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Items: 34

1.

Development of the essential genetic and genomic competencies for nurses with graduate degrees.

Greco KE, Tinley S, Seibert D.

Annu Rev Nurs Res. 2011;29:173-90. Review.

PMID:
22891504
2.

Barriers and facilitators to electronic documentation in a rural hospital.

Whittaker AA, Aufdenkamp M, Tinley S.

J Nurs Scholarsh. 2009;41(3):293-300. doi: 10.1111/j.1547-5069.2009.01278.x.

PMID:
19723278
3.

Five families living with hereditary breast and ovarian cancer risk.

Norris J, Spelic SS, Snyder C, Tinley S.

Clin J Oncol Nurs. 2009 Feb;13(1):73-80. doi: 10.1188/09.CJON.73-80.

PMID:
19193551
4.

Familial adenomatous polyposis in children younger than age ten years: a multidisciplinary clinic experience.

Attard TM, Tajouri T, Peterson KD, Tinley S, Thorson AG, Lynch HT.

Dis Colon Rectum. 2008 Feb;51(2):207-12. Epub 2007 Dec 22.

PMID:
18157572
5.

Three philosophical approaches to the study of spirituality.

Tinley ST, Kinney AY.

ANS Adv Nurs Sci. 2007 Jan-Mar;30(1):71-80. Review.

PMID:
17299286
6.

Challenging pedigrees seen in a hereditary cancer consultation center.

Lynch HT, Tinley ST, Lynch JF, Attard TM.

Cancer Genet Cytogenet. 2004 Sep;153(2):91-101.

PMID:
15350297
7.

The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations.

Howe JR, Sayed MG, Ahmed AF, Ringold J, Larsen-Haidle J, Merg A, Mitros FA, Vaccaro CA, Petersen GM, Giardiello FM, Tinley ST, Aaltonen LA, Lynch HT.

J Med Genet. 2004 Jul;41(7):484-91.

8.

Screening adherence in BRCA1/2 families is associated with primary physicians' behavior.

Tinley ST, Houfek J, Watson P, Wenzel L, Clark MB, Coughlin S, Lynch HT.

Am J Med Genet A. 2004 Feb 15;125A(1):5-11.

PMID:
14755459
9.

Challenging colonic polyposis pedigrees: differential diagnosis, surveillance, and management concerns.

Lynch HT, Tinley ST, Shaw TG, Lynch JF, Howe JR, Attard TM.

Cancer Genet Cytogenet. 2004 Jan 15;148(2):104-17.

PMID:
14734220
10.

Carrier risk status changes resulting from mutation testing in hereditary non-polyposis colorectal cancer and hereditary breast-ovarian cancer.

Watson P, Narod SA, Fodde R, Wagner A, Lynch JF, Tinley ST, Snyder CL, Coronel SA, Riley B, Kinarsky Y, Lynch HT.

J Med Genet. 2003 Aug;40(8):591-6.

11.

Germline SMAD4 or BMPR1A mutations and phenotype of juvenile polyposis.

Sayed MG, Ahmed AF, Ringold JR, Anderson ME, Bair JL, Mitros FA, Lynch HT, Tinley ST, Petersen GM, Giardiello FM, Vogelstein B, Howe JR.

Ann Surg Oncol. 2002 Nov;9(9):901-6.

PMID:
12417513
12.

Colon cancer in women.

Tinley ST.

AWHONN Lifelines. 2001 Jun-Jul;5(3):26-32. No abstract available.

PMID:
11982260
13.

Familial adenomatous polyposis and extracolonic cancer.

Lynch HT, Thorson AG, McComb RD, Franklin BA, Tinley ST, Lynch JF.

Dig Dis Sci. 2001 Nov;46(11):2325-32.

PMID:
11713930
14.

Cancer genetics and nursing practice: what every gastroenterology nurse needs to know.

Rieger PT, Tinley ST.

Gastroenterol Nurs. 2000 Jan-Feb;23(1):28-39. Review.

PMID:
11096805
15.

Hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay.

Sarroca C, Alfano N, Bendin GT, Della Valle A, Dominguez A, Quadrelli R, Vaglio A, Mechoso B, Tinley ST, Harty AE, Lynch JF, Franklin BA, Kristo P, Smyrk TC, Peltomäki P, Lynch HT.

Dis Colon Rectum. 2000 Mar;43(3):353-60; discussion 360-2.

PMID:
10733117
16.

Preparing the nursing profession for participation in a genetic paradigm in health care.

Anderson G, Monsen RB, Prows CA, Tinley S, Jenkins J.

Nurs Outlook. 2000 Jan-Feb;48(1):23-7. Review.

PMID:
10715078
17.

Integration of family history and medical management of patients with hereditary cancers.

Tinley ST, Lynch HT.

Cancer. 1999 Dec 1;86(11 Suppl):2525-32.

PMID:
10630178
18.

Clinical impact of molecular genetic diagnosis, genetic counseling, and management of hereditary cancer. Part II: Hereditary nonpolyposis colorectal carcinoma as a model.

Lynch HT, Watson P, Shaw TG, Lynch JF, Harty AE, Franklin BA, Kapler CR, Tinley ST, Liu B, Lerman C.

Cancer. 1999 Dec 1;86(11 Suppl):2457-63.

PMID:
10630171
19.

Clinical impact of molecular genetic diagnosis, genetic counseling, and management of hereditary cancer. Part I: Studies of cancer in families.

Lynch HT, Watson P, Shaw TG, Lynch JF, Harty AE, Franklin BA, Kapler CR, Tinley ST, Liu B.

Cancer. 1999 Dec 1;86(11 Suppl):2449-56.

PMID:
10630170
20.

An update on DNA-based BRCA1/BRCA2 genetic counseling in hereditary breast cancer.

Lynch HT, Watson P, Tinley S, Snyder C, Durham C, Lynch J, Kirnarsky Y, Serova O, Lenoir G, Lerman C, Narod SA.

Cancer Genet Cytogenet. 1999 Mar;109(2):91-8.

PMID:
10087939
21.

Medical genetic evaluation for the etiology of hearing loss in children.

Smith SD, Kimberling WJ, Schaefer GB, Horton MB, Tinley ST.

J Commun Disord. 1998 Sep-Oct;31(5):371-88; quiz 388-9. Review.

PMID:
9777485
22.

Prevention of osteoporosis in women treated for hereditary breast and ovarian carcinoma: a need that is overlooked.

Lappe JM, Tinley ST.

Cancer. 1998 Sep 1;83(5):830-4. No abstract available.

PMID:
9731880
23.

Genetics in the OR--implications for perioperative nursing practice.

Lea DH, Tinley ST.

AORN J. 1998 Jun;67(6):1175-80, 1183-6, 1189, passim.

PMID:
9629453
24.

Etiology, natural history, management and molecular genetics of hereditary nonpolyposis colorectal cancer (Lynch syndromes): genetic counseling implications.

Lynch HT, Lemon SJ, Karr B, Franklin B, Lynch JF, Watson P, Tinley S, Lerman C, Carter C.

Cancer Epidemiol Biomarkers Prev. 1997 Dec;6(12):987-91.

25.

A descriptive study of BRCA1 testing and reactions to disclosure of test results.

Lynch HT, Lemon SJ, Durham C, Tinley ST, Connolly C, Lynch JF, Surdam J, Orinion E, Slominski-Caster S, Watson P, Lerman C, Tonin P, Lenoir G, Serova O, Narod S.

Cancer. 1997 Jun 1;79(11):2219-28.

PMID:
9179070
26.

Narrowing the genetic interval and yeast artificial chromosome map in the branchio-oto-renal region on chromosome 8q.

Kumar S, Kimberling WJ, Lanyi A, Sumegi J, Pinnt J, Ing P, Tinley S, Marres HA, Cremers CW.

Genomics. 1996 Jan 1;31(1):71-9.

PMID:
8808282
27.

Refining the region of branchio-oto-renal syndrome and defining the flanking markers on chromosome 8q by genetic mapping.

Kumar S, Kimberling WJ, Connolly CJ, Tinley S, Marres HA, Cremers CW.

Am J Hum Genet. 1994 Dec;55(6):1188-94.

28.

Family planning: adults only?

Tinley S.

Nurs Stand. 1994 Jul 6-12;8(41):38-9. No abstract available.

PMID:
8060883
29.

Nursing and genetic health care.

Lea DH, Williams JK, Tinley ST.

J Genet Couns. 1994 Jun;3(2):113-24. doi: 10.1007/BF01423173.

PMID:
24233860
30.

Localization of the gene for branchiootorenal syndrome to chromosome 8q.

Smith RJ, Coppage KB, Ankerstjerne JK, Capper DT, Kumar S, Kenyon J, Tinley S, Comeau K, Kimberling WJ.

Genomics. 1992 Dec;14(4):841-4.

PMID:
1478663
31.

A comment on the analysis of families with prelinqual deafness.

Kimberling S, Smith SD, Ing PS, Tinley S.

Am J Hum Genet. 1989 Jul;45(1):157-60. No abstract available.

32.

Nurses' and geneticists' role expectations for the genetics nurse clinician.

Tinley ST.

J Pediatr Nurs. 1987 Aug;2(4):259-64. No abstract available.

PMID:
3649404
33.

Prenatal diagnosis in a Catholic facility.

Tinley ST.

Birth Defects Orig Artic Ser. 1987;23(6):262-6. No abstract available.

PMID:
3435772
34.

Genetics and medical emergencies: an interesting patient.

Lynch HT, Kimberling W, Grush M, Tinley S.

Nebr Med J. 1982 Feb;67(2):30-1. No abstract available.

PMID:
7045704

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