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Items: 1 to 50 of 197

1.

"A change in perspective": Exploring the experiences of adolescents with hereditary tumor predisposition.

Weber E, Shuman C, Wasserman JD, Barrera M, Patenaude AF, Fung K, Chitayat D, Malkin D, Druker H.

Pediatr Blood Cancer. 2018 Sep 11:e27445. doi: 10.1002/pbc.27445. [Epub ahead of print]

PMID:
30207072
2.

Disability Experiences and Perspectives Regarding Reproductive Decisions, Parenting, and the Utility of Genetic Services: a Qualitative Study.

Roadhouse C, Shuman C, Anstey K, Sappleton K, Chitayat D, Ignagni E.

J Genet Couns. 2018 Jun 16. doi: 10.1007/s10897-018-0265-1. [Epub ahead of print]

PMID:
29909595
3.

Associations among unit leadership and unit climates for implementation in acute care: a cross-sectional study.

Shuman CJ, Liu X, Aebersold ML, Tschannen D, Banaszak-Holl J, Titler MG.

Implement Sci. 2018 Apr 25;13(1):62. doi: 10.1186/s13012-018-0753-6.

4.

Informed Decision-Making in the Context of Prenatal Chromosomal Microarray.

Baker J, Shuman C, Chitayat D, Wasim S, Okun N, Keunen J, Hofstedter R, Silver R.

J Genet Couns. 2018 Sep;27(5):1130-1147. doi: 10.1007/s10897-018-0231-y. Epub 2018 Mar 7.

PMID:
29516345
5.

Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testing.

Costain G, Jobling R, Walker S, Reuter MS, Snell M, Bowdin S, Cohn RD, Dupuis L, Hewson S, Mercimek-Andrews S, Shuman C, Sondheimer N, Weksberg R, Yoon G, Meyn MS, Stavropoulos DJ, Scherer SW, Mendoza-Londono R, Marshall CR.

Eur J Hum Genet. 2018 May;26(5):740-744. doi: 10.1038/s41431-018-0114-6. Epub 2018 Feb 16.

PMID:
29453418
6.

Reply to Brioude et al.

Brzezinski J, Shuman C, Choufani S, Ray P, Stavropoulos DJ, Basran R, Steele L, Parkinson N, Grant R, Thorner P, Lorenzo A, Weksberg R.

Eur J Hum Genet. 2018 Apr;26(4):473-474. doi: 10.1038/s41431-017-0094-y. Epub 2018 Feb 15. No abstract available.

PMID:
29449717
7.

The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants.

Reuter MS, Walker S, Thiruvahindrapuram B, Whitney J, Cohn I, Sondheimer N, Yuen RKC, Trost B, Paton TA, Pereira SL, Herbrick JA, Wintle RF, Merico D, Howe J, MacDonald JR, Lu C, Nalpathamkalam T, Sung WWL, Wang Z, Patel RV, Pellecchia G, Wei J, Strug LJ, Bell S, Kellam B, Mahtani MM, Bassett AS, Bombard Y, Weksberg R, Shuman C, Cohn RD, Stavropoulos DJ, Bowdin S, Hildebrandt MR, Wei W, Romm A, Pasceri P, Ellis J, Ray P, Meyn MS, Monfared N, Hosseini SM, Joseph-George AM, Keeley FW, Cook RA, Fiume M, Lee HC, Marshall CR, Davies J, Hazell A, Buchanan JA, Szego MJ, Scherer SW.

CMAJ. 2018 Feb 5;190(5):E126-E136. doi: 10.1503/cmaj.171151.

8.

Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray.

Hayeems RZ, Bhawra J, Tsiplova K, Meyn MS, Monfared N, Bowdin S, Stavropoulos DJ, Marshall CR, Basran R, Shuman C, Ito S, Cohn I, Hum C, Girdea M, Brudno M, Cohn RD, Scherer SW, Ungar WJ.

Eur J Hum Genet. 2017 Dec;25(12):1303-1312. doi: 10.1038/s41431-017-0020-3. Epub 2017 Nov 20.

PMID:
29158552
9.

Registered Nurse and Nursing Assistant Perceptions of Limited English-Proficient Patient-Clinician Communication.

Shuman C, Montie M, Galinato J, Patak L, Titler M.

J Nurs Adm. 2017 Dec;47(12):589-591. doi: 10.1097/NNA.0000000000000549.

PMID:
29135845
10.

Sustainability of Evidence-Based Acute Pain Management Practices for Hospitalized Older Adults.

Shuman CJ, Xie XJ, Herr KA, Titler MG.

West J Nurs Res. 2017 Nov 1:193945917738781. doi: 10.1177/0193945917738781. [Epub ahead of print]

PMID:
29103368
11.

Conduits to care: call lights and patients' perceptions of communication.

Montie M, Shuman C, Galinato J, Patak L, Anderson CA, Titler MG.

J Multidiscip Healthc. 2017 Sep 18;10:359-366. doi: 10.2147/JMDH.S144152. eCollection 2017.

12.

Development and Testing of the Nurse Manager EBP Competency Scale.

Shuman CJ, Ploutz-Snyder RJ, Titler MG.

West J Nurs Res. 2018 Feb;40(2):175-190. doi: 10.1177/0193945917728249. Epub 2017 Aug 30.

PMID:
28854864
13.

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.

Lionel AC, Costain G, Monfared N, Walker S, Reuter MS, Hosseini SM, Thiruvahindrapuram B, Merico D, Jobling R, Nalpathamkalam T, Pellecchia G, Sung WWL, Wang Z, Bikangaga P, Boelman C, Carter MT, Cordeiro D, Cytrynbaum C, Dell SD, Dhir P, Dowling JJ, Heon E, Hewson S, Hiraki L, Inbar-Feigenberg M, Klatt R, Kronick J, Laxer RM, Licht C, MacDonald H, Mercimek-Andrews S, Mendoza-Londono R, Piscione T, Schneider R, Schulze A, Silverman E, Siriwardena K, Snead OC, Sondheimer N, Sutherland J, Vincent A, Wasserman JD, Weksberg R, Shuman C, Carew C, Szego MJ, Hayeems RZ, Basran R, Stavropoulos DJ, Ray PN, Bowdin S, Meyn MS, Cohn RD, Scherer SW, Marshall CR.

Genet Med. 2018 Apr;20(4):435-443. doi: 10.1038/gim.2017.119. Epub 2017 Aug 3.

14.

Wilms tumour in Beckwith-Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelines.

Brzezinski J, Shuman C, Choufani S, Ray P, Stavropoulos DJ, Basran R, Steele L, Parkinson N, Grant R, Thorner P, Lorenzo A, Weksberg R.

Eur J Hum Genet. 2017 Sep;25(9):1031-1039. doi: 10.1038/ejhg.2017.102. Epub 2017 Jul 12.

15.

Effectiveness of implementing a dyadic psychoeducational intervention for cancer patients and family caregivers.

Titler MG, Visovatti MA, Shuman C, Ellis KR, Banerjee T, Dockham B, Yakusheva O, Northouse L.

Support Care Cancer. 2017 Nov;25(11):3395-3406. doi: 10.1007/s00520-017-3758-9. Epub 2017 Jun 13.

16.

A rare cause of acute dysphagia: acute calcific tendonitis of the longus colli muscle.

Abou Dargham H, Bytyci F, Shuman C, Stolear A.

BMJ Case Rep. 2017 May 27;2017. pii: bcr-2017-219684. doi: 10.1136/bcr-2017-219684.

PMID:
28551599
17.

Optimization of intelligent infusion pump technology to minimize vasopressor pump programming errors.

Vadiei N, Shuman CA, Murthy MS, Daley MJ.

Expert Opin Drug Saf. 2017 Aug;16(8):891-895. doi: 10.1080/14740338.2017.1323866. Epub 2017 May 17.

PMID:
28443354
18.

Perspectives of Nurses on Patients With Limited English Proficiency and Their Call Light Use.

Galinato J, Montie M, Shuman C, Patak L, Titler M.

Glob Qual Nurs Res. 2016 Aug 12;3. doi: 10.1177/2333393616637764. Epub 2016 Mar 22.

19.

Does personal genome testing drive service utilization in an adult preventive medicine clinic?

Hoang N, Hayeems R, Davies J, Pu S, Wasim S, Velsher L, Aw J, Chénier S, Stavropoulos DJ, Babul-Hirji R, Weksberg R, Shuman C.

J Community Genet. 2017 Jul;8(3):151-158. doi: 10.1007/s12687-017-0297-5. Epub 2017 Apr 3.

20.

Perspectives of 30 English Patients on Call Light Technology, Eloquence Revisited.

Montie M, Shuman C, Galinato J, Patak L, Titler M.

Comput Inform Nurs. 2018 Jan;36(1):27-34. doi: 10.1097/CIN.0000000000000345.

PMID:
28306574
21.

Corrigendum to "The sooner the better: Genetic testing following ovarian cancer diagnosis" [Gynecol. Oncol. 137 (2015) 423-429].

Fox E, McCuaig J, Demsky R, Shuman C, Chitayat D, Maganti M, Murphy J, Rosen B, Ferguson S, Randall Armel S.

Gynecol Oncol. 2017 May;145(2):409. doi: 10.1016/j.ygyno.2017.02.021. Epub 2017 Feb 27. No abstract available.

PMID:
28256319
22.

Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?

Anderson JA, Meyn MS, Shuman C, Zlotnik Shaul R, Mantella LE, Szego MJ, Bowdin S, Monfared N, Hayeems RZ.

J Med Ethics. 2017 Aug;43(8):535-539. doi: 10.1136/medethics-2016-103564. Epub 2016 Nov 25.

PMID:
27888232
23.

Impact of Norepinephrine Weight-Based Dosing Compared With Non-Weight-Based Dosing in Achieving Time to Goal Mean Arterial Pressure in Obese Patients With Septic Shock.

Vadiei N, Daley MJ, Murthy MS, Shuman CS.

Ann Pharmacother. 2017 Mar;51(3):194-202. doi: 10.1177/1060028016682030. Epub 2016 Nov 25.

PMID:
27886982
24.

Recommendations for the integration of genomics into clinical practice.

Bowdin S, Gilbert A, Bedoukian E, Carew C, Adam MP, Belmont J, Bernhardt B, Biesecker L, Bjornsson HT, Blitzer M, D'Alessandro LC, Deardorff MA, Demmer L, Elliott A, Feldman GL, Glass IA, Herman G, Hindorff L, Hisama F, Hudgins L, Innes AM, Jackson L, Jarvik G, Kim R, Korf B, Ledbetter DH, Li M, Liston E, Marshall C, Medne L, Meyn MS, Monfared N, Morton C, Mulvihill JJ, Plon SE, Rehm H, Roberts A, Shuman C, Spinner NB, Stavropoulos DJ, Valverde K, Waggoner DJ, Wilkens A, Cohn RD, Krantz ID.

Genet Med. 2016 Nov;18(11):1075-1084. doi: 10.1038/gim.2016.17. Epub 2016 May 12. Review.

25.

Congenital limb deficiencies with vascular etiology: Possible association with maternal thrombophilia.

Ordal L, Keunen J, Martin N, Shehata N, Borschel GH, Clarke HM, Toi A, Shuman C, Chitayat D.

Am J Med Genet A. 2016 Dec;170(12):3083-3089. doi: 10.1002/ajmg.a.37890. Epub 2016 Aug 17.

PMID:
27530094
26.

Beckwith-Wiedemann Syndrome.

Shuman C, Beckwith JB, Weksberg R.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2000 Mar 3 [updated 2016 Aug 11].

27.

Patient perceptions and experiences with falls during hospitalization and after discharge.

Shuman C, Liu J, Montie M, Galinato JG, Todd MA, Hegstad M, Titler M.

Appl Nurs Res. 2016 Aug;31:79-85. doi: 10.1016/j.apnr.2016.01.009. Epub 2016 Feb 2.

PMID:
27397823
28.

Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell-Silver syndrome.

Cytrynbaum C, Chong K, Hannig V, Choufani S, Shuman C, Steele L, Morgan T, Scherer SW, Stavropoulos DJ, Basran RK, Weksberg R.

Am J Med Genet A. 2016 Oct;170(10):2731-9. doi: 10.1002/ajmg.a.37819. Epub 2016 Jul 4.

PMID:
27374371
29.

The Relationship Between Burnout and Occupational Stress in Genetic Counselors.

Johnstone B, Kaiser A, Injeyan MC, Sappleton K, Chitayat D, Stephens D, Shuman C.

J Genet Couns. 2016 Aug;25(4):731-41. doi: 10.1007/s10897-016-9968-3. Epub 2016 May 26.

PMID:
27228983
30.

Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine.

Stavropoulos DJ, Merico D, Jobling R, Bowdin S, Monfared N, Thiruvahindrapuram B, Nalpathamkalam T, Pellecchia G, Yuen RKC, Szego MJ, Hayeems RZ, Shaul RZ, Brudno M, Girdea M, Frey B, Alipanahi B, Ahmed S, Babul-Hirji R, Porras RB, Carter MT, Chad L, Chaudhry A, Chitayat D, Doust SJ, Cytrynbaum C, Dupuis L, Ejaz R, Fishman L, Guerin A, Hashemi B, Helal M, Hewson S, Inbar-Feigenberg M, Kannu P, Karp N, Kim R, Kronick J, Liston E, MacDonald H, Mercimek-Mahmutoglu S, Mendoza-Londono R, Nasr E, Nimmo G, Parkinson N, Quercia N, Raiman J, Roifman M, Schulze A, Shugar A, Shuman C, Sinajon P, Siriwardena K, Weksberg R, Yoon G, Carew C, Erickson R, Leach RA, Klein R, Ray PN, Meyn MS, Scherer SW, Cohn RD, Marshall CR.

NPJ Genom Med. 2016 Jan 13;1. pii: 15012. doi: 10.1038/npjgenmed.2015.12.

31.

Obsessive-Compulsive Disorder: The Process of Parental Adaptation and Implications for Genetic Counseling.

Andrighetti H, Semaka A, Stewart SE, Shuman C, Hayeems R, Austin J.

J Genet Couns. 2016 Oct;25(5):912-22. doi: 10.1007/s10897-015-9914-9. Epub 2015 Dec 7.

32.

Experience with genetic counseling: the adolescent perspective.

Pichini A, Shuman C, Sappleton K, Kaufman M, Chitayat D, Babul-Hirji R.

J Genet Couns. 2016 Jun;25(3):583-95. doi: 10.1007/s10897-015-9912-y. Epub 2015 Nov 17.

PMID:
26573304
33.

Parents' Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic Counseling.

Hayeems RZ, Babul-Hirji R, Hoang N, Weksberg R, Shuman C.

J Genet Couns. 2016 Apr;25(2):298-304. doi: 10.1007/s10897-015-9871-3. Epub 2015 Aug 12.

PMID:
26259530
34.

The sooner the better: Genetic testing following ovarian cancer diagnosis.

Fox E, McCuaig J, Demsky R, Shuman C, Chitayat D, Maganti M, Murphy J, Rosen B, Ferguson S, Randall Armel S.

Gynecol Oncol. 2015 Jun;137(3):423-9. doi: 10.1016/j.ygyno.2015.03.057. Epub 2015 Apr 11. Erratum in: Gynecol Oncol. 2017 May;145(2):409.

PMID:
25868966
35.

Greenland ice sheet melt from MODIS and associated atmospheric variability.

Häkkinen S, Hall DK, Shuman CA, Worthen DL, DiGirolamo NE.

Geophys Res Lett. 2014 Mar 16;41(5):1600-1607. Epub 2014 Mar 10.

36.

Capturing the clinical utility of genomic testing: medical recommendations following pediatric microarray.

Hayeems RZ, Hoang N, Chenier S, Stavropoulos DJ, Pu S, Weksberg R, Shuman C.

Eur J Hum Genet. 2015 Sep;23(9):1135-41. doi: 10.1038/ejhg.2014.260. Epub 2014 Dec 10.

37.

Paternal germline mosaicism for a GPC3 deletion in X-linked Simpson-Golabi-Behmel syndrome.

Agatep R, Shuman C, Steele L, Parkinson N, Weksberg R, Stockley TL.

Am J Med Genet A. 2014 Oct;164A(10):2682-4. doi: 10.1002/ajmg.a.36682. Epub 2014 Jul 29. No abstract available.

PMID:
25073799
38.

Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelines.

Anderson JA, Hayeems RZ, Shuman C, Szego MJ, Monfared N, Bowdin S, Zlotnik Shaul R, Meyn MS.

Clin Genet. 2015 Apr;87(4):301-10. doi: 10.1111/cge.12460. Epub 2014 Oct 7. Review.

PMID:
25046648
39.

Predictive genomic testing of children for adult onset disorders: a Canadian perspective.

Szego MJ, Meyn MS, Anderson JA, Hayeems R, Shuman C, Monfared N, Bowdin S, Shaul RZ.

Am J Bioeth. 2014;14(3):19-21. doi: 10.1080/15265161.2013.879960. No abstract available.

PMID:
24592833
40.

High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith-Wiedemann syndrome.

Baskin B, Choufani S, Chen YA, Shuman C, Parkinson N, Lemyre E, Micheil Innes A, Stavropoulos DJ, Ray PN, Weksberg R.

Hum Genet. 2014 Mar;133(3):321-30. doi: 10.1007/s00439-013-1379-z. Epub 2013 Oct 24.

PMID:
24154661
41.

Risk estimates for complex disorders: comparing personal genome testing and family history.

Aiyar L, Shuman C, Hayeems R, Dupuis A, Pu S, Wodak S, Chitayat D, Velsher L, Davies J.

Genet Med. 2014 Mar;16(3):231-7. doi: 10.1038/gim.2013.115. Epub 2013 Sep 5.

PMID:
24009002
42.

Molecular findings in Beckwith-Wiedemann syndrome.

Choufani S, Shuman C, Weksberg R.

Am J Med Genet C Semin Med Genet. 2013 May;163C(2):131-40. doi: 10.1002/ajmg.c.31363. Epub 2013 Apr 16. Review.

PMID:
23592339
43.

Clinical dilemmas and a review of strategies to manage drug shortages.

Rider AE, Templet DJ, Daley MJ, Shuman C, Smith LV.

J Pharm Pract. 2013 Jun;26(3):183-91. doi: 10.1177/0897190013482332. Epub 2013 Apr 3. Review.

PMID:
23553544
44.

Förster resonance energy transfer studies of calmodulin produced by native protein ligation reveal inter-domain electrostatic repulsion.

Hellstrand E, Kukora S, Shuman CF, Steenbergen S, Thulin E, Kohli A, Krouse B, Linse S, Åkerfeldt KS.

FEBS J. 2013 Jun;280(11):2675-87. doi: 10.1111/febs.12269. Epub 2013 Apr 29.

45.

Cigarette smoking in methadone maintained patients: an up-to-date review.

Zirakzadeh A, Shuman C, Stauter E, Hays JT, Ebbert JO.

Curr Drug Abuse Rev. 2013 Mar;6(1):77-84. Review.

PMID:
23506370
46.

Maternal age-based prenatal screening for chromosomal disorders: attitudes of women and health care providers toward changes.

Carroll JC, Rideout A, Wilson BJ, Allanson J, Blaine S, Esplen MJ, Farrell S, Graham GE, MacKenzie J, Meschino WS, Prakash P, Shuman C, Taylor S, Tobin S.

Can Fam Physician. 2013 Jan;59(1):e39-47.

47.

Mosaicism for genome-wide paternal uniparental disomy with features of multiple imprinting disorders: diagnostic and management issues.

Inbar-Feigenberg M, Choufani S, Cytrynbaum C, Chen YA, Steele L, Shuman C, Ray PN, Weksberg R.

Am J Med Genet A. 2013 Jan;161A(1):13-20. doi: 10.1002/ajmg.a.35651. Epub 2012 Dec 13.

PMID:
23239666
48.

Nephron sparing surgery for unilateral Wilms tumor in children with predisposing syndromes: single center experience over 10 years.

Romão RL, Pippi Salle JL, Shuman C, Weksberg R, Figueroa V, Weber B, Bägli DJ, Farhat WA, Grant R, Gerstle JT, Lorenzo AJ.

J Urol. 2012 Oct;188(4 Suppl):1493-8. doi: 10.1016/j.juro.2012.02.034. Epub 2012 Aug 19.

PMID:
22910237
49.

22q11.2 deletion syndrome: attitudes towards disclosing the risk of psychiatric illness.

Martin N, Mikhaelian M, Cytrynbaum C, Shuman C, Chitayat DA, Weksberg R, Bassett AS.

J Genet Couns. 2012 Dec;21(6):825-34. doi: 10.1007/s10897-012-9517-7. Epub 2012 Jul 26.

50.

Parents' perspectives on participating in genetic research in autism.

Trottier M, Roberts W, Drmic I, Scherer SW, Weksberg R, Cytrynbaum C, Chitayat D, Shuman C, Miller FA.

J Autism Dev Disord. 2013 Mar;43(3):556-68. doi: 10.1007/s10803-012-1592-y.

PMID:
22782649

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