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Risks of first and subsequent cancers among TP53 mutation carriers in the National Cancer Institute Li‐Fraumeni syndrome cohort

Cancer, 2016-12, Vol.122 (23), p.3673-3681

2016

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Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study

British journal of haematology, 2010-07, Vol.150 (2), p.179-188

2010

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Essential Elements of Genetic Cancer Risk Assessment, Counseling, and Testing: Updated Recommendations of the National Society of Genetic Counselors

Journal of genetic counseling, 2012-04, Vol.21 (2), p.151-161

2012

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Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita

Blood, 2007-09, Vol.110 (5), p.1439-1447

2007

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Characteristics of Health Information Gatherers, Disseminators, and Blockers Within Families at Risk of Hereditary Cancer: Implications for Family Health Communication Interventions

American journal of public health (1971), 2009-12, Vol.99 (12), p.2203-2209

2009

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A Pragmatic Testing-Eligibility Framework for Population Mutation Screening: The Example of BRCA1/2

Cancer epidemiology, biomarkers & prevention, 2019-02, Vol.28 (2), p.293-302

2019

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Special Issue Introduction: Dealing with Psychological and Social Complexity in Genetic Counseling

Journal of genetic counseling, 2017-04, Vol.26 (2), p.195-198

2017

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Prevalence of Cancer at Baseline Screening in the National Cancer Institute Li-Fraumeni Syndrome Cohort

JAMA oncology, 2017-12, Vol.3 (12), p.1640

2017

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Family Health Leaders: Lessons on Living with Li‐Fraumeni Syndrome across Generations

Family process, 2020-12, Vol.59 (4), p.1648-1663

2020

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Familial testicular germ cell tumors in adults: 2010 summary of genetic risk factors and clinical phenotype

Endocrine-related cancer, 2010-06, Vol.17 (2), p.R109-R121

2010

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Research participant interest in primary, secondary, and incidental genomic findings

Genetics in medicine, 2016-12, Vol.18 (12), p.1218-1225

2016

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Easing the Burden: Describing the Role of Social, Emotional and Spiritual Support in Research Families with Li-Fraumeni Syndrome

Journal of genetic counseling, 2016-06, Vol.25 (3), p.529-542

2016

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Couples coping with screening burden and diagnostic uncertainty in Li-Fraumeni syndrome: Connection versus independence

Journal of psychosocial oncology, 2019-03, Vol.37 (2), p.178-193

2019

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Sisters in hereditary breast and ovarian cancer families: communal coping, social integration, and psychological well-being

Psycho-oncology (Chichester, England), 2008-08, Vol.17 (8), p.812-821

2008

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Genetic Information-Seeking Behaviors and Knowledge among Family Members and Patients with Inherited Bone Marrow Failure Syndromes

Journal of genetic counseling, 2015-10, Vol.24 (5), p.760-770

2015

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Unpacking the Blockers: Understanding Perceptions and Social Constraints of Health Communication in Hereditary Breast Ovarian Cancer (HBOC) Susceptibility Families

Journal of genetic counseling, 2011-10, Vol.20 (5), p.450-464

2011

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Genetic Cancer Risk Assessment and Counseling: Recommendations of the National Society of Genetic Counselors

Journal of genetic counseling, 2004-04, Vol.13 (2), p.83-114

2004

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Referral to cancer genetic counseling: Are there stages of readiness?

American journal of medical genetics. Part C, Seminars in medical genetics, 2006-11, Vol.142C (4), p.221-231

2006

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Use of an educational computer program before genetic counseling for breast cancer susceptibility: Effects on duration and content of counseling sessions

Genetics in medicine, 2005-04, Vol.7 (4), p.221-229

2005

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Close ties: an exploratory Colored Eco-Genetic Relationship Map (CEGRM) study of social connections of men in Familial Testicular Cancer (FTC) families

Hereditary cancer in clinical practice, 2012-03, Vol.10 (1), p.2-2, Article 2

2012

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BRCA mutation-negative women from hereditary breast and ovarian cancer families: a qualitative study of the BRCA-negative experience

Health expectations : an international journal of public participation in health care and health policy, 2008-09, Vol.11 (3), p.220-231

2008

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Factors associated with testicular self-examination among unaffected men from multiple-case testicular cancer families

Hereditary cancer in clinical practice, 2009-05, Vol.7 (1), p.11-11, Article 11

2009

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Disclosure of Positive BRCA1/2-Mutation Status in Young Couples: The Journey From Uncertainty to Bonding Through Partner Support

Families systems & health, 2008-09, Vol.26 (3), p.296-316

2008

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Familial testicular germ cell tumor: no associated syndromic pattern identified

Hereditary cancer in clinical practice, 2014-02, Vol.12 (1), p.3-3, Article 3

2014

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Risks of first and subsequent cancers among TP53 mutation carriers in the National Cancer Institute Li‐Fraumeni syndrome cohort

Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study

Essential Elements of Genetic Cancer Risk Assessment, Counseling, and Testing: Updated Recommendations of the National Society of Genetic Counselors

Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita

Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging: A Meta-analysis

Characteristics of Health Information Gatherers, Disseminators, and Blockers Within Families at Risk of Hereditary Cancer: Implications for Family Health Communication Interventions

A Pragmatic Testing-Eligibility Framework for Population Mutation Screening: The Example of BRCA1/2

Special Issue Introduction: Dealing with Psychological and Social Complexity in Genetic Counseling

Prevalence of Cancer at Baseline Screening in the National Cancer Institute Li-Fraumeni Syndrome Cohort

Family Health Leaders: Lessons on Living with Li‐Fraumeni Syndrome across Generations

Familial testicular germ cell tumors in adults: 2010 summary of genetic risk factors and clinical phenotype

Research participant interest in primary, secondary, and incidental genomic findings

Easing the Burden: Describing the Role of Social, Emotional and Spiritual Support in Research Families with Li-Fraumeni Syndrome

Couples coping with screening burden and diagnostic uncertainty in Li-Fraumeni syndrome: Connection versus independence

Sisters in hereditary breast and ovarian cancer families: communal coping, social integration, and psychological well-being

Genetic Information-Seeking Behaviors and Knowledge among Family Members and Patients with Inherited Bone Marrow Failure Syndromes

Unpacking the Blockers: Understanding Perceptions and Social Constraints of Health Communication in Hereditary Breast Ovarian Cancer (HBOC) Susceptibility Families

Genetic Cancer Risk Assessment and Counseling: Recommendations of the National Society of Genetic Counselors

Referral to cancer genetic counseling: Are there stages of readiness?

Use of an educational computer program before genetic counseling for breast cancer susceptibility: Effects on duration and content of counseling sessions

Close ties: an exploratory Colored Eco-Genetic Relationship Map (CEGRM) study of social connections of men in Familial Testicular Cancer (FTC) families

BRCA mutation-negative women from hereditary breast and ovarian cancer families: a qualitative study of the BRCA-negative experience

Factors associated with testicular self-examination among unaffected men from multiple-case testicular cancer families

Disclosure of Positive BRCA1/2-Mutation Status in Young Couples: The Journey From Uncertainty to Bonding Through Partner Support

Familial testicular germ cell tumor: no associated syndromic pattern identified

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