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pro vyhledávání: '"Janice L. Berliner"'
The genetic counseling (GC) profession has seen exponential growth in recent years, although the core identity of practitioners, focusing on the interpersonal impact of genetics on their clients' lives, remains unchanged. This chapter familiarizes un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39c080176824214ab6234dfdc8aa9b31
https://doi.org/10.4018/978-1-7998-9617-3.ch001
https://doi.org/10.4018/978-1-7998-9617-3.ch001
Publikováno v:
Journal of genetic counselingREFERENCES. 30(2)
Cancer risk assessment and genetic counseling for hereditary breast and ovarian cancer (HBOC) are a communication process to inform and prepare patients for genetic test results and the related medical management. An increasing number of healthcare p
Autor:
Janice L. Berliner, Angela G. Arnold, Magan Trottier, Jennifer L. Hay, Kenneth Offit, Erin E. Salo-Mullen, Zsofia K. Stadler, M.E. Robson, N Sekhri, Noah D. Kauff, P Gaissert, M Harlan Fleischut, Vanessa Marcell, Kimberly Amoroso, Michael Walsh, Beth Siegel, Jada G. Hamilton, Margaret Sheehan
Publikováno v:
Cancer Research. 76:P2-09
Background: Multiplex genetic testing involves the simultaneous analysis of a panel of known cancer susceptibility genes. Although efficient and cost-effective, multiplex testing presents several challenges for patients and clinicians: these tests pr
Publikováno v:
Quality of Life Among Cancer Survivors ISBN: 9783319752228
This chapter will examine the complex psychosocial aspects of pre- and post-test counseling for cancer genetic syndromes with both adult and pediatric onset. Using case examples, we will illustrate some of the many issues that cancer patients face wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e759bd935428c3c09d83ddd5cfb9561a
https://doi.org/10.1007/978-3-319-75223-5_5
https://doi.org/10.1007/978-3-319-75223-5_5
Autor:
Kenneth Offit, Beth Siegel, Ebunoluwa Otegbeye, Noah D. Kauff, Erin E. Salo-Mullen, Janice L. Berliner, Liying Zhang, Kim Amoroso, Emily Glogowski, Margaret Sheehan, Megan Harlan Fleischut, Angela G. Arnold, Mark E. Robson, Sherry R. Boyar, Zsofia K. Stadler
Publikováno v:
Breast Cancer Research and Treatment. 145:625-634
BRCA1/2 large rearrangement (LR) testing has been available to patients since 2006. Three existing models commonly used in cancer genetics clinical and research settings (BRCAPRO, Penn II and Myriad II) have not been assessed for their performance in
Autor:
Todd Tillmanns, Angela Musial Fay, Janice L. Berliner, Shelly Cummings, Brittany Boldt Burnett
Publikováno v:
Journal of Genetic Counseling. 22:155-163
The purpose of this document is to present a current and comprehensive set of practice recommendations for effective genetic cancer risk assessment, counseling and testing for hereditary breast and ovarian cancer. The intended audience is genetic cou
Autor:
Janice L. Berliner, Angela Musial Fay
Publikováno v:
Journal of Genetic Counseling. 16:241-260
These cancer genetic counseling recommendations describe the medical, psychosocial and ethical implications of identifying at-risk individuals for hereditary breast and ovarian cancer (HBOC) through cancer risk assessment, with or without genetic sus
Autor:
Janice L. Berliner, Nathalie McIntosh
Publikováno v:
Journal of Genetic Counseling. 13:463-550
Autor:
Beth Siegel, Marjorie G. Zauderer, Diana Mandelker, Marc Ladanyi, Janice L. Berliner, Mariel A. DuBoff, Megan Harlan Fleischut, Angela G. Arnold, Mark E. Robson
Publikováno v:
Journal of Clinical Oncology. 35:e13118-e13118
e13118 Background: Somatic BAP1 mutations are very common in MM tumors (Bueno et al. Nat Genet 2016, Bott et al. Nature Genet 2011) and germline BAP1 mutations have also been shown to segregate in numerous families with clusters of malignancies inclu
Autor:
Faye N. Shapiro, George E. Houck, Janice L. Berliner, Xiaohua Ding, W. Ted Brown, Sarah L. Nolin, Susan Sklower Brooks, Carl Dobkin
Publikováno v:
Journal of Genetic Counseling. 3:233-244
Molecular analysis of the fragile X (FMR-1) gene identifies female fragile X carriers, but appropriate genetic counseling can only be provided if the limitations of the testing methods are understood. Molecular analysis of this gene is achieved with