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Experience of carrier couples identified through a population‐based carrier screening pilot program for four founder autosomal recessive diseases in Saguenay–Lac‐Saint‐Jean

Prenatal diagnosis, 2018-01, Vol.38 (1), p.67-74

2018

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Secondary findings from next-generation sequencing: what does actionable in childhood really mean?

Genetics in medicine, 2019-01, Vol.21 (1), p.124-132

2019

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Paediatricians’ expectations and perspectives regarding genetic testing for children with developmental disorders

Acta Paediatrica, 2018-05, Vol.107 (5), p.838-844

2018

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Retrospective analysis of fetal vertebral defects: Associated anomalies, etiologies, and outcome

American journal of medical genetics. Part A, 2020-04, Vol.182 (4), p.664-672

2020

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Homozygous/compound heterozygote RYR1 gene variants: Expanding the clinical spectrum

American journal of medical genetics. Part A, 2019-03, Vol.179 (3), p.386-396

2019

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A qualitative study of women and partners from Lebanon and Quebec regarding an expanded scope of noninvasive prenatal testing

BMC pregnancy and childbirth, 2021-01, Vol.21 (1), p.54-54, Article 54

2021

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The value of non-invasive prenatal testing: preferences of Canadian pregnant women, their partners, and health professionals regarding NIPT use and access

BMC pregnancy and childbirth, 2019-01, Vol.19 (1), p.22-22, Article 22

2019

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From Community-Based Carrier Programs to Opportunistic Carrier Screening: How the Objective of Carrier Screening Was Lost in Translation

American journal of bioethics, 2023-07, Vol.23 (7), p.123-126

Laberge, Anne-Marie

2023

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Metabolically healthy obesity in children enrolled in the CANadian Pediatric Weight management Registry (CANPWR): An exploratory secondary analysis of baseline data

Clinical obesity, 2022-02, Vol.12 (1), p.e12490-n/a

2022

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Implementation challenges for an ethical introduction of noninvasive prenatal testing: a qualitative study of healthcare professionals' views from Lebanon and Quebec

BMC medical ethics, 2020-02, Vol.21 (1), p.15-15, Article 15

2020

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Fibrodysplasia ossificans progressiva: bilateral hallux valgus on ultrasound a clue for the first prenatal diagnosis for this condition-clinical report and review of the literature

Prenatal diagnosis, 2015-03, Vol.35 (3), p.305-307

2015

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Views of Canadian healthcare professionals on the future uses of non-invasive prenatal testing: a mixed method study

European journal of human genetics : EJHG, 2022-11, Vol.30 (11), p.1269-1275

2022

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Recommending inclusion of HFE C282Y homozygotes in the ACMG actionable gene list: cop-out or stealth move toward population screening?

Genetics in medicine, 2018-04, Vol.20 (4), p.400-402

Laberge, Anne-Marie

2018

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Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groups

Journal of inherited metabolic disease, 2016-01, Vol.39 (1), p.139-147

2016

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Screening Children for Familial Aortopathies: Tread With Caution

Canadian journal of cardiology, 2016, Vol.32 (1), p.60-65

2016

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The CANadian Pediatric Weight management Registry (CANPWR): lessons learned from developing and initiating a national, multi-centre study embedded in pediatric clinical practice

BMC pediatrics, 2018-07, Vol.18 (1), p.237-237, Article 237

2018

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The Need to Consider Context: A Systematic Review of Factors Involved in the Consent Process for Genetic Tests from the Perspective of Patients

AJOB empirical bioethics, 2024-01, Vol.15 (2), p.93-107

2024

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A systematic review of the assessment of the clinical utility of genomic sequencing: Implications of the lack of standard definitions and measures of clinical utility

European journal of medical genetics, 2024-04, Vol.68, p.104925-104925, Article 104925

2024

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Going Back to Basics: What is the Target of Prenatal Screening?

American journal of bioethics, 2023-03, Vol.23 (3), p.50-52

2023

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Genetic Testing in Thoracic Aortic Disease—When, Why, and How?

Canadian journal of cardiology, 2016-01, Vol.32 (1), p.131-134

2016

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Variants in LSM7 impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease

HGG advances, 2021-07, Vol.2 (3), p.100034-100034, Article 100034

2021

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Genetic burden linked to founder effects in Saguenay-Lac-Saint-Jean illustrates the importance of genetic screening test availability

Journal of medical genetics, 2021-10, Vol.58 (10), p.653

2021

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Diagnostic and Therapeutic Misconception: Parental Expectations and Perspectives Regarding Genetic Testing for Developmental Disorders

Journal of autism and developmental disorders, 2019-01, Vol.49 (1), p.363-375

2019

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The Serious Factor in Expanded Prenatal Genetic Testing

American journal of bioethics, 2022-02, Vol.22 (2), p.23-25

2022

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Experience of carrier couples identified through a population‐based carrier screening pilot program for four founder autosomal recessive diseases in Saguenay–Lac‐Saint‐Jean

Secondary findings from next-generation sequencing: what does actionable in childhood really mean?

The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists

Paediatricians’ expectations and perspectives regarding genetic testing for children with developmental disorders

Retrospective analysis of fetal vertebral defects: Associated anomalies, etiologies, and outcome

Homozygous/compound heterozygote RYR1 gene variants: Expanding the clinical spectrum

A qualitative study of women and partners from Lebanon and Quebec regarding an expanded scope of noninvasive prenatal testing

The value of non-invasive prenatal testing: preferences of Canadian pregnant women, their partners, and health professionals regarding NIPT use and access

From Community-Based Carrier Programs to Opportunistic Carrier Screening: How the Objective of Carrier Screening Was Lost in Translation

Metabolically healthy obesity in children enrolled in the CANadian Pediatric Weight management Registry (CANPWR): An exploratory secondary analysis of baseline data

Implementation challenges for an ethical introduction of noninvasive prenatal testing: a qualitative study of healthcare professionals' views from Lebanon and Quebec

Fibrodysplasia ossificans progressiva: bilateral hallux valgus on ultrasound a clue for the first prenatal diagnosis for this condition-clinical report and review of the literature

Views of Canadian healthcare professionals on the future uses of non-invasive prenatal testing: a mixed method study

Recommending inclusion of HFE C282Y homozygotes in the ACMG actionable gene list: cop-out or stealth move toward population screening?

Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groups

Screening Children for Familial Aortopathies: Tread With Caution

The CANadian Pediatric Weight management Registry (CANPWR): lessons learned from developing and initiating a national, multi-centre study embedded in pediatric clinical practice

The Need to Consider Context: A Systematic Review of Factors Involved in the Consent Process for Genetic Tests from the Perspective of Patients

A systematic review of the assessment of the clinical utility of genomic sequencing: Implications of the lack of standard definitions and measures of clinical utility

Going Back to Basics: What is the Target of Prenatal Screening?

Genetic Testing in Thoracic Aortic Disease—When, Why, and How?

Variants in LSM7 impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease

Genetic burden linked to founder effects in Saguenay-Lac-Saint-Jean illustrates the importance of genetic screening test availability

Diagnostic and Therapeutic Misconception: Parental Expectations and Perspectives Regarding Genetic Testing for Developmental Disorders

The Serious Factor in Expanded Prenatal Genetic Testing

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