Search Results - "Farrell, Carolyn"

Genetic Cancer Risk Assessment and Counseling: Recommendations of the National Society of Genetic Counselors by Trepanier, Angela, Ahrens, Mary, McKinnon, Wendy, Peters, June, Stopfer, Jill, Grumet, Sherry Campbell, Manley, Susan, Culver, Julie O., Acton, Ronald, Larsen‐Haidle, Joy, Correia, Lori Ann, Bennett, Robin, Pettersen, Barbara, Ferlita, Terri Diamond, Costalas, Josephine Wagner, Hunt, Katherine, Donlon, Susan, Skrzynia, Cecile, Farrell, Carolyn, Callif‐Daley, Faith, Vockley, Catherine Walsh

“…These cancer genetic counseling recommendations describe the medical, psychosocial, and ethical ramifications of identifying at‐risk individuals through cancer…”
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Patients with a family history of cancer: identification and management by Eberl, Margaret M, Sunga, Annette Y, Farrell, Carolyn D, Mahoney, Martin C

“…A family history of certain malignancies, especially breast, ovarian, colorectal, and prostate cancers, can place persons at increased risk of developing these…”
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Genetic/familial high-risk assessment: breast and ovarian by Daly, Mary B, Axilbund, Jennifer E, Buys, Saundra, Crawford, Beth, Farrell, Carolyn D, Friedman, Susan, Garber, Judy E, Goorha, Salil, Gruber, Stephen B, Hampel, Heather, Kaklamani, Virginia, Kohlmann, Wendy, Kurian, Allison, Litton, Jennifer, Marcom, P Kelly, Nussbaum, Robert, Offit, Kenneth, Pal, Tuya, Pasche, Boris, Pilarski, Robert, Reiser, Gwen, Shannon, Kristen Mahoney, Smith, Jeffrey R, Swisher, Elizabeth, Weitzel, Jeffrey N

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Unsuspected Klinefelter syndrome diagnosed during oncologic evaluation: a case series by Eberl, Margaret M, Baer, Maria R, Mahoney, Martin C, Sait, Sheila N J, Block, Annemarie W, Farrell, Carolyn D

“…Klinefelter syndrome is an underdiagnosed chromosomal disorder that has significant implications for health and for medical management. This report presents 5…”
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Identifying and prioritising unanswered research questions for people with hyperacusis: James Lind Alliance Hyperacusis Priority Setting Partnership by Fackrell, Kathryn, Stratmann, Linda, Kennedy, Veronica, MacDonald, Carol, Hodgson, Hilary, Wray, Nic, Farrell, Carolyn, Meadows, Mike, Sheldrake, Jacqueline, Byrom, Peter, Baguley, David M, Kentish, Rosie, Chapman, Sarah, Marriage, Josephine, Phillips, John, Pollard, Tracey, Henshaw, Helen, Gronlund, Toto A, Hoare, Derek J

“…ObjectiveTo determine research priorities in hyperacusis that key stakeholders agree are the most important.Design/settingA priority setting partnership using…”
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Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia by ASHLEY-KOCH, Allison, BONNER, Erin R, MARCHUK, Douglas A, BOUSTANY, Rose-Mary N, VANCE, Jeffery M, SCOTT, William K, PERICAK-VANCE, Margaret A, GASKELL, P. Craig, WEST, Sandra G, TIM, Richard, WOLPERT, Chantelle M, JONES, Rodney, FARRELL, Carolyn D, NANCE, Martha, SVENSON, Ingrid K

“…We evaluated seven families segregating pure, autosomal dominant familial spastic paraplegia (SPG) for linkage to four recently identified SPG loci on…”
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Uterine Carcinosarcoma Associated With Hereditary Nonpolyposis Colorectal Cancer by South, Stacey A., Hutton, Mollie, Farrell, Carolyn, Mhawech-Fauceglia, Paulette, Rodabaugh, Kerry J.

“…Hereditary nonpolyposis colorectal cancer (HNPCC) was originally described as a genetic disorder predominantly involving colorectal cancer. Numerous neoplasms…”
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Consideration of hereditary nonpolyposis colorectal cancer in BRCA mutation‐negative familial ovarian cancers by South, Stacey A., Vance, Heidi, Farrell, Carolyn, DiCioccio, Richard A., Fahey, Cathy, Piver, M. Steven, Rodabaugh, Kerry J.

“…BACKGROUND: Inherited mutations account for approximately 10% of all epithelial ovarian cancers. Breast cancer (BRCA1 and BRACA2) gene mutations are…”
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Perceived health status, health values and health goals as influences on individual pursuit of DTC genome testing: Implications for healthcare of ill & healthy by Farrell, Carolyn Marie Dachs

“…This dissertation examines an individual's perceived health status, and health values, as influences on self-initiated health action, specifically the pursuit…”
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The role of hereditary nonpolyposis colorectal cancer in the management of familial ovarian cancer by Farrell, Carolyn, Lyman, Mollie, Freitag, Katherine, Fahey, Cathy, Piver, M. Steven, Rodabaugh, Kerry J.

“…Purpose: Familial ovarian cancer is most often associated with hereditary breast and ovarian cancer, implicating mutations in the BRCA1 and BRCA2 genes…”
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Genomic DNA-based hMSH2 and hMLH1 mutation screening in 32 Eastern United States hereditary nonpolyposis colorectal cancer pedigrees by WEBER, T. K, CONLON, W, ANDERSON, G, STOLER, D, YANDELL, D, PETRELLI, N. J, RODRIGUEZ-BIGAS, M, KEITZ, B, PAZIK, J, FARRELL, C, O'MALLEY, L, OSHALIM, M, ABDO, M

“…Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant cancer syndrome characterized by early age of onset colorectal cancer (mean 45…”
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Genetic/familial high-risk assessment: breast and ovarian by Daly, Mary B, Axilbund, Jennifer E, Bryant, Eileen, Buys, Saundra, Eng, Charis, Friedman, Susan, Esserman, Laura J, Farrell, Carolyn D, Ford, James M, Garber, Judy E, Jeter, Joanne M, Kohlmann, Wendy, Lynch, Patrick M, Marcom, P Kelly, Nabell, Lisle M, Offit, Kenneth, Osarogiagbon, Raymond U, Pasche, Boris, Reiser, Gwen, Sutphen, Rebecca, Weitzel, Jeffrey N

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Health, Life, and Disability Insurance and Hereditary Nonpolyposis Colorectal Cancer by Rodriguez-Bigas, Miguel A., Vasen, Hans F.A., O'Malley, Linda, Rosenblatt, Mary-Jo T., Farrell, Carolyn, Weber, Thomas K., Petrelli, Nicholas J.

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A cancer genetics education campaign: delivering parallel messages to clinicians and the public by Piniewski-Bond, Joanne, Celestino, Paul B, Mahoney, Martin C, Farrell, Carolyn D, Bauer, Joseph E, Hastrup, Janice L, Cummings, K Michael

“…Up to 10% of all cancers are thought to have a familial basis through complex interactions between genes and environment. A community-wide education campaign…”
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Reply to Niermeijer by Rodriguez-Bigas, Miguel A., Rosenblatt, Mary-Jo T., Farrell, Carolyn

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Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia by Scott, W K, Gaskell, P C, Lennon, F, Wolpert, C M, Menold, M M, Aylsworth, A S, Warner, C, Farrell, C D, Boustany, R M, Albright, S G, Boyd, E, Kingston, H M, Cumming, W J, Vance, J M, Pericak-Vance, M A

“…We examined 11 Caucasian pedigrees with autosomal dominant 'uncomplicated' familial spastic paraplegia (SPG) for linkage to the previously identified loci on…”
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Genetic counseling: the emerging reality by Farrell, C D

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