S. McCormick

发表

Toward a better understanding of the experience of patients with moderate penetrance breast cancer gene pathogenic/likely pathogenic variants: A focus on ATM and CHEK2

S. McCormick, Stephanie R Hicks, Mackenzie Wooters, 2022, Journal of genetic counseling.

Uptake of BRCA1/2 Genetic Testing in a Randomized Trial of Telephone Counseling

J. Garber, H. Valdimarsdottir, C. Isaacs, 2014, Genetics in Medicine.

Characteristics of individuals with breast cancer rearrangements in BRCA1 and BRCA2

R. Nussbaum, L. Esserman, N. Yi, 2014, Cancer.

New Insights into Melanoma Tumor Syndromes

H. Tsao, S. McCormick, Sameer Gupta, 2022, JID innovations : skin science from molecules to population health.

Motivation and family communication in hereditary prostate cancer genetic testing: Survey of patients from a US tertiary medical center

K. Niendorf, S. McCormick, L. Rodgers, 2022, Journal of genetic counseling.

Randomized noninferiority trial of telephone versus in-person genetic counseling for hereditary breast and ovarian cancer.

J. Garber, H. Valdimarsdottir, C. Isaacs, 2014, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Genotypic and Phenotypic Features of BAP1 Cancer Syndrome: A Report of 8 New Families and Review of Cases in the Literature

C. Shea, H. Rana, Raj Kumar, 2017, JAMA dermatology.

Intentions for risk‐reducing surgery among high‐risk women referred for BRCA1/BRCA2 genetic counseling

J. Garber, H. Valdimarsdottir, B. Peshkin, 2015, Psycho-oncology.

Uptake of BRCA1/2 Genetic Testing in a Randomized Trial of Telephone Counseling

J. Garber, H. Valdimarsdottir, C. Isaacs, 2014, Genetics in Medicine.

Randomized Noninferiority Trial of Telephone vs In-Person Genetic Counseling for Hereditary Breast and Ovarian Cancer: A 12-Month Follow-Up

J. Garber, H. Valdimarsdottir, C. Isaacs, 2017, JNCI cancer spectrum.

Telephone versus in-person genetic counseling for hereditary cancer risk: Patient predictors of differential outcomes

J. Garber, H. Valdimarsdottir, C. Isaacs, 2021, Journal of telemedicine and telecare.

Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer

H. Valdimarsdottir, B. Peshkin, M. Schwartz, 2016, Familial Cancer.

Patient Perceptions of Telephone vs. In-Person BRCA1/BRCA2 Genetic Counseling

J. Garber, H. Valdimarsdottir, C. Isaacs, 2016, Journal of Genetic Counseling.

Cancer risks associated with the germline MITF(E318K) variant

S. Guhan, L. Ellisen, M. Artomov, 2020, Scientific Reports.

Evidence for colorectal cancer micrometastases using reverse transcriptase-polymerase chain reaction analysis of MUC2 in lymph nodes.

R. Kratzke, G. Niehans, S. Frizelle, 2000, Cancer detection and prevention.

Impact of an Expanded Definition of Family History on Outcomes of Active Surveillance for Prostate Cancer

E. V. Van Allen, M. Blute, A. Zietman, 2023, The Journal of urology.

Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer

H. Valdimarsdottir, B. Peshkin, M. Schwartz, 2016, Familial Cancer.