Year |
Citation |
Score |
2009 |
Norris J, Spelic SS, Snyder C, Tinley S. Five families living with hereditary breast and ovarian cancer risk. Clinical Journal of Oncology Nursing. 13: 73-80. PMID 19193551 DOI: 10.1188/09.Cjon.73-80 |
0.457 |
|
2007 |
Tinley ST, Kinney AY. Three philosophical approaches to the study of spirituality. Ans. Advances in Nursing Science. 30: 71-80. PMID 17299286 DOI: 10.1097/00012272-200701000-00008 |
0.447 |
|
2004 |
Lynch HT, Tinley ST, Lynch JF, Attard TM. Challenging pedigrees seen in a hereditary cancer consultation center. Cancer Genetics and Cytogenetics. 153: 91-101. PMID 15350297 DOI: 10.1016/J.Cancergencyto.2004.01.011 |
0.483 |
|
2004 |
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. The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations. Journal of Medical Genetics. 41: 484-91. PMID 15235019 DOI: 10.1136/Jmg.2004.018598 |
0.328 |
|
2004 |
Tinley ST, Houfek J, Watson P, Wenzel L, Clark MB, Coughlin S, Lynch HT. Screening adherence in BRCA1/2 families is associated with primary physicians' behavior. American Journal of Medical Genetics. Part A. 125: 5-11. PMID 14755459 DOI: 10.1002/Ajmg.A.20431 |
0.398 |
|
2004 |
Lynch HT, Tinley ST, Shaw TG, Lynch JF, Howe JR, Attard TM. Challenging colonic polyposis pedigrees: differential diagnosis, surveillance, and management concerns. Cancer Genetics and Cytogenetics. 148: 104-17. PMID 14734220 DOI: 10.1016/S0165-4608(03)00280-2 |
0.444 |
|
2003 |
Watson P, Narod SA, Fodde R, Wagner A, Lynch JF, Tinley ST, Snyder CL, Coronel SA, Riley B, Kinarsky Y, Lynch HT. Carrier risk status changes resulting from mutation testing in hereditary non-polyposis colorectal cancer and hereditary breast-ovarian cancer. Journal of Medical Genetics. 40: 591-6. PMID 12920070 DOI: 10.1136/Jmg.40.8.591 |
0.455 |
|
2002 |
Sayed MG, Ahmed AF, Ringold JR, Anderson ME, Bair JL, Mitros FA, Lynch HT, Tinley ST, Petersen GM, Giardiello FM, Vogelstein B, Howe JR. Germline SMAD4 or BMPR1A mutations and phenotype of juvenile polyposis. Annals of Surgical Oncology. 9: 901-6. PMID 12417513 DOI: 10.1007/Bf02557528 |
0.35 |
|
2001 |
Tinley ST. Colon cancer in women Awhonn Lifelines / Association of Women's Health, Obstetric and Neonatal Nurses. 5: 26-32. PMID 11982260 DOI: 10.1111/J.1552-6356.2001.Tb01276.X |
0.332 |
|
2001 |
Lynch HT, Thorson AG, McComb RD, Franklin BA, Tinley ST, Lynch JF. Familial adenomatous polyposis and extracolonic cancer. Digestive Diseases and Sciences. 46: 2325-32. PMID 11713930 DOI: 10.1023/A:1012330626600 |
0.433 |
|
2000 |
Rieger PT, Tinley ST. Cancer genetics and nursing practice: what every gastroenterology nurse needs to know Gastroenterology Nursing : the Official Journal of the Society of Gastroenterology Nurses and Associates. 23: 28-39. PMID 11096805 |
0.4 |
|
2000 |
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, et al. Hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay Diseases of the Colon and Rectum. 43: 353-362. PMID 10733117 DOI: 10.1007/Bf02258301 |
0.502 |
|
1999 |
Tinley ST, Lynch HT. Integration of family history and medical management of patients with hereditary cancers Cancer. 86: 2525-2532. PMID 10630178 DOI: 10.1002/(Sici)1097-0142(19991201)86:11+<2525::Aid-Cncr9>3.0.Co;2-7 |
0.482 |
|
1999 |
Lynch HT, Watson P, Shaw TG, Lynch JF, Harty AE, Franklin BA, Kapler CR, Tinley ST, Liu B, Lerman C. Clinical impact of molecular genetic diagnosis, genetic counseling, and management of hereditary cancer: Part II: Hereditary nonpolyposis colorectal carcinoma as a model Cancer. 86: 2457-2463. PMID 10630171 DOI: 10.1002/(Sici)1097-0142(19991201)86:11+<2457::Aid-Cncr2>3.0.Co;2-I |
0.469 |
|
1999 |
Lynch HT, Watson P, Shaw TG, Lynch JF, Harty AE, Franklin BA, Kapler CR, Tinley ST, Liu B. Clinical impact of molecular genetic diagnosis, genetic counseling, and management of hereditary cancer: Part I: Studies of cancer in families Cancer. 86: 2449-2456. PMID 10630170 DOI: 10.1002/(Sici)1097-0142(19991201)86:11+<2449::Aid-Cncr1>3.0.Co;2-M |
0.527 |
|
1999 |
Lynch HT, Watson P, Tinley S, Snyder C, Durham C, Lynch J, Kirnarsky Y, Serova O, Lenoir G, Lerman C, Narod SA. An update on DNA-based BRCA1/BRCA2 genetic counseling in hereditary breast cancer. Cancer Genetics and Cytogenetics. 109: 91-8. PMID 10087939 DOI: 10.1016/S0165-4608(98)00165-4 |
0.495 |
|
1998 |
Lappe JM, Tinley ST. Prevention of osteoporosis in women treated for hereditary breast and ovarian carcinoma: A need that is overlooked Cancer. 83: 830-834. PMID 9731880 DOI: 10.1002/(Sici)1097-0142(19980901)83:5<830::Aid-Cncr2>3.0.Co;2-M |
0.322 |
|
1997 |
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. A descriptive study of BRCA1 testing and reactions to disclosure of test results. Cancer. 79: 2219-28. PMID 9179070 DOI: 10.1002/(Sici)1097-0142(19970601)79:11<2219::Aid-Cncr21>3.0.Co;2-Y |
0.342 |
|
1997 |
Lynch HT, Tinley ST, Lynch J, Vanderhoof J, Lemon SJ. Familial adenomatous polyposis: Discovery of a family and its management in a Cancer Genetics Clinic Cancer. 80: 614-620. DOI: 10.1002/(Sici)1097-0142(19970801)80:3+<614::Aid-Cncr11>3.0.Co;2-H |
0.478 |
|
1997 |
Lemon SJ, Tinley ST, Fusaro RM, Lynch HT. Cancer risk assessment in a Hereditary Cancer Prevention Clinic and its first year's experience Cancer. 80: 606-613. DOI: 10.1002/(Sici)1097-0142(19970801)80:3+<606::Aid-Cncr10>3.0.Co;2-I |
0.461 |
|
Low-probability matches (unlikely to be authored by this person) |
1998 |
Smith SD, Kimberling WJ, Schaefer GB, Horton MB, Tinley ST. Medical genetic evaluation for the etiology of hearing loss in children Journal of Communication Disorders. 31: 371-389. PMID 9777485 DOI: 10.1016/S0021-9924(98)00011-2 |
0.299 |
|
1997 |
Lynch HT, Lemon SJ, Tinley ST, Lynch JF, Watson P. Genetic susceptibility testing Cancer. 79: 2066-2066. DOI: 10.1002/(Sici)1097-0142(19970601)79:11<2066::Aid-Cncr2>3.0.Co;2-N |
0.293 |
|
2008 |
Attard TM, Tajouri T, Peterson KD, Tinley S, Thorson AG, Lynch HT. Familial adenomatous polyposis in children younger than age ten years: a multidisciplinary clinic experience. Diseases of the Colon and Rectum. 51: 207-12. PMID 18157572 DOI: 10.1007/S10350-007-9090-6 |
0.285 |
|
1994 |
Lea DH, Williams JK, Tinley ST. Nursing and genetic health care Journal of Genetic Counseling. 3: 113-124. DOI: 10.1007/BF01423173 |
0.241 |
|
1998 |
Lea DH, Tinley ST. Genetics in the OR--implications for perioperative nursing practice Aorn Journal. 67. PMID 9629453 |
0.215 |
|
2009 |
Whittaker AA, Aufdenkamp M, Tinley S. Barriers and facilitators to electronic documentation in a rural hospital. Journal of Nursing Scholarship : An Official Publication of Sigma Theta Tau International Honor Society of Nursing / Sigma Theta Tau. 41: 293-300. PMID 19723278 DOI: 10.1111/J.1547-5069.2009.01278.X |
0.206 |
|
2000 |
Anderson G, Monsen RB, Prows CA, Tinley S, Jenkins J. Preparing the nursing profession for participation in a genetic paradigm in health care. Nursing Outlook. 48: 23-7. PMID 10715078 DOI: 10.1067/mno.2000.99810 |
0.206 |
|
1997 |
Lerman C, Peters JA, Ades T, Fink D, Barr P, Biesecker BB, Brooks SW, Calzone KA, Croyle RT, Fine BA, Green B, Lemon SJ, Lynch HT, Narod SA, Offit K, ... ... Tinley ST, et al. Genetic counseling issues: Workshop No. 2 Cancer. 80: 628-629. |
0.203 |
|
2011 |
Greco KE, Tinley S, Seibert D. Development of the essential genetic and genomic competencies for nurses with graduate degrees Annual Review of Nursing Research. 29: 173-190. PMID 22891504 DOI: 10.1891/0739-6686.29.173 |
0.202 |
|
1997 |
Lerman C, Peters JA, Ades T, Fink D, Barr P, Biesecker BB, Brooks SW, Calzone KA, Croyle RT, Fine BA, Green B, Lemon SJ, Lynch HT, Narod SA, Offit K, ... ... Tinley ST, et al. Genetic counseling issues Cancer. 80: 628-629. DOI: 10.1002/(Sici)1097-0142(19970801)80:3+<628::Aid-Cncr14>3.0.Co;2-G |
0.201 |
|
1997 |
Freedman TG, Lynch HT, Lemon SJ, Tinley ST, Lynch JF, Watson P. Genetic susceptibility testing: A therapeutic illusion? Cancer. 79: 2063-2066. PMID 9179051 DOI: 10.1002/(SICI)1097-0142(19970601)79:11<2063::AID-CNCR1>3.0.CO;2-Q |
0.2 |
|
2005 |
Attard TM, Young RJ, Thorson AG, Tinley ST, Lynch HT. FAMILIAL ADENOMATOUS POLYPOSIS IN CHILDREN UNDER 10; PRESENTATION AND CLINICAL OUTCOME: WHO GOES TO COLECTOMY? Journal of Pediatric Gastroenterology and Nutrition. 41: 535. DOI: 10.1097/01.MPG.0000181992.45042.25 |
0.162 |
|
1987 |
Tinley ST. Nurses' and geneticists' role expectations for the genetics nurse clinician Journal of Pediatric Nursing. 2: 259-264. PMID 3649404 |
0.14 |
|
1993 |
Smith RJ, Coppage KB, Ankerstjerne JK, Capper DT, Kumar S, Kenyon J, Tinley S, Comeau K, Kimberling WJ. Localization of the gene for branchiootorenal syndrome to chromosome 8q. Genomics. 14: 841-4. PMID 1478663 DOI: 10.1016/S0888-7543(05)80102-8 |
0.112 |
|
1996 |
Kumar S, Kimberling WJ, Lanyi A, Sumegi J, Pinnt J, Ing P, Tinley S, Marres HA, Cremers CW. Narrowing the genetic interval and yeast artificial chromosome map in the branchio-oto-renal region on chromosome 8q. Genomics. 31: 71-9. PMID 8808282 DOI: 10.1006/geno.1996.0011 |
0.106 |
|
2000 |
Guillem JG, Sarroca C, Alfano N, Bendin GT, Valle AD, Dominguez A, Quadrelli R, Vaglio A, Mechoso B, Tinley ST, Harty AE, Lynch JF, Franklin BA, Smyrk TC, Lynch HT, et al. Invited editorial Diseases of the Colon & Rectum. 43: 360-362. DOI: 10.1007/bf02258302 |
0.075 |
|
1987 |
Tinley ST. Prenatal diagnosis in a Catholic facility Birth Defects Original Article Series. 23: 262-266. PMID 3435772 |
0.072 |
|
Hide low-probability matches. |