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Paternalism and the ACMG recommendations on genomic incidental findings: patients seen but not heard

Genetics in medicine, 2013-09, Vol.15 (9), p.751-752

2013

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Genetic counselling resources in non-english languages: A scoping review

PEC innovation, 2023-12, Vol.2, p.100135, Article 100135

2023

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Genetics professionals' perspectives on reporting incidental findings from clinical genome-wide sequencing

American journal of medical genetics. Part A, 2013-03, Vol.161A (3), p.542-549

2013

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Indigenous Peoples and genomics: Starting a conversation

Journal of genetic counseling, 2019-04, Vol.28 (2), p.407-418

2019

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Costs of caring for children with an intellectual developmental disorder

Disability and health journal, 2015-10, Vol.8 (4), p.646-651

2015

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A novel online genomic counseling and variant interpretation certificate: Learning design, learning analytics, and evaluation

Journal of genetic counseling, 2023-12, Vol.32 (6), p.1280-1287

2023

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Serial MRIs provide novel insight into natural history of optic pathway gliomas in patients with neurofibromatosis 1

Orphanet journal of rare diseases, 2018-04, Vol.13 (1), p.62-62, Article 62

2018

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Comparing the ability of OPTION12 and OPTION5 to assess shared decision-making in genetic counselling

Patient education and counseling, 2016-10, Vol.99 (10), p.1717-1723

2016

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Assessing an Interactive Online Tool to Support Parents' Genomic Testing Decisions

Journal of genetic counseling, 2019-02, Vol.28 (1), p.10-17

2019

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Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing

Journal of nursing scholarship, 2016-05, Vol.48 (3), p.265-275

2016

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A personalized genomic results e-booklet, co-designed and pilot-tested by families

PEC innovation, 2022-12, Vol.1, p.100039-100039, Article 100039

2022

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Comparing the ability of OPTION(12) and OPTION(5) to assess shared decision-making in genetic counselling

Patient education and counseling, 2016-10, Vol.99 (10), p.1717-1723

2016

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Assessing Shared Decision‐Making Clinical Behaviors Among Genetic Counsellors

Journal of genetic counseling, 2019-02, Vol.28 (1), p.40-49

2019

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Parental perceived value of a diagnosis for intellectual disability (ID): A qualitative comparison of families with and without a diagnosis for their child's ID

American journal of medical genetics. Part A, 2009-11, Vol.149A (11), p.2393-2402

2009

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Skeletal abnormalities in neurofibromatosis type 1: Approaches to therapeutic options

American journal of medical genetics. Part A, 2009-10, Vol.149A (10), p.2327-2338

2009

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The composition and capacity of the clinical genetics workforce in high-income countries: a scoping review

Genetics in medicine, 2020-09, Vol.22 (9), p.1437-1449

2020

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Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data

BMC bioinformatics, 2007-10, Vol.8 (1), p.368-368, Article 368

2007

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MIA is a potential biomarker for tumour load in neurofibromatosis type 1

BMC medicine, 2011-07, Vol.9 (1), p.82-82, Article 82

2011

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Genome-wide sequencing as a first-tier screening test for short tandem repeat expansions

Genome medicine, 2021-08, Vol.13 (1), p.126-126, Article 126

2021

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The stepwise process of integrating a genetic counsellor into primary care

European journal of human genetics : EJHG, 2022-07, Vol.30 (7), p.772-781

2022

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Experiences With Genetic Counseling, Testing, and Diagnosis Among Adolescents With a Genetic Condition: A Scoping Review

JAMA pediatrics, 2022-02, Vol.176 (2), p.185

2022

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The long‐term impact of receiving incidental findings on parents undergoing genome‐wide sequencing

Journal of genetic counseling, 2022-08, Vol.31 (4), p.887-900

2022

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Out‐of‐pocket and private pay in clinical genetic testing: A scoping review

Clinical genetics, 2021-11, Vol.100 (5), p.504-521

2021

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Development and pilot testing of a tool to calculate parental and societal costs of raising a child with intellectual disability

Journal of intellectual & developmental disability, 2016-01, Vol.41 (1), p.11-20

2016

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Paternalism and the ACMG recommendations on genomic incidental findings: patients seen but not heard

Genetic counselling resources in non-english languages: A scoping review

Genetics professionals' perspectives on reporting incidental findings from clinical genome-wide sequencing

Indigenous Peoples and genomics: Starting a conversation

Costs of caring for children with an intellectual developmental disorder

A novel online genomic counseling and variant interpretation certificate: Learning design, learning analytics, and evaluation

Serial MRIs provide novel insight into natural history of optic pathway gliomas in patients with neurofibromatosis 1

Comparing the ability of OPTION12 and OPTION5 to assess shared decision-making in genetic counselling

Assessing an Interactive Online Tool to Support Parents' Genomic Testing Decisions

Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing

A personalized genomic results e-booklet, co-designed and pilot-tested by families

Comparing the ability of OPTION(12) and OPTION(5) to assess shared decision-making in genetic counselling

Assessing Shared Decision‐Making Clinical Behaviors Among Genetic Counsellors

Parental perceived value of a diagnosis for intellectual disability (ID): A qualitative comparison of families with and without a diagnosis for their child's ID

Skeletal abnormalities in neurofibromatosis type 1: Approaches to therapeutic options

The composition and capacity of the clinical genetics workforce in high-income countries: a scoping review

Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data

MIA is a potential biomarker for tumour load in neurofibromatosis type 1

Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization

Genome-wide sequencing as a first-tier screening test for short tandem repeat expansions

The stepwise process of integrating a genetic counsellor into primary care

Experiences With Genetic Counseling, Testing, and Diagnosis Among Adolescents With a Genetic Condition: A Scoping Review

The long‐term impact of receiving incidental findings on parents undergoing genome‐wide sequencing

Out‐of‐pocket and private pay in clinical genetic testing: A scoping review

Development and pilot testing of a tool to calculate parental and societal costs of raising a child with intellectual disability

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