Detalhe da pesquisa
1.
Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease.
Am J Hum Genet
; 104(6): 1116-1126, 2019 06 06.
Artigo
Inglês
| MEDLINE | ID: mdl-31104771
2.
Reflections of parents of children with 22q11.2 Deletion Syndrome on the experience of receiving psychiatric genetic counseling: 'Awareness to Act'.
J Genet Couns
; 31(1): 140-152, 2022 02.
Artigo
Inglês
| MEDLINE | ID: mdl-34224608
3.
Patient perspectives on the process and outcomes of psychiatric genetic counseling: An "Empowering Encounter".
J Genet Couns
; 28(4): 856-868, 2019 08.
Artigo
Inglês
| MEDLINE | ID: mdl-31050075
4.
The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population.
Am J Med Genet B Neuropsychiatr Genet
; 177(3): 346-357, 2018 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29460498
5.
Women's experiences of participating in a prospective, longitudinal postpartum depression study: insights for perinatal mental health researchers.
Arch Womens Ment Health
; 20(4): 547-559, 2017 08.
Artigo
Inglês
| MEDLINE | ID: mdl-28600644
6.
Obsessive-Compulsive Disorder: The Process of Parental Adaptation and Implications for Genetic Counseling.
J Genet Couns
; 25(5): 912-22, 2016 10.
Artigo
Inglês
| MEDLINE | ID: mdl-26639756
7.
CAG size-specific risk estimates for intermediate allele repeat instability in Huntington disease.
J Med Genet
; 50(10): 696-703, 2013 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-23896435
8.
Conceptualizing genetic counseling as psychotherapy in the era of genomic medicine.
J Genet Couns
; 23(6): 903-9, 2014 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-24841456
9.
High frequency of intermediate alleles on Huntington disease-associated haplotypes in British Columbia's general population.
Am J Med Genet B Neuropsychiatr Genet
; 162B(8): 864-71, 2013 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-24038799
10.
CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup.
Am J Hum Genet
; 84(3): 351-66, 2009 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-19249009
11.
A new mutation for Huntington disease following maternal transmission of an intermediate allele.
Eur J Med Genet
; 58(1): 28-30, 2015 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-25464109
12.
Re: Autopsy-proven Huntington's disease with 29 trinucleotide repeats.
Mov Disord
; 23(12): 1794-5; author reply 1793, 2008 Sep 15.
Artigo
Inglês
| MEDLINE | ID: mdl-18548612
13.
Huntington disease in the South African population occurs on diverse and ethnically distinct genetic haplotypes.
Eur J Hum Genet
; 21(10): 1120-7, 2013 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-23463025
14.
When they hear what we say: ethical challenges in presenting research findings to the Huntington disease community.
J Empir Res Hum Res Ethics
; 6(3): 47-54, 2011 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-21931237
15.
De novo Huntington disease caused by 26-44 CAG repeat expansion on a low-risk haplotype.
Neurology
; 81(12): 1099-100, 2013 Sep 17.
Artigo
Inglês
| MEDLINE | ID: mdl-23946314