Ballard L, Doheny S, Dimond R, Lucassen A, Clarke A
J Genet Couns. 2024; 34(1):e1911.
PMID: 38741209
PMC: 11735177.
DOI: 10.1002/jgc4.1911.
Howard J, Forrest Keenan K, Mazanderani F, Turner M, Locock L
J Genet Couns. 2024; 34(1):e1904.
PMID: 38628040
PMC: 11735176.
DOI: 10.1002/jgc4.1904.
Howard J, Mazanderani F, Forrest Keenan K, Turner M, Locock L
Health Expect. 2024; 27(2):e14024.
PMID: 38528673
PMC: 10963887.
DOI: 10.1111/hex.14024.
Velissaris S, Davis M, Fisher F, Gluyas C, Stout J
J Community Genet. 2023; 14(4):395-405.
PMID: 37458974
PMC: 10444936.
DOI: 10.1007/s12687-023-00651-1.
Dale M, Wood A, Zarotti N, Eccles F, Gunn S, Kiani R
J Pers Med. 2022; 12(8).
PMID: 35893316
PMC: 9332789.
DOI: 10.3390/jpm12081222.
Family Communication Patterns and Challenges of Huntington's Disease Risk, the Decision to Pursue Presymptomatic Testing, and Test Results.
Stuttgen K, Bollinger J, McCague A, Dvoskin R, Mathews D
J Huntingtons Dis. 2020; 9(3):265-274.
PMID: 32568103
PMC: 7569676.
DOI: 10.3233/JHD-200402.
Presymptomatic genetic testing for hereditary cancer in young adults: a survey of young adults and parents.
Godino L, Turchetti D, Jackson L, Hennessy C, Skirton H
Eur J Hum Genet. 2018; 27(2):291-299.
PMID: 30287899
PMC: 6336858.
DOI: 10.1038/s41431-018-0262-8.
Perspectives on Genetic Testing and Return of Results from the First Cohort of Presymptomatically Tested Individuals At Risk of Huntington Disease.
Stuttgen K, Bollinger J, Dvoskin R, McCague A, Shpritz B, Brandt J
J Genet Couns. 2018; 27(6):1428-1437.
PMID: 29967967
PMC: 6212306.
DOI: 10.1007/s10897-018-0274-0.
Decision making and experiences of young adults undergoing presymptomatic genetic testing for familial cancer: a longitudinal grounded theory study.
Godino L, Jackson L, Turchetti D, Hennessy C, Skirton H
Eur J Hum Genet. 2017; 26(1):44-53.
PMID: 29162934
PMC: 5839040.
DOI: 10.1038/s41431-017-0030-1.
Psychological Impact of Predictive Genetic Testing in VCP Inclusion Body Myopathy, Paget Disease of Bone and Frontotemporal Dementia.
Surampalli A, Khare M, Kubrussi G, Wencel M, Tanaja J, Donkervoort S
J Genet Couns. 2015; 24(5):842-50.
PMID: 25716352
PMC: 5565393.
DOI: 10.1007/s10897-015-9819-7.
PRECREST: a phase II prevention and biomarker trial of creatine in at-risk Huntington disease.
Rosas H, Doros G, Gevorkian S, Malarick K, Reuter M, Coutu J
Neurology. 2014; 82(10):850-7.
PMID: 24510496
PMC: 3959748.
DOI: 10.1212/WNL.0000000000000187.
Strategies used by teens growing up in families with Huntington disease.
Williams J, Driessnack M, Barnette J, Sparbel K, Leserman A, Thompson S
J Pediatr Nurs. 2013; 28(5):464-9.
PMID: 23531469
PMC: 3759611.
DOI: 10.1016/j.pedn.2013.02.030.
How do partners find out about the risk of Huntington's disease in couple relationships?.
Forrest Keenan K, Simpson S, Miedzybrodzka Z, Alexander D, Semper J
J Genet Couns. 2013; 22(3):336-44.
PMID: 23297124
DOI: 10.1007/s10897-012-9562-2.
Development of the HD-Teen Inventory.
Driessnack M, Williams J, Barnette J, Sparbel K, Paulsen J
Clin Nurs Res. 2011; 21(2):213-23.
PMID: 21632913
PMC: 3806303.
DOI: 10.1177/1054773811409397.
Impact of presymptomatic genetic testing for familial amyotrophic lateral sclerosis.
Fanos J, Gronka S, Wuu J, Stanislaw C, Andersen P, Benatar M
Genet Med. 2011; 13(4):342-8.
PMID: 21285887
PMC: 4039017.
DOI: 10.1097/GIM.0b013e318204d004.
What were you thinking?: individuals at risk for Huntington Disease talk about having children.
Quaid K, Swenson M, Sims S, Harrison J, Moskowitz C, Stepanov N
J Genet Couns. 2010; 19(6):606-17.
PMID: 20734119
PMC: 3686108.
DOI: 10.1007/s10897-010-9312-2.
Potential stigma associated with inclusion of the psychosis risk syndrome in the DSM-V: an empirical question.
Yang L, Wonpat-Borja A, Opler M, Corcoran C
Schizophr Res. 2010; 120(1-3):42-8.
PMID: 20399610
PMC: 2921374.
DOI: 10.1016/j.schres.2010.03.012.
Experiences of teens living in the shadow of Huntington Disease.
Sparbel K, Driessnack M, Williams J, Schutte D, Tripp-Reimer T, McGonigal-Kenney M
J Genet Couns. 2008; 17(4):327-35.
PMID: 18347962
PMC: 2811873.
DOI: 10.1007/s10897-008-9151-6.