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Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease

American journal of human genetics, 2019-06, Vol.104 (6), p.1116-1126

2019

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The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2018-04, Vol.177 (3), p.346-357

2018

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CAG size-specific risk estimates for intermediate allele repeat instability in Huntington disease

Journal of medical genetics, 2013-10, Vol.50 (10), p.696-703

2013

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Patient perspectives on the process and outcomes of psychiatric genetic counseling: An “Empowering Encounter”

Journal of genetic counseling, 2019-08, Vol.28 (4), p.856-868

2019

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Conceptualizing Genetic Counseling as Psychotherapy in the Era of Genomic Medicine

Journal of genetic counseling, 2014-12, Vol.23 (6), p.903-909

2014

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GENETIC COUNSELING AS A WAY TO ENGAGE PEOPLE IN BEHAVIOUR CHANGE TO REDUCE RISK FOR COMMON COMPLEX DISEASE: RATIONALE FOR ITS POTENTIAL EFFECTIVENESS WHERE GENETIC INFORMATION HAS FAILED

European neuropsychopharmacology, 2019, Vol.29, p.S1029-S1029

2019

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Reflections of parents of children with 22q11.2 Deletion Syndrome on the experience of receiving psychiatric genetic counseling: ‘Awareness to Act’

Journal of genetic counseling, 2022-02, Vol.31 (1), p.140-152

2022

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T37PSYCHIATRIC GENETIC COUNSELLING FOR PARENTS OF CHILDREN WITH 22Q11DS ACTIVATES AN “AWARENESS TO ACT”

European neuropsychopharmacology, 2019-10, Vol.29, p.S236-S237

2019

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Women’s experiences of participating in a prospective, longitudinal postpartum depression study: insights for perinatal mental health researchers

Archives of women's mental health, 2017-08, Vol.20 (4), p.547-559

2017

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CAG Expansion in the Huntington Disease Gene Is Associated with a Specific and Targetable Predisposing Haplogroup

American journal of human genetics, 2009-03, Vol.84 (3), p.351-366

2009

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Recommendations for the predictive genetic test in Huntington's disease

Clinical genetics, 2013-03, Vol.83 (3), p.221-231

2013

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High frequency of intermediate alleles on huntington disease-associated haplotypes in British Columbia's general population

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2013-12, Vol.162B (8), p.864-871

2013

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De novo Huntington disease caused by 26-44 CAG repeat expansion on a low-risk haplotype

Neurology, 2013-09, Vol.81 (12), p.1099

2013

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Huntington disease in the South African population occurs on diverse and ethnically distinct genetic haplotypes

European journal of human genetics : EJHG, 2013-10, Vol.21 (10), p.1120-1127

2013

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

Journal of genetic counseling, 2016-10, Vol.25 (5), p.912-922

2016

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A new mutation for Huntington disease following maternal transmission of an intermediate allele

European journal of medical genetics, 2015-01, Vol.58 (1), p.28-30

2015

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When They Hear What We Say: Ethical Challenges in Presenting Research Findings to the Huntington Disease Community

Journal of empirical research on human research ethics, 2011-09, Vol.6 (3), p.47-54

2011

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Re: Autopsy-proven Huntington's disease with 29 trinucleotide repeats

Movement disorders, 2008-09, Vol.23 (12), p.1794-1795

2008

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GAG Expansion in the Huntington Disease Gene Is Associated with a Specific and Targetable Predisposing Haplogroup

American journal of human genetics, 2009-03, Vol.84 (3), p.351

2009

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Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease

The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population

CAG size-specific risk estimates for intermediate allele repeat instability in Huntington disease

Patient perspectives on the process and outcomes of psychiatric genetic counseling: An “Empowering Encounter”

Conceptualizing Genetic Counseling as Psychotherapy in the Era of Genomic Medicine

GENETIC COUNSELING AS A WAY TO ENGAGE PEOPLE IN BEHAVIOUR CHANGE TO REDUCE RISK FOR COMMON COMPLEX DISEASE: RATIONALE FOR ITS POTENTIAL EFFECTIVENESS WHERE GENETIC INFORMATION HAS FAILED

Reflections of parents of children with 22q11.2 Deletion Syndrome on the experience of receiving psychiatric genetic counseling: ‘Awareness to Act’

T37PSYCHIATRIC GENETIC COUNSELLING FOR PARENTS OF CHILDREN WITH 22Q11DS ACTIVATES AN “AWARENESS TO ACT”

Women’s experiences of participating in a prospective, longitudinal postpartum depression study: insights for perinatal mental health researchers

CAG Expansion in the Huntington Disease Gene Is Associated with a Specific and Targetable Predisposing Haplogroup

Recommendations for the predictive genetic test in Huntington's disease

High frequency of intermediate alleles on huntington disease-associated haplotypes in British Columbia's general population

De novo Huntington disease caused by 26-44 CAG repeat expansion on a low-risk haplotype

Huntington disease in the South African population occurs on diverse and ethnically distinct genetic haplotypes

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

A new mutation for Huntington disease following maternal transmission of an intermediate allele

When They Hear What We Say: Ethical Challenges in Presenting Research Findings to the Huntington Disease Community

Re: Autopsy-proven Huntington's disease with 29 trinucleotide repeats

GAG Expansion in the Huntington Disease Gene Is Associated with a Specific and Targetable Predisposing Haplogroup

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