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A novel approach to offering additional genomic findings-A protocol to test a two-step approach in the healthcare system.

Martyn M, Kanga-Parabia A, Lynch E, James PA, Macciocca I, Trainer AH, Halliday J, Keogh L, Wale J, Winship I, Bogwitz M, Valente G, Walsh M, Downie L, Amor D, Wallis M, Cunningham F, Burgess M, Brown NJ, Jarmolowicz A, Lunke S, Goranitis I; Melbourne Genomics Health Alliance, Gaff CL.

J Genet Couns. 2019 Apr;28(2):388-397. doi: 10.1002/jgc4.1102. Epub 2019 Feb 18.


Genetic Counseling in the Era of Genomics: What's all the Fuss about?

Brett GR, Wilkins EJ, Creed ET, West K, Jarmolowicz A, Valente GM, Prawer Y, Lynch E, Macciocca I.

J Genet Couns. 2018 Sep;27(5):1010-1021. doi: 10.1007/s10897-018-0216-x. Epub 2018 Jan 24.


A qualitative systematic review of internal and external influences on shared decision-making in all health care settings.

Truglio-Londrigan M, Slyer JT, Singleton JK, Worral P.

JBI Libr Syst Rev. 2012;10(58):4633-4646.


Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial.

Shickh S, Clausen M, Mighton C, Casalino S, Joshi E, Glogowski E, Schrader KA, Scheer A, Elser C, Panchal S, Eisen A, Graham T, Aronson M, Semotiuk KM, Winter-Paquette L, Evans M, Lerner-Ellis J, Carroll JC, Hamilton JG, Offit K, Robson M, Thorpe KE, Laupacis A, Bombard Y.

BMJ Open. 2018 Apr 26;8(4):e021876. doi: 10.1136/bmjopen-2018-021876.


Adoptees' Pursuit of Genomic Testing to Fill Gaps in Family Health History and Reduce Healthcare Disparity.

Casas KA.

Narrat Inq Bioeth. 2018;8(2):131-135. doi: 10.1353/nib.2018.0050.


The PiGeOn project: protocol of a longitudinal study examining psychosocial and ethical issues and outcomes in germline genomic sequencing for cancer.

Best M, Newson AJ, Meiser B, Juraskova I, Goldstein D, Tucker K, Ballinger ML, Hess D, Schlub TE, Biesecker B, Vines R, Vines K, Thomas D, Young MA, Savard J, Jacobs C, Butow P.

BMC Cancer. 2018 Apr 23;18(1):454. doi: 10.1186/s12885-018-4366-x.


Improving the referral process for familial breast cancer genetic counselling: findings of three randomised controlled trials of two interventions.

Wilson BJ, Torrance N, Mollison J, Wordsworth S, Gray JR, Haites NE, Grant A, Campbell MK, Miedyzbrodzka Z, Clarke A, Watson MS, Douglas A.

Health Technol Assess. 2005 Feb;9(3):iii-iv, 1-126. Review.


Evidence Brief: Effectiveness of Intensive Primary Care Programs.

Peterson K, Helfand M, Humphrey L, Christensen V, Carson S.

VA Evidence Synthesis Program Evidence Briefs [Internet]. Washington (DC): Department of Veterans Affairs (US); 2011-.
2013 Feb.


Evidence Brief: Comparative Effectiveness of Appointment Recall Reminder Procedures for Follow-up Appointments.

Peterson K, McCleery E, Anderson J, Waldrip K, Helfand M.

VA Evidence Synthesis Program Evidence Briefs [Internet]. Washington (DC): Department of Veterans Affairs (US); 2011-.
2015 Jul.


Identification of Delivery Models for the Provision of Predictive Genetic Testing in Europe: Protocol for a Multicentre Qualitative Study and a Systematic Review of the Literature.

Unim B, Lagerberg T, Pitini E, De Vito C, Vacchio MR, Adamo G, Rosso A, D'Andrea E, Marzuillo C, Villari P.

Front Public Health. 2017 Aug 22;5:223. doi: 10.3389/fpubh.2017.00223. eCollection 2017.


Role and practice evolution for genetic counseling in the genomic era: The experience of Australian and UK genetics practitioners.

Dwarte T, Barlow-Stewart K, O'Shea R, Dinger ME, Terrill B.

J Genet Couns. 2019 Apr;28(2):378-387. doi: 10.1002/jgc4.1053. Epub 2018 Dec 15.


Genetic counseling for consumer-driven whole exome and whole genome sequencing: A commentary on early experiences.

Schmidt JL, Maas R, Altmeyer SR.

J Genet Couns. 2019 Apr;28(2):449-455. doi: 10.1002/jgc4.1109. Epub 2019 Mar 12.


Genomic medicine and risk prediction across the disease spectrum.

Kotze MJ, Lückhoff HK, Peeters AV, Baatjes K, Schoeman M, van der Merwe L, Grant KA, Fisher LR, van der Merwe N, Pretorius J, van Velden DP, Myburgh EJ, Pienaar FM, van Rensburg SJ, Yako YY, September AV, Moremi KE, Cronje FJ, Tiffin N, Bouwens CS, Bezuidenhout J, Apffelstaedt JP, Hough FS, Erasmus RT, Schneider JW.

Crit Rev Clin Lab Sci. 2015;52(3):120-37. doi: 10.3109/10408363.2014.997930. Epub 2015 Jan 19. Review.


Risk management frameworks for human health and environmental risks.

Jardine C, Hrudey S, Shortreed J, Craig L, Krewski D, Furgal C, McColl S.

J Toxicol Environ Health B Crit Rev. 2003 Nov-Dec;6(6):569-720. Review.


Shared decision making: Implications for return of results from whole-exome and whole-genome sequencing.

Vadaparampil ST, Cragun D.

Transl Behav Med. 2018 Jan 29;8(1):80-84. doi: 10.1093/tbm/ibx048.


Exploring the Issues Surrounding Clinical Exome Sequencing in the Prenatal Setting.

Narayanan S, Blumberg B, Clayman ML, Pan V, Wicklund C.

J Genet Couns. 2018 Sep;27(5):1228-1237. doi: 10.1007/s10897-018-0245-5. Epub 2018 Mar 10.


The use of a risk assessment and decision support tool (CRISP) compared with usual care in general practice to increase risk-stratified colorectal cancer screening: study protocol for a randomised controlled trial.

Walker JG, Macrae F, Winship I, Oberoi J, Saya S, Milton S, Bickerstaffe A, Dowty JG, De Abreu Lourenço R, Clark M, Galloway L, Fishman G, Walter FM, Flander L, Chondros P, Ait Ouakrim D, Pirotta M, Trevena L, Jenkins MA, Emery JD.

Trials. 2018 Jul 25;19(1):397. doi: 10.1186/s13063-018-2764-7.


Evaluating parents' decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol.

Milko LV, Rini C, Lewis MA, Butterfield RM, Lin FC, Paquin RS, Powell BC, Roche MI, Souris KJ, Bailey DB Jr, Berg JS, Powell CM.

Trials. 2018 Jun 28;19(1):344. doi: 10.1186/s13063-018-2686-4.

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