M
Mary Ahrens
Researcher at University of Minnesota
Publications - 7
Citations - 372
Mary Ahrens is an academic researcher from University of Minnesota. The author has contributed to research in topics: Genetic counseling & Cancer. The author has an hindex of 6, co-authored 7 publications receiving 355 citations.
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Journal ArticleDOI
Genetic Cancer Risk Assessment and Counseling: Recommendations of the National Society of Genetic Counselors
Angela Trepanier,Mary Ahrens,Wendy McKinnon,June A. Peters,Jill Stopfer,Sherry C. Grumet,Susan Manley,Julie O. Culver,Ronald T. Acton,Joy Larsen-Haidle,Lori Ann Correia,Robin L. Bennett,Barbara Pettersen,Terri Diamond Ferlita,Josephine Wagner Costalas,Katherine Hunt,Susan Donlon,Cécile Skrzynia,Carolyn Farrell,Faith Callif-Daley,Catherine Walsh Vockley +20 more
TL;DR: These cancer genetic counseling recommendations describe the medical, psychosocial, and ethical ramifications of identifying at-risk individuals through cancer risk assessment with or without genetic testing.
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Genetic Services for Familial Cancer Patients: A Survey of National Cancer Institute Cancer Centers
Julie A. Thompson,Thomas A. Sellers,Celine M. Vachon,Mary Ahrens,Mary Sumpmann,John H. Kersey,Georgia L. Wiesner,John D. Potter +7 more
TL;DR: There is interest in developing clinical programs for familial cancers by NCI-supported cancer centers, but most of these programs are in developmental stages; a base line has been established to monitor future progress for the provision of cancer genetic services.
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Complete and sustained response of adult medulloblastoma to first-line sonic hedgehog inhibition with vismodegib
TL;DR: Findings indicate that vismodegib may also block alternate, non-canonical forms of downstream SHH pathway activation, which provides strong impetus for further investigation of vismODEgib in clinical trials in the first-line setting for pediatric and adult forms of medulloblastoma.
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Clinical and biochemical heterogeneity in females of a large pedigree with ornithine transcarbamylase deficiency due to the R141Q mutation
Mary Ahrens,Susan A. Berry,Chester B. Whitley,Dorothy Markowitz,Robert J. Plante,Mendel Tuchman +5 more
TL;DR: A higher than expected proportion of female heterozygous for the R141Q mutation were clinically and biochemically symptomatic but remained undiagnosed for many years and should be performed in females who present with a combination of relatively non-specific symptoms.
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"What would you do if you were me?" Effects of counselor self-disclosure versus non-disclosure in a hypothetical genetic counseling session.
Amy L. Paine,Patricia McCarthy Veach,Ian M. MacFarlane,Brittany C. Thomas,Mary Ahrens,Bonnie S. LeRoy +5 more
TL;DR: Analysis of written responses yielded four themes: Made Decision, Sought Information, Expressed Thoughts/Feelings, and No Decision, which rated the non-disclosing counselor significantly lower in social attractiveness than either disclosing counselor, and less satisfying than the professional disclosing counselor.