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Cost–utility analysis of risk-reducing strategies to prevent breast and ovarian cancer in BRCA-mutation carriers in Switzerland

The European journal of health economics, 2022-07, Vol.23 (5), p.807-821

2022

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Levels of plasma circulating cell free nuclear and mitochondrial DNA as potential biomarkers for breast tumors

Molecular cancer, 2009-11, Vol.8 (1), p.105-105, Article 105

2009

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Hypermethylation of tumor suppressor genes involved in critical regulatory pathways for developing a blood-based test in breast cancer

PloS one, 2011-01, Vol.6 (1), p.e16080-e16080

2011

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Genetic counselling and testing of susceptibility genes for therapeutic decision-making in breast cancer—an European consensus statement and expert recommendations

European journal of cancer (1990), 2019-01, Vol.106, p.54-60

2019

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Routine Genetic Testing of Germline Breast Cancer Susceptibility ─ Challenges and Opportunities

Healthbook TIMES. Oncology Hematology, 2023-10, Vol.17 (17)

2023

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The Communication Chain of Genetic Risk: Analyses of Narrative Data Exploring Proband–Provider and Proband–Family Communication in Hereditary Breast and Ovarian Cancer

Journal of personalized medicine, 2022-08, Vol.12 (8), p.1249

2022

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Genetic Literacy and Communication of Genetic Information in Families Concerned with Hereditary Breast and Ovarian Cancer: A Cross-Study Comparison in Two Countries and within a Timeframe of More Than 10 Years

Cancers, 2021-12, Vol.13 (24), p.6254

2021

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Molekulare Früherkennung in der Gynäkologie – Hereditäres Mamma- und Ovarialkarzinom: Indikationen für genetische Beratung und Gentests

Therapeutische Umschau, 2010-07, Vol.67 (7), p.359-366

Bürki, Nicole

2010

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Examining information-seeking behavior in genetic testing for cancer predisposition: A qualitative interview study

Patient education and counseling, 2021-02, Vol.104 (2), p.257-264

2021

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S143. Steroid Hormone Analysis of Retrospective Maternal Hair and Newborn Nail Samples Indicate Effects of Prenatal Stress on Postpartum Well-being of Mother and Offspring

Biological psychiatry (1969), 2018-05, Vol.83 (9), p.S403-S404

2018

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Hereditary breast and ovarian cancer - indications for genetic testing, counseling and options for mutation carriers

Therapeutische Umschau, 2010-07, Vol.67 (7), p.359

Bürki, Nicole

2010

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Predicting Openness of Communication in Families With Hereditary Breast and Ovarian Cancer Syndrome: Natural Language Processing Analysis

JMIR formative research, 2023-01, Vol.7, p.e38399-e38399

2023

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Relatives from Hereditary Breast and Ovarian Cancer and Lynch Syndrome Families Forgoing Genetic Testing: Findings from the Swiss CASCADE Cohort

Journal of personalized medicine, 2022-10, Vol.12 (10), p.1740

2022

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Placental α-microglobulin-1 to detect uncertain rupture of membranes in a European cohort of pregnancies

Archives of gynecology and obstetrics, 2012, Vol.285 (1), p.21-25

2012

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Comparative genomic hybridization of fine needle aspirates from breast carcinomas

International journal of cancer, 2000-11, Vol.88 (4), p.607-613

2000

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Well-Differentiated Mucinous Carcinoma of the Ovary and a Coexisting Brenner Tumor Both Exhibit Amplification of 12q14–21 by Comparative Genomic Hybridization

Gynecologic oncology, 1999-07, Vol.74 (1), p.134-137

1999

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Impact of breast cancer family history on tumor detection and tumor size in women newly-diagnosed with invasive breast cancer

Familial cancer, 2014-03, Vol.13 (1), p.99-107

2014

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Hypercalcemic-type of small cell carcinoma of the ovary: characterization of a new tumor line

Anticancer research, 2001-09, Vol.21 (5), p.3253

2001

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Problems in Umbilical Cord Blood Collection

Transfusion medicine and hemotherapy, 2007-01, Vol.34 (2), p.95-98

2007

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Behandlung des Mammakarzinoms

Pharma-kritik, 2003-11, Vol.25 (12)

Masche, Urspeter

2003

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Cost–utility analysis of risk-reducing strategies to prevent breast and ovarian cancer in BRCA-mutation carriers in Switzerland

Levels of plasma circulating cell free nuclear and mitochondrial DNA as potential biomarkers for breast tumors

Hypermethylation of tumor suppressor genes involved in critical regulatory pathways for developing a blood-based test in breast cancer

Genetic counselling and testing of susceptibility genes for therapeutic decision-making in breast cancer—an European consensus statement and expert recommendations

Routine Genetic Testing of Germline Breast Cancer Susceptibility ─ Challenges and Opportunities

Intention to Inform Relatives, Rates of Cascade Testing, and Preference for Patient-Mediated Communication in Families Concerned with Hereditary Breast and Ovarian Cancer and Lynch Syndrome: The Swiss CASCADE Cohort

The Communication Chain of Genetic Risk: Analyses of Narrative Data Exploring Proband–Provider and Proband–Family Communication in Hereditary Breast and Ovarian Cancer

Genetic Literacy and Communication of Genetic Information in Families Concerned with Hereditary Breast and Ovarian Cancer: A Cross-Study Comparison in Two Countries and within a Timeframe of More Than 10 Years

Acceptability and Usability of the Family Gene Toolkit for Swiss and Korean Families Harboring BRCA1/BRAC2 Pathogenic Variants: A Web-Based Platform for Cascade Genetic Testing

Using a Tailored Digital Health Intervention for Family Communication and Cascade Genetic Testing in Swiss and Korean Families With Hereditary Breast and Ovarian Cancer: Protocol for the DIALOGUE Study

Molekulare Früherkennung in der Gynäkologie – Hereditäres Mamma- und Ovarialkarzinom: Indikationen für genetische Beratung und Gentests

Examining information-seeking behavior in genetic testing for cancer predisposition: A qualitative interview study

S143. Steroid Hormone Analysis of Retrospective Maternal Hair and Newborn Nail Samples Indicate Effects of Prenatal Stress on Postpartum Well-being of Mother and Offspring

Hereditary breast and ovarian cancer - indications for genetic testing, counseling and options for mutation carriers

Acceptability and Usability of the Family Gene Toolkit for Swiss and Korean Families Harboring IBRCA1/BRAC2/I Pathogenic Variants: A Web-Based Platform for Cascade Genetic Testing

Predicting Openness of Communication in Families With Hereditary Breast and Ovarian Cancer Syndrome: Natural Language Processing Analysis

Relatives from Hereditary Breast and Ovarian Cancer and Lynch Syndrome Families Forgoing Genetic Testing: Findings from the Swiss CASCADE Cohort

Placental α-microglobulin-1 to detect uncertain rupture of membranes in a European cohort of pregnancies

Comparative genomic hybridization of fine needle aspirates from breast carcinomas

Challenges and Opportunities for Cancer Predisposition Cascade Screening for Hereditary Breast and Ovarian Cancer and Lynch Syndrome in Switzerland: Findings from an International Workshop

Well-Differentiated Mucinous Carcinoma of the Ovary and a Coexisting Brenner Tumor Both Exhibit Amplification of 12q14–21 by Comparative Genomic Hybridization

Impact of breast cancer family history on tumor detection and tumor size in women newly-diagnosed with invasive breast cancer

Hypercalcemic-type of small cell carcinoma of the ovary: characterization of a new tumor line

Problems in Umbilical Cord Blood Collection

Behandlung des Mammakarzinoms

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