017 1516
Facilitating decision-making in women undergoing genetic testing for hereditary breast cancer: BRECONDA randomized controlled trial results.   Sherman Kerry A et al. Breast (Edinburgh, Scotland) 2017 Oct 3679-85
Expanding the spectrum of germline variants in cancer.   Siraj Abdul K et al. Human genetics 2017 Oct
Video Education on Hereditary Breast and Ovarian Cancer (HBOC) for Physicians: an Interventional Study.   Krishnamachari Bhuma et al. Journal of cancer education : the official journal of the American Association for Cancer Education 2017 Jun
Hereditary and non-hereditary branches of family eligible for BRCA test: cancers in other sites.   Digennaro M et al. Hereditary cancer in clinical practice 2017 157
Identification and Management of TP53 Gene Carriers Detected Through Multigene Panel Testing.   Pal Tuya et al. Southern medical journal 2017 Oct 110(10) 643-648
Evaluation of psychosocial aspects in participants of cancer genetic counseling.   González-Ramírez Leivy Patricia et al. Hereditary cancer in clinical practice 2017 1513
Breadth of Genetic Testing Selected by Patients at Risk of Hereditary Breast and Ovarian Cancer.   Szender J Brian et al. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society 2017 Sep
Increased Identification of Candidates for High-Risk Breast Cancer Screening Through Expanded Genetic Testing.   Rosenthal Eric T et al. Journal of the American College of Radiology : JACR 2017 Apr 14(4) 561-568
A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.   Rossi Benedito Mauro et al. BMC cancer 2017 Sep 17(1) 623
CADD score has limited clinical validity for the identification of pathogenic variants in noncoding regions in a hereditary cancer panel.   Mather Cheryl A et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Dec 18(12) 1269-1275
Family history in ovarian cancer referral population.   Berg L A et al. Journal of genetic counseling 1996 Mar 5(1) 27-38
Preoperative genetic testing impacts surgical decision making in BRCA mutation carriers with breast cancer: a retrospective cohort analysis.   Yadav Siddhartha et al. Hereditary cancer in clinical practice 2017 1511
Preoperative Panel Testing for Hereditary Cancer Syndromes Does Not Significantly Impact Time to Surgery for Newly Diagnosed Breast Cancer Patients Compared with BRCA1/2 Testing.   Murphy Amy E et al. Annals of surgical oncology 2017 Aug
Expanded Gene Panel Use for Women With Breast Cancer: Identification and Intervention Beyond Breast Cancer Risk.   O'Leary Erin et al. Annals of surgical oncology 2017 Aug
Advances in the diagnosis of hereditary kidney cancer: Initial results of a multigene panel test.   Nguyen Kevin A et al. Cancer 2017 Aug
Racial/ethnic differences in multiple-gene sequencing results for hereditary cancer risk.   Caswell-Jin Jennifer L et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Jul
Is no news good news? Inconclusive genetic test results in BRCA1 and BRCA2 from patients and professionals' perspectives.   Ardern-Jones Audrey et al. Hereditary cancer in clinical practice 2010 Jan 8(1) 1
A randomized controlled trial of disclosing genetic risk information for Alzheimer disease via telephone.   Christensen Kurt D et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Jul
A multi-gene panel study in hereditary breast and ovarian cancer in Colombia.   Cock-Rada A M et al. Familial cancer 2017 May
Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity.   Houlleberghs Hellen et al. PLoS genetics 2017 May 13(5) e1006765
Adherence to Recommended Risk Management among Unaffected Women with a BRCA Mutation.   Buchanan Adam H et al. Journal of genetic counseling 2017 Feb 26(1) 79-92
Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer.   Couch Fergus J et al. JAMA oncology 2017 Apr
Clinical Variant Classification: A Comparison of Public Databases and a Commercial Testing Laboratory.   Gradishar William et al. The oncologist 2017 Apr
Clinical utility of a self-administered questionnaire for assessment of hereditary gynecologic cancer.   Masuda Kenta et al. Japanese journal of clinical oncology 2017 Dec 1-6
Payer Coverage for Hereditary Cancer Panels: Barriers, Opportunities, and Implications for the Precision Medicine Initiative.   Trosman Julia R et al. Journal of the National Comprehensive Cancer Network : JNCCN 2017 Feb 15(2) 219-228
Recruiting families at risk for hereditary breast and ovarian cancer from a statewide cancer registry: a methodological study.   Katapodi Maria C et al. Cancer causes & control : CCC 2017 Feb
Family History in Colonoscopy Patients: Feasibility and Performance of Electronic and Paper-based Surveys for Colorectal Cancer Risk Assessment in the Outpatient Setting.   Guivatchian Tannaz et al. Gastrointestinal endoscopy 2017 Feb
Impact of hereditary multigene panel testing for cancer survivors.   Swisher Jennifer et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2016 Jan 34(3_suppl) 261
"It was an Emotional Baby": Previvors' Family Planning Decision-Making Styles about Hereditary Breast and Ovarian Cancer Risk.   Dean Marleah et al. Journal of genetic counseling 2017 Jan
The Use of Social Media to Recruit Participants With Rare Conditions: Lynch Syndrome as an Example.   Burton-Chase Allison M et al. JMIR research protocols 2017 Jan 6(1) e12
Anxiety and depression symptoms among women attending group-based patient education courses for hereditary breast and ovarian cancer.   Listøl Wenche et al. Hereditary cancer in clinical practice 2017 152
Li-Fraumeni syndrome: a paradigm for the understanding of hereditary cancer predisposition.   Valdez Jessica M et al. British journal of haematology 2016 Dec
Cancer Genetic Counselors' Current Practices and Attitudes Related to the Use of Tumor Profiling.   Goedde LeAnne Noelle et al. Journal of genetic counseling 2017 Jan
A study of over 35,000 women with breast cancer tested with a 25-gene panel of hereditary cancer genes.   Buys Saundra S et al. Cancer 2017 Jan
Impact of Payer Constraints on Access to Genetic Testing.   Whitworth Pat et al. Journal of oncology practice 2017 Jan 13(1) e47-e56
How does genetic risk information for Lynch syndrome translate to risk management behaviours?   Steel Emma et al. Hereditary cancer in clinical practice 2017 151
Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.   Pearlman Rachel et al. JAMA oncology 2016 Dec
Five Years of Multidisciplinary Care in Hereditary Cancer: Our Experience in a Spanish University Hospital.   Márquez-Rodas I et al. Oncology 2016 Nov
Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands.   Dommering Charlotte J et al. Familial cancer 2016 Nov
Novel BRCA1 and BRCA2 Tumour Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas.   Weren Robbert D A et al. Human mutation 2016 Oct
Challenges to clinical utilization of hereditary cancer gene panel testing: perspectives from the front lines.   Marcus Rebecca K et al. Familial cancer 2015 Dec 14(4) 641-9
Changing patterns of referrals and outcomes of genetic participation in gynaecological-oncology multidisciplinary care.   Pokharel Hanoon P et al. The Australian & New Zealand journal of obstetrics & gynaecology 2016 Aug
Evolution of Hereditary Breast Cancer Genetic Services: Are Changes Reflected in the Knowledge and Clinical Practices of Florida Providers?   Cragun Deborah et al. Genetic testing and molecular biomarkers 2016 Aug
Lynch syndrome: barriers to and facilitators of screening and disease management.   Watkins Kathy E et al. Hereditary cancer in clinical practice 2011 98
Genomics of Hereditary Colorectal Cancer: Lessons Learnt from 25 Years of the Singapore Polyposis Registry.   Chew Min Hoe et al. Annals of the Academy of Medicine, Singapore 2015 Aug 44(8) 290-6
Multi-gene panel testing for hereditary cancer susceptibility in a rural Familial Cancer Program.   Hermel David J et al. Familial cancer 2016 Jul
Successful implementation of Lynch syndrome screening in a safety net institution.   Kidambi Trilokesh D et al. Journal of community genetics 2016 Jul
Classification of genetic variants in genes associated with Lynch syndrome using a clinical history weighting algorithm.   Morris Brian et al. BMC genetics 2016 17(1) 99
A model for patient-direct screening and referral for familial cancer risk.   Niendorf Kristin B et al. Familial cancer 2016 Jun
The Clinical Utility of Next Generation Sequencing Results in a Community-Based Hereditary Cancer Risk Program.   Bunnell A E et al. Journal of genetic counseling 2016 Jun
Self-reported cancer family history is a useful tool for identification of individuals at risk of hereditary cancer predisposition syndrome at primary care centers in middle-income settings: a longitudinal study.   Flória-Santos Milena et al. Genetics and molecular biology 2016 Jun 0
Exome sequencing reveals frequent deleterious germline variants in cancer susceptibility genes in women with invasive breast cancer undergoing neoadjuvant chemotherapy.   Ellingson Marissa S et al. Breast cancer research and treatment 2015 Sep 153(2) 435-43
The Impact of Angelina Jolie (AJ)'s Story on Genetic Referral and Testing at an Academic Cancer Centre in Canada.   Raphael Jacques et al. Journal of genetic counseling 2016 May
Evaluation of Patients and Families With Concern for Predispositions to Hematologic Malignancies Within the Hereditary Hematologic Malignancy Clinic (HHMC).   DiNardo Courtney D et al. Clinical lymphoma, myeloma & leukemia 2016 Apr
Use of panel tests in place of single gene tests in the cancer genetics clinic.   Yorczyk A et al. Clinical genetics 2015 Sep 88(3) 278-82
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.   Maxwell Kara N et al. American journal of human genetics 2016 May 98(5) 801-17
Assessing biases of information contained in pedigrees for the classification of BRCA-genetic variants: a study arising from the ENIGMA analytical working group.   Kerkhofs C H H et al. Hereditary cancer in clinical practice 2016 1410
Identifying Women at Risk for Hereditary Breast and Ovarian Cancer Syndrome Utilizing Breast Care Nurse Navigation at Mammography and Imaging Centers.   Appel Susan J et al. Journal of National Black Nurses' Association : JNBNA 2015 Dec 26(2) 17-26
Adherence to the breast cancer surveillance program for women at risk for familial breast and ovarian cancer versus overscreening: a monocenter study in Germany.   Vetter Lisa et al. Breast cancer research and treatment 2016 Mar
Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registry.   Vasen Hans F A et al. Familial cancer 2016 Mar
Clinical utility of a Web-enabled risk-assessment and clinical decision support program.   Orlando Lori A et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Mar
Knowledge regarding basic concepts of hereditary cancers, and the available genetic counselling and testing services: A survey of general practitioners in Johannesburg, South Africa.   Van Wyk Chantel et al. South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 2016 106(3) 268-71